Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 167691 |
| ensemblid | ENSG00000135338.14 |
| hgncid | 31923 |
| symbol | LCA5 |
| name | lebercilin LCA5 |
| refseq_nuc | NM_001122769.3 |
| refseq_prot | NP_001116241.1 |
| ensembl_nuc | ENST00000369846.9 |
| ensembl_prot | ENSP00000358861.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 79484991 |
| end | 79537430 |
| strand | - |
| ver | v1.2 |
| region | chr6:79484991-79537430 |
| region5000 | chr6:79479991-79542430 |
| regionname0 | LCA5_chr6_79484991_79537430 |
| regionname5000 | LCA5_chr6_79479991_79542430 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 697 | 202 | 34 | 34 | 97 | 7 | 29 | 80 | LCA5_chr6_79479991_79542430 | LCA5 | MGERA others(692): Show |
chr6 | 79479991 | 79542430 |
| a0002 | 0/0 | 697 | 73 | 11 | 12 | 43 | 1 | 6 | 36 | LCA5_chr6_79479991_79542430 | LCA5 | MGERA others(692): Show |
chr6 | 79479991 | 79542430 |
| a0003 | 0/0 | 697 | 69 | 29 | 8 | 28 | 2 | 2 | 27 | LCA5_chr6_79479991_79542430 | LCA5 | MGERA others(692): Show |
chr6 | 79479991 | 79542430 |
| a0004 | 1/0 | 697 | 33 | 7 | 12 | 5 | 4 | 4 | 2 | LCA5_chr6_79479991_79542430 | LCA5 | MGERA others(692): Show |
chr6 | 79479991 | 79542430 |
| a0005 | 0/0 | 697 | 11 | 11 | 0 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | MGERA others(692): Show |
chr6 | 79479991 | 79542430 |
| a0006 | 0/0 | 697 | 5 | 0 | 0 | 4 | 0 | 1 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | MGERA others(692): Show |
chr6 | 79479991 | 79542430 |
| a0007 | 0/0 | 697 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | MGERA others(692): Show |
chr6 | 79479991 | 79542430 |
| a0008 | 0/0 | 697 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | MGERA others(692): Show |
chr6 | 79479991 | 79542430 |
| a0009 | 0/0 | 697 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | MGERA others(692): Show |
chr6 | 79479991 | 79542430 |
| a0010 | 0/0 | 697 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | MGERA others(692): Show |
chr6 | 79479991 | 79542430 |
| a0011 | 0/0 | 697 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | MGERA others(692): Show |
chr6 | 79479991 | 79542430 |
| a0012 | 0/0 | 314 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | MGERA others(309): Show |
chr6 | 79479991 | 79542430 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2091 | 201 | 34 | 34 | 96 | 7 | 29 | LCA5_chr6_79479991_79542430 | LCA5 | ATGGG others(2086): Show |
chr6 | 79479991 | 79542430 | ||
| a0001c0009 | 0/0 | 2091 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | ATGGG others(2086): Show |
chr6 | 79479991 | 79542430 | ||
| a0002c0002 | 0/0 | 2091 | 72 | 11 | 12 | 43 | 1 | 5 | LCA5_chr6_79479991_79542430 | LCA5 | ATGGG others(2086): Show |
chr6 | 79479991 | 79542430 | ||
| a0002c0013 | 0/0 | 2091 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | ATGGG others(2086): Show |
chr6 | 79479991 | 79542430 | ||
| a0003c0003 | 0/0 | 2091 | 67 | 27 | 8 | 28 | 2 | 2 | LCA5_chr6_79479991_79542430 | LCA5 | ATGGG others(2086): Show |
chr6 | 79479991 | 79542430 | ||
| a0003c0008 | 0/0 | 2091 | 2 | 2 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | ATGGG others(2086): Show |
chr6 | 79479991 | 79542430 | ||
| a0004c0004 | 1/0 | 2091 | 32 | 6 | 12 | 5 | 4 | 4 | LCA5_chr6_79479991_79542430 | LCA5 | ATGGG others(2086): Show |
chr6 | 79479991 | 79542430 | ||
| a0004c0015 | 0/0 | 2091 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | ATGGG others(2086): Show |
chr6 | 79479991 | 79542430 | ||
| a0005c0005 | 0/0 | 2091 | 11 | 11 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | ATGGG others(2086): Show |
chr6 | 79479991 | 79542430 | ||
| a0006c0006 | 0/0 | 2091 | 5 | 0 | 0 | 4 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | ATGGG others(2086): Show |
chr6 | 79479991 | 79542430 | ||
| a0007c0007 | 0/0 | 2091 | 2 | 2 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | ATGGG others(2086): Show |
chr6 | 79479991 | 79542430 | ||
| a0008c0014 | 0/0 | 2091 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | ATGGG others(2086): Show |
chr6 | 79479991 | 79542430 | ||
| a0009c0011 | 0/0 | 2091 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | ATGGG others(2086): Show |
chr6 | 79479991 | 79542430 | ||
| a0010c0016 | 0/0 | 2091 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | ATGGG others(2086): Show |
chr6 | 79479991 | 79542430 | ||
| a0011c0010 | 0/0 | 2091 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | ATGGG others(2086): Show |
chr6 | 79479991 | 79542430 | ||
| a0012c0012 | 0/0 | 2091 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | ATGGG others(2086): Show |
chr6 | 79479991 | 79542430 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4564 | 87 | 3 | 18 | 58 | 1 | 7 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0001c0001t0002 | 0/1 | 4564 | 102 | 25 | 15 | 33 | 6 | 22 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0001c0001t0007 | 0/0 | 4564 | 6 | 6 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0001c0001t0010 | 0/0 | 4564 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0001c0001t0013 | 0/0 | 4564 | 2 | 0 | 0 | 2 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0001c0001t0014 | 0/0 | 4564 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0001c0001t0016 | 0/0 | 4564 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0001c0001t0017 | 0/0 | 4564 | 1 | 0 | 1 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0001c0009t0001 | 0/0 | 4564 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0002c0002t0001 | 0/0 | 4564 | 61 | 1 | 11 | 43 | 1 | 5 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0002c0002t0006 | 0/0 | 4564 | 10 | 9 | 1 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0002c0002t0015 | 0/0 | 4564 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0002c0013t0001 | 0/0 | 4564 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0003c0003t0001 | 0/0 | 4564 | 11 | 11 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0003c0003t0004 | 0/0 | 4564 | 28 | 9 | 5 | 11 | 2 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0003c0003t0005 | 0/0 | 4564 | 21 | 0 | 3 | 17 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0003c0003t0009 | 0/0 | 4563 | 3 | 3 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4558): Show |
chr6 | 79479991 | 79542430 |
| a0003c0003t0011 | 0/0 | 4564 | 2 | 2 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0003c0003t0012 | 0/0 | 4564 | 2 | 2 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0003c0008t0001 | 0/0 | 4564 | 2 | 2 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0004c0004t0003 | 1/0 | 4564 | 27 | 6 | 7 | 5 | 4 | 4 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0004c0004t0008 | 0/0 | 4564 | 5 | 0 | 5 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0004c0015t0003 | 0/0 | 4564 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0005c0005t0001 | 0/0 | 4564 | 11 | 11 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0006c0006t0001 | 0/0 | 4564 | 5 | 0 | 0 | 4 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0007c0007t0007 | 0/0 | 4564 | 2 | 2 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0008c0014t0010 | 0/0 | 4564 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0009c0011t0001 | 0/0 | 4564 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0010c0016t0003 | 0/0 | 4564 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0011c0010t0002 | 0/0 | 4564 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| a0012c0012t0001 | 0/0 | 4564 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | AGTCT others(4559): Show |
chr6 | 79479991 | 79542430 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 34 | 1 | 10 | 19 | 1 | 3 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0002 | 0/0 | 15 | 0 | 0 | 14 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0007 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0017 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0028 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0031 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0127 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0007g0009 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0010g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0013g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0013g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0014g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0016g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0001t0017g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0001c0009t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0003 | 0/0 | 14 | 0 | 0 | 13 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0008 | 0/0 | 6 | 1 | 3 | 0 | 1 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0006g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0006g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0006g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0002t0015g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0002c0013t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0004g0006 | 0/0 | 9 | 2 | 1 | 6 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0004g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0004g0030 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0004g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0004g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0004g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0005g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0005g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0005g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0005g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0005g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0005g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0005g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0005g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0005g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0005g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0005g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0005g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0009g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0009g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0009g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0011g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0011g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0012g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0003t0012g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0008t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0003c0008t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0004c0004t0003g0004 | 1/0 | 10 | 2 | 6 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0004c0004t0003g0026 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0004c0004t0003g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0004c0004t0003g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0004c0004t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0004c0004t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0004c0004t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0004c0004t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0004c0004t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0004c0004t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0004c0004t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0004c0004t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0004c0004t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0004c0004t0008g0025 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0004c0004t0008g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0004c0004t0008g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0004c0015t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0005c0005t0001g0005 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0005c0005t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0005c0005t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0006c0006t0001g0014 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0006c0006t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0007c0007t0007g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0007c0007t0007g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0008c0014t0010g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0009c0011t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0010c0016t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0011c0010t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| a0012c0012t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0004 | c0004 | t0003 | g0026 | EUR | GBR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG00140 | hp2 | a0003 | c0003 | t0004 | g0030 | EUR | GBR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG00280 | hp1 | a0004 | c0004 | t0003 | g0026 | EUR | FIN | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0008 | EUR | FIN | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0144 | EUR | FIN | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | CHS | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG00438 | hp2 | a0001 | c0001 | t0016 | g0076 | EAS | CHS | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | CHS | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG00642 | hp1 | a0003 | c0003 | t0004 | g0030 | AMR | PUR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG00733 | hp1 | a0003 | c0003 | t0004 | g0197 | AMR | PUR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG00733 | hp2 | a0004 | c0004 | t0003 | g0004 | AMR | PUR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0022 | AMR | PUR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0105 | AMR | PUR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0106 | AMR | PUR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01071 | hp2 | a0004 | c0004 | t0003 | g0004 | AMR | PUR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01074 | hp2 | a0003 | c0003 | t0004 | g0006 | AMR | PUR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | PUR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01099 | hp1 | a0003 | c0003 | t0005 | g0209 | AMR | PUR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01106 | hp2 | a0003 | c0003 | t0004 | g0198 | AMR | PUR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01167 | hp1 | a0004 | c0004 | t0008 | g0146 | AMR | PUR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01169 | hp2 | a0004 | c0004 | t0003 | g0004 | AMR | PUR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01175 | hp2 | a0004 | c0004 | t0003 | g0004 | AMR | PUR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01192 | hp1 | a0004 | c0004 | t0008 | g0025 | AMR | PUR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0111 | AMR | CLM | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01256 | hp1 | a0004 | c0004 | t0008 | g0025 | AMR | CLM | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01256 | hp2 | a0003 | c0003 | t0005 | g0053 | AMR | CLM | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01257 | hp1 | a0001 | c0001 | t0017 | g0084 | AMR | CLM | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | CLM | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | CLM | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01258 | hp2 | a0004 | c0004 | t0008 | g0025 | AMR | CLM | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | CLM | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01346 | hp2 | a0002 | c0002 | t0006 | g0102 | AMR | CLM | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01358 | hp1 | a0003 | c0003 | t0005 | g0213 | AMR | CLM | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01358 | hp2 | a0004 | c0004 | t0008 | g0155 | AMR | CLM | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | CLM | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01496 | hp1 | a0004 | c0004 | t0003 | g0004 | AMR | CLM | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01515 | hp1 | a0004 | c0004 | t0003 | g0038 | EUR | IBS | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0040 | EUR | IBS | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0171 | EUR | IBS | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0140 | EUR | IBS | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01517 | hp1 | a0004 | c0004 | t0003 | g0038 | EUR | IBS | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0017 | EUR | IBS | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01884 | hp1 | a0005 | c0005 | t0001 | g0005 | AFR | ACB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0009 | AFR | ACB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01891 | hp1 | a0002 | c0002 | t0006 | g0021 | AFR | ACB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01891 | hp2 | a0003 | c0003 | t0001 | g0219 | AFR | ACB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01934 | hp1 | a0004 | c0004 | t0003 | g0004 | AMR | PEL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0109 | AMR | PEL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01943 | hp1 | a0004 | c0004 | t0003 | g0147 | AMR | PEL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0022 | AMR | PEL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PEL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0101 | AMR | PEL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PEL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0022 | AMR | PEL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PEL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02015 | hp2 | a0004 | c0004 | t0003 | g0027 | EAS | KHV | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02027 | hp2 | a0004 | c0004 | t0003 | g0152 | EAS | KHV | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | ACB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02055 | hp2 | a0003 | c0003 | t0009 | g0222 | AFR | ACB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02056 | hp1 | a0006 | c0006 | t0001 | g0014 | EAS | KHV | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0119 | EAS | KHV | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0110 | EAS | KHV | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02132 | hp2 | a0006 | c0006 | t0001 | g0077 | EAS | KHV | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02135 | hp1 | a0003 | c0003 | t0005 | g0010 | EAS | KHV | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02135 | hp2 | a0006 | c0006 | t0001 | g0014 | EAS | KHV | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | ACB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PEL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CDX | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02165 | hp1 | a0006 | c0006 | t0001 | g0014 | EAS | CDX | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | CDX | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02257 | hp1 | a0003 | c0008 | t0001 | g0143 | AFR | ACB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02258 | hp1 | a0002 | c0002 | t0006 | g0015 | AFR | ACB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | ACB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02280 | hp1 | a0005 | c0005 | t0001 | g0005 | AFR | ACB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02280 | hp2 | a0003 | c0003 | t0009 | g0223 | AFR | ACB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | ACB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02451 | hp2 | a0002 | c0002 | t0015 | g0050 | AFR | ACB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | KHV | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02572 | hp1 | a0003 | c0003 | t0001 | g0097 | AFR | GWD | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02572 | hp2 | a0003 | c0003 | t0004 | g0187 | AFR | GWD | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | PJL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0037 | SAS | PJL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02615 | hp1 | a0004 | c0015 | t0003 | g0154 | AFR | GWD | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0009 | AFR | GWD | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0009 | AFR | GWD | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02622 | hp2 | a0003 | c0003 | t0011 | g0099 | AFR | GWD | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02630 | hp1 | a0007 | c0007 | t0007 | g0204 | AFR | GWD | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02630 | hp2 | a0003 | c0003 | t0012 | g0095 | AFR | GWD | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02683 | hp1 | a0004 | c0004 | t0003 | g0004 | SAS | PJL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0008 | SAS | PJL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0145 | SAS | PJL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02723 | hp1 | a0003 | c0003 | t0012 | g0096 | AFR | GWD | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | GWD | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02735 | hp1 | a0003 | c0003 | t0004 | g0030 | SAS | PJL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0037 | SAS | PJL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02809 | hp1 | a0003 | c0003 | t0009 | g0221 | AFR | GWD | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | GWD | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02818 | hp1 | a0003 | c0003 | t0004 | g0185 | AFR | GWD | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02818 | hp2 | a0003 | c0008 | t0001 | g0142 | AFR | GWD | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02886 | hp1 | a0003 | c0003 | t0001 | g0218 | AFR | GWD | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | GWD | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02895 | hp1 | a0005 | c0005 | t0001 | g0091 | AFR | GWD | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02895 | hp2 | a0002 | c0002 | t0006 | g0104 | AFR | GWD | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02896 | hp1 | a0003 | c0003 | t0001 | g0044 | AFR | GWD | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02897 | hp1 | a0003 | c0003 | t0001 | g0044 | AFR | GWD | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02897 | hp2 | a0005 | c0005 | t0001 | g0090 | AFR | GWD | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | ESN | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0009 | AFR | ESN | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02965 | hp1 | a0005 | c0005 | t0001 | g0005 | AFR | ESN | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | ESN | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02970 | hp1 | a0003 | c0003 | t0004 | g0180 | AFR | ESN | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0009 | AFR | ESN | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02976 | hp1 | a0003 | c0003 | t0004 | g0188 | AFR | ESN | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02976 | hp2 | a0005 | c0005 | t0001 | g0005 | AFR | ESN | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0100 | SAS | PJL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | GWD | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03041 | hp2 | a0004 | c0004 | t0003 | g0004 | AFR | GWD | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03098 | hp1 | a0002 | c0002 | t0006 | g0015 | AFR | MSL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | MSL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03130 | hp1 | a0002 | c0002 | t0006 | g0021 | AFR | ESN | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03130 | hp2 | a0007 | c0007 | t0007 | g0205 | AFR | ESN | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03139 | hp1 | a0003 | c0003 | t0001 | g0045 | AFR | ESN | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03139 | hp2 | a0002 | c0002 | t0006 | g0021 | AFR | ESN | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | ESN | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03195 | hp2 | a0003 | c0003 | t0001 | g0220 | AFR | ESN | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03209 | hp1 | a0003 | c0003 | t0001 | g0045 | AFR | MSL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03209 | hp2 | a0008 | c0014 | t0010 | g0153 | AFR | MSL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03225 | hp1 | a0004 | c0004 | t0003 | g0216 | AFR | MSL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | MSL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | MSL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0009 | AFR | MSL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | MSL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03486 | hp2 | a0003 | c0003 | t0004 | g0183 | AFR | MSL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03491 | hp2 | a0003 | c0003 | t0005 | g0211 | SAS | PJL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | PJL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03516 | hp1 | a0004 | c0004 | t0003 | g0004 | AFR | ESN | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03516 | hp2 | a0003 | c0003 | t0004 | g0184 | AFR | ESN | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03540 | hp2 | a0003 | c0003 | t0004 | g0006 | AFR | GWD | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | MSL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03579 | hp2 | a0003 | c0003 | t0001 | g0201 | AFR | MSL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0168 | SAS | PJL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | STU | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0167 | SAS | STU | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | PJL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | PJL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0132 | SAS | BEB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0165 | SAS | BEB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03834 | hp1 | a0002 | c0013 | t0001 | g0117 | SAS | BEB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03927 | hp1 | a0009 | c0011 | t0001 | g0083 | SAS | BEB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | BEB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03942 | hp1 | a0004 | c0004 | t0003 | g0215 | SAS | BEB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0162 | SAS | BEB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG04115 | hp1 | a0004 | c0004 | t0003 | g0151 | SAS | STU | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0159 | SAS | STU | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | STU | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0170 | SAS | STU | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG04204 | hp1 | a0010 | c0016 | t0003 | g0150 | SAS | STU | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG04204 | hp2 | a0006 | c0006 | t0001 | g0014 | SAS | STU | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | STU | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG04228 | hp2 | a0004 | c0004 | t0003 | g0149 | SAS | STU | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18522 | hp1 | a0005 | c0005 | t0001 | g0005 | AFR | YRI | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | YRI | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | CHB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18747 | hp1 | a0004 | c0004 | t0003 | g0027 | EAS | CHB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18906 | hp1 | a0005 | c0005 | t0001 | g0005 | AFR | YRI | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | YRI | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18945 | hp1 | a0003 | c0003 | t0005 | g0010 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18947 | hp1 | a0003 | c0003 | t0004 | g0029 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18951 | hp1 | a0003 | c0003 | t0005 | g0212 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18954 | hp1 | a0003 | c0003 | t0004 | g0029 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18957 | hp1 | a0003 | c0003 | t0004 | g0006 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18957 | hp2 | a0003 | c0003 | t0005 | g0010 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18964 | hp2 | a0003 | c0003 | t0004 | g0182 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18966 | hp2 | a0003 | c0003 | t0004 | g0006 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18967 | hp1 | a0012 | c0012 | t0001 | g0114 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18969 | hp2 | a0003 | c0003 | t0005 | g0046 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18971 | hp2 | a0003 | c0003 | t0005 | g0047 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18983 | hp1 | a0003 | c0003 | t0005 | g0010 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18984 | hp1 | a0003 | c0003 | t0004 | g0006 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18984 | hp2 | a0001 | c0001 | t0013 | g0074 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18985 | hp1 | a0003 | c0003 | t0005 | g0048 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18986 | hp1 | a0003 | c0003 | t0005 | g0010 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18986 | hp2 | a0001 | c0001 | t0013 | g0075 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18987 | hp2 | a0003 | c0003 | t0004 | g0029 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18988 | hp2 | a0003 | c0003 | t0005 | g0046 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18993 | hp2 | a0003 | c0003 | t0005 | g0010 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18995 | hp1 | a0003 | c0003 | t0005 | g0048 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19005 | hp1 | a0003 | c0003 | t0005 | g0054 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19006 | hp2 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19010 | hp1 | a0004 | c0004 | t0003 | g0148 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | LWK | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19030 | hp2 | a0003 | c0003 | t0004 | g0006 | AFR | LWK | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | LWK | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19043 | hp2 | a0005 | c0005 | t0001 | g0005 | AFR | LWK | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19055 | hp2 | a0003 | c0003 | t0005 | g0208 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19057 | hp1 | a0003 | c0003 | t0004 | g0006 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19066 | hp2 | a0003 | c0003 | t0004 | g0006 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19068 | hp1 | a0003 | c0003 | t0005 | g0047 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19070 | hp2 | a0001 | c0001 | t0014 | g0049 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19072 | hp1 | a0003 | c0003 | t0005 | g0207 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19074 | hp1 | a0001 | c0001 | t0010 | g0061 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19074 | hp2 | a0003 | c0003 | t0005 | g0210 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19075 | hp2 | a0003 | c0003 | t0004 | g0006 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19077 | hp2 | a0001 | c0009 | t0001 | g0069 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19078 | hp2 | a0003 | c0003 | t0004 | g0186 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19080 | hp1 | a0004 | c0004 | t0003 | g0027 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA20129 | hp1 | a0003 | c0003 | t0004 | g0181 | AFR | ASW | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA20129 | hp2 | a0002 | c0002 | t0006 | g0103 | AFR | ASW | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0126 | EUR | TSI | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA20752 | hp2 | a0003 | c0003 | t0004 | g0200 | EUR | TSI | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0108 | SAS | GIH | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0043 | SAS | GIH | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG01123 | hp2 | a0003 | c0003 | t0004 | g0199 | AMR | CLM | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02109 | hp1 | a0005 | c0005 | t0001 | g0005 | AFR | ACB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02109 | hp2 | a0002 | c0002 | t0006 | g0015 | AFR | ACB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02486 | hp1 | a0005 | c0005 | t0001 | g0005 | AFR | ACB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02486 | hp2 | a0004 | c0004 | t0003 | g0026 | AFR | ACB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02559 | hp1 | a0004 | c0004 | t0003 | g0156 | AFR | ACB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG02559 | hp2 | a0003 | c0003 | t0011 | g0098 | AFR | ACB | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03471 | hp1 | a0003 | c0003 | t0001 | g0214 | AFR | MSL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG06807 | hp1 | a0011 | c0010 | t0002 | g0174 | AFR | USA | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | USA | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | USA | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA20300 | hp2 | a0002 | c0002 | t0006 | g0015 | AFR | USA | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA21309 | hp1 | a0004 | c0004 | t0003 | g0178 | AFR | LWK | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| NA21309 | hp2 | a0003 | c0003 | t0001 | g0217 | AFR | LWK | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0127 | REF | REF | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| homoSapiens | grch38p0 | a0004 | c0004 | t0003 | g0004 | REF | REF | LCA5_chr6_79479991_79542430 | LCA5 | chr6 | 79479991 | 79542430 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:79487131 | C | T | 5 | a0002 a0003 a0005 others(2): Show |
155 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(152): Show |
missense_variant | MODERATE | c.1967G>A | p.Gly656Asp | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 8/8 | 2424/4564 | 1967/2094 | 656/697 | chr6 | 79487131 | |||
| chr6:79487456 | G | A | 1 | a0006 | 5 | HG02056.hp1 HG02132.hp2 HG02135.hp2 others(2): Show |
missense_variant | MODERATE | c.1642C>T | p.Pro548Ser | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 8/8 | 2099/4564 | 1642/2094 | 548/697 | chr6 | 79487456 | |||
| chr6:79487519 | T | C | 1 | a0007 | 2 | HG02630.hp1 HG03130.hp2 |
missense_variant | MODERATE | c.1579A>G | p.Ile527Val | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 8/8 | 2036/4564 | 1579/2094 | 527/697 | chr6 | 79487519 | |||
| chr6:79491638 | T | C | 1 | a0011 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.1048A>G | p.Thr350Ala | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 6/8 | 1505/4564 | 1048/2094 | 350/697 | chr6 | 79491638 | |||
| chr6:79492559 | C | T | 1 | a0012 | 1 | NA18967.hp1 | missense_variant | MODERATE | c.947G>A | p.Arg316Lys | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 5/8 | 1404/4564 | 947/2094 | 316/697 | chr6 | 79492559 | |||
| chr6:79492560 | T | C | 1 | a0012 | 1 | NA18967.hp1 | missense_variant | MODERATE | c.946A>G | p.Arg316Gly | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 5/8 | 1403/4564 | 946/2094 | 316/697 | chr6 | 79492560 | |||
| chr6:79492562 | A | T | 1 | a0012 | 1 | NA18967.hp1 | stop_gained | HIGH | c.944T>A | p.Leu315* | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 5/8 | 1401/4564 | 944/2094 | 315/697 | chr6 | 79492562 | |||
| chr6:79513485 | C | A | 1 | a0010 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.447G>T | p.Lys149Asn | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/8 | 904/4564 | 447/2094 | 149/697 | chr6 | 79513485 | |||
| chr6:79513598 | T | C | 1 | a0009 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.334A>G | p.Ile112Val | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/8 | 791/4564 | 334/2094 | 112/697 | chr6 | 79513598 | |||
| chr6:79513735 | C | T | 1 | a0005 | 11 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(8): Show |
missense_variant | MODERATE | c.197G>A | p.Arg66Gln | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/8 | 654/4564 | 197/2094 | 66/697 | chr6 | 79513735 | |||
| chr6:79518818 | T | G | 2 | a0002 a0012 |
74 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(71): Show |
missense_variant | MODERATE | c.77A>C | p.Asp26Ala | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/8 | 534/4564 | 77/2094 | 26/697 | chr6 | 79518818 | |||
| chr6:79518824 | A | G | 9 | a0001 a0002 a0003 others(6): Show |
364 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(361): Show |
missense_variant | MODERATE | c.71T>C | p.Leu24Ser | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/8 | 528/4564 | 71/2094 | 24/697 | chr6 | 79518824 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:79487313 | A | T | 1 | a0002c0013 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.1785T>A | p.Ile595Ile | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 8/8 | 2242/4564 | 1785/2094 | 595/697 | chr6 | 79487313 | |||
| chr6:79487601 | T | C | 1 | a0001c0009 | 1 | NA19077.hp2 | synonymous_variant | LOW | c.1497A>G | p.Leu499Leu | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 8/8 | 1954/4564 | 1497/2094 | 499/697 | chr6 | 79487601 | |||
| chr6:79493730 | T | C | 1 | a0004c0015 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.741A>G | p.Glu247Glu | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 4/8 | 1198/4564 | 741/2094 | 247/697 | chr6 | 79493730 | |||
| chr6:79513346 | G | A | 1 | a0003c0008 | 2 | HG02257.hp1 HG02818.hp2 |
synonymous_variant | LOW | c.586C>T | p.Leu196Leu | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/8 | 1043/4564 | 586/2094 | 196/697 | chr6 | 79513346 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:79485393 | A | G | 1 | a0003c0003t0012 | 2 | HG02630.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1611T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 8/8 | 1611 | chr6 | 79485393 | ||||||
| chr6:79485431 | T | C | 1 | a0001c0001t0017 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1573A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 8/8 | 1573 | chr6 | 79485431 | ||||||
| chr6:79485476 | C | T | 1 | a0003c0003t0004 | 28 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1528G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 8/8 | 1528 | chr6 | 79485476 | ||||||
| chr6:79485509 | C | T | 2 | a0001c0001t0007 a0007c0007t0007 |
8 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1495G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 8/8 | 1495 | chr6 | 79485509 | ||||||
| chr6:79485558 | C | T | 1 | a0001c0001t0016 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1446G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 8/8 | 1446 | chr6 | 79485558 | ||||||
| chr6:79485561 | CT | C | 1 | a0003c0003t0009 | 3 | HG02055.hp2 HG02280.hp2 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1442delA | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 8/8 | 1442 | chr6 | 79485561 | ||||||
| chr6:79485704 | C | T | 1 | a0003c0003t0005 | 21 | HG01099.hp1 HG01256.hp2 HG01358.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1300G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 8/8 | 1300 | chr6 | 79485704 | ||||||
| chr6:79485712 | T | C | 1 | a0002c0002t0006 | 10 | HG01346.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1292A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 8/8 | 1292 | chr6 | 79485712 | ||||||
| chr6:79485960 | T | G | 1 | a0004c0004t0008 | 5 | HG01167.hp1 HG01192.hp1 HG01256.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1044A>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 8/8 | 1044 | chr6 | 79485960 | ||||||
| chr6:79486285 | T | C | 1 | a0001c0001t0013 | 2 | NA18984.hp2 NA18986.hp2 |
3_prime_UTR_variant | MODIFIER | c.*719A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 8/8 | 719 | chr6 | 79486285 | ||||||
| chr6:79486507 | C | T | 1 | a0003c0003t0011 | 2 | HG02559.hp2 HG02622.hp2 |
3_prime_UTR_variant | MODIFIER | c.*497G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 8/8 | 497 | chr6 | 79486507 | ||||||
| chr6:79486781 | T | C | 23 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0013 others(20): Show |
255 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(252): Show |
3_prime_UTR_variant | MODIFIER | c.*223A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 8/8 | 223 | chr6 | 79486781 | ||||||
| chr6:79518956 | T | C | 25 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 others(22): Show |
363 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(360): Show |
5_prime_UTR_variant | MODIFIER | c.-62A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/8 | 62 | chr6 | 79518956 | ||||||
| chr6:79537256 | G | T | 1 | a0002c0002t0015 | 1 | HG02451.hp2 | 5_prime_UTR_variant | MODIFIER | c.-283C>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/8 | 18362 | chr6 | 79537256 | ||||||
| chr6:79537307 | G | A | 1 | a0003c0003t0009 | 3 | HG02055.hp2 HG02280.hp2 HG02809.hp1 |
5_prime_UTR_variant | MODIFIER | c.-334C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/8 | 18413 | chr6 | 79537307 | ||||||
| chr6:79537394 | C | T | 1 | a0001c0001t0014 | 1 | NA19070.hp2 | 5_prime_UTR_variant | MODIFIER | c.-421G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/8 | 18500 | chr6 | 79537394 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:79488190 | T | C | 1 | a0001c0001t0002g0163 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1232-324A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 7/7 | chr6 | 79488190 | |||||||
| chr6:79488391 | CCT | C | 3 | a0003c0003t0009g0221 a0003c0003t0009g0222 a0003c0003t0009g0223 |
3 | HG02055.hp2 HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1232-527_1232-526d others(4): Show |
LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 7/7 | chr6 | 79488391 | |||||||
| chr6:79488404 | C | A | 28 | a0001c0001t0002g0108 a0001c0001t0002g0144 a0001c0001t0002g0145 others(25): Show |
36 | HG00323.hp2 HG01099.hp1 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.1232-538G>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 7/7 | chr6 | 79488404 | |||||||
| chr6:79488406 | A | C | 3 | a0005c0005t0001g0005 a0005c0005t0001g0090 a0005c0005t0001g0091 |
11 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1232-540T>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 7/7 | chr6 | 79488406 | |||||||
| chr6:79488500 | T | C | 1 | a0001c0001t0002g0129 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1231+584A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 7/7 | chr6 | 79488500 | |||||||
| chr6:79488545 | A | C | 1 | a0001c0001t0001g0073 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1231+539T>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 7/7 | chr6 | 79488545 | |||||||
| chr6:79488778 | C | T | 89 | a0002c0002t0001g0003 a0002c0002t0001g0008 a0002c0002t0001g0013 others(86): Show |
155 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(152): Show |
intron_variant | MODIFIER | c.1231+306G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 7/7 | chr6 | 79488778 | |||||||
| chr6:79488779 | A | G | 2 | a0003c0003t0001g0220 a0008c0014t0010g0153 |
2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1231+305T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 7/7 | chr6 | 79488779 | |||||||
| chr6:79488787 | AG | A | 89 | a0002c0002t0001g0003 a0002c0002t0001g0008 a0002c0002t0001g0013 others(86): Show |
155 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(152): Show |
intron_variant | MODIFIER | c.1231+296delC | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 7/7 | chr6 | 79488787 | |||||||
| chr6:79489228 | T | C | 3 | a0001c0001t0002g0162 a0001c0001t0002g0165 a0001c0001t0002g0167 |
3 | HG03688.hp2 HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1099-12A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 6/7 | chr6 | 79489228 | |||||||
| chr6:79489303 | T | A | 1 | a0002c0002t0001g0093 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1099-87A>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 6/7 | chr6 | 79489303 | |||||||
| chr6:79489303 | T | G | 3 | a0002c0002t0001g0022 a0002c0002t0001g0109 a0002c0002t0001g0111 |
5 | HG00735.hp1 HG01255.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.1099-87A>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 6/7 | chr6 | 79489303 | |||||||
| chr6:79489390 | C | T | 1 | a0003c0008t0001g0143 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1099-174G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 6/7 | chr6 | 79489390 | |||||||
| chr6:79489473 | G | C | 1 | a0002c0002t0001g0118 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1099-257C>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 6/7 | chr6 | 79489473 | |||||||
| chr6:79489514 | TGC | T | 6 | a0003c0003t0001g0214 a0003c0003t0001g0217 a0003c0003t0001g0218 others(3): Show |
6 | HG01891.hp2 HG02886.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1099-300_1099-299d others(4): Show |
LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 6/7 | chr6 | 79489514 | |||||||
| chr6:79489749 | A | G | 1 | a0001c0001t0002g0134 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1099-533T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 6/7 | chr6 | 79489749 | |||||||
| chr6:79489857 | A | G | 2 | a0001c0001t0002g0089 a0001c0001t0002g0173 |
2 | HG02055.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1099-641T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 6/7 | chr6 | 79489857 | |||||||
| chr6:79490200 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(132): Show |
255 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.1099-984A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 6/7 | chr6 | 79490200 | |||||||
| chr6:79490204 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1099-988G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 6/7 | chr6 | 79490204 | |||||||
| chr6:79490309 | G | GA | 135 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(132): Show |
255 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.1099-1094dupT | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 6/7 | chr6 | 79490309 | |||||||
| chr6:79490958 | C | G | 1 | a0003c0003t0001g0214 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1098+630G>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 6/7 | chr6 | 79490958 | |||||||
| chr6:79491049 | C | CA | 94 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(91): Show |
170 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.1098+538dupT | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 6/7 | chr6 | 79491049 | |||||||
| chr6:79491049 | C | CAA | 4 | a0003c0003t0004g0185 a0005c0005t0001g0005 a0005c0005t0001g0090 others(1): Show |
12 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1098+537_1098+538d others(4): Show |
LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 6/7 | chr6 | 79491049 | |||||||
| chr6:79491079 | C | T | 13 | a0003c0003t0005g0010 a0003c0003t0005g0046 a0003c0003t0005g0047 others(10): Show |
21 | HG01099.hp1 HG01256.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.1098+509G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 6/7 | chr6 | 79491079 | |||||||
| chr6:79491153 | G | A | 1 | a0001c0001t0002g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1098+435C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 6/7 | chr6 | 79491153 | |||||||
| chr6:79491278 | T | A | 1 | a0001c0001t0001g0086 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1098+310A>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 6/7 | chr6 | 79491278 | |||||||
| chr6:79491365 | G | A | 1 | a0001c0001t0002g0136 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1098+223C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 6/7 | chr6 | 79491365 | |||||||
| chr6:79491403 | A | G | 38 | a0002c0002t0001g0003 a0002c0002t0001g0008 a0002c0002t0001g0013 others(35): Show |
74 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.1098+185T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 6/7 | chr6 | 79491403 | |||||||
| chr6:79491558 | T | C | 2 | a0003c0008t0001g0142 a0003c0008t0001g0143 |
2 | HG02257.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1098+30A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 6/7 | chr6 | 79491558 | |||||||
| chr6:79491825 | T | G | 1 | a0001c0001t0002g0108 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.956-95A>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 5/7 | chr6 | 79491825 | |||||||
| chr6:79491861 | T | C | 2 | a0003c0003t0001g0044 a0003c0003t0001g0045 |
4 | HG02896.hp1 HG02897.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.956-131A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 5/7 | chr6 | 79491861 | |||||||
| chr6:79491861 | T | G | 2 | a0001c0001t0001g0034 a0001c0001t0010g0061 |
3 | NA18968.hp2 NA19074.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.956-131A>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 5/7 | chr6 | 79491861 | |||||||
| chr6:79491883 | T | A | 1 | a0001c0001t0002g0170 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.956-153A>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 5/7 | chr6 | 79491883 | |||||||
| chr6:79492070 | T | G | 1 | a0001c0001t0007g0009 | 6 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.956-340A>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 5/7 | chr6 | 79492070 | |||||||
| chr6:79492367 | GA | G | 5 | a0001c0001t0002g0202 a0001c0001t0002g0203 a0003c0003t0001g0217 others(2): Show |
5 | HG01891.hp2 HG02886.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.955+183delT | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 5/7 | chr6 | 79492367 | |||||||
| chr6:79492422 | T | G | 1 | a0012c0012t0001g0114 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.955+129A>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 5/7 | chr6 | 79492422 | |||||||
| chr6:79492492 | T | G | 1 | a0012c0012t0001g0114 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.955+59A>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 5/7 | chr6 | 79492492 | |||||||
| chr6:79492509 | A | T | 1 | a0012c0012t0001g0114 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.955+42T>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 5/7 | chr6 | 79492509 | |||||||
| chr6:79492519 | T | A | 1 | a0012c0012t0001g0114 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.955+32A>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 5/7 | chr6 | 79492519 | |||||||
| chr6:79492659 | C | G | 3 | a0005c0005t0001g0005 a0005c0005t0001g0090 a0005c0005t0001g0091 |
11 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.859-12G>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 4/7 | chr6 | 79492659 | |||||||
| chr6:79492754 | G | C | 1 | a0001c0001t0013g0075 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.859-107C>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 4/7 | chr6 | 79492754 | |||||||
| chr6:79492785 | T | C | 1 | a0003c0003t0005g0213 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.859-138A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 4/7 | chr6 | 79492785 | |||||||
| chr6:79492945 | A | T | 1 | a0012c0012t0001g0114 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.859-298T>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 4/7 | chr6 | 79492945 | |||||||
| chr6:79493071 | AAC | A | 3 | a0003c0003t0001g0097 a0003c0003t0012g0095 a0003c0003t0012g0096 |
3 | HG02572.hp1 HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.859-426_859-425del others(2): Show |
LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 4/7 | chr6 | 79493071 | |||||||
| chr6:79493400 | T | A | 1 | a0012c0012t0001g0114 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.858+213A>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 4/7 | chr6 | 79493400 | |||||||
| chr6:79493479 | C | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(86): Show |
165 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.858+134G>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 4/7 | chr6 | 79493479 | |||||||
| chr6:79493483 | AGAT | A | 38 | a0002c0002t0001g0003 a0002c0002t0001g0008 a0002c0002t0001g0013 others(35): Show |
74 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.858+127_858+129del others(3): Show |
LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 4/7 | chr6 | 79493483 | |||||||
| chr6:79493536 | G | A | 43 | a0002c0002t0001g0003 a0002c0002t0001g0008 a0002c0002t0001g0013 others(40): Show |
87 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.858+77C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 4/7 | chr6 | 79493536 | |||||||
| chr6:79493569 | G | A | 1 | a0004c0004t0008g0146 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.858+44C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 4/7 | chr6 | 79493569 | |||||||
| chr6:79493606 | T | A | 1 | a0002c0002t0001g0111 | 1 | HG01255.hp1 | splice_region_variant&intron_variant | LOW | c.858+7A>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 4/7 | chr6 | 79493606 | |||||||
| chr6:79493608 | C | G | 1 | a0002c0002t0001g0111 | 1 | HG01255.hp1 | splice_region_variant&intron_variant | LOW | c.858+5G>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 4/7 | chr6 | 79493608 | |||||||
| chr6:79494128 | G | A | 1 | a0012c0012t0001g0114 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.721-378C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79494128 | |||||||
| chr6:79494233 | T | TA | 46 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(43): Show |
100 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.721-484dupT | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79494233 | |||||||
| chr6:79494316 | G | A | 1 | a0003c0003t0012g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.721-566C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79494316 | |||||||
| chr6:79494320 | C | T | 3 | a0001c0001t0002g0160 a0001c0001t0002g0170 a0011c0010t0002g0174 |
3 | HG02683.hp2 HG04199.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.721-570G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79494320 | |||||||
| chr6:79494443 | C | T | 1 | a0001c0001t0007g0009 | 6 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.721-693G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79494443 | |||||||
| chr6:79494469 | C | T | 1 | a0003c0003t0011g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.721-719G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79494469 | |||||||
| chr6:79494470 | G | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(43): Show |
100 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.721-720C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79494470 | |||||||
| chr6:79494490 | TATAG | T | 4 | a0003c0003t0004g0197 a0003c0003t0009g0221 a0003c0003t0009g0222 others(1): Show |
4 | HG00733.hp1 HG02055.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-744_721-741del others(4): Show |
LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79494490 | |||||||
| chr6:79494689 | T | C | 1 | a0001c0001t0002g0132 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.721-939A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79494689 | |||||||
| chr6:79494778 | G | T | 43 | a0002c0002t0001g0003 a0002c0002t0001g0008 a0002c0002t0001g0013 others(40): Show |
87 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.721-1028C>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79494778 | |||||||
| chr6:79494783 | C | A | 1 | a0012c0012t0001g0114 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.721-1033G>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79494783 | |||||||
| chr6:79494783 | C | T | 3 | a0003c0003t0005g0047 a0003c0003t0005g0208 a0003c0003t0005g0212 |
4 | NA18951.hp1 NA18971.hp2 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-1033G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79494783 | |||||||
| chr6:79494878 | T | C | 16 | a0003c0003t0004g0006 a0003c0003t0004g0029 a0003c0003t0004g0030 others(13): Show |
28 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.721-1128A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79494878 | |||||||
| chr6:79494930 | A | C | 3 | a0001c0001t0007g0009 a0007c0007t0007g0204 a0007c0007t0007g0205 |
8 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.721-1180T>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79494930 | |||||||
| chr6:79495037 | C | A | 43 | a0002c0002t0001g0003 a0002c0002t0001g0008 a0002c0002t0001g0013 others(40): Show |
87 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.721-1287G>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79495037 | |||||||
| chr6:79495039 | G | A | 1 | a0001c0001t0016g0076 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.721-1289C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79495039 | |||||||
| chr6:79495285 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.721-1535G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79495285 | |||||||
| chr6:79495316 | G | C | 3 | a0005c0005t0001g0005 a0005c0005t0001g0090 a0005c0005t0001g0091 |
11 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.721-1566C>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79495316 | |||||||
| chr6:79495339 | T | G | 1 | a0004c0004t0008g0155 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.721-1589A>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79495339 | |||||||
| chr6:79495340 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.721-1590T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79495340 | |||||||
| chr6:79495477 | C | T | 3 | a0003c0003t0005g0209 a0003c0003t0005g0211 a0003c0003t0005g0213 |
3 | HG01099.hp1 HG01358.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.721-1727G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79495477 | |||||||
| chr6:79495478 | G | A | 1 | a0001c0001t0002g0043 | 2 | HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.721-1728C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79495478 | |||||||
| chr6:79495488 | A | G | 5 | a0002c0002t0006g0015 a0002c0002t0006g0021 a0002c0002t0006g0102 others(2): Show |
10 | HG01346.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.721-1738T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79495488 | |||||||
| chr6:79495489 | T | A | 1 | a0001c0001t0001g0060 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.721-1739A>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79495489 | |||||||
| chr6:79495567 | C | T | 1 | a0001c0001t0002g0136 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.721-1817G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79495567 | |||||||
| chr6:79495622 | G | A | 1 | a0001c0001t0002g0172 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.721-1872C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79495622 | |||||||
| chr6:79495750 | C | CAAA | 40 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0018 others(37): Show |
90 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.721-2003_721-2001d others(5): Show |
LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79495750 | |||||||
| chr6:79495750 | CA | C | 6 | a0001c0001t0002g0166 a0001c0001t0007g0009 a0003c0003t0005g0210 others(3): Show |
11 | HG01884.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.721-2001delT | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79495750 | |||||||
| chr6:79495773 | G | A | 1 | a0001c0001t0002g0138 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.721-2023C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79495773 | |||||||
| chr6:79495780 | C | T | 4 | a0001c0001t0001g0035 a0001c0001t0001g0062 a0001c0001t0001g0065 others(1): Show |
5 | HG00609.hp2 HG02027.hp1 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.721-2030G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79495780 | |||||||
| chr6:79495781 | G | A | 1 | a0004c0004t0003g0038 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.721-2031C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79495781 | |||||||
| chr6:79495941 | A | G | 13 | a0003c0003t0005g0010 a0003c0003t0005g0046 a0003c0003t0005g0047 others(10): Show |
21 | HG01099.hp1 HG01256.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.721-2191T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79495941 | |||||||
| chr6:79496043 | C | T | 5 | a0001c0001t0002g0024 a0001c0001t0002g0134 a0001c0001t0002g0135 others(2): Show |
7 | HG02809.hp2 HG02886.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.721-2293G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79496043 | |||||||
| chr6:79496139 | C | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(132): Show |
255 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.721-2389G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79496139 | |||||||
| chr6:79496182 | A | G | 1 | a0003c0003t0004g0200 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.721-2432T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79496182 | |||||||
| chr6:79496256 | T | C | 3 | a0003c0003t0009g0221 a0003c0003t0009g0222 a0003c0003t0009g0223 |
3 | HG02055.hp2 HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.721-2506A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79496256 | |||||||
| chr6:79496327 | C | T | 3 | a0003c0003t0001g0097 a0003c0003t0012g0095 a0003c0003t0012g0096 |
3 | HG02572.hp1 HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.721-2577G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79496327 | |||||||
| chr6:79496528 | G | C | 1 | a0009c0011t0001g0083 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.721-2778C>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79496528 | |||||||
| chr6:79497012 | G | T | 2 | a0003c0003t0012g0095 a0003c0003t0012g0096 |
2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.721-3262C>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79497012 | |||||||
| chr6:79497069 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(135): Show |
263 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.721-3319G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79497069 | |||||||
| chr6:79497190 | G | C | 16 | a0003c0003t0004g0006 a0003c0003t0004g0029 a0003c0003t0004g0030 others(13): Show |
28 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.721-3440C>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79497190 | |||||||
| chr6:79497205 | C | T | 1 | a0001c0001t0002g0144 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.721-3455G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79497205 | |||||||
| chr6:79497313 | T | C | 3 | a0005c0005t0001g0005 a0005c0005t0001g0090 a0005c0005t0001g0091 |
11 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.721-3563A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79497313 | |||||||
| chr6:79497494 | C | T | 1 | a0004c0004t0003g0215 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.721-3744G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79497494 | |||||||
| chr6:79497528 | T | C | 46 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(43): Show |
100 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.721-3778A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79497528 | |||||||
| chr6:79497532 | G | C | 1 | a0002c0002t0001g0111 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.721-3782C>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79497532 | |||||||
| chr6:79497609 | G | A | 2 | a0006c0006t0001g0014 a0006c0006t0001g0077 |
5 | HG02056.hp1 HG02132.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.721-3859C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79497609 | |||||||
| chr6:79497646 | T | C | 16 | a0003c0003t0004g0006 a0003c0003t0004g0029 a0003c0003t0004g0030 others(13): Show |
28 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.721-3896A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79497646 | |||||||
| chr6:79497706 | G | A | 3 | a0003c0003t0001g0097 a0003c0003t0012g0095 a0003c0003t0012g0096 |
3 | HG02572.hp1 HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.721-3956C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79497706 | |||||||
| chr6:79497743 | C | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(135): Show |
263 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.721-3993G>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79497743 | |||||||
| chr6:79497956 | C | CA | 35 | a0001c0001t0001g0078 a0001c0001t0002g0160 a0001c0001t0002g0170 others(32): Show |
49 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.721-4207dupT | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79497956 | |||||||
| chr6:79497956 | CA | C | 41 | a0001c0001t0002g0161 a0002c0002t0001g0003 a0002c0002t0001g0008 others(38): Show |
81 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.721-4207delT | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79497956 | |||||||
| chr6:79497970 | A | G | 13 | a0003c0003t0005g0010 a0003c0003t0005g0046 a0003c0003t0005g0047 others(10): Show |
21 | HG01099.hp1 HG01256.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.721-4220T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79497970 | |||||||
| chr6:79498119 | C | T | 1 | a0004c0004t0003g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.721-4369G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79498119 | |||||||
| chr6:79498147 | T | C | 2 | a0003c0003t0004g0197 a0003c0003t0004g0198 |
2 | HG00733.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.721-4397A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79498147 | |||||||
| chr6:79498172 | TA | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(136): Show |
261 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.721-4423delT | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79498172 | |||||||
| chr6:79498332 | C | T | 3 | a0003c0003t0001g0214 a0003c0003t0001g0220 a0008c0014t0010g0153 |
3 | HG03195.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.721-4582G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79498332 | |||||||
| chr6:79498393 | A | G | 43 | a0002c0002t0001g0003 a0002c0002t0001g0008 a0002c0002t0001g0013 others(40): Show |
87 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.721-4643T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79498393 | |||||||
| chr6:79498453 | C | T | 3 | a0003c0003t0001g0097 a0003c0003t0012g0095 a0003c0003t0012g0096 |
3 | HG02572.hp1 HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.721-4703G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79498453 | |||||||
| chr6:79498513 | G | A | 3 | a0005c0005t0001g0005 a0005c0005t0001g0090 a0005c0005t0001g0091 |
11 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.721-4763C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79498513 | |||||||
| chr6:79498532 | T | C | 1 | a0003c0003t0005g0048 | 2 | NA18985.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.721-4782A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79498532 | |||||||
| chr6:79498719 | T | A | 3 | a0003c0003t0001g0097 a0003c0003t0012g0095 a0003c0003t0012g0096 |
3 | HG02572.hp1 HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.721-4969A>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79498719 | |||||||
| chr6:79498797 | G | T | 2 | a0001c0001t0002g0042 a0001c0001t0002g0094 |
3 | HG02647.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.721-5047C>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79498797 | |||||||
| chr6:79498928 | T | C | 1 | a0007c0007t0007g0205 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.721-5178A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79498928 | |||||||
| chr6:79499196 | C | G | 46 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(43): Show |
100 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.721-5446G>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79499196 | |||||||
| chr6:79499211 | T | C | 1 | a0003c0003t0001g0201 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.721-5461A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79499211 | |||||||
| chr6:79499302 | TA | T | 46 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(43): Show |
100 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.721-5553delT | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79499302 | |||||||
| chr6:79499436 | A | G | 1 | a0003c0003t0004g0183 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.721-5686T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79499436 | |||||||
| chr6:79499462 | C | G | 3 | a0001c0001t0002g0042 a0001c0001t0002g0094 a0001c0001t0002g0176 |
4 | HG02451.hp1 HG02647.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-5712G>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79499462 | |||||||
| chr6:79499476 | A | G | 1 | a0001c0001t0001g0071 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.721-5726T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79499476 | |||||||
| chr6:79499478 | A | G | 1 | a0002c0002t0001g0116 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.721-5728T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79499478 | |||||||
| chr6:79499489 | C | T | 1 | a0002c0002t0001g0092 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.721-5739G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79499489 | |||||||
| chr6:79499606 | TAAGG | T | 63 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0017 others(60): Show |
99 | HG00323.hp2 HG00438.hp1 HG00738.hp1 others(96): Show |
intron_variant | MODIFIER | c.721-5860_721-5857d others(6): Show |
LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79499606 | |||||||
| chr6:79499637 | C | T | 2 | a0003c0008t0001g0142 a0003c0008t0001g0143 |
2 | HG02257.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.721-5887G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79499637 | |||||||
| chr6:79499638 | G | A | 2 | a0003c0003t0011g0098 a0003c0003t0011g0099 |
2 | HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.721-5888C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79499638 | |||||||
| chr6:79499852 | C | A | 1 | a0001c0001t0001g0079 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.721-6102G>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79499852 | |||||||
| chr6:79499854 | A | T | 1 | a0001c0001t0001g0079 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.721-6104T>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79499854 | |||||||
| chr6:79499860 | C | A | 1 | a0001c0001t0001g0079 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.721-6110G>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79499860 | |||||||
| chr6:79500019 | C | T | 1 | a0004c0004t0003g0147 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.721-6269G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79500019 | |||||||
| chr6:79500044 | G | A | 13 | a0003c0003t0005g0010 a0003c0003t0005g0046 a0003c0003t0005g0047 others(10): Show |
21 | HG01099.hp1 HG01256.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.721-6294C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79500044 | |||||||
| chr6:79500093 | C | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(132): Show |
255 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.721-6343G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79500093 | |||||||
| chr6:79500146 | G | A | 3 | a0003c0003t0001g0097 a0003c0003t0012g0095 a0003c0003t0012g0096 |
3 | HG02572.hp1 HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.721-6396C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79500146 | |||||||
| chr6:79500372 | G | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(131): Show |
254 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.721-6622C>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79500372 | |||||||
| chr6:79500514 | G | T | 1 | a0003c0003t0001g0218 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.721-6764C>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79500514 | |||||||
| chr6:79500574 | C | T | 24 | a0003c0003t0001g0214 a0003c0003t0001g0217 a0003c0003t0001g0218 others(21): Show |
36 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.721-6824G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79500574 | |||||||
| chr6:79500720 | A | T | 46 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(43): Show |
100 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.721-6970T>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79500720 | |||||||
| chr6:79500827 | A | AT | 17 | a0001c0001t0002g0024 a0001c0001t0002g0052 a0001c0001t0002g0128 others(14): Show |
19 | HG01081.hp1 HG01175.hp1 HG01516.hp1 others(16): Show |
intron_variant | MODIFIER | c.721-7078dupA | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79500827 | |||||||
| chr6:79500916 | CAT | C | 5 | a0003c0003t0004g0030 a0003c0003t0004g0197 a0003c0003t0004g0198 others(2): Show |
7 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.721-7168_721-7167d others(4): Show |
LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79500916 | |||||||
| chr6:79500920 | T | C | 1 | a0003c0003t0004g0182 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.721-7170A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79500920 | |||||||
| chr6:79500941 | C | A | 3 | a0003c0003t0001g0217 a0003c0003t0001g0218 a0003c0003t0001g0219 |
3 | HG01891.hp2 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.721-7191G>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79500941 | |||||||
| chr6:79501051 | G | C | 4 | a0003c0003t0004g0183 a0003c0003t0004g0184 a0003c0003t0004g0185 others(1): Show |
4 | HG02818.hp1 HG02976.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-7301C>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79501051 | |||||||
| chr6:79501085 | A | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0081 |
2 | NA19009.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.721-7335T>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79501085 | |||||||
| chr6:79501691 | T | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(133): Show |
261 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.721-7941A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79501691 | |||||||
| chr6:79501730 | TCTATAA | T | 2 | a0001c0001t0001g0033 a0001c0001t0002g0052 |
3 | HG01069.hp2 HG01433.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.721-7986_721-7981d others(8): Show |
LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79501730 | |||||||
| chr6:79501812 | C | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(133): Show |
261 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.721-8062G>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79501812 | |||||||
| chr6:79501906 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.721-8156C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79501906 | |||||||
| chr6:79501990 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(135): Show |
263 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.721-8240T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79501990 | |||||||
| chr6:79502205 | C | T | 1 | a0001c0001t0002g0133 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.721-8455G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79502205 | |||||||
| chr6:79502402 | T | A | 1 | a0001c0001t0002g0166 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.721-8652A>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79502402 | |||||||
| chr6:79502573 | G | C | 1 | a0001c0001t0002g0137 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.721-8823C>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79502573 | |||||||
| chr6:79502629 | A | T | 2 | a0003c0003t0011g0098 a0003c0003t0011g0099 |
2 | HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.721-8879T>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79502629 | |||||||
| chr6:79502784 | A | G | 1 | a0002c0002t0001g0116 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.721-9034T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79502784 | |||||||
| chr6:79502860 | C | T | 2 | a0003c0003t0005g0047 a0003c0003t0005g0208 |
3 | NA18971.hp2 NA19055.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.721-9110G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79502860 | |||||||
| chr6:79502993 | G | C | 13 | a0003c0003t0005g0010 a0003c0003t0005g0046 a0003c0003t0005g0047 others(10): Show |
21 | HG01099.hp1 HG01256.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.721-9243C>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79502993 | |||||||
| chr6:79502998 | G | A | 1 | a0001c0001t0002g0135 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.721-9248C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79502998 | |||||||
| chr6:79503006 | G | A | 1 | a0003c0003t0001g0097 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.721-9256C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79503006 | |||||||
| chr6:79503083 | T | C | 2 | a0001c0001t0002g0128 a0001c0001t0002g0129 |
2 | HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.721-9333A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79503083 | |||||||
| chr6:79503110 | G | A | 1 | a0002c0002t0001g0121 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.721-9360C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79503110 | |||||||
| chr6:79503159 | G | C | 2 | a0001c0001t0002g0206 a0001c0001t0007g0009 |
7 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.721-9409C>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79503159 | |||||||
| chr6:79503220 | A | G | 2 | a0005c0005t0001g0090 a0005c0005t0001g0091 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.721-9470T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79503220 | |||||||
| chr6:79503434 | C | T | 1 | a0002c0002t0001g0115 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.721-9684G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79503434 | |||||||
| chr6:79503797 | T | C | 3 | a0003c0003t0001g0097 a0003c0003t0012g0095 a0003c0003t0012g0096 |
3 | HG02572.hp1 HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.720+9415A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79503797 | |||||||
| chr6:79503801 | C | T | 44 | a0002c0002t0001g0003 a0002c0002t0001g0008 a0002c0002t0001g0013 others(41): Show |
88 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.720+9411G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79503801 | |||||||
| chr6:79503999 | T | C | 5 | a0003c0003t0011g0098 a0003c0003t0011g0099 a0005c0005t0001g0005 others(2): Show |
13 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.720+9213A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79503999 | |||||||
| chr6:79504180 | A | G | 2 | a0001c0001t0002g0206 a0001c0001t0007g0009 |
7 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.720+9032T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79504180 | |||||||
| chr6:79504378 | T | C | 1 | a0003c0003t0011g0098 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.720+8834A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79504378 | |||||||
| chr6:79504656 | T | C | 2 | a0003c0003t0004g0197 a0003c0003t0004g0198 |
2 | HG00733.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.720+8556A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79504656 | |||||||
| chr6:79504736 | T | C | 1 | a0001c0001t0002g0167 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.720+8476A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79504736 | |||||||
| chr6:79504753 | A | G | 1 | a0002c0002t0006g0015 | 4 | HG02109.hp2 HG02258.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+8459T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79504753 | |||||||
| chr6:79504803 | T | C | 2 | a0003c0008t0001g0142 a0003c0008t0001g0143 |
2 | HG02257.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.720+8409A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79504803 | |||||||
| chr6:79504839 | T | C | 1 | a0003c0003t0005g0212 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.720+8373A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79504839 | |||||||
| chr6:79504880 | A | G | 3 | a0004c0004t0008g0025 a0004c0004t0008g0146 a0004c0004t0008g0155 |
5 | HG01167.hp1 HG01192.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+8332T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79504880 | |||||||
| chr6:79504926 | C | T | 13 | a0003c0003t0005g0010 a0003c0003t0005g0046 a0003c0003t0005g0047 others(10): Show |
21 | HG01099.hp1 HG01256.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.720+8286G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79504926 | |||||||
| chr6:79505034 | G | A | 43 | a0002c0002t0001g0003 a0002c0002t0001g0008 a0002c0002t0001g0013 others(40): Show |
87 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.720+8178C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79505034 | |||||||
| chr6:79505110 | C | T | 3 | a0003c0003t0001g0044 a0003c0003t0001g0045 a0003c0003t0001g0201 |
5 | HG02896.hp1 HG02897.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+8102G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79505110 | |||||||
| chr6:79505168 | C | A | 65 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0017 others(62): Show |
101 | HG00323.hp2 HG00438.hp1 HG00738.hp1 others(98): Show |
intron_variant | MODIFIER | c.720+8044G>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79505168 | |||||||
| chr6:79505173 | G | T | 1 | a0001c0001t0001g0070 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.720+8039C>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79505173 | |||||||
| chr6:79505209 | A | G | 1 | a0002c0002t0001g0101 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.720+8003T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79505209 | |||||||
| chr6:79505214 | T | C | 7 | a0001c0001t0002g0052 a0001c0001t0002g0132 a0001c0001t0002g0133 others(4): Show |
7 | HG01081.hp1 HG01175.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.720+7998A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79505214 | |||||||
| chr6:79505242 | A | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(133): Show |
261 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.720+7970T>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79505242 | |||||||
| chr6:79505473 | T | C | 1 | a0001c0001t0002g0161 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.720+7739A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79505473 | |||||||
| chr6:79505540 | G | A | 5 | a0002c0002t0006g0015 a0002c0002t0006g0021 a0002c0002t0006g0102 others(2): Show |
10 | HG01346.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.720+7672C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79505540 | |||||||
| chr6:79505616 | C | T | 3 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0009t0001g0069 |
3 | NA18972.hp1 NA18982.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.720+7596G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79505616 | |||||||
| chr6:79505693 | A | G | 1 | a0001c0001t0002g0175 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.720+7519T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79505693 | |||||||
| chr6:79505698 | C | T | 1 | a0001c0001t0002g0162 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.720+7514G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79505698 | |||||||
| chr6:79505858 | C | G | 23 | a0001c0001t0002g0007 a0001c0001t0002g0017 a0001c0001t0002g0028 others(20): Show |
39 | HG00738.hp1 HG01074.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.720+7354G>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79505858 | |||||||
| chr6:79506129 | C | G | 2 | a0001c0001t0002g0206 a0001c0001t0007g0009 |
7 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.720+7083G>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79506129 | |||||||
| chr6:79506189 | A | T | 48 | a0001c0001t0001g0067 a0001c0001t0002g0206 a0001c0001t0007g0009 others(45): Show |
97 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.720+7023T>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79506189 | |||||||
| chr6:79506377 | C | T | 1 | a0003c0003t0004g0180 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.720+6835G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79506377 | |||||||
| chr6:79506594 | T | C | 1 | a0001c0001t0002g0131 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.720+6618A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79506594 | |||||||
| chr6:79506619 | A | G | 1 | a0001c0001t0002g0041 | 2 | HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.720+6593T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79506619 | |||||||
| chr6:79506627 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.720+6585G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79506627 | |||||||
| chr6:79506893 | A | G | 2 | a0002c0002t0001g0113 a0012c0012t0001g0114 |
2 | HG00609.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.720+6319T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79506893 | |||||||
| chr6:79506957 | G | A | 3 | a0003c0003t0009g0221 a0003c0003t0009g0222 a0003c0003t0009g0223 |
3 | HG02055.hp2 HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.720+6255C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79506957 | |||||||
| chr6:79507014 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0081 |
2 | NA19009.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.720+6198A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79507014 | |||||||
| chr6:79507081 | A | G | 65 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0017 others(62): Show |
101 | HG00323.hp2 HG00438.hp1 HG00738.hp1 others(98): Show |
intron_variant | MODIFIER | c.720+6131T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79507081 | |||||||
| chr6:79507123 | T | C | 59 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(56): Show |
121 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(118): Show |
intron_variant | MODIFIER | c.720+6089A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79507123 | |||||||
| chr6:79507264 | T | C | 38 | a0002c0002t0001g0003 a0002c0002t0001g0008 a0002c0002t0001g0013 others(35): Show |
74 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.720+5948A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79507264 | |||||||
| chr6:79507398 | G | A | 1 | a0001c0001t0002g0157 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.720+5814C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79507398 | |||||||
| chr6:79507555 | T | C | 4 | a0001c0001t0001g0035 a0001c0001t0001g0062 a0001c0001t0001g0065 others(1): Show |
5 | HG00609.hp2 HG02027.hp1 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.720+5657A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79507555 | |||||||
| chr6:79507559 | T | C | 46 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(43): Show |
100 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.720+5653A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79507559 | |||||||
| chr6:79507599 | C | G | 1 | a0001c0001t0002g0131 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.720+5613G>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79507599 | |||||||
| chr6:79507599 | C | T | 2 | a0001c0001t0002g0206 a0001c0001t0007g0009 |
7 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.720+5613G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79507599 | |||||||
| chr6:79507859 | T | C | 1 | a0001c0001t0002g0168 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.720+5353A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79507859 | |||||||
| chr6:79507956 | G | C | 3 | a0003c0003t0009g0221 a0003c0003t0009g0222 a0003c0003t0009g0223 |
3 | HG02055.hp2 HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.720+5256C>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79507956 | |||||||
| chr6:79508027 | T | C | 1 | a0001c0001t0002g0138 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.720+5185A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79508027 | |||||||
| chr6:79508137 | C | T | 2 | a0001c0001t0002g0206 a0001c0001t0007g0009 |
7 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.720+5075G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79508137 | |||||||
| chr6:79508161 | T | C | 3 | a0005c0005t0001g0005 a0005c0005t0001g0090 a0005c0005t0001g0091 |
11 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.720+5051A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79508161 | |||||||
| chr6:79508405 | G | A | 2 | a0003c0003t0011g0098 a0003c0003t0011g0099 |
2 | HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.720+4807C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79508405 | |||||||
| chr6:79508629 | GA | G | 36 | a0001c0001t0014g0049 a0002c0002t0001g0003 a0002c0002t0001g0008 others(33): Show |
67 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.720+4582delT | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79508629 | |||||||
| chr6:79508668 | T | G | 2 | a0007c0007t0007g0204 a0007c0007t0007g0205 |
2 | HG02630.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.720+4544A>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79508668 | |||||||
| chr6:79508867 | T | C | 1 | a0001c0001t0002g0129 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.720+4345A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79508867 | |||||||
| chr6:79509402 | C | T | 27 | a0003c0003t0001g0044 a0003c0003t0001g0045 a0003c0003t0001g0201 others(24): Show |
41 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.720+3810G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79509402 | |||||||
| chr6:79509448 | C | T | 1 | a0003c0008t0001g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.720+3764G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79509448 | |||||||
| chr6:79509453 | C | CA | 56 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(53): Show |
115 | HG00280.hp2 HG00438.hp2 HG00642.hp2 others(112): Show |
intron_variant | MODIFIER | c.720+3758dupT | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79509453 | |||||||
| chr6:79509453 | CA | C | 30 | a0001c0001t0002g0190 a0002c0002t0001g0023 a0002c0002t0001g0105 others(27): Show |
52 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.720+3758delT | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79509453 | |||||||
| chr6:79509469 | A | G | 1 | a0004c0004t0003g0151 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.720+3743T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79509469 | |||||||
| chr6:79509508 | A | G | 1 | a0002c0002t0001g0037 | 2 | HG02602.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.720+3704T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79509508 | |||||||
| chr6:79510026 | A | G | 1 | a0001c0001t0001g0060 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.720+3186T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79510026 | |||||||
| chr6:79510065 | A | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(129): Show |
252 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.720+3147T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79510065 | |||||||
| chr6:79510083 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.720+3129G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79510083 | |||||||
| chr6:79510244 | T | C | 27 | a0003c0003t0001g0044 a0003c0003t0001g0045 a0003c0003t0001g0201 others(24): Show |
41 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.720+2968A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79510244 | |||||||
| chr6:79510842 | A | G | 2 | a0003c0003t0012g0095 a0003c0003t0012g0096 |
2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.720+2370T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79510842 | |||||||
| chr6:79510891 | G | T | 65 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0017 others(62): Show |
101 | HG00323.hp2 HG00438.hp1 HG00738.hp1 others(98): Show |
intron_variant | MODIFIER | c.720+2321C>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79510891 | |||||||
| chr6:79510967 | G | A | 12 | a0001c0001t0002g0024 a0001c0001t0002g0052 a0001c0001t0002g0132 others(9): Show |
14 | HG01081.hp1 HG01175.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.720+2245C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79510967 | |||||||
| chr6:79510968 | G | A | 4 | a0001c0001t0002g0206 a0001c0001t0007g0009 a0007c0007t0007g0204 others(1): Show |
9 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.720+2244C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79510968 | |||||||
| chr6:79511198 | T | C | 1 | a0003c0003t0001g0201 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.720+2014A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79511198 | |||||||
| chr6:79511836 | A | C | 3 | a0005c0005t0001g0005 a0005c0005t0001g0090 a0005c0005t0001g0091 |
11 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.720+1376T>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79511836 | |||||||
| chr6:79512015 | C | A | 1 | a0001c0001t0002g0193 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.720+1197G>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79512015 | |||||||
| chr6:79512053 | T | C | 1 | a0002c0002t0001g0122 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.720+1159A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79512053 | |||||||
| chr6:79512079 | T | C | 2 | a0003c0003t0001g0214 a0003c0003t0001g0220 |
2 | HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.720+1133A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79512079 | |||||||
| chr6:79512120 | C | A | 2 | a0001c0001t0002g0202 a0001c0001t0002g0203 |
2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.720+1092G>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79512120 | |||||||
| chr6:79512376 | T | A | 1 | a0003c0003t0005g0213 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.720+836A>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79512376 | |||||||
| chr6:79512418 | AT | A | 2 | a0001c0001t0002g0206 a0001c0001t0007g0009 |
7 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.720+793delA | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79512418 | |||||||
| chr6:79512621 | C | CAT | 43 | a0002c0002t0001g0003 a0002c0002t0001g0008 a0002c0002t0001g0013 others(40): Show |
87 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.720+589_720+590dup others(2): Show |
LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79512621 | |||||||
| chr6:79512644 | C | G | 2 | a0001c0001t0002g0206 a0001c0001t0007g0009 |
7 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.720+568G>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79512644 | |||||||
| chr6:79512785 | G | A | 3 | a0003c0003t0001g0097 a0003c0003t0012g0095 a0003c0003t0012g0096 |
3 | HG02572.hp1 HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.720+427C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79512785 | |||||||
| chr6:79512927 | T | C | 1 | a0003c0003t0001g0214 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.720+285A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79512927 | |||||||
| chr6:79513087 | G | C | 38 | a0002c0002t0001g0003 a0002c0002t0001g0008 a0002c0002t0001g0013 others(35): Show |
74 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.720+125C>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 3/7 | chr6 | 79513087 | |||||||
| chr6:79513879 | G | A | 2 | a0001c0001t0002g0206 a0001c0001t0007g0009 |
7 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.191-138C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79513879 | |||||||
| chr6:79513965 | T | C | 1 | a0003c0003t0001g0220 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.191-224A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79513965 | |||||||
| chr6:79513999 | A | C | 1 | a0001c0001t0001g0062 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.191-258T>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79513999 | |||||||
| chr6:79514247 | A | C | 1 | a0001c0001t0001g0020 | 3 | HG03491.hp1 HG03492.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.191-506T>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79514247 | |||||||
| chr6:79514247 | A | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(128): Show |
249 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.191-506T>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79514247 | |||||||
| chr6:79514320 | G | A | 1 | a0001c0001t0002g0170 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.191-579C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79514320 | |||||||
| chr6:79514324 | A | G | 1 | a0003c0003t0004g0029 | 3 | NA18947.hp1 NA18954.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.191-583T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79514324 | |||||||
| chr6:79514520 | C | T | 1 | a0002c0002t0001g0109 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.191-779G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79514520 | |||||||
| chr6:79514659 | C | T | 1 | a0004c0004t0003g0151 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.191-918G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79514659 | |||||||
| chr6:79515050 | T | C | 1 | a0008c0014t0010g0153 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.191-1309A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79515050 | |||||||
| chr6:79515311 | G | C | 46 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(43): Show |
100 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.191-1570C>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79515311 | |||||||
| chr6:79515394 | G | T | 2 | a0003c0003t0001g0044 a0003c0003t0001g0045 |
4 | HG02896.hp1 HG02897.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.191-1653C>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79515394 | |||||||
| chr6:79515763 | C | T | 2 | a0003c0003t0011g0098 a0003c0003t0011g0099 |
2 | HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.191-2022G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79515763 | |||||||
| chr6:79515774 | T | A | 2 | a0007c0007t0007g0204 a0007c0007t0007g0205 |
2 | HG02630.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.191-2033A>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79515774 | |||||||
| chr6:79515787 | G | T | 1 | a0003c0003t0001g0097 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.191-2046C>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79515787 | |||||||
| chr6:79515809 | A | AT | 2 | a0002c0002t0001g0013 a0002c0002t0001g0112 |
6 | NA18979.hp1 NA18998.hp1 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.191-2069dupA | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79515809 | |||||||
| chr6:79515820 | T | C | 1 | a0004c0015t0003g0154 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.191-2079A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79515820 | |||||||
| chr6:79515982 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(135): Show |
263 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.191-2241G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79515982 | |||||||
| chr6:79515985 | G | C | 1 | a0003c0003t0001g0201 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.191-2244C>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79515985 | |||||||
| chr6:79516114 | T | C | 1 | a0001c0001t0002g0139 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.191-2373A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79516114 | |||||||
| chr6:79516125 | GT | G | 3 | a0001c0001t0002g0017 a0001c0001t0002g0140 a0001c0001t0002g0171 |
6 | HG01074.hp1 HG01346.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.191-2385delA | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79516125 | |||||||
| chr6:79516126 | T | G | 1 | a0002c0002t0001g0003 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.191-2385A>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79516126 | |||||||
| chr6:79516164 | C | T | 1 | a0001c0001t0002g0133 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.191-2423G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79516164 | |||||||
| chr6:79516167 | A | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(133): Show |
261 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.191-2426T>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79516167 | |||||||
| chr6:79516516 | G | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(129): Show |
252 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.190+2189C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79516516 | |||||||
| chr6:79516744 | C | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(133): Show |
261 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.190+1961G>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79516744 | |||||||
| chr6:79516857 | A | G | 1 | a0003c0003t0001g0097 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.190+1848T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79516857 | |||||||
| chr6:79516920 | G | A | 2 | a0003c0008t0001g0142 a0003c0008t0001g0143 |
2 | HG02257.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.190+1785C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79516920 | |||||||
| chr6:79516969 | T | C | 1 | a0002c0002t0006g0021 | 3 | HG01891.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.190+1736A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79516969 | |||||||
| chr6:79516980 | C | CA | 4 | a0001c0001t0002g0206 a0001c0001t0007g0009 a0007c0007t0007g0204 others(1): Show |
9 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.190+1724dupT | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79516980 | |||||||
| chr6:79517052 | A | G | 38 | a0002c0002t0001g0003 a0002c0002t0001g0008 a0002c0002t0001g0013 others(35): Show |
74 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.190+1653T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79517052 | |||||||
| chr6:79517165 | A | C | 1 | a0003c0003t0001g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.190+1540T>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79517165 | |||||||
| chr6:79517240 | A | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(133): Show |
261 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.190+1465T>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79517240 | |||||||
| chr6:79517430 | A | T | 2 | a0001c0001t0002g0040 a0001c0001t0002g0159 |
3 | HG01433.hp1 HG01515.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.190+1275T>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79517430 | |||||||
| chr6:79517777 | T | G | 2 | a0003c0003t0012g0095 a0003c0003t0012g0096 |
2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.190+928A>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79517777 | |||||||
| chr6:79517783 | T | A | 2 | a0001c0001t0002g0202 a0001c0001t0002g0203 |
2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.190+922A>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79517783 | |||||||
| chr6:79517797 | T | A | 1 | a0002c0002t0015g0050 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.190+908A>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79517797 | |||||||
| chr6:79517818 | C | T | 1 | a0001c0001t0002g0132 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.190+887G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79517818 | |||||||
| chr6:79517845 | G | C | 1 | a0001c0001t0017g0084 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.190+860C>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79517845 | |||||||
| chr6:79517861 | A | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(127): Show |
250 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.190+844T>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79517861 | |||||||
| chr6:79517972 | G | A | 27 | a0003c0003t0001g0044 a0003c0003t0001g0045 a0003c0003t0001g0201 others(24): Show |
41 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.190+733C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79517972 | |||||||
| chr6:79518004 | TC | T | 4 | a0002c0002t0001g0022 a0002c0002t0001g0109 a0002c0002t0001g0110 others(1): Show |
6 | HG00735.hp1 HG01255.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.190+700delG | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79518004 | |||||||
| chr6:79518045 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.190+660A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79518045 | |||||||
| chr6:79518630 | T | A | 2 | a0001c0001t0002g0206 a0001c0001t0007g0009 |
7 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.190+75A>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 2/7 | chr6 | 79518630 | |||||||
| chr6:79519268 | T | C | 1 | a0001c0001t0002g0203 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-191-183A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79519268 | |||||||
| chr6:79519305 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-191-220G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79519305 | |||||||
| chr6:79519635 | C | T | 1 | a0003c0003t0001g0044 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-191-550G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79519635 | |||||||
| chr6:79519650 | G | A | 1 | a0004c0004t0003g0178 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-191-565C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79519650 | |||||||
| chr6:79519715 | C | CA | 8 | a0002c0002t0001g0123 a0002c0002t0006g0104 a0003c0003t0001g0044 others(5): Show |
10 | HG01123.hp2 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-191-631dupT | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79519715 | |||||||
| chr6:79519715 | CA | C | 17 | a0001c0001t0001g0011 a0001c0001t0001g0060 a0001c0001t0002g0141 others(14): Show |
23 | HG01069.hp1 HG01891.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.-191-631delT | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79519715 | |||||||
| chr6:79520106 | T | A | 1 | a0003c0003t0001g0097 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-191-1021A>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79520106 | |||||||
| chr6:79520162 | T | C | 2 | a0003c0008t0001g0142 a0003c0008t0001g0143 |
2 | HG02257.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-191-1077A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79520162 | |||||||
| chr6:79520168 | T | C | 1 | a0003c0003t0011g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-191-1083A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79520168 | |||||||
| chr6:79520255 | C | T | 44 | a0001c0001t0002g0108 a0002c0002t0001g0003 a0002c0002t0001g0008 others(41): Show |
88 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.-191-1170G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79520255 | |||||||
| chr6:79520343 | A | G | 1 | a0001c0001t0002g0130 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-191-1258T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79520343 | |||||||
| chr6:79520450 | T | C | 1 | a0001c0001t0002g0194 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-191-1365A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79520450 | |||||||
| chr6:79520766 | T | C | 2 | a0003c0008t0001g0142 a0003c0008t0001g0143 |
2 | HG02257.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-191-1681A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79520766 | |||||||
| chr6:79520822 | G | A | 39 | a0001c0001t0002g0108 a0002c0002t0001g0003 a0002c0002t0001g0008 others(36): Show |
75 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.-191-1737C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79520822 | |||||||
| chr6:79520890 | T | C | 2 | a0003c0003t0001g0044 a0003c0003t0001g0045 |
4 | HG02896.hp1 HG02897.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-191-1805A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79520890 | |||||||
| chr6:79520908 | G | A | 4 | a0001c0001t0002g0206 a0001c0001t0007g0009 a0007c0007t0007g0204 others(1): Show |
9 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-191-1823C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79520908 | |||||||
| chr6:79521239 | A | G | 2 | a0001c0001t0002g0202 a0001c0001t0002g0203 |
2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-191-2154T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79521239 | |||||||
| chr6:79521387 | T | G | 13 | a0003c0003t0005g0010 a0003c0003t0005g0046 a0003c0003t0005g0047 others(10): Show |
21 | HG01099.hp1 HG01256.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.-191-2302A>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79521387 | |||||||
| chr6:79521794 | T | G | 1 | a0001c0001t0002g0172 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-191-2709A>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79521794 | |||||||
| chr6:79521918 | A | G | 3 | a0003c0003t0001g0217 a0003c0003t0001g0218 a0003c0003t0001g0219 |
3 | HG01891.hp2 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-191-2833T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79521918 | |||||||
| chr6:79522061 | AAGATTCT others(28): Show |
A | 1 | a0002c0002t0001g0125 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-191-3011_-191-297 others(39): Show |
LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79522061 | |||||||
| chr6:79522798 | C | T | 2 | a0001c0001t0002g0128 a0001c0001t0002g0129 |
2 | HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-191-3713G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79522798 | |||||||
| chr6:79522815 | G | C | 2 | a0003c0003t0001g0044 a0003c0003t0001g0045 |
4 | HG02896.hp1 HG02897.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-191-3730C>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79522815 | |||||||
| chr6:79522904 | CT | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(194): Show |
358 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(355): Show |
intron_variant | MODIFIER | c.-191-3820delA | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79522904 | |||||||
| chr6:79523006 | T | C | 2 | a0001c0001t0002g0089 a0001c0001t0002g0173 |
2 | HG02055.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-191-3921A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79523006 | |||||||
| chr6:79523051 | T | G | 46 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(43): Show |
100 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.-191-3966A>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79523051 | |||||||
| chr6:79523170 | T | A | 1 | a0001c0001t0002g0141 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-191-4085A>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79523170 | |||||||
| chr6:79523183 | C | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(200): Show |
364 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(361): Show |
intron_variant | MODIFIER | c.-191-4098G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79523183 | |||||||
| chr6:79523336 | AG | A | 3 | a0003c0003t0001g0097 a0003c0003t0012g0095 a0003c0003t0012g0096 |
3 | HG02572.hp1 HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-191-4252delC | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79523336 | |||||||
| chr6:79523416 | A | G | 1 | a0001c0001t0002g0052 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-191-4331T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79523416 | |||||||
| chr6:79523651 | C | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(130): Show |
253 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.-191-4566G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79523651 | |||||||
| chr6:79523747 | CT | C | 3 | a0003c0003t0001g0097 a0003c0003t0012g0095 a0003c0003t0012g0096 |
3 | HG02572.hp1 HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-191-4663delA | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79523747 | |||||||
| chr6:79523796 | C | G | 2 | a0007c0007t0007g0204 a0007c0007t0007g0205 |
2 | HG02630.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-191-4711G>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79523796 | |||||||
| chr6:79523799 | T | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(43): Show |
100 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.-191-4714A>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79523799 | |||||||
| chr6:79523830 | A | T | 1 | a0001c0001t0002g0157 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-191-4745T>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79523830 | |||||||
| chr6:79523880 | A | C | 2 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
2 | HG00323.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.-191-4795T>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79523880 | |||||||
| chr6:79523920 | A | G | 2 | a0001c0001t0002g0206 a0001c0001t0007g0009 |
7 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-191-4835T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79523920 | |||||||
| chr6:79523947 | T | C | 1 | a0011c0010t0002g0174 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-191-4862A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79523947 | |||||||
| chr6:79524089 | A | C | 44 | a0001c0001t0002g0108 a0002c0002t0001g0003 a0002c0002t0001g0008 others(41): Show |
88 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.-191-5004T>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79524089 | |||||||
| chr6:79524231 | T | C | 24 | a0003c0003t0001g0214 a0003c0003t0001g0217 a0003c0003t0001g0218 others(21): Show |
36 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.-191-5146A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79524231 | |||||||
| chr6:79524293 | T | C | 44 | a0001c0001t0002g0108 a0002c0002t0001g0003 a0002c0002t0001g0008 others(41): Show |
88 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.-191-5208A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79524293 | |||||||
| chr6:79524295 | A | C | 2 | a0001c0001t0002g0206 a0001c0001t0007g0009 |
7 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-191-5210T>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79524295 | |||||||
| chr6:79524582 | A | T | 5 | a0004c0004t0003g0026 a0004c0004t0003g0147 a0004c0004t0008g0025 others(2): Show |
9 | HG00140.hp1 HG00280.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.-191-5497T>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79524582 | |||||||
| chr6:79524600 | A | G | 3 | a0003c0003t0001g0097 a0003c0003t0012g0095 a0003c0003t0012g0096 |
3 | HG02572.hp1 HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-191-5515T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79524600 | |||||||
| chr6:79524601 | T | C | 1 | a0004c0004t0003g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-191-5516A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79524601 | |||||||
| chr6:79524626 | A | G | 5 | a0003c0003t0001g0214 a0003c0003t0001g0217 a0003c0003t0001g0218 others(2): Show |
5 | HG01891.hp2 HG02886.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-191-5541T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79524626 | |||||||
| chr6:79524750 | C | A | 1 | a0003c0003t0011g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-191-5665G>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79524750 | |||||||
| chr6:79525052 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-191-5967G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79525052 | |||||||
| chr6:79525093 | A | C | 62 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(59): Show |
124 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(121): Show |
intron_variant | MODIFIER | c.-191-6008T>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79525093 | |||||||
| chr6:79525097 | T | C | 1 | a0004c0004t0008g0155 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-191-6012A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79525097 | |||||||
| chr6:79525287 | G | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(68): Show |
146 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(143): Show |
intron_variant | MODIFIER | c.-191-6202C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79525287 | |||||||
| chr6:79525477 | C | A | 1 | a0001c0001t0002g0175 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-191-6392G>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79525477 | |||||||
| chr6:79525569 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-191-6484C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79525569 | |||||||
| chr6:79525764 | TTTGTAAC others(12): Show |
T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(72): Show |
152 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(149): Show |
intron_variant | MODIFIER | c.-191-6698_-191-668 others(23): Show |
LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79525764 | |||||||
| chr6:79526167 | A | G | 1 | a0001c0001t0002g0039 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-191-7082T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79526167 | |||||||
| chr6:79526405 | G | A | 2 | a0007c0007t0007g0204 a0007c0007t0007g0205 |
2 | HG02630.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-191-7320C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79526405 | |||||||
| chr6:79526457 | T | C | 2 | a0003c0003t0012g0095 a0003c0003t0012g0096 |
2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-191-7372A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79526457 | |||||||
| chr6:79526530 | C | A | 1 | a0004c0004t0003g0156 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-191-7445G>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79526530 | |||||||
| chr6:79526629 | C | A | 1 | a0002c0002t0001g0124 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-191-7544G>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79526629 | |||||||
| chr6:79526827 | C | A | 1 | a0002c0002t0001g0125 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-191-7742G>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79526827 | |||||||
| chr6:79526828 | A | G | 1 | a0002c0002t0001g0125 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-191-7743T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79526828 | |||||||
| chr6:79526830 | G | A | 1 | a0002c0002t0001g0125 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-191-7745C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79526830 | |||||||
| chr6:79526858 | G | A | 1 | a0001c0001t0002g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-191-7773C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79526858 | |||||||
| chr6:79527067 | T | A | 1 | a0001c0001t0001g0056 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-191-7982A>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79527067 | |||||||
| chr6:79527252 | A | G | 1 | a0001c0001t0001g0057 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-191-8167T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79527252 | |||||||
| chr6:79527295 | A | G | 1 | a0002c0002t0001g0125 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-191-8210T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79527295 | |||||||
| chr6:79527296 | G | A | 1 | a0002c0002t0001g0125 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-191-8211C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79527296 | |||||||
| chr6:79527790 | T | G | 64 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0017 others(61): Show |
100 | HG00323.hp2 HG00438.hp1 HG00738.hp1 others(97): Show |
intron_variant | MODIFIER | c.-191-8705A>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79527790 | |||||||
| chr6:79527836 | G | A | 1 | a0001c0001t0002g0177 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-191-8751C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79527836 | |||||||
| chr6:79527885 | A | C | 1 | a0002c0002t0001g0125 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-191-8800T>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79527885 | |||||||
| chr6:79527886 | C | T | 2 | a0001c0001t0002g0206 a0001c0001t0007g0009 |
7 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-191-8801G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79527886 | |||||||
| chr6:79527970 | C | T | 46 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(43): Show |
100 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.-191-8885G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79527970 | |||||||
| chr6:79527993 | A | C | 1 | a0002c0002t0001g0125 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-191-8908T>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79527993 | |||||||
| chr6:79527994 | G | A | 1 | a0002c0002t0001g0125 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-191-8909C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79527994 | |||||||
| chr6:79528055 | C | A | 1 | a0001c0001t0001g0086 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-191-8970G>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79528055 | |||||||
| chr6:79528073 | G | A | 1 | a0003c0003t0001g0214 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-191-8988C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79528073 | |||||||
| chr6:79528104 | C | T | 1 | a0003c0003t0001g0097 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-191-9019G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79528104 | |||||||
| chr6:79528138 | G | A | 2 | a0003c0003t0012g0095 a0003c0003t0012g0096 |
2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-192+9027C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79528138 | |||||||
| chr6:79528271 | C | T | 1 | a0001c0001t0001g0032 | 2 | NA18941.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.-192+8894G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79528271 | |||||||
| chr6:79528294 | G | T | 13 | a0003c0003t0005g0010 a0003c0003t0005g0046 a0003c0003t0005g0047 others(10): Show |
21 | HG01099.hp1 HG01256.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.-192+8871C>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79528294 | |||||||
| chr6:79528391 | A | G | 1 | a0001c0001t0002g0051 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-192+8774T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79528391 | |||||||
| chr6:79528484 | T | C | 2 | a0002c0002t0001g0016 a0002c0002t0001g0124 |
5 | NA18942.hp1 NA18944.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.-192+8681A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79528484 | |||||||
| chr6:79528668 | T | C | 1 | a0002c0002t0001g0125 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-192+8497A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79528668 | |||||||
| chr6:79528673 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-192+8492A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79528673 | |||||||
| chr6:79528687 | T | C | 2 | a0003c0003t0011g0098 a0003c0003t0011g0099 |
2 | HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-192+8478A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79528687 | |||||||
| chr6:79528842 | A | G | 2 | a0007c0007t0007g0204 a0007c0007t0007g0205 |
2 | HG02630.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-192+8323T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79528842 | |||||||
| chr6:79528878 | G | A | 2 | a0007c0007t0007g0204 a0007c0007t0007g0205 |
2 | HG02630.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-192+8287C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79528878 | |||||||
| chr6:79528879 | T | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(43): Show |
100 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.-192+8286A>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79528879 | |||||||
| chr6:79529060 | A | AT | 3 | a0002c0002t0001g0008 a0002c0002t0001g0100 a0002c0002t0001g0101 |
8 | HG00323.hp1 HG01192.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.-192+8104dupA | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79529060 | |||||||
| chr6:79529127 | A | G | 2 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
2 | HG00323.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.-192+8038T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79529127 | |||||||
| chr6:79529137 | T | A | 3 | a0003c0003t0001g0044 a0003c0003t0001g0045 a0003c0003t0001g0201 |
5 | HG02896.hp1 HG02897.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-192+8028A>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79529137 | |||||||
| chr6:79529142 | C | T | 13 | a0003c0003t0005g0010 a0003c0003t0005g0046 a0003c0003t0005g0047 others(10): Show |
21 | HG01099.hp1 HG01256.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.-192+8023G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79529142 | |||||||
| chr6:79529276 | A | C | 2 | a0003c0008t0001g0142 a0003c0008t0001g0143 |
2 | HG02257.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-192+7889T>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79529276 | |||||||
| chr6:79529548 | T | C | 13 | a0003c0003t0005g0010 a0003c0003t0005g0046 a0003c0003t0005g0047 others(10): Show |
21 | HG01099.hp1 HG01256.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.-192+7617A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79529548 | |||||||
| chr6:79529715 | CA | C | 13 | a0003c0003t0005g0010 a0003c0003t0005g0046 a0003c0003t0005g0047 others(10): Show |
21 | HG01099.hp1 HG01256.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.-192+7449delT | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79529715 | |||||||
| chr6:79529824 | T | A | 1 | a0003c0003t0012g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-192+7341A>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79529824 | |||||||
| chr6:79529829 | T | G | 1 | a0004c0004t0003g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-192+7336A>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79529829 | |||||||
| chr6:79529896 | A | G | 1 | a0003c0003t0005g0053 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-192+7269T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79529896 | |||||||
| chr6:79530288 | T | G | 1 | a0004c0004t0003g0178 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-192+6877A>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79530288 | |||||||
| chr6:79530324 | T | C | 3 | a0003c0003t0001g0044 a0003c0003t0001g0045 a0003c0003t0001g0201 |
5 | HG02896.hp1 HG02897.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-192+6841A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79530324 | |||||||
| chr6:79530398 | C | T | 1 | a0002c0002t0001g0100 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-192+6767G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79530398 | |||||||
| chr6:79530616 | C | T | 2 | a0001c0001t0002g0206 a0001c0001t0007g0009 |
7 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-192+6549G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79530616 | |||||||
| chr6:79530617 | G | A | 16 | a0003c0003t0004g0006 a0003c0003t0004g0029 a0003c0003t0004g0030 others(13): Show |
28 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.-192+6548C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79530617 | |||||||
| chr6:79530627 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-192+6538A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79530627 | |||||||
| chr6:79530712 | G | A | 1 | a0003c0003t0004g0188 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-192+6453C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79530712 | |||||||
| chr6:79530764 | G | C | 2 | a0003c0003t0011g0098 a0003c0003t0011g0099 |
2 | HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-192+6401C>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79530764 | |||||||
| chr6:79530828 | A | G | 1 | a0003c0008t0001g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-192+6337T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79530828 | |||||||
| chr6:79531067 | A | G | 1 | a0003c0003t0001g0097 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-192+6098T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79531067 | |||||||
| chr6:79531234 | C | T | 16 | a0001c0001t0002g0024 a0001c0001t0002g0052 a0001c0001t0002g0128 others(13): Show |
18 | HG01081.hp1 HG01175.hp1 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.-192+5931G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79531234 | |||||||
| chr6:79531302 | T | A | 39 | a0001c0001t0002g0108 a0002c0002t0001g0003 a0002c0002t0001g0008 others(36): Show |
75 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.-192+5863A>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79531302 | |||||||
| chr6:79531340 | G | A | 1 | a0001c0001t0002g0179 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-192+5825C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79531340 | |||||||
| chr6:79531419 | C | T | 4 | a0001c0001t0002g0206 a0001c0001t0007g0009 a0007c0007t0007g0204 others(1): Show |
9 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-192+5746G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79531419 | |||||||
| chr6:79531448 | T | C | 2 | a0003c0003t0001g0044 a0003c0003t0001g0045 |
4 | HG02896.hp1 HG02897.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-192+5717A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79531448 | |||||||
| chr6:79531459 | A | G | 1 | a0001c0001t0002g0126 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-192+5706T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79531459 | |||||||
| chr6:79531460 | A | G | 1 | a0001c0001t0002g0051 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-192+5705T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79531460 | |||||||
| chr6:79531579 | G | A | 13 | a0003c0003t0005g0010 a0003c0003t0005g0046 a0003c0003t0005g0047 others(10): Show |
21 | HG01099.hp1 HG01256.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.-192+5586C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79531579 | |||||||
| chr6:79531656 | C | T | 2 | a0003c0003t0012g0095 a0003c0003t0012g0096 |
2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-192+5509G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79531656 | |||||||
| chr6:79531798 | C | T | 4 | a0003c0003t0001g0217 a0003c0003t0001g0218 a0003c0003t0001g0219 others(1): Show |
4 | HG01891.hp2 HG02886.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-192+5367G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79531798 | |||||||
| chr6:79531878 | C | A | 24 | a0003c0003t0001g0214 a0003c0003t0001g0217 a0003c0003t0001g0218 others(21): Show |
36 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.-192+5287G>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79531878 | |||||||
| chr6:79531964 | T | C | 13 | a0003c0003t0005g0010 a0003c0003t0005g0046 a0003c0003t0005g0047 others(10): Show |
21 | HG01099.hp1 HG01256.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.-192+5201A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79531964 | |||||||
| chr6:79532125 | T | C | 1 | a0003c0003t0004g0200 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-192+5040A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79532125 | |||||||
| chr6:79532795 | A | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(106): Show |
217 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(214): Show |
intron_variant | MODIFIER | c.-192+4370T>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79532795 | |||||||
| chr6:79532967 | A | T | 1 | a0001c0001t0002g0094 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-192+4198T>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79532967 | |||||||
| chr6:79533054 | T | G | 1 | a0001c0001t0002g0189 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-192+4111A>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79533054 | |||||||
| chr6:79533152 | C | A | 1 | a0003c0003t0001g0214 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-192+4013G>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79533152 | |||||||
| chr6:79533199 | A | C | 3 | a0002c0002t0001g0036 a0002c0002t0001g0092 a0002c0002t0001g0093 |
4 | HG02165.hp2 HG02523.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.-192+3966T>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79533199 | |||||||
| chr6:79533276 | T | C | 7 | a0001c0001t0002g0007 a0001c0001t0002g0031 a0001c0001t0002g0190 others(4): Show |
17 | HG01255.hp2 HG01261.hp2 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.-192+3889A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79533276 | |||||||
| chr6:79533635 | C | CA | 6 | a0001c0001t0002g0195 a0001c0001t0002g0196 a0003c0003t0001g0044 others(3): Show |
8 | HG01257.hp2 HG01258.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-192+3529dupT | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79533635 | |||||||
| chr6:79533635 | CA | C | 13 | a0003c0003t0005g0010 a0003c0003t0005g0046 a0003c0003t0005g0047 others(10): Show |
21 | HG01099.hp1 HG01256.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.-192+3529delT | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79533635 | |||||||
| chr6:79533865 | G | C | 2 | a0001c0001t0002g0206 a0001c0001t0007g0009 |
7 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-192+3300C>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79533865 | |||||||
| chr6:79533922 | C | T | 46 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(43): Show |
100 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.-192+3243G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79533922 | |||||||
| chr6:79534062 | TTACACTG | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0056 |
4 | NA18940.hp2 NA18953.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-192+3096_-192+310 others(11): Show |
LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79534062 | |||||||
| chr6:79534067 | C | G | 30 | a0001c0001t0001g0062 a0001c0001t0002g0206 a0001c0001t0007g0009 others(27): Show |
47 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.-192+3098G>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79534067 | |||||||
| chr6:79534133 | C | T | 3 | a0005c0005t0001g0005 a0005c0005t0001g0090 a0005c0005t0001g0091 |
11 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-192+3032G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79534133 | |||||||
| chr6:79534139 | G | A | 5 | a0003c0003t0004g0030 a0003c0003t0004g0197 a0003c0003t0004g0198 others(2): Show |
7 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.-192+3026C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79534139 | |||||||
| chr6:79534349 | C | T | 1 | a0001c0001t0002g0089 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-192+2816G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79534349 | |||||||
| chr6:79534462 | G | A | 3 | a0003c0003t0001g0044 a0003c0003t0001g0045 a0003c0003t0001g0201 |
5 | HG02896.hp1 HG02897.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-192+2703C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79534462 | |||||||
| chr6:79534469 | G | A | 2 | a0001c0001t0002g0202 a0001c0001t0002g0203 |
2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-192+2696C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79534469 | |||||||
| chr6:79534718 | T | C | 2 | a0007c0007t0007g0204 a0007c0007t0007g0205 |
2 | HG02630.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-192+2447A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79534718 | |||||||
| chr6:79534831 | A | G | 46 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(43): Show |
100 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.-192+2334T>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79534831 | |||||||
| chr6:79535099 | A | T | 1 | a0001c0001t0001g0055 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-192+2066T>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79535099 | |||||||
| chr6:79535424 | T | C | 2 | a0001c0001t0002g0206 a0001c0001t0007g0009 |
7 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-192+1741A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79535424 | |||||||
| chr6:79535688 | C | T | 13 | a0003c0003t0005g0010 a0003c0003t0005g0046 a0003c0003t0005g0047 others(10): Show |
21 | HG01099.hp1 HG01256.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.-192+1477G>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79535688 | |||||||
| chr6:79535740 | G | C | 1 | a0001c0001t0002g0031 | 3 | HG01255.hp2 HG01261.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.-192+1425C>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79535740 | |||||||
| chr6:79536189 | G | A | 13 | a0003c0003t0005g0010 a0003c0003t0005g0046 a0003c0003t0005g0047 others(10): Show |
21 | HG01099.hp1 HG01256.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.-192+976C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79536189 | |||||||
| chr6:79536250 | G | A | 4 | a0003c0003t0001g0217 a0003c0003t0001g0218 a0003c0003t0001g0219 others(1): Show |
4 | HG01891.hp2 HG02886.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-192+915C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79536250 | |||||||
| chr6:79536357 | A | C | 2 | a0003c0003t0005g0053 a0003c0003t0005g0054 |
2 | HG01256.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-192+808T>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79536357 | |||||||
| chr6:79536413 | T | C | 1 | a0003c0003t0001g0214 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-192+752A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79536413 | |||||||
| chr6:79536512 | C | G | 1 | a0001c0001t0002g0052 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-192+653G>C | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79536512 | |||||||
| chr6:79536575 | T | C | 1 | a0004c0004t0003g0215 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-192+590A>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79536575 | |||||||
| chr6:79536768 | A | T | 1 | a0001c0001t0002g0051 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-192+397T>A | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79536768 | |||||||
| chr6:79537095 | G | A | 5 | a0003c0003t0001g0217 a0003c0003t0001g0218 a0003c0003t0001g0219 others(2): Show |
5 | HG01891.hp2 HG02886.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-192+70C>T | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79537095 | |||||||
| chr6:79537103 | A | C | 1 | a0006c0006t0001g0014 | 4 | HG02056.hp1 HG02135.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.-192+62T>G | LCA5 | ENSG00000135338.14 | transcript | ENST00000369846.9 | protein_coding | 1/7 | chr6 | 79537103 |