Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 163882 |
| ensemblid | ENSG00000162852.14 |
| hgncid | 26486 |
| symbol | CNST |
| name | consortin, connexin sorting protein |
| refseq_nuc | NM_152609.3 |
| refseq_prot | NP_689822.2 |
| ensembl_nuc | ENST00000366513.9 |
| ensembl_prot | ENSP00000355470.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 246566456 |
| end | 246668595 |
| strand | + |
| ver | v1.2 |
| region | chr1:246566456-246668595 |
| region5000 | chr1:246561456-246673595 |
| regionname0 | CNST_chr1_246566456_246668595 |
| regionname5000 | CNST_chr1_246561456_246673595 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 725 | 253 | 59 | 64 | 85 | 13 | 31 | 58 | CNST_chr1_246561456_246673595 | CNST | MDDSD others(720): Show |
chr1 | 246561456 | 246673595 |
| a0002 | 1/0 | 725 | 43 | 13 | 6 | 18 | 3 | 2 | 11 | CNST_chr1_246561456_246673595 | CNST | MDDSD others(720): Show |
chr1 | 246561456 | 246673595 |
| a0003 | 0/0 | 725 | 12 | 10 | 2 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | MDDSD others(720): Show |
chr1 | 246561456 | 246673595 |
| a0004 | 0/0 | 725 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | MDDSD others(720): Show |
chr1 | 246561456 | 246673595 |
| a0005 | 0/0 | 725 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | MDDSD others(720): Show |
chr1 | 246561456 | 246673595 |
| a0006 | 0/0 | 725 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | MDDSD others(720): Show |
chr1 | 246561456 | 246673595 |
| a0007 | 0/0 | 725 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | MDDSD others(720): Show |
chr1 | 246561456 | 246673595 |
| a0008 | 0/0 | 725 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | MDDSD others(720): Show |
chr1 | 246561456 | 246673595 |
| a0009 | 0/0 | 725 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | MDDSD others(720): Show |
chr1 | 246561456 | 246673595 |
| a0010 | 0/0 | 725 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | MDDSD others(720): Show |
chr1 | 246561456 | 246673595 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2175 | 250 | 58 | 64 | 83 | 13 | 31 | CNST_chr1_246561456_246673595 | CNST | ATGGA others(2170): Show |
chr1 | 246561456 | 246673595 | ||
| a0001c0006 | 0/0 | 2175 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | ATGGA others(2170): Show |
chr1 | 246561456 | 246673595 | ||
| a0001c0009 | 0/0 | 2175 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | ATGGA others(2170): Show |
chr1 | 246561456 | 246673595 | ||
| a0001c0012 | 0/0 | 2175 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | ATGGA others(2170): Show |
chr1 | 246561456 | 246673595 | ||
| a0002c0002 | 1/0 | 2175 | 43 | 13 | 6 | 18 | 3 | 2 | CNST_chr1_246561456_246673595 | CNST | ATGGA others(2170): Show |
chr1 | 246561456 | 246673595 | ||
| a0003c0003 | 0/0 | 2175 | 12 | 10 | 2 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | ATGGA others(2170): Show |
chr1 | 246561456 | 246673595 | ||
| a0004c0004 | 0/0 | 2175 | 6 | 6 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | ATGGA others(2170): Show |
chr1 | 246561456 | 246673595 | ||
| a0005c0010 | 0/0 | 2175 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | ATGGA others(2170): Show |
chr1 | 246561456 | 246673595 | ||
| a0006c0007 | 0/0 | 2175 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | ATGGA others(2170): Show |
chr1 | 246561456 | 246673595 | ||
| a0007c0005 | 0/0 | 2175 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | ATGGA others(2170): Show |
chr1 | 246561456 | 246673595 | ||
| a0008c0011 | 0/0 | 2175 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | ATGGA others(2170): Show |
chr1 | 246561456 | 246673595 | ||
| a0009c0013 | 0/0 | 2175 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | ATGGA others(2170): Show |
chr1 | 246561456 | 246673595 | ||
| a0010c0008 | 0/0 | 2175 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | ATGGA others(2170): Show |
chr1 | 246561456 | 246673595 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5127 | 89 | 19 | 21 | 34 | 7 | 8 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0001c0001t0002 | 0/1 | 5127 | 61 | 3 | 23 | 21 | 3 | 10 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0001c0001t0003 | 0/0 | 5127 | 47 | 2 | 13 | 19 | 3 | 10 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0001c0001t0004 | 0/0 | 5127 | 22 | 21 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0001c0001t0005 | 0/0 | 5127 | 5 | 4 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0001c0001t0007 | 0/0 | 5127 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0001c0001t0008 | 0/0 | 5127 | 3 | 3 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0001c0001t0009 | 0/0 | 5127 | 3 | 3 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0001c0001t0010 | 0/0 | 5127 | 3 | 0 | 0 | 3 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0001c0001t0011 | 0/0 | 5127 | 3 | 1 | 1 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0001c0001t0012 | 0/0 | 5127 | 2 | 0 | 2 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0001c0001t0013 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0001c0001t0014 | 0/0 | 5127 | 2 | 0 | 0 | 2 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0001c0001t0016 | 0/0 | 5127 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0001c0001t0017 | 0/0 | 5127 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0001c0001t0018 | 0/0 | 5127 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0001c0001t0019 | 0/0 | 5127 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0001c0001t0020 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0001c0001t0022 | 0/0 | 5127 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0001c0001t0024 | 0/0 | 5127 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0001c0001t0025 | 0/0 | 5127 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0001c0006t0001 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0001c0009t0001 | 0/0 | 5127 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0001c0012t0002 | 0/0 | 5127 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0002c0002t0001 | 0/0 | 5127 | 32 | 8 | 6 | 14 | 2 | 2 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0002c0002t0002 | 1/0 | 5127 | 4 | 0 | 0 | 2 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0002c0002t0006 | 0/0 | 5127 | 3 | 3 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0002c0002t0007 | 0/0 | 5127 | 2 | 0 | 0 | 2 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0002c0002t0013 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0002c0002t0015 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0003c0003t0001 | 0/0 | 5127 | 8 | 7 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0003c0003t0004 | 0/0 | 5127 | 4 | 3 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0004c0004t0003 | 0/0 | 5127 | 5 | 5 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0004c0004t0021 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0005c0010t0002 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0006c0007t0003 | 0/0 | 5127 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0007c0005t0023 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0008c0011t0015 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0009c0013t0001 | 0/0 | 5127 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| a0010c0008t0001 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | GCGGT others(5122): Show |
chr1 | 246561456 | 246673595 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0107 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0007g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0008g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0008g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0009g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0009g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0009g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0010g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0010g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0010g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0011g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0011g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0011g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0012g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0013g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0014g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0014g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0016g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0017g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0018g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0019g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0020g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0022g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0024g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0001t0025g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0006t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0009t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0001c0012t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0002g0179 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0007g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0013g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0002c0002t0015g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0003c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0003c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0003c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0003c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0003c0003t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0003c0003t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0003c0003t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0003c0003t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0003c0003t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0003c0003t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0003c0003t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0003c0003t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0004c0004t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0004c0004t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0004c0004t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0004c0004t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0004c0004t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0004c0004t0021g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0005c0010t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0006c0007t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0007c0005t0023g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0008c0011t0015g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0009c0013t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| a0010c0008t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | GBR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0103 | EUR | GBR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0058 | EUR | FIN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0262 | EUR | FIN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0198 | EUR | FIN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0304 | EUR | FIN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | CHS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | CHS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | CHS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00423 | hp2 | a0001 | c0001 | t0014 | g0163 | EAS | CHS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | CHS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00558 | hp2 | a0001 | c0001 | t0010 | g0224 | EAS | CHS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0124 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0274 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | CHS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | CHS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00733 | hp1 | a0003 | c0003 | t0001 | g0042 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0098 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0029 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01069 | hp2 | a0001 | c0001 | t0012 | g0001 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0250 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01071 | hp1 | a0001 | c0001 | t0012 | g0001 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0108 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0156 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0104 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0149 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0069 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0283 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01243 | hp1 | a0003 | c0003 | t0004 | g0037 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01243 | hp2 | a0001 | c0001 | t0016 | g0133 | AMR | PUR | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0067 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0049 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0050 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0269 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0201 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | IBS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0057 | EUR | IBS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | IBS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0280 | EUR | IBS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | IBS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | IBS | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01891 | hp2 | a0003 | c0003 | t0001 | g0041 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01934 | hp1 | a0001 | c0001 | t0011 | g0210 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0052 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0094 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01981 | hp1 | a0001 | c0001 | t0017 | g0010 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0072 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0068 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0116 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02080 | hp2 | a0001 | c0001 | t0010 | g0284 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02083 | hp1 | a0001 | c0001 | t0007 | g0065 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02129 | hp2 | a0001 | c0001 | t0010 | g0225 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0295 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0176 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0073 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0273 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02257 | hp2 | a0003 | c0003 | t0001 | g0043 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0148 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0155 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0053 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0071 | AMR | PEL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02451 | hp1 | a0003 | c0003 | t0001 | g0035 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02451 | hp2 | a0004 | c0004 | t0003 | g0190 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | KHV | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0105 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02615 | hp1 | a0002 | c0002 | t0006 | g0033 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02622 | hp1 | a0002 | c0002 | t0015 | g0166 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02622 | hp2 | a0002 | c0002 | t0006 | g0031 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02630 | hp2 | a0004 | c0004 | t0021 | g0150 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02647 | hp2 | a0001 | c0001 | t0008 | g0023 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0144 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0259 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0109 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02717 | hp1 | a0003 | c0003 | t0004 | g0160 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02723 | hp1 | a0003 | c0003 | t0001 | g0040 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0143 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02818 | hp2 | a0004 | c0004 | t0003 | g0117 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02896 | hp1 | a0003 | c0003 | t0004 | g0038 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02896 | hp2 | a0004 | c0004 | t0003 | g0182 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0134 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02897 | hp2 | a0004 | c0004 | t0003 | g0183 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0021 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02922 | hp2 | a0005 | c0010 | t0002 | g0030 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02965 | hp1 | a0001 | c0001 | t0013 | g0194 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02965 | hp2 | a0001 | c0001 | t0008 | g0174 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0012 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0315 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03017 | hp2 | a0006 | c0007 | t0003 | g0265 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0015 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03098 | hp1 | a0003 | c0003 | t0001 | g0039 | AFR | MSL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0152 | AFR | MSL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03130 | hp1 | a0003 | c0003 | t0001 | g0046 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03139 | hp1 | a0001 | c0001 | t0009 | g0014 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0200 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0128 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03209 | hp1 | a0001 | c0001 | t0020 | g0026 | AFR | MSL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03209 | hp2 | a0007 | c0005 | t0023 | g0045 | AFR | MSL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0120 | AFR | MSL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03225 | hp2 | a0002 | c0002 | t0013 | g0178 | AFR | MSL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03239 | hp2 | a0001 | c0001 | t0022 | g0087 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03486 | hp1 | a0008 | c0011 | t0015 | g0211 | AFR | MSL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03486 | hp2 | a0002 | c0002 | t0006 | g0032 | AFR | MSL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | ESN | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0153 | AFR | GWD | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0177 | AFR | MSL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03579 | hp2 | a0003 | c0003 | t0001 | g0034 | AFR | MSL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0236 | SAS | STU | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0218 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0257 | SAS | PJL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0079 | SAS | BEB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0271 | SAS | BEB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | BEB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0207 | SAS | STU | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0282 | SAS | STU | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | BEB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0279 | SAS | BEB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0256 | SAS | STU | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0248 | SAS | STU | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0204 | SAS | STU | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0314 | SAS | STU | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG04228 | hp1 | a0001 | c0001 | t0019 | g0106 | SAS | STU | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0086 | SAS | STU | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18522 | hp2 | a0003 | c0003 | t0004 | g0036 | AFR | YRI | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | CHB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18612 | hp2 | a0002 | c0002 | t0007 | g0140 | EAS | CHB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | CHB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | CHB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0022 | AFR | YRI | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0126 | AFR | YRI | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18943 | hp2 | a0001 | c0012 | t0002 | g0276 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18952 | hp1 | a0001 | c0009 | t0001 | g0189 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18960 | hp1 | a0001 | c0001 | t0025 | g0286 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18971 | hp1 | a0001 | c0001 | t0011 | g0220 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18979 | hp2 | a0002 | c0002 | t0007 | g0141 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19009 | hp1 | a0001 | c0001 | t0014 | g0162 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | LWK | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0100 | AFR | LWK | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0025 | AFR | LWK | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0131 | AFR | LWK | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19085 | hp2 | a0009 | c0013 | t0001 | g0136 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0203 | AFR | YRI | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ASW | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0290 | AFR | ASW | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0146 | EUR | TSI | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0121 | EUR | TSI | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0059 | EUR | TSI | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0161 | EUR | TSI | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0064 | SAS | GIH | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA20905 | hp2 | a0001 | c0001 | t0024 | g0270 | SAS | GIH | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0151 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0169 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02486 | hp2 | a0001 | c0006 | t0001 | g0011 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0145 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0157 | AFR | ACB | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | MSL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG03471 | hp2 | a0004 | c0004 | t0003 | g0191 | AFR | MSL | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0115 | AFR | USA | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | USA | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA18955 | hp2 | a0001 | c0001 | t0018 | g0254 | EAS | JPT | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0172 | AFR | USA | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA20300 | hp2 | a0001 | c0001 | t0011 | g0206 | AFR | USA | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA21309 | hp1 | a0010 | c0008 | t0001 | g0159 | AFR | LWK | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | LWK | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0107 | REF | REF | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0179 | REF | REF | CNST_chr1_246561456_246673595 | CNST | chr1 | 246561456 | 246673595 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:246591579 | C | G | 1 | a0009 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.17C>G | p.Thr6Ser | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/11 | 276/5127 | 17/2178 | 6/725 | chr1 | 246591579 | |||
| chr1:246591645 | G | A | 2 | a0003 a0007 |
13 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
missense_variant | MODERATE | c.83G>A | p.Ser28Asn | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/11 | 342/5127 | 83/2178 | 28/725 | chr1 | 246591645 | |||
| chr1:246591822 | T | C | 5 | a0001 a0004 a0005 others(2): Show |
261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
missense_variant | MODERATE | c.260T>C | p.Leu87Ser | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/11 | 519/5127 | 260/2178 | 87/725 | chr1 | 246591822 | |||
| chr1:246591902 | C | T | 1 | a0005 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.340C>T | p.Pro114Ser | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/11 | 599/5127 | 340/2178 | 114/725 | chr1 | 246591902 | |||
| chr1:246621597 | A | G | 1 | a0004 | 6 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
missense_variant | MODERATE | c.548A>G | p.Gln183Arg | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/11 | 807/5127 | 548/2178 | 183/725 | chr1 | 246621597 | |||
| chr1:246634514 | C | G | 1 | a0008 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.745C>G | p.Leu249Val | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/11 | 1004/5127 | 745/2178 | 249/725 | chr1 | 246634514 | |||
| chr1:246641963 | A | G | 1 | a0010 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.863A>G | p.Gln288Arg | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/11 | 1122/5127 | 863/2178 | 288/725 | chr1 | 246641963 | |||
| chr1:246647186 | A | C | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.985A>C | p.Thr329Pro | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/11 | 1244/5127 | 985/2178 | 329/725 | chr1 | 246647186 | |||
| chr1:246647396 | C | T | 1 | a0004 | 6 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
missense_variant | MODERATE | c.1195C>T | p.Arg399Cys | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/11 | 1454/5127 | 1195/2178 | 399/725 | chr1 | 246647396 | |||
| chr1:246660289 | A | C | 1 | a0006 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.1927A>C | p.Lys643Gln | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/11 | 2186/5127 | 1927/2178 | 643/725 | chr1 | 246660289 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:246591718 | C | T | 1 | a0001c0012 | 1 | NA18943.hp2 | synonymous_variant | LOW | c.156C>T | p.Thr52Thr | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/11 | 415/5127 | 156/2178 | 52/725 | chr1 | 246591718 | |||
| chr1:246633994 | C | T | 1 | a0001c0009 | 1 | NA18952.hp1 | synonymous_variant | LOW | c.687C>T | p.Ala229Ala | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 5/11 | 946/5127 | 687/2178 | 229/725 | chr1 | 246633994 | |||
| chr1:246647290 | G | A | 1 | a0001c0006 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.1089G>A | p.Leu363Leu | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/11 | 1348/5127 | 1089/2178 | 363/725 | chr1 | 246647290 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:246566584 | G | A | 1 | a0001c0001t0016 | 1 | HG01243.hp2 | 5_prime_UTR_variant | MODIFIER | c.-131G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/11 | 24979 | chr1 | 246566584 | ||||||
| chr1:246566590 | C | A | 2 | a0001c0001t0017 a0002c0002t0006 |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-125C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/11 | 24973 | chr1 | 246566590 | ||||||
| chr1:246666020 | G | A | 2 | a0001c0001t0007 a0002c0002t0007 |
3 | HG02083.hp1 NA18612.hp2 NA18979.hp2 |
3_prime_UTR_variant | MODIFIER | c.*115G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 115 | chr1 | 246666020 | ||||||
| chr1:246666168 | T | G | 1 | a0001c0001t0018 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*263T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 263 | chr1 | 246666168 | ||||||
| chr1:246666307 | A | G | 1 | a0001c0001t0025 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*402A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 402 | chr1 | 246666307 | ||||||
| chr1:246666314 | T | C | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(19): Show |
205 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*409T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 409 | chr1 | 246666314 | ||||||
| chr1:246666380 | T | A | 1 | a0001c0001t0008 | 3 | HG02647.hp2 HG02965.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*475T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 475 | chr1 | 246666380 | ||||||
| chr1:246666440 | T | C | 31 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(28): Show |
244 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*535T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 535 | chr1 | 246666440 | ||||||
| chr1:246666459 | A | G | 1 | a0001c0001t0009 | 3 | HG02976.hp1 HG03041.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*554A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 554 | chr1 | 246666459 | ||||||
| chr1:246666468 | C | T | 1 | a0001c0001t0011 | 3 | HG01934.hp1 NA18971.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*563C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 563 | chr1 | 246666468 | ||||||
| chr1:246666553 | T | C | 1 | a0001c0001t0012 | 2 | HG01069.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*648T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 648 | chr1 | 246666553 | ||||||
| chr1:246666571 | G | A | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(19): Show |
205 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*666G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 666 | chr1 | 246666571 | ||||||
| chr1:246666656 | A | T | 1 | a0001c0001t0008 | 3 | HG02647.hp2 HG02965.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*751A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 751 | chr1 | 246666656 | ||||||
| chr1:246666715 | C | T | 5 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0016 others(2): Show |
33 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*810C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 810 | chr1 | 246666715 | ||||||
| chr1:246666732 | G | C | 1 | a0001c0001t0019 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*827G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 827 | chr1 | 246666732 | ||||||
| chr1:246666991 | A | G | 31 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(28): Show |
244 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*1086A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 1086 | chr1 | 246666991 | ||||||
| chr1:246666999 | A | G | 1 | a0001c0001t0014 | 2 | HG00423.hp2 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1094A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 1094 | chr1 | 246666999 | ||||||
| chr1:246667186 | T | C | 31 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(28): Show |
244 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*1281T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 1281 | chr1 | 246667186 | ||||||
| chr1:246667325 | T | C | 3 | a0001c0001t0005 a0001c0001t0013 a0002c0002t0013 |
7 | HG01433.hp1 HG02965.hp1 HG03098.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1420T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 1420 | chr1 | 246667325 | ||||||
| chr1:246667422 | C | T | 2 | a0001c0001t0022 a0004c0004t0021 |
2 | HG02630.hp2 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1517C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 1517 | chr1 | 246667422 | ||||||
| chr1:246667725 | A | G | 1 | a0001c0001t0020 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1820A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 1820 | chr1 | 246667725 | ||||||
| chr1:246667751 | C | T | 1 | a0001c0001t0010 | 3 | HG00558.hp2 HG02080.hp2 HG02129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1846C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 1846 | chr1 | 246667751 | ||||||
| chr1:246667752 | A | G | 2 | a0001c0001t0013 a0002c0002t0013 |
2 | HG02965.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1847A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 1847 | chr1 | 246667752 | ||||||
| chr1:246667946 | C | T | 3 | a0001c0001t0008 a0002c0002t0015 a0008c0011t0015 |
5 | HG02622.hp1 HG02647.hp2 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2041C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 2041 | chr1 | 246667946 | ||||||
| chr1:246668054 | G | A | 6 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0014 others(3): Show |
58 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*2149G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 2149 | chr1 | 246668054 | ||||||
| chr1:246668060 | G | A | 1 | a0001c0001t0024 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2155G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 11/11 | 2155 | chr1 | 246668060 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:246566688 | A | G | 125 | a0001c0001t0001g0192 a0001c0001t0001g0195 a0001c0001t0001g0196 others(122): Show |
125 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.-52+25A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246566688 | |||||||
| chr1:246566777 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-52+114C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246566777 | |||||||
| chr1:246566788 | G | C | 288 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(285): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.-52+125G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246566788 | |||||||
| chr1:246566872 | C | G | 1 | a0001c0001t0001g0164 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-52+209C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246566872 | |||||||
| chr1:246566931 | C | A | 1 | a0001c0001t0003g0005 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-52+268C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246566931 | |||||||
| chr1:246567059 | T | G | 1 | a0001c0001t0004g0006 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-52+396T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246567059 | |||||||
| chr1:246567062 | C | T | 2 | a0001c0001t0014g0162 a0001c0001t0014g0163 |
2 | HG00423.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-52+399C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246567062 | |||||||
| chr1:246567090 | G | A | 5 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(2): Show |
5 | HG02486.hp1 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+427G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246567090 | |||||||
| chr1:246567165 | A | G | 2 | a0001c0001t0003g0314 a0001c0001t0003g0315 |
2 | HG03017.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-52+502A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246567165 | |||||||
| chr1:246567353 | C | CT | 132 | a0001c0001t0001g0154 a0001c0001t0001g0158 a0001c0001t0001g0202 others(129): Show |
132 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.-52+701dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246567353 | ||||||
| chr1:246567384 | A | G | 2 | a0001c0001t0001g0313 a0001c0001t0002g0312 |
2 | HG00673.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.-52+721A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246567384 | |||||||
| chr1:246567435 | C | G | 23 | a0001c0001t0001g0196 a0001c0001t0001g0291 a0001c0001t0001g0293 others(20): Show |
23 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(20): Show |
intron_variant | MODIFIER | c.-52+772C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246567435 | |||||||
| chr1:246567435 | C | T | 50 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0130 others(47): Show |
52 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.-52+772C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246567435 | |||||||
| chr1:246567591 | C | T | 1 | a0001c0001t0003g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-52+928C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246567591 | |||||||
| chr1:246567614 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0002g0099 |
3 | HG00642.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-52+951C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246567614 | |||||||
| chr1:246567782 | C | T | 1 | a0002c0002t0001g0147 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-52+1119C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246567782 | |||||||
| chr1:246567788 | GAC | G | 4 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(1): Show |
4 | HG02622.hp1 HG02809.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+1127_-52+1128d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246567788 | ||||||
| chr1:246567807 | CTT | C | 5 | a0001c0001t0001g0291 a0001c0001t0001g0293 a0001c0001t0001g0294 others(2): Show |
5 | HG00621.hp1 HG02135.hp1 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.-52+1146_-52+1147d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246567807 | ||||||
| chr1:246568001 | T | A | 135 | a0001c0001t0001g0154 a0001c0001t0001g0158 a0001c0001t0001g0192 others(132): Show |
135 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.-52+1338T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246568001 | |||||||
| chr1:246568039 | G | A | 1 | a0001c0001t0001g0296 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-52+1376G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246568039 | |||||||
| chr1:246568202 | A | G | 1 | a0001c0001t0003g0098 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-52+1539A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246568202 | |||||||
| chr1:246568520 | G | T | 1 | a0001c0001t0001g0289 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-52+1857G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246568520 | |||||||
| chr1:246568624 | C | T | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-52+1961C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246568624 | |||||||
| chr1:246568625 | G | A | 1 | a0001c0001t0004g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-52+1962G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246568625 | |||||||
| chr1:246568668 | C | T | 13 | a0001c0001t0001g0309 a0001c0001t0002g0184 a0001c0001t0002g0185 others(10): Show |
13 | HG00423.hp1 HG02451.hp2 HG02896.hp2 others(10): Show |
intron_variant | MODIFIER | c.-52+2005C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246568668 | |||||||
| chr1:246568947 | T | C | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-52+2284T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246568947 | |||||||
| chr1:246569022 | C | T | 1 | a0001c0001t0025g0286 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-52+2359C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246569022 | |||||||
| chr1:246569156 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-52+2493A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246569156 | |||||||
| chr1:246569175 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-52+2512C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246569175 | |||||||
| chr1:246569208 | G | A | 139 | a0001c0001t0001g0154 a0001c0001t0001g0158 a0001c0001t0001g0192 others(136): Show |
139 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.-52+2545G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246569208 | |||||||
| chr1:246569511 | C | T | 43 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0130 others(40): Show |
44 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.-52+2848C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246569511 | |||||||
| chr1:246569645 | G | A | 8 | a0001c0001t0002g0003 a0001c0001t0002g0101 a0001c0001t0002g0102 others(5): Show |
9 | HG00140.hp2 HG00733.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.-52+2982G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246569645 | |||||||
| chr1:246569755 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-52+3092C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246569755 | |||||||
| chr1:246569776 | A | C | 4 | a0001c0001t0002g0170 a0001c0001t0002g0173 a0001c0001t0004g0171 others(1): Show |
4 | HG01884.hp2 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+3113A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246569776 | |||||||
| chr1:246570069 | A | G | 13 | a0001c0001t0001g0309 a0001c0001t0002g0184 a0001c0001t0002g0185 others(10): Show |
13 | HG00423.hp1 HG02451.hp2 HG02896.hp2 others(10): Show |
intron_variant | MODIFIER | c.-52+3406A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246570069 | |||||||
| chr1:246570177 | A | G | 1 | a0001c0001t0003g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-52+3514A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246570177 | |||||||
| chr1:246570266 | C | T | 1 | a0004c0004t0003g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-52+3603C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246570266 | |||||||
| chr1:246570568 | A | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(71): Show |
76 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.-52+3905A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246570568 | |||||||
| chr1:246570674 | G | T | 87 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(84): Show |
89 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.-52+4011G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246570674 | |||||||
| chr1:246570679 | A | G | 87 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(84): Show |
89 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.-52+4016A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246570679 | |||||||
| chr1:246570680 | T | TGA | 87 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(84): Show |
89 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.-52+4017_-52+4018i others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246570680 | |||||||
| chr1:246570681 | A | G | 87 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(84): Show |
89 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.-52+4018A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246570681 | |||||||
| chr1:246570697 | T | A | 1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-52+4034T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246570697 | |||||||
| chr1:246570795 | A | C | 4 | a0001c0001t0002g0170 a0001c0001t0002g0173 a0001c0001t0004g0171 others(1): Show |
4 | HG01884.hp2 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+4132A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246570795 | |||||||
| chr1:246570897 | C | T | 2 | a0002c0002t0001g0145 a0002c0002t0001g0146 |
2 | HG02559.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-52+4234C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246570897 | |||||||
| chr1:246571185 | C | T | 135 | a0001c0001t0001g0154 a0001c0001t0001g0158 a0001c0001t0001g0192 others(132): Show |
135 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.-52+4522C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246571185 | |||||||
| chr1:246571350 | A | G | 8 | a0001c0001t0002g0003 a0001c0001t0002g0101 a0001c0001t0002g0102 others(5): Show |
9 | HG00140.hp2 HG00733.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.-52+4687A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246571350 | |||||||
| chr1:246571452 | A | G | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+4789A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246571452 | |||||||
| chr1:246571685 | ATTTACTT others(9): Show |
A | 1 | a0001c0001t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-52+5023_-52+5038d others(18): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246571685 | |||||||
| chr1:246572093 | C | T | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-52+5430C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246572093 | |||||||
| chr1:246572162 | G | A | 1 | a0001c0001t0002g0199 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-52+5499G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246572162 | |||||||
| chr1:246572224 | G | T | 7 | a0001c0001t0004g0044 a0003c0003t0001g0040 a0003c0003t0001g0041 others(4): Show |
7 | HG00733.hp1 HG01891.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-52+5561G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246572224 | |||||||
| chr1:246572251 | A | G | 1 | a0005c0010t0002g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-52+5588A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246572251 | |||||||
| chr1:246572262 | A | G | 1 | a0001c0001t0003g0094 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-52+5599A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246572262 | |||||||
| chr1:246572532 | T | TTAAA | 305 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(302): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-52+5871_-52+5872i others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246572532 | ||||||
| chr1:246572601 | T | C | 51 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(48): Show |
53 | HG00280.hp1 HG00423.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.-52+5938T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246572601 | |||||||
| chr1:246572631 | G | A | 1 | a0001c0006t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-52+5968G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246572631 | |||||||
| chr1:246572722 | T | A | 1 | a0001c0001t0009g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-52+6059T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246572722 | |||||||
| chr1:246572831 | G | A | 2 | a0001c0001t0001g0013 a0005c0010t0002g0030 |
2 | HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-52+6168G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246572831 | |||||||
| chr1:246572917 | T | C | 12 | a0001c0001t0004g0044 a0003c0003t0001g0034 a0003c0003t0001g0035 others(9): Show |
12 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-52+6254T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246572917 | |||||||
| chr1:246572968 | C | T | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+6305C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246572968 | |||||||
| chr1:246573018 | G | T | 2 | a0001c0001t0001g0002 a0001c0001t0002g0099 |
3 | HG00642.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-52+6355G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246573018 | |||||||
| chr1:246573025 | C | T | 13 | a0001c0001t0004g0044 a0003c0003t0001g0034 a0003c0003t0001g0035 others(10): Show |
13 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-52+6362C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246573025 | |||||||
| chr1:246573113 | C | A | 3 | a0001c0001t0003g0109 a0002c0002t0001g0108 a0002c0002t0001g0198 |
3 | HG00323.hp1 HG01074.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.-52+6450C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246573113 | |||||||
| chr1:246573270 | A | G | 1 | a0001c0001t0004g0006 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-52+6607A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246573270 | |||||||
| chr1:246573280 | C | T | 2 | a0001c0001t0001g0013 a0005c0010t0002g0030 |
2 | HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-52+6617C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246573280 | |||||||
| chr1:246573521 | T | G | 1 | a0001c0001t0001g0192 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-52+6858T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246573521 | |||||||
| chr1:246573624 | G | A | 303 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(300): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.-52+6961G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246573624 | |||||||
| chr1:246573687 | T | C | 1 | a0001c0001t0004g0006 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-52+7024T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246573687 | |||||||
| chr1:246573784 | C | T | 4 | a0002c0002t0001g0143 a0002c0002t0001g0144 a0002c0002t0001g0145 others(1): Show |
4 | HG02559.hp1 HG02683.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+7121C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246573784 | |||||||
| chr1:246573785 | G | A | 4 | a0001c0001t0001g0202 a0001c0001t0005g0200 a0001c0001t0005g0201 others(1): Show |
4 | HG01261.hp1 HG01433.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+7122G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246573785 | |||||||
| chr1:246573861 | G | GA | 51 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(48): Show |
53 | HG00280.hp1 HG00423.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.-52+7204dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246573861 | ||||||
| chr1:246573992 | C | T | 2 | a0001c0001t0001g0013 a0005c0010t0002g0030 |
2 | HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-52+7329C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246573992 | |||||||
| chr1:246574047 | T | C | 1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-52+7384T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574047 | |||||||
| chr1:246574171 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-52+7508G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574171 | |||||||
| chr1:246574185 | G | A | 1 | a0002c0002t0001g0110 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-52+7522G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574185 | |||||||
| chr1:246574235 | A | C | 1 | a0002c0002t0001g0110 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-52+7572A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574235 | |||||||
| chr1:246574275 | T | C | 13 | a0001c0001t0004g0044 a0003c0003t0001g0034 a0003c0003t0001g0035 others(10): Show |
13 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-52+7612T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574275 | |||||||
| chr1:246574331 | G | A | 2 | a0001c0001t0001g0313 a0001c0001t0002g0312 |
2 | HG00673.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.-52+7668G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574331 | |||||||
| chr1:246574434 | A | T | 1 | a0001c0001t0010g0284 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-52+7771A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574434 | |||||||
| chr1:246574438 | T | G | 1 | a0001c0001t0003g0204 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-52+7775T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574438 | |||||||
| chr1:246574445 | A | G | 1 | a0001c0001t0002g0283 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-52+7782A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574445 | |||||||
| chr1:246574530 | A | G | 1 | a0001c0001t0002g0085 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-52+7867A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574530 | |||||||
| chr1:246574530 | A | T | 1 | a0001c0006t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-52+7867A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574530 | |||||||
| chr1:246574808 | GTCCT | G | 6 | a0001c0001t0002g0099 a0001c0001t0002g0101 a0001c0001t0002g0102 others(3): Show |
6 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52+8150_-52+8153d others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246574808 | ||||||
| chr1:246574827 | T | C | 13 | a0001c0001t0001g0309 a0001c0001t0002g0184 a0001c0001t0002g0185 others(10): Show |
13 | HG00423.hp1 HG02451.hp2 HG02896.hp2 others(10): Show |
intron_variant | MODIFIER | c.-52+8164T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574827 | |||||||
| chr1:246574839 | T | C | 6 | a0002c0002t0001g0004 a0002c0002t0001g0111 a0002c0002t0001g0113 others(3): Show |
7 | HG02040.hp1 HG02074.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.-52+8176T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574839 | |||||||
| chr1:246574842 | C | T | 311 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(308): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.-52+8179C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574842 | |||||||
| chr1:246574908 | A | G | 2 | a0001c0001t0003g0083 a0001c0001t0003g0084 |
2 | NA18943.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-52+8245A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574908 | |||||||
| chr1:246574938 | C | G | 8 | a0001c0001t0003g0142 a0002c0002t0001g0110 a0002c0002t0001g0137 others(5): Show |
8 | HG02129.hp1 NA18612.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.-52+8275C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246574938 | |||||||
| chr1:246574972 | T | TTTTA | 61 | a0001c0001t0001g0078 a0001c0001t0001g0091 a0001c0001t0001g0092 others(58): Show |
61 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.-52+8345_-52+8348d others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246574972 | ||||||
| chr1:246574972 | T | TTTTATTT others(1): Show |
129 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(126): Show |
132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.-52+8341_-52+8348d others(10): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246574972 | ||||||
| chr1:246574972 | T | TTTTATTT others(5): Show |
90 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0214 others(87): Show |
91 | HG00558.hp1 HG00558.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.-52+8337_-52+8348d others(14): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246574972 | ||||||
| chr1:246574972 | T | TTTTATTT others(9): Show |
2 | a0001c0001t0001g0205 a0001c0001t0011g0206 |
2 | HG02040.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-52+8333_-52+8348d others(18): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246574972 | ||||||
| chr1:246574972 | TTTTA | T | 14 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0175 others(11): Show |
14 | HG00735.hp1 HG00741.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-52+8345_-52+8348d others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246574972 | ||||||
| chr1:246574972 | TTTTATTT others(1): Show |
T | 4 | a0001c0001t0004g0006 a0003c0003t0004g0036 a0003c0003t0004g0037 others(1): Show |
4 | HG01243.hp1 HG02896.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+8341_-52+8348d others(10): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246574972 | ||||||
| chr1:246574972 | TTTTATTT others(5): Show |
T | 1 | a0001c0001t0010g0284 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-52+8337_-52+8348d others(14): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246574972 | ||||||
| chr1:246574976 | A | ATTTATTT others(5): Show |
1 | a0001c0001t0002g0082 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-52+8324_-52+8325i others(14): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246574976 | ||||||
| chr1:246575057 | A | G | 43 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0130 others(40): Show |
44 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.-52+8394A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246575057 | |||||||
| chr1:246575376 | C | A | 1 | a0005c0010t0002g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-52+8713C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246575376 | |||||||
| chr1:246575411 | A | C | 1 | a0001c0001t0001g0175 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-52+8748A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246575411 | |||||||
| chr1:246575432 | G | C | 2 | a0001c0001t0001g0013 a0005c0010t0002g0030 |
2 | HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-52+8769G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246575432 | |||||||
| chr1:246575624 | A | G | 1 | a0001c0001t0004g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-52+8961A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246575624 | |||||||
| chr1:246575631 | C | T | 1 | a0004c0004t0003g0117 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-52+8968C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246575631 | |||||||
| chr1:246575739 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-52+9076C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246575739 | |||||||
| chr1:246575785 | A | G | 1 | a0001c0001t0004g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-52+9122A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246575785 | |||||||
| chr1:246575853 | A | C | 4 | a0001c0001t0001g0164 a0001c0001t0009g0012 a0001c0001t0009g0014 others(1): Show |
4 | HG02976.hp1 HG03041.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+9190A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246575853 | |||||||
| chr1:246575876 | T | C | 16 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0175 others(13): Show |
16 | HG00735.hp1 HG00741.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-52+9213T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246575876 | |||||||
| chr1:246575881 | T | C | 1 | a0001c0001t0002g0207 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-52+9218T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246575881 | |||||||
| chr1:246575903 | T | C | 13 | a0001c0001t0001g0309 a0001c0001t0002g0184 a0001c0001t0002g0185 others(10): Show |
13 | HG00423.hp1 HG02451.hp2 HG02896.hp2 others(10): Show |
intron_variant | MODIFIER | c.-52+9240T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246575903 | |||||||
| chr1:246575973 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-52+9310G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246575973 | |||||||
| chr1:246576007 | A | G | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9344A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576007 | |||||||
| chr1:246576010 | A | G | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9347A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576010 | |||||||
| chr1:246576016 | CTT | C | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9354_-52+9355d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576016 | |||||||
| chr1:246576029 | A | G | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9366A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576029 | |||||||
| chr1:246576030 | T | A | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9367T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576030 | |||||||
| chr1:246576033 | A | G | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9370A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576033 | |||||||
| chr1:246576040 | G | T | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9377G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576040 | |||||||
| chr1:246576042 | C | G | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9379C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576042 | |||||||
| chr1:246576047 | C | T | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9384C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576047 | |||||||
| chr1:246576052 | T | C | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9389T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576052 | |||||||
| chr1:246576062 | G | C | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9399G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576062 | |||||||
| chr1:246576063 | T | C | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9400T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576063 | |||||||
| chr1:246576067 | C | T | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9404C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576067 | |||||||
| chr1:246576079 | G | A | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9416G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576079 | |||||||
| chr1:246576080 | C | CA | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9422dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576080 | ||||||
| chr1:246576091 | C | T | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9428C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576091 | |||||||
| chr1:246576092 | A | G | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9429A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576092 | |||||||
| chr1:246576096 | A | G | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9433A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576096 | |||||||
| chr1:246576098 | G | A | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9435G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576098 | |||||||
| chr1:246576113 | T | C | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9450T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576113 | |||||||
| chr1:246576115 | A | G | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9452A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576115 | |||||||
| chr1:246576122 | A | C | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9459A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576122 | |||||||
| chr1:246576128 | T | G | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9465T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576128 | |||||||
| chr1:246576149 | T | G | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9486T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576149 | |||||||
| chr1:246576151 | G | C | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9488G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576151 | |||||||
| chr1:246576152 | T | G | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9489T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576152 | |||||||
| chr1:246576166 | T | C | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9503T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576166 | |||||||
| chr1:246576183 | C | T | 1 | a0001c0001t0011g0206 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-52+9520C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576183 | |||||||
| chr1:246576186 | A | G | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9523A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576186 | |||||||
| chr1:246576187 | A | G | 1 | a0001c0001t0002g0256 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-52+9524A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576187 | |||||||
| chr1:246576189 | G | C | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9526G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576189 | |||||||
| chr1:246576190 | G | C | 4 | a0001c0001t0017g0010 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9527G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576190 | |||||||
| chr1:246576190 | G | GCGCCACC others(412): Show |
1 | a0001c0001t0011g0206 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-52+9532_-52+9533i others(421): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576190 | ||||||
| chr1:246576190 | G | GCGCCACC others(410): Show |
1 | a0001c0001t0014g0162 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-52+9532_-52+9533i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576190 | ||||||
| chr1:246576195 | A | ACCGCACT others(411): Show |
1 | a0001c0001t0001g0195 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-52+9532_-52+9533i others(420): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576195 | |||||||
| chr1:246576195 | A | ACCGCACT others(410): Show |
2 | a0001c0001t0003g0075 a0001c0001t0003g0076 |
2 | HG02071.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.-52+9532_-52+9533i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576195 | |||||||
| chr1:246576195 | A | ACCGCACT others(410): Show |
1 | a0001c0001t0003g0053 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-52+9532_-52+9533i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576195 | |||||||
| chr1:246576195 | A | ACCGCACT others(412): Show |
1 | a0001c0001t0003g0083 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-52+9532_-52+9533i others(421): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576195 | |||||||
| chr1:246576195 | A | ACCGCACT others(411): Show |
3 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0003g0084 |
3 | HG00738.hp1 HG01978.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.-52+9532_-52+9533i others(420): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576195 | |||||||
| chr1:246576195 | A | ACCGCACT others(409): Show |
4 | a0001c0001t0001g0078 a0001c0001t0002g0181 a0001c0001t0003g0056 others(1): Show |
4 | HG01891.hp1 HG01934.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+9532_-52+9533i others(418): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576195 | |||||||
| chr1:246576195 | A | ACCGCACT others(410): Show |
1 | a0001c0001t0003g0057 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-52+9532_-52+9533i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576195 | |||||||
| chr1:246576195 | A | ACCGCACT others(410): Show |
22 | a0001c0001t0001g0002 a0001c0001t0001g0060 a0001c0001t0001g0061 others(19): Show |
24 | HG00280.hp1 HG00423.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.-52+9532_-52+9533i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576195 | |||||||
| chr1:246576195 | A | ACCGCACT others(410): Show |
1 | a0001c0001t0002g0082 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-52+9532_-52+9533i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576195 | |||||||
| chr1:246576195 | A | ACCGCACT others(410): Show |
1 | a0001c0001t0002g0080 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-52+9532_-52+9533i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576195 | |||||||
| chr1:246576195 | A | ACCGCACT others(409): Show |
8 | a0001c0001t0002g0070 a0001c0001t0003g0052 a0001c0001t0003g0068 others(5): Show |
8 | HG01192.hp1 HG01943.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.-52+9532_-52+9533i others(418): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576195 | |||||||
| chr1:246576195 | A | ACCGCACT others(410): Show |
2 | a0001c0001t0002g0074 a0001c0001t0003g0081 |
2 | HG01099.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.-52+9532_-52+9533i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576195 | |||||||
| chr1:246576196 | T | C | 53 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(50): Show |
55 | HG00280.hp1 HG00423.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.-52+9533T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576196 | |||||||
| chr1:246576196 | T | TTGCACTC others(411): Show |
1 | a0003c0003t0001g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(420): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576196 | ||||||
| chr1:246576196 | T | TTGCACTC others(411): Show |
1 | a0003c0003t0001g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(420): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576196 | ||||||
| chr1:246576196 | T | TTGCACTC others(412): Show |
1 | a0008c0011t0015g0211 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(421): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576196 | ||||||
| chr1:246576196 | T | TTGCACTC others(411): Show |
1 | a0001c0001t0003g0257 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(420): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576196 | ||||||
| chr1:246576196 | T | TTGCACTC others(410): Show |
3 | a0001c0001t0004g0044 a0003c0003t0001g0042 a0003c0003t0001g0043 |
3 | HG00733.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576196 | ||||||
| chr1:246576196 | T | TTGCACTC others(410): Show |
4 | a0003c0003t0001g0035 a0003c0003t0004g0036 a0003c0003t0004g0037 others(1): Show |
4 | HG01243.hp1 HG02451.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576196 | ||||||
| chr1:246576196 | T | TTGCACTC others(411): Show |
1 | a0003c0003t0001g0040 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(420): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576196 | ||||||
| chr1:246576196 | T | TTGCACTC others(411): Show |
1 | a0001c0001t0003g0218 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(420): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576196 | ||||||
| chr1:246576196 | T | TTGCACTC others(409): Show |
1 | a0003c0003t0004g0038 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(418): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576196 | ||||||
| chr1:246576196 | T | TTGCACTC others(410): Show |
1 | a0004c0004t0003g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576196 | ||||||
| chr1:246576196 | T | TTGCACTC others(412): Show |
1 | a0001c0001t0001g0164 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(421): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576196 | ||||||
| chr1:246576196 | T | TTGCACTC others(410): Show |
1 | a0004c0004t0003g0190 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576196 | ||||||
| chr1:246576196 | T | TTGCACTC others(410): Show |
1 | a0003c0003t0001g0039 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576196 | ||||||
| chr1:246576200 | A | ACTCAAGC others(415): Show |
1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-52+9540_-52+9541i others(424): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(417): Show |
1 | a0001c0001t0002g0099 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(426): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(413): Show |
2 | a0001c0001t0001g0154 a0002c0002t0001g0149 |
2 | HG01175.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(422): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(414): Show |
1 | a0001c0001t0019g0106 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(423): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(415): Show |
5 | a0001c0001t0002g0003 a0001c0001t0002g0101 a0001c0001t0002g0102 others(2): Show |
6 | HG00140.hp2 HG00733.hp2 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(424): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(416): Show |
1 | a0001c0001t0002g0105 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(425): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(412): Show |
11 | a0001c0001t0001g0208 a0001c0001t0001g0313 a0001c0001t0002g0312 others(8): Show |
11 | HG00673.hp2 HG01934.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(421): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(412): Show |
4 | a0001c0001t0001g0158 a0001c0001t0004g0155 a0001c0001t0004g0156 others(1): Show |
4 | HG01109.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(421): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(413): Show |
1 | a0001c0001t0002g0212 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(422): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(413): Show |
6 | a0001c0001t0001g0213 a0001c0001t0001g0287 a0001c0001t0001g0297 others(3): Show |
6 | HG01175.hp1 HG02145.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(422): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(412): Show |
1 | a0001c0001t0002g0184 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(421): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(410): Show |
6 | a0001c0001t0001g0291 a0001c0001t0004g0018 a0001c0001t0004g0019 others(3): Show |
6 | HG02630.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(411): Show |
9 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0216 others(6): Show |
9 | HG00558.hp1 HG00673.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(420): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(411): Show |
82 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0175 others(79): Show |
82 | HG00280.hp2 HG00558.hp2 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(420): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(412): Show |
2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | NA18969.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(421): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(412): Show |
18 | a0001c0001t0001g0196 a0001c0001t0001g0253 a0001c0001t0001g0272 others(15): Show |
18 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(15): Show |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(421): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(411): Show |
1 | a0001c0001t0004g0273 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(420): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(411): Show |
2 | a0001c0001t0003g0204 a0001c0001t0013g0194 |
2 | HG02965.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(420): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(411): Show |
1 | a0001c0001t0002g0274 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(420): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(412): Show |
1 | a0001c0001t0003g0280 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(421): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(411): Show |
1 | a0001c0001t0002g0283 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(420): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(409): Show |
1 | a0001c0001t0002g0185 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(418): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(410): Show |
2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(410): Show |
3 | a0001c0001t0001g0275 a0001c0001t0001g0281 a0001c0001t0002g0170 |
3 | HG02886.hp2 HG03491.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(411): Show |
3 | a0001c0001t0004g0171 a0001c0001t0004g0172 a0001c0001t0009g0012 |
3 | HG01884.hp2 HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(420): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(412): Show |
2 | a0001c0001t0002g0173 a0001c0001t0009g0015 |
2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(421): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(413): Show |
1 | a0001c0001t0009g0014 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(422): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(410): Show |
2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(410): Show |
4 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0093 others(1): Show |
4 | HG01261.hp2 HG01433.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(410): Show |
2 | a0004c0004t0003g0182 a0004c0004t0003g0183 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(410): Show |
6 | a0001c0001t0001g0309 a0001c0001t0002g0186 a0001c0001t0002g0187 others(3): Show |
6 | NA18950.hp2 NA18952.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(419): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(408): Show |
34 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0002g0127 others(31): Show |
35 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(417): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(408): Show |
3 | a0001c0001t0001g0132 a0001c0001t0004g0134 a0001c0001t0016g0133 |
3 | HG01243.hp2 HG02897.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(417): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(409): Show |
4 | a0001c0001t0001g0255 a0001c0001t0003g0135 a0002c0002t0001g0137 others(1): Show |
4 | HG01884.hp1 NA18960.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(418): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(409): Show |
1 | a0001c0001t0001g0090 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(418): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(409): Show |
1 | a0001c0001t0002g0311 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(418): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(412): Show |
1 | a0001c0001t0001g0013 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(421): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(413): Show |
1 | a0005c0010t0002g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(422): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(407): Show |
1 | a0001c0001t0002g0129 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-52+9549_-52+9550i others(416): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | ACTCCAGC others(407): Show |
2 | a0001c0001t0001g0130 a0002c0002t0001g0139 |
2 | HG02735.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.-52+9549_-52+9550i others(416): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576200 | ||||||
| chr1:246576200 | A | G | 53 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(50): Show |
55 | HG00280.hp1 HG00423.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.-52+9537A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576200 | |||||||
| chr1:246576213 | C | A | 2 | a0001c0001t0003g0218 a0001c0001t0003g0257 |
2 | HG03704.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-52+9550C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576213 | |||||||
| chr1:246576213 | C | T | 56 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(53): Show |
58 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.-52+9550C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576213 | |||||||
| chr1:246576214 | G | T | 2 | a0004c0004t0003g0190 a0004c0004t0003g0191 |
2 | HG02451.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-52+9551G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576214 | |||||||
| chr1:246576219 | A | G | 6 | a0001c0001t0004g0148 a0001c0001t0004g0151 a0001c0001t0004g0153 others(3): Show |
6 | HG01175.hp2 HG02109.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52+9556A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576219 | |||||||
| chr1:246576222 | C | G | 21 | a0001c0001t0002g0170 a0001c0001t0003g0295 a0001c0001t0004g0044 others(18): Show |
21 | HG00733.hp1 HG01175.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.-52+9559C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576222 | |||||||
| chr1:246576229 | C | T | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+9566C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576229 | |||||||
| chr1:246576234 | C | A | 1 | a0003c0003t0004g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-52+9571C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576234 | |||||||
| chr1:246576234 | C | CA | 172 | a0001c0001t0001g0013 a0001c0001t0001g0119 a0001c0001t0001g0125 others(169): Show |
174 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.-52+9590dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576234 | ||||||
| chr1:246576234 | C | CAA | 49 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0132 others(46): Show |
49 | HG00642.hp1 HG00733.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.-52+9589_-52+9590d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576234 | ||||||
| chr1:246576234 | C | CAAA | 71 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(68): Show |
73 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.-52+9588_-52+9590d others(5): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576234 | ||||||
| chr1:246576234 | C | G | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-52+9571C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576234 | |||||||
| chr1:246576258 | C | A | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+9595C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576258 | |||||||
| chr1:246576265 | TTCTCAGT others(1650): Show |
T | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+9606_-52+11262 others(3): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576265 | ||||||
| chr1:246576445 | TTTTGGTT others(8): Show |
T | 136 | a0001c0001t0001g0154 a0001c0001t0001g0158 a0001c0001t0001g0192 others(133): Show |
136 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.-52+9785_-52+9799d others(17): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246576445 | ||||||
| chr1:246576605 | C | T | 1 | a0001c0001t0002g0070 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-52+9942C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576605 | |||||||
| chr1:246576610 | C | G | 2 | a0001c0001t0014g0162 a0001c0001t0014g0163 |
2 | HG00423.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-52+9947C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576610 | |||||||
| chr1:246576677 | A | G | 82 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(79): Show |
84 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.-52+10014A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576677 | |||||||
| chr1:246576735 | C | G | 1 | a0001c0001t0004g0006 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-52+10072C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576735 | |||||||
| chr1:246576990 | T | C | 4 | a0001c0001t0002g0244 a0001c0001t0003g0245 a0001c0001t0003g0246 others(1): Show |
4 | NA18985.hp1 NA18999.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+10327T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246576990 | |||||||
| chr1:246577069 | G | A | 1 | a0001c0012t0002g0276 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-52+10406G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577069 | |||||||
| chr1:246577114 | G | T | 3 | a0001c0001t0009g0012 a0001c0001t0009g0014 a0001c0001t0009g0015 |
3 | HG02976.hp1 HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-52+10451G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577114 | |||||||
| chr1:246577245 | C | T | 5 | a0001c0001t0001g0263 a0001c0001t0001g0267 a0001c0001t0001g0268 others(2): Show |
5 | HG02145.hp1 HG02647.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+10582C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577245 | |||||||
| chr1:246577295 | G | A | 1 | a0001c0001t0004g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-52+10632G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577295 | |||||||
| chr1:246577301 | C | A | 1 | a0001c0001t0002g0279 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-52+10638C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577301 | |||||||
| chr1:246577351 | C | T | 51 | a0001c0001t0001g0002 a0001c0001t0001g0055 a0001c0001t0001g0063 others(48): Show |
52 | HG00140.hp1 HG00423.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.-52+10688C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577351 | |||||||
| chr1:246577361 | T | C | 4 | a0001c0001t0001g0158 a0001c0001t0004g0155 a0001c0001t0004g0156 others(1): Show |
4 | HG01109.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52+10698T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577361 | |||||||
| chr1:246577373 | A | G | 1 | a0001c0001t0003g0086 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-52+10710A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577373 | |||||||
| chr1:246577455 | T | C | 1 | a0003c0003t0001g0039 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-52+10792T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577455 | |||||||
| chr1:246577553 | G | A | 1 | a0001c0001t0004g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-52+10890G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577553 | |||||||
| chr1:246577637 | G | T | 3 | a0002c0002t0006g0031 a0002c0002t0006g0032 a0002c0002t0006g0033 |
3 | HG02615.hp1 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-52+10974G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577637 | |||||||
| chr1:246577798 | G | T | 1 | a0001c0001t0002g0074 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-52+11135G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577798 | |||||||
| chr1:246577803 | A | G | 10 | a0001c0001t0001g0132 a0001c0001t0002g0170 a0001c0001t0002g0173 others(7): Show |
10 | HG01243.hp2 HG01884.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-52+11140A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577803 | |||||||
| chr1:246577808 | A | G | 1 | a0001c0001t0002g0219 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-52+11145A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577808 | |||||||
| chr1:246577845 | C | T | 16 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0175 others(13): Show |
16 | HG00735.hp1 HG00741.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-52+11182C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577845 | |||||||
| chr1:246577925 | T | A | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11262T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577925 | |||||||
| chr1:246577928 | T | G | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11265T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577928 | |||||||
| chr1:246577935 | T | G | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11272T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577935 | |||||||
| chr1:246577938 | C | G | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11275C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577938 | |||||||
| chr1:246577939 | C | T | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11276C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577939 | |||||||
| chr1:246577940 | C | A | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11277C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577940 | |||||||
| chr1:246577967 | T | G | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11304T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577967 | |||||||
| chr1:246577973 | T | G | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11310T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577973 | |||||||
| chr1:246577974 | T | G | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11311T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577974 | |||||||
| chr1:246577975 | T | G | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11312T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577975 | |||||||
| chr1:246577976 | T | G | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11313T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577976 | |||||||
| chr1:246577976 | TTTG | T | 10 | a0001c0001t0001g0132 a0001c0001t0002g0170 a0001c0001t0002g0173 others(7): Show |
10 | HG01243.hp2 HG01884.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-52+11319_-52+1132 others(7): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246577976 | ||||||
| chr1:246577977 | T | G | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11314T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577977 | |||||||
| chr1:246577978 | T | G | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11315T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577978 | |||||||
| chr1:246577980 | T | G | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11317T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577980 | |||||||
| chr1:246577981 | T | A | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11318T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577981 | |||||||
| chr1:246577987 | G | A | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11324G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577987 | |||||||
| chr1:246577989 | A | T | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11326A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577989 | |||||||
| chr1:246577990 | C | A | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11327C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577990 | |||||||
| chr1:246577995 | T | TGCCTTTG others(4): Show |
1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11332_-52+1133 others(15): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246577995 | |||||||
| chr1:246578005 | C | G | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11342C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578005 | |||||||
| chr1:246578010 | G | T | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11347G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578010 | |||||||
| chr1:246578014 | T | A | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11351T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578014 | |||||||
| chr1:246578016 | T | C | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11353T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578016 | |||||||
| chr1:246578019 | C | A | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11356C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578019 | |||||||
| chr1:246578024 | TTTTTCTA others(356): Show |
T | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11364_-52+1172 others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246578024 | ||||||
| chr1:246578290 | A | G | 1 | a0001c0001t0004g0006 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-52+11627A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578290 | |||||||
| chr1:246578388 | T | C | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11725T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578388 | |||||||
| chr1:246578391 | G | A | 2 | a0001c0001t0001g0277 a0001c0001t0002g0199 |
2 | HG00673.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-52+11728G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578391 | |||||||
| chr1:246578394 | T | C | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11731T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578394 | |||||||
| chr1:246578400 | T | C | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11737T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578400 | |||||||
| chr1:246578438 | T | C | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11775T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578438 | |||||||
| chr1:246578443 | T | C | 4 | a0001c0001t0001g0164 a0001c0001t0009g0012 a0001c0001t0009g0014 others(1): Show |
4 | HG02976.hp1 HG03130.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-52+11780T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578443 | |||||||
| chr1:246578454 | T | C | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11791T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578454 | |||||||
| chr1:246578468 | G | A | 302 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0027 others(299): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.-52+11805G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578468 | |||||||
| chr1:246578477 | C | G | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11814C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578477 | |||||||
| chr1:246578490 | T | C | 9 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(6): Show |
9 | HG00140.hp1 HG01261.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.-52+11827T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578490 | |||||||
| chr1:246578511 | C | A | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11848C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578511 | |||||||
| chr1:246578527 | T | C | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11864T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578527 | |||||||
| chr1:246578531 | T | C | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11868T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578531 | |||||||
| chr1:246578532 | G | A | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11869G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578532 | |||||||
| chr1:246578540 | A | G | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11877A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578540 | |||||||
| chr1:246578541 | C | G | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11878C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578541 | |||||||
| chr1:246578542 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-52+11879G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578542 | |||||||
| chr1:246578543 | T | C | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-52+11880T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578543 | |||||||
| chr1:246578569 | G | T | 67 | a0001c0001t0001g0002 a0001c0001t0001g0055 a0001c0001t0001g0063 others(64): Show |
68 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.-52+11906G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578569 | |||||||
| chr1:246578621 | A | G | 3 | a0001c0001t0003g0086 a0001c0001t0003g0248 a0001c0001t0003g0271 |
3 | HG03942.hp1 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-52+11958A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578621 | |||||||
| chr1:246578658 | G | C | 174 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0130 others(171): Show |
175 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.-52+11995G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578658 | |||||||
| chr1:246578668 | C | CA | 12 | a0001c0001t0001g0132 a0001c0001t0001g0154 a0001c0001t0001g0208 others(9): Show |
12 | HG01243.hp2 HG01884.hp2 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-52+12018dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246578668 | ||||||
| chr1:246578827 | A | G | 1 | a0001c0001t0001g0247 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-52+12164A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578827 | |||||||
| chr1:246578855 | C | T | 21 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0060 others(18): Show |
23 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.-52+12192C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578855 | |||||||
| chr1:246578886 | G | A | 6 | a0001c0001t0004g0148 a0001c0001t0004g0151 a0001c0001t0004g0153 others(3): Show |
6 | HG01175.hp2 HG02109.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52+12223G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578886 | |||||||
| chr1:246578922 | A | G | 2 | a0001c0001t0003g0049 a0001c0001t0003g0050 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-52+12259A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246578922 | |||||||
| chr1:246579148 | T | A | 21 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0060 others(18): Show |
23 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.-51-12364T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246579148 | |||||||
| chr1:246579250 | T | A | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-51-12262T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246579250 | |||||||
| chr1:246579307 | T | C | 1 | a0001c0006t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-51-12205T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246579307 | |||||||
| chr1:246579435 | G | C | 1 | a0001c0001t0004g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-51-12077G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246579435 | |||||||
| chr1:246579499 | T | C | 10 | a0001c0001t0001g0132 a0001c0001t0002g0170 a0001c0001t0002g0173 others(7): Show |
10 | HG01243.hp2 HG01884.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-51-12013T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246579499 | |||||||
| chr1:246579555 | G | A | 1 | a0003c0003t0001g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-51-11957G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246579555 | |||||||
| chr1:246579733 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-51-11779C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246579733 | |||||||
| chr1:246579818 | G | A | 1 | a0001c0001t0004g0006 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-51-11694G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246579818 | |||||||
| chr1:246580076 | G | A | 1 | a0002c0002t0001g0118 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-51-11436G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246580076 | |||||||
| chr1:246580374 | C | A | 1 | a0001c0006t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-51-11138C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246580374 | |||||||
| chr1:246580389 | TACAG | T | 3 | a0002c0002t0006g0031 a0002c0002t0006g0032 a0002c0002t0006g0033 |
3 | HG02615.hp1 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-51-11118_-51-1111 others(8): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246580389 | ||||||
| chr1:246580428 | C | CT | 63 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0078 others(60): Show |
64 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.-51-11075dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246580428 | ||||||
| chr1:246580432 | T | C | 1 | a0001c0006t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-51-11080T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246580432 | |||||||
| chr1:246580465 | G | C | 10 | a0001c0001t0001g0132 a0001c0001t0002g0170 a0001c0001t0002g0173 others(7): Show |
10 | HG01243.hp2 HG01884.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-51-11047G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246580465 | |||||||
| chr1:246580514 | G | T | 83 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(80): Show |
86 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.-51-10998G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246580514 | |||||||
| chr1:246580740 | T | C | 1 | a0001c0001t0001g0309 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-51-10772T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246580740 | |||||||
| chr1:246580751 | C | T | 1 | a0001c0001t0001g0297 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-51-10761C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246580751 | |||||||
| chr1:246580832 | C | T | 1 | a0001c0001t0003g0056 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-51-10680C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246580832 | |||||||
| chr1:246580985 | C | A | 1 | a0001c0001t0001g0013 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-51-10527C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246580985 | |||||||
| chr1:246581030 | C | T | 1 | a0002c0002t0001g0116 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-51-10482C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246581030 | |||||||
| chr1:246581054 | A | G | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-51-10458A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246581054 | |||||||
| chr1:246581246 | T | C | 12 | a0001c0001t0004g0044 a0003c0003t0001g0034 a0003c0003t0001g0035 others(9): Show |
12 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-51-10266T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246581246 | |||||||
| chr1:246581263 | C | G | 1 | a0001c0001t0003g0098 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-51-10249C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246581263 | |||||||
| chr1:246581358 | G | C | 21 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0060 others(18): Show |
23 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.-51-10154G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246581358 | |||||||
| chr1:246581455 | G | T | 41 | a0001c0001t0001g0125 a0001c0001t0001g0130 a0001c0001t0001g0285 others(38): Show |
42 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.-51-10057G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246581455 | |||||||
| chr1:246581683 | A | G | 2 | a0001c0001t0004g0008 a0004c0004t0003g0117 |
2 | HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-51-9829A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246581683 | |||||||
| chr1:246581699 | T | C | 303 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0027 others(300): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.-51-9813T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246581699 | |||||||
| chr1:246581709 | A | G | 1 | a0001c0001t0004g0006 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-51-9803A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246581709 | |||||||
| chr1:246581792 | G | A | 47 | a0001c0001t0001g0063 a0001c0001t0001g0078 a0001c0001t0001g0088 others(44): Show |
47 | HG00140.hp1 HG00423.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.-51-9720G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246581792 | |||||||
| chr1:246581877 | T | G | 1 | a0001c0006t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-51-9635T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246581877 | |||||||
| chr1:246581957 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-51-9555G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246581957 | |||||||
| chr1:246582001 | G | A | 4 | a0002c0002t0001g0143 a0002c0002t0001g0144 a0002c0002t0001g0145 others(1): Show |
4 | HG02559.hp1 HG02683.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-9511G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582001 | |||||||
| chr1:246582169 | C | T | 1 | a0001c0001t0003g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-51-9343C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582169 | |||||||
| chr1:246582261 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-51-9251C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582261 | |||||||
| chr1:246582356 | C | CT | 20 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0175 others(17): Show |
20 | HG00735.hp1 HG00741.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.-51-9142dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246582356 | ||||||
| chr1:246582356 | CT | C | 119 | a0001c0001t0001g0090 a0001c0001t0001g0119 a0001c0001t0001g0154 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.-51-9142delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246582356 | ||||||
| chr1:246582419 | G | GCTCCCTG others(10): Show |
4 | a0001c0001t0001g0158 a0001c0001t0004g0155 a0001c0001t0004g0156 others(1): Show |
4 | HG01109.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-9087_-51-9071d others(19): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246582419 | ||||||
| chr1:246582675 | T | C | 1 | a0001c0001t0004g0273 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-51-8837T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582675 | |||||||
| chr1:246582707 | A | G | 1 | a0001c0001t0004g0006 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-51-8805A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582707 | |||||||
| chr1:246582715 | G | A | 27 | a0001c0001t0001g0024 a0001c0001t0001g0175 a0001c0001t0004g0016 others(24): Show |
27 | HG00733.hp1 HG00735.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.-51-8797G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582715 | |||||||
| chr1:246582763 | C | T | 1 | a0001c0001t0002g0127 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-51-8749C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582763 | |||||||
| chr1:246582799 | C | G | 2 | a0001c0001t0003g0049 a0001c0001t0003g0050 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-51-8713C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582799 | |||||||
| chr1:246582799 | C | T | 118 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0027 others(115): Show |
120 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.-51-8713C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582799 | |||||||
| chr1:246582831 | G | A | 1 | a0001c0001t0004g0006 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-51-8681G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582831 | |||||||
| chr1:246582849 | C | T | 1 | a0001c0001t0001g0296 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-51-8663C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582849 | |||||||
| chr1:246582869 | A | G | 79 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0063 others(76): Show |
80 | HG00423.hp2 HG00642.hp1 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.-51-8643A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582869 | |||||||
| chr1:246582931 | G | A | 1 | a0001c0001t0004g0018 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-51-8581G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582931 | |||||||
| chr1:246582995 | G | C | 1 | a0001c0001t0001g0297 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-51-8517G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582995 | |||||||
| chr1:246582996 | C | G | 1 | a0001c0001t0001g0297 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-51-8516C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246582996 | |||||||
| chr1:246583110 | A | C | 2 | a0001c0001t0004g0020 a0001c0001t0004g0021 |
2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-51-8402A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246583110 | |||||||
| chr1:246583157 | T | TTTGGTGG others(23): Show |
1 | a0001c0001t0001g0297 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-51-8353_-51-8324d others(32): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246583157 | ||||||
| chr1:246583301 | A | G | 11 | a0001c0001t0001g0027 a0001c0001t0004g0008 a0001c0001t0004g0028 others(8): Show |
11 | HG01981.hp1 HG02615.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-51-8211A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246583301 | |||||||
| chr1:246583435 | A | C | 13 | a0001c0001t0001g0013 a0001c0001t0001g0165 a0001c0001t0001g0167 others(10): Show |
13 | HG01884.hp2 HG01981.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-51-8077A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246583435 | |||||||
| chr1:246583639 | G | A | 16 | a0001c0001t0001g0078 a0001c0001t0001g0119 a0001c0001t0001g0302 others(13): Show |
16 | HG00558.hp2 HG01934.hp2 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-51-7873G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246583639 | |||||||
| chr1:246583836 | G | A | 13 | a0001c0001t0001g0013 a0001c0001t0001g0165 a0001c0001t0001g0167 others(10): Show |
13 | HG01884.hp2 HG01981.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-51-7676G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246583836 | |||||||
| chr1:246583880 | T | G | 3 | a0002c0002t0001g0029 a0002c0002t0001g0120 a0002c0002t0001g0128 |
3 | HG00741.hp2 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-51-7632T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246583880 | |||||||
| chr1:246583929 | G | T | 11 | a0003c0003t0001g0034 a0003c0003t0001g0035 a0003c0003t0001g0039 others(8): Show |
11 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-51-7583G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246583929 | |||||||
| chr1:246583930 | C | T | 11 | a0003c0003t0001g0034 a0003c0003t0001g0035 a0003c0003t0001g0039 others(8): Show |
11 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-51-7582C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246583930 | |||||||
| chr1:246583986 | G | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(90): Show |
96 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.-51-7526G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246583986 | |||||||
| chr1:246584036 | CT | C | 274 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(271): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.-51-7473delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246584036 | ||||||
| chr1:246584039 | T | C | 274 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(271): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.-51-7473T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246584039 | |||||||
| chr1:246584179 | C | T | 1 | a0001c0001t0004g0028 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-51-7333C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246584179 | |||||||
| chr1:246584250 | C | T | 1 | a0001c0001t0003g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-51-7262C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246584250 | |||||||
| chr1:246584278 | G | A | 2 | a0001c0001t0017g0010 a0001c0006t0001g0011 |
2 | HG01981.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-51-7234G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246584278 | |||||||
| chr1:246584284 | G | A | 129 | a0001c0001t0001g0024 a0001c0001t0001g0132 a0001c0001t0001g0154 others(126): Show |
129 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.-51-7228G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246584284 | |||||||
| chr1:246584388 | T | G | 1 | a0001c0001t0002g0219 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-51-7124T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246584388 | |||||||
| chr1:246584419 | G | A | 1 | a0001c0001t0002g0003 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-51-7093G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246584419 | |||||||
| chr1:246584576 | T | C | 1 | a0001c0001t0001g0293 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-51-6936T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246584576 | |||||||
| chr1:246584640 | G | A | 10 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(7): Show |
10 | HG00735.hp1 HG02630.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-51-6872G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246584640 | |||||||
| chr1:246584812 | G | A | 41 | a0001c0001t0001g0013 a0001c0001t0001g0164 a0001c0001t0001g0165 others(38): Show |
41 | HG00733.hp1 HG00735.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.-51-6700G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246584812 | |||||||
| chr1:246584828 | A | G | 2 | a0001c0001t0002g0282 a0002c0002t0001g0131 |
2 | HG04115.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-51-6684A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246584828 | |||||||
| chr1:246585034 | T | A | 2 | a0002c0002t0001g0108 a0002c0002t0002g0121 |
2 | HG01074.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-51-6478T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585034 | |||||||
| chr1:246585140 | C | T | 1 | a0002c0002t0001g0108 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-51-6372C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585140 | |||||||
| chr1:246585175 | C | T | 85 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0055 others(82): Show |
88 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-51-6337C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585175 | |||||||
| chr1:246585382 | CACATCTG others(426): Show |
C | 1 | a0001c0001t0001g0243 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-51-6116_-51-5684d others(2): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585382 | ||||||
| chr1:246585552 | C | T | 4 | a0001c0001t0003g0056 a0001c0001t0003g0075 a0001c0001t0003g0076 others(1): Show |
4 | HG02071.hp1 HG02074.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-5960C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585552 | |||||||
| chr1:246585561 | C | G | 2 | a0002c0002t0015g0166 a0008c0011t0015g0211 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-51-5951C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585561 | |||||||
| chr1:246585590 | G | A | 1 | a0001c0001t0002g0231 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-51-5922G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585590 | |||||||
| chr1:246585641 | C | CA | 13 | a0001c0001t0001g0192 a0001c0001t0001g0252 a0001c0001t0001g0291 others(10): Show |
13 | HG00140.hp2 HG00621.hp1 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.-51-5849dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585641 | ||||||
| chr1:246585641 | CA | C | 20 | a0001c0001t0001g0154 a0001c0001t0001g0164 a0001c0001t0001g0202 others(17): Show |
20 | HG00558.hp1 HG01074.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.-51-5849delA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585641 | ||||||
| chr1:246585641 | CAA | C | 7 | a0001c0001t0001g0132 a0001c0001t0004g0006 a0001c0001t0004g0134 others(4): Show |
7 | HG01243.hp2 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-51-5850_-51-5849d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585641 | ||||||
| chr1:246585641 | CAAA | C | 11 | a0001c0001t0001g0289 a0001c0001t0004g0044 a0001c0001t0004g0148 others(8): Show |
11 | HG01175.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-51-5851_-51-5849d others(5): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585641 | ||||||
| chr1:246585641 | CAAAAA | C | 9 | a0001c0001t0004g0171 a0001c0001t0005g0152 a0001c0001t0005g0200 others(6): Show |
9 | HG01433.hp1 HG01884.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51-5853_-51-5849d others(7): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585641 | ||||||
| chr1:246585656 | A | T | 2 | a0001c0001t0004g0008 a0003c0003t0004g0036 |
2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-51-5856A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585656 | |||||||
| chr1:246585658 | A | T | 9 | a0001c0001t0004g0008 a0003c0003t0001g0039 a0003c0003t0001g0040 others(6): Show |
9 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51-5854A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585658 | |||||||
| chr1:246585660 | A | T | 21 | a0001c0001t0001g0027 a0001c0001t0003g0290 a0001c0001t0004g0008 others(18): Show |
21 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-51-5852A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585660 | |||||||
| chr1:246585661 | AAAT | A | 16 | a0001c0001t0001g0165 a0001c0001t0002g0080 a0001c0001t0002g0101 others(13): Show |
16 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.-51-5849_-51-5847d others(5): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585661 | ||||||
| chr1:246585661 | AAATATAC others(4): Show |
A | 8 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0168 others(5): Show |
8 | HG01515.hp1 HG01517.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-51-5849_-51-5839d others(13): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585661 | ||||||
| chr1:246585661 | AAATATAC others(18): Show |
A | 2 | a0001c0001t0001g0125 a0002c0002t0001g0115 |
2 | HG03688.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-51-5849_-51-5825d others(27): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585661 | ||||||
| chr1:246585662 | A | AT | 3 | a0001c0001t0001g0299 a0001c0001t0003g0081 a0002c0002t0001g0113 |
3 | HG02015.hp2 HG02074.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.-51-5850_-51-5849i others(3): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585662 | |||||||
| chr1:246585662 | A | T | 23 | a0001c0001t0001g0027 a0001c0001t0003g0290 a0001c0001t0004g0008 others(20): Show |
23 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.-51-5850A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585662 | |||||||
| chr1:246585663 | ATATAC | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0180 others(5): Show |
8 | HG01257.hp2 HG01346.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-51-5848_-51-5844d others(7): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585663 | |||||||
| chr1:246585663 | ATATACAC others(10): Show |
A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0175 |
2 | HG00735.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-51-5848_-51-5832d others(19): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585663 | |||||||
| chr1:246585664 | T | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0288 |
2 | HG01978.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-51-5848T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585664 | |||||||
| chr1:246585664 | T | C | 3 | a0001c0001t0001g0299 a0001c0001t0003g0081 a0002c0002t0001g0113 |
3 | HG02015.hp2 HG02074.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.-51-5848T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585664 | |||||||
| chr1:246585664 | TATAC | T | 4 | a0001c0001t0002g0007 a0001c0001t0002g0129 a0001c0001t0002g0282 others(1): Show |
4 | HG00741.hp1 HG03942.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-5846_-51-5843d others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585664 | ||||||
| chr1:246585664 | TATACACA others(3): Show |
T | 3 | a0001c0001t0001g0167 a0001c0001t0003g0071 a0002c0002t0006g0032 |
3 | HG02300.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-51-5846_-51-5837d others(12): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585664 | ||||||
| chr1:246585666 | T | C | 15 | a0001c0001t0001g0202 a0001c0001t0001g0299 a0001c0001t0002g0074 others(12): Show |
15 | HG01099.hp2 HG01261.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.-51-5846T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585666 | |||||||
| chr1:246585666 | TAC | T | 19 | a0001c0001t0001g0242 a0001c0001t0001g0255 a0001c0001t0001g0258 others(16): Show |
19 | HG00280.hp1 HG00558.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.-51-5801_-51-5800d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585666 | ||||||
| chr1:246585666 | TACAC | T | 46 | a0001c0001t0001g0055 a0001c0001t0001g0078 a0001c0001t0001g0089 others(43): Show |
47 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.-51-5803_-51-5800d others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585666 | ||||||
| chr1:246585666 | TACACAC | T | 99 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0061 others(96): Show |
100 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.-51-5805_-51-5800d others(8): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585666 | ||||||
| chr1:246585666 | TACACACA others(1): Show |
T | 24 | a0001c0001t0001g0024 a0001c0001t0001g0060 a0001c0001t0001g0088 others(21): Show |
24 | HG01070.hp2 HG01074.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.-51-5807_-51-5800d others(10): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585666 | ||||||
| chr1:246585666 | TACACACA others(3): Show |
T | 5 | a0001c0001t0001g0158 a0001c0001t0002g0312 a0001c0001t0003g0142 others(2): Show |
5 | HG02015.hp1 HG02257.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-5809_-51-5800d others(12): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585666 | ||||||
| chr1:246585666 | TACACACA others(5): Show |
T | 7 | a0001c0001t0001g0208 a0001c0001t0001g0239 a0001c0001t0004g0273 others(4): Show |
7 | HG02257.hp1 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-51-5811_-51-5800d others(14): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585666 | ||||||
| chr1:246585666 | TACACACA others(7): Show |
T | 15 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0018 others(12): Show |
15 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.-51-5813_-51-5800d others(16): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585666 | ||||||
| chr1:246585666 | TACACACA others(9): Show |
T | 6 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0002g0187 others(3): Show |
6 | HG02647.hp1 HG02976.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51-5815_-51-5800d others(18): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585666 | ||||||
| chr1:246585666 | TACACACA others(11): Show |
T | 4 | a0001c0001t0001g0154 a0001c0001t0001g0164 a0003c0003t0004g0160 others(1): Show |
4 | HG02717.hp1 HG03209.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-5817_-51-5800d others(20): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585666 | ||||||
| chr1:246585666 | TACACACA others(13): Show |
T | 1 | a0001c0001t0003g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-51-5819_-51-5800d others(22): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246585666 | ||||||
| chr1:246585668 | C | T | 9 | a0001c0001t0001g0027 a0001c0001t0002g0181 a0001c0001t0004g0008 others(6): Show |
9 | HG01891.hp1 HG01981.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51-5844C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585668 | |||||||
| chr1:246585670 | C | T | 18 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0063 others(15): Show |
18 | HG00140.hp1 HG01257.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.-51-5842C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585670 | |||||||
| chr1:246585672 | C | T | 16 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0055 others(13): Show |
16 | HG01257.hp2 HG01346.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.-51-5840C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585672 | |||||||
| chr1:246585674 | C | T | 13 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0168 others(10): Show |
13 | HG01515.hp1 HG01517.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51-5838C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585674 | |||||||
| chr1:246585676 | C | T | 5 | a0001c0001t0009g0012 a0001c0001t0009g0014 a0001c0001t0017g0010 others(2): Show |
5 | HG01981.hp1 HG02486.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-5836C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585676 | |||||||
| chr1:246585678 | C | T | 6 | a0001c0001t0009g0012 a0001c0001t0009g0014 a0001c0001t0017g0010 others(3): Show |
6 | HG01981.hp1 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51-5834C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585678 | |||||||
| chr1:246585680 | C | T | 4 | a0001c0006t0001g0011 a0002c0002t0006g0031 a0002c0002t0006g0033 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-5832C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585680 | |||||||
| chr1:246585682 | C | T | 11 | a0001c0001t0001g0013 a0001c0001t0001g0175 a0003c0003t0001g0039 others(8): Show |
11 | HG00733.hp1 HG00735.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.-51-5830C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585682 | |||||||
| chr1:246585684 | C | T | 13 | a0001c0001t0001g0013 a0001c0001t0001g0175 a0001c0001t0001g0288 others(10): Show |
13 | HG00733.hp1 HG00735.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51-5828C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585684 | |||||||
| chr1:246585686 | C | T | 7 | a0001c0001t0001g0013 a0001c0001t0001g0154 a0001c0001t0001g0164 others(4): Show |
7 | HG00735.hp1 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-51-5826C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585686 | |||||||
| chr1:246585688 | C | T | 2 | a0001c0001t0001g0125 a0002c0002t0001g0115 |
2 | HG03688.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-51-5824C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585688 | |||||||
| chr1:246585709 | A | T | 1 | a0002c0002t0001g0095 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-51-5803A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585709 | |||||||
| chr1:246585767 | G | A | 1 | a0001c0001t0002g0199 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-51-5745G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246585767 | |||||||
| chr1:246586105 | A | ATGTGTGT others(3): Show |
1 | a0003c0003t0004g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-51-5406_-51-5405i others(12): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586105 | ||||||
| chr1:246586107 | A | ATGTGTGT others(1): Show |
6 | a0001c0001t0004g0006 a0001c0001t0004g0028 a0001c0001t0004g0172 others(3): Show |
6 | HG02818.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51-5404_-51-5403i others(10): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586107 | ||||||
| chr1:246586107 | A | ATGTGTGT others(5): Show |
4 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
4 | HG01515.hp1 HG01517.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-5404_-51-5403i others(14): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586107 | ||||||
| chr1:246586107 | A | ATGTGTGT others(7): Show |
1 | a0001c0001t0001g0090 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-51-5404_-51-5403i others(16): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586107 | ||||||
| chr1:246586107 | A | G | 1 | a0003c0003t0004g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-51-5405A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246586107 | |||||||
| chr1:246586109 | A | ATG | 49 | a0001c0001t0001g0078 a0001c0001t0001g0089 a0001c0001t0001g0096 others(46): Show |
49 | HG00423.hp2 HG01099.hp2 HG01169.hp1 others(46): Show |
intron_variant | MODIFIER | c.-51-5402_-51-5401i others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586109 | ||||||
| chr1:246586109 | A | ATGTG | 29 | a0001c0001t0001g0002 a0001c0001t0001g0055 a0001c0001t0001g0060 others(26): Show |
31 | HG00140.hp2 HG00423.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.-51-5402_-51-5401i others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586109 | ||||||
| chr1:246586109 | A | ATGTGTG | 4 | a0001c0001t0001g0168 a0001c0001t0001g0309 a0001c0001t0002g0099 others(1): Show |
4 | HG00642.hp2 HG01515.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-5402_-51-5401i others(8): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586109 | ||||||
| chr1:246586109 | A | ATGTGTGT others(1): Show |
3 | a0001c0001t0002g0170 a0001c0001t0003g0176 a0001c0001t0003g0314 |
3 | HG02145.hp2 HG02886.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-51-5402_-51-5401i others(10): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586109 | ||||||
| chr1:246586109 | A | ATGTGTGT others(3): Show |
3 | a0001c0001t0002g0173 a0001c0001t0004g0171 a0002c0002t0001g0169 |
3 | HG01884.hp2 HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-51-5402_-51-5401i others(12): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586109 | ||||||
| chr1:246586109 | A | ATGTGTGT others(7): Show |
1 | a0001c0001t0002g0079 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-51-5402_-51-5401i others(16): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586109 | ||||||
| chr1:246586109 | A | G | 16 | a0001c0001t0001g0027 a0001c0001t0001g0090 a0001c0001t0001g0091 others(13): Show |
17 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.-51-5403A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246586109 | |||||||
| chr1:246586109 | ATATG | A | 10 | a0001c0001t0001g0205 a0001c0001t0002g0283 a0001c0001t0002g0300 others(7): Show |
10 | HG00558.hp2 HG01192.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.-51-5401_-51-5398d others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586109 | ||||||
| chr1:246586109 | ATATGTG | A | 111 | a0001c0001t0001g0024 a0001c0001t0001g0132 a0001c0001t0001g0154 others(108): Show |
111 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.-51-5401_-51-5396d others(8): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586109 | ||||||
| chr1:246586111 | A | ATATATGT others(3): Show |
1 | a0003c0003t0004g0037 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-51-5400_-51-5399i others(12): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586111 | ||||||
| chr1:246586111 | A | ATATATGT others(5): Show |
2 | a0003c0003t0004g0036 a0003c0003t0004g0038 |
2 | HG02896.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-51-5400_-51-5399i others(14): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586111 | ||||||
| chr1:246586111 | A | ATATATGT others(7): Show |
1 | a0003c0003t0001g0035 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-51-5400_-51-5399i others(16): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586111 | ||||||
| chr1:246586111 | A | ATATATGT others(9): Show |
5 | a0003c0003t0001g0040 a0003c0003t0001g0041 a0003c0003t0001g0042 others(2): Show |
5 | HG00733.hp1 HG01891.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.-51-5400_-51-5399i others(18): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586111 | ||||||
| chr1:246586111 | A | ATATATGT others(11): Show |
1 | a0003c0003t0001g0039 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-51-5400_-51-5399i others(20): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586111 | ||||||
| chr1:246586111 | A | ATATGTGT others(9): Show |
1 | a0002c0002t0006g0033 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-51-5400_-51-5399i others(18): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586111 | ||||||
| chr1:246586111 | A | ATGTGTG | 6 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0165 others(3): Show |
6 | HG00738.hp1 HG02647.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51-5375_-51-5370d others(8): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586111 | ||||||
| chr1:246586111 | A | ATGTGTGT others(1): Show |
7 | a0001c0001t0001g0180 a0001c0001t0004g0016 a0001c0001t0004g0017 others(4): Show |
7 | HG01981.hp1 HG02630.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-51-5377_-51-5370d others(10): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586111 | ||||||
| chr1:246586111 | A | ATGTGTGT others(3): Show |
2 | a0001c0001t0001g0175 a0001c0001t0004g0019 |
2 | HG00735.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-51-5379_-51-5370d others(12): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586111 | ||||||
| chr1:246586111 | A | ATGTGTGT others(7): Show |
2 | a0002c0002t0006g0031 a0002c0002t0006g0032 |
2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-51-5383_-51-5370d others(16): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586111 | ||||||
| chr1:246586111 | A | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0055 others(108): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.-51-5401A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246586111 | |||||||
| chr1:246586141 | G | A | 120 | a0001c0001t0001g0024 a0001c0001t0001g0132 a0001c0001t0001g0154 others(117): Show |
120 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.-51-5371G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246586141 | |||||||
| chr1:246586141 | G | GTA | 6 | a0001c0001t0002g0058 a0004c0004t0003g0117 a0004c0004t0003g0182 others(3): Show |
6 | HG00280.hp1 HG02451.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51-5365_-51-5364d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586141 | ||||||
| chr1:246586143 | A | G | 10 | a0001c0001t0002g0051 a0002c0002t0001g0143 a0002c0002t0001g0144 others(7): Show |
10 | HG01256.hp1 HG02486.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-51-5369A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246586143 | |||||||
| chr1:246586213 | G | C | 13 | a0003c0003t0001g0034 a0003c0003t0001g0035 a0003c0003t0001g0039 others(10): Show |
13 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-51-5299G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246586213 | |||||||
| chr1:246586224 | A | G | 2 | a0001c0001t0001g0027 a0001c0001t0004g0028 |
2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-51-5288A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246586224 | |||||||
| chr1:246586285 | C | A | 1 | a0001c0001t0001g0164 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-51-5227C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246586285 | |||||||
| chr1:246586397 | A | G | 1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-51-5115A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246586397 | |||||||
| chr1:246586405 | CAT | C | 14 | a0001c0001t0001g0242 a0003c0003t0001g0034 a0003c0003t0001g0035 others(11): Show |
14 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-51-5104_-51-5103d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246586405 | ||||||
| chr1:246586408 | A | G | 1 | a0001c0001t0005g0152 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-51-5104A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246586408 | |||||||
| chr1:246587097 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-51-4415T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246587097 | |||||||
| chr1:246587327 | T | C | 29 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0060 others(26): Show |
30 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.-51-4185T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246587327 | |||||||
| chr1:246587695 | C | T | 13 | a0003c0003t0001g0034 a0003c0003t0001g0035 a0003c0003t0001g0039 others(10): Show |
13 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-51-3817C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246587695 | |||||||
| chr1:246587790 | G | A | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-51-3722G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246587790 | |||||||
| chr1:246587864 | T | C | 7 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(4): Show |
7 | HG00140.hp1 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.-51-3648T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246587864 | |||||||
| chr1:246587885 | T | C | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0002c0002t0001g0131 |
3 | HG02970.hp1 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-51-3627T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246587885 | |||||||
| chr1:246587953 | G | A | 2 | a0001c0001t0003g0049 a0001c0001t0003g0050 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-51-3559G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246587953 | |||||||
| chr1:246588159 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0167 |
2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-51-3353G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246588159 | |||||||
| chr1:246588488 | A | G | 137 | a0001c0001t0001g0024 a0001c0001t0001g0132 a0001c0001t0001g0154 others(134): Show |
137 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.-51-3024A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246588488 | |||||||
| chr1:246588502 | A | T | 1 | a0001c0001t0002g0308 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-51-3010A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246588502 | |||||||
| chr1:246588555 | A | G | 10 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(7): Show |
10 | HG00735.hp1 HG02630.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-51-2957A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246588555 | |||||||
| chr1:246588702 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-51-2810A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246588702 | |||||||
| chr1:246588828 | A | G | 2 | a0001c0001t0001g0164 a0001c0001t0003g0290 |
2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-51-2684A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246588828 | |||||||
| chr1:246589004 | T | C | 1 | a0001c0001t0003g0135 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-51-2508T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589004 | |||||||
| chr1:246589222 | G | A | 2 | a0001c0001t0001g0302 a0001c0001t0003g0197 |
2 | NA18969.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-51-2290G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589222 | |||||||
| chr1:246589265 | T | TC | 13 | a0001c0001t0001g0125 a0001c0001t0002g0185 a0001c0001t0002g0241 others(10): Show |
13 | HG01099.hp1 HG01192.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51-2241dupC | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246589265 | ||||||
| chr1:246589402 | A | G | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-51-2110A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589402 | |||||||
| chr1:246589410 | C | T | 8 | a0002c0002t0001g0110 a0002c0002t0001g0124 a0002c0002t0001g0137 others(5): Show |
8 | HG00639.hp2 HG02129.hp1 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.-51-2102C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589410 | |||||||
| chr1:246589421 | A | T | 1 | a0001c0001t0003g0135 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-51-2091A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589421 | |||||||
| chr1:246589427 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-51-2085C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589427 | |||||||
| chr1:246589449 | A | C | 1 | a0006c0007t0003g0265 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-51-2063A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589449 | |||||||
| chr1:246589460 | A | C | 7 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(4): Show |
7 | HG00140.hp1 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.-51-2052A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589460 | |||||||
| chr1:246589507 | T | C | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-51-2005T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589507 | |||||||
| chr1:246589516 | G | T | 13 | a0003c0003t0001g0034 a0003c0003t0001g0035 a0003c0003t0001g0039 others(10): Show |
13 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-51-1996G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589516 | |||||||
| chr1:246589528 | C | G | 271 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(268): Show |
274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.-51-1984C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589528 | |||||||
| chr1:246589551 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-51-1961T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589551 | |||||||
| chr1:246589587 | G | A | 13 | a0003c0003t0001g0034 a0003c0003t0001g0035 a0003c0003t0001g0039 others(10): Show |
13 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-51-1925G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589587 | |||||||
| chr1:246589641 | G | A | 1 | a0001c0001t0024g0270 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-51-1871G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589641 | |||||||
| chr1:246589832 | C | G | 10 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(7): Show |
10 | HG00735.hp1 HG02630.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-51-1680C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589832 | |||||||
| chr1:246589832 | C | T | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-51-1680C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589832 | |||||||
| chr1:246589908 | G | A | 8 | a0001c0001t0001g0309 a0001c0001t0002g0184 a0001c0001t0002g0185 others(5): Show |
8 | HG00423.hp1 NA18950.hp2 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.-51-1604G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589908 | |||||||
| chr1:246589941 | C | T | 6 | a0004c0004t0003g0117 a0004c0004t0003g0182 a0004c0004t0003g0183 others(3): Show |
6 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51-1571C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589941 | |||||||
| chr1:246589998 | G | A | 2 | a0001c0001t0001g0226 a0001c0001t0001g0281 |
2 | NA18945.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-51-1514G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246589998 | |||||||
| chr1:246590078 | C | T | 1 | a0007c0005t0023g0045 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-51-1434C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246590078 | |||||||
| chr1:246590237 | C | T | 2 | a0002c0002t0015g0166 a0008c0011t0015g0211 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-51-1275C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246590237 | |||||||
| chr1:246590282 | G | A | 1 | a0001c0001t0004g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-51-1230G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246590282 | |||||||
| chr1:246590450 | T | G | 1 | a0001c0001t0001g0119 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-51-1062T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246590450 | |||||||
| chr1:246590488 | G | A | 1 | a0008c0011t0015g0211 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-51-1024G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246590488 | |||||||
| chr1:246590512 | C | T | 8 | a0001c0001t0001g0132 a0001c0001t0004g0044 a0001c0001t0004g0100 others(5): Show |
8 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-51-1000C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246590512 | |||||||
| chr1:246590621 | A | G | 100 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0054 others(97): Show |
103 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.-51-891A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246590621 | |||||||
| chr1:246590738 | G | A | 1 | a0001c0001t0003g0257 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-51-774G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246590738 | |||||||
| chr1:246590859 | C | CT | 103 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0054 others(100): Show |
106 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.-51-636dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246590859 | ||||||
| chr1:246590859 | CTTTT | C | 7 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(4): Show |
7 | HG00140.hp1 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.-51-639_-51-636del others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246590859 | ||||||
| chr1:246590944 | A | G | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-51-568A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246590944 | |||||||
| chr1:246590962 | A | T | 1 | a0001c0001t0001g0054 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-51-550A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246590962 | |||||||
| chr1:246591015 | T | A | 1 | a0001c0001t0001g0164 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-51-497T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246591015 | |||||||
| chr1:246591016 | A | T | 149 | a0001c0001t0001g0024 a0001c0001t0001g0090 a0001c0001t0001g0091 others(146): Show |
149 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.-51-496A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246591016 | |||||||
| chr1:246591113 | T | C | 2 | a0002c0002t0001g0137 a0002c0002t0001g0138 |
2 | NA18960.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-51-399T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246591113 | |||||||
| chr1:246591314 | C | T | 2 | a0001c0001t0003g0049 a0001c0001t0003g0050 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-51-198C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246591314 | |||||||
| chr1:246591440 | G | A | 1 | a0001c0001t0025g0286 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-51-72G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | 246591440 | |||||||
| chr1:246591476 | G | GA | 137 | a0001c0001t0001g0024 a0001c0001t0001g0132 a0001c0001t0001g0154 others(134): Show |
137 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.-51-32dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 246591476 | ||||||
| chr1:246591979 | A | T | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.379+38A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246591979 | |||||||
| chr1:246592198 | C | G | 2 | a0001c0001t0001g0164 a0001c0001t0003g0290 |
2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.379+257C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246592198 | |||||||
| chr1:246592211 | G | A | 1 | a0001c0001t0003g0266 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.379+270G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246592211 | |||||||
| chr1:246592217 | G | A | 4 | a0001c0001t0002g0170 a0001c0001t0002g0173 a0001c0001t0004g0171 others(1): Show |
4 | HG01884.hp2 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.379+276G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246592217 | |||||||
| chr1:246592226 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.379+285C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246592226 | |||||||
| chr1:246592574 | C | T | 1 | a0001c0001t0003g0245 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.379+633C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246592574 | |||||||
| chr1:246592705 | C | T | 1 | a0002c0002t0001g0118 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.379+764C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246592705 | |||||||
| chr1:246592813 | T | C | 2 | a0001c0001t0001g0168 a0001c0001t0003g0176 |
2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.379+872T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246592813 | |||||||
| chr1:246592822 | G | A | 1 | a0001c0006t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.379+881G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246592822 | |||||||
| chr1:246592862 | G | C | 1 | a0001c0001t0002g0227 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.379+921G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246592862 | |||||||
| chr1:246593261 | C | T | 241 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0054 others(238): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.379+1320C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246593261 | |||||||
| chr1:246593319 | CT | C | 57 | a0001c0001t0001g0192 a0001c0001t0001g0205 a0001c0001t0001g0213 others(54): Show |
57 | HG00280.hp2 HG00558.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.379+1391delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246593319 | ||||||
| chr1:246593408 | C | T | 2 | a0001c0001t0017g0010 a0001c0006t0001g0011 |
2 | HG01981.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.379+1467C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246593408 | |||||||
| chr1:246593558 | G | T | 1 | a0001c0001t0002g0199 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.379+1617G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246593558 | |||||||
| chr1:246593631 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.379+1690C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246593631 | |||||||
| chr1:246593741 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.379+1800C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246593741 | |||||||
| chr1:246593865 | C | T | 2 | a0001c0001t0001g0272 a0001c0001t0003g0005 |
2 | HG02109.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.379+1924C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246593865 | |||||||
| chr1:246594012 | C | T | 2 | a0001c0001t0001g0306 a0001c0001t0001g0307 |
2 | HG00408.hp1 HG00408.hp2 |
intron_variant | MODIFIER | c.379+2071C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246594012 | |||||||
| chr1:246594026 | C | T | 1 | a0007c0005t0023g0045 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.379+2085C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246594026 | |||||||
| chr1:246594147 | T | C | 273 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(270): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.379+2206T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246594147 | |||||||
| chr1:246594248 | C | G | 1 | a0001c0006t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.379+2307C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246594248 | |||||||
| chr1:246594281 | C | G | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.379+2340C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246594281 | |||||||
| chr1:246594385 | A | G | 2 | a0001c0001t0001g0192 a0001c0001t0001g0205 |
2 | HG00621.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.379+2444A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246594385 | |||||||
| chr1:246594731 | T | A | 3 | a0003c0003t0004g0036 a0003c0003t0004g0037 a0003c0003t0004g0038 |
3 | HG01243.hp1 HG02896.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.379+2790T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246594731 | |||||||
| chr1:246594860 | C | T | 277 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(274): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.379+2919C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246594860 | |||||||
| chr1:246595000 | G | A | 1 | a0001c0001t0002g0241 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.379+3059G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246595000 | |||||||
| chr1:246595484 | C | T | 2 | a0002c0002t0015g0166 a0008c0011t0015g0211 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.379+3543C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246595484 | |||||||
| chr1:246595591 | T | C | 2 | a0001c0001t0003g0005 a0001c0001t0003g0209 |
2 | NA18962.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.379+3650T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246595591 | |||||||
| chr1:246595635 | T | C | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG02056.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.379+3694T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246595635 | |||||||
| chr1:246595817 | G | T | 1 | a0001c0001t0001g0089 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.379+3876G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246595817 | |||||||
| chr1:246595991 | G | C | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.379+4050G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246595991 | |||||||
| chr1:246596151 | C | T | 1 | a0001c0001t0003g0084 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.379+4210C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246596151 | |||||||
| chr1:246596341 | G | A | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.379+4400G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246596341 | |||||||
| chr1:246596397 | C | CA | 8 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(5): Show |
8 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.379+4469dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246596397 | ||||||
| chr1:246596780 | C | T | 277 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(274): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.379+4839C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246596780 | |||||||
| chr1:246596821 | A | T | 1 | a0001c0001t0011g0210 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.379+4880A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246596821 | |||||||
| chr1:246596829 | A | T | 271 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(268): Show |
274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.379+4888A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246596829 | |||||||
| chr1:246596910 | T | C | 1 | a0001c0001t0003g0292 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.379+4969T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246596910 | |||||||
| chr1:246596971 | G | C | 13 | a0003c0003t0001g0034 a0003c0003t0001g0035 a0003c0003t0001g0039 others(10): Show |
13 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.379+5030G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246596971 | |||||||
| chr1:246597165 | G | T | 9 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(6): Show |
9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.379+5224G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246597165 | |||||||
| chr1:246597250 | C | T | 7 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(4): Show |
7 | HG00140.hp1 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.379+5309C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246597250 | |||||||
| chr1:246597268 | C | G | 100 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0054 others(97): Show |
103 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.379+5327C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246597268 | |||||||
| chr1:246597342 | C | A | 7 | a0001c0001t0001g0027 a0001c0001t0004g0006 a0001c0001t0004g0008 others(4): Show |
7 | HG02723.hp2 HG02818.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.379+5401C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246597342 | |||||||
| chr1:246597542 | G | A | 1 | a0001c0001t0002g0007 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.379+5601G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246597542 | |||||||
| chr1:246597601 | T | C | 2 | a0002c0002t0015g0166 a0008c0011t0015g0211 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.379+5660T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246597601 | |||||||
| chr1:246597649 | T | C | 6 | a0001c0001t0002g0244 a0001c0001t0003g0245 a0001c0001t0003g0246 others(3): Show |
6 | HG00423.hp2 NA18985.hp1 NA18999.hp2 others(3): Show |
intron_variant | MODIFIER | c.379+5708T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246597649 | |||||||
| chr1:246597973 | GTATT | G | 268 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(265): Show |
271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.379+6055_379+6058d others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246597973 | ||||||
| chr1:246597973 | GTATTTAT others(5): Show |
G | 4 | a0002c0002t0001g0169 a0002c0002t0006g0031 a0002c0002t0006g0032 others(1): Show |
4 | HG02486.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.379+6047_379+6058d others(14): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246597973 | ||||||
| chr1:246598087 | T | G | 1 | a0001c0001t0003g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.379+6146T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246598087 | |||||||
| chr1:246598149 | A | AT | 13 | a0001c0001t0001g0167 a0001c0001t0001g0297 a0003c0003t0001g0034 others(10): Show |
13 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.379+6224dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246598149 | ||||||
| chr1:246598149 | AT | A | 208 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0054 others(205): Show |
211 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.379+6224delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246598149 | ||||||
| chr1:246598477 | A | G | 1 | a0001c0001t0003g0204 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.379+6536A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246598477 | |||||||
| chr1:246598615 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0288 |
2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.379+6674G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246598615 | |||||||
| chr1:246598719 | T | C | 17 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0165 others(14): Show |
17 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.379+6778T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246598719 | |||||||
| chr1:246599129 | T | A | 1 | a0001c0001t0004g0155 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.379+7188T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246599129 | |||||||
| chr1:246599176 | GA | G | 19 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0165 others(16): Show |
19 | HG01884.hp2 HG02040.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.379+7249delA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246599176 | ||||||
| chr1:246599232 | A | G | 2 | a0002c0002t0015g0166 a0008c0011t0015g0211 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.379+7291A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246599232 | |||||||
| chr1:246599283 | C | T | 1 | a0002c0002t0001g0169 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.379+7342C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246599283 | |||||||
| chr1:246599388 | G | A | 2 | a0001c0001t0002g0102 a0001c0001t0002g0103 |
2 | HG00140.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.379+7447G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246599388 | |||||||
| chr1:246599437 | C | G | 9 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.379+7496C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246599437 | |||||||
| chr1:246599480 | G | C | 1 | a0001c0001t0022g0087 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.379+7539G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246599480 | |||||||
| chr1:246599552 | G | A | 1 | a0002c0002t0001g0118 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.379+7611G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246599552 | |||||||
| chr1:246599600 | T | C | 1 | a0002c0002t0001g0144 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.379+7659T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246599600 | |||||||
| chr1:246599680 | A | G | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.379+7739A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246599680 | |||||||
| chr1:246599756 | T | G | 1 | a0001c0001t0003g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.379+7815T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246599756 | |||||||
| chr1:246599837 | A | T | 1 | a0001c0001t0003g0142 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.379+7896A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246599837 | |||||||
| chr1:246600164 | G | A | 1 | a0001c0001t0008g0023 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.379+8223G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246600164 | |||||||
| chr1:246600191 | G | A | 1 | a0001c0001t0004g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.379+8250G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246600191 | |||||||
| chr1:246600308 | T | C | 1 | a0001c0012t0002g0276 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.379+8367T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246600308 | |||||||
| chr1:246600748 | G | A | 1 | a0001c0001t0003g0057 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.379+8807G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246600748 | |||||||
| chr1:246600751 | G | A | 1 | a0001c0001t0024g0270 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.379+8810G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246600751 | |||||||
| chr1:246601101 | T | C | 5 | a0003c0003t0001g0034 a0003c0003t0001g0035 a0003c0003t0004g0036 others(2): Show |
5 | HG01243.hp1 HG02451.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.379+9160T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246601101 | |||||||
| chr1:246601163 | G | C | 1 | a0001c0001t0003g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.379+9222G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246601163 | |||||||
| chr1:246601323 | C | T | 7 | a0001c0001t0001g0175 a0001c0001t0004g0019 a0001c0001t0004g0020 others(4): Show |
7 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.379+9382C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246601323 | |||||||
| chr1:246601337 | G | T | 1 | a0001c0001t0001g0264 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.379+9396G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246601337 | |||||||
| chr1:246601372 | C | CACCAACT others(7): Show |
1 | a0001c0001t0018g0254 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.379+9433_379+9446d others(16): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246601372 | ||||||
| chr1:246601555 | G | A | 13 | a0003c0003t0001g0034 a0003c0003t0001g0035 a0003c0003t0001g0039 others(10): Show |
13 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.379+9614G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246601555 | |||||||
| chr1:246601624 | A | G | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.379+9683A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246601624 | |||||||
| chr1:246601637 | A | G | 1 | a0002c0002t0001g0126 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.379+9696A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246601637 | |||||||
| chr1:246601655 | G | A | 1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.379+9714G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246601655 | |||||||
| chr1:246601660 | G | A | 7 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(4): Show |
7 | HG00140.hp1 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.379+9719G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246601660 | |||||||
| chr1:246601700 | G | A | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.379+9759G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246601700 | |||||||
| chr1:246601845 | A | G | 1 | a0001c0001t0003g0083 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.379+9904A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246601845 | |||||||
| chr1:246601895 | A | C | 8 | a0001c0001t0001g0132 a0001c0001t0004g0018 a0001c0001t0004g0044 others(5): Show |
8 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.379+9954A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246601895 | |||||||
| chr1:246602075 | T | G | 1 | a0001c0001t0004g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.379+10134T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246602075 | |||||||
| chr1:246602504 | A | G | 26 | a0001c0001t0001g0196 a0001c0001t0001g0208 a0001c0001t0001g0217 others(23): Show |
26 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(23): Show |
intron_variant | MODIFIER | c.379+10563A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246602504 | |||||||
| chr1:246602535 | C | G | 1 | a0001c0001t0001g0281 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.379+10594C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246602535 | |||||||
| chr1:246602706 | C | T | 7 | a0001c0001t0003g0005 a0003c0003t0001g0034 a0003c0003t0001g0035 others(4): Show |
7 | HG00733.hp1 HG01891.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.379+10765C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246602706 | |||||||
| chr1:246602836 | G | C | 3 | a0001c0001t0001g0214 a0001c0001t0001g0251 a0001c0001t0002g0199 |
3 | HG00673.hp1 NA18969.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.379+10895G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246602836 | |||||||
| chr1:246602897 | G | GT | 150 | a0001c0001t0001g0024 a0001c0001t0001g0090 a0001c0001t0001g0091 others(147): Show |
150 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.379+10968dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246602897 | ||||||
| chr1:246602897 | GT | G | 95 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(92): Show |
98 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.379+10968delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246602897 | ||||||
| chr1:246602953 | G | T | 1 | a0006c0007t0003g0265 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.379+11012G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246602953 | |||||||
| chr1:246602968 | A | G | 1 | a0001c0001t0004g0155 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.379+11027A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246602968 | |||||||
| chr1:246602970 | G | A | 7 | a0001c0001t0001g0175 a0001c0001t0004g0019 a0001c0001t0004g0020 others(4): Show |
7 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.379+11029G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246602970 | |||||||
| chr1:246603133 | A | G | 271 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(268): Show |
274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.379+11192A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246603133 | |||||||
| chr1:246603345 | CTAAA | C | 125 | a0001c0001t0001g0024 a0001c0001t0001g0132 a0001c0001t0001g0154 others(122): Show |
125 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.379+11407_379+1141 others(8): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246603345 | ||||||
| chr1:246603508 | T | TTTAAACA others(11): Show |
1 | a0001c0001t0002g0300 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.379+11568_379+1158 others(22): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246603508 | ||||||
| chr1:246603585 | A | T | 2 | a0002c0002t0015g0166 a0008c0011t0015g0211 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.379+11644A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246603585 | |||||||
| chr1:246603696 | A | T | 271 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(268): Show |
274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.379+11755A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246603696 | |||||||
| chr1:246603742 | A | G | 3 | a0002c0002t0015g0166 a0008c0011t0015g0211 a0010c0008t0001g0159 |
3 | HG02622.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.379+11801A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246603742 | |||||||
| chr1:246603889 | C | T | 273 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(270): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.379+11948C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246603889 | |||||||
| chr1:246603975 | C | T | 1 | a0003c0003t0001g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.379+12034C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246603975 | |||||||
| chr1:246603994 | C | T | 7 | a0001c0001t0001g0175 a0001c0001t0004g0019 a0001c0001t0004g0020 others(4): Show |
7 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.379+12053C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246603994 | |||||||
| chr1:246604238 | C | T | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.379+12297C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246604238 | |||||||
| chr1:246604272 | A | G | 4 | a0001c0001t0003g0072 a0001c0001t0003g0094 a0002c0002t0015g0166 others(1): Show |
4 | HG01952.hp2 HG01981.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.379+12331A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246604272 | |||||||
| chr1:246604304 | A | AAGAAACG others(53): Show |
1 | a0001c0001t0001g0091 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.379+12365_379+1242 others(64): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246604304 | ||||||
| chr1:246604628 | A | T | 1 | a0001c0001t0013g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.379+12687A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246604628 | |||||||
| chr1:246604673 | AT | A | 4 | a0001c0001t0001g0158 a0001c0001t0004g0155 a0001c0001t0004g0156 others(1): Show |
4 | HG01109.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.379+12734delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246604673 | ||||||
| chr1:246604681 | T | TATTTTGA others(36): Show |
2 | a0002c0002t0015g0166 a0008c0011t0015g0211 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.379+12743_379+1278 others(47): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246604681 | ||||||
| chr1:246604697 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.379+12756C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246604697 | |||||||
| chr1:246604723 | C | T | 1 | a0001c0001t0003g0098 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.379+12782C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246604723 | |||||||
| chr1:246604729 | C | T | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.379+12788C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246604729 | |||||||
| chr1:246604743 | A | C | 2 | a0001c0001t0001g0154 a0001c0001t0001g0289 |
2 | HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.379+12802A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246604743 | |||||||
| chr1:246604831 | G | A | 1 | a0001c0001t0005g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.379+12890G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246604831 | |||||||
| chr1:246604838 | T | G | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.379+12897T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246604838 | |||||||
| chr1:246605043 | C | A | 1 | a0001c0001t0002g0181 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.379+13102C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605043 | |||||||
| chr1:246605182 | A | T | 2 | a0003c0003t0004g0160 a0007c0005t0023g0045 |
2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.379+13241A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605182 | |||||||
| chr1:246605203 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.379+13262A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605203 | |||||||
| chr1:246605304 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0003g0176 |
2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.379+13363G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605304 | |||||||
| chr1:246605360 | G | C | 59 | a0001c0001t0001g0063 a0001c0001t0001g0078 a0001c0001t0001g0088 others(56): Show |
60 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.379+13419G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605360 | |||||||
| chr1:246605363 | T | A | 1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.379+13422T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605363 | |||||||
| chr1:246605368 | G | T | 5 | a0002c0002t0001g0029 a0002c0002t0001g0120 a0002c0002t0001g0128 others(2): Show |
5 | HG00741.hp2 HG01175.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.379+13427G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605368 | |||||||
| chr1:246605437 | C | T | 1 | a0001c0001t0004g0017 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.379+13496C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605437 | |||||||
| chr1:246605467 | G | A | 3 | a0001c0001t0002g0256 a0001c0001t0002g0259 a0001c0001t0002g0282 |
3 | HG02698.hp1 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.379+13526G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605467 | |||||||
| chr1:246605487 | T | A | 1 | a0001c0001t0003g0280 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.379+13546T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605487 | |||||||
| chr1:246605503 | T | C | 1 | a0001c0001t0002g0279 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.379+13562T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605503 | |||||||
| chr1:246605536 | G | A | 3 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0007g0141 |
3 | NA18960.hp2 NA18979.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.379+13595G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605536 | |||||||
| chr1:246605541 | A | G | 276 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(273): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.379+13600A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605541 | |||||||
| chr1:246605549 | G | A | 9 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(6): Show |
9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.379+13608G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605549 | |||||||
| chr1:246605571 | C | T | 1 | a0001c0001t0002g0007 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.379+13630C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605571 | |||||||
| chr1:246605641 | C | T | 1 | a0001c0001t0002g0074 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.379+13700C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605641 | |||||||
| chr1:246605648 | GGGTGTCT others(73): Show |
G | 72 | a0001c0001t0001g0027 a0001c0001t0001g0063 a0001c0001t0001g0078 others(69): Show |
73 | HG00423.hp2 HG00558.hp2 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.379+13787_379+1386 others(84): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605648 | ||||||
| chr1:246605666 | G | T | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.379+13725G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605666 | |||||||
| chr1:246605669 | CGTGTCTT others(13): Show |
C | 15 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(12): Show |
15 | HG00735.hp1 HG00741.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.379+13787_379+1380 others(24): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605669 | ||||||
| chr1:246605688 | A | G | 2 | a0001c0001t0001g0164 a0001c0001t0003g0290 |
2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.379+13747A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605688 | |||||||
| chr1:246605689 | G | C | 2 | a0001c0001t0001g0164 a0001c0001t0003g0290 |
2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.379+13748G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605689 | |||||||
| chr1:246605709 | G | GGTGTCTT others(13): Show |
4 | a0001c0001t0001g0208 a0001c0001t0001g0239 a0001c0001t0002g0227 others(1): Show |
4 | HG00735.hp2 HG02056.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.379+13786_379+1378 others(24): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605709 | ||||||
| chr1:246605709 | GGTGTCTT others(33): Show |
G | 1 | a0001c0001t0001g0164 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.379+13807_379+1384 others(44): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605709 | ||||||
| chr1:246605723 | GGGGTAGG others(72): Show |
G | 1 | a0001c0001t0003g0068 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.379+13786_379+1386 others(83): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605723 | ||||||
| chr1:246605728 | A | G | 30 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(27): Show |
32 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.379+13787A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605728 | |||||||
| chr1:246605729 | G | C | 30 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(27): Show |
32 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.379+13788G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605729 | |||||||
| chr1:246605729 | GGTGTCTT others(13): Show |
G | 1 | a0001c0001t0003g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.379+13807_379+1382 others(24): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605729 | ||||||
| chr1:246605738 | C | T | 12 | a0003c0003t0001g0034 a0003c0003t0001g0035 a0003c0003t0001g0039 others(9): Show |
12 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.379+13797C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605738 | |||||||
| chr1:246605748 | G | A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(31): Show |
36 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.379+13807G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605748 | |||||||
| chr1:246605749 | C | CGTGTCTT others(13): Show |
5 | a0001c0001t0001g0202 a0001c0001t0002g0300 a0001c0001t0005g0152 others(2): Show |
5 | HG01261.hp1 HG01433.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.379+13847_379+1386 others(24): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605749 | ||||||
| chr1:246605749 | C | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(31): Show |
36 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.379+13808C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605749 | |||||||
| chr1:246605758 | C | T | 1 | a0001c0001t0002g0241 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.379+13817C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605758 | |||||||
| chr1:246605759 | GGCCGGGG others(53): Show |
G | 30 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(27): Show |
32 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.379+13847_379+1390 others(64): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605759 | ||||||
| chr1:246605762 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0165 a0001c0001t0001g0167 others(2): Show |
5 | HG02647.hp1 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.379+13821C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605762 | |||||||
| chr1:246605768 | A | G | 14 | a0001c0001t0001g0013 a0001c0001t0001g0165 a0001c0001t0001g0167 others(11): Show |
14 | HG01884.hp2 HG01981.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.379+13827A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605768 | |||||||
| chr1:246605769 | G | C | 14 | a0001c0001t0001g0013 a0001c0001t0001g0165 a0001c0001t0001g0167 others(11): Show |
14 | HG01884.hp2 HG01981.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.379+13828G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605769 | |||||||
| chr1:246605776 | T | C | 1 | a0001c0001t0003g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.379+13835T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605776 | |||||||
| chr1:246605788 | A | G | 4 | a0001c0001t0001g0208 a0001c0001t0001g0239 a0001c0001t0002g0227 others(1): Show |
4 | HG00735.hp2 HG02056.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.379+13847A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605788 | |||||||
| chr1:246605789 | G | C | 4 | a0001c0001t0001g0208 a0001c0001t0001g0239 a0001c0001t0002g0227 others(1): Show |
4 | HG00735.hp2 HG02056.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.379+13848G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605789 | |||||||
| chr1:246605789 | G | GGTGTCTT others(33): Show |
103 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(100): Show |
103 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.379+13866_379+1386 others(44): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605789 | ||||||
| chr1:246605789 | G | GGTGTCTT others(53): Show |
1 | a0001c0001t0002g0207 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.379+13866_379+1386 others(64): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605789 | ||||||
| chr1:246605789 | G | GGTGTCTT others(13): Show |
14 | a0001c0001t0005g0203 a0003c0003t0001g0034 a0003c0003t0001g0035 others(11): Show |
14 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.379+13858_379+1387 others(24): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605789 | ||||||
| chr1:246605789 | G | GGTGTCTT others(33): Show |
9 | a0001c0001t0001g0132 a0001c0001t0004g0018 a0001c0001t0004g0044 others(6): Show |
9 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.379+13877_379+1387 others(44): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605789 | ||||||
| chr1:246605799 | GGCCGGGG others(13): Show |
G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0288 |
2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.379+13867_379+1388 others(24): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605799 | ||||||
| chr1:246605802 | C | CGGGGTAG others(34): Show |
1 | a0001c0001t0003g0292 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.379+13866_379+1386 others(45): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605802 | ||||||
| chr1:246605808 | G | A | 1 | a0001c0001t0018g0254 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.379+13867G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605808 | |||||||
| chr1:246605809 | C | G | 1 | a0001c0001t0018g0254 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.379+13868C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605809 | |||||||
| chr1:246605817 | C | T | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.379+13876C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605817 | |||||||
| chr1:246605819 | A | G | 236 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0063 others(233): Show |
237 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.379+13878A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605819 | |||||||
| chr1:246605825 | G | GGTGCGTG others(19): Show |
1 | a0001c0001t0018g0254 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.379+13886_379+1388 others(30): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605825 | ||||||
| chr1:246605828 | A | G | 31 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(28): Show |
33 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.379+13887A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605828 | |||||||
| chr1:246605829 | G | C | 31 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(28): Show |
33 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.379+13888G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605829 | |||||||
| chr1:246605912 | C | T | 249 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0027 others(246): Show |
252 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.379+13971C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605912 | |||||||
| chr1:246605973 | G | A | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.379+14032G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605973 | |||||||
| chr1:246605974 | GC | G | 5 | a0001c0001t0004g0018 a0001c0001t0004g0044 a0001c0001t0004g0148 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.379+14037delC | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246605974 | ||||||
| chr1:246605978 | C | T | 1 | a0001c0001t0002g0181 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.379+14037C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246605978 | |||||||
| chr1:246606001 | C | T | 2 | a0004c0004t0003g0190 a0004c0004t0003g0191 |
2 | HG02451.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.379+14060C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606001 | |||||||
| chr1:246606066 | G | A | 1 | a0001c0001t0002g0311 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.379+14125G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606066 | |||||||
| chr1:246606068 | G | A | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.379+14127G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606068 | |||||||
| chr1:246606100 | A | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0054 others(98): Show |
104 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.379+14159A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606100 | |||||||
| chr1:246606108 | G | A | 3 | a0001c0001t0001g0168 a0001c0001t0003g0135 a0001c0001t0003g0176 |
3 | HG02145.hp2 HG03195.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.379+14167G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606108 | |||||||
| chr1:246606143 | G | A | 125 | a0001c0001t0001g0024 a0001c0001t0001g0132 a0001c0001t0001g0154 others(122): Show |
125 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.379+14202G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606143 | |||||||
| chr1:246606207 | G | A | 2 | a0002c0002t0015g0166 a0008c0011t0015g0211 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.379+14266G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606207 | |||||||
| chr1:246606246 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.379+14305G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606246 | |||||||
| chr1:246606291 | T | G | 13 | a0003c0003t0001g0034 a0003c0003t0001g0035 a0003c0003t0001g0039 others(10): Show |
13 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.379+14350T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606291 | |||||||
| chr1:246606312 | C | A | 1 | a0001c0001t0004g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.379+14371C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606312 | |||||||
| chr1:246606364 | C | T | 1 | a0001c0001t0003g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.379+14423C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606364 | |||||||
| chr1:246606403 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.379+14462G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606403 | |||||||
| chr1:246606417 | A | G | 1 | a0001c0001t0003g0218 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.379+14476A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606417 | |||||||
| chr1:246606441 | C | G | 267 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(264): Show |
270 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.379+14500C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606441 | |||||||
| chr1:246606454 | G | C | 3 | a0001c0001t0002g0207 a0004c0004t0003g0182 a0004c0004t0003g0183 |
3 | HG02896.hp2 HG02897.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.379+14513G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606454 | |||||||
| chr1:246606462 | C | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0287 a0001c0001t0008g0022 others(1): Show |
4 | HG02145.hp1 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.379+14521C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606462 | |||||||
| chr1:246606542 | C | T | 9 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(6): Show |
9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.379+14601C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606542 | |||||||
| chr1:246606596 | G | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0054 others(98): Show |
104 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.379+14655G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606596 | |||||||
| chr1:246606597 | T | C | 1 | a0001c0001t0001g0253 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.379+14656T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606597 | |||||||
| chr1:246606612 | A | G | 100 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0054 others(97): Show |
103 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.379+14671A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606612 | |||||||
| chr1:246606618 | G | C | 103 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0054 others(100): Show |
106 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.379+14677G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606618 | |||||||
| chr1:246606674 | C | T | 2 | a0001c0001t0004g0273 a0002c0002t0001g0169 |
2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.379+14733C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606674 | |||||||
| chr1:246606718 | G | A | 2 | a0001c0001t0001g0164 a0001c0001t0003g0290 |
2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.380-14711G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606718 | |||||||
| chr1:246606811 | G | A | 1 | a0002c0002t0001g0115 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.380-14618G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606811 | |||||||
| chr1:246606813 | T | C | 1 | a0002c0002t0001g0115 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.380-14616T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606813 | |||||||
| chr1:246606864 | C | T | 6 | a0004c0004t0003g0117 a0004c0004t0003g0182 a0004c0004t0003g0183 others(3): Show |
6 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.380-14565C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606864 | |||||||
| chr1:246606909 | G | A | 312 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(309): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.380-14520G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606909 | |||||||
| chr1:246606957 | C | G | 251 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0027 others(248): Show |
254 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.380-14472C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606957 | |||||||
| chr1:246606960 | A | G | 1 | a0001c0001t0001g0247 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.380-14469A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606960 | |||||||
| chr1:246606963 | T | C | 1 | a0001c0001t0001g0164 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.380-14466T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606963 | |||||||
| chr1:246606974 | TTAG | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0054 others(98): Show |
104 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.380-14453_380-1445 others(7): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246606974 | ||||||
| chr1:246606999 | C | T | 1 | a0001c0001t0002g0230 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.380-14430C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246606999 | |||||||
| chr1:246607043 | G | T | 9 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(6): Show |
9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.380-14386G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607043 | |||||||
| chr1:246607054 | G | A | 10 | a0001c0001t0001g0130 a0001c0001t0003g0064 a0001c0001t0003g0067 others(7): Show |
10 | HG00423.hp2 HG01255.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.380-14375G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607054 | |||||||
| chr1:246607268 | G | T | 1 | a0001c0001t0001g0261 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.380-14161G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607268 | |||||||
| chr1:246607302 | C | T | 6 | a0004c0004t0003g0117 a0004c0004t0003g0182 a0004c0004t0003g0183 others(3): Show |
6 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.380-14127C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607302 | |||||||
| chr1:246607325 | A | G | 125 | a0001c0001t0001g0024 a0001c0001t0001g0132 a0001c0001t0001g0154 others(122): Show |
125 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.380-14104A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607325 | |||||||
| chr1:246607334 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0288 |
2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.380-14095A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607334 | |||||||
| chr1:246607407 | G | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(85): Show |
91 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.380-14022G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607407 | |||||||
| chr1:246607586 | G | A | 1 | a0001c0001t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.380-13843G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607586 | |||||||
| chr1:246607600 | C | T | 6 | a0002c0002t0001g0004 a0002c0002t0001g0111 a0002c0002t0001g0113 others(3): Show |
7 | HG02040.hp1 HG02074.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.380-13829C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607600 | |||||||
| chr1:246607678 | A | AT | 267 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(264): Show |
270 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.380-13751_380-1375 others(5): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607678 | |||||||
| chr1:246607687 | C | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0054 others(97): Show |
103 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.380-13742C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607687 | |||||||
| chr1:246607803 | C | T | 1 | a0001c0001t0002g0279 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.380-13626C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607803 | |||||||
| chr1:246607881 | G | T | 14 | a0001c0001t0001g0013 a0001c0001t0001g0165 a0001c0001t0001g0167 others(11): Show |
14 | HG01884.hp2 HG01981.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.380-13548G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607881 | |||||||
| chr1:246607919 | G | A | 1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.380-13510G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607919 | |||||||
| chr1:246607930 | A | C | 1 | a0001c0001t0004g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.380-13499A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607930 | |||||||
| chr1:246607984 | G | A | 13 | a0003c0003t0001g0034 a0003c0003t0001g0035 a0003c0003t0001g0039 others(10): Show |
13 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.380-13445G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246607984 | |||||||
| chr1:246608030 | G | A | 1 | a0001c0001t0002g0283 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.380-13399G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246608030 | |||||||
| chr1:246608056 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.380-13373G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246608056 | |||||||
| chr1:246608136 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0004g0028 |
2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.380-13293C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246608136 | |||||||
| chr1:246608160 | A | C | 1 | a0001c0006t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.380-13269A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246608160 | |||||||
| chr1:246608165 | AAATAAAT others(4): Show |
A | 1 | a0001c0001t0004g0006 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.380-13249_380-1323 others(15): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246608165 | ||||||
| chr1:246608178 | AT | A | 11 | a0003c0003t0001g0034 a0003c0003t0001g0035 a0003c0003t0001g0039 others(8): Show |
11 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.380-13250delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246608178 | |||||||
| chr1:246608387 | T | C | 9 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(6): Show |
9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.380-13042T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246608387 | |||||||
| chr1:246608647 | C | G | 1 | a0001c0001t0001g0132 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.380-12782C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246608647 | |||||||
| chr1:246608649 | C | T | 1 | a0001c0001t0004g0006 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.380-12780C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246608649 | |||||||
| chr1:246608702 | G | A | 1 | a0001c0001t0002g0129 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.380-12727G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246608702 | |||||||
| chr1:246608717 | G | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0054 others(99): Show |
105 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.380-12712G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246608717 | |||||||
| chr1:246608909 | C | T | 11 | a0003c0003t0001g0034 a0003c0003t0001g0035 a0003c0003t0001g0039 others(8): Show |
11 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.380-12520C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246608909 | |||||||
| chr1:246609056 | G | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0054 others(98): Show |
104 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.380-12373G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246609056 | |||||||
| chr1:246609352 | G | T | 9 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(6): Show |
9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.380-12077G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246609352 | |||||||
| chr1:246609404 | C | T | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.380-12025C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246609404 | |||||||
| chr1:246610102 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.380-11327G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610102 | |||||||
| chr1:246610125 | A | G | 1 | a0001c0001t0022g0087 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.380-11304A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610125 | |||||||
| chr1:246610149 | G | A | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.380-11280G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610149 | |||||||
| chr1:246610282 | AAAAC | A | 10 | a0001c0001t0001g0027 a0001c0001t0001g0168 a0001c0001t0001g0243 others(7): Show |
10 | HG02083.hp2 HG02145.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.380-11131_380-1112 others(8): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246610282 | ||||||
| chr1:246610441 | A | T | 1 | a0001c0001t0001g0164 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.380-10988A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610441 | |||||||
| chr1:246610503 | C | G | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.380-10926C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610503 | |||||||
| chr1:246610515 | G | GT | 4 | a0001c0001t0001g0242 a0001c0001t0004g0016 a0001c0001t0004g0134 others(1): Show |
4 | HG02074.hp2 HG02602.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.380-10907dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246610515 | ||||||
| chr1:246610538 | G | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0054 others(99): Show |
105 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.380-10891G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610538 | |||||||
| chr1:246610556 | G | A | 2 | a0001c0001t0003g0248 a0001c0001t0003g0271 |
2 | HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.380-10873G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610556 | |||||||
| chr1:246610604 | C | G | 1 | a0001c0001t0002g0230 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.380-10825C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610604 | |||||||
| chr1:246610614 | G | A | 1 | a0001c0001t0003g0077 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.380-10815G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610614 | |||||||
| chr1:246610770 | C | T | 2 | a0001c0001t0010g0224 a0001c0001t0010g0225 |
2 | HG00558.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.380-10659C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610770 | |||||||
| chr1:246610786 | G | A | 2 | a0001c0001t0001g0313 a0001c0001t0002g0312 |
2 | HG00673.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.380-10643G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610786 | |||||||
| chr1:246610790 | G | A | 3 | a0001c0001t0002g0256 a0001c0001t0002g0259 a0001c0001t0002g0282 |
3 | HG02698.hp1 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.380-10639G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610790 | |||||||
| chr1:246610809 | C | T | 2 | a0003c0003t0004g0160 a0007c0005t0023g0045 |
2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.380-10620C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610809 | |||||||
| chr1:246610810 | G | A | 2 | a0001c0001t0001g0309 a0001c0001t0002g0310 |
2 | NA18993.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.380-10619G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610810 | |||||||
| chr1:246610826 | T | C | 1 | a0001c0001t0004g0134 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.380-10603T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610826 | |||||||
| chr1:246610827 | C | T | 1 | a0001c0001t0004g0134 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.380-10602C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610827 | |||||||
| chr1:246610856 | C | T | 1 | a0001c0001t0002g0236 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.380-10573C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610856 | |||||||
| chr1:246610912 | G | A | 2 | a0002c0002t0015g0166 a0008c0011t0015g0211 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.380-10517G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610912 | |||||||
| chr1:246610926 | C | T | 1 | a0002c0002t0001g0169 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.380-10503C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610926 | |||||||
| chr1:246610979 | A | G | 12 | a0001c0001t0001g0013 a0001c0001t0001g0165 a0001c0001t0001g0167 others(9): Show |
12 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.380-10450A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610979 | |||||||
| chr1:246610998 | C | T | 1 | a0003c0003t0004g0036 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.380-10431C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246610998 | |||||||
| chr1:246611262 | G | A | 1 | a0007c0005t0023g0045 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.380-10167G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246611262 | |||||||
| chr1:246611298 | T | C | 103 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0054 others(100): Show |
106 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.380-10131T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246611298 | |||||||
| chr1:246611317 | A | G | 1 | a0001c0001t0009g0015 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.380-10112A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246611317 | |||||||
| chr1:246611325 | T | C | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.380-10104T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246611325 | |||||||
| chr1:246611339 | G | GT | 7 | a0002c0002t0001g0139 a0004c0004t0003g0117 a0004c0004t0003g0182 others(4): Show |
7 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.380-10081dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246611339 | ||||||
| chr1:246611348 | T | A | 3 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0003g0314 |
3 | HG02809.hp1 HG03516.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.380-10081T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246611348 | |||||||
| chr1:246611349 | A | T | 6 | a0004c0004t0003g0117 a0004c0004t0003g0182 a0004c0004t0003g0183 others(3): Show |
6 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.380-10080A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246611349 | |||||||
| chr1:246611393 | G | A | 9 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(6): Show |
9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.380-10036G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246611393 | |||||||
| chr1:246611459 | G | A | 1 | a0002c0002t0001g0269 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.380-9970G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246611459 | |||||||
| chr1:246611490 | A | C | 1 | a0001c0001t0003g0068 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.380-9939A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246611490 | |||||||
| chr1:246611607 | G | GA | 6 | a0001c0001t0001g0214 a0001c0001t0001g0305 a0001c0001t0002g0101 others(3): Show |
6 | HG00733.hp2 HG02083.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.380-9815dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246611607 | ||||||
| chr1:246611615 | C | A | 98 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(95): Show |
101 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.380-9814C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246611615 | |||||||
| chr1:246611778 | C | G | 1 | a0001c0001t0001g0304 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.380-9651C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246611778 | |||||||
| chr1:246611786 | C | CATAGCAG others(19): Show |
1 | a0001c0001t0002g0219 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.380-9641_380-9616d others(28): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246611786 | ||||||
| chr1:246612124 | G | A | 1 | a0001c0001t0001g0302 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.380-9305G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246612124 | |||||||
| chr1:246612148 | T | C | 2 | a0001c0001t0001g0164 a0001c0001t0003g0290 |
2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.380-9281T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246612148 | |||||||
| chr1:246612183 | T | C | 6 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0093 others(3): Show |
6 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.380-9246T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246612183 | |||||||
| chr1:246612328 | A | G | 1 | a0001c0001t0002g0222 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.380-9101A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246612328 | |||||||
| chr1:246612566 | T | A | 1 | a0001c0001t0002g0240 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.380-8863T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246612566 | |||||||
| chr1:246612569 | GT | G | 4 | a0001c0001t0003g0048 a0002c0002t0001g0137 a0004c0004t0003g0117 others(1): Show |
4 | HG02818.hp2 HG02896.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.380-8853delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246612569 | ||||||
| chr1:246612684 | C | T | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.380-8745C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246612684 | |||||||
| chr1:246612686 | A | AGACCAGT others(20): Show |
1 | a0001c0001t0001g0305 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.380-8742_380-8716d others(29): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246612686 | ||||||
| chr1:246612751 | G | T | 9 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(6): Show |
9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.380-8678G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246612751 | |||||||
| chr1:246612765 | G | A | 2 | a0001c0001t0001g0091 a0001c0001t0003g0057 |
2 | HG01515.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.380-8664G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246612765 | |||||||
| chr1:246612898 | A | T | 1 | a0001c0001t0001g0253 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.380-8531A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246612898 | |||||||
| chr1:246612899 | T | A | 1 | a0001c0001t0001g0253 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.380-8530T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246612899 | |||||||
| chr1:246612930 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.380-8499A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246612930 | |||||||
| chr1:246613055 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(86): Show |
92 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.380-8374C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613055 | |||||||
| chr1:246613131 | G | T | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.380-8298G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613131 | |||||||
| chr1:246613179 | C | G | 185 | a0001c0001t0001g0024 a0001c0001t0001g0054 a0001c0001t0001g0055 others(182): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.380-8250C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613179 | |||||||
| chr1:246613428 | G | T | 1 | a0001c0001t0002g0219 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.380-8001G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613428 | |||||||
| chr1:246613431 | T | G | 1 | a0001c0001t0002g0219 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.380-7998T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613431 | |||||||
| chr1:246613466 | C | T | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.380-7963C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613466 | |||||||
| chr1:246613577 | AGGGTACT others(15): Show |
A | 1 | a0001c0001t0001g0214 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.380-7851_380-7830d others(24): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613577 | |||||||
| chr1:246613654 | T | TCCCCCTC others(914): Show |
1 | a0001c0001t0001g0251 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.380-7774_380-7773i others(923): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613654 | ||||||
| chr1:246613656 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.380-7773T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613656 | |||||||
| chr1:246613656 | T | TCTCCCCC others(1188): Show |
1 | a0002c0002t0001g0269 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.380-7770_380-7769i others(1197): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(958): Show |
1 | a0001c0001t0001g0298 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(967): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(957): Show |
2 | a0001c0001t0001g0264 a0001c0001t0001g0301 |
2 | NA18942.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.380-7767_380-7766i others(966): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(949): Show |
1 | a0001c0001t0001g0299 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(958): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(990): Show |
1 | a0001c0001t0004g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(999): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(977): Show |
1 | a0001c0001t0002g0244 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(986): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(971): Show |
1 | a0001c0001t0001g0096 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(980): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(960): Show |
1 | a0001c0001t0004g0273 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(969): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(965): Show |
1 | a0001c0001t0002g0187 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(974): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(964): Show |
1 | a0001c0001t0002g0103 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(973): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(961): Show |
1 | a0001c0001t0001g0255 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(970): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(1170): Show |
1 | a0003c0003t0001g0039 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1179): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(992): Show |
1 | a0001c0001t0003g0176 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1001): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(960): Show |
1 | a0001c0001t0001g0267 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(969): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(967): Show |
1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(976): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(980): Show |
1 | a0001c0001t0003g0083 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(989): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(979): Show |
1 | a0001c0001t0003g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(988): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(963): Show |
1 | a0001c0001t0004g0156 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(972): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(975): Show |
1 | a0002c0002t0001g0111 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(984): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(980): Show |
1 | a0001c0001t0003g0005 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(989): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(959): Show |
1 | a0001c0001t0001g0223 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(968): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(975): Show |
1 | a0001c0001t0003g0069 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(984): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(963): Show |
1 | a0001c0001t0002g0185 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(972): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(968): Show |
1 | a0001c0001t0001g0097 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(977): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(974): Show |
1 | a0002c0002t0001g0149 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(983): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(1362): Show |
1 | a0001c0001t0001g0305 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1371): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(931): Show |
1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(940): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(895): Show |
1 | a0001c0001t0001g0272 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(904): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(970): Show |
1 | a0001c0001t0003g0109 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(979): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(957): Show |
1 | a0001c0001t0003g0292 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(966): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(969): Show |
1 | a0001c0001t0003g0314 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(978): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(953): Show |
1 | a0001c0001t0001g0268 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(962): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(963): Show |
1 | a0001c0001t0002g0051 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(972): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(963): Show |
1 | a0001c0001t0002g0099 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(972): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(964): Show |
1 | a0001c0001t0019g0106 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(973): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(964): Show |
1 | a0001c0001t0002g0184 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(973): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(962): Show |
18 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0060 others(15): Show |
19 | HG00280.hp1 HG00738.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.380-7767_380-7766i others(971): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(961): Show |
1 | a0001c0001t0002g0310 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(970): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(961): Show |
1 | a0001c0001t0002g0062 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(970): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(961): Show |
1 | a0001c0001t0001g0309 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(970): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(969): Show |
1 | a0001c0001t0003g0073 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(978): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(970): Show |
1 | a0001c0001t0003g0135 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(979): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(969): Show |
1 | a0001c0001t0001g0302 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(978): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(1577): Show |
1 | a0001c0001t0008g0174 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1586): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(1579): Show |
1 | a0001c0001t0001g0287 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1588): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(998): Show |
1 | a0001c0001t0001g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1007): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(970): Show |
2 | a0001c0001t0001g0013 a0001c0001t0001g0288 |
2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.380-7767_380-7766i others(979): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(959): Show |
1 | a0001c0001t0001g0154 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(968): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(1469): Show |
1 | a0001c0001t0001g0294 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1478): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(958): Show |
29 | a0001c0001t0001g0158 a0001c0001t0001g0196 a0001c0001t0001g0202 others(26): Show |
29 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.380-7767_380-7766i others(967): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(969): Show |
1 | a0001c0001t0002g0080 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(978): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(969): Show |
1 | a0001c0001t0003g0072 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(978): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(968): Show |
39 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0078 others(36): Show |
40 | HG00423.hp2 HG00558.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.380-7767_380-7766i others(977): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(958): Show |
1 | a0001c0001t0002g0282 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(967): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(950): Show |
1 | a0005c0010t0002g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(959): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(932): Show |
1 | a0001c0001t0002g0181 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(941): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(978): Show |
1 | a0001c0001t0002g0173 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(987): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(957): Show |
1 | a0001c0001t0001g0291 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(966): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(968): Show |
1 | a0001c0001t0012g0001 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.380-7767_380-7766i others(977): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(969): Show |
3 | a0001c0001t0004g0018 a0001c0001t0004g0044 a0001c0001t0004g0148 |
3 | HG02280.hp1 HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.380-7767_380-7766i others(978): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(933): Show |
1 | a0001c0001t0001g0263 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(942): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(978): Show |
2 | a0003c0003t0001g0034 a0003c0003t0001g0035 |
2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.380-7767_380-7766i others(987): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(1403): Show |
1 | a0003c0003t0004g0038 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1412): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(1403): Show |
2 | a0003c0003t0004g0036 a0003c0003t0004g0037 |
2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.380-7767_380-7766i others(1412): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(1168): Show |
3 | a0003c0003t0001g0040 a0003c0003t0001g0041 a0003c0003t0001g0046 |
3 | HG01891.hp2 HG02723.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.380-7767_380-7766i others(1177): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(960): Show |
2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.380-7767_380-7766i others(969): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(973): Show |
1 | a0002c0002t0001g0122 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(982): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(973): Show |
1 | a0002c0002t0001g0169 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(982): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(972): Show |
2 | a0002c0002t0001g0177 a0002c0002t0013g0178 |
2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.380-7767_380-7766i others(981): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(973): Show |
1 | a0002c0002t0001g0113 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(982): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(973): Show |
1 | a0002c0002t0001g0095 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(982): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(972): Show |
25 | a0002c0002t0001g0004 a0002c0002t0001g0029 a0002c0002t0001g0108 others(22): Show |
26 | HG00639.hp2 HG00741.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.380-7767_380-7766i others(981): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(972): Show |
1 | a0002c0002t0001g0118 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(981): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(955): Show |
1 | a0001c0001t0001g0195 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(964): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(972): Show |
1 | a0002c0002t0006g0033 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(981): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(1168): Show |
1 | a0003c0003t0001g0042 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1177): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(1575): Show |
1 | a0001c0001t0008g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1584): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(970): Show |
1 | a0001c0001t0003g0068 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(979): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(970): Show |
1 | a0001c0001t0022g0087 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(979): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(971): Show |
1 | a0001c0001t0001g0090 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(980): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(970): Show |
3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0002g0079 |
3 | HG01517.hp1 HG03239.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.380-7767_380-7766i others(979): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(993): Show |
1 | a0001c0001t0004g0171 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1002): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(993): Show |
1 | a0001c0001t0001g0168 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1002): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(1031): Show |
5 | a0001c0001t0001g0027 a0001c0001t0004g0028 a0001c0001t0009g0012 others(2): Show |
5 | HG02818.hp1 HG02976.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.380-7767_380-7766i others(1040): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(992): Show |
1 | a0001c0001t0001g0167 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1001): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(991): Show |
1 | a0001c0001t0001g0180 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1000): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(992): Show |
1 | a0001c0001t0001g0164 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1001): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(1103): Show |
1 | a0001c0001t0004g0172 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1112): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(991): Show |
1 | a0001c0001t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1000): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(981): Show |
1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(990): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(983): Show |
1 | a0007c0005t0023g0045 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(992): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(1072): Show |
1 | a0003c0003t0004g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1081): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(969): Show |
1 | a0001c0001t0004g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(978): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(967): Show |
1 | a0001c0001t0004g0006 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(976): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(673): Show |
5 | a0004c0004t0003g0117 a0004c0004t0003g0183 a0004c0004t0003g0190 others(2): Show |
5 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.380-7767_380-7766i others(682): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(961): Show |
1 | a0001c0001t0002g0102 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(970): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(965): Show |
1 | a0001c0001t0004g0016 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(974): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(964): Show |
1 | a0008c0011t0015g0211 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(973): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(963): Show |
1 | a0002c0002t0015g0166 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(972): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(965): Show |
1 | a0001c0001t0001g0175 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(974): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(988): Show |
2 | a0001c0001t0004g0020 a0001c0001t0004g0021 |
2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.380-7767_380-7766i others(997): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(964): Show |
5 | a0001c0001t0004g0017 a0001c0001t0004g0019 a0001c0001t0005g0025 others(2): Show |
5 | HG02647.hp2 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.380-7767_380-7766i others(973): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(972): Show |
1 | a0001c0001t0001g0165 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(981): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(964): Show |
1 | a0001c0001t0004g0153 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(973): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(968): Show |
1 | a0001c0001t0003g0104 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(977): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(973): Show |
1 | a0002c0002t0001g0139 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(982): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(955): Show |
1 | a0001c0001t0001g0217 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(964): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(944): Show |
1 | a0001c0001t0014g0162 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(953): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(967): Show |
1 | a0001c0001t0004g0151 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(976): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(968): Show |
1 | a0001c0001t0002g0101 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(977): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(971): Show |
1 | a0002c0002t0001g0198 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(980): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(677): Show |
1 | a0004c0004t0003g0182 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(686): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(933): Show |
1 | a0001c0001t0002g0219 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(942): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(1193): Show |
1 | a0001c0006t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1202): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(1163): Show |
1 | a0003c0003t0001g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1172): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(959): Show |
1 | a0001c0001t0002g0193 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(968): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(961): Show |
1 | a0001c0001t0002g0231 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(970): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(998): Show |
1 | a0001c0001t0001g0213 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(1007): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(959): Show |
1 | a0001c0001t0002g0222 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(968): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(960): Show |
1 | a0001c0001t0002g0236 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(969): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(959): Show |
2 | a0001c0001t0001g0192 a0001c0001t0001g0232 |
2 | HG00621.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.380-7767_380-7766i others(968): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(959): Show |
1 | a0001c0001t0001g0296 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.380-7767_380-7766i others(968): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(959): Show |
1 | a0001c0001t0001g0258 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(968): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(935): Show |
1 | a0001c0001t0002g0241 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(944): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(973): Show |
1 | a0001c0001t0025g0286 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(982): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(972): Show |
2 | a0001c0001t0002g0300 a0001c0001t0018g0254 |
2 | NA18955.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.380-7767_380-7766i others(981): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(959): Show |
1 | a0001c0001t0001g0228 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(968): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(959): Show |
1 | a0001c0001t0003g0295 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(968): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(959): Show |
1 | a0001c0001t0003g0221 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(968): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(958): Show |
36 | a0001c0001t0001g0205 a0001c0001t0001g0216 a0001c0001t0001g0229 others(33): Show |
36 | HG00280.hp2 HG00642.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.380-7767_380-7766i others(967): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(957): Show |
1 | a0001c0001t0001g0242 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(966): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(958): Show |
2 | a0001c0001t0002g0256 a0001c0001t0002g0259 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.380-7767_380-7766i others(967): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(958): Show |
1 | a0001c0001t0001g0316 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(967): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCCC others(966): Show |
1 | a0001c0001t0001g0253 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.380-7767_380-7766i others(975): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCTC others(986): Show |
1 | a0002c0002t0001g0137 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.380-7768_380-7767i others(995): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCTC others(978): Show |
1 | a0001c0001t0001g0125 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.380-7768_380-7767i others(987): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCTC others(964): Show |
1 | a0001c0001t0002g0283 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.380-7768_380-7767i others(973): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613656 | T | TCTCTCTC others(982): Show |
1 | a0001c0001t0001g0214 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.380-7768_380-7767i others(991): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613656 | ||||||
| chr1:246613663 | T | C | 5 | a0001c0001t0001g0132 a0001c0001t0004g0134 a0001c0001t0016g0133 others(2): Show |
5 | HG01243.hp2 HG02622.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.380-7766T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613663 | |||||||
| chr1:246613666 | T | C | 3 | a0001c0001t0001g0132 a0001c0001t0004g0134 a0002c0002t0006g0031 |
3 | HG02622.hp2 HG02897.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.380-7763T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613666 | |||||||
| chr1:246613670 | T | TCTCCCTC others(953): Show |
2 | a0001c0001t0001g0132 a0002c0002t0006g0031 |
2 | HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.380-7759_380-7758i others(962): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613670 | |||||||
| chr1:246613670 | T | TCTCCCTC others(949): Show |
1 | a0001c0001t0004g0134 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.380-7759_380-7758i others(958): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613670 | |||||||
| chr1:246613671 | A | C | 5 | a0001c0001t0001g0132 a0001c0001t0004g0134 a0001c0001t0016g0133 others(2): Show |
5 | HG01243.hp2 HG02622.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.380-7758A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613671 | |||||||
| chr1:246613679 | T | C | 2 | a0001c0001t0016g0133 a0002c0002t0006g0032 |
2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.380-7750T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613679 | |||||||
| chr1:246613680 | C | T | 2 | a0001c0001t0016g0133 a0002c0002t0006g0032 |
2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.380-7749C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613680 | |||||||
| chr1:246613681 | C | CACCTCCT others(958): Show |
1 | a0002c0002t0006g0032 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.380-7748_380-7747i others(967): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613681 | |||||||
| chr1:246613681 | C | CACCTCCT others(957): Show |
1 | a0001c0001t0016g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.380-7748_380-7747i others(966): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613681 | |||||||
| chr1:246613681 | C | CTCTCTA | 3 | a0001c0001t0001g0132 a0001c0001t0004g0134 a0002c0002t0006g0031 |
3 | HG02622.hp2 HG02897.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.380-7743_380-7742i others(8): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246613681 | ||||||
| chr1:246613734 | T | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(97): Show |
103 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.380-7695T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613734 | |||||||
| chr1:246613737 | A | G | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.380-7692A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613737 | |||||||
| chr1:246613826 | T | G | 1 | a0001c0001t0001g0275 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.380-7603T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613826 | |||||||
| chr1:246613878 | A | T | 1 | a0004c0004t0003g0182 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.380-7551A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613878 | |||||||
| chr1:246613914 | G | A | 1 | a0001c0001t0003g0248 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.380-7515G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613914 | |||||||
| chr1:246613939 | C | T | 5 | a0001c0001t0001g0132 a0001c0001t0004g0134 a0001c0001t0016g0133 others(2): Show |
5 | HG01243.hp2 HG02622.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.380-7490C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613939 | |||||||
| chr1:246613983 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.380-7446T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246613983 | |||||||
| chr1:246614143 | A | C | 1 | a0001c0001t0003g0005 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.380-7286A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614143 | |||||||
| chr1:246614147 | T | G | 1 | a0001c0001t0003g0005 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.380-7282T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614147 | |||||||
| chr1:246614148 | T | A | 1 | a0001c0001t0003g0005 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.380-7281T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614148 | |||||||
| chr1:246614149 | C | G | 1 | a0001c0001t0003g0005 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.380-7280C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614149 | |||||||
| chr1:246614150 | G | A | 1 | a0001c0001t0003g0005 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.380-7279G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614150 | |||||||
| chr1:246614151 | C | G | 1 | a0001c0001t0003g0005 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.380-7278C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614151 | |||||||
| chr1:246614183 | C | T | 7 | a0001c0001t0001g0168 a0001c0001t0002g0170 a0001c0001t0002g0173 others(4): Show |
7 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.380-7246C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614183 | |||||||
| chr1:246614300 | A | C | 2 | a0001c0001t0001g0164 a0001c0001t0003g0290 |
2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.380-7129A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614300 | |||||||
| chr1:246614315 | G | A | 9 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(6): Show |
9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.380-7114G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614315 | |||||||
| chr1:246614512 | AT | A | 114 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0027 others(111): Show |
117 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.380-6900delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246614512 | ||||||
| chr1:246614512 | ATT | A | 151 | a0001c0001t0001g0024 a0001c0001t0001g0090 a0001c0001t0001g0092 others(148): Show |
151 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.380-6901_380-6900d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246614512 | ||||||
| chr1:246614512 | ATTT | A | 10 | a0001c0001t0001g0223 a0001c0001t0001g0262 a0001c0001t0001g0263 others(7): Show |
10 | HG00280.hp2 HG00558.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.380-6902_380-6900d others(5): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246614512 | ||||||
| chr1:246614526 | T | C | 2 | a0001c0001t0002g0007 a0001c0001t0002g0274 |
2 | HG00642.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.380-6903T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614526 | |||||||
| chr1:246614535 | C | T | 1 | a0001c0001t0003g0218 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.380-6894C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614535 | |||||||
| chr1:246614589 | A | G | 1 | a0001c0001t0002g0102 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.380-6840A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614589 | |||||||
| chr1:246614611 | A | G | 1 | a0001c0001t0003g0221 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.380-6818A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614611 | |||||||
| chr1:246614620 | C | G | 1 | a0001c0001t0001g0217 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.380-6809C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614620 | |||||||
| chr1:246614623 | C | T | 1 | a0001c0001t0002g0080 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.380-6806C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614623 | |||||||
| chr1:246614664 | G | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.380-6765G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614664 | |||||||
| chr1:246614875 | A | G | 1 | a0001c0001t0002g0102 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.380-6554A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246614875 | |||||||
| chr1:246615113 | A | G | 1 | a0001c0001t0003g0005 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.380-6316A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246615113 | |||||||
| chr1:246615121 | A | T | 1 | a0001c0001t0001g0213 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.380-6308A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246615121 | |||||||
| chr1:246615168 | T | C | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.380-6261T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246615168 | |||||||
| chr1:246615170 | C | CA | 6 | a0001c0001t0001g0195 a0001c0001t0001g0253 a0001c0001t0002g0062 others(3): Show |
6 | HG01109.hp1 HG01255.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.380-6249dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246615170 | ||||||
| chr1:246615199 | G | A | 9 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(6): Show |
9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.380-6230G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246615199 | |||||||
| chr1:246615206 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.380-6223C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246615206 | |||||||
| chr1:246615215 | A | G | 10 | a0001c0001t0001g0132 a0001c0001t0004g0018 a0001c0001t0004g0044 others(7): Show |
10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.380-6214A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246615215 | |||||||
| chr1:246615228 | C | T | 10 | a0001c0001t0001g0132 a0001c0001t0004g0018 a0001c0001t0004g0044 others(7): Show |
10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.380-6201C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246615228 | |||||||
| chr1:246615302 | C | T | 1 | a0002c0002t0001g0131 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.380-6127C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246615302 | |||||||
| chr1:246615470 | C | T | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.380-5959C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246615470 | |||||||
| chr1:246615471 | G | A | 1 | a0001c0006t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.380-5958G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246615471 | |||||||
| chr1:246615673 | G | A | 3 | a0001c0001t0017g0010 a0002c0002t0015g0166 a0008c0011t0015g0211 |
3 | HG01981.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.380-5756G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246615673 | |||||||
| chr1:246615818 | C | T | 1 | a0005c0010t0002g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.380-5611C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246615818 | |||||||
| chr1:246615819 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0288 |
2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.380-5610G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246615819 | |||||||
| chr1:246615879 | C | CA | 6 | a0001c0001t0001g0232 a0001c0001t0002g0074 a0001c0001t0002g0103 others(3): Show |
6 | HG00140.hp2 HG01099.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.380-5539dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246615879 | ||||||
| chr1:246616088 | G | A | 1 | a0001c0001t0001g0002 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.380-5341G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246616088 | |||||||
| chr1:246616322 | G | C | 1 | a0001c0001t0002g0102 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.380-5107G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246616322 | |||||||
| chr1:246616323 | A | G | 1 | a0001c0001t0001g0301 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.380-5106A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246616323 | |||||||
| chr1:246616424 | G | T | 9 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(6): Show |
9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.380-5005G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246616424 | |||||||
| chr1:246616511 | T | C | 154 | a0001c0001t0001g0024 a0001c0001t0001g0090 a0001c0001t0001g0092 others(151): Show |
154 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.380-4918T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246616511 | |||||||
| chr1:246616524 | C | T | 3 | a0001c0001t0011g0206 a0001c0001t0011g0210 a0001c0001t0011g0220 |
3 | HG01934.hp1 NA18971.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.380-4905C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246616524 | |||||||
| chr1:246616755 | A | G | 1 | a0002c0002t0013g0178 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.380-4674A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246616755 | |||||||
| chr1:246616916 | AT | A | 3 | a0001c0001t0001g0097 a0001c0001t0001g0165 a0001c0001t0001g0309 |
3 | HG01516.hp1 HG02809.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.380-4507delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246616916 | ||||||
| chr1:246616953 | C | T | 6 | a0004c0004t0003g0117 a0004c0004t0003g0182 a0004c0004t0003g0183 others(3): Show |
6 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.380-4476C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246616953 | |||||||
| chr1:246617255 | C | G | 109 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(106): Show |
112 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.380-4174C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246617255 | |||||||
| chr1:246617317 | T | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(108): Show |
114 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.380-4112T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246617317 | |||||||
| chr1:246617346 | T | C | 1 | a0001c0006t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.380-4083T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246617346 | |||||||
| chr1:246617499 | A | AG | 6 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0093 others(3): Show |
6 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.380-3926dupG | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246617499 | ||||||
| chr1:246617725 | C | A | 1 | a0001c0001t0002g0193 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.380-3704C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246617725 | |||||||
| chr1:246617725 | C | G | 1 | a0001c0001t0001g0180 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.380-3704C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246617725 | |||||||
| chr1:246617751 | A | G | 4 | a0001c0001t0001g0158 a0001c0001t0004g0155 a0001c0001t0004g0156 others(1): Show |
4 | HG01109.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.380-3678A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246617751 | |||||||
| chr1:246617773 | C | T | 17 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0165 others(14): Show |
17 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.380-3656C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246617773 | |||||||
| chr1:246618018 | A | T | 1 | a0001c0001t0002g0230 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.380-3411A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246618018 | |||||||
| chr1:246618088 | A | G | 1 | a0002c0002t0001g0144 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.380-3341A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246618088 | |||||||
| chr1:246618098 | T | C | 1 | a0002c0002t0007g0140 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.380-3331T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246618098 | |||||||
| chr1:246618769 | G | A | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.380-2660G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246618769 | |||||||
| chr1:246618810 | C | T | 3 | a0002c0002t0015g0166 a0008c0011t0015g0211 a0010c0008t0001g0159 |
3 | HG02622.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.380-2619C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246618810 | |||||||
| chr1:246618829 | G | A | 7 | a0001c0001t0001g0119 a0001c0001t0003g0135 a0001c0001t0003g0245 others(4): Show |
7 | HG00423.hp2 NA18985.hp2 NA18999.hp2 others(4): Show |
intron_variant | MODIFIER | c.380-2600G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246618829 | |||||||
| chr1:246618929 | T | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(106): Show |
112 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.380-2500T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246618929 | |||||||
| chr1:246619104 | A | G | 24 | a0001c0001t0001g0164 a0001c0001t0001g0175 a0001c0001t0003g0290 others(21): Show |
24 | HG00735.hp1 HG02451.hp2 HG02622.hp1 others(21): Show |
intron_variant | MODIFIER | c.380-2325A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246619104 | |||||||
| chr1:246619154 | G | GA | 119 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0054 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.380-2263dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246619154 | ||||||
| chr1:246619154 | G | GAA | 16 | a0001c0001t0001g0175 a0001c0001t0001g0281 a0001c0001t0001g0291 others(13): Show |
16 | HG00735.hp1 HG00741.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.380-2264_380-2263d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246619154 | ||||||
| chr1:246619154 | G | GAAA | 8 | a0001c0001t0004g0016 a0004c0004t0003g0117 a0004c0004t0003g0182 others(5): Show |
8 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.380-2265_380-2263d others(5): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246619154 | ||||||
| chr1:246619198 | C | T | 21 | a0001c0001t0001g0192 a0001c0001t0001g0205 a0001c0001t0001g0213 others(18): Show |
21 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.380-2231C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246619198 | |||||||
| chr1:246619246 | A | G | 1 | a0001c0001t0002g0047 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.380-2183A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246619246 | |||||||
| chr1:246619248 | G | A | 1 | a0006c0007t0003g0265 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.380-2181G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246619248 | |||||||
| chr1:246619315 | G | A | 6 | a0004c0004t0003g0117 a0004c0004t0003g0182 a0004c0004t0003g0183 others(3): Show |
6 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.380-2114G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246619315 | |||||||
| chr1:246619839 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.380-1590C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246619839 | |||||||
| chr1:246619852 | GGTGCATA others(47): Show |
G | 1 | a0001c0001t0001g0175 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.380-1551_380-1498d others(56): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246619852 | ||||||
| chr1:246619852 | GGTGCATA others(153): Show |
G | 2 | a0001c0001t0001g0168 a0001c0001t0003g0176 |
2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.380-1473_380-1314d others(2): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246619852 | ||||||
| chr1:246619876 | G | A | 1 | a0001c0001t0004g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.380-1553G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246619876 | |||||||
| chr1:246619878 | CACACTCT others(369): Show |
C | 10 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0093 others(7): Show |
10 | HG00140.hp1 HG01517.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.380-1205_380-830de others(1): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246619878 | ||||||
| chr1:246619912 | TAC | T | 3 | a0002c0002t0015g0166 a0008c0011t0015g0211 a0010c0008t0001g0159 |
3 | HG02622.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.380-1512_380-1511d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246619912 | ||||||
| chr1:246619932 | AACACTAC others(637): Show |
A | 1 | a0001c0001t0003g0218 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.380-1391_380-748de others(1): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246619932 | ||||||
| chr1:246619948 | C | T | 21 | a0001c0001t0001g0013 a0001c0001t0001g0165 a0001c0001t0001g0167 others(18): Show |
21 | HG00733.hp1 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.380-1481C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246619948 | |||||||
| chr1:246619958 | C | T | 3 | a0002c0002t0015g0166 a0008c0011t0015g0211 a0010c0008t0001g0159 |
3 | HG02622.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.380-1471C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246619958 | |||||||
| chr1:246619984 | A | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(103): Show |
109 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.380-1445A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246619984 | |||||||
| chr1:246620002 | C | T | 106 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(103): Show |
109 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.380-1427C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620002 | |||||||
| chr1:246620024 | C | T | 2 | a0002c0002t0001g0115 a0002c0002t0001g0116 |
2 | HG02004.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.380-1405C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620024 | |||||||
| chr1:246620038 | C | A | 3 | a0001c0001t0001g0303 a0001c0001t0002g0007 a0001c0001t0002g0274 |
3 | HG00642.hp1 HG00741.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.380-1391C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620038 | |||||||
| chr1:246620038 | CACACTCT others(583): Show |
C | 1 | a0002c0002t0001g0114 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.380-1313_380-724de others(1): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620038 | ||||||
| chr1:246620041 | ACT | A | 3 | a0001c0001t0001g0303 a0002c0002t0001g0126 a0004c0004t0003g0182 |
3 | HG02135.hp2 HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.380-1385_380-1384d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620041 | ||||||
| chr1:246620041 | ACTCTACA others(211): Show |
A | 5 | a0004c0004t0003g0117 a0004c0004t0003g0183 a0004c0004t0003g0190 others(2): Show |
5 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.380-1385_380-1168d others(2): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620041 | ||||||
| chr1:246620043 | TCTACAGG others(45): Show |
T | 1 | a0001c0001t0002g0279 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.380-1365_380-1314d others(54): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620043 | ||||||
| chr1:246620066 | C | G | 2 | a0002c0002t0015g0166 a0008c0011t0015g0211 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.380-1363C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620066 | |||||||
| chr1:246620069 | GCATACAC others(366): Show |
G | 1 | a0001c0001t0001g0303 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.380-1359_380-987de others(1): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620069 | |||||||
| chr1:246620092 | A | C | 3 | a0001c0001t0002g0007 a0001c0001t0002g0274 a0010c0008t0001g0159 |
3 | HG00642.hp1 HG00741.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.380-1337A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620092 | |||||||
| chr1:246620095 | A | ACT | 5 | a0001c0001t0002g0007 a0001c0001t0002g0274 a0002c0002t0015g0166 others(2): Show |
5 | HG00642.hp1 HG00741.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.380-1333_380-1332d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620095 | ||||||
| chr1:246620102 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.380-1327G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620102 | |||||||
| chr1:246620106 | G | A | 2 | a0002c0002t0015g0166 a0008c0011t0015g0211 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.380-1323G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620106 | |||||||
| chr1:246620115 | A | AG | 3 | a0001c0001t0003g0204 a0001c0001t0003g0257 a0006c0007t0003g0265 |
3 | HG03017.hp2 HG03704.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.380-1314_380-1313i others(3): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620115 | |||||||
| chr1:246620115 | ATC | A | 5 | a0001c0001t0002g0007 a0001c0001t0002g0274 a0002c0002t0015g0166 others(2): Show |
5 | HG00642.hp1 HG00741.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.380-1313_380-1312d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620115 | |||||||
| chr1:246620120 | G | C | 5 | a0001c0001t0002g0007 a0001c0001t0002g0274 a0002c0002t0015g0166 others(2): Show |
5 | HG00642.hp1 HG00741.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.380-1309G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620120 | |||||||
| chr1:246620126 | T | C | 3 | a0001c0001t0003g0204 a0001c0001t0003g0257 a0006c0007t0003g0265 |
3 | HG03017.hp2 HG03704.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.380-1303T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620126 | |||||||
| chr1:246620146 | A | C | 2 | a0002c0002t0015g0166 a0008c0011t0015g0211 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.380-1283A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620146 | |||||||
| chr1:246620149 | ACTACAGG others(103): Show |
A | 30 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0060 others(27): Show |
31 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.380-1259_380-1150d others(2): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620149 | ||||||
| chr1:246620149 | ACTACAGG others(209): Show |
A | 4 | a0001c0001t0003g0083 a0001c0001t0003g0104 a0001c0001t0014g0162 others(1): Show |
4 | HG01169.hp1 HG02896.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.380-1259_380-1044d others(2): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620149 | ||||||
| chr1:246620149 | ACTACAGG others(263): Show |
A | 8 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(5): Show |
8 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.380-1259_380-990de others(1): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620149 | ||||||
| chr1:246620149 | ACTACAGG others(477): Show |
A | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.380-1259_380-776de others(1): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620149 | ||||||
| chr1:246620151 | TACAGGGA others(582): Show |
T | 3 | a0001c0001t0003g0204 a0001c0001t0003g0257 a0006c0007t0003g0265 |
3 | HG03017.hp2 HG03704.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.380-1277_380-689de others(1): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620151 | |||||||
| chr1:246620162 | C | T | 1 | a0005c0010t0002g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.380-1267C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620162 | |||||||
| chr1:246620163 | G | A | 5 | a0003c0003t0001g0040 a0003c0003t0001g0041 a0003c0003t0001g0042 others(2): Show |
5 | HG00733.hp1 HG01891.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.380-1266G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620163 | |||||||
| chr1:246620169 | ATCGTGGT others(49): Show |
A | 57 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0078 others(54): Show |
59 | HG00423.hp2 HG00558.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.380-1259_380-1204d others(58): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620169 | |||||||
| chr1:246620171 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.380-1258C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620171 | |||||||
| chr1:246620174 | G | C | 1 | a0001c0001t0004g0021 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.380-1255G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620174 | |||||||
| chr1:246620190 | G | A | 121 | a0001c0001t0001g0024 a0001c0001t0001g0132 a0001c0001t0001g0154 others(118): Show |
121 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.380-1239G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620190 | |||||||
| chr1:246620198 | GGCACACT others(50): Show |
G | 1 | a0001c0001t0001g0305 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.380-1230_380-1174d others(59): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620198 | |||||||
| chr1:246620200 | C | A | 4 | a0001c0001t0002g0007 a0001c0001t0002g0274 a0001c0001t0004g0021 others(1): Show |
4 | HG00642.hp1 HG00741.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.380-1229C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620200 | |||||||
| chr1:246620203 | A | T | 2 | a0002c0002t0015g0166 a0008c0011t0015g0211 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.380-1226A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620203 | |||||||
| chr1:246620223 | ATC | A | 122 | a0001c0001t0001g0024 a0001c0001t0001g0132 a0001c0001t0001g0154 others(119): Show |
122 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.380-1205_380-1204d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620223 | |||||||
| chr1:246620228 | G | C | 179 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0063 others(176): Show |
181 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.380-1201G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620228 | |||||||
| chr1:246620228 | GGTGCATA others(47): Show |
G | 1 | a0001c0001t0004g0021 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.380-1169_380-1116d others(56): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620228 | ||||||
| chr1:246620244 | G | A | 2 | a0001c0001t0002g0007 a0001c0001t0002g0274 |
2 | HG00642.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.380-1185G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620244 | |||||||
| chr1:246620254 | A | C | 3 | a0002c0002t0015g0166 a0008c0011t0015g0211 a0010c0008t0001g0159 |
3 | HG02622.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.380-1175A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620254 | |||||||
| chr1:246620257 | ACTCTACA others(155): Show |
A | 56 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0078 others(53): Show |
58 | HG00423.hp2 HG00558.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.380-1169_380-1008d others(2): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620257 | ||||||
| chr1:246620259 | T | A | 3 | a0001c0001t0001g0305 a0001c0001t0002g0007 a0001c0001t0002g0274 |
3 | HG00642.hp1 HG00741.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.380-1170T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620259 | |||||||
| chr1:246620259 | TCTACAGG others(45): Show |
T | 1 | a0001c0001t0008g0174 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.380-1115_380-1064d others(54): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620259 | ||||||
| chr1:246620269 | G | A | 2 | a0002c0002t0015g0166 a0008c0011t0015g0211 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.380-1160G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620269 | |||||||
| chr1:246620308 | A | C | 1 | a0001c0001t0004g0021 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.380-1121A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620308 | |||||||
| chr1:246620311 | A | ACT | 6 | a0001c0001t0001g0305 a0001c0001t0002g0007 a0001c0001t0002g0274 others(3): Show |
6 | HG00642.hp1 HG00741.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.380-1117_380-1116d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620311 | ||||||
| chr1:246620311 | ACTACAGG others(315): Show |
A | 1 | a0001c0001t0001g0180 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.380-1063_380-742de others(1): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620311 | ||||||
| chr1:246620324 | C | T | 2 | a0003c0003t0004g0160 a0007c0005t0023g0045 |
2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.380-1105C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620324 | |||||||
| chr1:246620331 | A | ATC | 6 | a0001c0001t0001g0096 a0004c0004t0003g0117 a0004c0004t0003g0183 others(3): Show |
6 | HG01517.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.380-1098_380-1097i others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620331 | |||||||
| chr1:246620334 | C | G | 6 | a0001c0001t0001g0096 a0004c0004t0003g0117 a0004c0004t0003g0183 others(3): Show |
6 | HG01517.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.380-1095C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620334 | |||||||
| chr1:246620337 | GCATACAC others(44): Show |
G | 1 | a0001c0001t0011g0206 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.380-1091_380-1041d others(53): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620337 | |||||||
| chr1:246620337 | GCATACAC others(98): Show |
G | 118 | a0001c0001t0001g0024 a0001c0001t0001g0132 a0001c0001t0001g0154 others(115): Show |
118 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.380-1091_380-987de others(1): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620337 | |||||||
| chr1:246620360 | A | C | 3 | a0001c0001t0004g0021 a0002c0002t0015g0166 a0008c0011t0015g0211 |
3 | HG02622.hp1 HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.380-1069A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620360 | |||||||
| chr1:246620360 | AACACTCT others(47): Show |
A | 1 | a0001c0001t0009g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.380-1015_380-962de others(55): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620360 | ||||||
| chr1:246620363 | ACT | A | 40 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0060 others(37): Show |
41 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.380-1063_380-1062d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620363 | ||||||
| chr1:246620365 | T | A | 1 | a0001c0001t0001g0096 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.380-1064T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620365 | |||||||
| chr1:246620385 | A | ATC | 30 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0060 others(27): Show |
31 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.380-1044_380-1043i others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620385 | |||||||
| chr1:246620386 | GTCGTGCA others(152): Show |
G | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.380-1037_380-879de others(1): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620386 | ||||||
| chr1:246620388 | C | G | 30 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0060 others(27): Show |
31 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.380-1041C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620388 | |||||||
| chr1:246620391 | GCATACAC others(44): Show |
G | 4 | a0001c0001t0001g0305 a0001c0001t0002g0007 a0001c0001t0002g0274 others(1): Show |
4 | HG00642.hp1 HG00741.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.380-1037_380-987de others(52): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620391 | |||||||
| chr1:246620394 | T | C | 1 | a0001c0001t0011g0206 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.380-1035T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620394 | |||||||
| chr1:246620414 | C | A | 11 | a0001c0001t0003g0083 a0001c0001t0003g0104 a0001c0001t0004g0021 others(8): Show |
11 | HG01169.hp1 HG02451.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.380-1015C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620414 | |||||||
| chr1:246620417 | ACT | A | 40 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0060 others(37): Show |
41 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.380-1009_380-1008d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620417 | ||||||
| chr1:246620419 | T | C | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.380-1010T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620419 | |||||||
| chr1:246620419 | TCTACAGG others(153): Show |
T | 1 | a0001c0001t0001g0096 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.380-955_380-796del | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620419 | ||||||
| chr1:246620440 | G | A | 1 | a0001c0001t0011g0206 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.380-989G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620440 | |||||||
| chr1:246620442 | C | CGTGCATA others(209): Show |
1 | a0003c0003t0001g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.380-908_380-907ins others(216): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620442 | ||||||
| chr1:246620442 | C | G | 1 | a0001c0001t0011g0206 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.380-987C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620442 | |||||||
| chr1:246620448 | T | C | 123 | a0001c0001t0001g0024 a0001c0001t0001g0132 a0001c0001t0001g0154 others(120): Show |
123 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.380-981T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620448 | |||||||
| chr1:246620468 | A | C | 30 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0060 others(27): Show |
31 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.380-961A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620468 | |||||||
| chr1:246620471 | A | ACT | 30 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0060 others(27): Show |
31 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.380-957_380-956dup others(2): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620471 | ||||||
| chr1:246620491 | ATC | A | 3 | a0001c0001t0004g0021 a0002c0002t0015g0166 a0008c0011t0015g0211 |
3 | HG02622.hp1 HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.380-937_380-936del others(2): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620491 | |||||||
| chr1:246620494 | G | A | 110 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(107): Show |
110 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.380-935G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620494 | |||||||
| chr1:246620496 | G | C | 3 | a0001c0001t0004g0021 a0002c0002t0015g0166 a0008c0011t0015g0211 |
3 | HG02622.hp1 HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.380-933G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620496 | |||||||
| chr1:246620522 | A | C | 104 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(101): Show |
107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.380-907A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620522 | |||||||
| chr1:246620545 | ATC | A | 104 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(101): Show |
107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.380-883_380-882del others(2): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620545 | |||||||
| chr1:246620550 | G | C | 104 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(101): Show |
107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.380-879G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620550 | |||||||
| chr1:246620556 | T | C | 2 | a0001c0001t0011g0206 a0010c0008t0001g0159 |
2 | NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.380-873T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620556 | |||||||
| chr1:246620563 | G | T | 1 | a0001c0001t0003g0104 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.380-866G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620563 | |||||||
| chr1:246620579 | A | ACT | 74 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0078 others(71): Show |
76 | HG00423.hp2 HG00558.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.380-849_380-848dup others(2): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620579 | ||||||
| chr1:246620579 | A | ACTCTACA others(431): Show |
2 | a0002c0002t0015g0166 a0008c0011t0015g0211 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.380-848_380-847ins others(438): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620579 | ||||||
| chr1:246620579 | A | T | 1 | a0001c0001t0011g0206 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.380-850A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620579 | |||||||
| chr1:246620608 | T | C | 123 | a0001c0001t0001g0024 a0001c0001t0001g0132 a0001c0001t0001g0154 others(120): Show |
123 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.380-821T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620608 | |||||||
| chr1:246620628 | A | C | 1 | a0001c0001t0003g0218 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.380-801A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620628 | |||||||
| chr1:246620630 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0003g0290 |
2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.380-799C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620630 | |||||||
| chr1:246620656 | CGTGCATA others(48): Show |
C | 5 | a0001c0001t0001g0027 a0001c0001t0004g0028 a0001c0001t0009g0012 others(2): Show |
5 | HG02818.hp1 HG02976.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.380-730_380-676del others(55): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620656 | ||||||
| chr1:246620662 | T | C | 1 | a0001c0001t0011g0206 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.380-767T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620662 | |||||||
| chr1:246620699 | G | A | 1 | a0001c0001t0011g0206 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.380-730G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620699 | |||||||
| chr1:246620709 | G | A | 4 | a0001c0001t0001g0158 a0001c0001t0004g0155 a0001c0001t0004g0156 others(1): Show |
4 | HG01109.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.380-720G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620709 | |||||||
| chr1:246620712 | G | A | 1 | a0001c0001t0011g0206 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.380-717G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620712 | |||||||
| chr1:246620717 | T | C | 134 | a0001c0001t0001g0024 a0001c0001t0001g0090 a0001c0001t0001g0092 others(131): Show |
134 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.380-712T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620717 | |||||||
| chr1:246620737 | A | C | 1 | a0001c0001t0011g0206 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.380-692A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620737 | |||||||
| chr1:246620740 | A | ACT | 132 | a0001c0001t0001g0024 a0001c0001t0001g0090 a0001c0001t0001g0092 others(129): Show |
132 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.380-688_380-687dup others(2): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 246620740 | ||||||
| chr1:246620750 | G | A | 1 | a0001c0001t0011g0206 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.380-679G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620750 | |||||||
| chr1:246620754 | A | G | 11 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(8): Show |
11 | HG00735.hp1 HG02486.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.380-675A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620754 | |||||||
| chr1:246620764 | A | G | 1 | a0001c0001t0011g0206 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.380-665A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620764 | |||||||
| chr1:246620768 | A | G | 13 | a0001c0001t0001g0132 a0001c0001t0004g0018 a0001c0001t0004g0044 others(10): Show |
13 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.380-661A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620768 | |||||||
| chr1:246620778 | T | C | 1 | a0001c0001t0011g0206 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.380-651T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620778 | |||||||
| chr1:246620781 | G | A | 5 | a0001c0001t0001g0027 a0001c0001t0004g0028 a0001c0001t0009g0012 others(2): Show |
5 | HG02818.hp1 HG02976.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.380-648G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620781 | |||||||
| chr1:246620818 | G | A | 1 | a0001c0001t0010g0284 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.380-611G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620818 | |||||||
| chr1:246620832 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(86): Show |
92 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.380-597C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620832 | |||||||
| chr1:246620885 | A | G | 2 | a0001c0001t0003g0005 a0001c0001t0003g0209 |
2 | NA18962.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.380-544A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620885 | |||||||
| chr1:246620965 | G | A | 3 | a0002c0002t0015g0166 a0008c0011t0015g0211 a0010c0008t0001g0159 |
3 | HG02622.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.380-464G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246620965 | |||||||
| chr1:246621373 | T | C | 1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.380-56T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | chr1 | 246621373 | |||||||
| chr1:246621723 | A | C | 1 | a0001c0001t0003g0104 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.585+89A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246621723 | |||||||
| chr1:246621811 | A | C | 115 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(112): Show |
115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.585+177A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246621811 | |||||||
| chr1:246621892 | G | A | 2 | a0003c0003t0004g0160 a0007c0005t0023g0045 |
2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.585+258G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246621892 | |||||||
| chr1:246621896 | A | G | 2 | a0002c0002t0015g0166 a0008c0011t0015g0211 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.585+262A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246621896 | |||||||
| chr1:246622043 | G | C | 1 | a0002c0002t0001g0144 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.585+409G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246622043 | |||||||
| chr1:246622094 | C | T | 6 | a0001c0001t0002g0099 a0001c0001t0002g0101 a0001c0001t0002g0102 others(3): Show |
6 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.585+460C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246622094 | |||||||
| chr1:246622146 | C | A | 97 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(94): Show |
100 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.585+512C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246622146 | |||||||
| chr1:246622226 | A | G | 275 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(272): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.585+592A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246622226 | |||||||
| chr1:246622259 | A | C | 6 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0093 others(3): Show |
6 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.585+625A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246622259 | |||||||
| chr1:246622309 | C | T | 97 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(94): Show |
100 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.585+675C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246622309 | |||||||
| chr1:246622444 | G | T | 9 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(6): Show |
9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.585+810G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246622444 | |||||||
| chr1:246622531 | A | G | 1 | a0001c0006t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.585+897A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246622531 | |||||||
| chr1:246622575 | G | T | 1 | a0001c0001t0003g0295 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.585+941G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246622575 | |||||||
| chr1:246622681 | G | A | 11 | a0003c0003t0001g0034 a0003c0003t0001g0035 a0003c0003t0001g0039 others(8): Show |
11 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.585+1047G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246622681 | |||||||
| chr1:246622731 | C | T | 6 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0093 others(3): Show |
6 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.585+1097C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246622731 | |||||||
| chr1:246622745 | CT | C | 113 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(110): Show |
113 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.585+1121delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246622745 | ||||||
| chr1:246622794 | C | A | 4 | a0001c0001t0001g0158 a0001c0001t0004g0155 a0001c0001t0004g0156 others(1): Show |
4 | HG01109.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.585+1160C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246622794 | |||||||
| chr1:246622867 | A | G | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.585+1233A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246622867 | |||||||
| chr1:246622970 | C | T | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.585+1336C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246622970 | |||||||
| chr1:246623002 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.585+1368T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623002 | |||||||
| chr1:246623145 | A | G | 97 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(94): Show |
100 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.585+1511A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623145 | |||||||
| chr1:246623213 | A | C | 2 | a0001c0001t0001g0154 a0001c0001t0001g0289 |
2 | HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.585+1579A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623213 | |||||||
| chr1:246623223 | C | T | 29 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0165 others(26): Show |
29 | HG00733.hp1 HG01243.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.585+1589C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623223 | |||||||
| chr1:246623296 | G | A | 106 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(103): Show |
109 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.585+1662G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623296 | |||||||
| chr1:246623343 | C | G | 107 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(104): Show |
110 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.585+1709C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623343 | |||||||
| chr1:246623473 | A | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(107): Show |
113 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.585+1839A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623473 | |||||||
| chr1:246623527 | G | A | 1 | a0002c0002t0001g0120 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.585+1893G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623527 | |||||||
| chr1:246623601 | C | T | 4 | a0003c0003t0001g0040 a0003c0003t0001g0041 a0003c0003t0001g0042 others(1): Show |
4 | HG00733.hp1 HG01891.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.585+1967C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623601 | |||||||
| chr1:246623605 | C | A | 1 | a0001c0001t0004g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.585+1971C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623605 | |||||||
| chr1:246623721 | C | G | 28 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0165 others(25): Show |
28 | HG00733.hp1 HG01243.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.585+2087C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623721 | |||||||
| chr1:246623797 | T | G | 1 | a0007c0005t0023g0045 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.585+2163T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623797 | |||||||
| chr1:246623818 | C | T | 1 | a0001c0001t0019g0106 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.585+2184C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623818 | |||||||
| chr1:246623841 | T | C | 5 | a0003c0003t0001g0034 a0003c0003t0001g0035 a0003c0003t0004g0036 others(2): Show |
5 | HG01243.hp1 HG02451.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.585+2207T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623841 | |||||||
| chr1:246623898 | C | CA | 132 | a0001c0001t0001g0024 a0001c0001t0001g0090 a0001c0001t0001g0092 others(129): Show |
132 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.585+2278dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246623898 | ||||||
| chr1:246623898 | C | CAA | 95 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(92): Show |
98 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.585+2277_585+2278d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246623898 | ||||||
| chr1:246623898 | C | CAAA | 6 | a0001c0001t0002g0059 a0001c0001t0002g0103 a0001c0001t0003g0056 others(3): Show |
6 | HG00140.hp2 HG02071.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.585+2276_585+2278d others(5): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246623898 | ||||||
| chr1:246623926 | G | A | 28 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0165 others(25): Show |
28 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.585+2292G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623926 | |||||||
| chr1:246623960 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.585+2326C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623960 | |||||||
| chr1:246623978 | G | A | 6 | a0001c0001t0004g0018 a0001c0001t0004g0044 a0001c0001t0004g0148 others(3): Show |
6 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.585+2344G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246623978 | |||||||
| chr1:246624040 | G | A | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG00639.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.585+2406G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246624040 | |||||||
| chr1:246624058 | A | G | 275 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(272): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.585+2424A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246624058 | |||||||
| chr1:246624146 | C | T | 97 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(94): Show |
100 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.585+2512C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246624146 | |||||||
| chr1:246624353 | C | T | 1 | a0001c0001t0002g0102 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.585+2719C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246624353 | |||||||
| chr1:246624677 | G | A | 6 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0093 others(3): Show |
6 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.585+3043G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246624677 | |||||||
| chr1:246624729 | T | C | 97 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(94): Show |
100 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.585+3095T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246624729 | |||||||
| chr1:246624905 | T | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(108): Show |
114 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.585+3271T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246624905 | |||||||
| chr1:246624975 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.585+3341G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246624975 | |||||||
| chr1:246625323 | G | A | 128 | a0001c0001t0001g0024 a0001c0001t0001g0132 a0001c0001t0001g0154 others(125): Show |
128 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.585+3689G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246625323 | |||||||
| chr1:246625414 | CT | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(131): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.585+3805delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246625414 | ||||||
| chr1:246625414 | CTT | C | 168 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0027 others(165): Show |
168 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.585+3804_585+3805d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246625414 | ||||||
| chr1:246625414 | CTTT | C | 7 | a0001c0001t0002g0222 a0001c0001t0004g0009 a0001c0001t0009g0015 others(4): Show |
7 | HG02258.hp1 HG02622.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.585+3803_585+3805d others(5): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246625414 | ||||||
| chr1:246625420 | T | C | 2 | a0001c0001t0003g0290 a0001c0001t0004g0019 |
2 | HG02809.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.585+3786T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246625420 | |||||||
| chr1:246625482 | C | T | 4 | a0001c0001t0001g0196 a0001c0001t0001g0223 a0001c0001t0001g0303 others(1): Show |
4 | HG00323.hp2 HG01081.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.585+3848C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246625482 | |||||||
| chr1:246625578 | C | T | 2 | a0002c0002t0015g0166 a0008c0011t0015g0211 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.585+3944C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246625578 | |||||||
| chr1:246625631 | A | AG | 6 | a0004c0004t0003g0117 a0004c0004t0003g0182 a0004c0004t0003g0183 others(3): Show |
6 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.585+3999dupG | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246625631 | ||||||
| chr1:246625641 | C | T | 27 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0165 others(24): Show |
27 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.585+4007C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246625641 | |||||||
| chr1:246625642 | G | A | 5 | a0001c0001t0001g0132 a0001c0001t0004g0134 a0001c0001t0016g0133 others(2): Show |
5 | HG01243.hp2 HG02622.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.585+4008G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246625642 | |||||||
| chr1:246625662 | C | T | 1 | a0004c0004t0003g0117 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.585+4028C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246625662 | |||||||
| chr1:246625716 | G | A | 2 | a0001c0001t0004g0006 a0001c0001t0004g0008 |
2 | HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.585+4082G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246625716 | |||||||
| chr1:246625799 | C | T | 2 | a0002c0002t0001g0004 a0002c0002t0002g0112 |
3 | NA18944.hp1 NA18948.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.585+4165C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246625799 | |||||||
| chr1:246625845 | A | G | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.585+4211A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246625845 | |||||||
| chr1:246625934 | C | T | 2 | a0001c0001t0004g0006 a0001c0001t0004g0008 |
2 | HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.585+4300C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246625934 | |||||||
| chr1:246625951 | A | G | 2 | a0001c0001t0009g0012 a0001c0001t0009g0014 |
2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.585+4317A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246625951 | |||||||
| chr1:246626015 | C | T | 1 | a0001c0001t0005g0203 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.585+4381C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626015 | |||||||
| chr1:246626016 | A | G | 3 | a0002c0002t0015g0166 a0008c0011t0015g0211 a0010c0008t0001g0159 |
3 | HG02622.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.585+4382A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626016 | |||||||
| chr1:246626037 | C | T | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.585+4403C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626037 | |||||||
| chr1:246626066 | CT | C | 28 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0165 others(25): Show |
28 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.585+4444delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246626066 | ||||||
| chr1:246626088 | T | C | 115 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(112): Show |
115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.585+4454T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626088 | |||||||
| chr1:246626118 | C | T | 1 | a0001c0001t0002g0101 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.585+4484C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626118 | |||||||
| chr1:246626145 | G | A | 1 | a0001c0001t0003g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.585+4511G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626145 | |||||||
| chr1:246626149 | A | G | 2 | a0002c0002t0001g0108 a0002c0002t0002g0121 |
2 | HG01074.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.585+4515A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626149 | |||||||
| chr1:246626271 | G | A | 2 | a0001c0001t0005g0025 a0001c0001t0020g0026 |
2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.585+4637G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626271 | |||||||
| chr1:246626438 | C | T | 1 | a0001c0001t0002g0079 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.585+4804C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626438 | |||||||
| chr1:246626451 | C | CT | 54 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0090 others(51): Show |
54 | HG00140.hp1 HG00558.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.585+4841dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246626451 | ||||||
| chr1:246626451 | C | CTT | 87 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(84): Show |
90 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.585+4840_585+4841d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246626451 | ||||||
| chr1:246626451 | C | CTTT | 13 | a0001c0001t0002g0082 a0001c0001t0003g0069 a0001c0001t0003g0071 others(10): Show |
13 | HG01169.hp1 HG01192.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.585+4839_585+4841d others(5): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246626451 | ||||||
| chr1:246626451 | CT | C | 6 | a0001c0001t0001g0024 a0001c0001t0001g0291 a0002c0002t0001g0124 others(3): Show |
6 | HG00639.hp2 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.585+4841delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246626451 | ||||||
| chr1:246626451 | CTTTTTTT others(5): Show |
C | 15 | a0001c0001t0001g0132 a0001c0001t0004g0018 a0001c0001t0004g0044 others(12): Show |
15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.585+4830_585+4841d others(14): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246626451 | ||||||
| chr1:246626525 | T | G | 3 | a0002c0002t0015g0166 a0008c0011t0015g0211 a0010c0008t0001g0159 |
3 | HG02622.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.585+4891T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626525 | |||||||
| chr1:246626544 | G | A | 1 | a0001c0001t0003g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.585+4910G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626544 | |||||||
| chr1:246626603 | C | T | 2 | a0001c0001t0001g0158 a0001c0001t0001g0255 |
2 | HG01884.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.585+4969C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626603 | |||||||
| chr1:246626604 | G | A | 1 | a0001c0001t0002g0199 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.585+4970G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626604 | |||||||
| chr1:246626752 | C | T | 1 | a0001c0001t0005g0203 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.585+5118C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626752 | |||||||
| chr1:246626842 | C | A | 3 | a0002c0002t0015g0166 a0008c0011t0015g0211 a0010c0008t0001g0159 |
3 | HG02622.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.586-5052C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626842 | |||||||
| chr1:246626911 | G | A | 266 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(263): Show |
269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.586-4983G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626911 | |||||||
| chr1:246626946 | G | C | 3 | a0002c0002t0015g0166 a0008c0011t0015g0211 a0010c0008t0001g0159 |
3 | HG02622.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.586-4948G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246626946 | |||||||
| chr1:246627055 | C | T | 9 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(6): Show |
9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.586-4839C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246627055 | |||||||
| chr1:246627072 | A | G | 1 | a0001c0001t0012g0001 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.586-4822A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246627072 | |||||||
| chr1:246627187 | A | G | 15 | a0001c0001t0001g0132 a0001c0001t0004g0018 a0001c0001t0004g0044 others(12): Show |
15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.586-4707A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246627187 | |||||||
| chr1:246627225 | C | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0296 a0001c0001t0002g0215 |
4 | HG01257.hp2 HG01258.hp2 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.586-4669C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246627225 | |||||||
| chr1:246627269 | C | T | 1 | a0002c0002t0002g0249 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.586-4625C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246627269 | |||||||
| chr1:246627335 | C | T | 1 | a0001c0001t0002g0236 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.586-4559C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246627335 | |||||||
| chr1:246627400 | C | T | 7 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0093 others(4): Show |
7 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.586-4494C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246627400 | |||||||
| chr1:246627454 | G | A | 167 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0027 others(164): Show |
167 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.586-4440G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246627454 | |||||||
| chr1:246627884 | G | GAACTCAT others(50): Show |
2 | a0002c0002t0015g0166 a0008c0011t0015g0211 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.586-3975_586-3974i others(59): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246627884 | ||||||
| chr1:246627884 | G | GAACTCAT others(68): Show |
1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.586-3964_586-3963i others(77): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246627884 | ||||||
| chr1:246627893 | G | A | 7 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0093 others(4): Show |
7 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.586-4001G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246627893 | |||||||
| chr1:246627977 | A | C | 2 | a0001c0001t0004g0006 a0001c0001t0004g0008 |
2 | HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.586-3917A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246627977 | |||||||
| chr1:246628076 | G | T | 8 | a0001c0001t0001g0213 a0001c0001t0001g0232 a0001c0001t0001g0235 others(5): Show |
8 | HG01109.hp1 HG01175.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.586-3818G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246628076 | |||||||
| chr1:246628078 | G | A | 4 | a0001c0001t0003g0290 a0002c0002t0015g0166 a0008c0011t0015g0211 others(1): Show |
4 | HG02622.hp1 HG03486.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.586-3816G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246628078 | |||||||
| chr1:246628110 | C | G | 7 | a0001c0001t0001g0168 a0001c0001t0002g0170 a0001c0001t0002g0173 others(4): Show |
7 | HG02145.hp2 HG02258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.586-3784C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246628110 | |||||||
| chr1:246628114 | C | T | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.586-3780C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246628114 | |||||||
| chr1:246628200 | A | G | 1 | a0001c0001t0004g0006 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.586-3694A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246628200 | |||||||
| chr1:246628241 | C | T | 115 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(112): Show |
115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.586-3653C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246628241 | |||||||
| chr1:246628409 | G | A | 1 | a0001c0001t0002g0240 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.586-3485G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246628409 | |||||||
| chr1:246628640 | C | T | 26 | a0001c0001t0001g0132 a0001c0001t0004g0018 a0001c0001t0004g0044 others(23): Show |
26 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.586-3254C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246628640 | |||||||
| chr1:246628830 | C | A | 1 | a0001c0001t0001g0272 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.586-3064C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246628830 | |||||||
| chr1:246628830 | C | G | 274 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(271): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.586-3064C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246628830 | |||||||
| chr1:246628926 | C | T | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.586-2968C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246628926 | |||||||
| chr1:246628933 | T | A | 11 | a0003c0003t0001g0034 a0003c0003t0001g0035 a0003c0003t0001g0039 others(8): Show |
11 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.586-2961T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246628933 | |||||||
| chr1:246629018 | T | C | 9 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(6): Show |
9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.586-2876T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246629018 | |||||||
| chr1:246629399 | A | ATGTC | 275 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(272): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.586-2494_586-2493i others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246629399 | ||||||
| chr1:246629439 | A | G | 19 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0165 others(16): Show |
19 | HG01981.hp1 HG02145.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.586-2455A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246629439 | |||||||
| chr1:246629511 | G | T | 3 | a0002c0002t0015g0166 a0008c0011t0015g0211 a0010c0008t0001g0159 |
3 | HG02622.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.586-2383G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246629511 | |||||||
| chr1:246629628 | A | G | 1 | a0001c0001t0003g0161 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.586-2266A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246629628 | |||||||
| chr1:246629786 | C | G | 1 | a0001c0001t0008g0023 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.586-2108C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246629786 | |||||||
| chr1:246629838 | T | G | 9 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(6): Show |
9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.586-2056T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246629838 | |||||||
| chr1:246629879 | A | C | 3 | a0002c0002t0015g0166 a0008c0011t0015g0211 a0010c0008t0001g0159 |
3 | HG02622.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.586-2015A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246629879 | |||||||
| chr1:246629913 | G | T | 1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.586-1981G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246629913 | |||||||
| chr1:246629928 | C | T | 157 | a0001c0001t0001g0024 a0001c0001t0001g0090 a0001c0001t0001g0092 others(154): Show |
157 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.586-1966C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246629928 | |||||||
| chr1:246629983 | C | T | 7 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0093 others(4): Show |
7 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.586-1911C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246629983 | |||||||
| chr1:246630027 | C | T | 4 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0096 others(1): Show |
4 | HG01261.hp2 HG01433.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.586-1867C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246630027 | |||||||
| chr1:246630257 | T | C | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.586-1637T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246630257 | |||||||
| chr1:246630402 | C | A | 1 | a0001c0006t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.586-1492C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246630402 | |||||||
| chr1:246630447 | A | C | 179 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0027 others(176): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.586-1447A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246630447 | |||||||
| chr1:246630481 | C | T | 179 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0027 others(176): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.586-1413C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246630481 | |||||||
| chr1:246630578 | A | G | 179 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0027 others(176): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.586-1316A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246630578 | |||||||
| chr1:246630653 | G | A | 1 | a0001c0001t0003g0067 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.586-1241G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246630653 | |||||||
| chr1:246630677 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.586-1217T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246630677 | |||||||
| chr1:246630699 | C | CT | 179 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0027 others(176): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.586-1188dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 246630699 | ||||||
| chr1:246630730 | A | G | 179 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0027 others(176): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.586-1164A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246630730 | |||||||
| chr1:246630731 | T | G | 11 | a0001c0001t0001g0013 a0001c0001t0001g0165 a0001c0001t0001g0167 others(8): Show |
11 | HG02145.hp2 HG02258.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.586-1163T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246630731 | |||||||
| chr1:246630832 | A | G | 179 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0027 others(176): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.586-1062A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246630832 | |||||||
| chr1:246630887 | A | G | 1 | a0001c0001t0001g0288 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.586-1007A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246630887 | |||||||
| chr1:246630993 | A | G | 179 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0027 others(176): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.586-901A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246630993 | |||||||
| chr1:246631025 | C | T | 2 | a0001c0001t0004g0006 a0001c0001t0004g0008 |
2 | HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.586-869C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246631025 | |||||||
| chr1:246631069 | G | A | 115 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(112): Show |
115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.586-825G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246631069 | |||||||
| chr1:246631125 | A | G | 1 | a0001c0001t0003g0142 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.586-769A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246631125 | |||||||
| chr1:246631173 | A | G | 1 | a0001c0001t0003g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.586-721A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246631173 | |||||||
| chr1:246631392 | C | T | 1 | a0001c0001t0002g0311 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.586-502C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246631392 | |||||||
| chr1:246631393 | G | A | 2 | a0004c0004t0003g0182 a0004c0004t0003g0183 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.586-501G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246631393 | |||||||
| chr1:246631599 | T | C | 1 | a0001c0001t0003g0073 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.586-295T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246631599 | |||||||
| chr1:246631645 | G | A | 177 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0027 others(174): Show |
177 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.586-249G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 3/10 | chr1 | 246631645 | |||||||
| chr1:246632161 | T | G | 179 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0027 others(176): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.616+237T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246632161 | |||||||
| chr1:246632581 | A | T | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.616+657A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246632581 | |||||||
| chr1:246632591 | G | A | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.616+667G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246632591 | |||||||
| chr1:246632796 | G | C | 115 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(112): Show |
115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.616+872G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246632796 | |||||||
| chr1:246633147 | C | T | 1 | a0001c0001t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.617-777C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246633147 | |||||||
| chr1:246633175 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.617-749C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246633175 | |||||||
| chr1:246633187 | C | T | 7 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0093 others(4): Show |
7 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.617-737C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246633187 | |||||||
| chr1:246633301 | G | T | 275 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(272): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.617-623G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246633301 | |||||||
| chr1:246633305 | C | T | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.617-619C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246633305 | |||||||
| chr1:246633341 | C | G | 1 | a0001c0001t0001g0165 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617-583C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246633341 | |||||||
| chr1:246633424 | C | G | 277 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(274): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.617-500C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246633424 | |||||||
| chr1:246633603 | C | T | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.617-321C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246633603 | |||||||
| chr1:246633637 | G | A | 1 | a0001c0001t0003g0209 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.617-287G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246633637 | |||||||
| chr1:246633668 | G | A | 2 | a0001c0001t0003g0049 a0001c0001t0003g0050 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.617-256G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246633668 | |||||||
| chr1:246633746 | GA | G | 10 | a0001c0001t0002g0233 a0001c0001t0004g0018 a0001c0001t0004g0044 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.617-163delA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 246633746 | ||||||
| chr1:246633799 | A | G | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.617-125A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246633799 | |||||||
| chr1:246633853 | G | A | 1 | a0001c0001t0022g0087 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.617-71G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246633853 | |||||||
| chr1:246633906 | C | T | 1 | a0001c0001t0002g0181 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.617-18C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 4/10 | chr1 | 246633906 | |||||||
| chr1:246634123 | A | G | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.703+113A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 5/10 | chr1 | 246634123 | |||||||
| chr1:246634343 | T | C | 4 | a0001c0001t0003g0204 a0001c0001t0003g0218 a0001c0001t0003g0257 others(1): Show |
4 | HG03017.hp2 HG03704.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-130T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 5/10 | chr1 | 246634343 | |||||||
| chr1:246634391 | G | A | 1 | a0003c0003t0004g0036 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.704-82G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 5/10 | chr1 | 246634391 | |||||||
| chr1:246634408 | G | T | 116 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(113): Show |
116 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.704-65G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 5/10 | chr1 | 246634408 | |||||||
| chr1:246634412 | G | GT | 115 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(112): Show |
115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.704-54dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 246634412 | ||||||
| chr1:246634672 | T | A | 116 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(113): Show |
116 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.818+85T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246634672 | |||||||
| chr1:246634747 | G | A | 115 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(112): Show |
115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.818+160G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246634747 | |||||||
| chr1:246634783 | A | C | 24 | a0001c0001t0001g0196 a0001c0001t0001g0208 a0001c0001t0001g0217 others(21): Show |
24 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(21): Show |
intron_variant | MODIFIER | c.818+196A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246634783 | |||||||
| chr1:246634788 | G | A | 2 | a0002c0002t0015g0166 a0008c0011t0015g0211 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.818+201G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246634788 | |||||||
| chr1:246634848 | G | A | 115 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(112): Show |
115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.818+261G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246634848 | |||||||
| chr1:246634863 | G | A | 2 | a0001c0001t0002g0074 a0001c0001t0003g0086 |
2 | HG01099.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.818+276G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246634863 | |||||||
| chr1:246634935 | C | T | 6 | a0001c0001t0001g0232 a0001c0001t0001g0235 a0001c0001t0001g0253 others(3): Show |
6 | HG01109.hp1 HG01943.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.818+348C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246634935 | |||||||
| chr1:246634951 | T | TGGTGGGT others(13): Show |
114 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(111): Show |
114 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.818+368_818+369ins others(20): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 246634951 | ||||||
| chr1:246634951 | T | TGGTGTGT others(13): Show |
1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.818+368_818+369ins others(20): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 246634951 | ||||||
| chr1:246634951 | TGGTGCGT others(13): Show |
T | 1 | a0002c0002t0001g0145 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.818+385_818+404del others(20): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 246634951 | ||||||
| chr1:246634956 | C | CGTGTCTT others(13): Show |
125 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0027 others(122): Show |
128 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.818+387_818+388ins others(20): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 246634956 | ||||||
| chr1:246634956 | C | CGTGTCTT others(13): Show |
1 | a0001c0006t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.818+377_818+378ins others(20): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 246634956 | ||||||
| chr1:246634956 | C | G | 1 | a0005c0010t0002g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.818+369C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246634956 | |||||||
| chr1:246634967 | G | T | 1 | a0001c0006t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.818+380G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246634967 | |||||||
| chr1:246634969 | C | CGGGGTAG others(13): Show |
33 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0093 others(30): Show |
33 | HG00140.hp1 HG00733.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.818+387_818+388ins others(20): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 246634969 | ||||||
| chr1:246634977 | G | C | 7 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0093 others(4): Show |
7 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.818+390G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246634977 | |||||||
| chr1:246634990 | G | A | 116 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(113): Show |
116 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.818+403G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246634990 | |||||||
| chr1:246635047 | C | T | 1 | a0001c0001t0003g0104 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.818+460C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635047 | |||||||
| chr1:246635083 | C | T | 116 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(113): Show |
116 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.818+496C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635083 | |||||||
| chr1:246635105 | T | C | 1 | a0002c0002t0001g0198 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.818+518T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635105 | |||||||
| chr1:246635155 | A | G | 117 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(114): Show |
117 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.818+568A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635155 | |||||||
| chr1:246635163 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.818+576C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635163 | |||||||
| chr1:246635208 | G | A | 115 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(112): Show |
115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.818+621G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635208 | |||||||
| chr1:246635244 | T | A | 168 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0027 others(165): Show |
168 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.818+657T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635244 | |||||||
| chr1:246635266 | G | A | 116 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(113): Show |
116 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.818+679G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635266 | |||||||
| chr1:246635283 | G | A | 96 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(93): Show |
99 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.818+696G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635283 | |||||||
| chr1:246635289 | A | G | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.818+702A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635289 | |||||||
| chr1:246635300 | A | G | 17 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0165 others(14): Show |
17 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.818+713A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635300 | |||||||
| chr1:246635358 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0002g0051 |
2 | HG01256.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.818+771G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635358 | |||||||
| chr1:246635374 | C | G | 1 | a0002c0002t0001g0118 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.818+787C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635374 | |||||||
| chr1:246635379 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.818+792A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635379 | |||||||
| chr1:246635414 | T | A | 115 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(112): Show |
115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.818+827T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635414 | |||||||
| chr1:246635487 | C | T | 52 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0090 others(49): Show |
52 | HG00140.hp1 HG00733.hp1 HG01243.hp1 others(49): Show |
intron_variant | MODIFIER | c.818+900C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635487 | |||||||
| chr1:246635646 | A | G | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.818+1059A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635646 | |||||||
| chr1:246635664 | G | A | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.818+1077G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635664 | |||||||
| chr1:246635678 | C | G | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.818+1091C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635678 | |||||||
| chr1:246635683 | G | A | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.818+1096G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635683 | |||||||
| chr1:246635719 | T | G | 2 | a0001c0001t0001g0180 a0001c0001t0017g0010 |
2 | HG01981.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.818+1132T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635719 | |||||||
| chr1:246635741 | C | G | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.818+1154C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635741 | |||||||
| chr1:246635756 | G | A | 2 | a0001c0001t0001g0226 a0001c0001t0001g0281 |
2 | NA18945.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.818+1169G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635756 | |||||||
| chr1:246635758 | G | A | 1 | a0007c0005t0023g0045 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.818+1171G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635758 | |||||||
| chr1:246635767 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0003g0176 |
2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.818+1180G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635767 | |||||||
| chr1:246635778 | T | G | 1 | a0001c0001t0003g0314 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.818+1191T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635778 | |||||||
| chr1:246635807 | G | A | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.818+1220G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635807 | |||||||
| chr1:246635819 | C | T | 30 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0060 others(27): Show |
31 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.818+1232C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635819 | |||||||
| chr1:246635840 | C | T | 8 | a0001c0001t0001g0213 a0001c0001t0001g0232 a0001c0001t0001g0235 others(5): Show |
8 | HG01109.hp1 HG01175.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.818+1253C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635840 | |||||||
| chr1:246635903 | C | T | 9 | a0001c0001t0001g0299 a0002c0002t0001g0110 a0002c0002t0001g0124 others(6): Show |
9 | HG00639.hp2 HG02015.hp2 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.818+1316C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635903 | |||||||
| chr1:246635916 | C | T | 1 | a0002c0002t0001g0169 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.818+1329C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635916 | |||||||
| chr1:246635957 | A | G | 118 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(115): Show |
118 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.818+1370A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635957 | |||||||
| chr1:246635982 | G | A | 1 | a0001c0001t0002g0283 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.818+1395G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246635982 | |||||||
| chr1:246636035 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.818+1448G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636035 | |||||||
| chr1:246636086 | C | T | 26 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0090 others(23): Show |
26 | HG00140.hp1 HG00408.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.818+1499C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636086 | |||||||
| chr1:246636139 | C | G | 1 | a0001c0001t0004g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.818+1552C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636139 | |||||||
| chr1:246636176 | C | T | 8 | a0001c0001t0001g0213 a0001c0001t0001g0232 a0001c0001t0001g0235 others(5): Show |
8 | HG01109.hp1 HG01175.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.818+1589C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636176 | |||||||
| chr1:246636177 | A | G | 116 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(113): Show |
116 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.818+1590A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636177 | |||||||
| chr1:246636235 | CAG | C | 5 | a0003c0003t0001g0040 a0003c0003t0001g0041 a0003c0003t0001g0042 others(2): Show |
5 | HG00733.hp1 HG01891.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.818+1649_818+1650d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636235 | |||||||
| chr1:246636252 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.818+1665G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636252 | |||||||
| chr1:246636256 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.818+1669C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636256 | |||||||
| chr1:246636275 | A | G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0287 a0001c0001t0008g0022 others(1): Show |
4 | HG02145.hp1 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.818+1688A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636275 | |||||||
| chr1:246636281 | G | A | 2 | a0002c0002t0015g0166 a0008c0011t0015g0211 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.818+1694G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636281 | |||||||
| chr1:246636295 | G | A | 9 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(6): Show |
9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.818+1708G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636295 | |||||||
| chr1:246636409 | G | A | 1 | a0001c0001t0002g0101 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.818+1822G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636409 | |||||||
| chr1:246636427 | C | T | 96 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(93): Show |
99 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.818+1840C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636427 | |||||||
| chr1:246636448 | C | T | 2 | a0002c0002t0001g0004 a0002c0002t0002g0112 |
3 | NA18944.hp1 NA18948.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.818+1861C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636448 | |||||||
| chr1:246636472 | G | A | 4 | a0001c0001t0001g0119 a0001c0001t0010g0224 a0001c0001t0010g0225 others(1): Show |
4 | HG00558.hp2 HG02080.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.818+1885G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636472 | |||||||
| chr1:246636504 | T | G | 1 | a0001c0001t0004g0006 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.818+1917T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636504 | |||||||
| chr1:246636532 | G | A | 1 | a0001c0001t0003g0292 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.818+1945G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636532 | |||||||
| chr1:246636561 | A | G | 1 | a0001c0001t0025g0286 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.818+1974A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636561 | |||||||
| chr1:246636605 | T | C | 1 | a0001c0001t0001g0307 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.818+2018T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636605 | |||||||
| chr1:246636631 | T | C | 1 | a0003c0003t0004g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.818+2044T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636631 | |||||||
| chr1:246636652 | G | A | 1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.818+2065G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636652 | |||||||
| chr1:246636654 | G | A | 1 | a0001c0001t0002g0207 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.818+2067G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636654 | |||||||
| chr1:246636696 | T | G | 24 | a0001c0001t0001g0196 a0001c0001t0001g0208 a0001c0001t0001g0217 others(21): Show |
24 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(21): Show |
intron_variant | MODIFIER | c.818+2109T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636696 | |||||||
| chr1:246636708 | A | G | 116 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(113): Show |
116 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.818+2121A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636708 | |||||||
| chr1:246636720 | A | G | 116 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(113): Show |
116 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.818+2133A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636720 | |||||||
| chr1:246636937 | G | A | 116 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(113): Show |
116 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.818+2350G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636937 | |||||||
| chr1:246636952 | C | G | 7 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0093 others(4): Show |
7 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.818+2365C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246636952 | |||||||
| chr1:246637027 | T | A | 115 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(112): Show |
115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.818+2440T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246637027 | |||||||
| chr1:246637106 | G | T | 1 | a0001c0001t0003g0218 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.818+2519G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246637106 | |||||||
| chr1:246637268 | A | G | 3 | a0001c0001t0001g0093 a0001c0001t0001g0125 a0001c0001t0002g0079 |
3 | HG03239.hp1 HG03688.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.818+2681A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246637268 | |||||||
| chr1:246637303 | T | G | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.818+2716T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246637303 | |||||||
| chr1:246637479 | G | A | 1 | a0001c0001t0003g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.818+2892G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246637479 | |||||||
| chr1:246637545 | G | A | 9 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(6): Show |
9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.818+2958G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246637545 | |||||||
| chr1:246637687 | C | T | 275 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(272): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.818+3100C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246637687 | |||||||
| chr1:246637702 | T | G | 170 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0027 others(167): Show |
170 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.818+3115T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246637702 | |||||||
| chr1:246637703 | C | T | 170 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0027 others(167): Show |
170 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.818+3116C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246637703 | |||||||
| chr1:246637782 | A | G | 2 | a0002c0002t0015g0166 a0008c0011t0015g0211 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.818+3195A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246637782 | |||||||
| chr1:246637808 | A | G | 7 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0093 others(4): Show |
7 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.818+3221A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246637808 | |||||||
| chr1:246637887 | G | A | 7 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0093 others(4): Show |
7 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.818+3300G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246637887 | |||||||
| chr1:246637938 | T | G | 7 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0093 others(4): Show |
7 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.818+3351T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246637938 | |||||||
| chr1:246638119 | C | T | 9 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(6): Show |
9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.818+3532C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246638119 | |||||||
| chr1:246638293 | C | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0288 |
2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.819-3456C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246638293 | |||||||
| chr1:246638305 | G | A | 1 | a0001c0001t0012g0001 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.819-3444G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246638305 | |||||||
| chr1:246638346 | G | A | 275 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(272): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.819-3403G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246638346 | |||||||
| chr1:246638356 | C | T | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.819-3393C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246638356 | |||||||
| chr1:246638416 | A | C | 1 | a0001c0001t0003g0245 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.819-3333A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246638416 | |||||||
| chr1:246638491 | C | G | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.819-3258C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246638491 | |||||||
| chr1:246638558 | T | C | 26 | a0001c0001t0001g0132 a0001c0001t0004g0018 a0001c0001t0004g0044 others(23): Show |
26 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.819-3191T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246638558 | |||||||
| chr1:246638886 | G | A | 1 | a0001c0001t0001g0013 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.819-2863G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246638886 | |||||||
| chr1:246639090 | G | A | 2 | a0001c0001t0001g0258 a0001c0001t0001g0316 |
2 | HG00558.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.819-2659G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639090 | |||||||
| chr1:246639154 | T | C | 1 | a0001c0009t0001g0189 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.819-2595T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639154 | |||||||
| chr1:246639176 | T | C | 115 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(112): Show |
115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.819-2573T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639176 | |||||||
| chr1:246639180 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.819-2569C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639180 | |||||||
| chr1:246639183 | C | A | 7 | a0001c0001t0004g0018 a0001c0001t0004g0044 a0001c0001t0004g0148 others(4): Show |
7 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.819-2566C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639183 | |||||||
| chr1:246639183 | C | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(93): Show |
99 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.819-2566C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639183 | |||||||
| chr1:246639197 | G | A | 3 | a0003c0003t0004g0036 a0003c0003t0004g0037 a0003c0003t0004g0038 |
3 | HG01243.hp1 HG02896.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.819-2552G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639197 | |||||||
| chr1:246639266 | G | A | 2 | a0001c0001t0002g0238 a0001c0001t0002g0250 |
2 | HG01070.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.819-2483G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639266 | |||||||
| chr1:246639391 | C | A | 1 | a0001c0001t0002g0236 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.819-2358C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639391 | |||||||
| chr1:246639423 | C | T | 1 | a0001c0001t0002g0236 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.819-2326C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639423 | |||||||
| chr1:246639455 | G | A | 4 | a0001c0001t0001g0195 a0001c0001t0001g0272 a0001c0001t0001g0275 others(1): Show |
4 | HG02109.hp2 HG03491.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.819-2294G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639455 | |||||||
| chr1:246639566 | A | G | 179 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0027 others(176): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.819-2183A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639566 | |||||||
| chr1:246639704 | G | A | 4 | a0001c0001t0005g0152 a0001c0001t0005g0200 a0001c0001t0005g0201 others(1): Show |
4 | HG01433.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.819-2045G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639704 | |||||||
| chr1:246639769 | C | T | 2 | a0002c0002t0015g0166 a0008c0011t0015g0211 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.819-1980C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639769 | |||||||
| chr1:246639915 | T | C | 115 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(112): Show |
115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.819-1834T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246639915 | |||||||
| chr1:246640074 | T | G | 4 | a0002c0002t0001g0143 a0002c0002t0001g0144 a0002c0002t0001g0145 others(1): Show |
4 | HG02559.hp1 HG02683.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.819-1675T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246640074 | |||||||
| chr1:246640420 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0255 |
2 | HG01884.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.819-1329A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246640420 | |||||||
| chr1:246640488 | T | A | 1 | a0002c0002t0001g0122 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.819-1261T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246640488 | |||||||
| chr1:246640548 | T | C | 1 | a0001c0001t0003g0069 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.819-1201T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246640548 | |||||||
| chr1:246640604 | A | G | 1 | a0002c0002t0001g0124 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.819-1145A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246640604 | |||||||
| chr1:246640618 | A | G | 1 | a0001c0001t0003g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.819-1131A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246640618 | |||||||
| chr1:246640918 | G | T | 2 | a0002c0002t0015g0166 a0008c0011t0015g0211 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.819-831G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246640918 | |||||||
| chr1:246640935 | T | TGGAACAT others(54): Show |
1 | a0001c0001t0004g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.819-813_819-753dup others(61): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 246640935 | ||||||
| chr1:246640983 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.819-766C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246640983 | |||||||
| chr1:246640999 | A | G | 1 | a0001c0001t0003g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.819-750A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246640999 | |||||||
| chr1:246641188 | A | G | 9 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(6): Show |
9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.819-561A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246641188 | |||||||
| chr1:246641288 | A | G | 3 | a0002c0002t0015g0166 a0008c0011t0015g0211 a0010c0008t0001g0159 |
3 | HG02622.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.819-461A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246641288 | |||||||
| chr1:246641431 | T | A | 1 | a0001c0001t0001g0285 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.819-318T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246641431 | |||||||
| chr1:246641522 | T | C | 115 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(112): Show |
115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.819-227T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 6/10 | chr1 | 246641522 | |||||||
| chr1:246641895 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.841-46C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 7/10 | chr1 | 246641895 | |||||||
| chr1:246642131 | TG | T | 94 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(91): Show |
94 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.937+96delG | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642131 | ||||||
| chr1:246642132 | G | GTT | 8 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(5): Show |
8 | HG00140.hp1 HG00741.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.937+95_937+96insTT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642132 | |||||||
| chr1:246642132 | G | GTTTTTT | 9 | a0001c0001t0001g0132 a0001c0001t0004g0044 a0001c0001t0004g0134 others(6): Show |
9 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.937+95_937+96insTT others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642132 | |||||||
| chr1:246642132 | G | GTTTTTTT | 14 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0148 others(11): Show |
14 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.937+95_937+96insTT others(5): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642132 | |||||||
| chr1:246642132 | G | GTTTTTTT others(1): Show |
4 | a0001c0001t0004g0100 a0003c0003t0001g0034 a0003c0003t0001g0043 others(1): Show |
4 | HG02257.hp2 HG02896.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.937+95_937+96insTT others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642132 | |||||||
| chr1:246642132 | G | GTTTTTTT others(4): Show |
1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.937+95_937+96insTT others(9): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642132 | |||||||
| chr1:246642132 | G | GTTTTTTT others(5): Show |
3 | a0001c0001t0004g0019 a0001c0001t0005g0025 a0001c0001t0020g0026 |
3 | HG02809.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.937+95_937+96insTT others(10): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642132 | |||||||
| chr1:246642132 | G | GTTTTTTT others(6): Show |
6 | a0001c0001t0001g0175 a0001c0001t0001g0180 a0001c0001t0004g0016 others(3): Show |
6 | HG00735.hp1 HG02647.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.937+95_937+96insTT others(11): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642132 | |||||||
| chr1:246642132 | G | GTTTTTTT others(8): Show |
2 | a0001c0001t0001g0168 a0001c0001t0004g0009 |
2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.937+95_937+96insTT others(13): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642132 | |||||||
| chr1:246642132 | G | GTTTTTTT others(9): Show |
5 | a0001c0001t0001g0165 a0001c0001t0002g0170 a0001c0001t0002g0173 others(2): Show |
5 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.937+95_937+96insTT others(14): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642132 | |||||||
| chr1:246642132 | G | GTTTTTTT others(10): Show |
1 | a0001c0001t0009g0015 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.937+95_937+96insTT others(15): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642132 | |||||||
| chr1:246642132 | G | GTTTTTTT others(11): Show |
5 | a0001c0001t0001g0027 a0001c0001t0001g0167 a0001c0001t0004g0028 others(2): Show |
5 | HG02818.hp1 HG02976.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.937+95_937+96insTT others(16): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642132 | |||||||
| chr1:246642132 | G | GTTTTTTT others(15): Show |
2 | a0001c0001t0001g0013 a0001c0001t0003g0290 |
2 | NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.937+95_937+96insTT others(20): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642132 | |||||||
| chr1:246642132 | G | GTTTTTTT others(16): Show |
1 | a0001c0001t0001g0288 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.937+95_937+96insTT others(21): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642132 | |||||||
| chr1:246642132 | GGT | G | 7 | a0001c0001t0001g0242 a0001c0001t0005g0152 a0001c0001t0005g0200 others(4): Show |
7 | HG01433.hp1 HG02602.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.937+96_937+97delGT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642132 | |||||||
| chr1:246642133 | G | GT | 10 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0309 others(7): Show |
10 | HG01978.hp2 HG01981.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.937+117dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642133 | ||||||
| chr1:246642133 | G | T | 78 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0090 others(75): Show |
78 | HG00140.hp1 HG00621.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.937+96G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642133 | |||||||
| chr1:246642143 | T | G | 1 | a0001c0001t0002g0082 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.937+106T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642143 | |||||||
| chr1:246642259 | A | C | 1 | a0001c0001t0001g0195 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.937+222A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642259 | |||||||
| chr1:246642379 | A | G | 1 | a0001c0001t0001g0002 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.937+342A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642379 | |||||||
| chr1:246642383 | A | G | 1 | a0001c0001t0003g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.937+346A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642383 | |||||||
| chr1:246642764 | T | G | 1 | a0001c0001t0002g0186 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.937+727T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642764 | |||||||
| chr1:246642780 | A | G | 1 | a0001c0006t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.937+743A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642780 | |||||||
| chr1:246642837 | G | GGTGGTGG others(889): Show |
3 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 |
3 | HG01109.hp2 HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.937+801_937+802ins others(896): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(886): Show |
1 | a0001c0001t0001g0281 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(893): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(892): Show |
1 | a0001c0001t0002g0231 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(899): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(883): Show |
1 | a0005c0010t0002g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(890): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(877): Show |
2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG02056.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.937+801_937+802ins others(884): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(880): Show |
1 | a0001c0001t0002g0230 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(887): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(886): Show |
1 | a0001c0001t0001g0258 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(893): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(889): Show |
1 | a0001c0001t0002g0207 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(896): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(883): Show |
1 | a0001c0001t0001g0313 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(890): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(889): Show |
2 | a0001c0001t0005g0152 a0001c0001t0005g0201 |
2 | HG01433.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.937+801_937+802ins others(896): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(889): Show |
5 | a0001c0001t0001g0158 a0001c0001t0001g0226 a0001c0001t0001g0255 others(2): Show |
5 | HG01884.hp1 HG03130.hp2 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.937+801_937+802ins others(896): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(889): Show |
1 | a0001c0001t0002g0236 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(896): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(892): Show |
1 | a0001c0001t0001g0289 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(899): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(891): Show |
1 | a0001c0001t0002g0199 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(898): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(892): Show |
3 | a0001c0001t0002g0238 a0001c0001t0002g0244 a0001c0001t0002g0250 |
3 | HG01070.hp2 HG01081.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.937+801_937+802ins others(899): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(889): Show |
1 | a0001c0001t0001g0267 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(896): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(889): Show |
1 | a0001c0001t0001g0262 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(896): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(892): Show |
1 | a0001c0001t0001g0205 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(899): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(886): Show |
1 | a0001c0001t0001g0294 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(893): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(886): Show |
4 | a0001c0001t0001g0235 a0001c0001t0001g0253 a0001c0001t0001g0261 others(1): Show |
4 | HG01109.hp1 HG01943.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.937+801_937+802ins others(893): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(883): Show |
1 | a0001c0001t0001g0232 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(890): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(883): Show |
1 | a0001c0001t0001g0260 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(890): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(892): Show |
1 | a0001c0001t0001g0264 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(899): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(883): Show |
2 | a0001c0001t0001g0154 a0001c0012t0002g0276 |
2 | NA18943.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.937+801_937+802ins others(890): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(880): Show |
1 | a0001c0001t0002g0241 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(887): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(892): Show |
1 | a0001c0001t0011g0220 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(899): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(892): Show |
1 | a0008c0011t0015g0211 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(899): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(886): Show |
1 | a0002c0002t0015g0166 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(893): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(898): Show |
1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(905): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(889): Show |
1 | a0001c0001t0001g0263 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(896): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(919): Show |
32 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0060 others(29): Show |
33 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.937+801_937+802ins others(926): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(916): Show |
1 | a0001c0001t0002g0186 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(923): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(916): Show |
1 | a0001c0001t0002g0059 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(923): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(916): Show |
1 | a0001c0001t0002g0066 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(923): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(910): Show |
7 | a0002c0002t0001g0029 a0002c0002t0001g0120 a0002c0002t0001g0128 others(4): Show |
7 | HG00741.hp2 HG01175.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.937+801_937+802ins others(917): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(901): Show |
6 | a0002c0002t0001g0004 a0002c0002t0001g0111 a0002c0002t0001g0113 others(3): Show |
7 | HG02040.hp1 HG02074.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.937+801_937+802ins others(908): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(904): Show |
19 | a0001c0001t0001g0299 a0002c0002t0001g0108 a0002c0002t0001g0110 others(16): Show |
19 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.937+801_937+802ins others(911): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(904): Show |
1 | a0002c0002t0001g0269 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(911): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(958): Show |
1 | a0002c0002t0007g0140 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(965): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(901): Show |
2 | a0002c0002t0001g0095 a0002c0002t0001g0123 |
2 | NA18747.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.937+801_937+802ins others(908): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(910): Show |
2 | a0002c0002t0001g0169 a0002c0002t0006g0033 |
2 | HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.937+801_937+802ins others(917): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(895): Show |
1 | a0002c0002t0001g0144 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(902): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(994): Show |
1 | a0001c0001t0003g0246 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(1001): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(994): Show |
1 | a0001c0001t0010g0224 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(1001): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(982): Show |
2 | a0001c0001t0002g0074 a0001c0001t0003g0086 |
2 | HG01099.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.937+801_937+802ins others(989): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(994): Show |
48 | a0001c0001t0001g0063 a0001c0001t0001g0078 a0001c0001t0001g0088 others(45): Show |
49 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.937+801_937+802ins others(1001): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(994): Show |
1 | a0001c0001t0003g0084 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(1001): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(1213): Show |
1 | a0001c0001t0001g0002 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.937+801_937+802ins others(1220): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(991): Show |
1 | a0001c0001t0003g0056 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(998): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(991): Show |
1 | a0001c0001t0003g0005 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(998): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(991): Show |
1 | a0001c0001t0002g0181 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(998): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(991): Show |
1 | a0001c0001t0003g0271 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(998): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(874): Show |
1 | a0001c0001t0013g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(881): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(784): Show |
2 | a0001c0001t0001g0168 a0001c0001t0003g0176 |
2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.937+801_937+802ins others(791): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(904): Show |
1 | a0001c0001t0004g0006 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(911): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(895): Show |
1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(902): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(910): Show |
2 | a0003c0003t0004g0160 a0007c0005t0023g0045 |
2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.937+801_937+802ins others(917): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(901): Show |
9 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(6): Show |
9 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.937+801_937+802ins others(908): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(883): Show |
7 | a0001c0001t0004g0018 a0001c0001t0004g0044 a0001c0001t0004g0148 others(4): Show |
7 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.937+801_937+802ins others(890): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(883): Show |
5 | a0001c0001t0001g0132 a0001c0001t0004g0134 a0001c0001t0016g0133 others(2): Show |
5 | HG01243.hp2 HG02622.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.937+801_937+802ins others(890): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(787): Show |
1 | a0001c0001t0002g0173 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(794): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(790): Show |
1 | a0001c0001t0001g0288 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(797): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(979): Show |
1 | a0001c0001t0004g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(986): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(796): Show |
2 | a0001c0001t0002g0170 a0001c0001t0004g0172 |
2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.937+801_937+802ins others(803): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(793): Show |
2 | a0001c0001t0001g0165 a0001c0001t0001g0167 |
2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.937+801_937+802ins others(800): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(799): Show |
1 | a0001c0001t0001g0013 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(806): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(796): Show |
1 | a0001c0001t0001g0180 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(803): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(820): Show |
4 | a0001c0001t0001g0027 a0001c0001t0004g0028 a0001c0001t0009g0014 others(1): Show |
4 | HG02818.hp1 HG03041.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.937+801_937+802ins others(827): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(817): Show |
1 | a0001c0001t0009g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(824): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(904): Show |
1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(911): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(811): Show |
1 | a0001c0006t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(818): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(904): Show |
1 | a0001c0001t0003g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(911): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(883): Show |
1 | a0003c0003t0001g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(890): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(886): Show |
9 | a0003c0003t0001g0034 a0003c0003t0001g0035 a0003c0003t0001g0039 others(6): Show |
9 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.937+801_937+802ins others(893): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(871): Show |
1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.937+801_937+802ins others(878): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(892): Show |
5 | a0001c0001t0001g0093 a0001c0001t0001g0125 a0001c0001t0001g0285 others(2): Show |
5 | HG03239.hp1 HG03239.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.937+801_937+802ins others(899): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(889): Show |
2 | a0001c0001t0001g0090 a0001c0001t0001g0092 |
2 | HG00140.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.937+801_937+802ins others(896): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642837 | G | GGTGGTGG others(907): Show |
1 | a0001c0001t0004g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.937+801_937+802ins others(914): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642837 | ||||||
| chr1:246642839 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.937+802A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642839 | |||||||
| chr1:246642857 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.937+820G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642857 | |||||||
| chr1:246642858 | T | TGGTGATG others(903): Show |
1 | a0001c0001t0001g0091 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.937+822_937+823ins others(910): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642858 | ||||||
| chr1:246642887 | CT | C | 6 | a0003c0003t0001g0039 a0003c0003t0001g0040 a0003c0003t0001g0041 others(3): Show |
6 | HG00733.hp1 HG01891.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.937+856delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246642887 | ||||||
| chr1:246642900 | T | A | 1 | a0001c0001t0001g0091 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.937+863T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642900 | |||||||
| chr1:246642925 | G | A | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG00639.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.937+888G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642925 | |||||||
| chr1:246642973 | C | T | 1 | a0003c0003t0004g0037 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.937+936C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246642973 | |||||||
| chr1:246643040 | C | T | 2 | a0001c0001t0003g0072 a0001c0001t0003g0094 |
2 | HG01952.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.937+1003C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643040 | |||||||
| chr1:246643068 | T | G | 1 | a0001c0001t0003g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.937+1031T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643068 | |||||||
| chr1:246643084 | G | T | 26 | a0001c0001t0001g0132 a0001c0001t0004g0018 a0001c0001t0004g0044 others(23): Show |
26 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.937+1047G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643084 | |||||||
| chr1:246643092 | A | G | 18 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0165 others(15): Show |
18 | HG01981.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.937+1055A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643092 | |||||||
| chr1:246643128 | G | A | 8 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(5): Show |
8 | HG00735.hp1 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.937+1091G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643128 | |||||||
| chr1:246643304 | G | T | 1 | a0002c0002t0001g0029 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.937+1267G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643304 | |||||||
| chr1:246643312 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.937+1275G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643312 | |||||||
| chr1:246643379 | A | T | 1 | a0001c0001t0002g0079 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.937+1342A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643379 | |||||||
| chr1:246643498 | G | A | 2 | a0001c0001t0001g0158 a0001c0001t0001g0255 |
2 | HG01884.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.937+1461G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643498 | |||||||
| chr1:246643559 | G | A | 9 | a0001c0001t0001g0024 a0001c0001t0001g0202 a0001c0001t0001g0263 others(6): Show |
9 | HG01261.hp1 HG02145.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.937+1522G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643559 | |||||||
| chr1:246643637 | C | G | 1 | a0001c0001t0002g0283 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.937+1600C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643637 | |||||||
| chr1:246643759 | C | G | 10 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(7): Show |
10 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.937+1722C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643759 | |||||||
| chr1:246643812 | A | G | 60 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0090 others(57): Show |
60 | HG00140.hp1 HG00733.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.937+1775A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643812 | |||||||
| chr1:246643836 | A | G | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.937+1799A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643836 | |||||||
| chr1:246643847 | G | A | 16 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0165 others(13): Show |
16 | HG01981.hp1 HG02486.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.937+1810G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246643847 | |||||||
| chr1:246644124 | G | A | 1 | a0001c0001t0003g0094 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.937+2087G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246644124 | |||||||
| chr1:246644128 | C | T | 10 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(7): Show |
10 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.937+2091C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246644128 | |||||||
| chr1:246644176 | G | A | 13 | a0001c0001t0001g0130 a0001c0001t0002g0070 a0001c0001t0003g0052 others(10): Show |
13 | HG01192.hp1 HG01255.hp1 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.937+2139G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246644176 | |||||||
| chr1:246644341 | A | G | 4 | a0001c0001t0005g0152 a0001c0001t0005g0200 a0001c0001t0005g0201 others(1): Show |
4 | HG01433.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.937+2304A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246644341 | |||||||
| chr1:246644367 | G | A | 1 | a0001c0001t0024g0270 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.937+2330G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246644367 | |||||||
| chr1:246644388 | C | CA | 88 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(85): Show |
91 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.937+2374dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246644388 | ||||||
| chr1:246644388 | C | CAA | 14 | a0001c0001t0001g0060 a0001c0001t0002g0066 a0001c0001t0002g0105 others(11): Show |
14 | HG00738.hp2 HG01358.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.937+2373_937+2374d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246644388 | ||||||
| chr1:246644388 | CA | C | 108 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0154 others(105): Show |
108 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.937+2374delA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246644388 | ||||||
| chr1:246644388 | CAA | C | 13 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(10): Show |
13 | HG00140.hp1 HG01515.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.937+2373_937+2374d others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246644388 | ||||||
| chr1:246644388 | CAAA | C | 32 | a0001c0001t0001g0132 a0001c0001t0001g0175 a0001c0001t0004g0016 others(29): Show |
32 | HG00733.hp1 HG00735.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.937+2372_937+2374d others(5): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246644388 | ||||||
| chr1:246644388 | CAAAAAAA | C | 29 | a0001c0001t0001g0299 a0002c0002t0001g0004 a0002c0002t0001g0095 others(26): Show |
30 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.937+2368_937+2374d others(9): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246644388 | ||||||
| chr1:246644450 | A | G | 1 | a0006c0007t0003g0265 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.937+2413A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246644450 | |||||||
| chr1:246644728 | C | T | 1 | a0001c0001t0004g0006 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.938-2411C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246644728 | |||||||
| chr1:246644766 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.938-2373T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246644766 | |||||||
| chr1:246644906 | G | A | 1 | a0001c0006t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.938-2233G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246644906 | |||||||
| chr1:246644953 | A | G | 60 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0090 others(57): Show |
60 | HG00140.hp1 HG00733.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.938-2186A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246644953 | |||||||
| chr1:246645053 | C | T | 1 | a0001c0001t0003g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.938-2086C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645053 | |||||||
| chr1:246645111 | A | G | 1 | a0001c0001t0016g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.938-2028A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645111 | |||||||
| chr1:246645240 | T | A | 1 | a0001c0001t0003g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.938-1899T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645240 | |||||||
| chr1:246645296 | GA | G | 100 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(97): Show |
103 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.938-1840delA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246645296 | ||||||
| chr1:246645423 | A | ATT | 28 | a0001c0001t0001g0132 a0001c0001t0004g0016 a0001c0001t0004g0017 others(25): Show |
28 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.938-1716_938-1715i others(4): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645423 | |||||||
| chr1:246645423 | A | ATTT | 7 | a0001c0001t0001g0175 a0001c0001t0004g0020 a0001c0001t0004g0100 others(4): Show |
7 | HG00735.hp1 HG02109.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.938-1716_938-1715i others(5): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645423 | |||||||
| chr1:246645424 | C | CT | 32 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0060 others(29): Show |
33 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.938-1694dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246645424 | ||||||
| chr1:246645424 | C | CTTTTTT | 9 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0165 others(6): Show |
9 | HG02647.hp1 HG02809.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.938-1699_938-1694d others(8): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246645424 | ||||||
| chr1:246645424 | C | T | 42 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0093 others(39): Show |
42 | HG00140.hp1 HG00733.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.938-1715C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645424 | |||||||
| chr1:246645426 | T | TTTA | 113 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(110): Show |
113 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.938-1711_938-1710i others(5): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246645426 | ||||||
| chr1:246645430 | T | A | 113 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(110): Show |
113 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.938-1709T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645430 | |||||||
| chr1:246645431 | T | A | 2 | a0001c0001t0002g0193 a0001c0001t0025g0286 |
2 | HG02300.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.938-1708T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645431 | |||||||
| chr1:246645434 | T | A | 3 | a0001c0001t0001g0196 a0001c0001t0001g0223 a0001c0001t0001g0304 |
3 | HG00323.hp2 HG01081.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.938-1705T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645434 | |||||||
| chr1:246645450 | T | C | 3 | a0002c0002t0001g0114 a0002c0002t0015g0166 a0008c0011t0015g0211 |
3 | HG02040.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.938-1689T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645450 | |||||||
| chr1:246645466 | C | T | 1 | a0001c0001t0003g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.938-1673C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645466 | |||||||
| chr1:246645513 | C | T | 97 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(94): Show |
100 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.938-1626C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645513 | |||||||
| chr1:246645514 | G | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0289 |
2 | HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.938-1625G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645514 | |||||||
| chr1:246645521 | G | A | 275 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(272): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.938-1618G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645521 | |||||||
| chr1:246645529 | G | A | 275 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(272): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.938-1610G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645529 | |||||||
| chr1:246645553 | G | T | 5 | a0001c0001t0001g0027 a0001c0001t0004g0028 a0001c0001t0009g0012 others(2): Show |
5 | HG02818.hp1 HG02976.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.938-1586G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645553 | |||||||
| chr1:246645583 | G | A | 1 | a0003c0003t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.938-1556G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645583 | |||||||
| chr1:246645585 | G | A | 115 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(112): Show |
115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.938-1554G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645585 | |||||||
| chr1:246645588 | C | T | 1 | a0001c0001t0002g0080 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.938-1551C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645588 | |||||||
| chr1:246645695 | G | A | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.938-1444G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645695 | |||||||
| chr1:246645717 | G | A | 6 | a0004c0004t0003g0117 a0004c0004t0003g0182 a0004c0004t0003g0183 others(3): Show |
6 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.938-1422G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645717 | |||||||
| chr1:246645799 | T | C | 5 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0061 others(2): Show |
5 | HG00738.hp1 HG01255.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.938-1340T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645799 | |||||||
| chr1:246645891 | T | C | 1 | a0001c0001t0002g0207 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.938-1248T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645891 | |||||||
| chr1:246645915 | A | T | 2 | a0001c0001t0003g0048 a0001c0001t0003g0081 |
2 | NA18942.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.938-1224A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246645915 | |||||||
| chr1:246646005 | C | T | 34 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(31): Show |
34 | HG00140.hp1 HG00621.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.938-1134C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646005 | |||||||
| chr1:246646018 | G | A | 1 | a0001c0001t0002g0003 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.938-1121G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646018 | |||||||
| chr1:246646055 | A | G | 60 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0090 others(57): Show |
60 | HG00140.hp1 HG00733.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.938-1084A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646055 | |||||||
| chr1:246646209 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.938-930G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646209 | |||||||
| chr1:246646212 | G | A | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.938-927G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646212 | |||||||
| chr1:246646279 | C | CAAA | 8 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(5): Show |
8 | HG00140.hp1 HG01515.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.938-847_938-845dup others(3): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246646279 | ||||||
| chr1:246646279 | C | CAAAAAAA | 9 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(6): Show |
9 | HG00735.hp1 HG02809.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.938-851_938-845dup others(7): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246646279 | ||||||
| chr1:246646279 | C | CAAAAAAA others(3): Show |
47 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0001t0001g0214 others(44): Show |
47 | HG00280.hp2 HG00558.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.938-854_938-845dup others(10): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246646279 | ||||||
| chr1:246646279 | C | CAAAAAAA others(4): Show |
62 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(59): Show |
62 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.938-855_938-845dup others(11): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246646279 | ||||||
| chr1:246646279 | C | CAAAAAAA others(5): Show |
4 | a0001c0001t0001g0195 a0001c0001t0001g0267 a0001c0001t0001g0297 others(1): Show |
4 | HG02970.hp1 HG03017.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.938-856_938-845dup others(12): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246646279 | ||||||
| chr1:246646279 | C | CAAAAAAA others(6): Show |
26 | a0001c0001t0001g0013 a0001c0001t0001g0132 a0001c0001t0001g0165 others(23): Show |
26 | HG00733.hp1 HG01243.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.938-857_938-845dup others(13): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246646279 | ||||||
| chr1:246646279 | C | CAAAAAAA others(7): Show |
13 | a0001c0001t0001g0027 a0001c0001t0001g0288 a0001c0001t0002g0170 others(10): Show |
13 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.938-858_938-845dup others(14): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246646279 | ||||||
| chr1:246646279 | C | CAAAAAAA others(8): Show |
3 | a0001c0001t0004g0044 a0001c0001t0004g0151 a0001c0006t0001g0011 |
3 | HG02109.hp1 HG02486.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.938-859_938-845dup others(15): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 246646279 | ||||||
| chr1:246646361 | C | T | 1 | a0001c0001t0003g0245 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.938-778C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646361 | |||||||
| chr1:246646427 | T | C | 1 | a0007c0005t0023g0045 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.938-712T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646427 | |||||||
| chr1:246646445 | C | G | 1 | a0001c0001t0001g0304 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.938-694C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646445 | |||||||
| chr1:246646541 | C | T | 2 | a0002c0002t0001g0169 a0002c0002t0006g0033 |
2 | HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.938-598C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646541 | |||||||
| chr1:246646550 | A | C | 43 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(40): Show |
43 | HG00140.hp1 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.938-589A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646550 | |||||||
| chr1:246646566 | C | T | 1 | a0001c0006t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.938-573C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646566 | |||||||
| chr1:246646574 | G | A | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.938-565G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646574 | |||||||
| chr1:246646575 | G | T | 2 | a0001c0001t0018g0254 a0002c0002t0002g0249 |
2 | NA18945.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.938-564G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646575 | |||||||
| chr1:246646654 | G | A | 274 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(271): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.938-485G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646654 | |||||||
| chr1:246646792 | C | A | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.938-347C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | 246646792 | |||||||
| chr1:246648394 | A | G | 114 | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(111): Show |
114 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.1836+357A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246648394 | |||||||
| chr1:246648402 | C | T | 97 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(94): Show |
100 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1836+365C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246648402 | |||||||
| chr1:246648463 | T | C | 1 | a0001c0001t0016g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1836+426T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246648463 | |||||||
| chr1:246648648 | C | T | 37 | a0001c0001t0001g0027 a0001c0001t0001g0093 a0001c0001t0001g0125 others(34): Show |
37 | HG00735.hp1 HG01884.hp2 HG02109.hp1 others(34): Show |
intron_variant | MODIFIER | c.1836+611C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246648648 | |||||||
| chr1:246648888 | A | G | 1 | a0007c0005t0023g0045 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1836+851A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246648888 | |||||||
| chr1:246648940 | G | C | 1 | a0001c0001t0002g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1836+903G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246648940 | |||||||
| chr1:246649091 | A | C | 1 | a0001c0001t0001g0253 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1836+1054A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246649091 | |||||||
| chr1:246649105 | T | G | 1 | a0001c0001t0005g0203 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1836+1068T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246649105 | |||||||
| chr1:246649112 | A | G | 26 | a0001c0001t0001g0132 a0001c0001t0004g0018 a0001c0001t0004g0044 others(23): Show |
26 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.1836+1075A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246649112 | |||||||
| chr1:246649160 | TG | T | 13 | a0001c0001t0001g0078 a0001c0001t0001g0302 a0001c0001t0003g0056 others(10): Show |
13 | HG01934.hp2 HG02071.hp1 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1836+1124delG | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246649160 | |||||||
| chr1:246649161 | G | T | 53 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0088 others(50): Show |
55 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.1836+1124G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246649161 | |||||||
| chr1:246649161 | GT | G | 218 | a0001c0001t0001g0024 a0001c0001t0001g0054 a0001c0001t0001g0055 others(215): Show |
220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1836+1139delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246649161 | ||||||
| chr1:246649247 | A | G | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1836+1210A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246649247 | |||||||
| chr1:246649258 | A | G | 26 | a0001c0001t0001g0132 a0001c0001t0004g0018 a0001c0001t0004g0044 others(23): Show |
26 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.1836+1221A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246649258 | |||||||
| chr1:246649375 | G | C | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1836+1338G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246649375 | |||||||
| chr1:246649576 | C | T | 1 | a0002c0002t0001g0169 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1836+1539C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246649576 | |||||||
| chr1:246649614 | TGAA | T | 10 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(7): Show |
10 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1836+1585_1836+158 others(7): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246649614 | ||||||
| chr1:246649808 | C | T | 1 | a0001c0001t0003g0204 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1836+1771C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246649808 | |||||||
| chr1:246649929 | T | C | 1 | a0001c0001t0002g0219 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1836+1892T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246649929 | |||||||
| chr1:246650162 | G | A | 1 | a0002c0002t0001g0169 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1836+2125G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246650162 | |||||||
| chr1:246650175 | A | C | 225 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0054 others(222): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1836+2138A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246650175 | |||||||
| chr1:246650676 | C | CT | 227 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0027 others(224): Show |
229 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.1836+2658dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246650676 | ||||||
| chr1:246650676 | C | CTT | 11 | a0001c0001t0001g0195 a0001c0001t0001g0262 a0001c0001t0002g0102 others(8): Show |
11 | HG00140.hp2 HG00280.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1836+2657_1836+265 others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246650676 | ||||||
| chr1:246650676 | C | CTTT | 7 | a0001c0001t0003g0049 a0001c0001t0003g0068 a0004c0004t0003g0117 others(4): Show |
7 | HG01256.hp2 HG01993.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1836+2656_1836+265 others(7): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246650676 | ||||||
| chr1:246650676 | C | CTTTT | 47 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0088 others(44): Show |
49 | HG00423.hp2 HG01069.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.1836+2655_1836+265 others(8): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246650676 | ||||||
| chr1:246650735 | C | T | 14 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0165 others(11): Show |
14 | HG02486.hp2 HG02615.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.1836+2698C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246650735 | |||||||
| chr1:246650835 | G | A | 149 | a0001c0001t0001g0024 a0001c0001t0001g0054 a0001c0001t0001g0055 others(146): Show |
150 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.1836+2798G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246650835 | |||||||
| chr1:246650992 | C | A | 2 | a0001c0001t0003g0048 a0001c0001t0003g0081 |
2 | NA18942.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1836+2955C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246650992 | |||||||
| chr1:246651070 | T | A | 35 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(32): Show |
35 | HG00140.hp1 HG00733.hp1 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.1836+3033T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246651070 | |||||||
| chr1:246651074 | G | C | 274 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(271): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1836+3037G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246651074 | |||||||
| chr1:246651136 | AT | A | 14 | a0001c0001t0001g0013 a0001c0001t0001g0165 a0001c0001t0001g0167 others(11): Show |
14 | HG01109.hp1 HG01175.hp1 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1836+3108delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246651136 | ||||||
| chr1:246651254 | GC | G | 7 | a0001c0001t0004g0018 a0001c0001t0004g0044 a0001c0001t0004g0148 others(4): Show |
7 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1836+3222delC | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246651254 | ||||||
| chr1:246651399 | G | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0289 |
2 | HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1836+3362G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246651399 | |||||||
| chr1:246651440 | G | A | 2 | a0003c0003t0001g0034 a0003c0003t0001g0035 |
2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1836+3403G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246651440 | |||||||
| chr1:246651504 | A | G | 59 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0090 others(56): Show |
59 | HG00140.hp1 HG00733.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.1836+3467A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246651504 | |||||||
| chr1:246651644 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1836+3607A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246651644 | |||||||
| chr1:246651680 | C | T | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1836+3643C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246651680 | |||||||
| chr1:246651774 | A | G | 2 | a0001c0001t0001g0291 a0001c0001t0001g0294 |
2 | HG00621.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.1836+3737A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246651774 | |||||||
| chr1:246651872 | C | A | 1 | a0001c0001t0001g0063 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1836+3835C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246651872 | |||||||
| chr1:246652056 | C | T | 1 | a0001c0001t0005g0203 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1836+4019C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652056 | |||||||
| chr1:246652119 | G | A | 5 | a0001c0001t0001g0243 a0001c0001t0001g0293 a0001c0001t0001g0305 others(2): Show |
5 | HG00408.hp1 HG02083.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.1836+4082G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652119 | |||||||
| chr1:246652294 | G | T | 62 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0088 others(59): Show |
64 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.1836+4257G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652294 | |||||||
| chr1:246652299 | G | C | 2 | a0002c0002t0015g0166 a0008c0011t0015g0211 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1836+4262G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652299 | |||||||
| chr1:246652372 | T | C | 140 | a0001c0001t0001g0024 a0001c0001t0001g0054 a0001c0001t0001g0055 others(137): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1836+4335T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652372 | |||||||
| chr1:246652726 | C | T | 3 | a0001c0001t0001g0208 a0001c0001t0001g0239 a0001c0001t0003g0005 |
3 | NA18950.hp1 NA18983.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1836+4689C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652726 | |||||||
| chr1:246652730 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1836+4693C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652730 | |||||||
| chr1:246652731 | A | G | 116 | a0001c0001t0001g0024 a0001c0001t0001g0054 a0001c0001t0001g0055 others(113): Show |
116 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1836+4694A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652731 | |||||||
| chr1:246652733 | A | G | 114 | a0001c0001t0001g0024 a0001c0001t0001g0054 a0001c0001t0001g0055 others(111): Show |
114 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.1836+4696A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652733 | |||||||
| chr1:246652737 | G | C | 1 | a0001c0001t0004g0006 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1836+4700G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652737 | |||||||
| chr1:246652743 | G | A | 1 | a0001c0001t0001g0301 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1836+4706G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652743 | |||||||
| chr1:246652771 | A | G | 117 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0063 others(114): Show |
120 | HG00140.hp1 HG00423.hp2 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.1836+4734A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652771 | |||||||
| chr1:246652775 | C | A | 137 | a0001c0001t0001g0024 a0001c0001t0001g0054 a0001c0001t0001g0055 others(134): Show |
137 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.1836+4738C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652775 | |||||||
| chr1:246652779 | C | T | 12 | a0001c0001t0001g0027 a0001c0001t0001g0165 a0001c0001t0001g0167 others(9): Show |
12 | HG01981.hp1 HG02615.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.1836+4742C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652779 | |||||||
| chr1:246652780 | G | A | 65 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0088 others(62): Show |
67 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.1836+4743G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652780 | |||||||
| chr1:246652786 | C | CAAGGTCA others(259): Show |
1 | a0001c0001t0001g0287 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1836+4749_1836+475 others(270): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652786 | |||||||
| chr1:246652786 | C | CAAGGTCA others(126): Show |
17 | a0001c0001t0001g0024 a0001c0001t0001g0158 a0001c0001t0001g0243 others(14): Show |
17 | HG00408.hp2 HG01884.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.1836+4749_1836+475 others(137): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652786 | |||||||
| chr1:246652786 | C | CAAGGTCA others(259): Show |
1 | a0001c0009t0001g0189 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1836+4749_1836+475 others(270): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652786 | |||||||
| chr1:246652786 | C | CAAGGTCA others(126): Show |
1 | a0001c0001t0001g0252 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1836+4749_1836+475 others(137): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652786 | |||||||
| chr1:246652786 | C | CAAGGTCA others(392): Show |
1 | a0001c0001t0001g0305 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1836+4749_1836+475 others(403): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652786 | |||||||
| chr1:246652786 | C | CGAGGTCA others(126): Show |
5 | a0001c0001t0001g0054 a0001c0001t0001g0061 a0001c0001t0002g0047 others(2): Show |
5 | HG00280.hp1 HG00738.hp1 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.1836+4762_1836+476 others(137): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246652786 | ||||||
| chr1:246652786 | C | CGAGGTCA others(127): Show |
1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1836+4762_1836+476 others(138): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246652786 | ||||||
| chr1:246652787 | G | A | 45 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(42): Show |
45 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.1836+4750G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652787 | |||||||
| chr1:246652792 | C | T | 2 | a0002c0002t0001g0095 a0002c0002t0001g0123 |
2 | NA18747.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1836+4755C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652792 | |||||||
| chr1:246652800 | C | G | 68 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0090 others(65): Show |
69 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.1836+4763C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652800 | |||||||
| chr1:246652801 | G | A | 1 | a0002c0002t0001g0169 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1836+4764G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652801 | |||||||
| chr1:246652805 | C | A | 1 | a0001c0001t0001g0267 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1836+4768C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652805 | |||||||
| chr1:246652807 | A | G | 26 | a0001c0001t0001g0132 a0001c0001t0004g0018 a0001c0001t0004g0044 others(23): Show |
26 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.1836+4770A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652807 | |||||||
| chr1:246652807 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1836+4770A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652807 | |||||||
| chr1:246652810 | C | CTGGCTGA others(126): Show |
3 | a0001c0001t0001g0217 a0001c0001t0001g0297 a0001c0001t0001g0298 |
3 | NA18946.hp1 NA18951.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1836+4778_1836+477 others(137): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246652810 | ||||||
| chr1:246652811 | T | C | 5 | a0002c0002t0001g0029 a0002c0002t0001g0120 a0002c0002t0001g0131 others(2): Show |
5 | HG00741.hp2 HG01175.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1836+4774T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652811 | |||||||
| chr1:246652813 | G | A | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1836+4776G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652813 | |||||||
| chr1:246652816 | A | G | 204 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0054 others(201): Show |
206 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1836+4779A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652816 | |||||||
| chr1:246652820 | C | T | 2 | a0002c0002t0001g0147 a0002c0002t0007g0140 |
2 | NA18612.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.1836+4783C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652820 | |||||||
| chr1:246652821 | G | A | 1 | a0008c0011t0015g0211 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1836+4784G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652821 | |||||||
| chr1:246652831 | C | A | 1 | a0001c0001t0002g0105 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1836+4794C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652831 | |||||||
| chr1:246652832 | G | A | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1836+4795G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652832 | |||||||
| chr1:246652853 | A | C | 3 | a0001c0001t0001g0304 a0001c0001t0003g0221 a0002c0002t0001g0126 |
3 | HG00323.hp2 NA18906.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1836+4816A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652853 | |||||||
| chr1:246652855 | C | T | 272 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(269): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.1836+4818C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652855 | |||||||
| chr1:246652861 | G | A | 1 | a0003c0003t0004g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1836+4824G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652861 | |||||||
| chr1:246652865 | G | A | 61 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0027 others(58): Show |
61 | HG00140.hp1 HG00408.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.1836+4828G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652865 | |||||||
| chr1:246652866 | T | G | 26 | a0001c0001t0001g0024 a0001c0001t0001g0158 a0001c0001t0001g0243 others(23): Show |
26 | HG00408.hp2 HG01884.hp1 HG02083.hp2 others(23): Show |
intron_variant | MODIFIER | c.1836+4829T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652866 | |||||||
| chr1:246652866 | T | TGGCGGGC others(123): Show |
1 | a0001c0001t0002g0283 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1836+4831_1836+483 others(134): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246652866 | ||||||
| chr1:246652866 | T | TGGTGGCG others(126): Show |
3 | a0001c0001t0004g0156 a0001c0001t0004g0157 a0001c0001t0004g0172 |
3 | HG01109.hp2 HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1836+4846_1836+484 others(137): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246652866 | ||||||
| chr1:246652866 | T | TGGTGGCG others(126): Show |
72 | a0001c0001t0001g0055 a0001c0001t0001g0119 a0001c0001t0001g0164 others(69): Show |
72 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.1836+4846_1836+484 others(137): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246652866 | ||||||
| chr1:246652866 | T | TGGTGGCG others(259): Show |
6 | a0001c0001t0002g0099 a0001c0001t0002g0101 a0001c0001t0002g0102 others(3): Show |
6 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.1836+4846_1836+484 others(270): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246652866 | ||||||
| chr1:246652866 | T | TGGTGGCG others(259): Show |
16 | a0001c0001t0001g0060 a0001c0001t0001g0309 a0001c0001t0002g0051 others(13): Show |
16 | HG00423.hp1 HG01074.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.1836+4846_1836+484 others(270): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246652866 | ||||||
| chr1:246652866 | T | TGGTGGCG others(392): Show |
1 | a0001c0001t0002g0003 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1836+4846_1836+484 others(403): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246652866 | ||||||
| chr1:246652866 | T | TGGTGGCG others(259): Show |
1 | a0001c0001t0001g0306 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1836+4846_1836+484 others(270): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246652866 | ||||||
| chr1:246652866 | T | TGGTGGCG others(126): Show |
1 | a0001c0001t0005g0203 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1836+4846_1836+484 others(137): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246652866 | ||||||
| chr1:246652866 | T | TGGTGGCG others(126): Show |
1 | a0001c0001t0002g0212 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1836+4854_1836+485 others(137): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246652866 | ||||||
| chr1:246652873 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1836+4836G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652873 | |||||||
| chr1:246652874 | G | GGCGCCTG others(126): Show |
1 | a0001c0001t0005g0152 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1836+4846_1836+484 others(137): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246652874 | ||||||
| chr1:246652877 | G | A | 2 | a0001c0001t0003g0314 a0001c0001t0003g0315 |
2 | HG03017.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1836+4840G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652877 | |||||||
| chr1:246652884 | G | A | 2 | a0001c0001t0001g0208 a0001c0001t0001g0239 |
2 | NA18950.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1836+4847G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652884 | |||||||
| chr1:246652928 | T | C | 13 | a0001c0001t0001g0175 a0001c0001t0003g0176 a0001c0001t0004g0006 others(10): Show |
13 | HG00735.hp1 HG02145.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.1836+4891T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652928 | |||||||
| chr1:246652940 | C | G | 2 | a0002c0002t0015g0166 a0008c0011t0015g0211 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1836+4903C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652940 | |||||||
| chr1:246652940 | C | T | 10 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(7): Show |
10 | HG00735.hp1 HG02647.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1836+4903C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652940 | |||||||
| chr1:246652958 | T | C | 2 | a0001c0001t0002g0231 a0001c0006t0001g0011 |
2 | HG02486.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1836+4921T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652958 | |||||||
| chr1:246652959 | G | A | 1 | a0001c0006t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1836+4922G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652959 | |||||||
| chr1:246652961 | A | G | 1 | a0001c0006t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1836+4924A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652961 | |||||||
| chr1:246652983 | T | G | 1 | a0001c0001t0024g0270 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1836+4946T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246652983 | |||||||
| chr1:246653003 | CA | C | 11 | a0001c0006t0001g0011 a0002c0002t0006g0033 a0003c0003t0004g0036 others(8): Show |
11 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1836+4981delA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246653003 | ||||||
| chr1:246653015 | AAAAG | A | 9 | a0001c0001t0001g0024 a0001c0001t0001g0202 a0001c0001t0001g0263 others(6): Show |
9 | HG01261.hp1 HG02145.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1836+4983_1836+498 others(8): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246653015 | ||||||
| chr1:246653041 | A | G | 1 | a0010c0008t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1836+5004A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246653041 | |||||||
| chr1:246653363 | C | T | 3 | a0001c0001t0003g0176 a0001c0001t0004g0006 a0001c0001t0004g0008 |
3 | HG02145.hp2 HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1836+5326C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246653363 | |||||||
| chr1:246653407 | C | T | 1 | a0001c0001t0009g0014 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1836+5370C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246653407 | |||||||
| chr1:246653583 | G | A | 1 | a0007c0005t0023g0045 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1836+5546G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246653583 | |||||||
| chr1:246653704 | C | T | 13 | a0001c0001t0001g0132 a0001c0001t0004g0018 a0001c0001t0004g0044 others(10): Show |
13 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1836+5667C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246653704 | |||||||
| chr1:246653705 | G | A | 204 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0054 others(201): Show |
207 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.1836+5668G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246653705 | |||||||
| chr1:246653771 | C | G | 26 | a0001c0001t0001g0132 a0001c0001t0004g0018 a0001c0001t0004g0044 others(23): Show |
26 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.1836+5734C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246653771 | |||||||
| chr1:246653879 | C | T | 1 | a0001c0006t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1836+5842C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246653879 | |||||||
| chr1:246653907 | A | G | 1 | a0005c0010t0002g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1836+5870A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246653907 | |||||||
| chr1:246653949 | C | T | 1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1836+5912C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246653949 | |||||||
| chr1:246653995 | C | T | 1 | a0001c0001t0005g0203 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1836+5958C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246653995 | |||||||
| chr1:246654060 | A | T | 2 | a0002c0002t0001g0120 a0002c0002t0001g0149 |
2 | HG01175.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1836+6023A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246654060 | |||||||
| chr1:246654086 | C | T | 1 | a0001c0001t0013g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1836+6049C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246654086 | |||||||
| chr1:246654089 | C | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0167 |
2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1836+6052C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246654089 | |||||||
| chr1:246654150 | C | T | 1 | a0001c0001t0002g0259 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1837-6049C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246654150 | |||||||
| chr1:246654166 | A | G | 60 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0088 others(57): Show |
62 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.1837-6033A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246654166 | |||||||
| chr1:246654236 | C | A | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1837-5963C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246654236 | |||||||
| chr1:246654253 | C | T | 7 | a0001c0001t0004g0018 a0001c0001t0004g0044 a0001c0001t0004g0148 others(4): Show |
7 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1837-5946C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246654253 | |||||||
| chr1:246654415 | G | C | 26 | a0001c0001t0001g0132 a0001c0001t0004g0018 a0001c0001t0004g0044 others(23): Show |
26 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.1837-5784G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246654415 | |||||||
| chr1:246654468 | C | T | 6 | a0004c0004t0003g0117 a0004c0004t0003g0182 a0004c0004t0003g0183 others(3): Show |
6 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1837-5731C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246654468 | |||||||
| chr1:246654553 | G | A | 1 | a0002c0002t0001g0131 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1837-5646G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246654553 | |||||||
| chr1:246654580 | A | G | 1 | a0001c0001t0020g0026 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1837-5619A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246654580 | |||||||
| chr1:246654793 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1837-5406G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246654793 | |||||||
| chr1:246654823 | GT | G | 264 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(261): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1837-5365delT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246654823 | ||||||
| chr1:246654942 | A | T | 62 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0090 others(59): Show |
62 | HG00140.hp1 HG00733.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.1837-5257A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246654942 | |||||||
| chr1:246654947 | C | T | 3 | a0001c0001t0003g0248 a0002c0002t0001g0095 a0002c0002t0001g0123 |
3 | HG04199.hp2 NA18747.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1837-5252C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246654947 | |||||||
| chr1:246655086 | A | G | 1 | a0001c0001t0003g0005 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1837-5113A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246655086 | |||||||
| chr1:246655332 | A | G | 140 | a0001c0001t0001g0024 a0001c0001t0001g0054 a0001c0001t0001g0055 others(137): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1837-4867A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246655332 | |||||||
| chr1:246655425 | T | A | 1 | a0001c0006t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1837-4774T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246655425 | |||||||
| chr1:246655707 | A | C | 1 | a0001c0001t0003g0109 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1837-4492A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246655707 | |||||||
| chr1:246655853 | G | A | 62 | a0001c0001t0001g0119 a0001c0001t0001g0192 a0001c0001t0001g0205 others(59): Show |
62 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.1837-4346G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246655853 | |||||||
| chr1:246655857 | T | A | 14 | a0001c0001t0001g0002 a0001c0001t0001g0302 a0001c0001t0003g0005 others(11): Show |
15 | HG01257.hp2 HG01258.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1837-4342T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246655857 | |||||||
| chr1:246656114 | G | A | 1 | a0001c0001t0002g0215 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1837-4085G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246656114 | |||||||
| chr1:246656166 | A | G | 1 | a0001c0012t0002g0276 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1837-4033A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246656166 | |||||||
| chr1:246656233 | AG | A | 45 | a0001c0001t0001g0027 a0001c0001t0001g0132 a0001c0001t0001g0175 others(42): Show |
45 | HG00733.hp1 HG00735.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.1837-3965delG | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246656233 | |||||||
| chr1:246656265 | A | T | 1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1837-3934A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246656265 | |||||||
| chr1:246656293 | C | T | 27 | a0001c0001t0001g0132 a0001c0001t0004g0018 a0001c0001t0004g0044 others(24): Show |
27 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.1837-3906C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246656293 | |||||||
| chr1:246656417 | T | C | 4 | a0001c0001t0005g0025 a0001c0001t0020g0026 a0001c0006t0001g0011 others(1): Show |
4 | HG02486.hp1 HG02486.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1837-3782T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246656417 | |||||||
| chr1:246656679 | G | A | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1837-3520G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246656679 | |||||||
| chr1:246656801 | G | C | 267 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(264): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.1837-3398G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246656801 | |||||||
| chr1:246656838 | G | T | 2 | a0001c0001t0003g0048 a0001c0001t0003g0081 |
2 | NA18942.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1837-3361G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246656838 | |||||||
| chr1:246656852 | C | T | 1 | a0001c0001t0017g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1837-3347C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246656852 | |||||||
| chr1:246656918 | C | T | 1 | a0001c0001t0002g0256 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1837-3281C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246656918 | |||||||
| chr1:246656919 | G | A | 24 | a0001c0001t0001g0013 a0001c0001t0001g0165 a0001c0001t0001g0167 others(21): Show |
24 | HG00558.hp1 HG00621.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.1837-3280G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246656919 | |||||||
| chr1:246656943 | A | G | 11 | a0001c0001t0001g0175 a0001c0001t0004g0016 a0001c0001t0004g0017 others(8): Show |
11 | HG00735.hp1 HG00741.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1837-3256A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246656943 | |||||||
| chr1:246657139 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1837-3060T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246657139 | |||||||
| chr1:246657208 | C | T | 1 | a0001c0001t0002g0003 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1837-2991C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246657208 | |||||||
| chr1:246657209 | G | A | 1 | a0002c0002t0001g0145 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1837-2990G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246657209 | |||||||
| chr1:246657236 | C | T | 6 | a0004c0004t0003g0117 a0004c0004t0003g0182 a0004c0004t0003g0183 others(3): Show |
6 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1837-2963C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246657236 | |||||||
| chr1:246657512 | C | T | 2 | a0001c0001t0001g0208 a0001c0001t0001g0239 |
2 | NA18950.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1837-2687C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246657512 | |||||||
| chr1:246657555 | A | C | 8 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(5): Show |
8 | HG00140.hp1 HG01515.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.1837-2644A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246657555 | |||||||
| chr1:246657730 | G | A | 28 | a0001c0001t0004g0009 a0001c0001t0004g0018 a0001c0001t0004g0044 others(25): Show |
28 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1837-2469G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246657730 | |||||||
| chr1:246657770 | A | G | 2 | a0002c0002t0015g0166 a0008c0011t0015g0211 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1837-2429A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246657770 | |||||||
| chr1:246657807 | A | G | 24 | a0001c0001t0001g0013 a0001c0001t0001g0061 a0001c0001t0001g0165 others(21): Show |
24 | HG00558.hp1 HG00621.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.1837-2392A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246657807 | |||||||
| chr1:246658099 | T | A | 1 | a0006c0007t0003g0265 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1837-2100T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246658099 | |||||||
| chr1:246658204 | T | C | 8 | a0003c0003t0001g0034 a0003c0003t0001g0035 a0003c0003t0001g0040 others(5): Show |
8 | HG00733.hp1 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1837-1995T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246658204 | |||||||
| chr1:246658273 | CCT | C | 25 | a0001c0001t0001g0013 a0001c0001t0001g0061 a0001c0001t0001g0165 others(22): Show |
25 | HG00558.hp1 HG00621.hp2 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.1837-1922_1837-192 others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246658273 | ||||||
| chr1:246658297 | A | G | 90 | a0001c0001t0001g0027 a0001c0001t0001g0132 a0001c0001t0001g0288 others(87): Show |
91 | HG00423.hp2 HG00733.hp1 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.1837-1902A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246658297 | |||||||
| chr1:246658465 | CTTGTTGA others(3): Show |
C | 1 | a0007c0005t0023g0045 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1837-1731_1837-172 others(14): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246658465 | ||||||
| chr1:246658472 | A | AT | 21 | a0001c0001t0001g0027 a0001c0001t0001g0060 a0001c0001t0001g0061 others(18): Show |
21 | HG01175.hp2 HG01978.hp2 HG02293.hp1 others(18): Show |
intron_variant | MODIFIER | c.1837-1717dupT | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246658472 | ||||||
| chr1:246658558 | C | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0288 |
2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1837-1641C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246658558 | |||||||
| chr1:246658582 | C | T | 1 | a0001c0001t0002g0308 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1837-1617C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246658582 | |||||||
| chr1:246658614 | C | T | 1 | a0001c0001t0003g0218 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1837-1585C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246658614 | |||||||
| chr1:246658670 | A | G | 1 | a0001c0001t0016g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1837-1529A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246658670 | |||||||
| chr1:246658687 | C | A | 1 | a0001c0001t0002g0085 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1837-1512C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246658687 | |||||||
| chr1:246658709 | GGCCAGCA others(10): Show |
G | 7 | a0003c0003t0001g0039 a0004c0004t0003g0117 a0004c0004t0003g0182 others(4): Show |
7 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1837-1474_1837-145 others(21): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246658709 | ||||||
| chr1:246658721 | ACTGATGC others(15): Show |
A | 54 | a0001c0001t0001g0168 a0001c0001t0001g0302 a0001c0001t0002g0181 others(51): Show |
55 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.1837-1457_1837-143 others(26): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246658721 | ||||||
| chr1:246658912 | C | T | 1 | a0007c0005t0023g0045 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1837-1287C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246658912 | |||||||
| chr1:246658976 | G | T | 7 | a0003c0003t0001g0039 a0004c0004t0003g0117 a0004c0004t0003g0182 others(4): Show |
7 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1837-1223G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246658976 | |||||||
| chr1:246659004 | TAGGC | T | 8 | a0001c0001t0001g0027 a0001c0001t0001g0132 a0001c0001t0004g0028 others(5): Show |
8 | HG02486.hp1 HG02486.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1837-1191_1837-118 others(8): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246659004 | ||||||
| chr1:246659151 | G | A | 1 | a0003c0003t0001g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1837-1048G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659151 | |||||||
| chr1:246659184 | C | T | 1 | a0001c0012t0002g0276 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1837-1015C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659184 | |||||||
| chr1:246659203 | G | A | 4 | a0001c0001t0003g0135 a0001c0001t0003g0245 a0001c0001t0003g0246 others(1): Show |
4 | NA18985.hp2 NA18999.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1837-996G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659203 | |||||||
| chr1:246659247 | G | C | 1 | a0001c0006t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1837-952G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659247 | |||||||
| chr1:246659251 | T | G | 1 | a0001c0001t0003g0292 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1837-948T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659251 | |||||||
| chr1:246659319 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1837-880G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659319 | |||||||
| chr1:246659320 | T | C | 106 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0060 others(103): Show |
107 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1837-879T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659320 | |||||||
| chr1:246659321 | G | A | 3 | a0001c0001t0010g0224 a0001c0001t0010g0225 a0001c0001t0010g0284 |
3 | HG00558.hp2 HG02080.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1837-878G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659321 | |||||||
| chr1:246659322 | C | T | 1 | a0001c0006t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1837-877C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659322 | |||||||
| chr1:246659323 | G | C | 3 | a0001c0001t0010g0224 a0001c0001t0010g0225 a0001c0001t0010g0284 |
3 | HG00558.hp2 HG02080.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1837-876G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659323 | |||||||
| chr1:246659333 | A | G | 29 | a0001c0001t0003g0056 a0001c0001t0003g0075 a0001c0001t0003g0076 others(26): Show |
29 | HG00733.hp1 HG00741.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.1837-866A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659333 | |||||||
| chr1:246659361 | A | G | 20 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0018 others(17): Show |
20 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1837-838A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659361 | |||||||
| chr1:246659365 | C | A | 1 | a0002c0002t0001g0110 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1837-834C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659365 | |||||||
| chr1:246659369 | C | T | 1 | a0002c0002t0001g0110 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1837-830C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659369 | |||||||
| chr1:246659370 | A | G | 2 | a0001c0006t0001g0011 a0002c0002t0001g0110 |
2 | HG02129.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1837-829A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659370 | |||||||
| chr1:246659376 | C | T | 13 | a0001c0001t0001g0027 a0001c0001t0001g0090 a0001c0001t0001g0091 others(10): Show |
13 | HG00140.hp1 HG01515.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.1837-823C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659376 | |||||||
| chr1:246659377 | G | T | 14 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0018 others(11): Show |
14 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1837-822G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659377 | |||||||
| chr1:246659390 | C | G | 33 | a0001c0001t0001g0027 a0001c0001t0001g0090 a0001c0001t0001g0091 others(30): Show |
33 | HG00140.hp1 HG00733.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.1837-809C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659390 | |||||||
| chr1:246659403 | G | A | 2 | a0001c0001t0001g0060 a0010c0008t0001g0159 |
2 | HG01978.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1837-796G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659403 | |||||||
| chr1:246659405 | T | A | 24 | a0001c0001t0001g0013 a0001c0001t0001g0090 a0001c0001t0001g0091 others(21): Show |
24 | HG00140.hp1 HG00558.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.1837-794T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659405 | |||||||
| chr1:246659405 | T | C | 59 | a0001c0001t0001g0168 a0001c0001t0001g0196 a0001c0001t0001g0302 others(56): Show |
60 | HG00423.hp2 HG00738.hp2 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.1837-794T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659405 | |||||||
| chr1:246659409 | T | A | 134 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(131): Show |
136 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1837-790T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659409 | |||||||
| chr1:246659411 | G | A | 17 | a0001c0001t0001g0013 a0001c0001t0001g0165 a0001c0001t0001g0167 others(14): Show |
17 | HG00558.hp1 HG00621.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.1837-788G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659411 | |||||||
| chr1:246659421 | C | T | 208 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(205): Show |
211 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.1837-778C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659421 | |||||||
| chr1:246659431 | G | A | 4 | a0001c0001t0001g0217 a0001c0001t0001g0297 a0001c0001t0002g0193 others(1): Show |
4 | HG02300.hp1 NA18951.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1837-768G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659431 | |||||||
| chr1:246659438 | C | G | 2 | a0001c0001t0001g0217 a0001c0001t0001g0297 |
2 | NA18951.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1837-761C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659438 | |||||||
| chr1:246659464 | G | A | 4 | a0002c0002t0006g0033 a0003c0003t0004g0036 a0003c0003t0004g0037 others(1): Show |
4 | HG01243.hp1 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1837-735G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659464 | |||||||
| chr1:246659467 | T | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1837-732T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659467 | |||||||
| chr1:246659467 | T | C | 1 | a0001c0001t0004g0006 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1837-732T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659467 | |||||||
| chr1:246659527 | G | A | 1 | a0001c0006t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1837-672G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659527 | |||||||
| chr1:246659531 | A | G | 1 | a0001c0006t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1837-668A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659531 | |||||||
| chr1:246659573 | C | T | 1 | a0001c0001t0024g0270 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1837-626C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659573 | |||||||
| chr1:246659579 | A | G | 1 | a0001c0001t0024g0270 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1837-620A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659579 | |||||||
| chr1:246659582 | A | G | 61 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0061 others(58): Show |
61 | HG00558.hp1 HG00621.hp2 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.1837-617A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659582 | |||||||
| chr1:246659589 | T | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0167 |
2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1837-610T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246659589 | |||||||
| chr1:246659594 | C | CA | 9 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(6): Show |
9 | HG00140.hp1 HG01515.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1837-591dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246659594 | ||||||
| chr1:246659594 | CA | C | 23 | a0001c0001t0001g0060 a0001c0001t0001g0154 a0001c0001t0001g0289 others(20): Show |
23 | HG01175.hp2 HG01243.hp1 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.1837-591delA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 246659594 | ||||||
| chr1:246660011 | G | A | 44 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0061 others(41): Show |
44 | HG00558.hp1 HG00621.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.1837-188G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 9/10 | chr1 | 246660011 | |||||||
| chr1:246660445 | G | A | 1 | a0001c0001t0002g0129 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1972+111G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246660445 | |||||||
| chr1:246660447 | C | G | 1 | a0004c0004t0021g0150 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1972+113C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246660447 | |||||||
| chr1:246660496 | C | T | 1 | a0007c0005t0023g0045 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1972+162C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246660496 | |||||||
| chr1:246660555 | G | A | 94 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0061 others(91): Show |
95 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.1972+221G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246660555 | |||||||
| chr1:246660632 | G | A | 1 | a0001c0001t0003g0142 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1972+298G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246660632 | |||||||
| chr1:246660676 | G | T | 30 | a0001c0001t0001g0060 a0001c0001t0001g0154 a0001c0001t0001g0289 others(27): Show |
30 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.1972+342G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246660676 | |||||||
| chr1:246660783 | A | C | 1 | a0004c0004t0021g0150 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1972+449A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246660783 | |||||||
| chr1:246661021 | T | G | 135 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0060 others(132): Show |
136 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(133): Show |
intron_variant | MODIFIER | c.1972+687T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246661021 | |||||||
| chr1:246661319 | T | C | 8 | a0002c0002t0001g0029 a0003c0003t0001g0034 a0003c0003t0001g0035 others(5): Show |
8 | HG00733.hp1 HG00741.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1972+985T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246661319 | |||||||
| chr1:246661442 | A | G | 1 | a0001c0001t0002g0079 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1972+1108A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246661442 | |||||||
| chr1:246661538 | T | A | 298 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(295): Show |
301 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.1972+1204T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246661538 | |||||||
| chr1:246661618 | A | G | 1 | a0001c0001t0002g0127 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1972+1284A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246661618 | |||||||
| chr1:246661752 | T | TA | 4 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(1): Show |
4 | HG01109.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1972+1422dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 246661752 | ||||||
| chr1:246661888 | C | G | 10 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0019 others(7): Show |
10 | HG02622.hp1 HG02647.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1972+1554C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246661888 | |||||||
| chr1:246662031 | C | T | 1 | a0007c0005t0023g0045 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1972+1697C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246662031 | |||||||
| chr1:246662118 | A | G | 31 | a0001c0001t0001g0060 a0001c0001t0001g0154 a0001c0001t0001g0175 others(28): Show |
31 | HG00735.hp1 HG01109.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.1972+1784A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246662118 | |||||||
| chr1:246662177 | G | T | 3 | a0001c0001t0002g0170 a0001c0001t0002g0173 a0001c0001t0002g0181 |
3 | HG01891.hp1 HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1972+1843G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246662177 | |||||||
| chr1:246662540 | C | G | 1 | a0001c0001t0004g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1972+2206C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246662540 | |||||||
| chr1:246662543 | G | C | 128 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0061 others(125): Show |
129 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(126): Show |
intron_variant | MODIFIER | c.1972+2209G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246662543 | |||||||
| chr1:246662545 | C | T | 2 | a0001c0001t0003g0221 a0007c0005t0023g0045 |
2 | HG03209.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1972+2211C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246662545 | |||||||
| chr1:246662681 | G | A | 10 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0019 others(7): Show |
10 | HG02622.hp1 HG02647.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1972+2347G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246662681 | |||||||
| chr1:246662877 | C | T | 75 | a0001c0001t0001g0061 a0001c0001t0001g0078 a0001c0001t0001g0165 others(72): Show |
76 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.1972+2543C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246662877 | |||||||
| chr1:246663109 | T | G | 11 | a0001c0001t0004g0028 a0001c0001t0004g0155 a0001c0001t0004g0156 others(8): Show |
11 | HG01109.hp2 HG01243.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1973-2591T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246663109 | |||||||
| chr1:246663111 | C | T | 7 | a0003c0003t0001g0039 a0004c0004t0003g0117 a0004c0004t0003g0182 others(4): Show |
7 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1973-2589C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246663111 | |||||||
| chr1:246663213 | G | A | 12 | a0001c0001t0004g0009 a0001c0001t0004g0018 a0001c0001t0004g0044 others(9): Show |
12 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1973-2487G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246663213 | |||||||
| chr1:246663234 | T | G | 313 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(310): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.1973-2466T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246663234 | |||||||
| chr1:246663270 | T | C | 8 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0019 others(5): Show |
8 | HG02647.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1973-2430T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246663270 | |||||||
| chr1:246663271 | C | T | 4 | a0001c0001t0007g0065 a0002c0002t0001g0139 a0002c0002t0007g0140 others(1): Show |
4 | HG02083.hp1 NA18612.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.1973-2429C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246663271 | |||||||
| chr1:246663272 | G | A | 7 | a0003c0003t0001g0039 a0004c0004t0003g0117 a0004c0004t0003g0182 others(4): Show |
7 | HG02451.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1973-2428G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246663272 | |||||||
| chr1:246663336 | T | TA | 14 | a0001c0001t0004g0009 a0001c0001t0004g0018 a0001c0001t0004g0044 others(11): Show |
14 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1973-2348dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 246663336 | ||||||
| chr1:246663336 | T | TAA | 7 | a0001c0001t0003g0084 a0001c0001t0004g0028 a0002c0002t0006g0033 others(4): Show |
7 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1973-2349_1973-234 others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 246663336 | ||||||
| chr1:246663365 | C | T | 242 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(239): Show |
245 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.1973-2335C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246663365 | |||||||
| chr1:246663368 | A | G | 3 | a0001c0001t0001g0214 a0001c0001t0001g0251 a0001c0001t0001g0299 |
3 | HG02015.hp2 NA18969.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1973-2332A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246663368 | |||||||
| chr1:246663740 | C | CA | 11 | a0001c0001t0002g0308 a0002c0002t0001g0120 a0002c0002t0001g0149 others(8): Show |
11 | HG01175.hp2 HG02451.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1973-1949dupA | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 246663740 | ||||||
| chr1:246663749 | A | C | 1 | a0001c0001t0002g0051 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1973-1951A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246663749 | |||||||
| chr1:246663900 | G | A | 135 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0060 others(132): Show |
136 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(133): Show |
intron_variant | MODIFIER | c.1973-1800G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246663900 | |||||||
| chr1:246663929 | T | C | 2 | a0001c0001t0002g0259 a0001c0001t0002g0282 |
2 | HG02698.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1973-1771T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246663929 | |||||||
| chr1:246663937 | T | C | 22 | a0001c0001t0004g0009 a0001c0001t0004g0018 a0001c0001t0004g0028 others(19): Show |
22 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.1973-1763T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246663937 | |||||||
| chr1:246664254 | A | G | 3 | a0002c0002t0001g0120 a0002c0002t0001g0131 a0002c0002t0001g0149 |
3 | HG01175.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1973-1446A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664254 | |||||||
| chr1:246664350 | T | G | 2 | a0001c0001t0001g0252 a0001c0001t0001g0307 |
2 | HG00408.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1973-1350T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664350 | |||||||
| chr1:246664375 | G | A | 4 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(1): Show |
4 | HG01109.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1973-1325G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664375 | |||||||
| chr1:246664431 | C | CTT | 14 | a0001c0001t0001g0060 a0001c0001t0001g0090 a0001c0001t0001g0091 others(11): Show |
14 | HG00140.hp1 HG01175.hp2 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.1973-1257_1973-125 others(6): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 246664431 | ||||||
| chr1:246664449 | A | T | 1 | a0001c0001t0001g0301 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1973-1251A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664449 | |||||||
| chr1:246664496 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1973-1204A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664496 | |||||||
| chr1:246664503 | T | G | 1 | a0001c0001t0001g0267 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1973-1197T>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664503 | |||||||
| chr1:246664512 | C | T | 1 | a0001c0001t0022g0087 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1973-1188C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664512 | |||||||
| chr1:246664527 | T | C | 37 | a0001c0001t0001g0060 a0001c0001t0001g0090 a0001c0001t0001g0091 others(34): Show |
37 | HG00140.hp1 HG01109.hp2 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.1973-1173T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664527 | |||||||
| chr1:246664551 | T | C | 1 | a0001c0001t0003g0292 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1973-1149T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664551 | |||||||
| chr1:246664581 | C | T | 1 | a0001c0001t0019g0106 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1973-1119C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664581 | |||||||
| chr1:246664583 | C | T | 3 | a0001c0001t0009g0012 a0001c0001t0009g0014 a0001c0001t0009g0015 |
3 | HG02976.hp1 HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1973-1117C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664583 | |||||||
| chr1:246664600 | A | G | 74 | a0001c0001t0001g0027 a0001c0001t0001g0132 a0001c0001t0001g0235 others(71): Show |
76 | HG00738.hp2 HG00741.hp2 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.1973-1100A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664600 | |||||||
| chr1:246664616 | C | T | 7 | a0001c0001t0001g0061 a0001c0001t0001g0213 a0001c0001t0001g0232 others(4): Show |
7 | HG01109.hp1 HG01175.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.1973-1084C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664616 | |||||||
| chr1:246664617 | G | A | 33 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(30): Show |
33 | HG00140.hp1 HG00733.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.1973-1083G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664617 | |||||||
| chr1:246664619 | G | A | 6 | a0001c0001t0001g0061 a0001c0001t0001g0213 a0001c0001t0001g0232 others(3): Show |
6 | HG01109.hp1 HG01175.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.1973-1081G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664619 | |||||||
| chr1:246664628 | G | A | 1 | a0002c0002t0007g0140 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1973-1072G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664628 | |||||||
| chr1:246664628 | G | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0288 |
2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1973-1072G>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664628 | |||||||
| chr1:246664632 | C | T | 233 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0027 others(230): Show |
235 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.1973-1068C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664632 | |||||||
| chr1:246664633 | A | G | 1 | a0002c0002t0007g0140 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1973-1067A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664633 | |||||||
| chr1:246664637 | A | G | 17 | a0001c0001t0001g0027 a0001c0001t0001g0090 a0001c0001t0001g0091 others(14): Show |
17 | HG00140.hp1 HG01175.hp2 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.1973-1063A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664637 | |||||||
| chr1:246664640 | A | C | 1 | a0001c0001t0001g0272 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1973-1060A>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664640 | |||||||
| chr1:246664643 | G | A | 4 | a0001c0001t0003g0056 a0001c0001t0003g0075 a0001c0001t0003g0077 others(1): Show |
4 | HG02071.hp1 HG02135.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.1973-1057G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664643 | |||||||
| chr1:246664647 | C | G | 3 | a0001c0001t0001g0078 a0001c0001t0001g0226 a0001c0001t0001g0281 |
3 | HG01934.hp2 NA18945.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1973-1053C>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664647 | |||||||
| chr1:246664647 | C | T | 1 | a0001c0001t0003g0086 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1973-1053C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664647 | |||||||
| chr1:246664648 | G | C | 26 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0303 others(23): Show |
26 | HG00738.hp2 HG01109.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.1973-1052G>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664648 | |||||||
| chr1:246664661 | C | T | 62 | a0001c0001t0001g0024 a0001c0001t0001g0060 a0001c0001t0001g0090 others(59): Show |
62 | HG00140.hp1 HG00733.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.1973-1039C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664661 | |||||||
| chr1:246664662 | G | A | 1 | a0001c0001t0003g0086 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1973-1038G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664662 | |||||||
| chr1:246664669 | G | A | 1 | a0001c0001t0003g0280 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1973-1031G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664669 | |||||||
| chr1:246664672 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0287 a0001c0001t0001g0298 |
3 | HG02145.hp1 HG02258.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.1973-1028C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664672 | |||||||
| chr1:246664673 | G | A | 3 | a0001c0001t0001g0305 a0001c0001t0003g0086 a0001c0001t0022g0087 |
3 | HG03239.hp2 HG04228.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1973-1027G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664673 | |||||||
| chr1:246664677 | C | T | 162 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0027 others(159): Show |
165 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1973-1023C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664677 | |||||||
| chr1:246664678 | A | G | 232 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0024 others(229): Show |
235 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.1973-1022A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664678 | |||||||
| chr1:246664716 | A | G | 6 | a0001c0001t0001g0154 a0001c0001t0001g0232 a0001c0001t0001g0289 others(3): Show |
6 | HG01255.hp1 HG01952.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1973-984A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664716 | |||||||
| chr1:246664718 | A | G | 14 | a0001c0001t0001g0013 a0001c0001t0001g0154 a0001c0001t0001g0289 others(11): Show |
14 | HG00733.hp1 HG00741.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.1973-982A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664718 | |||||||
| chr1:246664722 | A | G | 3 | a0001c0001t0001g0154 a0001c0001t0001g0289 a0001c0001t0003g0067 |
3 | HG01255.hp1 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1973-978A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664722 | |||||||
| chr1:246664887 | T | A | 2 | a0001c0001t0001g0263 a0005c0010t0002g0030 |
2 | HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1973-813T>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664887 | |||||||
| chr1:246664888 | A | T | 2 | a0001c0001t0003g0049 a0001c0001t0003g0050 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1973-812A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664888 | |||||||
| chr1:246664991 | T | C | 14 | a0001c0001t0001g0060 a0001c0001t0001g0090 a0001c0001t0001g0091 others(11): Show |
14 | HG00140.hp1 HG01175.hp2 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.1973-709T>C | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246664991 | |||||||
| chr1:246665087 | G | A | 31 | a0001c0001t0004g0009 a0001c0001t0004g0018 a0001c0001t0004g0028 others(28): Show |
31 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1973-613G>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246665087 | |||||||
| chr1:246665105 | C | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0167 |
2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1973-595C>A | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246665105 | |||||||
| chr1:246665135 | C | T | 3 | a0001c0001t0001g0294 a0002c0002t0001g0111 a0002c0002t0001g0147 |
3 | HG00621.hp1 NA18946.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.1973-565C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246665135 | |||||||
| chr1:246665246 | G | GC | 14 | a0001c0001t0001g0060 a0001c0001t0001g0090 a0001c0001t0001g0091 others(11): Show |
14 | HG00140.hp1 HG01175.hp2 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.1973-452dupC | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 246665246 | ||||||
| chr1:246665396 | A | T | 1 | a0002c0002t0001g0177 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1973-304A>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246665396 | |||||||
| chr1:246665588 | C | T | 1 | a0001c0001t0002g0051 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1973-112C>T | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246665588 | |||||||
| chr1:246665670 | A | G | 1 | a0001c0001t0003g0135 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1973-30A>G | CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 10/10 | chr1 | 246665670 |