Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 90678 |
| ensemblid | ENSG00000148356.15 |
| hgncid | 25135 |
| symbol | LRSAM1 |
| name | leucine rich repeat and sterile alpha motif containing 1 |
| refseq_nuc | NM_001005373.4 |
| refseq_prot | NP_001005373.1 |
| ensembl_nuc | ENST00000300417.11 |
| ensembl_prot | ENSP00000300417.6 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 127451510 |
| end | 127503499 |
| strand | + |
| ver | v1.2 |
| region | chr9:127451510-127503499 |
| region5000 | chr9:127446510-127508499 |
| regionname0 | LRSAM1_chr9_127451510_127503499 |
| regionname5000 | LRSAM1_chr9_127446510_127508499 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 723 | 219 | 41 | 46 | 96 | 12 | 23 | 74 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | MPLFF others(718): Show |
chr9 | 127446510 | 127508499 |
| a0002 | 1/0 | 723 | 102 | 32 | 19 | 35 | 4 | 11 | 29 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | MPLFF others(718): Show |
chr9 | 127446510 | 127508499 |
| a0003 | 0/0 | 723 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | MPLFF others(718): Show |
chr9 | 127446510 | 127508499 |
| a0004 | 0/0 | 723 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | MPLFF others(718): Show |
chr9 | 127446510 | 127508499 |
| a0005 | 0/0 | 723 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | MPLFF others(718): Show |
chr9 | 127446510 | 127508499 |
| a0006 | 0/0 | 723 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | MPLFF others(718): Show |
chr9 | 127446510 | 127508499 |
| a0007 | 0/0 | 723 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | MPLFF others(718): Show |
chr9 | 127446510 | 127508499 |
| a0008 | 0/0 | 723 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | MPLFF others(718): Show |
chr9 | 127446510 | 127508499 |
| a0009 | 0/0 | 723 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | MPLFF others(718): Show |
chr9 | 127446510 | 127508499 |
| a0010 | 0/0 | 723 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | MPLFF others(718): Show |
chr9 | 127446510 | 127508499 |
| a0011 | 0/0 | 723 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | MPLFF others(718): Show |
chr9 | 127446510 | 127508499 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2169 | 163 | 35 | 31 | 73 | 7 | 16 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | ATGCC others(2164): Show |
chr9 | 127446510 | 127508499 | ||
| a0001c0003 | 0/0 | 2169 | 51 | 4 | 14 | 22 | 5 | 6 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | ATGCC others(2164): Show |
chr9 | 127446510 | 127508499 | ||
| a0001c0007 | 0/0 | 2169 | 3 | 2 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | ATGCC others(2164): Show |
chr9 | 127446510 | 127508499 | ||
| a0001c0013 | 0/0 | 2169 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | ATGCC others(2164): Show |
chr9 | 127446510 | 127508499 | ||
| a0001c0016 | 0/0 | 2169 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | ATGCC others(2164): Show |
chr9 | 127446510 | 127508499 | ||
| a0002c0002 | 1/0 | 2169 | 99 | 30 | 19 | 35 | 4 | 10 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | ATGCC others(2164): Show |
chr9 | 127446510 | 127508499 | ||
| a0002c0005 | 0/0 | 2169 | 3 | 2 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | ATGCC others(2164): Show |
chr9 | 127446510 | 127508499 | ||
| a0003c0004 | 0/0 | 2169 | 9 | 9 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | ATGCC others(2164): Show |
chr9 | 127446510 | 127508499 | ||
| a0004c0006 | 0/0 | 2169 | 3 | 0 | 0 | 3 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | ATGCC others(2164): Show |
chr9 | 127446510 | 127508499 | ||
| a0005c0010 | 0/0 | 2169 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | ATGCC others(2164): Show |
chr9 | 127446510 | 127508499 | ||
| a0006c0008 | 0/0 | 2169 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | ATGCC others(2164): Show |
chr9 | 127446510 | 127508499 | ||
| a0007c0012 | 0/0 | 2169 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | ATGCC others(2164): Show |
chr9 | 127446510 | 127508499 | ||
| a0008c0015 | 0/0 | 2169 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | ATGCC others(2164): Show |
chr9 | 127446510 | 127508499 | ||
| a0009c0011 | 0/0 | 2169 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | ATGCC others(2164): Show |
chr9 | 127446510 | 127508499 | ||
| a0010c0009 | 0/0 | 2169 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | ATGCC others(2164): Show |
chr9 | 127446510 | 127508499 | ||
| a0011c0014 | 0/0 | 2169 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | ATGCC others(2164): Show |
chr9 | 127446510 | 127508499 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3120 | 162 | 34 | 31 | 73 | 7 | 16 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | GTTGT others(3115): Show |
chr9 | 127446510 | 127508499 |
| a0001c0001t0002 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | GTTGT others(3115): Show |
chr9 | 127446510 | 127508499 |
| a0001c0003t0001 | 0/0 | 3120 | 51 | 4 | 14 | 22 | 5 | 6 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | GTTGT others(3115): Show |
chr9 | 127446510 | 127508499 |
| a0001c0007t0001 | 0/0 | 3120 | 3 | 2 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | GTTGT others(3115): Show |
chr9 | 127446510 | 127508499 |
| a0001c0013t0001 | 0/0 | 3120 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | GTTGT others(3115): Show |
chr9 | 127446510 | 127508499 |
| a0001c0016t0001 | 0/0 | 3120 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | GTTGT others(3115): Show |
chr9 | 127446510 | 127508499 |
| a0002c0002t0001 | 1/0 | 3120 | 97 | 30 | 18 | 34 | 4 | 10 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | GTTGT others(3115): Show |
chr9 | 127446510 | 127508499 |
| a0002c0002t0003 | 0/0 | 3120 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | GTTGT others(3115): Show |
chr9 | 127446510 | 127508499 |
| a0002c0002t0005 | 0/0 | 3120 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | GTTGT others(3115): Show |
chr9 | 127446510 | 127508499 |
| a0002c0005t0001 | 0/0 | 3120 | 2 | 1 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | GTTGT others(3115): Show |
chr9 | 127446510 | 127508499 |
| a0002c0005t0002 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | GTTGT others(3115): Show |
chr9 | 127446510 | 127508499 |
| a0003c0004t0001 | 0/0 | 3120 | 7 | 7 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | GTTGT others(3115): Show |
chr9 | 127446510 | 127508499 |
| a0003c0004t0002 | 0/0 | 3120 | 2 | 2 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | GTTGT others(3115): Show |
chr9 | 127446510 | 127508499 |
| a0004c0006t0001 | 0/0 | 3120 | 2 | 0 | 0 | 2 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | GTTGT others(3115): Show |
chr9 | 127446510 | 127508499 |
| a0004c0006t0004 | 0/0 | 3070 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | GTTGT others(3065): Show |
chr9 | 127446510 | 127508499 |
| a0005c0010t0001 | 0/0 | 3120 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | GTTGT others(3115): Show |
chr9 | 127446510 | 127508499 |
| a0006c0008t0001 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | GTTGT others(3115): Show |
chr9 | 127446510 | 127508499 |
| a0007c0012t0001 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | GTTGT others(3115): Show |
chr9 | 127446510 | 127508499 |
| a0008c0015t0001 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | GTTGT others(3115): Show |
chr9 | 127446510 | 127508499 |
| a0009c0011t0001 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | GTTGT others(3115): Show |
chr9 | 127446510 | 127508499 |
| a0010c0009t0001 | 0/0 | 3120 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | GTTGT others(3115): Show |
chr9 | 127446510 | 127508499 |
| a0011c0014t0001 | 0/0 | 3120 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | GTTGT others(3115): Show |
chr9 | 127446510 | 127508499 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0262 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0007t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0007t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0007t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0013t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0001c0016t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0221 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0002t0005g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0005t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0005t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0002c0005t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0003c0004t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0003c0004t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0003c0004t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0003c0004t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0003c0004t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0003c0004t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0003c0004t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0003c0004t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0003c0004t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0004c0006t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0004c0006t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0004c0006t0004g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0005c0010t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0006c0008t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0007c0012t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0008c0015t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0009c0011t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0010c0009t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| a0011c0014t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0100 | EUR | GBR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00140 | hp2 | a0001 | c0003 | t0001 | g0144 | EUR | GBR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0232 | EUR | FIN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0225 | EUR | FIN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0317 | EUR | FIN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00323 | hp2 | a0001 | c0003 | t0001 | g0196 | EUR | FIN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | CHS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | CHS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | CHS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00558 | hp1 | a0001 | c0003 | t0001 | g0138 | EAS | CHS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | CHS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00609 | hp2 | a0001 | c0003 | t0001 | g0099 | EAS | CHS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | CHS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0210 | EAS | CHS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00673 | hp1 | a0001 | c0013 | t0001 | g0201 | EAS | CHS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0103 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0111 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0168 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG00741 | hp2 | a0001 | c0003 | t0001 | g0153 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01070 | hp1 | a0001 | c0003 | t0001 | g0154 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01070 | hp2 | a0001 | c0003 | t0001 | g0163 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01071 | hp2 | a0001 | c0003 | t0001 | g0155 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01074 | hp1 | a0001 | c0003 | t0001 | g0159 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0156 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0224 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0169 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01106 | hp1 | a0005 | c0010 | t0001 | g0112 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01109 | hp1 | a0001 | c0007 | t0001 | g0329 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0126 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0227 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0167 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0107 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0113 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01175 | hp2 | a0001 | c0003 | t0001 | g0207 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01192 | hp1 | a0002 | c0002 | t0005 | g0104 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0132 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01255 | hp1 | a0001 | c0003 | t0001 | g0192 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0188 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0213 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0114 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0164 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0233 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0212 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01433 | hp2 | a0001 | c0003 | t0001 | g0211 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0124 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | IBS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01515 | hp2 | a0001 | c0003 | t0001 | g0004 | EUR | IBS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0004 | EUR | IBS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0259 | EUR | IBS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0162 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01884 | hp2 | a0003 | c0004 | t0001 | g0082 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01952 | hp1 | a0001 | c0003 | t0001 | g0183 | AMR | PEL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0110 | AMR | PEL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0105 | AMR | PEL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0106 | AMR | PEL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PEL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02004 | hp2 | a0001 | c0003 | t0001 | g0171 | AMR | PEL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02015 | hp1 | a0001 | c0003 | t0001 | g0186 | EAS | KHV | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0229 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02055 | hp2 | a0003 | c0004 | t0002 | g0083 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0101 | EAS | KHV | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02083 | hp2 | a0001 | c0003 | t0001 | g0178 | EAS | KHV | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | KHV | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0116 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CDX | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | CDX | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | CDX | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0145 | EAS | CDX | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0157 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0234 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0095 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0195 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02451 | hp2 | a0003 | c0004 | t0001 | g0077 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | KHV | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | KHV | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0120 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0148 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0115 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0128 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0133 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0090 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02630 | hp1 | a0003 | c0004 | t0001 | g0087 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0206 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0172 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02698 | hp2 | a0001 | c0003 | t0001 | g0170 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02723 | hp2 | a0001 | c0007 | t0001 | g0327 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0139 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02735 | hp2 | a0002 | c0005 | t0001 | g0272 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02738 | hp2 | a0001 | c0003 | t0001 | g0208 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0096 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0129 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0209 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02895 | hp2 | a0003 | c0004 | t0001 | g0089 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02897 | hp2 | a0003 | c0004 | t0001 | g0088 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02922 | hp2 | a0006 | c0008 | t0001 | g0149 | AFR | ESN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02976 | hp2 | a0003 | c0004 | t0001 | g0078 | AFR | ESN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0184 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0093 | AFR | MSL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0220 | AFR | MSL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0185 | AFR | ESN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03139 | hp2 | a0001 | c0007 | t0001 | g0326 | AFR | ESN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03195 | hp1 | a0007 | c0012 | t0001 | g0175 | AFR | ESN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03239 | hp2 | a0001 | c0003 | t0001 | g0222 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | MSL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03486 | hp1 | a0008 | c0015 | t0001 | g0160 | AFR | MSL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03486 | hp2 | a0002 | c0005 | t0001 | g0076 | AFR | MSL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0223 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | ESN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0094 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0118 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03579 | hp1 | a0009 | c0011 | t0001 | g0228 | AFR | MSL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | MSL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0123 | SAS | BEB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0119 | SAS | BEB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03834 | hp1 | a0001 | c0016 | t0001 | g0137 | SAS | BEB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0108 | SAS | BEB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0198 | SAS | BEB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0122 | SAS | BEB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03942 | hp2 | a0001 | c0003 | t0001 | g0136 | SAS | BEB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0302 | SAS | BEB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0182 | SAS | BEB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG04228 | hp2 | a0001 | c0003 | t0001 | g0098 | SAS | STU | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18522 | hp1 | a0003 | c0004 | t0001 | g0073 | AFR | YRI | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0150 | AFR | YRI | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | YRI | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | YRI | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18942 | hp2 | a0001 | c0003 | t0001 | g0147 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18944 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18945 | hp1 | a0001 | c0003 | t0001 | g0176 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18952 | hp1 | a0001 | c0003 | t0001 | g0173 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18971 | hp1 | a0001 | c0003 | t0001 | g0199 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18973 | hp2 | a0001 | c0003 | t0001 | g0165 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18974 | hp2 | a0004 | c0006 | t0004 | g0013 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18975 | hp2 | a0001 | c0003 | t0001 | g0191 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18978 | hp2 | a0001 | c0003 | t0001 | g0215 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18980 | hp1 | a0001 | c0003 | t0001 | g0146 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18984 | hp1 | a0001 | c0003 | t0001 | g0151 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18989 | hp1 | a0004 | c0006 | t0001 | g0070 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18997 | hp2 | a0001 | c0003 | t0001 | g0214 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19000 | hp1 | a0001 | c0003 | t0001 | g0231 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19001 | hp2 | a0010 | c0009 | t0001 | g0152 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19012 | hp1 | a0001 | c0003 | t0001 | g0143 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0235 | AFR | LWK | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | LWK | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | LWK | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19056 | hp1 | a0001 | c0003 | t0001 | g0131 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19064 | hp1 | a0011 | c0014 | t0001 | g0287 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19074 | hp2 | a0001 | c0003 | t0001 | g0187 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19075 | hp1 | a0002 | c0002 | t0003 | g0226 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19078 | hp2 | a0001 | c0003 | t0001 | g0091 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19079 | hp2 | a0001 | c0003 | t0001 | g0142 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19088 | hp1 | a0004 | c0006 | t0001 | g0072 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0127 | AFR | YRI | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | YRI | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0117 | AFR | ASW | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0158 | AFR | ASW | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0283 | EUR | TSI | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | TSI | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0109 | EUR | TSI | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA20805 | hp2 | a0001 | c0003 | t0001 | g0140 | EUR | TSI | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | GIH | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | GIH | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0161 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0121 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0205 | AFR | MSL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG06807 | hp1 | a0003 | c0004 | t0002 | g0084 | AFR | USA | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0219 | AFR | USA | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA20300 | hp1 | a0002 | c0005 | t0002 | g0086 | AFR | USA | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | USA | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0262 | REF | REF | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0221 | REF | REF | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:127454589 | A | G | 1 | a0008 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.62A>G | p.Gln21Arg | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 3/26 | 410/3120 | 62/2172 | 21/723 | chr9 | 127454589 | |||
| chr9:127467759 | C | T | 1 | a0003 | 9 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(6): Show |
missense_variant | MODERATE | c.548C>T | p.Ser183Leu | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/26 | 896/3120 | 548/2172 | 183/723 | chr9 | 127467759 | |||
| chr9:127473897 | C | G | 1 | a0007 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.716C>G | p.Thr239Arg | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/26 | 1064/3120 | 716/2172 | 239/723 | chr9 | 127473897 | |||
| chr9:127479852 | T | G | 1 | a0006 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.917T>G | p.Leu306Arg | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 14/26 | 1265/3120 | 917/2172 | 306/723 | chr9 | 127479852 | |||
| chr9:127479887 | A | G | 5 | a0001 a0003 a0004 others(2): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
missense_variant | MODERATE | c.952A>G | p.Asn318Asp | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 14/26 | 1300/3120 | 952/2172 | 318/723 | chr9 | 127479887 | |||
| chr9:127489447 | G | A | 1 | a0010 | 1 | NA19001.hp2 | missense_variant | MODERATE | c.1351G>A | p.Ala451Thr | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/26 | 1699/3120 | 1351/2172 | 451/723 | chr9 | 127489447 | |||
| chr9:127489478 | A | T | 1 | a0011 | 1 | NA19064.hp1 | missense_variant | MODERATE | c.1382A>T | p.Gln461Leu | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/26 | 1730/3120 | 1382/2172 | 461/723 | chr9 | 127489478 | |||
| chr9:127489502 | G | A | 1 | a0009 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.1406G>A | p.Arg469Gln | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/26 | 1754/3120 | 1406/2172 | 469/723 | chr9 | 127489502 | |||
| chr9:127501072 | G | A | 1 | a0004 | 3 | NA18974.hp2 NA18989.hp1 NA19088.hp1 |
missense_variant | MODERATE | c.1975G>A | p.Val659Met | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/26 | 2323/3120 | 1975/2172 | 659/723 | chr9 | 127501072 | |||
| chr9:127501139 | G | A | 1 | a0005 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.2042G>A | p.Arg681Gln | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/26 | 2390/3120 | 2042/2172 | 681/723 | chr9 | 127501139 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:127454536 | C | T | 1 | a0001c0016 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.9C>T | p.Leu3Leu | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 3/26 | 357/3120 | 9/2172 | 3/723 | chr9 | 127454536 | |||
| chr9:127457390 | C | T | 6 | a0001c0001 a0001c0007 a0002c0005 others(3): Show |
181 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(178): Show |
synonymous_variant | LOW | c.249C>T | p.Ile83Ile | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/26 | 597/3120 | 249/2172 | 83/723 | chr9 | 127457390 | |||
| chr9:127462325 | C | T | 1 | a0001c0013 | 1 | HG00673.hp1 | synonymous_variant | LOW | c.480C>T | p.Asn160Asn | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/26 | 828/3120 | 480/2172 | 160/723 | chr9 | 127462325 | |||
| chr9:127502884 | C | T | 1 | a0001c0007 | 3 | HG01109.hp1 HG02723.hp2 HG03139.hp2 |
synonymous_variant | LOW | c.2157C>T | p.Ile719Ile | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 26/26 | 2505/3120 | 2157/2172 | 719/723 | chr9 | 127502884 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:127451542 | C | T | 3 | a0001c0001t0002 a0002c0005t0002 a0003c0004t0002 |
4 | HG02055.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-316C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 1/26 | 2986 | chr9 | 127451542 | ||||||
| chr9:127451550 | G | A | 1 | a0002c0002t0003 | 1 | NA19075.hp1 | 5_prime_UTR_variant | MODIFIER | c.-308G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 1/26 | 2978 | chr9 | 127451550 | ||||||
| chr9:127452034 | GGGTGCAC others(396): Show |
G | 1 | a0004c0006t0004 | 1 | NA18974.hp2 | splice_donor_variant&splice_region_variant&5_prime_UTR_variant&intron_variant | HIGH | c.-80_-33+355del | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/26 | 2089 | INFO_REALIGN_3_PRIME | chr9 | 127452034 | |||||
| chr9:127502956 | G | A | 1 | a0002c0002t0005 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*57G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 26/26 | 57 | chr9 | 127502956 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:127451684 | G | A | 1 | a0002c0002t0001g0012 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-189+15G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 1/25 | chr9 | 127451684 | |||||||
| chr9:127452135 | C | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(54): Show |
59 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.-33+51C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | chr9 | 127452135 | |||||||
| chr9:127452325 | T | C | 1 | a0001c0003t0001g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-33+241T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | chr9 | 127452325 | |||||||
| chr9:127452325 | T | TG | 57 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(54): Show |
59 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.-33+246dupG | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 127452325 | ||||||
| chr9:127452529 | G | T | 4 | a0001c0001t0001g0328 a0001c0007t0001g0326 a0001c0007t0001g0327 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+445G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | chr9 | 127452529 | |||||||
| chr9:127452644 | G | A | 1 | a0001c0003t0001g0014 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-33+560G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | chr9 | 127452644 | |||||||
| chr9:127452970 | C | T | 93 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(90): Show |
97 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.-33+886C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | chr9 | 127452970 | |||||||
| chr9:127453000 | G | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(172): Show |
181 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.-33+916G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | chr9 | 127453000 | |||||||
| chr9:127453071 | C | CTTTA | 4 | a0001c0001t0001g0328 a0001c0007t0001g0326 a0001c0007t0001g0327 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+1002_-33+1005d others(6): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 127453071 | ||||||
| chr9:127453238 | C | T | 1 | a0002c0002t0001g0235 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-33+1154C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | chr9 | 127453238 | |||||||
| chr9:127453432 | C | CT | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(172): Show |
181 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.-32-1064_-32-1063i others(3): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | chr9 | 127453432 | |||||||
| chr9:127453517 | T | A | 1 | a0001c0001t0001g0015 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-32-979T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | chr9 | 127453517 | |||||||
| chr9:127453571 | G | A | 1 | a0002c0002t0001g0090 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-32-925G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | chr9 | 127453571 | |||||||
| chr9:127453647 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-32-849T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | chr9 | 127453647 | |||||||
| chr9:127453841 | G | T | 93 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(90): Show |
97 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.-32-655G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | chr9 | 127453841 | |||||||
| chr9:127453975 | C | T | 3 | a0002c0002t0001g0232 a0002c0002t0001g0233 a0002c0002t0001g0234 |
3 | HG00280.hp1 HG01358.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-32-521C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | chr9 | 127453975 | |||||||
| chr9:127454047 | A | ATAGAAAG others(28): Show |
82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(79): Show |
84 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.-32-427_-32-426ins others(35): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 127454047 | ||||||
| chr9:127454106 | C | T | 1 | a0001c0001t0001g0325 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-32-390C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | chr9 | 127454106 | |||||||
| chr9:127454644 | C | T | 1 | a0001c0001t0001g0324 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.72+45C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 3/25 | chr9 | 127454644 | |||||||
| chr9:127454672 | G | T | 82 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(79): Show |
85 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.72+73G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 3/25 | chr9 | 127454672 | |||||||
| chr9:127454771 | C | G | 70 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(67): Show |
73 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.72+172C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 3/25 | chr9 | 127454771 | |||||||
| chr9:127454968 | A | C | 19 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0074 others(16): Show |
19 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.73-30A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 3/25 | chr9 | 127454968 | |||||||
| chr9:127455172 | G | A | 1 | a0001c0001t0001g0018 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.129+118G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 4/25 | chr9 | 127455172 | |||||||
| chr9:127455182 | C | T | 4 | a0001c0001t0001g0328 a0001c0007t0001g0326 a0001c0007t0001g0327 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+128C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 4/25 | chr9 | 127455182 | |||||||
| chr9:127455238 | C | T | 1 | a0001c0003t0001g0231 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.129+184C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 4/25 | chr9 | 127455238 | |||||||
| chr9:127455247 | C | CA | 4 | a0001c0001t0001g0328 a0001c0007t0001g0326 a0001c0007t0001g0327 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+195dupA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr9 | 127455247 | ||||||
| chr9:127455382 | A | G | 1 | a0002c0002t0001g0230 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.130-194A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 4/25 | chr9 | 127455382 | |||||||
| chr9:127456015 | G | A | 1 | a0001c0003t0001g0091 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.174+395G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | chr9 | 127456015 | |||||||
| chr9:127456057 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.174+437C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | chr9 | 127456057 | |||||||
| chr9:127456093 | G | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(79): Show |
84 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.174+473G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | chr9 | 127456093 | |||||||
| chr9:127456116 | C | G | 2 | a0001c0001t0001g0322 a0001c0001t0001g0323 |
2 | HG00423.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.174+496C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | chr9 | 127456116 | |||||||
| chr9:127456162 | C | CA | 6 | a0002c0002t0001g0092 a0002c0002t0001g0093 a0002c0002t0001g0094 others(3): Show |
6 | HG02258.hp1 HG02523.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.174+562dupA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr9 | 127456162 | ||||||
| chr9:127456162 | CA | C | 23 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(20): Show |
23 | HG00735.hp2 HG01168.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.174+562delA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr9 | 127456162 | ||||||
| chr9:127456162 | CAA | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(144): Show |
153 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.174+561_174+562del others(2): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr9 | 127456162 | ||||||
| chr9:127456162 | CAAA | C | 9 | a0001c0001t0001g0071 a0001c0001t0001g0245 a0001c0001t0001g0257 others(6): Show |
9 | HG01109.hp1 HG02129.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.174+560_174+562del others(3): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr9 | 127456162 | ||||||
| chr9:127456234 | G | GT | 6 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0001g0320 others(3): Show |
6 | HG00609.hp1 HG00621.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.174+629dupT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr9 | 127456234 | ||||||
| chr9:127456259 | C | T | 11 | a0001c0001t0001g0008 a0001c0001t0001g0236 a0001c0001t0001g0237 others(8): Show |
12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.174+639C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | chr9 | 127456259 | |||||||
| chr9:127456412 | T | TTAG | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(174): Show |
183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.174+793_174+795dup others(3): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr9 | 127456412 | ||||||
| chr9:127456426 | T | C | 1 | a0001c0003t0001g0098 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.174+806T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | chr9 | 127456426 | |||||||
| chr9:127456448 | C | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(55): Show |
60 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.174+828C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | chr9 | 127456448 | |||||||
| chr9:127456523 | G | A | 15 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0074 others(12): Show |
15 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.175-793G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | chr9 | 127456523 | |||||||
| chr9:127456670 | C | T | 2 | a0002c0002t0001g0224 a0002c0002t0001g0225 |
2 | HG00280.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.175-646C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | chr9 | 127456670 | |||||||
| chr9:127456766 | C | T | 19 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0074 others(16): Show |
19 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.175-550C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | chr9 | 127456766 | |||||||
| chr9:127456779 | T | A | 1 | a0002c0002t0001g0097 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.175-537T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | chr9 | 127456779 | |||||||
| chr9:127456865 | CA | C | 8 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0256 others(5): Show |
9 | HG00323.hp1 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.175-436delA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr9 | 127456865 | ||||||
| chr9:127456873 | A | C | 1 | a0001c0001t0001g0244 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.175-443A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | chr9 | 127456873 | |||||||
| chr9:127456878 | A | T | 9 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(6): Show |
9 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.175-438A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | chr9 | 127456878 | |||||||
| chr9:127457130 | G | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(55): Show |
60 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.175-186G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | chr9 | 127457130 | |||||||
| chr9:127457443 | C | A | 2 | a0001c0003t0001g0229 a0009c0011t0001g0228 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.252+50C>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127457443 | |||||||
| chr9:127457444 | G | A | 4 | a0001c0001t0001g0328 a0001c0007t0001g0326 a0001c0007t0001g0327 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+51G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127457444 | |||||||
| chr9:127457464 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(175): Show |
184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.252+71T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127457464 | |||||||
| chr9:127457704 | G | C | 1 | a0001c0001t0001g0259 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.252+311G>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127457704 | |||||||
| chr9:127457711 | G | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(172): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.252+318G>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127457711 | |||||||
| chr9:127457857 | C | T | 7 | a0001c0001t0001g0011 a0001c0001t0001g0311 a0001c0001t0001g0312 others(4): Show |
8 | HG01099.hp2 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.252+464C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127457857 | |||||||
| chr9:127457898 | T | G | 1 | a0001c0003t0001g0101 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.252+505T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127457898 | |||||||
| chr9:127457932 | A | G | 9 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0062 others(6): Show |
10 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.252+539A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127457932 | |||||||
| chr9:127457963 | T | G | 2 | a0001c0003t0001g0229 a0009c0011t0001g0228 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.252+570T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127457963 | |||||||
| chr9:127457968 | C | CT | 95 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(92): Show |
98 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.252+589dupT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 127457968 | ||||||
| chr9:127458072 | G | A | 2 | a0001c0003t0001g0229 a0009c0011t0001g0228 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.252+679G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458072 | |||||||
| chr9:127458090 | A | G | 1 | a0001c0001t0001g0310 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.252+697A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458090 | |||||||
| chr9:127458205 | A | T | 6 | a0001c0001t0001g0328 a0001c0003t0001g0229 a0001c0007t0001g0326 others(3): Show |
6 | HG01109.hp1 HG02055.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.253-798A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458205 | |||||||
| chr9:127458314 | G | A | 2 | a0002c0002t0001g0092 a0002c0002t0001g0102 |
2 | HG00438.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.253-689G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458314 | |||||||
| chr9:127458359 | G | A | 20 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0074 others(17): Show |
20 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.253-644G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458359 | |||||||
| chr9:127458367 | C | T | 2 | a0001c0001t0001g0308 a0001c0001t0001g0309 |
2 | HG02145.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.253-636C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458367 | |||||||
| chr9:127458368 | G | A | 2 | a0001c0003t0001g0229 a0009c0011t0001g0228 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.253-635G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458368 | |||||||
| chr9:127458382 | T | C | 325 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(322): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.253-621T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458382 | |||||||
| chr9:127458384 | G | A | 26 | a0002c0002t0001g0093 a0002c0002t0001g0100 a0002c0002t0001g0103 others(23): Show |
26 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.253-619G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458384 | |||||||
| chr9:127458388 | C | CA | 17 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(14): Show |
18 | HG00438.hp1 HG02129.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.253-610dupA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 127458388 | ||||||
| chr9:127458393 | AC | A | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0009c0011t0001g0228 |
3 | HG00639.hp2 HG03579.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.253-609delC | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458393 | |||||||
| chr9:127458394 | C | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(171): Show |
180 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.253-609C>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458394 | |||||||
| chr9:127458399 | C | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(174): Show |
183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.253-604C>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458399 | |||||||
| chr9:127458404 | C | A | 25 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0074 others(22): Show |
25 | HG00639.hp2 HG01884.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.253-599C>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458404 | |||||||
| chr9:127458417 | A | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(170): Show |
179 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.253-586A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458417 | |||||||
| chr9:127458419 | C | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(172): Show |
181 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.253-584C>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458419 | |||||||
| chr9:127458424 | A | C | 1 | a0002c0002t0001g0218 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.253-579A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458424 | |||||||
| chr9:127458439 | G | A | 19 | a0002c0002t0001g0100 a0002c0002t0001g0103 a0002c0002t0001g0105 others(16): Show |
19 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.253-564G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458439 | |||||||
| chr9:127458600 | A | T | 82 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(79): Show |
85 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.253-403A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458600 | |||||||
| chr9:127458677 | G | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(174): Show |
183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.253-326G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458677 | |||||||
| chr9:127458905 | G | A | 2 | a0003c0004t0002g0083 a0003c0004t0002g0084 |
2 | HG02055.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.253-98G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458905 | |||||||
| chr9:127458986 | G | T | 1 | a0001c0001t0001g0241 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.253-17G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458986 | |||||||
| chr9:127459109 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(174): Show |
183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.321+38T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127459109 | |||||||
| chr9:127459172 | A | T | 1 | a0002c0002t0001g0121 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.321+101A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127459172 | |||||||
| chr9:127459217 | G | GT | 111 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(108): Show |
114 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.321+163dupT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr9 | 127459217 | ||||||
| chr9:127459217 | G | GTT | 18 | a0001c0001t0001g0255 a0001c0001t0001g0263 a0001c0001t0001g0298 others(15): Show |
18 | HG00423.hp1 HG00642.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.321+162_321+163dup others(2): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr9 | 127459217 | ||||||
| chr9:127459240 | A | C | 1 | a0001c0001t0001g0297 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.321+169A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127459240 | |||||||
| chr9:127459253 | G | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(79): Show |
84 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.321+182G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127459253 | |||||||
| chr9:127459419 | T | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(172): Show |
181 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.321+348T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127459419 | |||||||
| chr9:127459455 | G | GT | 4 | a0001c0001t0001g0071 a0004c0006t0001g0070 a0004c0006t0001g0072 others(1): Show |
4 | HG02129.hp1 NA18974.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.321+386dupT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr9 | 127459455 | ||||||
| chr9:127459760 | T | C | 1 | a0002c0002t0001g0124 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.321+689T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127459760 | |||||||
| chr9:127459933 | T | A | 1 | a0001c0001t0001g0025 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.321+862T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127459933 | |||||||
| chr9:127460093 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.321+1022G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460093 | |||||||
| chr9:127460173 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(172): Show |
181 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.322-1000A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460173 | |||||||
| chr9:127460174 | T | C | 1 | a0002c0002t0001g0125 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.322-999T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460174 | |||||||
| chr9:127460287 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.322-886C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460287 | |||||||
| chr9:127460348 | C | G | 1 | a0001c0001t0001g0241 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.322-825C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460348 | |||||||
| chr9:127460451 | C | T | 2 | a0002c0002t0001g0204 a0002c0002t0001g0217 |
2 | NA18955.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.322-722C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460451 | |||||||
| chr9:127460480 | C | G | 1 | a0001c0001t0001g0296 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.322-693C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460480 | |||||||
| chr9:127460544 | C | A | 12 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(9): Show |
12 | HG02486.hp2 HG02717.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.322-629C>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460544 | |||||||
| chr9:127460636 | C | G | 1 | a0002c0002t0001g0203 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.322-537C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460636 | |||||||
| chr9:127460769 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.322-404G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460769 | |||||||
| chr9:127460773 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0002c0005t0001g0076 others(1): Show |
4 | HG03041.hp1 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.322-400G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460773 | |||||||
| chr9:127460790 | G | A | 5 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0027 others(2): Show |
5 | NA18959.hp1 NA18979.hp1 NA19057.hp2 others(2): Show |
intron_variant | MODIFIER | c.322-383G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460790 | |||||||
| chr9:127460847 | C | CT | 25 | a0001c0001t0001g0008 a0001c0001t0001g0237 a0001c0001t0001g0238 others(22): Show |
26 | HG00323.hp1 HG00323.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.322-300dupT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr9 | 127460847 | ||||||
| chr9:127460847 | C | CTT | 47 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0019 others(44): Show |
49 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.322-301_322-300dup others(2): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr9 | 127460847 | ||||||
| chr9:127460847 | C | CTTT | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(74): Show |
80 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.322-302_322-300dup others(3): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr9 | 127460847 | ||||||
| chr9:127460847 | C | CTTTT | 24 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0023 others(21): Show |
24 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.322-303_322-300dup others(4): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr9 | 127460847 | ||||||
| chr9:127460847 | C | CTTTTTTT others(2592): Show |
1 | a0001c0001t0001g0285 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.322-300_322-299ins others(2599): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr9 | 127460847 | ||||||
| chr9:127460847 | CTTTTTTT others(3): Show |
C | 11 | a0001c0001t0001g0311 a0002c0002t0001g0003 a0002c0002t0001g0094 others(8): Show |
12 | HG01109.hp2 HG02258.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.322-309_322-300del others(10): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr9 | 127460847 | ||||||
| chr9:127460847 | CTTTTTTT others(4): Show |
C | 1 | a0001c0003t0001g0091 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.322-310_322-300del others(11): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr9 | 127460847 | ||||||
| chr9:127460872 | T | C | 4 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
4 | HG02886.hp1 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.322-301T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460872 | |||||||
| chr9:127460872 | T | TC | 8 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 others(5): Show |
8 | HG02486.hp2 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.322-301_322-300ins others(1): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460872 | |||||||
| chr9:127460904 | G | A | 12 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(9): Show |
12 | HG02486.hp2 HG02717.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.322-269G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460904 | |||||||
| chr9:127461122 | G | A | 1 | a0001c0001t0001g0328 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.322-51G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127461122 | |||||||
| chr9:127461136 | A | G | 1 | a0001c0001t0001g0285 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.322-37A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127461136 | |||||||
| chr9:127461280 | C | T | 11 | a0001c0001t0001g0008 a0001c0001t0001g0236 a0001c0001t0001g0237 others(8): Show |
12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.406+23C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 8/25 | chr9 | 127461280 | |||||||
| chr9:127461281 | G | A | 3 | a0002c0002t0001g0125 a0002c0002t0001g0130 a0002c0002t0001g0193 |
3 | NA18946.hp2 NA18974.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.406+24G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 8/25 | chr9 | 127461281 | |||||||
| chr9:127461473 | C | T | 1 | a0002c0002t0001g0092 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.406+216C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 8/25 | chr9 | 127461473 | |||||||
| chr9:127461475 | G | A | 52 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0259 others(49): Show |
54 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.406+218G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 8/25 | chr9 | 127461475 | |||||||
| chr9:127461543 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(55): Show |
60 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.406+286G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 8/25 | chr9 | 127461543 | |||||||
| chr9:127461605 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.406+348A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 8/25 | chr9 | 127461605 | |||||||
| chr9:127461649 | G | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0236 a0001c0001t0001g0237 others(8): Show |
12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.406+392G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 8/25 | chr9 | 127461649 | |||||||
| chr9:127461846 | A | C | 1 | a0001c0003t0001g0192 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.407-406A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 8/25 | chr9 | 127461846 | |||||||
| chr9:127462098 | T | G | 1 | a0002c0002t0001g0097 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.407-154T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 8/25 | chr9 | 127462098 | |||||||
| chr9:127462217 | T | G | 2 | a0001c0003t0001g0091 a0001c0003t0001g0131 |
2 | NA19056.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.407-35T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 8/25 | chr9 | 127462217 | |||||||
| chr9:127462450 | T | C | 1 | a0002c0002t0001g0103 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.528+77T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127462450 | |||||||
| chr9:127462506 | G | C | 9 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(6): Show |
9 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.528+133G>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127462506 | |||||||
| chr9:127462626 | A | G | 1 | a0001c0003t0001g0191 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.528+253A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127462626 | |||||||
| chr9:127462648 | A | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(174): Show |
183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.528+275A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127462648 | |||||||
| chr9:127462855 | TA | T | 6 | a0001c0001t0001g0028 a0001c0001t0001g0244 a0001c0001t0001g0321 others(3): Show |
6 | HG01168.hp1 HG02523.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.528+495delA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127462855 | ||||||
| chr9:127462883 | G | C | 1 | a0001c0001t0001g0328 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.528+510G>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127462883 | |||||||
| chr9:127462892 | T | C | 2 | a0001c0003t0001g0229 a0009c0011t0001g0228 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.528+519T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127462892 | |||||||
| chr9:127462948 | C | A | 1 | a0001c0003t0001g0101 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.528+575C>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127462948 | |||||||
| chr9:127462949 | A | G | 10 | a0002c0002t0001g0003 a0002c0002t0001g0094 a0002c0002t0001g0095 others(7): Show |
11 | HG01109.hp2 HG02258.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.528+576A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127462949 | |||||||
| chr9:127463148 | G | A | 2 | a0001c0001t0001g0328 a0002c0002t0001g0124 |
2 | HG01496.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.528+775G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127463148 | |||||||
| chr9:127463156 | G | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0236 a0001c0001t0001g0237 others(8): Show |
12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.528+783G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127463156 | |||||||
| chr9:127463198 | C | CA | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(83): Show |
89 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.528+848dupA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127463198 | ||||||
| chr9:127463198 | CA | C | 90 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(87): Show |
94 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.528+848delA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127463198 | ||||||
| chr9:127463227 | A | G | 1 | a0001c0001t0001g0002 | 2 | HG00099.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.528+854A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127463227 | |||||||
| chr9:127463233 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0256 |
2 | HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.528+860C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127463233 | |||||||
| chr9:127463341 | A | C | 1 | a0002c0002t0001g0234 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.528+968A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127463341 | |||||||
| chr9:127463433 | G | A | 2 | a0001c0003t0001g0229 a0009c0011t0001g0228 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.528+1060G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127463433 | |||||||
| chr9:127463497 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.528+1124G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127463497 | |||||||
| chr9:127464016 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.528+1643C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127464016 | |||||||
| chr9:127464234 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0002c0005t0001g0076 others(1): Show |
4 | HG03041.hp1 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.528+1861G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127464234 | |||||||
| chr9:127464289 | A | G | 2 | a0001c0003t0001g0229 a0009c0011t0001g0228 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.528+1916A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127464289 | |||||||
| chr9:127464362 | TGACCGTG others(49): Show |
T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(73): Show |
78 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.528+2011_528+2066d others(58): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127464362 | ||||||
| chr9:127464380 | C | T | 3 | a0001c0003t0001g0146 a0001c0003t0001g0229 a0009c0011t0001g0228 |
3 | HG02055.hp1 HG03579.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.528+2007C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127464380 | |||||||
| chr9:127464422 | C | G | 2 | a0001c0003t0001g0229 a0009c0011t0001g0228 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.528+2049C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127464422 | |||||||
| chr9:127464475 | A | T | 2 | a0001c0003t0001g0229 a0009c0011t0001g0228 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.528+2102A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127464475 | |||||||
| chr9:127464579 | A | G | 1 | a0002c0002t0001g0185 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.528+2206A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127464579 | |||||||
| chr9:127464594 | A | C | 1 | a0002c0002t0001g0121 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.528+2221A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127464594 | |||||||
| chr9:127464630 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(174): Show |
183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.528+2257T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127464630 | |||||||
| chr9:127464800 | T | A | 101 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(98): Show |
105 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.528+2427T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127464800 | |||||||
| chr9:127465075 | G | A | 1 | a0001c0001t0001g0032 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.529-2665G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127465075 | |||||||
| chr9:127465077 | C | CA | 4 | a0001c0001t0001g0328 a0001c0007t0001g0326 a0001c0007t0001g0327 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-2662dupA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127465077 | ||||||
| chr9:127465083 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.529-2657C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127465083 | |||||||
| chr9:127465275 | T | C | 2 | a0001c0003t0001g0229 a0009c0011t0001g0228 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.529-2465T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127465275 | |||||||
| chr9:127465374 | A | T | 1 | a0002c0002t0001g0184 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.529-2366A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127465374 | |||||||
| chr9:127465665 | G | A | 2 | a0001c0003t0001g0136 a0001c0016t0001g0137 |
2 | HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.529-2075G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127465665 | |||||||
| chr9:127465808 | G | T | 4 | a0001c0001t0001g0265 a0001c0001t0001g0280 a0001c0001t0001g0281 others(1): Show |
4 | NA18957.hp1 NA18989.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.529-1932G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127465808 | |||||||
| chr9:127465996 | C | CA | 85 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(82): Show |
88 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.529-1736dupA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127465996 | ||||||
| chr9:127466005 | T | C | 9 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(6): Show |
9 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.529-1735T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466005 | |||||||
| chr9:127466165 | C | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(174): Show |
183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.529-1575C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466165 | |||||||
| chr9:127466166 | G | A | 1 | a0001c0003t0001g0138 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.529-1574G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466166 | |||||||
| chr9:127466216 | A | G | 101 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(98): Show |
105 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.529-1524A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466216 | |||||||
| chr9:127466232 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(174): Show |
183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.529-1508T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466232 | |||||||
| chr9:127466290 | C | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(174): Show |
183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.529-1450C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466290 | |||||||
| chr9:127466474 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.529-1266T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466474 | |||||||
| chr9:127466475 | C | CAT | 9 | a0001c0003t0001g0091 a0001c0003t0001g0163 a0001c0003t0001g0170 others(6): Show |
9 | HG00323.hp2 HG01070.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.529-1236_529-1235d others(4): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466475 | ||||||
| chr9:127466475 | C | CATAT | 8 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0245 others(5): Show |
9 | HG01255.hp1 HG02886.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.529-1238_529-1235d others(6): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466475 | ||||||
| chr9:127466475 | C | CATATAT | 17 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0058 others(14): Show |
18 | HG01106.hp2 HG01884.hp2 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.529-1240_529-1235d others(8): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466475 | ||||||
| chr9:127466475 | C | CATATATA others(1): Show |
5 | a0001c0003t0001g0140 a0001c0003t0001g0222 a0002c0002t0001g0090 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.529-1242_529-1235d others(10): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466475 | ||||||
| chr9:127466475 | C | CATATATA others(3): Show |
1 | a0001c0003t0001g0207 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.529-1244_529-1235d others(12): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466475 | ||||||
| chr9:127466475 | C | CATATATA others(7): Show |
2 | a0002c0002t0001g0119 a0002c0002t0001g0224 |
2 | HG01081.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.529-1248_529-1235d others(16): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466475 | ||||||
| chr9:127466475 | C | CATATATA others(9): Show |
1 | a0002c0002t0001g0139 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.529-1250_529-1235d others(18): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466475 | ||||||
| chr9:127466475 | CAT | C | 3 | a0001c0001t0001g0257 a0001c0001t0001g0260 a0002c0002t0001g0181 |
3 | HG00639.hp2 NA19043.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.529-1236_529-1235d others(4): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466475 | ||||||
| chr9:127466475 | CATATATA others(1): Show |
C | 25 | a0001c0001t0001g0259 a0001c0001t0001g0273 a0001c0001t0001g0276 others(22): Show |
26 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.529-1242_529-1235d others(10): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466475 | ||||||
| chr9:127466475 | CATATATA others(3): Show |
C | 7 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0320 others(4): Show |
7 | HG00423.hp1 HG00609.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.529-1244_529-1235d others(12): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466475 | ||||||
| chr9:127466492 | ATATATAT others(11): Show |
A | 1 | a0001c0003t0001g0214 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.529-1246_529-1229d others(20): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466492 | ||||||
| chr9:127466493 | TATATATA others(2): Show |
T | 5 | a0001c0001t0001g0281 a0001c0001t0001g0321 a0002c0002t0001g0094 others(2): Show |
5 | HG01109.hp2 HG02523.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.529-1246_529-1238d others(11): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466493 | |||||||
| chr9:127466494 | ATATATAT others(4): Show |
A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0267 a0001c0001t0001g0304 |
3 | HG00642.hp2 HG00738.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.529-1244_529-1234d others(13): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466494 | ||||||
| chr9:127466494 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0265 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.529-1244_529-1228d others(19): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466494 | ||||||
| chr9:127466494 | ATATATAT others(11): Show |
A | 1 | a0002c0005t0001g0272 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.529-1244_529-1227d others(20): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466494 | ||||||
| chr9:127466495 | TATATATA | T | 4 | a0001c0001t0001g0258 a0001c0001t0001g0263 a0001c0001t0001g0282 others(1): Show |
4 | HG00735.hp2 HG01358.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-1244_529-1238d others(9): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466495 | |||||||
| chr9:127466495 | TATATATA others(2): Show |
T | 12 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0266 others(9): Show |
12 | HG00099.hp2 HG00323.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.529-1244_529-1236d others(11): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466495 | |||||||
| chr9:127466496 | ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0309 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.529-1242_529-1231d others(14): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466496 | ||||||
| chr9:127466496 | ATATATAT others(13): Show |
A | 1 | a0001c0001t0001g0269 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.529-1242_529-1223d others(22): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466496 | ||||||
| chr9:127466497 | TATATATA | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0270 others(4): Show |
7 | HG01261.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.529-1242_529-1236d others(9): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466497 | |||||||
| chr9:127466498 | ATATATAT others(5): Show |
A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0308 |
2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.529-1240_529-1229d others(14): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466498 | ||||||
| chr9:127466498 | ATATATAT others(6): Show |
A | 1 | a0001c0001t0001g0079 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.529-1240_529-1228d others(15): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466498 | ||||||
| chr9:127466500 | A | T | 2 | a0002c0002t0001g0003 a0002c0002t0001g0205 |
3 | HG03471.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.529-1240A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466500 | |||||||
| chr9:127466500 | ATATATTT others(4): Show |
A | 1 | a0001c0001t0001g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.529-1238_529-1228d others(13): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466500 | ||||||
| chr9:127466502 | A | ATT | 3 | a0002c0002t0001g0204 a0002c0002t0001g0217 a0002c0002t0003g0226 |
3 | NA18955.hp2 NA19066.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.529-1237_529-1236i others(4): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466502 | ||||||
| chr9:127466502 | A | T | 14 | a0001c0001t0001g0279 a0001c0001t0001g0292 a0001c0001t0001g0300 others(11): Show |
15 | HG01952.hp1 HG01981.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.529-1238A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466502 | |||||||
| chr9:127466504 | A | ATATATAT others(6): Show |
1 | a0001c0003t0001g0136 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.529-1235_529-1234i others(15): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | ||||||
| chr9:127466504 | A | ATATATAT others(8): Show |
2 | a0002c0002t0001g0225 a0002c0002t0001g0232 |
2 | HG00280.hp1 HG00280.hp2 |
intron_variant | MODIFIER | c.529-1235_529-1234i others(17): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | ||||||
| chr9:127466504 | A | ATATATAT others(10): Show |
1 | a0001c0001t0002g0085 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529-1235_529-1234i others(19): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | ||||||
| chr9:127466504 | A | ATATATAT others(16): Show |
1 | a0002c0002t0005g0104 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.529-1235_529-1234i others(25): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | ||||||
| chr9:127466504 | A | ATATATAT others(13): Show |
1 | a0002c0002t0001g0103 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.529-1235_529-1234i others(22): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | ||||||
| chr9:127466504 | A | ATATATAT others(13): Show |
1 | a0001c0003t0001g0004 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.529-1235_529-1234i others(22): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | ||||||
| chr9:127466504 | A | ATATATAT others(9): Show |
1 | a0002c0002t0001g0106 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.529-1235_529-1234i others(18): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | ||||||
| chr9:127466504 | A | ATATATAT others(10): Show |
1 | a0002c0002t0001g0120 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.529-1235_529-1234i others(19): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | ||||||
| chr9:127466504 | A | ATATATAT others(8): Show |
3 | a0002c0002t0001g0107 a0002c0002t0001g0114 a0002c0005t0002g0086 |
3 | HG01169.hp2 HG01258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.529-1235_529-1234i others(17): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | ||||||
| chr9:127466504 | A | ATATATAT others(10): Show |
2 | a0002c0002t0001g0108 a0002c0002t0001g0117 |
2 | HG03834.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.529-1235_529-1234i others(19): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | ||||||
| chr9:127466504 | A | ATATATAT others(5): Show |
2 | a0002c0002t0001g0115 a0002c0002t0001g0233 |
2 | HG01358.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.529-1235_529-1234i others(14): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | ||||||
| chr9:127466504 | A | ATATATAT others(6): Show |
1 | a0002c0002t0001g0109 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.529-1235_529-1234i others(15): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | ||||||
| chr9:127466504 | A | ATATATAT others(3): Show |
1 | a0002c0002t0001g0100 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.529-1235_529-1234i others(12): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | ||||||
| chr9:127466504 | A | ATATATAT others(4): Show |
3 | a0002c0002t0001g0093 a0002c0002t0001g0110 a0002c0002t0001g0123 |
3 | HG01952.hp2 HG03098.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.529-1235_529-1234i others(13): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | ||||||
| chr9:127466504 | A | ATATATAT others(5): Show |
4 | a0002c0002t0001g0111 a0002c0002t0001g0113 a0002c0002t0001g0234 others(1): Show |
4 | HG00738.hp2 HG01106.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.529-1235_529-1234i others(14): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | ||||||
| chr9:127466504 | A | ATATATAT others(6): Show |
3 | a0001c0003t0001g0132 a0001c0003t0001g0144 a0002c0002t0001g0121 |
3 | HG00140.hp2 HG01192.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.529-1235_529-1234i others(15): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | ||||||
| chr9:127466504 | A | ATATATAT others(5): Show |
3 | a0001c0003t0001g0153 a0001c0003t0001g0154 a0001c0003t0001g0155 |
3 | HG00741.hp2 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.529-1235_529-1234i others(14): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | ||||||
| chr9:127466504 | A | ATATATTT others(7): Show |
1 | a0002c0002t0001g0118 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.529-1235_529-1234i others(16): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | ||||||
| chr9:127466504 | A | ATATTTTT others(8): Show |
1 | a0002c0002t0001g0116 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.529-1235_529-1234i others(17): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | ||||||
| chr9:127466504 | A | ATT | 7 | a0001c0003t0001g0014 a0001c0003t0001g0178 a0001c0003t0001g0231 others(4): Show |
7 | HG00438.hp2 HG02083.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.529-1211_529-1210d others(4): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | ||||||
| chr9:127466504 | A | T | 48 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0261 others(45): Show |
50 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.529-1236A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466504 | |||||||
| chr9:127466504 | AT | A | 6 | a0001c0003t0001g0157 a0001c0003t0001g0171 a0001c0003t0001g0199 others(3): Show |
6 | HG02004.hp2 HG02257.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.529-1210delT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | ||||||
| chr9:127466505 | T | TA | 27 | a0001c0001t0001g0015 a0001c0001t0001g0021 a0001c0001t0001g0023 others(24): Show |
27 | HG00621.hp2 HG00639.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.529-1235_529-1234i others(3): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466505 | |||||||
| chr9:127466505 | T | TATA | 21 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0041 others(18): Show |
21 | HG00558.hp1 HG01255.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.529-1235_529-1234i others(5): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466505 | |||||||
| chr9:127466505 | T | TATATA | 13 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0034 others(10): Show |
13 | HG00558.hp2 HG00642.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.529-1235_529-1234i others(7): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466505 | |||||||
| chr9:127466505 | T | TATATATA | 8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0037 others(5): Show |
10 | HG00099.hp1 HG01361.hp2 HG03669.hp2 others(7): Show |
intron_variant | MODIFIER | c.529-1235_529-1234i others(9): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466505 | |||||||
| chr9:127466505 | T | TATATATA others(6): Show |
2 | a0001c0001t0001g0048 a0001c0001t0001g0069 |
2 | HG01981.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.529-1235_529-1234i others(15): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466505 | |||||||
| chr9:127466505 | T | TATATATA others(10): Show |
1 | a0002c0002t0001g0105 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.529-1235_529-1234i others(19): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466505 | |||||||
| chr9:127466506 | T | A | 67 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0019 others(64): Show |
69 | HG00323.hp2 HG00438.hp1 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.529-1234T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466506 | |||||||
| chr9:127466507 | T | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(59): Show |
64 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.529-1233T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466507 | |||||||
| chr9:127466508 | T | A | 53 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0020 others(50): Show |
55 | HG00438.hp1 HG01106.hp2 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.529-1232T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466508 | |||||||
| chr9:127466509 | T | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(41): Show |
46 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.529-1231T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466509 | |||||||
| chr9:127466510 | T | A | 50 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0020 others(47): Show |
52 | HG00438.hp1 HG01106.hp2 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.529-1230T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466510 | |||||||
| chr9:127466511 | T | A | 38 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(35): Show |
40 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.529-1229T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466511 | |||||||
| chr9:127466511 | T | TAC | 3 | a0001c0007t0001g0326 a0001c0007t0001g0327 a0001c0007t0001g0329 |
3 | HG01109.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.529-1229_529-1228i others(4): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466511 | |||||||
| chr9:127466512 | T | A | 42 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0020 others(39): Show |
43 | HG00438.hp1 HG01081.hp1 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.529-1228T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466512 | |||||||
| chr9:127466513 | T | A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(34): Show |
39 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.529-1227T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466513 | |||||||
| chr9:127466514 | T | A | 25 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0022 others(22): Show |
26 | HG00438.hp1 HG01106.hp2 HG01943.hp1 others(23): Show |
intron_variant | MODIFIER | c.529-1226T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466514 | |||||||
| chr9:127466515 | T | A | 34 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(31): Show |
36 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.529-1225T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466515 | |||||||
| chr9:127466516 | T | A | 16 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0032 others(13): Show |
18 | HG00438.hp1 HG01106.hp2 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.529-1224T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466516 | |||||||
| chr9:127466516 | TTTTTTTT others(8): Show |
T | 1 | a0001c0001t0001g0052 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.529-1223_529-1209d others(17): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466516 | |||||||
| chr9:127466517 | T | A | 18 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(15): Show |
18 | HG00558.hp2 HG00639.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.529-1223T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466517 | |||||||
| chr9:127466518 | T | A | 4 | a0001c0001t0001g0038 a0001c0001t0001g0047 a0001c0001t0001g0058 others(1): Show |
4 | HG01106.hp2 HG02129.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.529-1222T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466518 | |||||||
| chr9:127466519 | T | A | 9 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0030 others(6): Show |
9 | HG00558.hp2 HG02155.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.529-1221T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466519 | |||||||
| chr9:127466520 | T | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0047 a0001c0001t0001g0237 |
3 | HG02129.hp2 NA18999.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.529-1220T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466520 | |||||||
| chr9:127466521 | T | A | 1 | a0001c0001t0001g0023 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.529-1219T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466521 | |||||||
| chr9:127466522 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.529-1218T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466522 | |||||||
| chr9:127466530 | T | C | 1 | a0009c0011t0001g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.529-1210T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466530 | |||||||
| chr9:127466530 | TC | T | 13 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0026 others(10): Show |
13 | HG00438.hp1 HG01943.hp1 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.529-1208delC | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466530 | ||||||
| chr9:127466531 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(148): Show |
157 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.529-1209C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466531 | |||||||
| chr9:127466567 | G | A | 4 | a0001c0001t0001g0265 a0001c0001t0001g0280 a0001c0001t0001g0281 others(1): Show |
4 | NA18957.hp1 NA18989.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.529-1173G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466567 | |||||||
| chr9:127466707 | T | C | 3 | a0001c0007t0001g0326 a0001c0007t0001g0327 a0001c0007t0001g0329 |
3 | HG01109.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.529-1033T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466707 | |||||||
| chr9:127466862 | G | T | 4 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0001g0320 others(1): Show |
4 | HG00609.hp1 HG00621.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.529-878G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466862 | |||||||
| chr9:127466876 | G | T | 1 | a0001c0001t0001g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.529-864G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466876 | |||||||
| chr9:127466886 | C | T | 2 | a0002c0002t0001g0177 a0002c0002t0001g0181 |
2 | NA18948.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.529-854C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466886 | |||||||
| chr9:127466951 | C | T | 1 | a0002c0002t0001g0090 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.529-789C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466951 | |||||||
| chr9:127466975 | C | T | 1 | a0009c0011t0001g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.529-765C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466975 | |||||||
| chr9:127466983 | A | G | 101 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(98): Show |
105 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.529-757A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466983 | |||||||
| chr9:127467058 | C | T | 1 | a0002c0002t0001g0092 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.529-682C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127467058 | |||||||
| chr9:127467127 | T | C | 17 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0079 others(14): Show |
17 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.529-613T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127467127 | |||||||
| chr9:127467128 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.529-612T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127467128 | |||||||
| chr9:127467130 | G | T | 1 | a0001c0001t0001g0278 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.529-610G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127467130 | |||||||
| chr9:127467285 | C | A | 95 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(92): Show |
99 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.529-455C>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127467285 | |||||||
| chr9:127467373 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(176): Show |
185 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.529-367A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127467373 | |||||||
| chr9:127467374 | C | T | 1 | a0003c0004t0001g0073 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.529-366C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127467374 | |||||||
| chr9:127467494 | C | T | 3 | a0001c0007t0001g0326 a0001c0007t0001g0327 a0001c0007t0001g0329 |
3 | HG01109.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.529-246C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127467494 | |||||||
| chr9:127467718 | C | T | 1 | a0002c0002t0001g0184 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.529-22C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127467718 | |||||||
| chr9:127467843 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0029 |
2 | NA18979.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.619+13C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127467843 | |||||||
| chr9:127468030 | C | T | 3 | a0002c0002t0001g0177 a0002c0002t0001g0181 a0002c0002t0001g0230 |
3 | NA18948.hp1 NA19064.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.619+200C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127468030 | |||||||
| chr9:127468235 | A | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(178): Show |
187 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.619+405A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127468235 | |||||||
| chr9:127468367 | G | A | 5 | a0002c0002t0001g0164 a0002c0002t0001g0167 a0002c0002t0001g0188 others(2): Show |
5 | HG01168.hp1 HG01169.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.619+537G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127468367 | |||||||
| chr9:127468432 | G | A | 12 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(9): Show |
12 | HG02486.hp2 HG02717.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.619+602G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127468432 | |||||||
| chr9:127468810 | C | CA | 56 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0022 others(53): Show |
57 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.619+1009dupA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127468810 | ||||||
| chr9:127468810 | C | CAAA | 6 | a0001c0001t0001g0008 a0001c0001t0001g0238 a0001c0001t0001g0240 others(3): Show |
7 | HG03942.hp2 NA18959.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.619+1007_619+1009d others(5): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127468810 | ||||||
| chr9:127468810 | CAAAAAAA others(2): Show |
C | 6 | a0001c0001t0001g0328 a0001c0007t0001g0326 a0001c0007t0001g0327 others(3): Show |
6 | HG00733.hp2 HG01109.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.619+1001_619+1009d others(11): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127468810 | ||||||
| chr9:127468810 | CAAAAAAA others(8): Show |
C | 5 | a0001c0001t0001g0023 a0001c0001t0001g0030 a0001c0001t0001g0035 others(2): Show |
5 | NA18943.hp2 NA18948.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.619+995_619+1009de others(16): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127468810 | ||||||
| chr9:127468834 | A | AAC | 19 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0265 others(16): Show |
19 | HG00621.hp1 HG00738.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.619+1005_619+1006i others(4): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127468834 | ||||||
| chr9:127468834 | A | AC | 61 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(58): Show |
64 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.619+1004_619+1005i others(3): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127468834 | |||||||
| chr9:127468834 | A | C | 2 | a0001c0001t0001g0258 a0001c0001t0001g0300 |
2 | HG00735.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.619+1004A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127468834 | |||||||
| chr9:127469138 | A | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(174): Show |
183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.619+1308A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127469138 | |||||||
| chr9:127469326 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.619+1496T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127469326 | |||||||
| chr9:127469356 | G | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.619+1526G>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127469356 | |||||||
| chr9:127469435 | A | G | 320 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(317): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.619+1605A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127469435 | |||||||
| chr9:127469593 | C | T | 10 | a0001c0001t0001g0020 a0001c0003t0001g0004 a0001c0003t0001g0132 others(7): Show |
11 | HG00140.hp2 HG00741.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.619+1763C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127469593 | |||||||
| chr9:127469620 | G | GA | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(183): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.619+1801dupA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127469620 | ||||||
| chr9:127469688 | G | A | 1 | a0002c0002t0001g0184 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.619+1858G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127469688 | |||||||
| chr9:127469790 | T | C | 2 | a0001c0001t0002g0085 a0002c0005t0002g0086 |
2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.619+1960T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127469790 | |||||||
| chr9:127469836 | G | A | 1 | a0002c0002t0001g0128 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.619+2006G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127469836 | |||||||
| chr9:127469878 | T | C | 1 | a0002c0002t0001g0172 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.619+2048T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127469878 | |||||||
| chr9:127469889 | C | T | 1 | a0002c0002t0001g0180 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.619+2059C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127469889 | |||||||
| chr9:127469913 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.619+2083C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127469913 | |||||||
| chr9:127469920 | GCGCCACT others(1815): Show |
G | 1 | a0001c0001t0001g0296 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.619+2113_620-2037d others(2): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127469920 | ||||||
| chr9:127469943 | A | C | 1 | a0001c0001t0001g0032 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.619+2113A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127469943 | |||||||
| chr9:127469944 | T | G | 1 | a0001c0001t0001g0032 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.619+2114T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127469944 | |||||||
| chr9:127470144 | T | C | 16 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0079 others(13): Show |
16 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.619+2314T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127470144 | |||||||
| chr9:127470182 | G | A | 5 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0027 others(2): Show |
5 | NA18959.hp1 NA18979.hp1 NA19057.hp2 others(2): Show |
intron_variant | MODIFIER | c.619+2352G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127470182 | |||||||
| chr9:127470459 | A | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(64): Show |
70 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.619+2629A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127470459 | |||||||
| chr9:127470488 | G | A | 2 | a0001c0003t0001g0229 a0009c0011t0001g0228 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.619+2658G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127470488 | |||||||
| chr9:127470611 | T | A | 70 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(67): Show |
73 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.619+2781T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127470611 | |||||||
| chr9:127470630 | G | C | 70 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(67): Show |
73 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.619+2800G>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127470630 | |||||||
| chr9:127470676 | G | A | 1 | a0002c0002t0001g0119 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.619+2846G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127470676 | |||||||
| chr9:127470769 | T | C | 1 | a0009c0011t0001g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.619+2939T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127470769 | |||||||
| chr9:127470770 | G | C | 1 | a0001c0001t0001g0259 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.619+2940G>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127470770 | |||||||
| chr9:127470837 | T | C | 1 | a0001c0003t0001g0156 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.620-2964T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127470837 | |||||||
| chr9:127470963 | C | G | 16 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0079 others(13): Show |
16 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.620-2838C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127470963 | |||||||
| chr9:127471019 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(51): Show |
56 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.620-2782C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127471019 | |||||||
| chr9:127471111 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.620-2690C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127471111 | |||||||
| chr9:127471472 | T | TA | 38 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(35): Show |
39 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.620-2304dupA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127471472 | ||||||
| chr9:127471472 | TA | T | 36 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0022 others(33): Show |
36 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.620-2304delA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127471472 | ||||||
| chr9:127471472 | TAA | T | 70 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(67): Show |
73 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.620-2305_620-2304d others(4): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127471472 | ||||||
| chr9:127471472 | TAAA | T | 31 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0237 others(28): Show |
32 | HG01099.hp2 HG01109.hp1 HG01515.hp2 others(29): Show |
intron_variant | MODIFIER | c.620-2306_620-2304d others(5): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127471472 | ||||||
| chr9:127471514 | C | T | 16 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0079 others(13): Show |
16 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.620-2287C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127471514 | |||||||
| chr9:127471550 | G | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0236 a0001c0001t0001g0237 others(8): Show |
12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.620-2251G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127471550 | |||||||
| chr9:127471677 | C | T | 82 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(79): Show |
85 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.620-2124C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127471677 | |||||||
| chr9:127471714 | G | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(54): Show |
59 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.620-2087G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127471714 | |||||||
| chr9:127471875 | G | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(175): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.620-1926G>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127471875 | |||||||
| chr9:127471954 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.620-1847C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127471954 | |||||||
| chr9:127472000 | C | T | 11 | a0001c0001t0001g0008 a0001c0001t0001g0236 a0001c0001t0001g0237 others(8): Show |
12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.620-1801C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472000 | |||||||
| chr9:127472096 | G | T | 1 | a0002c0002t0001g0118 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.620-1705G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472096 | |||||||
| chr9:127472119 | G | A | 2 | a0001c0003t0001g0229 a0009c0011t0001g0228 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.620-1682G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472119 | |||||||
| chr9:127472252 | G | A | 16 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0079 others(13): Show |
16 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.620-1549G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472252 | |||||||
| chr9:127472297 | G | GTA | 11 | a0001c0001t0001g0008 a0001c0001t0001g0236 a0001c0001t0001g0237 others(8): Show |
12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.620-1488_620-1487d others(4): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127472297 | ||||||
| chr9:127472297 | GTA | G | 31 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0020 others(28): Show |
32 | HG00140.hp2 HG00741.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.620-1488_620-1487d others(4): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127472297 | ||||||
| chr9:127472313 | A | G | 1 | a0001c0001t0001g0047 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.620-1488A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472313 | |||||||
| chr9:127472313 | ATG | A | 82 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(79): Show |
85 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.620-1480_620-1479d others(4): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127472313 | ||||||
| chr9:127472315 | G | A | 12 | a0001c0001t0001g0008 a0001c0001t0001g0236 a0001c0001t0001g0237 others(9): Show |
13 | HG02129.hp2 HG03654.hp1 NA18950.hp1 others(10): Show |
intron_variant | MODIFIER | c.620-1486G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472315 | |||||||
| chr9:127472317 | G | A | 94 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(91): Show |
98 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.620-1484G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472317 | |||||||
| chr9:127472355 | A | G | 94 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(91): Show |
98 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.620-1446A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472355 | |||||||
| chr9:127472368 | A | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(180): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.620-1433A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472368 | |||||||
| chr9:127472442 | G | A | 1 | a0002c0002t0001g0139 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.620-1359G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472442 | |||||||
| chr9:127472632 | C | G | 6 | a0002c0002t0001g0093 a0002c0002t0001g0116 a0002c0002t0001g0117 others(3): Show |
6 | HG02145.hp1 HG02486.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.620-1169C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472632 | |||||||
| chr9:127472759 | C | T | 2 | a0003c0004t0002g0083 a0003c0004t0002g0084 |
2 | HG02055.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.620-1042C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472759 | |||||||
| chr9:127472774 | G | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(81): Show |
87 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.620-1027G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472774 | |||||||
| chr9:127472794 | C | T | 2 | a0002c0002t0001g0188 a0002c0002t0001g0213 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.620-1007C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472794 | |||||||
| chr9:127472924 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.620-877G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472924 | |||||||
| chr9:127473006 | AC | A | 6 | a0002c0002t0001g0007 a0002c0002t0001g0124 a0002c0002t0001g0133 others(3): Show |
7 | HG01496.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.620-793delC | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127473006 | ||||||
| chr9:127473173 | T | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(55): Show |
60 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.620-628T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127473173 | |||||||
| chr9:127473505 | C | T | 9 | a0001c0003t0001g0004 a0001c0003t0001g0132 a0001c0003t0001g0140 others(6): Show |
10 | HG00140.hp2 HG00741.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.620-296C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127473505 | |||||||
| chr9:127473522 | A | T | 1 | a0001c0003t0001g0153 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.620-279A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127473522 | |||||||
| chr9:127473581 | C | T | 11 | a0001c0001t0001g0008 a0001c0001t0001g0236 a0001c0001t0001g0237 others(8): Show |
12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.620-220C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127473581 | |||||||
| chr9:127473618 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(55): Show |
60 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.620-183G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127473618 | |||||||
| chr9:127473964 | G | A | 94 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(91): Show |
98 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.750+33G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127473964 | |||||||
| chr9:127474244 | G | A | 4 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
4 | HG02886.hp1 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.750+313G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127474244 | |||||||
| chr9:127474260 | CT | C | 93 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(90): Show |
97 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.750+345delT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 127474260 | ||||||
| chr9:127474310 | C | G | 96 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(93): Show |
100 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.750+379C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127474310 | |||||||
| chr9:127474329 | G | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0043 others(5): Show |
9 | NA18942.hp1 NA18962.hp1 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.750+398G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127474329 | |||||||
| chr9:127474382 | C | T | 1 | a0001c0003t0001g0176 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.750+451C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127474382 | |||||||
| chr9:127474603 | T | G | 1 | a0002c0005t0001g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.750+672T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127474603 | |||||||
| chr9:127474661 | C | T | 1 | a0001c0001t0001g0299 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.750+730C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127474661 | |||||||
| chr9:127474704 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.750+773C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127474704 | |||||||
| chr9:127474709 | C | T | 1 | a0001c0001t0001g0310 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.750+778C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127474709 | |||||||
| chr9:127474771 | C | T | 2 | a0001c0001t0001g0279 a0001c0001t0001g0282 |
2 | HG03239.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.750+840C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127474771 | |||||||
| chr9:127474789 | G | A | 9 | a0001c0003t0001g0004 a0001c0003t0001g0132 a0001c0003t0001g0140 others(6): Show |
10 | HG00140.hp2 HG00741.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.750+858G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127474789 | |||||||
| chr9:127474809 | C | T | 1 | a0001c0003t0001g0187 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.750+878C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127474809 | |||||||
| chr9:127474967 | T | A | 3 | a0001c0001t0001g0263 a0001c0001t0001g0291 a0001c0001t0001g0301 |
3 | HG01978.hp1 HG02738.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.750+1036T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127474967 | |||||||
| chr9:127475047 | T | TTTA | 100 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(97): Show |
104 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.750+1140_750+1142d others(5): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 127475047 | ||||||
| chr9:127475047 | T | TTTATTA | 4 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0243 others(1): Show |
4 | HG02258.hp2 HG02738.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.750+1137_750+1142d others(8): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 127475047 | ||||||
| chr9:127475077 | T | C | 96 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(93): Show |
100 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.750+1146T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127475077 | |||||||
| chr9:127475319 | T | G | 9 | a0002c0002t0001g0097 a0002c0002t0001g0141 a0002c0002t0001g0145 others(6): Show |
9 | HG00621.hp2 HG02165.hp2 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.750+1388T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127475319 | |||||||
| chr9:127475342 | T | G | 16 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0079 others(13): Show |
16 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.750+1411T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127475342 | |||||||
| chr9:127475413 | T | G | 1 | a0002c0002t0001g0172 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.750+1482T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127475413 | |||||||
| chr9:127475448 | G | A | 1 | a0001c0001t0002g0085 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.750+1517G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127475448 | |||||||
| chr9:127475493 | TCAAA | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(83): Show |
89 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.750+1581_750+1584d others(6): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 127475493 | ||||||
| chr9:127475745 | T | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(181): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.750+1814T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127475745 | |||||||
| chr9:127475749 | A | AT | 6 | a0002c0002t0001g0093 a0002c0002t0001g0116 a0002c0002t0001g0117 others(3): Show |
6 | HG02145.hp1 HG02486.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.750+1827dupT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 127475749 | ||||||
| chr9:127475749 | A | T | 1 | a0001c0001t0001g0021 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.750+1818A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127475749 | |||||||
| chr9:127475833 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.750+1902C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127475833 | |||||||
| chr9:127475834 | G | A | 1 | a0001c0003t0001g0142 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.750+1903G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127475834 | |||||||
| chr9:127475843 | T | C | 96 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(93): Show |
100 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.750+1912T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127475843 | |||||||
| chr9:127475881 | C | T | 96 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(93): Show |
100 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.750+1950C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127475881 | |||||||
| chr9:127475902 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.750+1971G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127475902 | |||||||
| chr9:127475912 | G | A | 42 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0003t0001g0014 others(39): Show |
42 | HG00323.hp2 HG00558.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.750+1981G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127475912 | |||||||
| chr9:127476015 | C | T | 4 | a0001c0001t0001g0071 a0004c0006t0001g0070 a0004c0006t0001g0072 others(1): Show |
4 | HG02129.hp1 NA18974.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.750+2084C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127476015 | |||||||
| chr9:127476189 | A | C | 1 | a0002c0005t0001g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.750+2258A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127476189 | |||||||
| chr9:127476248 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.750+2317G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127476248 | |||||||
| chr9:127476261 | A | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(180): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.750+2330A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127476261 | |||||||
| chr9:127476297 | A | G | 3 | a0001c0007t0001g0326 a0001c0007t0001g0327 a0001c0007t0001g0329 |
3 | HG01109.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.750+2366A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127476297 | |||||||
| chr9:127476366 | C | G | 83 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(80): Show |
86 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.750+2435C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127476366 | |||||||
| chr9:127476425 | G | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(81): Show |
87 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.750+2494G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127476425 | |||||||
| chr9:127476550 | A | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0003c0004t0001g0073 |
3 | HG03041.hp1 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.751-2384A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127476550 | |||||||
| chr9:127476651 | G | A | 1 | a0002c0005t0001g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.751-2283G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127476651 | |||||||
| chr9:127476680 | T | C | 16 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0079 others(13): Show |
16 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.751-2254T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127476680 | |||||||
| chr9:127476809 | G | T | 1 | a0001c0001t0001g0074 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.751-2125G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127476809 | |||||||
| chr9:127476955 | G | A | 1 | a0002c0005t0001g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.751-1979G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127476955 | |||||||
| chr9:127477052 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.751-1882A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127477052 | |||||||
| chr9:127477054 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.751-1880T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127477054 | |||||||
| chr9:127477063 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(55): Show |
60 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.751-1871G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127477063 | |||||||
| chr9:127477087 | C | T | 2 | a0001c0003t0001g0229 a0009c0011t0001g0228 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.751-1847C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127477087 | |||||||
| chr9:127477224 | G | T | 2 | a0001c0003t0001g0229 a0009c0011t0001g0228 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.751-1710G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127477224 | |||||||
| chr9:127477408 | A | G | 1 | a0003c0004t0001g0073 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.751-1526A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127477408 | |||||||
| chr9:127477515 | C | T | 1 | a0002c0005t0001g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.751-1419C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127477515 | |||||||
| chr9:127477621 | G | A | 94 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(91): Show |
98 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.751-1313G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127477621 | |||||||
| chr9:127477692 | G | A | 1 | a0001c0001t0001g0261 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.751-1242G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127477692 | |||||||
| chr9:127477697 | C | T | 3 | a0001c0007t0001g0326 a0001c0007t0001g0327 a0001c0007t0001g0329 |
3 | HG01109.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.751-1237C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127477697 | |||||||
| chr9:127477755 | A | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0003c0004t0001g0073 |
3 | HG03041.hp1 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.751-1179A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127477755 | |||||||
| chr9:127477770 | G | A | 16 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0079 others(13): Show |
16 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.751-1164G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127477770 | |||||||
| chr9:127477774 | G | A | 1 | a0002c0002t0001g0220 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.751-1160G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127477774 | |||||||
| chr9:127477906 | G | A | 12 | a0001c0003t0001g0004 a0001c0003t0001g0132 a0001c0003t0001g0140 others(9): Show |
13 | HG00140.hp2 HG00741.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.751-1028G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127477906 | |||||||
| chr9:127478040 | A | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(222): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.751-894A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127478040 | |||||||
| chr9:127478052 | C | CA | 15 | a0001c0001t0001g0018 a0001c0001t0001g0254 a0001c0001t0001g0265 others(12): Show |
15 | HG01192.hp2 HG01433.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.751-864dupA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 127478052 | ||||||
| chr9:127478052 | CA | C | 21 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0236 others(18): Show |
22 | HG00639.hp2 HG00741.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.751-864delA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 127478052 | ||||||
| chr9:127478460 | G | A | 2 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.751-474G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127478460 | |||||||
| chr9:127478479 | T | C | 1 | a0002c0002t0001g0090 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.751-455T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127478479 | |||||||
| chr9:127478500 | T | C | 1 | a0002c0002t0001g0094 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.751-434T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127478500 | |||||||
| chr9:127478502 | G | T | 10 | a0001c0001t0001g0008 a0001c0001t0001g0236 a0001c0001t0001g0238 others(7): Show |
11 | NA18950.hp1 NA18955.hp1 NA18959.hp2 others(8): Show |
intron_variant | MODIFIER | c.751-432G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127478502 | |||||||
| chr9:127478624 | A | G | 1 | a0001c0001t0001g0242 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.751-310A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127478624 | |||||||
| chr9:127478687 | A | C | 16 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0079 others(13): Show |
16 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.751-247A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127478687 | |||||||
| chr9:127478701 | A | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(223): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.751-233A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127478701 | |||||||
| chr9:127479043 | G | T | 10 | a0002c0002t0001g0003 a0002c0002t0001g0094 a0002c0002t0001g0095 others(7): Show |
11 | HG01109.hp2 HG02258.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.780+80G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 12/25 | chr9 | 127479043 | |||||||
| chr9:127479095 | G | GCA | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(223): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.780+133_780+134dup others(2): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 12/25 | INFO_REALIGN_3_PRIME | chr9 | 127479095 | ||||||
| chr9:127479160 | C | T | 1 | a0002c0002t0001g0197 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.780+197C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 12/25 | chr9 | 127479160 | |||||||
| chr9:127479257 | T | C | 2 | a0001c0003t0001g0171 a0001c0003t0001g0183 |
2 | HG01952.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.781-126T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 12/25 | chr9 | 127479257 | |||||||
| chr9:127479543 | T | C | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(222): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.903+38T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 13/25 | chr9 | 127479543 | |||||||
| chr9:127479598 | A | G | 12 | a0001c0003t0001g0014 a0001c0003t0001g0101 a0001c0003t0001g0159 others(9): Show |
12 | HG00673.hp1 HG00741.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.903+93A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 13/25 | chr9 | 127479598 | |||||||
| chr9:127479774 | A | G | 11 | a0001c0001t0001g0008 a0001c0001t0001g0236 a0001c0001t0001g0237 others(8): Show |
12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.904-65A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 13/25 | chr9 | 127479774 | |||||||
| chr9:127479791 | G | A | 3 | a0001c0007t0001g0326 a0001c0007t0001g0327 a0001c0007t0001g0329 |
3 | HG01109.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.904-48G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 13/25 | chr9 | 127479791 | |||||||
| chr9:127479830 | C | T | 94 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(91): Show |
98 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.904-9C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 13/25 | chr9 | 127479830 | |||||||
| chr9:127480033 | G | A | 1 | a0001c0003t0001g0165 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1043+55G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 14/25 | chr9 | 127480033 | |||||||
| chr9:127480082 | C | T | 3 | a0001c0007t0001g0326 a0001c0007t0001g0327 a0001c0007t0001g0329 |
3 | HG01109.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1043+104C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 14/25 | chr9 | 127480082 | |||||||
| chr9:127480593 | G | A | 1 | a0001c0001t0001g0312 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1044-590G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 14/25 | chr9 | 127480593 | |||||||
| chr9:127480799 | T | G | 1 | a0002c0002t0001g0093 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1044-384T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 14/25 | chr9 | 127480799 | |||||||
| chr9:127480870 | G | A | 4 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
4 | HG02886.hp1 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1044-313G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 14/25 | chr9 | 127480870 | |||||||
| chr9:127480871 | G | A | 1 | a0002c0002t0001g0148 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1044-312G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 14/25 | chr9 | 127480871 | |||||||
| chr9:127480953 | A | G | 1 | a0002c0002t0001g0225 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1044-230A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 14/25 | chr9 | 127480953 | |||||||
| chr9:127481174 | T | C | 1 | a0001c0001t0002g0085 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1044-9T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 14/25 | chr9 | 127481174 | |||||||
| chr9:127481255 | A | AT | 12 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0023 others(9): Show |
13 | HG01099.hp2 HG02109.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1088+44dupT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr9 | 127481255 | ||||||
| chr9:127481255 | AT | A | 16 | a0001c0001t0001g0008 a0001c0001t0001g0027 a0001c0001t0001g0236 others(13): Show |
17 | HG01884.hp2 HG02055.hp1 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.1088+44delT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr9 | 127481255 | ||||||
| chr9:127481341 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(55): Show |
60 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1088+114C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127481341 | |||||||
| chr9:127481544 | G | A | 1 | a0001c0001t0001g0325 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1088+317G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127481544 | |||||||
| chr9:127481567 | G | A | 96 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(93): Show |
100 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1088+340G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127481567 | |||||||
| chr9:127481711 | T | C | 1 | a0001c0001t0001g0319 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1088+484T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127481711 | |||||||
| chr9:127481734 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0042 |
2 | NA18978.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1088+507A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127481734 | |||||||
| chr9:127481927 | C | T | 5 | a0002c0002t0001g0148 a0002c0002t0001g0150 a0002c0002t0001g0161 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1088+700C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127481927 | |||||||
| chr9:127481931 | T | C | 1 | a0001c0001t0001g0294 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1088+704T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127481931 | |||||||
| chr9:127481950 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1088+723A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127481950 | |||||||
| chr9:127481976 | A | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(181): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.1088+749A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127481976 | |||||||
| chr9:127482113 | A | G | 1 | a0002c0005t0001g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1089-837A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127482113 | |||||||
| chr9:127482136 | A | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(55): Show |
60 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1089-814A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127482136 | |||||||
| chr9:127482140 | C | CT | 60 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(57): Show |
62 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1089-790dupT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr9 | 127482140 | ||||||
| chr9:127482140 | CT | C | 89 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(86): Show |
92 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1089-790delT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr9 | 127482140 | ||||||
| chr9:127482140 | CTT | C | 11 | a0001c0001t0001g0008 a0001c0001t0001g0237 a0001c0001t0001g0239 others(8): Show |
12 | HG00639.hp2 HG02129.hp2 HG03491.hp1 others(9): Show |
intron_variant | MODIFIER | c.1089-791_1089-790d others(4): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr9 | 127482140 | ||||||
| chr9:127482166 | G | A | 5 | a0002c0002t0001g0164 a0002c0002t0001g0167 a0002c0002t0001g0188 others(2): Show |
5 | HG01168.hp1 HG01169.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1089-784G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127482166 | |||||||
| chr9:127482523 | T | G | 1 | a0001c0001t0001g0261 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1089-427T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127482523 | |||||||
| chr9:127482525 | C | G | 1 | a0001c0001t0001g0067 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1089-425C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127482525 | |||||||
| chr9:127482633 | A | G | 1 | a0001c0003t0001g0169 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1089-317A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127482633 | |||||||
| chr9:127482659 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1089-291A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127482659 | |||||||
| chr9:127482910 | A | G | 1 | a0001c0001t0001g0026 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1089-40A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127482910 | |||||||
| chr9:127482938 | A | G | 1 | a0002c0002t0001g0103 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1089-12A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127482938 | |||||||
| chr9:127483266 | G | C | 96 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(93): Show |
100 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1159+246G>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127483266 | |||||||
| chr9:127483508 | G | T | 94 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(91): Show |
98 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1159+488G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127483508 | |||||||
| chr9:127483512 | T | G | 3 | a0001c0007t0001g0326 a0001c0007t0001g0327 a0001c0007t0001g0329 |
3 | HG01109.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1159+492T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127483512 | |||||||
| chr9:127483564 | G | C | 2 | a0004c0006t0001g0070 a0004c0006t0001g0072 |
2 | NA18989.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1159+544G>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127483564 | |||||||
| chr9:127483913 | CAACCTCC others(2): Show |
C | 11 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(8): Show |
11 | HG02486.hp2 HG02717.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1159+896_1159+904d others(11): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr9 | 127483913 | ||||||
| chr9:127484222 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(84): Show |
90 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1159+1202C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127484222 | |||||||
| chr9:127484263 | C | CT | 129 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(126): Show |
134 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.1159+1260dupT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr9 | 127484263 | ||||||
| chr9:127484263 | C | CTT | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(55): Show |
60 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1159+1259_1159+126 others(6): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr9 | 127484263 | ||||||
| chr9:127484263 | CT | C | 10 | a0001c0003t0001g0159 a0002c0002t0001g0093 a0002c0002t0001g0114 others(7): Show |
10 | HG00280.hp1 HG01074.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1159+1260delT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr9 | 127484263 | ||||||
| chr9:127484285 | C | T | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(237): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1159+1265C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127484285 | |||||||
| chr9:127484381 | T | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(223): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.1160-1355T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127484381 | |||||||
| chr9:127484620 | G | A | 2 | a0001c0001t0001g0297 a0001c0001t0001g0307 |
2 | NA19066.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1160-1116G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127484620 | |||||||
| chr9:127484657 | C | T | 2 | a0001c0003t0001g0229 a0009c0011t0001g0228 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1160-1079C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127484657 | |||||||
| chr9:127484658 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1160-1078G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127484658 | |||||||
| chr9:127484802 | CT | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0236 a0001c0001t0001g0237 others(19): Show |
23 | HG02129.hp2 HG02486.hp2 HG02717.hp2 others(20): Show |
intron_variant | MODIFIER | c.1160-927delT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr9 | 127484802 | ||||||
| chr9:127484808 | T | TC | 67 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(64): Show |
69 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.1160-928_1160-927i others(3): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127484808 | |||||||
| chr9:127484809 | T | C | 2 | a0001c0001t0001g0239 a0001c0001t0001g0309 |
2 | HG02145.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1160-927T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127484809 | |||||||
| chr9:127484810 | C | T | 71 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(68): Show |
74 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1160-926C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127484810 | |||||||
| chr9:127484815 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1160-921T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127484815 | |||||||
| chr9:127484835 | G | A | 1 | a0002c0002t0001g0095 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1160-901G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127484835 | |||||||
| chr9:127484885 | G | A | 10 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(7): Show |
10 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1160-851G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127484885 | |||||||
| chr9:127484901 | G | A | 3 | a0001c0001t0002g0085 a0003c0004t0002g0083 a0003c0004t0002g0084 |
3 | HG02055.hp2 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1160-835G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127484901 | |||||||
| chr9:127484997 | A | G | 1 | a0002c0002t0001g0164 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1160-739A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127484997 | |||||||
| chr9:127485076 | G | T | 72 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(69): Show |
75 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.1160-660G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127485076 | |||||||
| chr9:127485306 | C | G | 1 | a0001c0001t0001g0313 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1160-430C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127485306 | |||||||
| chr9:127485375 | G | C | 1 | a0002c0002t0001g0210 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1160-361G>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127485375 | |||||||
| chr9:127485468 | A | G | 1 | a0002c0002t0001g0197 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1160-268A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127485468 | |||||||
| chr9:127485472 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1160-264C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127485472 | |||||||
| chr9:127485562 | C | T | 1 | a0001c0003t0001g0147 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1160-174C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127485562 | |||||||
| chr9:127485611 | G | T | 10 | a0002c0002t0001g0003 a0002c0002t0001g0094 a0002c0002t0001g0095 others(7): Show |
11 | HG01109.hp2 HG02258.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1160-125G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127485611 | |||||||
| chr9:127485619 | C | T | 1 | a0001c0003t0001g0101 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1160-117C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127485619 | |||||||
| chr9:127486022 | G | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0236 a0001c0001t0001g0237 others(8): Show |
12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.1259+187G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127486022 | |||||||
| chr9:127486087 | T | A | 97 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(94): Show |
101 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1259+252T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127486087 | |||||||
| chr9:127486178 | T | C | 2 | a0001c0003t0001g0229 a0009c0011t0001g0228 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1259+343T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127486178 | |||||||
| chr9:127486359 | G | A | 1 | a0002c0005t0001g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1259+524G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127486359 | |||||||
| chr9:127486366 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1259+531G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127486366 | |||||||
| chr9:127486372 | C | T | 3 | a0001c0007t0001g0326 a0001c0007t0001g0327 a0001c0007t0001g0329 |
3 | HG01109.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1259+537C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127486372 | |||||||
| chr9:127486606 | T | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(133): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1259+771T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127486606 | |||||||
| chr9:127486774 | T | C | 1 | a0002c0002t0001g0216 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1260-902T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127486774 | |||||||
| chr9:127486793 | A | G | 1 | a0002c0005t0001g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1260-883A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127486793 | |||||||
| chr9:127486833 | T | G | 2 | a0001c0003t0001g0229 a0009c0011t0001g0228 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1260-843T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127486833 | |||||||
| chr9:127486865 | C | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(181): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.1260-811C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127486865 | |||||||
| chr9:127487143 | C | G | 1 | a0002c0005t0002g0086 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1260-533C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127487143 | |||||||
| chr9:127487183 | C | CA | 19 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0058 others(16): Show |
19 | HG00323.hp2 HG00741.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.1260-476dupA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr9 | 127487183 | ||||||
| chr9:127487183 | CA | C | 77 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(74): Show |
80 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1260-476delA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr9 | 127487183 | ||||||
| chr9:127487200 | A | G | 1 | a0001c0001t0001g0321 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1260-476A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127487200 | |||||||
| chr9:127487291 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1260-385G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127487291 | |||||||
| chr9:127487619 | A | G | 1 | a0002c0005t0001g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1260-57A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127487619 | |||||||
| chr9:127487842 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1347+79C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 18/25 | chr9 | 127487842 | |||||||
| chr9:127487843 | G | A | 2 | a0001c0003t0001g0229 a0009c0011t0001g0228 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1347+80G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 18/25 | chr9 | 127487843 | |||||||
| chr9:127488207 | C | T | 1 | a0002c0002t0001g0127 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1347+444C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 18/25 | chr9 | 127488207 | |||||||
| chr9:127488498 | C | T | 1 | a0002c0002t0001g0181 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1347+735C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 18/25 | chr9 | 127488498 | |||||||
| chr9:127488552 | G | A | 2 | a0001c0003t0001g0229 a0009c0011t0001g0228 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1347+789G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 18/25 | chr9 | 127488552 | |||||||
| chr9:127488599 | C | CT | 15 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0079 others(12): Show |
15 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1348-832dupT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr9 | 127488599 | ||||||
| chr9:127488599 | CT | C | 98 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(95): Show |
102 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.1348-832delT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr9 | 127488599 | ||||||
| chr9:127488696 | C | A | 1 | a0002c0002t0001g0126 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1348-748C>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 18/25 | chr9 | 127488696 | |||||||
| chr9:127488758 | T | G | 51 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0003t0001g0004 others(48): Show |
52 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.1348-686T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 18/25 | chr9 | 127488758 | |||||||
| chr9:127489205 | G | A | 1 | a0002c0002t0001g0179 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1348-239G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 18/25 | chr9 | 127489205 | |||||||
| chr9:127489233 | G | A | 97 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(94): Show |
101 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1348-211G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 18/25 | chr9 | 127489233 | |||||||
| chr9:127489336 | C | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(81): Show |
87 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1348-108C>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 18/25 | chr9 | 127489336 | |||||||
| chr9:127489410 | G | A | 10 | a0001c0001t0001g0020 a0001c0003t0001g0004 a0001c0003t0001g0132 others(7): Show |
11 | HG00140.hp2 HG00741.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.1348-34G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 18/25 | chr9 | 127489410 | |||||||
| chr9:127489556 | CAG | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(84): Show |
90 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1422+42_1422+43del others(2): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 127489556 | ||||||
| chr9:127489585 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1422+67G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127489585 | |||||||
| chr9:127489604 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1422+86G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127489604 | |||||||
| chr9:127489645 | G | T | 1 | a0002c0002t0001g0117 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1422+127G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127489645 | |||||||
| chr9:127489647 | C | T | 3 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 |
3 | HG02809.hp2 HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1422+129C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127489647 | |||||||
| chr9:127489821 | T | C | 11 | a0001c0001t0001g0008 a0001c0001t0001g0236 a0001c0001t0001g0237 others(8): Show |
12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.1422+303T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127489821 | |||||||
| chr9:127489856 | C | T | 1 | a0001c0003t0001g0199 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1422+338C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127489856 | |||||||
| chr9:127489876 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1422+358G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127489876 | |||||||
| chr9:127489971 | G | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(238): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1422+453G>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127489971 | |||||||
| chr9:127490007 | C | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(81): Show |
87 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1422+489C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127490007 | |||||||
| chr9:127490028 | T | A | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(219): Show |
228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.1422+510T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127490028 | |||||||
| chr9:127490033 | C | T | 39 | a0002c0002t0001g0097 a0002c0002t0001g0100 a0002c0002t0001g0103 others(36): Show |
39 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.1422+515C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127490033 | |||||||
| chr9:127490091 | G | GCTAT | 98 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(95): Show |
102 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.1422+574_1422+575i others(6): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 127490091 | ||||||
| chr9:127490176 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1422+658T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127490176 | |||||||
| chr9:127490246 | T | TTTTC | 6 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(3): Show |
6 | HG01884.hp2 HG02809.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1422+756_1422+759d others(6): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 127490246 | ||||||
| chr9:127490246 | T | TTTTCTTT others(1): Show |
4 | a0003c0004t0001g0077 a0003c0004t0001g0087 a0003c0004t0001g0088 others(1): Show |
4 | HG02451.hp2 HG02630.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1422+752_1422+759d others(10): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 127490246 | ||||||
| chr9:127490246 | TTTTC | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(152): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.1422+756_1422+759d others(6): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 127490246 | ||||||
| chr9:127490378 | G | T | 1 | a0002c0002t0001g0012 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1423-837G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127490378 | |||||||
| chr9:127490602 | T | C | 2 | a0002c0002t0001g0141 a0002c0002t0001g0189 |
2 | NA18957.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1423-613T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127490602 | |||||||
| chr9:127491007 | G | GA | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(225): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.1423-208_1423-207i others(3): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127491007 | |||||||
| chr9:127491075 | G | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0236 a0001c0001t0001g0237 others(8): Show |
12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.1423-140G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127491075 | |||||||
| chr9:127491392 | A | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1503+97A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 20/25 | chr9 | 127491392 | |||||||
| chr9:127491511 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(55): Show |
60 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1503+216C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 20/25 | chr9 | 127491511 | |||||||
| chr9:127491652 | A | G | 97 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(94): Show |
101 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1503+357A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 20/25 | chr9 | 127491652 | |||||||
| chr9:127492108 | G | A | 16 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0079 others(13): Show |
16 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1504-694G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 20/25 | chr9 | 127492108 | |||||||
| chr9:127492264 | G | T | 2 | a0001c0003t0001g0229 a0009c0011t0001g0228 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1504-538G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 20/25 | chr9 | 127492264 | |||||||
| chr9:127492401 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(55): Show |
60 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1504-401G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 20/25 | chr9 | 127492401 | |||||||
| chr9:127493190 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1599+293T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127493190 | |||||||
| chr9:127493227 | A | G | 54 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0001g0051 others(51): Show |
55 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.1599+330A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127493227 | |||||||
| chr9:127493289 | C | T | 86 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(83): Show |
89 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.1599+392C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127493289 | |||||||
| chr9:127493439 | G | A | 1 | a0001c0001t0001g0302 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1599+542G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127493439 | |||||||
| chr9:127493477 | G | A | 1 | a0001c0001t0001g0315 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1599+580G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127493477 | |||||||
| chr9:127493527 | C | T | 11 | a0001c0001t0001g0008 a0001c0001t0001g0236 a0001c0001t0001g0237 others(8): Show |
12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.1599+630C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127493527 | |||||||
| chr9:127493531 | C | G | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(225): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.1599+634C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127493531 | |||||||
| chr9:127493543 | T | C | 1 | a0005c0010t0001g0112 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1599+646T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127493543 | |||||||
| chr9:127493948 | G | A | 10 | a0001c0001t0001g0020 a0001c0003t0001g0004 a0001c0003t0001g0132 others(7): Show |
11 | HG00140.hp2 HG00741.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.1599+1051G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127493948 | |||||||
| chr9:127494032 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1599+1135C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127494032 | |||||||
| chr9:127494109 | T | C | 1 | a0001c0003t0001g0186 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1600-1211T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127494109 | |||||||
| chr9:127494219 | G | A | 2 | a0001c0003t0001g0229 a0009c0011t0001g0228 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1600-1101G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127494219 | |||||||
| chr9:127494527 | C | T | 11 | a0001c0001t0001g0008 a0001c0001t0001g0236 a0001c0001t0001g0237 others(8): Show |
12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.1600-793C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127494527 | |||||||
| chr9:127494746 | C | G | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(123): Show |
129 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1600-574C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127494746 | |||||||
| chr9:127494837 | C | T | 1 | a0001c0003t0001g0101 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1600-483C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127494837 | |||||||
| chr9:127494912 | G | A | 95 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(92): Show |
99 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1600-408G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127494912 | |||||||
| chr9:127494926 | G | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(181): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.1600-394G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127494926 | |||||||
| chr9:127494950 | T | G | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1600-370T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127494950 | |||||||
| chr9:127494981 | C | T | 1 | a0002c0002t0001g0223 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1600-339C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127494981 | |||||||
| chr9:127495123 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1600-197G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127495123 | |||||||
| chr9:127495153 | A | G | 1 | a0002c0005t0001g0272 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1600-167A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127495153 | |||||||
| chr9:127495168 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0003c0004t0001g0073 |
3 | HG03041.hp1 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1600-152G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127495168 | |||||||
| chr9:127495180 | C | T | 1 | a0003c0004t0001g0073 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1600-140C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127495180 | |||||||
| chr9:127495208 | C | A | 1 | a0002c0005t0001g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1600-112C>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127495208 | |||||||
| chr9:127495211 | C | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1600-109C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127495211 | |||||||
| chr9:127495214 | A | G | 1 | a0001c0003t0001g0140 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1600-106A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127495214 | |||||||
| chr9:127495288 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1600-32G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127495288 | |||||||
| chr9:127495657 | A | G | 11 | a0001c0001t0001g0008 a0001c0001t0001g0236 a0001c0001t0001g0237 others(8): Show |
12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.1698+239A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 22/25 | chr9 | 127495657 | |||||||
| chr9:127495673 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1698+255C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 22/25 | chr9 | 127495673 | |||||||
| chr9:127495796 | G | A | 3 | a0001c0001t0002g0085 a0003c0004t0002g0083 a0003c0004t0002g0084 |
3 | HG02055.hp2 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1699-168G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 22/25 | chr9 | 127495796 | |||||||
| chr9:127495881 | A | T | 97 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(94): Show |
101 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1699-83A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 22/25 | chr9 | 127495881 | |||||||
| chr9:127496101 | C | T | 6 | a0002c0002t0001g0108 a0002c0002t0001g0109 a0002c0002t0001g0114 others(3): Show |
6 | HG00280.hp1 HG01258.hp2 HG01358.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1830+6C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 23/25 | chr9 | 127496101 | |||||||
| chr9:127496131 | C | T | 11 | a0001c0001t0001g0008 a0001c0001t0001g0236 a0001c0001t0001g0237 others(8): Show |
12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.1830+36C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 23/25 | chr9 | 127496131 | |||||||
| chr9:127496515 | C | T | 12 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(9): Show |
12 | HG02486.hp2 HG02717.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1830+420C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 23/25 | chr9 | 127496515 | |||||||
| chr9:127496552 | G | A | 2 | a0002c0002t0001g0106 a0002c0002t0005g0104 |
2 | HG01192.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1830+457G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 23/25 | chr9 | 127496552 | |||||||
| chr9:127496631 | A | C | 1 | a0001c0001t0001g0027 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1830+536A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 23/25 | chr9 | 127496631 | |||||||
| chr9:127496726 | G | A | 1 | a0002c0005t0002g0086 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1831-527G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 23/25 | chr9 | 127496726 | |||||||
| chr9:127496732 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1831-521G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 23/25 | chr9 | 127496732 | |||||||
| chr9:127496818 | A | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(72): Show |
77 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.1831-435A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 23/25 | chr9 | 127496818 | |||||||
| chr9:127496837 | C | T | 1 | a0001c0003t0001g0163 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1831-416C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 23/25 | chr9 | 127496837 | |||||||
| chr9:127496869 | T | C | 3 | a0001c0007t0001g0326 a0001c0007t0001g0327 a0001c0007t0001g0329 |
3 | HG01109.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1831-384T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 23/25 | chr9 | 127496869 | |||||||
| chr9:127497031 | T | C | 11 | a0001c0001t0001g0008 a0001c0001t0001g0236 a0001c0001t0001g0237 others(8): Show |
12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.1831-222T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 23/25 | chr9 | 127497031 | |||||||
| chr9:127497187 | C | T | 3 | a0001c0007t0001g0326 a0001c0007t0001g0327 a0001c0007t0001g0329 |
3 | HG01109.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1831-66C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 23/25 | chr9 | 127497187 | |||||||
| chr9:127497195 | A | G | 4 | a0003c0004t0001g0077 a0003c0004t0001g0087 a0003c0004t0001g0088 others(1): Show |
4 | HG02451.hp2 HG02630.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1831-58A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 23/25 | chr9 | 127497195 | |||||||
| chr9:127497206 | C | T | 2 | a0001c0003t0001g0229 a0009c0011t0001g0228 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1831-47C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 23/25 | chr9 | 127497206 | |||||||
| chr9:127497339 | A | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(225): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
splice_region_variant&intron_variant | LOW | c.1912+5A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127497339 | |||||||
| chr9:127497369 | C | T | 1 | a0002c0002t0001g0195 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1912+35C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127497369 | |||||||
| chr9:127497377 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(55): Show |
60 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1912+43G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127497377 | |||||||
| chr9:127497479 | A | G | 1 | a0003c0004t0002g0083 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1912+145A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127497479 | |||||||
| chr9:127497551 | C | A | 10 | a0001c0001t0001g0020 a0001c0003t0001g0004 a0001c0003t0001g0132 others(7): Show |
11 | HG00140.hp2 HG00741.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.1912+217C>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127497551 | |||||||
| chr9:127497681 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0256 |
2 | HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1912+347C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127497681 | |||||||
| chr9:127498185 | C | T | 3 | a0001c0007t0001g0326 a0001c0007t0001g0327 a0001c0007t0001g0329 |
3 | HG01109.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1912+851C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127498185 | |||||||
| chr9:127498381 | A | C | 11 | a0001c0001t0001g0008 a0001c0001t0001g0236 a0001c0001t0001g0237 others(8): Show |
12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.1912+1047A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127498381 | |||||||
| chr9:127498492 | C | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1912+1158C>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127498492 | |||||||
| chr9:127498509 | C | T | 94 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(91): Show |
98 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1912+1175C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127498509 | |||||||
| chr9:127498536 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1912+1202C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127498536 | |||||||
| chr9:127498611 | G | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0236 a0001c0001t0001g0237 others(8): Show |
12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.1912+1277G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127498611 | |||||||
| chr9:127498638 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1912+1304G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127498638 | |||||||
| chr9:127498650 | T | C | 10 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(7): Show |
10 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1912+1316T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127498650 | |||||||
| chr9:127498806 | C | T | 71 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(68): Show |
74 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1912+1472C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127498806 | |||||||
| chr9:127498834 | G | A | 10 | a0001c0001t0001g0020 a0001c0003t0001g0004 a0001c0003t0001g0132 others(7): Show |
11 | HG00140.hp2 HG00741.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.1912+1500G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127498834 | |||||||
| chr9:127498849 | A | G | 1 | a0001c0001t0001g0317 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1912+1515A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127498849 | |||||||
| chr9:127498931 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1912+1597C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127498931 | |||||||
| chr9:127499055 | C | CA | 11 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(8): Show |
11 | HG02717.hp2 HG02723.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1912+1733dupA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127499055 | ||||||
| chr9:127499055 | C | CAA | 62 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0074 others(59): Show |
64 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1912+1732_1912+173 others(6): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127499055 | ||||||
| chr9:127499055 | C | CAAA | 9 | a0001c0001t0001g0011 a0001c0001t0001g0264 a0001c0001t0001g0303 others(6): Show |
10 | HG01099.hp2 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1912+1731_1912+173 others(7): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127499055 | ||||||
| chr9:127499099 | T | C | 1 | a0002c0005t0001g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1912+1765T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499099 | |||||||
| chr9:127499141 | C | T | 2 | a0001c0003t0001g0229 a0009c0011t0001g0228 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1912+1807C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499141 | |||||||
| chr9:127499270 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1913-1740G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499270 | |||||||
| chr9:127499283 | A | G | 2 | a0002c0002t0001g0134 a0002c0002t0001g0230 |
2 | NA18991.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1913-1727A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499283 | |||||||
| chr9:127499524 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(55): Show |
60 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1913-1486C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499524 | |||||||
| chr9:127499529 | T | TAA | 10 | a0001c0001t0001g0008 a0001c0001t0001g0236 a0001c0001t0001g0237 others(7): Show |
11 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(8): Show |
intron_variant | MODIFIER | c.1913-1473_1913-147 others(6): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127499529 | ||||||
| chr9:127499529 | TA | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(50): Show |
55 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.1913-1472delA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127499529 | ||||||
| chr9:127499537 | A | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0003t0001g0143 |
3 | HG03041.hp1 HG03471.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1913-1473A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499537 | |||||||
| chr9:127499538 | AT | A | 106 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(103): Show |
110 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.1913-1471delT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499538 | |||||||
| chr9:127499539 | T | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0236 a0001c0001t0001g0237 others(19): Show |
23 | HG01109.hp1 HG01433.hp2 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.1913-1471T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499539 | |||||||
| chr9:127499541 | T | A | 91 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(88): Show |
96 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.1913-1469T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499541 | |||||||
| chr9:127499543 | T | A | 3 | a0001c0007t0001g0326 a0001c0007t0001g0327 a0001c0007t0001g0329 |
3 | HG01109.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1913-1467T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499543 | |||||||
| chr9:127499556 | A | G | 1 | a0002c0005t0001g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1913-1454A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499556 | |||||||
| chr9:127499569 | C | T | 11 | a0001c0001t0001g0008 a0001c0001t0001g0236 a0001c0001t0001g0237 others(8): Show |
12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.1913-1441C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499569 | |||||||
| chr9:127499652 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1913-1358C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499652 | |||||||
| chr9:127499797 | A | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(177): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1913-1213A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499797 | |||||||
| chr9:127499810 | C | T | 1 | a0001c0003t0001g0186 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1913-1200C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499810 | |||||||
| chr9:127499873 | C | T | 1 | a0001c0001t0001g0283 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1913-1137C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499873 | |||||||
| chr9:127499925 | A | G | 2 | a0001c0001t0001g0253 a0001c0001t0001g0255 |
2 | HG02818.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1913-1085A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499925 | |||||||
| chr9:127499933 | A | G | 3 | a0001c0003t0001g0219 a0003c0004t0001g0078 a0003c0004t0001g0082 |
3 | HG01884.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1913-1077A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499933 | |||||||
| chr9:127500140 | C | G | 1 | a0002c0002t0001g0090 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1913-870C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127500140 | |||||||
| chr9:127500150 | CA | C | 96 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(93): Show |
100 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1913-856delA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127500150 | ||||||
| chr9:127500151 | A | G | 1 | a0002c0005t0001g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1913-859A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127500151 | |||||||
| chr9:127500155 | G | T | 96 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(93): Show |
100 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1913-855G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127500155 | |||||||
| chr9:127500310 | G | A | 2 | a0002c0002t0001g0122 a0002c0002t0001g0123 |
2 | HG03831.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1913-700G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127500310 | |||||||
| chr9:127500318 | G | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(180): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.1913-692G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127500318 | |||||||
| chr9:127500351 | A | ACT | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(177): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1913-658_1913-657d others(4): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127500351 | ||||||
| chr9:127500358 | C | CAAAAA | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(51): Show |
56 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.1913-639_1913-635d others(7): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127500358 | ||||||
| chr9:127500358 | C | CAAAAAAA others(3): Show |
3 | a0001c0001t0001g0080 a0001c0001t0001g0308 a0001c0001t0001g0309 |
3 | HG02145.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1913-644_1913-635d others(12): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127500358 | ||||||
| chr9:127500358 | C | CAAAAAAA others(4): Show |
23 | a0001c0001t0001g0074 a0001c0001t0001g0079 a0001c0001t0001g0081 others(20): Show |
23 | HG01168.hp2 HG02451.hp2 HG02630.hp1 others(20): Show |
intron_variant | MODIFIER | c.1913-645_1913-635d others(13): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127500358 | ||||||
| chr9:127500358 | C | CAAAAAAA others(5): Show |
58 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(55): Show |
61 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.1913-646_1913-635d others(14): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127500358 | ||||||
| chr9:127500358 | C | CAAAAAAA others(6): Show |
10 | a0001c0001t0001g0259 a0001c0001t0001g0265 a0001c0001t0001g0274 others(7): Show |
10 | HG01071.hp2 HG01256.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.1913-647_1913-635d others(15): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127500358 | ||||||
| chr9:127500358 | C | CAAAAAAA others(7): Show |
7 | a0001c0001t0001g0300 a0001c0003t0001g0004 a0001c0003t0001g0132 others(4): Show |
8 | HG00140.hp2 HG01070.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.1913-648_1913-635d others(16): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127500358 | ||||||
| chr9:127500358 | C | CAAAAAAA others(8): Show |
2 | a0001c0003t0001g0153 a0001c0003t0001g0207 |
2 | HG00741.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.1913-649_1913-635d others(17): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127500358 | ||||||
| chr9:127500358 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1913-650_1913-635d others(18): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127500358 | ||||||
| chr9:127500358 | CA | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0007t0001g0326 others(5): Show |
8 | HG01109.hp1 HG02723.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1913-635delA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127500358 | ||||||
| chr9:127500374 | A | AAAAAAAA others(4): Show |
3 | a0001c0001t0001g0236 a0001c0001t0001g0244 a0001c0001t0001g0245 |
3 | NA18959.hp2 NA18991.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1913-635_1913-634i others(13): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127500374 | ||||||
| chr9:127500374 | A | AAAAAAAA others(3): Show |
7 | a0001c0001t0001g0008 a0001c0001t0001g0237 a0001c0001t0001g0238 others(4): Show |
8 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.1913-635_1913-634i others(12): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127500374 | ||||||
| chr9:127500543 | A | T | 1 | a0001c0001t0001g0237 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1913-467A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127500543 | |||||||
| chr9:127500761 | C | T | 12 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(9): Show |
12 | HG02486.hp2 HG02717.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1913-249C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127500761 | |||||||
| chr9:127500821 | G | A | 12 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(9): Show |
12 | HG02486.hp2 HG02717.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1913-189G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127500821 | |||||||
| chr9:127501175 | C | T | 11 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(8): Show |
11 | HG02486.hp2 HG02717.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.2046+32C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127501175 | |||||||
| chr9:127501227 | G | A | 1 | a0001c0003t0001g0208 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2046+84G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127501227 | |||||||
| chr9:127501548 | A | G | 1 | a0001c0003t0001g0140 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2046+405A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127501548 | |||||||
| chr9:127501623 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2046+480T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127501623 | |||||||
| chr9:127501678 | G | T | 1 | a0001c0001t0001g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2046+535G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127501678 | |||||||
| chr9:127501682 | A | G | 1 | a0001c0001t0001g0270 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2046+539A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127501682 | |||||||
| chr9:127501774 | A | T | 1 | a0001c0001t0001g0328 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2046+631A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127501774 | |||||||
| chr9:127501881 | G | A | 2 | a0001c0003t0001g0229 a0009c0011t0001g0228 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2046+738G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127501881 | |||||||
| chr9:127501888 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2046+745G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127501888 | |||||||
| chr9:127502053 | C | T | 2 | a0001c0003t0001g0229 a0009c0011t0001g0228 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2047-721C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127502053 | |||||||
| chr9:127502061 | G | A | 12 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(9): Show |
12 | HG02486.hp2 HG02717.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.2047-713G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127502061 | |||||||
| chr9:127502151 | G | A | 3 | a0001c0001t0001g0259 a0001c0001t0001g0271 a0002c0002t0001g0184 |
3 | HG01168.hp2 HG01517.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.2047-623G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127502151 | |||||||
| chr9:127502207 | T | C | 1 | a0002c0002t0001g0184 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2047-567T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127502207 | |||||||
| chr9:127502466 | C | T | 1 | a0002c0005t0001g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2047-308C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127502466 | |||||||
| chr9:127502686 | C | CA | 24 | a0001c0003t0001g0091 a0001c0003t0001g0146 a0001c0003t0001g0168 others(21): Show |
24 | HG00140.hp1 HG00741.hp1 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.2047-64dupA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr9 | 127502686 | ||||||
| chr9:127502686 | CA | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(154): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.2047-64delA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr9 | 127502686 | ||||||
| chr9:127502735 | C | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(50): Show |
55 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.2047-39C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127502735 | |||||||
| chr9:127502751 | A | C | 1 | a0001c0001t0001g0254 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2047-23A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127502751 |