Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 341883 |
| ensemblid | ENSG00000131951.12 |
| hgncid | 19848 |
| symbol | LRRC9 |
| name | leucine rich repeat containing 9 |
| refseq_nuc | NM_001395648.1 |
| refseq_prot | NP_001382577.1 |
| ensembl_nuc | ENST00000570145.2 |
| ensembl_prot | ENSP00000457773.2 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 59920144 |
| end | 60066817 |
| strand | + |
| ver | v1.2 |
| region | chr14:59920144-60066817 |
| region5000 | chr14:59915144-60071817 |
| regionname0 | LRRC9_chr14_59920144_60066817 |
| regionname5000 | LRRC9_chr14_59915144_60071817 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1494 | 280 | 61 | 54 | 125 | 10 | 28 | 95 | LRRC9_chr14_59915144_60071817 | LRRC9 | MIESE others(1489): Show |
chr14 | 59915144 | 60071817 |
| a0002 | 0/0 | 1494 | 21 | 0 | 0 | 21 | 0 | 0 | 21 | LRRC9_chr14_59915144_60071817 | LRRC9 | MIESE others(1489): Show |
chr14 | 59915144 | 60071817 |
| a0003 | 0/0 | 1494 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | LRRC9_chr14_59915144_60071817 | LRRC9 | MIESE others(1489): Show |
chr14 | 59915144 | 60071817 |
| a0004 | 0/0 | 1494 | 3 | 0 | 0 | 2 | 0 | 1 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | MIESE others(1489): Show |
chr14 | 59915144 | 60071817 |
| a0005 | 0/0 | 1037 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | MIESE others(1032): Show |
chr14 | 59915144 | 60071817 |
| a0006 | 0/0 | 1494 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | MIESE others(1489): Show |
chr14 | 59915144 | 60071817 |
| a0007 | 0/0 | 1494 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | MIESE others(1489): Show |
chr14 | 59915144 | 60071817 |
| a0008 | 0/0 | 1494 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | MIESE others(1489): Show |
chr14 | 59915144 | 60071817 |
| a0009 | 0/0 | 1494 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | MIESE others(1489): Show |
chr14 | 59915144 | 60071817 |
| a0010 | 0/0 | 1494 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | MIESE others(1489): Show |
chr14 | 59915144 | 60071817 |
| a0011 | 0/0 | 1494 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | MIESE others(1489): Show |
chr14 | 59915144 | 60071817 |
| a0012 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | MIESE others(1489): Show |
chr14 | 59915144 | 60071817 |
| a0013 | 0/0 | 1494 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | MIESE others(1489): Show |
chr14 | 59915144 | 60071817 |
| a0014 | 0/0 | 1494 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | MIESE others(1489): Show |
chr14 | 59915144 | 60071817 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 4482 | 158 | 28 | 36 | 70 | 9 | 14 | LRRC9_chr14_59915144_60071817 | LRRC9 | ATGAT others(4477): Show |
chr14 | 59915144 | 60071817 | ||
| a0001c0002 | 1/0 | 4482 | 97 | 28 | 14 | 46 | 0 | 8 | LRRC9_chr14_59915144_60071817 | LRRC9 | ATGAT others(4477): Show |
chr14 | 59915144 | 60071817 | ||
| a0001c0004 | 0/0 | 4482 | 10 | 0 | 3 | 4 | 1 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | ATGAT others(4477): Show |
chr14 | 59915144 | 60071817 | ||
| a0001c0005 | 0/0 | 4482 | 8 | 5 | 1 | 0 | 0 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | ATGAT others(4477): Show |
chr14 | 59915144 | 60071817 | ||
| a0001c0006 | 0/0 | 4482 | 5 | 0 | 0 | 5 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | ATGAT others(4477): Show |
chr14 | 59915144 | 60071817 | ||
| a0001c0012 | 0/0 | 4482 | 2 | 0 | 0 | 0 | 0 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | ATGAT others(4477): Show |
chr14 | 59915144 | 60071817 | ||
| a0002c0003 | 0/0 | 4482 | 21 | 0 | 0 | 21 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | ATGAT others(4477): Show |
chr14 | 59915144 | 60071817 | ||
| a0003c0007 | 0/0 | 4482 | 4 | 0 | 0 | 4 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | ATGAT others(4477): Show |
chr14 | 59915144 | 60071817 | ||
| a0004c0008 | 0/0 | 4482 | 3 | 0 | 0 | 2 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | ATGAT others(4477): Show |
chr14 | 59915144 | 60071817 | ||
| a0005c0011 | 0/0 | 4482 | 2 | 0 | 0 | 0 | 2 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | ATGAT others(4477): Show |
chr14 | 59915144 | 60071817 | ||
| a0006c0010 | 0/0 | 4482 | 2 | 2 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | ATGAT others(4477): Show |
chr14 | 59915144 | 60071817 | ||
| a0007c0013 | 0/0 | 4482 | 2 | 2 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | ATGAT others(4477): Show |
chr14 | 59915144 | 60071817 | ||
| a0008c0009 | 0/0 | 4482 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | ATGAT others(4477): Show |
chr14 | 59915144 | 60071817 | ||
| a0009c0017 | 0/0 | 4482 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | ATGAT others(4477): Show |
chr14 | 59915144 | 60071817 | ||
| a0010c0015 | 0/0 | 4482 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | ATGAT others(4477): Show |
chr14 | 59915144 | 60071817 | ||
| a0011c0014 | 0/0 | 4482 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | ATGAT others(4477): Show |
chr14 | 59915144 | 60071817 | ||
| a0012c0018 | 0/0 | 4482 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | ATGAT others(4477): Show |
chr14 | 59915144 | 60071817 | ||
| a0013c0016 | 0/0 | 4482 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | ATGAT others(4477): Show |
chr14 | 59915144 | 60071817 | ||
| a0014c0019 | 0/0 | 4482 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | ATGAT others(4477): Show |
chr14 | 59915144 | 60071817 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 8425 | 52 | 17 | 3 | 27 | 1 | 3 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8420): Show |
chr14 | 59915144 | 60071817 |
| a0001c0001t0003 | 0/0 | 8426 | 31 | 2 | 14 | 9 | 4 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8421): Show |
chr14 | 59915144 | 60071817 |
| a0001c0001t0006 | 0/0 | 8427 | 10 | 1 | 4 | 3 | 0 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8422): Show |
chr14 | 59915144 | 60071817 |
| a0001c0001t0008 | 0/0 | 8425 | 11 | 1 | 5 | 0 | 3 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8420): Show |
chr14 | 59915144 | 60071817 |
| a0001c0001t0010 | 0/0 | 8425 | 8 | 0 | 1 | 7 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8420): Show |
chr14 | 59915144 | 60071817 |
| a0001c0001t0011 | 0/0 | 8413 | 8 | 4 | 0 | 4 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8408): Show |
chr14 | 59915144 | 60071817 |
| a0001c0001t0014 | 0/0 | 8427 | 7 | 1 | 2 | 3 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8422): Show |
chr14 | 59915144 | 60071817 |
| a0001c0001t0015 | 0/0 | 8426 | 4 | 0 | 0 | 4 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8421): Show |
chr14 | 59915144 | 60071817 |
| a0001c0001t0016 | 0/0 | 8424 | 4 | 0 | 2 | 2 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8419): Show |
chr14 | 59915144 | 60071817 |
| a0001c0001t0019 | 0/0 | 8426 | 3 | 1 | 0 | 1 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8421): Show |
chr14 | 59915144 | 60071817 |
| a0001c0001t0023 | 0/0 | 8414 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8409): Show |
chr14 | 59915144 | 60071817 |
| a0001c0001t0027 | 0/0 | 8424 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8419): Show |
chr14 | 59915144 | 60071817 |
| a0001c0001t0028 | 0/0 | 8425 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8420): Show |
chr14 | 59915144 | 60071817 |
| a0001c0001t0030 | 0/0 | 8426 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8421): Show |
chr14 | 59915144 | 60071817 |
| a0001c0001t0031 | 0/0 | 8425 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8420): Show |
chr14 | 59915144 | 60071817 |
| a0001c0001t0032 | 0/0 | 8425 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8420): Show |
chr14 | 59915144 | 60071817 |
| a0001c0001t0033 | 0/0 | 8425 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8420): Show |
chr14 | 59915144 | 60071817 |
| a0001c0001t0034 | 0/0 | 8428 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8423): Show |
chr14 | 59915144 | 60071817 |
| a0001c0001t0035 | 0/0 | 8103 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8098): Show |
chr14 | 59915144 | 60071817 |
| a0001c0001t0036 | 0/0 | 8427 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8422): Show |
chr14 | 59915144 | 60071817 |
| a0001c0001t0037 | 0/0 | 8426 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8421): Show |
chr14 | 59915144 | 60071817 |
| a0001c0001t0039 | 0/0 | 8427 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8422): Show |
chr14 | 59915144 | 60071817 |
| a0001c0001t0040 | 0/0 | 8426 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8421): Show |
chr14 | 59915144 | 60071817 |
| a0001c0001t0041 | 0/0 | 8425 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8420): Show |
chr14 | 59915144 | 60071817 |
| a0001c0001t0042 | 0/0 | 8426 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8421): Show |
chr14 | 59915144 | 60071817 |
| a0001c0001t0043 | 0/0 | 8426 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8421): Show |
chr14 | 59915144 | 60071817 |
| a0001c0001t0044 | 0/0 | 8424 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8419): Show |
chr14 | 59915144 | 60071817 |
| a0001c0001t0045 | 0/0 | 8425 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8420): Show |
chr14 | 59915144 | 60071817 |
| a0001c0002t0002 | 0/0 | 8102 | 37 | 9 | 12 | 9 | 0 | 7 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8097): Show |
chr14 | 59915144 | 60071817 |
| a0001c0002t0004 | 0/0 | 8102 | 24 | 4 | 1 | 19 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8097): Show |
chr14 | 59915144 | 60071817 |
| a0001c0002t0007 | 0/0 | 8102 | 11 | 0 | 0 | 11 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8097): Show |
chr14 | 59915144 | 60071817 |
| a0001c0002t0012 | 0/0 | 8102 | 8 | 8 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8097): Show |
chr14 | 59915144 | 60071817 |
| a0001c0002t0017 | 0/0 | 8102 | 4 | 3 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8097): Show |
chr14 | 59915144 | 60071817 |
| a0001c0002t0020 | 0/0 | 8101 | 3 | 0 | 0 | 3 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8096): Show |
chr14 | 59915144 | 60071817 |
| a0001c0002t0021 | 0/0 | 8103 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8098): Show |
chr14 | 59915144 | 60071817 |
| a0001c0002t0022 | 0/0 | 8103 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8098): Show |
chr14 | 59915144 | 60071817 |
| a0001c0002t0024 | 1/0 | 8103 | 2 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8098): Show |
chr14 | 59915144 | 60071817 |
| a0001c0002t0025 | 0/0 | 8103 | 2 | 1 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8098): Show |
chr14 | 59915144 | 60071817 |
| a0001c0002t0026 | 0/0 | 8102 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8097): Show |
chr14 | 59915144 | 60071817 |
| a0001c0002t0029 | 0/0 | 8102 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8097): Show |
chr14 | 59915144 | 60071817 |
| a0001c0004t0009 | 0/0 | 8103 | 10 | 0 | 3 | 4 | 1 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8098): Show |
chr14 | 59915144 | 60071817 |
| a0001c0005t0013 | 0/0 | 8102 | 7 | 4 | 1 | 0 | 0 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8097): Show |
chr14 | 59915144 | 60071817 |
| a0001c0005t0038 | 0/0 | 8102 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8097): Show |
chr14 | 59915144 | 60071817 |
| a0001c0006t0002 | 0/0 | 8102 | 5 | 0 | 0 | 5 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8097): Show |
chr14 | 59915144 | 60071817 |
| a0001c0012t0002 | 0/0 | 8102 | 2 | 0 | 0 | 0 | 0 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8097): Show |
chr14 | 59915144 | 60071817 |
| a0002c0003t0005 | 0/0 | 8101 | 21 | 0 | 0 | 21 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8096): Show |
chr14 | 59915144 | 60071817 |
| a0003c0007t0004 | 0/0 | 8102 | 4 | 0 | 0 | 4 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8097): Show |
chr14 | 59915144 | 60071817 |
| a0004c0008t0010 | 0/0 | 8425 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8420): Show |
chr14 | 59915144 | 60071817 |
| a0004c0008t0015 | 0/0 | 8426 | 2 | 0 | 0 | 1 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8421): Show |
chr14 | 59915144 | 60071817 |
| a0005c0011t0003 | 0/0 | 8426 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8421): Show |
chr14 | 59915144 | 60071817 |
| a0005c0011t0006 | 0/0 | 8427 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8422): Show |
chr14 | 59915144 | 60071817 |
| a0006c0010t0018 | 0/0 | 8102 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8097): Show |
chr14 | 59915144 | 60071817 |
| a0006c0010t0021 | 0/0 | 8103 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8098): Show |
chr14 | 59915144 | 60071817 |
| a0007c0013t0018 | 0/0 | 8102 | 2 | 2 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8097): Show |
chr14 | 59915144 | 60071817 |
| a0008c0009t0005 | 0/0 | 8101 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8096): Show |
chr14 | 59915144 | 60071817 |
| a0009c0017t0003 | 0/0 | 8426 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8421): Show |
chr14 | 59915144 | 60071817 |
| a0010c0015t0003 | 0/0 | 8426 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8421): Show |
chr14 | 59915144 | 60071817 |
| a0011c0014t0006 | 0/0 | 8427 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8422): Show |
chr14 | 59915144 | 60071817 |
| a0012c0018t0003 | 0/0 | 8426 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8421): Show |
chr14 | 59915144 | 60071817 |
| a0013c0016t0004 | 0/0 | 8102 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8097): Show |
chr14 | 59915144 | 60071817 |
| a0014c0019t0005 | 0/0 | 8101 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | AGTCT others(8096): Show |
chr14 | 59915144 | 60071817 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0220 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0006g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0006g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0006g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0006g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0006g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0006g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0006g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0006g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0006g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0008g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0008g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0008g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0008g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0008g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0008g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0008g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0008g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0008g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0008g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0008g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0010g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0010g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0010g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0010g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0010g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0010g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0010g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0010g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0011g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0011g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0011g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0011g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0011g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0011g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0011g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0011g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0014g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0014g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0014g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0014g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0014g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0014g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0014g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0015g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0015g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0015g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0015g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0016g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0016g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0016g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0016g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0019g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0019g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0019g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0023g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0023g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0027g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0027g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0028g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0030g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0031g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0032g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0033g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0034g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0035g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0036g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0037g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0039g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0040g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0041g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0042g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0043g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0044g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0045g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0007g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0007g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0007g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0007g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0007g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0007g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0007g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0007g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0007g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0007g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0012g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0012g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0012g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0012g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0012g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0012g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0012g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0012g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0017g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0017g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0017g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0017g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0020g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0020g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0020g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0021g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0022g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0022g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0024g0101 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0024g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0025g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0025g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0026g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0026g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0029g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0004t0009g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0004t0009g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0004t0009g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0004t0009g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0004t0009g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0004t0009g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0004t0009g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0004t0009g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0004t0009g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0004t0009g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0005t0013g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0005t0013g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0005t0013g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0005t0013g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0005t0013g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0005t0013g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0005t0013g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0005t0038g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0006t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0006t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0006t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0006t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0006t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0012t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0012t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0003c0007t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0003c0007t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0003c0007t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0003c0007t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0004c0008t0010g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0004c0008t0015g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0004c0008t0015g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0005c0011t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0005c0011t0006g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0006c0010t0018g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0006c0010t0021g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0007c0013t0018g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0007c0013t0018g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0008c0009t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0008c0009t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0009c0017t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0010c0015t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0011c0014t0006g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0012c0018t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0013c0016t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0014c0019t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0005 | c0011 | t0003 | g0211 | EUR | GBR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0039 | EUR | GBR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00280 | hp1 | a0001 | c0001 | t0008 | g0041 | EUR | FIN | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00280 | hp2 | a0005 | c0011 | t0006 | g0212 | EUR | FIN | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0259 | EUR | FIN | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00323 | hp2 | a0001 | c0004 | t0009 | g0304 | EUR | FIN | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00423 | hp1 | a0001 | c0001 | t0010 | g0028 | EAS | CHS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00423 | hp2 | a0001 | c0001 | t0006 | g0071 | EAS | CHS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00558 | hp2 | a0001 | c0002 | t0020 | g0282 | EAS | CHS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00609 | hp1 | a0001 | c0002 | t0004 | g0319 | EAS | CHS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00621 | hp1 | a0001 | c0001 | t0016 | g0051 | EAS | CHS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00621 | hp2 | a0001 | c0001 | t0016 | g0206 | EAS | CHS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0178 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00639 | hp2 | a0001 | c0001 | t0008 | g0011 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00642 | hp1 | a0001 | c0004 | t0009 | g0309 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0296 | EAS | CHS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00673 | hp2 | a0001 | c0001 | t0014 | g0249 | EAS | CHS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00735 | hp1 | a0001 | c0004 | t0009 | g0302 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0258 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0255 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00738 | hp2 | a0001 | c0001 | t0010 | g0067 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00741 | hp1 | a0001 | c0001 | t0006 | g0244 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00741 | hp2 | a0001 | c0001 | t0043 | g0012 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01074 | hp1 | a0001 | c0001 | t0016 | g0105 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01074 | hp2 | a0001 | c0001 | t0016 | g0023 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01081 | hp2 | a0001 | c0001 | t0008 | g0010 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0131 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01109 | hp2 | a0001 | c0002 | t0017 | g0141 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01168 | hp1 | a0001 | c0001 | t0008 | g0013 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0262 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01169 | hp2 | a0009 | c0017 | t0003 | g0065 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0107 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01175 | hp2 | a0001 | c0001 | t0008 | g0032 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0216 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0119 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0145 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01243 | hp2 | a0001 | c0002 | t0004 | g0004 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0177 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0038 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0138 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01258 | hp1 | a0001 | c0001 | t0008 | g0007 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0139 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0137 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0024 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01358 | hp1 | a0001 | c0001 | t0014 | g0103 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01358 | hp2 | a0001 | c0005 | t0013 | g0151 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01361 | hp1 | a0001 | c0001 | t0034 | g0098 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01361 | hp2 | a0001 | c0004 | t0009 | g0303 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0174 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01496 | hp1 | a0001 | c0001 | t0039 | g0068 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01496 | hp2 | a0001 | c0001 | t0035 | g0156 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01515 | hp1 | a0001 | c0001 | t0008 | g0009 | EUR | IBS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0254 | EUR | IBS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01516 | hp1 | a0001 | c0001 | t0008 | g0155 | EUR | IBS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0261 | EUR | IBS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0260 | EUR | IBS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01517 | hp2 | a0001 | c0001 | t0044 | g0008 | EUR | IBS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0112 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0242 | AMR | PEL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01928 | hp2 | a0001 | c0001 | t0006 | g0099 | AMR | PEL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01934 | hp1 | a0010 | c0015 | t0003 | g0164 | AMR | PEL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01934 | hp2 | a0001 | c0001 | t0014 | g0248 | AMR | PEL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0170 | AMR | PEL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0239 | AMR | PEL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0149 | AMR | PEL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0228 | AMR | PEL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0102 | AMR | PEL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0245 | AMR | PEL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02015 | hp2 | a0001 | c0002 | t0007 | g0275 | EAS | KHV | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02040 | hp1 | a0001 | c0002 | t0004 | g0289 | EAS | KHV | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02040 | hp2 | a0001 | c0001 | t0014 | g0035 | EAS | KHV | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02055 | hp1 | a0001 | c0005 | t0013 | g0179 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0006 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02071 | hp1 | a0001 | c0002 | t0004 | g0273 | EAS | KHV | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02074 | hp1 | a0001 | c0006 | t0002 | g0114 | EAS | KHV | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02074 | hp2 | a0001 | c0001 | t0023 | g0049 | EAS | KHV | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02080 | hp1 | a0001 | c0006 | t0002 | g0109 | EAS | KHV | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02080 | hp2 | a0001 | c0002 | t0022 | g0270 | EAS | KHV | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02132 | hp1 | a0001 | c0002 | t0022 | g0269 | EAS | KHV | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02132 | hp2 | a0001 | c0006 | t0002 | g0116 | EAS | KHV | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02145 | hp1 | a0001 | c0005 | t0013 | g0180 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02145 | hp2 | a0001 | c0002 | t0025 | g0113 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0064 | AMR | PEL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0312 | AMR | PEL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0128 | EAS | CDX | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02155 | hp2 | a0001 | c0001 | t0010 | g0026 | EAS | CDX | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02165 | hp1 | a0001 | c0001 | t0010 | g0076 | EAS | CDX | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02165 | hp2 | a0001 | c0002 | t0004 | g0287 | EAS | CDX | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02257 | hp1 | a0001 | c0002 | t0021 | g0161 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02258 | hp1 | a0001 | c0001 | t0033 | g0063 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0146 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0168 | AMR | PEL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02273 | hp2 | a0001 | c0001 | t0040 | g0104 | AMR | PEL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02280 | hp1 | a0001 | c0005 | t0013 | g0181 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02572 | hp2 | a0001 | c0002 | t0004 | g0310 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02602 | hp1 | a0001 | c0001 | t0042 | g0184 | SAS | PJL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02602 | hp2 | a0001 | c0012 | t0002 | g0106 | SAS | PJL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0152 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0169 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02622 | hp2 | a0001 | c0002 | t0012 | g0122 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02683 | hp1 | a0001 | c0002 | t0025 | g0135 | SAS | PJL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02683 | hp2 | a0001 | c0001 | t0008 | g0031 | SAS | PJL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02717 | hp2 | a0001 | c0002 | t0012 | g0147 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02735 | hp1 | a0011 | c0014 | t0006 | g0162 | SAS | PJL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02735 | hp2 | a0001 | c0005 | t0013 | g0172 | SAS | PJL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0158 | SAS | PJL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02738 | hp2 | a0004 | c0008 | t0015 | g0167 | SAS | PJL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02809 | hp1 | a0001 | c0002 | t0012 | g0121 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0095 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02818 | hp1 | a0001 | c0002 | t0017 | g0117 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02895 | hp1 | a0001 | c0002 | t0012 | g0123 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02896 | hp2 | a0001 | c0002 | t0012 | g0125 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0207 | AFR | ESN | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02922 | hp2 | a0001 | c0001 | t0011 | g0079 | AFR | ESN | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03139 | hp1 | a0007 | c0013 | t0018 | g0110 | AFR | ESN | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03139 | hp2 | a0001 | c0001 | t0011 | g0021 | AFR | ESN | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03195 | hp1 | a0012 | c0018 | t0003 | g0230 | AFR | ESN | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03195 | hp2 | a0001 | c0002 | t0017 | g0142 | AFR | ESN | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03209 | hp1 | a0001 | c0002 | t0012 | g0148 | AFR | MSL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03453 | hp1 | a0001 | c0002 | t0029 | g0017 | AFR | MSL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03453 | hp2 | a0001 | c0002 | t0012 | g0120 | AFR | MSL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03516 | hp1 | a0001 | c0001 | t0019 | g0083 | AFR | ESN | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03516 | hp2 | a0001 | c0002 | t0024 | g0157 | AFR | ESN | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03540 | hp1 | a0001 | c0005 | t0013 | g0182 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0159 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03579 | hp1 | a0001 | c0002 | t0017 | g0175 | AFR | MSL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03579 | hp2 | a0001 | c0001 | t0014 | g0066 | AFR | MSL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0136 | SAS | PJL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0022 | SAS | PJL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03669 | hp1 | a0001 | c0001 | t0006 | g0163 | SAS | PJL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0256 | SAS | PJL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03688 | hp1 | a0001 | c0001 | t0019 | g0315 | SAS | STU | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0176 | SAS | STU | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03710 | hp1 | a0001 | c0001 | t0032 | g0320 | SAS | PJL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03710 | hp2 | a0001 | c0004 | t0009 | g0308 | SAS | PJL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | BEB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0233 | SAS | BEB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03834 | hp2 | a0001 | c0012 | t0002 | g0140 | SAS | BEB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03927 | hp1 | a0001 | c0001 | t0014 | g0046 | SAS | BEB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0127 | SAS | BEB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03942 | hp1 | a0001 | c0005 | t0013 | g0171 | SAS | BEB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03942 | hp2 | a0001 | c0001 | t0030 | g0160 | SAS | BEB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | STU | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG04199 | hp2 | a0001 | c0001 | t0006 | g0241 | SAS | STU | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG04204 | hp1 | a0001 | c0004 | t0009 | g0307 | SAS | STU | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG04204 | hp2 | a0001 | c0001 | t0008 | g0154 | SAS | STU | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0133 | SAS | STU | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | STU | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0144 | AFR | YRI | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | YRI | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18612 | hp1 | a0001 | c0001 | t0010 | g0053 | EAS | CHB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18612 | hp2 | a0001 | c0006 | t0002 | g0115 | EAS | CHB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18747 | hp1 | a0001 | c0001 | t0037 | g0247 | EAS | CHB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18747 | hp2 | a0001 | c0001 | t0023 | g0059 | EAS | CHB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | YRI | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18906 | hp2 | a0001 | c0002 | t0004 | g0214 | AFR | YRI | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18939 | hp1 | a0001 | c0001 | t0041 | g0229 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18939 | hp2 | a0002 | c0003 | t0005 | g0001 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0134 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18941 | hp2 | a0002 | c0003 | t0005 | g0205 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18942 | hp1 | a0001 | c0001 | t0011 | g0073 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18942 | hp2 | a0001 | c0002 | t0020 | g0283 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18943 | hp1 | a0001 | c0002 | t0004 | g0265 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0118 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18945 | hp1 | a0001 | c0001 | t0006 | g0020 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18945 | hp2 | a0002 | c0003 | t0005 | g0202 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18946 | hp2 | a0001 | c0004 | t0009 | g0306 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18948 | hp1 | a0001 | c0004 | t0009 | g0305 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18950 | hp1 | a0001 | c0001 | t0011 | g0074 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18950 | hp2 | a0001 | c0002 | t0004 | g0278 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18960 | hp2 | a0002 | c0003 | t0005 | g0001 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18961 | hp2 | a0003 | c0007 | t0004 | g0276 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18962 | hp1 | a0003 | c0007 | t0004 | g0277 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18962 | hp2 | a0001 | c0004 | t0009 | g0209 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18964 | hp1 | a0001 | c0002 | t0004 | g0318 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18964 | hp2 | a0002 | c0003 | t0005 | g0199 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18966 | hp1 | a0013 | c0016 | t0004 | g0267 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18966 | hp2 | a0001 | c0001 | t0015 | g0052 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18968 | hp2 | a0001 | c0002 | t0004 | g0285 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18975 | hp2 | a0002 | c0003 | t0005 | g0190 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18977 | hp1 | a0002 | c0003 | t0005 | g0188 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18977 | hp2 | a0001 | c0001 | t0010 | g0043 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18978 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18978 | hp2 | a0004 | c0008 | t0010 | g0055 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18979 | hp2 | a0001 | c0002 | t0004 | g0284 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18980 | hp1 | a0001 | c0002 | t0004 | g0281 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18981 | hp1 | a0001 | c0002 | t0004 | g0300 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0129 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18983 | hp2 | a0008 | c0009 | t0005 | g0191 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18984 | hp1 | a0002 | c0003 | t0005 | g0186 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18986 | hp2 | a0003 | c0007 | t0004 | g0280 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18988 | hp1 | a0002 | c0003 | t0005 | g0196 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18988 | hp2 | a0001 | c0002 | t0004 | g0295 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18989 | hp1 | a0001 | c0002 | t0007 | g0290 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18989 | hp2 | a0001 | c0001 | t0011 | g0075 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18990 | hp2 | a0001 | c0002 | t0004 | g0288 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18992 | hp1 | a0002 | c0003 | t0005 | g0195 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18992 | hp2 | a0001 | c0002 | t0020 | g0301 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18993 | hp1 | a0001 | c0001 | t0028 | g0030 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18993 | hp2 | a0001 | c0002 | t0004 | g0286 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18994 | hp1 | a0001 | c0001 | t0010 | g0034 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18994 | hp2 | a0001 | c0002 | t0004 | g0268 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18995 | hp1 | a0002 | c0003 | t0005 | g0187 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18995 | hp2 | a0001 | c0001 | t0031 | g0219 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18998 | hp1 | a0001 | c0002 | t0007 | g0002 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18999 | hp2 | a0002 | c0003 | t0005 | g0201 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19002 | hp1 | a0001 | c0001 | t0045 | g0232 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0297 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19004 | hp1 | a0002 | c0003 | t0005 | g0197 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19006 | hp1 | a0001 | c0002 | t0007 | g0266 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19006 | hp2 | a0001 | c0001 | t0015 | g0060 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19007 | hp2 | a0001 | c0002 | t0007 | g0294 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0126 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19011 | hp2 | a0001 | c0001 | t0015 | g0062 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19012 | hp1 | a0001 | c0001 | t0006 | g0072 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19012 | hp2 | a0002 | c0003 | t0005 | g0185 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0215 | AFR | LWK | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | LWK | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19055 | hp1 | a0001 | c0004 | t0009 | g0210 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19055 | hp2 | a0002 | c0003 | t0005 | g0189 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19057 | hp2 | a0001 | c0002 | t0007 | g0274 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19059 | hp1 | a0001 | c0002 | t0004 | g0272 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19059 | hp2 | a0001 | c0001 | t0014 | g0040 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19065 | hp1 | a0001 | c0002 | t0026 | g0132 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19065 | hp2 | a0002 | c0003 | t0005 | g0192 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19066 | hp1 | a0001 | c0002 | t0026 | g0130 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19067 | hp1 | a0004 | c0008 | t0015 | g0036 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19067 | hp2 | a0001 | c0002 | t0007 | g0317 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19068 | hp2 | a0002 | c0003 | t0005 | g0198 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19070 | hp1 | a0002 | c0003 | t0005 | g0200 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19075 | hp1 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19075 | hp2 | a0001 | c0002 | t0007 | g0293 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19078 | hp1 | a0001 | c0002 | t0004 | g0316 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19078 | hp2 | a0001 | c0001 | t0036 | g0314 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19079 | hp1 | a0002 | c0003 | t0005 | g0194 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19079 | hp2 | a0001 | c0001 | t0015 | g0096 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19080 | hp2 | a0001 | c0002 | t0004 | g0298 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19081 | hp1 | a0014 | c0019 | t0005 | g0042 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19081 | hp2 | a0001 | c0002 | t0007 | g0292 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19082 | hp1 | a0001 | c0006 | t0002 | g0108 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19083 | hp1 | a0001 | c0002 | t0004 | g0271 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19084 | hp2 | a0001 | c0002 | t0007 | g0002 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19085 | hp2 | a0002 | c0003 | t0005 | g0193 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19086 | hp1 | a0002 | c0003 | t0005 | g0204 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19087 | hp1 | a0001 | c0001 | t0010 | g0054 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19087 | hp2 | a0003 | c0007 | t0004 | g0279 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19088 | hp1 | a0008 | c0009 | t0005 | g0203 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19088 | hp2 | a0001 | c0001 | t0027 | g0235 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19090 | hp1 | a0001 | c0001 | t0019 | g0311 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19090 | hp2 | a0001 | c0002 | t0007 | g0291 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | YRI | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19240 | hp2 | a0001 | c0005 | t0038 | g0150 | AFR | YRI | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ASW | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0143 | AFR | ASW | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02486 | hp1 | a0001 | c0002 | t0012 | g0124 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02486 | hp2 | a0006 | c0010 | t0021 | g0033 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02559 | hp1 | a0001 | c0002 | t0004 | g0153 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02559 | hp2 | a0001 | c0001 | t0011 | g0097 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03471 | hp1 | a0006 | c0010 | t0018 | g0166 | AFR | MSL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0173 | AFR | MSL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | USA | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | USA | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18955 | hp1 | a0001 | c0001 | t0027 | g0246 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18955 | hp2 | a0001 | c0001 | t0011 | g0050 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0100 | AFR | USA | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA20300 | hp2 | a0007 | c0013 | t0018 | g0111 | AFR | USA | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA21309 | hp1 | a0001 | c0001 | t0011 | g0078 | AFR | LWK | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA21309 | hp2 | a0001 | c0002 | t0004 | g0015 | AFR | LWK | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0220 | REF | REF | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0024 | g0101 | REF | REF | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:59931987 | A | G | 2 | a0004 a0014 |
4 | HG02738.hp2 NA18978.hp2 NA19067.hp1 others(1): Show |
missense_variant | MODERATE | c.491A>G | p.Asn164Ser | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/33 | 654/8103 | 491/4485 | 164/1494 | chr14 | 59931987 | |||
| chr14:59960963 | G | A | 1 | a0011 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.1129G>A | p.Gly377Ser | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/33 | 1292/8103 | 1129/4485 | 377/1494 | chr14 | 59960963 | |||
| chr14:59981854 | G | C | 1 | a0010 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.1885G>C | p.Ala629Pro | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/33 | 2048/8103 | 1885/4485 | 629/1494 | chr14 | 59981854 | |||
| chr14:59981881 | A | C | 1 | a0007 | 2 | HG03139.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.1912A>C | p.Asn638His | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/33 | 2075/8103 | 1912/4485 | 638/1494 | chr14 | 59981881 | |||
| chr14:59982016 | A | G | 1 | a0008 | 2 | NA18983.hp2 NA19088.hp1 |
missense_variant | MODERATE | c.2047A>G | p.Thr683Ala | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/33 | 2210/8103 | 2047/4485 | 683/1494 | chr14 | 59982016 | |||
| chr14:59985158 | A | T | 1 | a0003 | 4 | NA18961.hp2 NA18962.hp1 NA18986.hp2 others(1): Show |
missense_variant | MODERATE | c.2145A>T | p.Leu715Phe | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/33 | 2308/8103 | 2145/4485 | 715/1494 | chr14 | 59985158 | |||
| chr14:60001972 | C | T | 1 | a0012 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.2536C>T | p.Leu846Phe | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 20/33 | 2699/8103 | 2536/4485 | 846/1494 | chr14 | 60001972 | |||
| chr14:60002045 | C | A | 1 | a0006 | 2 | HG02486.hp2 HG03471.hp1 |
missense_variant | MODERATE | c.2609C>A | p.Thr870Lys | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 20/33 | 2772/8103 | 2609/4485 | 870/1494 | chr14 | 60002045 | |||
| chr14:60006505 | T | C | 1 | a0013 | 1 | NA18966.hp1 | missense_variant | MODERATE | c.2951T>C | p.Leu984Pro | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 22/33 | 3114/8103 | 2951/4485 | 984/1494 | chr14 | 60006505 | |||
| chr14:60008141 | G | A | 1 | a0005 | 2 | HG00099.hp1 HG00280.hp2 |
stop_gained | HIGH | c.3113G>A | p.Trp1038* | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/33 | 3276/8103 | 3113/4485 | 1038/1494 | chr14 | 60008141 | |||
| chr14:60057944 | G | A | 3 | a0002 a0008 a0014 |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
missense_variant | MODERATE | c.4198G>A | p.Glu1400Lys | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/33 | 4361/8103 | 4198/4485 | 1400/1494 | chr14 | 60057944 | |||
| chr14:60062015 | A | C | 1 | a0009 | 1 | HG01169.hp2 | missense_variant | MODERATE | c.4281A>C | p.Lys1427Asn | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 32/33 | 4444/8103 | 4281/4485 | 1427/1494 | chr14 | 60062015 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:59928369 | A | G | 1 | a0001c0005 | 8 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
synonymous_variant | LOW | c.150A>G | p.Leu50Leu | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 3/33 | 313/8103 | 150/4485 | 50/1494 | chr14 | 59928369 | |||
| chr14:59938560 | G | A | 1 | a0001c0004 | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
synonymous_variant | LOW | c.714G>A | p.Lys238Lys | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/33 | 877/8103 | 714/4485 | 238/1494 | chr14 | 59938560 | |||
| chr14:59977331 | T | C | 3 | a0002c0003 a0008c0009 a0014c0019 |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
synonymous_variant | LOW | c.1746T>C | p.Pro582Pro | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 14/33 | 1909/8103 | 1746/4485 | 582/1494 | chr14 | 59977331 | |||
| chr14:60032021 | C | T | 1 | a0001c0006 | 5 | HG02074.hp1 HG02080.hp1 HG02132.hp2 others(2): Show |
synonymous_variant | LOW | c.3948C>T | p.Asp1316Asp | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/33 | 4111/8103 | 3948/4485 | 1316/1494 | chr14 | 60032021 | |||
| chr14:60053202 | C | T | 10 | a0001c0001 a0002c0003 a0004c0008 others(7): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
synonymous_variant | LOW | c.4128C>T | p.Asn1376Asn | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/33 | 4291/8103 | 4128/4485 | 1376/1494 | chr14 | 60053202 | |||
| chr14:60057997 | C | T | 1 | a0001c0012 | 2 | HG02602.hp2 HG03834.hp2 |
synonymous_variant | LOW | c.4251C>T | p.Asp1417Asp | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/33 | 4414/8103 | 4251/4485 | 1417/1494 | chr14 | 60057997 | |||
| chr14:60062039 | G | A | 1 | a0001c0004 | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
synonymous_variant | LOW | c.4305G>A | p.Leu1435Leu | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 32/33 | 4468/8103 | 4305/4485 | 1435/1494 | chr14 | 60062039 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:59920168 | C | T | 1 | a0001c0001t0045 | 1 | NA19002.hp1 | 5_prime_UTR_variant | MODIFIER | c.-139C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/33 | 7776 | chr14 | 59920168 | ||||||
| chr14:60063389 | C | T | 4 | a0001c0001t0008 a0001c0001t0042 a0001c0001t0043 others(1): Show |
14 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*27C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 27 | chr14 | 60063389 | ||||||
| chr14:60063442 | TA | T | 7 | a0001c0001t0027 a0001c0001t0041 a0001c0001t0044 others(4): Show |
31 | HG00558.hp2 HG01517.hp2 NA18939.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*96delA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 96 | INFO_REALIGN_3_PRIME | chr14 | 60063442 | |||||
| chr14:60063596 | T | C | 1 | a0001c0005t0013 | 7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*234T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 234 | chr14 | 60063596 | ||||||
| chr14:60063627 | C | T | 6 | a0001c0001t0010 a0001c0001t0015 a0001c0001t0039 others(3): Show |
17 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*265C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 265 | chr14 | 60063627 | ||||||
| chr14:60064004 | G | A | 1 | a0001c0001t0028 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*642G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 642 | chr14 | 60064004 | ||||||
| chr14:60064108 | C | A | 3 | a0002c0003t0005 a0008c0009t0005 a0014c0019t0005 |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*746C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 746 | chr14 | 60064108 | ||||||
| chr14:60064120 | T | C | 53 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(50): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
3_prime_UTR_variant | MODIFIER | c.*758T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 758 | chr14 | 60064120 | ||||||
| chr14:60064369 | A | G | 40 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(37): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*1007A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 1007 | chr14 | 60064369 | ||||||
| chr14:60064541 | C | A | 40 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(37): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*1179C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 1179 | chr14 | 60064541 | ||||||
| chr14:60064587 | T | C | 1 | a0001c0001t0030 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1225T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 1225 | chr14 | 60064587 | ||||||
| chr14:60065083 | T | A | 1 | a0001c0001t0031 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1721T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 1721 | chr14 | 60065083 | ||||||
| chr14:60065111 | G | A | 1 | a0001c0002t0012 | 8 | HG02486.hp1 HG02622.hp2 HG02717.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1749G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 1749 | chr14 | 60065111 | ||||||
| chr14:60065241 | G | A | 1 | a0001c0002t0029 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1879G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 1879 | chr14 | 60065241 | ||||||
| chr14:60065257 | G | A | 4 | a0001c0002t0021 a0006c0010t0018 a0006c0010t0021 others(1): Show |
5 | HG02257.hp1 HG02486.hp2 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1895G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 1895 | chr14 | 60065257 | ||||||
| chr14:60065433 | A | C | 3 | a0002c0003t0005 a0008c0009t0005 a0014c0019t0005 |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2071A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 2071 | chr14 | 60065433 | ||||||
| chr14:60065440 | G | C | 1 | a0001c0001t0032 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2078G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 2078 | chr14 | 60065440 | ||||||
| chr14:60065573 | G | A | 1 | a0001c0001t0033 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2211G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 2211 | chr14 | 60065573 | ||||||
| chr14:60065647 | CA | C | 48 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(45): Show |
287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
3_prime_UTR_variant | MODIFIER | c.*2304delA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 2304 | INFO_REALIGN_3_PRIME | chr14 | 60065647 | |||||
| chr14:60065670 | T | TAAAAGAG others(304): Show |
2 | a0001c0001t0011 a0001c0001t0023 |
10 | HG02074.hp2 HG02559.hp2 HG02922.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2326_*2327insGGCC others(307): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 2327 | INFO_REALIGN_3_PRIME | chr14 | 60065670 | |||||
| chr14:60065670 | T | TAAAAGAG others(315): Show |
1 | a0001c0001t0016 | 4 | HG00621.hp1 HG00621.hp2 HG01074.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2326_*2327insGGCC others(318): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 2327 | INFO_REALIGN_3_PRIME | chr14 | 60065670 | |||||
| chr14:60065670 | T | TAAAAGAG others(316): Show |
14 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0010 others(11): Show |
84 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*2326_*2327insGGCC others(319): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 2327 | INFO_REALIGN_3_PRIME | chr14 | 60065670 | |||||
| chr14:60065670 | T | TAAAAGAG others(317): Show |
12 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0015 others(9): Show |
52 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*2326_*2327insGGCC others(320): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 2327 | INFO_REALIGN_3_PRIME | chr14 | 60065670 | |||||
| chr14:60065670 | T | TAAAAGAG others(318): Show |
6 | a0001c0001t0006 a0001c0001t0034 a0001c0001t0036 others(3): Show |
15 | HG00280.hp2 HG00423.hp2 HG00735.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2326_*2327insGGCC others(321): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 2327 | INFO_REALIGN_3_PRIME | chr14 | 60065670 | |||||
| chr14:60065806 | T | C | 1 | a0001c0001t0040 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2444T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 2444 | chr14 | 60065806 | ||||||
| chr14:60065847 | T | C | 1 | a0001c0002t0026 | 2 | NA19065.hp1 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2485T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 2485 | chr14 | 60065847 | ||||||
| chr14:60065893 | G | A | 1 | a0001c0004t0009 | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2531G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 2531 | chr14 | 60065893 | ||||||
| chr14:60065994 | T | A | 1 | a0001c0001t0030 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2632T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 2632 | chr14 | 60065994 | ||||||
| chr14:60066319 | G | A | 2 | a0001c0001t0036 a0001c0001t0037 |
2 | NA18747.hp1 NA19078.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2957G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 2957 | chr14 | 60066319 | ||||||
| chr14:60066512 | G | A | 37 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(34): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*3150G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 3150 | chr14 | 60066512 | ||||||
| chr14:60066526 | A | G | 1 | a0001c0001t0034 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3164A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 3164 | chr14 | 60066526 | ||||||
| chr14:60066577 | T | C | 37 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(34): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*3215T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 3215 | chr14 | 60066577 | ||||||
| chr14:60066641 | C | T | 37 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(34): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*3279C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 3279 | chr14 | 60066641 | ||||||
| chr14:60066648 | C | T | 58 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(55): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*3286C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 3286 | chr14 | 60066648 | ||||||
| chr14:60066797 | A | C | 1 | a0001c0002t0007 | 11 | HG02015.hp2 NA18989.hp1 NA18998.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3435A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 3435 | chr14 | 60066797 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:59920466 | A | G | 1 | a0001c0001t0032g0320 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-34+193A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59920466 | |||||||
| chr14:59920500 | T | C | 1 | a0001c0002t0002g0003 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-34+227T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59920500 | |||||||
| chr14:59920622 | C | T | 115 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(112): Show |
116 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-34+349C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59920622 | |||||||
| chr14:59921015 | C | T | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.-34+742C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59921015 | |||||||
| chr14:59921023 | A | C | 115 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(112): Show |
116 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-34+750A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59921023 | |||||||
| chr14:59921149 | A | C | 2 | a0001c0002t0004g0318 a0001c0002t0004g0319 |
2 | HG00609.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.-34+876A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59921149 | |||||||
| chr14:59921186 | T | TC | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.-34+915dupC | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr14 | 59921186 | ||||||
| chr14:59921717 | A | AT | 41 | a0001c0001t0001g0165 a0001c0001t0001g0313 a0001c0001t0003g0168 others(38): Show |
41 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.-34+1465dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr14 | 59921717 | ||||||
| chr14:59921717 | A | ATTTTT | 20 | a0002c0003t0005g0001 a0002c0003t0005g0187 a0002c0003t0005g0188 others(17): Show |
21 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(18): Show |
intron_variant | MODIFIER | c.-34+1461_-34+1465d others(7): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr14 | 59921717 | ||||||
| chr14:59922083 | C | CA | 9 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0009 others(6): Show |
9 | HG00621.hp2 HG00639.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.-34+1820dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr14 | 59922083 | ||||||
| chr14:59922090 | A | T | 65 | a0001c0001t0001g0299 a0001c0002t0002g0003 a0001c0002t0002g0296 others(62): Show |
67 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.-34+1817A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59922090 | |||||||
| chr14:59922094 | T | A | 2 | a0001c0002t0002g0005 a0001c0002t0004g0004 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.-34+1821T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59922094 | |||||||
| chr14:59922215 | C | T | 2 | a0001c0002t0002g0158 a0001c0002t0002g0159 |
2 | HG02738.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-34+1942C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59922215 | |||||||
| chr14:59922278 | G | C | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.-34+2005G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59922278 | |||||||
| chr14:59922802 | T | A | 1 | a0001c0001t0003g0014 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-34+2529T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59922802 | |||||||
| chr14:59923246 | T | C | 1 | a0001c0002t0004g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-34+2973T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59923246 | |||||||
| chr14:59923353 | G | C | 1 | a0001c0001t0003g0014 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-34+3080G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59923353 | |||||||
| chr14:59923514 | C | A | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.-34+3241C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59923514 | |||||||
| chr14:59923647 | T | C | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-34+3374T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59923647 | |||||||
| chr14:59923864 | C | A | 1 | a0001c0001t0001g0016 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-34+3591C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59923864 | |||||||
| chr14:59923895 | C | G | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.-34+3622C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59923895 | |||||||
| chr14:59923924 | A | C | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.-34+3651A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59923924 | |||||||
| chr14:59924185 | G | C | 1 | a0001c0001t0001g0208 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-33-3726G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59924185 | |||||||
| chr14:59924256 | G | A | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.-33-3655G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59924256 | |||||||
| chr14:59924309 | G | A | 115 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(112): Show |
116 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-33-3602G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59924309 | |||||||
| chr14:59924455 | A | G | 11 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0009 others(8): Show |
11 | HG00639.hp2 HG00741.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.-33-3456A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59924455 | |||||||
| chr14:59924458 | G | A | 1 | a0001c0001t0030g0160 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-33-3453G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59924458 | |||||||
| chr14:59924704 | A | G | 66 | a0001c0001t0030g0160 a0001c0002t0002g0005 a0001c0002t0002g0107 others(63): Show |
66 | HG00639.hp1 HG01081.hp1 HG01109.hp1 others(63): Show |
intron_variant | MODIFIER | c.-33-3207A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59924704 | |||||||
| chr14:59924789 | C | G | 116 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(113): Show |
117 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.-33-3122C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59924789 | |||||||
| chr14:59924899 | C | CT | 6 | a0001c0001t0019g0315 a0001c0001t0035g0156 a0001c0002t0002g0183 others(3): Show |
6 | HG01496.hp2 HG02559.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33-2998dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr14 | 59924899 | ||||||
| chr14:59924977 | C | A | 207 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(204): Show |
209 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.-33-2934C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59924977 | |||||||
| chr14:59924986 | G | A | 185 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(182): Show |
186 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.-33-2925G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59924986 | |||||||
| chr14:59925001 | G | C | 2 | a0001c0005t0013g0171 a0001c0005t0013g0172 |
2 | HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-33-2910G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59925001 | |||||||
| chr14:59925043 | T | C | 311 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(308): Show |
313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.-33-2868T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59925043 | |||||||
| chr14:59925056 | G | C | 185 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(182): Show |
186 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.-33-2855G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59925056 | |||||||
| chr14:59925592 | G | A | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.-33-2319G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59925592 | |||||||
| chr14:59925673 | A | C | 1 | a0001c0001t0011g0097 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-33-2238A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59925673 | |||||||
| chr14:59925954 | G | A | 1 | a0001c0002t0004g0265 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-33-1957G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59925954 | |||||||
| chr14:59925976 | C | G | 1 | a0001c0002t0002g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-33-1935C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59925976 | |||||||
| chr14:59926151 | G | A | 2 | a0005c0011t0003g0211 a0005c0011t0006g0212 |
2 | HG00099.hp1 HG00280.hp2 |
intron_variant | MODIFIER | c.-33-1760G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59926151 | |||||||
| chr14:59926232 | T | C | 1 | a0001c0002t0007g0266 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-33-1679T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59926232 | |||||||
| chr14:59926506 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-33-1405A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59926506 | |||||||
| chr14:59926567 | T | A | 212 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(209): Show |
214 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.-33-1344T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59926567 | |||||||
| chr14:59926658 | C | T | 185 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(182): Show |
186 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.-33-1253C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59926658 | |||||||
| chr14:59926785 | G | A | 2 | a0001c0001t0011g0021 a0001c0001t0011g0097 |
2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-33-1126G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59926785 | |||||||
| chr14:59926842 | A | T | 1 | a0001c0001t0015g0096 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-33-1069A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59926842 | |||||||
| chr14:59926852 | C | A | 2 | a0001c0001t0035g0156 a0001c0002t0024g0157 |
2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-33-1059C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59926852 | |||||||
| chr14:59926864 | A | G | 2 | a0001c0001t0001g0263 a0001c0001t0003g0262 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-33-1047A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59926864 | |||||||
| chr14:59926946 | T | A | 185 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(182): Show |
186 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.-33-965T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59926946 | |||||||
| chr14:59927651 | C | T | 9 | a0001c0002t0024g0157 a0001c0005t0013g0151 a0001c0005t0013g0171 others(6): Show |
9 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-33-260C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59927651 | |||||||
| chr14:59927762 | C | T | 1 | a0001c0002t0002g0149 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-33-149C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59927762 | |||||||
| chr14:59928110 | G | T | 231 | a0001c0001t0001g0016 a0001c0001t0001g0080 a0001c0001t0001g0081 others(228): Show |
233 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.48+119G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 2/32 | chr14 | 59928110 | |||||||
| chr14:59929311 | A | G | 2 | a0001c0002t0012g0147 a0001c0002t0012g0148 |
2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.267+825A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 3/32 | chr14 | 59929311 | |||||||
| chr14:59929338 | T | C | 69 | a0001c0001t0030g0160 a0001c0002t0002g0005 a0001c0002t0002g0107 others(66): Show |
69 | HG00639.hp1 HG01081.hp1 HG01109.hp1 others(66): Show |
intron_variant | MODIFIER | c.267+852T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 3/32 | chr14 | 59929338 | |||||||
| chr14:59929390 | A | T | 1 | a0001c0001t0001g0077 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.267+904A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 3/32 | chr14 | 59929390 | |||||||
| chr14:59929414 | C | CA | 189 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(186): Show |
191 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(188): Show |
intron_variant | MODIFIER | c.267+938dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr14 | 59929414 | ||||||
| chr14:59929428 | CAG | C | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.267+944_267+945del others(2): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr14 | 59929428 | ||||||
| chr14:59929629 | A | G | 1 | a0001c0002t0004g0300 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.267+1143A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 3/32 | chr14 | 59929629 | |||||||
| chr14:59929903 | G | A | 1 | a0001c0001t0016g0023 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.268-1015G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 3/32 | chr14 | 59929903 | |||||||
| chr14:59930027 | T | C | 3 | a0001c0001t0001g0213 a0001c0001t0001g0259 a0001c0001t0016g0105 |
3 | HG00323.hp1 HG01074.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.268-891T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 3/32 | chr14 | 59930027 | |||||||
| chr14:59930072 | T | A | 209 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(206): Show |
211 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.268-846T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 3/32 | chr14 | 59930072 | |||||||
| chr14:59930295 | C | A | 54 | a0001c0002t0002g0003 a0001c0002t0002g0207 a0001c0002t0002g0215 others(51): Show |
55 | HG00323.hp2 HG00558.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.268-623C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 3/32 | chr14 | 59930295 | |||||||
| chr14:59930322 | A | T | 1 | a0001c0001t0006g0258 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.268-596A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 3/32 | chr14 | 59930322 | |||||||
| chr14:59930765 | TA | T | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.268-152delA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 3/32 | chr14 | 59930765 | |||||||
| chr14:59930824 | T | C | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.268-94T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 3/32 | chr14 | 59930824 | |||||||
| chr14:59931168 | G | A | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.408+110G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 4/32 | chr14 | 59931168 | |||||||
| chr14:59931320 | T | G | 1 | a0001c0001t0006g0024 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.408+262T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 4/32 | chr14 | 59931320 | |||||||
| chr14:59931947 | T | A | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.473-22T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 5/32 | chr14 | 59931947 | |||||||
| chr14:59932364 | T | C | 66 | a0001c0001t0030g0160 a0001c0002t0002g0005 a0001c0002t0002g0107 others(63): Show |
66 | HG00639.hp1 HG01081.hp1 HG01109.hp1 others(63): Show |
intron_variant | MODIFIER | c.543+325T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59932364 | |||||||
| chr14:59932677 | A | G | 1 | a0001c0001t0010g0076 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.543+638A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59932677 | |||||||
| chr14:59932825 | C | T | 2 | a0001c0001t0035g0156 a0001c0002t0024g0157 |
2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.543+786C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59932825 | |||||||
| chr14:59932925 | T | C | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.543+886T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59932925 | |||||||
| chr14:59933028 | G | A | 1 | a0001c0001t0003g0025 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.543+989G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59933028 | |||||||
| chr14:59933126 | G | A | 1 | a0001c0001t0010g0026 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.543+1087G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59933126 | |||||||
| chr14:59933171 | T | C | 2 | a0001c0002t0004g0318 a0001c0002t0004g0319 |
2 | HG00609.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.543+1132T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59933171 | |||||||
| chr14:59933328 | G | T | 3 | a0001c0001t0011g0073 a0001c0001t0011g0074 a0001c0001t0011g0075 |
3 | NA18942.hp1 NA18950.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.543+1289G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59933328 | |||||||
| chr14:59933330 | T | C | 185 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(182): Show |
186 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.543+1291T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59933330 | |||||||
| chr14:59933333 | A | G | 3 | a0001c0001t0003g0070 a0001c0001t0006g0071 a0001c0001t0006g0072 |
3 | HG00423.hp2 NA18998.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.543+1294A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59933333 | |||||||
| chr14:59933370 | A | G | 185 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(182): Show |
186 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.543+1331A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59933370 | |||||||
| chr14:59933378 | A | G | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.543+1339A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59933378 | |||||||
| chr14:59933382 | A | G | 2 | a0001c0001t0003g0095 a0001c0001t0006g0169 |
2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.543+1343A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59933382 | |||||||
| chr14:59933478 | G | A | 1 | a0001c0005t0013g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.543+1439G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59933478 | |||||||
| chr14:59934082 | T | C | 1 | a0001c0002t0002g0159 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.543+2043T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59934082 | |||||||
| chr14:59934119 | G | A | 2 | a0001c0001t0035g0156 a0001c0002t0024g0157 |
2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.543+2080G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59934119 | |||||||
| chr14:59934399 | A | G | 45 | a0001c0002t0002g0003 a0001c0002t0002g0215 a0001c0002t0002g0296 others(42): Show |
46 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.543+2360A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59934399 | |||||||
| chr14:59934452 | T | C | 69 | a0001c0001t0030g0160 a0001c0002t0002g0005 a0001c0002t0002g0107 others(66): Show |
69 | HG00639.hp1 HG01081.hp1 HG01109.hp1 others(66): Show |
intron_variant | MODIFIER | c.543+2413T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59934452 | |||||||
| chr14:59934490 | C | T | 60 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(57): Show |
60 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.543+2451C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59934490 | |||||||
| chr14:59934752 | G | A | 1 | a0001c0001t0003g0216 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.543+2713G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59934752 | |||||||
| chr14:59935023 | C | T | 1 | a0002c0003t0005g0205 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.543+2984C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59935023 | |||||||
| chr14:59935052 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.543+3013G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59935052 | |||||||
| chr14:59935123 | T | TA | 30 | a0001c0001t0001g0027 a0001c0001t0003g0029 a0001c0001t0008g0006 others(27): Show |
31 | HG00423.hp1 HG02055.hp2 HG02572.hp2 others(28): Show |
intron_variant | MODIFIER | c.543+3105dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr14 | 59935123 | ||||||
| chr14:59935123 | TA | T | 135 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(132): Show |
135 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.543+3105delA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr14 | 59935123 | ||||||
| chr14:59935165 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.543+3126C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59935165 | |||||||
| chr14:59935293 | CA | C | 125 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(122): Show |
126 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.544-3083delA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr14 | 59935293 | ||||||
| chr14:59935293 | CAA | C | 67 | a0001c0001t0001g0257 a0001c0001t0030g0160 a0001c0002t0002g0005 others(64): Show |
67 | HG00639.hp1 HG01081.hp1 HG01109.hp1 others(64): Show |
intron_variant | MODIFIER | c.544-3084_544-3083d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr14 | 59935293 | ||||||
| chr14:59935375 | C | T | 1 | a0001c0002t0002g0159 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.544-3015C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59935375 | |||||||
| chr14:59935412 | C | T | 1 | a0001c0002t0002g0174 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.544-2978C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59935412 | |||||||
| chr14:59935418 | T | C | 2 | a0001c0001t0035g0156 a0001c0002t0024g0157 |
2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.544-2972T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59935418 | |||||||
| chr14:59935436 | T | C | 1 | a0001c0001t0008g0031 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.544-2954T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59935436 | |||||||
| chr14:59935902 | G | A | 1 | a0001c0002t0012g0147 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.544-2488G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59935902 | |||||||
| chr14:59936342 | G | A | 2 | a0001c0002t0022g0269 a0001c0002t0022g0270 |
2 | HG02080.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.544-2048G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59936342 | |||||||
| chr14:59936389 | C | T | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-2001C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59936389 | |||||||
| chr14:59936408 | A | G | 2 | a0001c0002t0017g0141 a0001c0002t0017g0142 |
2 | HG01109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.544-1982A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59936408 | |||||||
| chr14:59936596 | T | C | 209 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(206): Show |
211 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.544-1794T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59936596 | |||||||
| chr14:59936678 | C | A | 185 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(182): Show |
186 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.544-1712C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59936678 | |||||||
| chr14:59936815 | C | T | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.544-1575C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59936815 | |||||||
| chr14:59937195 | T | TA | 37 | a0001c0001t0001g0027 a0001c0001t0001g0217 a0001c0001t0001g0218 others(34): Show |
38 | HG01175.hp2 HG01243.hp2 HG02040.hp2 others(35): Show |
intron_variant | MODIFIER | c.544-1172dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr14 | 59937195 | ||||||
| chr14:59937195 | TA | T | 66 | a0001c0001t0008g0013 a0001c0001t0030g0160 a0001c0002t0002g0112 others(63): Show |
66 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.544-1172delA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr14 | 59937195 | ||||||
| chr14:59937197 | A | G | 1 | a0001c0005t0013g0182 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.544-1193A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59937197 | |||||||
| chr14:59937225 | T | C | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.544-1165T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59937225 | |||||||
| chr14:59937280 | T | A | 2 | a0001c0002t0004g0015 a0001c0002t0029g0017 |
2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.544-1110T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59937280 | |||||||
| chr14:59937290 | T | C | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-1100T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59937290 | |||||||
| chr14:59937318 | C | T | 1 | a0001c0002t0020g0301 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.544-1072C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59937318 | |||||||
| chr14:59937386 | A | G | 44 | a0001c0001t0030g0160 a0001c0002t0002g0107 a0001c0002t0002g0118 others(41): Show |
44 | HG00639.hp1 HG01109.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.544-1004A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59937386 | |||||||
| chr14:59937472 | A | G | 2 | a0001c0002t0002g0005 a0001c0002t0004g0004 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.544-918A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59937472 | |||||||
| chr14:59937566 | T | A | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.544-824T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59937566 | |||||||
| chr14:59937829 | A | G | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.544-561A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59937829 | |||||||
| chr14:59938121 | T | C | 2 | a0001c0002t0004g0318 a0001c0002t0004g0319 |
2 | HG00609.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.544-269T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59938121 | |||||||
| chr14:59938191 | G | A | 1 | a0001c0001t0001g0299 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.544-199G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59938191 | |||||||
| chr14:59938285 | G | A | 67 | a0001c0001t0001g0016 a0001c0001t0001g0080 a0001c0001t0001g0081 others(64): Show |
68 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.544-105G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59938285 | |||||||
| chr14:59938369 | T | C | 2 | a0001c0002t0022g0269 a0001c0002t0022g0270 |
2 | HG02080.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.544-21T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59938369 | |||||||
| chr14:59938667 | G | A | 185 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(182): Show |
186 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.726+95G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938667 | |||||||
| chr14:59938732 | A | G | 1 | a0001c0002t0025g0113 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.726+160A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938732 | |||||||
| chr14:59938777 | G | A | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.726+205G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938777 | |||||||
| chr14:59938848 | T | A | 1 | a0001c0002t0004g0272 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.726+276T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938848 | |||||||
| chr14:59938856 | A | ATAAT | 207 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(204): Show |
209 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.726+286_726+287ins others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59938856 | ||||||
| chr14:59938904 | CATATATA others(11): Show |
C | 5 | a0001c0006t0002g0108 a0001c0006t0002g0109 a0001c0006t0002g0114 others(2): Show |
5 | HG02074.hp1 HG02080.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.726+347_726+364del others(18): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59938904 | ||||||
| chr14:59938914 | C | CAT | 159 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(156): Show |
160 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.726+345_726+346dup others(2): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59938914 | ||||||
| chr14:59938914 | C | CATATATG others(23): Show |
1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.726+346_726+347ins others(30): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59938914 | ||||||
| chr14:59938914 | CATATGCA others(1): Show |
C | 43 | a0001c0002t0002g0003 a0001c0002t0002g0215 a0001c0002t0002g0296 others(40): Show |
44 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.726+347_726+354del others(8): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59938914 | ||||||
| chr14:59938914 | CATATGCA others(3): Show |
C | 1 | a0001c0001t0006g0258 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.726+347_726+356del others(10): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59938914 | ||||||
| chr14:59938929 | A | G | 43 | a0001c0002t0002g0003 a0001c0002t0002g0215 a0001c0002t0002g0296 others(40): Show |
44 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.726+357A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938929 | |||||||
| chr14:59938930 | C | T | 1 | a0001c0001t0006g0258 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.726+358C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938930 | |||||||
| chr14:59938931 | A | G | 1 | a0001c0001t0006g0258 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.726+359A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938931 | |||||||
| chr14:59938932 | C | T | 43 | a0001c0002t0002g0003 a0001c0002t0002g0215 a0001c0002t0002g0296 others(40): Show |
44 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.726+360C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938932 | |||||||
| chr14:59938938 | T | C | 2 | a0001c0001t0006g0258 a0001c0002t0004g0310 |
2 | HG00735.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.726+366T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938938 | |||||||
| chr14:59938940 | C | T | 2 | a0001c0001t0006g0258 a0001c0002t0004g0310 |
2 | HG00735.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.726+368C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938940 | |||||||
| chr14:59938942 | TATAC | T | 88 | a0001c0001t0030g0160 a0001c0002t0002g0107 a0001c0002t0002g0118 others(85): Show |
89 | HG00558.hp2 HG00609.hp1 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.726+378_726+381del others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59938942 | ||||||
| chr14:59938946 | C | CATAT | 93 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(90): Show |
93 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.726+377_726+378ins others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59938946 | ||||||
| chr14:59938948 | T | C | 3 | a0001c0001t0006g0258 a0001c0002t0002g0003 a0001c0002t0004g0310 |
3 | HG00735.hp2 HG02572.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.726+376T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938948 | |||||||
| chr14:59938952 | T | C | 93 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(90): Show |
93 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.726+380T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938952 | |||||||
| chr14:59938954 | T | C | 93 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(90): Show |
93 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.726+382T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938954 | |||||||
| chr14:59938956 | TACAC | T | 3 | a0001c0001t0006g0258 a0001c0002t0002g0003 a0001c0002t0004g0310 |
3 | HG00735.hp2 HG02572.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.726+388_726+391del others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59938956 | ||||||
| chr14:59938958 | C | T | 93 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(90): Show |
93 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.726+386C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938958 | |||||||
| chr14:59938960 | C | T | 94 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(91): Show |
94 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.726+388C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938960 | |||||||
| chr14:59938961 | A | G | 1 | a0001c0002t0002g0003 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.726+389A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938961 | |||||||
| chr14:59938979 | A | G | 3 | a0001c0001t0003g0070 a0001c0001t0006g0071 a0001c0001t0006g0072 |
3 | HG00423.hp2 NA18998.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.726+407A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938979 | |||||||
| chr14:59939020 | T | TAC | 3 | a0001c0001t0035g0156 a0001c0002t0004g0214 a0001c0002t0024g0157 |
3 | HG01496.hp2 HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.726+449_726+450ins others(2): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59939020 | ||||||
| chr14:59939020 | T | TATAC | 206 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(203): Show |
208 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.726+451_726+452ins others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59939020 | ||||||
| chr14:59939042 | T | C | 1 | a0001c0002t0004g0273 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.726+470T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59939042 | |||||||
| chr14:59939064 | C | T | 1 | a0001c0005t0013g0182 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.726+492C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59939064 | |||||||
| chr14:59939092 | CAT | C | 7 | a0001c0005t0013g0151 a0001c0005t0013g0171 a0001c0005t0013g0172 others(4): Show |
7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.726+528_726+529del others(2): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59939092 | ||||||
| chr14:59939100 | T | C | 178 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(175): Show |
179 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.726+528T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59939100 | |||||||
| chr14:59939106 | C | T | 178 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(175): Show |
179 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.726+534C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59939106 | |||||||
| chr14:59939114 | T | C | 178 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(175): Show |
179 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.726+542T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59939114 | |||||||
| chr14:59939116 | C | T | 178 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(175): Show |
179 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.726+544C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59939116 | |||||||
| chr14:59939639 | C | A | 56 | a0001c0001t0030g0160 a0001c0002t0002g0107 a0001c0002t0002g0112 others(53): Show |
56 | HG00639.hp1 HG01109.hp1 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.726+1067C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59939639 | |||||||
| chr14:59939700 | A | G | 209 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(206): Show |
211 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.726+1128A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59939700 | |||||||
| chr14:59940030 | G | C | 1 | a0001c0002t0017g0117 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.726+1458G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59940030 | |||||||
| chr14:59940378 | G | T | 2 | a0001c0002t0002g0005 a0001c0002t0004g0004 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.726+1806G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59940378 | |||||||
| chr14:59940430 | T | G | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.726+1858T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59940430 | |||||||
| chr14:59940665 | TG | T | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.726+2098delG | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59940665 | ||||||
| chr14:59940708 | T | A | 1 | a0001c0001t0008g0006 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.726+2136T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59940708 | |||||||
| chr14:59940933 | T | A | 1 | a0001c0001t0008g0154 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.726+2361T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59940933 | |||||||
| chr14:59940983 | C | T | 2 | a0001c0001t0035g0156 a0001c0002t0024g0157 |
2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.726+2411C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59940983 | |||||||
| chr14:59941042 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.726+2470T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59941042 | |||||||
| chr14:59941068 | C | CA | 27 | a0001c0001t0001g0027 a0001c0002t0004g0004 a0001c0002t0007g0266 others(24): Show |
28 | HG01243.hp2 NA18939.hp2 NA18941.hp2 others(25): Show |
intron_variant | MODIFIER | c.726+2506dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59941068 | ||||||
| chr14:59941326 | T | C | 1 | a0001c0001t0028g0030 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.726+2754T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59941326 | |||||||
| chr14:59941387 | T | G | 44 | a0001c0002t0002g0003 a0001c0002t0002g0215 a0001c0002t0002g0296 others(41): Show |
45 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.726+2815T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59941387 | |||||||
| chr14:59941480 | C | T | 3 | a0001c0001t0003g0254 a0001c0001t0003g0255 a0001c0001t0006g0258 |
3 | HG00735.hp2 HG00738.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.726+2908C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59941480 | |||||||
| chr14:59941696 | A | G | 1 | a0001c0002t0002g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.727-2893A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59941696 | |||||||
| chr14:59941771 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.727-2818A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59941771 | |||||||
| chr14:59942336 | T | A | 1 | a0001c0002t0004g0310 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.727-2253T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59942336 | |||||||
| chr14:59942435 | G | A | 2 | a0001c0001t0035g0156 a0001c0002t0024g0157 |
2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.727-2154G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59942435 | |||||||
| chr14:59942722 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.727-1867C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59942722 | |||||||
| chr14:59942774 | C | G | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.727-1815C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59942774 | |||||||
| chr14:59942776 | C | CT | 3 | a0001c0002t0002g0145 a0001c0002t0002g0146 a0001c0002t0004g0153 |
3 | HG01243.hp1 HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.727-1812dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59942776 | ||||||
| chr14:59942777 | TC | T | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.727-1811delC | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59942777 | |||||||
| chr14:59942778 | C | T | 185 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(182): Show |
186 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.727-1811C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59942778 | |||||||
| chr14:59942912 | G | GTA | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.727-1676_727-1675i others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59942912 | ||||||
| chr14:59942916 | G | T | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.727-1673G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59942916 | |||||||
| chr14:59943019 | GT | G | 185 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(182): Show |
186 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.727-1563delT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59943019 | ||||||
| chr14:59943048 | G | A | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.727-1541G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59943048 | |||||||
| chr14:59943097 | A | G | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.727-1492A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59943097 | |||||||
| chr14:59943220 | G | GTATTAGT others(7): Show |
24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.727-1365_727-1364i others(16): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59943220 | ||||||
| chr14:59943232 | A | T | 1 | a0001c0002t0004g0298 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.727-1357A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59943232 | |||||||
| chr14:59943247 | T | C | 209 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(206): Show |
211 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.727-1342T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59943247 | |||||||
| chr14:59943470 | G | GA | 11 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0009 others(8): Show |
11 | HG00639.hp2 HG00741.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.727-1110dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59943470 | ||||||
| chr14:59943504 | T | C | 2 | a0001c0002t0002g0118 a0001c0002t0002g0183 |
2 | NA18944.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.727-1085T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59943504 | |||||||
| chr14:59943783 | C | T | 56 | a0001c0001t0030g0160 a0001c0002t0002g0107 a0001c0002t0002g0112 others(53): Show |
56 | HG00639.hp1 HG01109.hp1 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.727-806C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59943783 | |||||||
| chr14:59943873 | T | C | 2 | a0001c0002t0002g0119 a0001c0002t0002g0174 |
2 | HG01192.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.727-716T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59943873 | |||||||
| chr14:59944050 | T | C | 4 | a0001c0001t0011g0021 a0001c0001t0011g0078 a0001c0001t0011g0079 others(1): Show |
4 | HG02559.hp2 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.727-539T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59944050 | |||||||
| chr14:59944141 | A | C | 1 | a0001c0006t0002g0109 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.727-448A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59944141 | |||||||
| chr14:59944172 | G | A | 2 | a0001c0001t0035g0156 a0001c0002t0024g0157 |
2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.727-417G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59944172 | |||||||
| chr14:59944211 | T | C | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.727-378T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59944211 | |||||||
| chr14:59944214 | A | C | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.727-375A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59944214 | |||||||
| chr14:59944539 | C | T | 43 | a0001c0002t0002g0003 a0001c0002t0002g0215 a0001c0002t0002g0296 others(40): Show |
44 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.727-50C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59944539 | |||||||
| chr14:59944831 | AT | A | 5 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(2): Show |
5 | HG00099.hp2 HG00642.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+88delT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59944831 | |||||||
| chr14:59944860 | ACACACT | A | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.882+122_882+127del others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr14 | 59944860 | ||||||
| chr14:59944866 | T | A | 42 | a0001c0002t0002g0003 a0001c0002t0002g0296 a0001c0002t0002g0297 others(39): Show |
43 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.882+122T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59944866 | |||||||
| chr14:59944866 | TCA | T | 140 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(137): Show |
140 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.882+141_882+142del others(2): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr14 | 59944866 | ||||||
| chr14:59944868 | A | T | 64 | a0001c0002t0002g0003 a0001c0002t0002g0296 a0001c0002t0002g0297 others(61): Show |
66 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.882+124A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59944868 | |||||||
| chr14:59944870 | A | T | 3 | a0001c0002t0002g0215 a0001c0002t0004g0015 a0001c0002t0029g0017 |
3 | HG03453.hp1 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.882+126A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59944870 | |||||||
| chr14:59944992 | A | G | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+248A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59944992 | |||||||
| chr14:59945025 | T | A | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+281T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59945025 | |||||||
| chr14:59945026 | A | T | 2 | a0005c0011t0003g0211 a0005c0011t0006g0212 |
2 | HG00099.hp1 HG00280.hp2 |
intron_variant | MODIFIER | c.882+282A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59945026 | |||||||
| chr14:59945042 | T | C | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.882+298T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59945042 | |||||||
| chr14:59945061 | T | C | 2 | a0001c0001t0035g0156 a0001c0002t0024g0157 |
2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.882+317T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59945061 | |||||||
| chr14:59945176 | C | T | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+432C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59945176 | |||||||
| chr14:59945289 | T | G | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+545T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59945289 | |||||||
| chr14:59945311 | G | A | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+567G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59945311 | |||||||
| chr14:59945463 | G | GA | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.882+727dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr14 | 59945463 | ||||||
| chr14:59945729 | C | T | 1 | a0001c0001t0014g0066 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.882+985C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59945729 | |||||||
| chr14:59945907 | G | A | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.882+1163G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59945907 | |||||||
| chr14:59946007 | A | C | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+1263A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59946007 | |||||||
| chr14:59946038 | C | G | 3 | a0001c0001t0003g0014 a0001c0001t0003g0064 a0009c0017t0003g0065 |
3 | HG01169.hp2 HG02148.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.882+1294C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59946038 | |||||||
| chr14:59946120 | A | T | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.882+1376A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59946120 | |||||||
| chr14:59946208 | A | C | 10 | a0001c0002t0002g0107 a0001c0002t0002g0119 a0001c0002t0002g0137 others(7): Show |
10 | HG00639.hp1 HG01175.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.882+1464A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59946208 | |||||||
| chr14:59946333 | T | G | 44 | a0001c0001t0030g0160 a0001c0002t0002g0107 a0001c0002t0002g0118 others(41): Show |
44 | HG00639.hp1 HG01109.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.882+1589T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59946333 | |||||||
| chr14:59946492 | C | CT | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+1757dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr14 | 59946492 | ||||||
| chr14:59946504 | CT | C | 13 | a0001c0001t0035g0156 a0001c0002t0007g0266 a0001c0002t0024g0157 others(10): Show |
13 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.882+1772delT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr14 | 59946504 | ||||||
| chr14:59946516 | T | C | 60 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(57): Show |
60 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.882+1772T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59946516 | |||||||
| chr14:59946622 | C | T | 1 | a0002c0003t0005g0200 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.882+1878C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59946622 | |||||||
| chr14:59946657 | T | G | 1 | a0001c0001t0008g0007 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.882+1913T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59946657 | |||||||
| chr14:59946662 | A | C | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+1918A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59946662 | |||||||
| chr14:59946667 | T | C | 209 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(206): Show |
211 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.882+1923T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59946667 | |||||||
| chr14:59946696 | C | T | 1 | a0001c0001t0008g0155 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.882+1952C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59946696 | |||||||
| chr14:59946844 | T | C | 2 | a0001c0001t0035g0156 a0001c0002t0024g0157 |
2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.882+2100T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59946844 | |||||||
| chr14:59946925 | G | C | 2 | a0001c0001t0035g0156 a0001c0002t0024g0157 |
2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.882+2181G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59946925 | |||||||
| chr14:59947283 | T | G | 1 | a0001c0001t0001g0080 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.882+2539T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59947283 | |||||||
| chr14:59947310 | G | T | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.882+2566G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59947310 | |||||||
| chr14:59947333 | C | T | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.882+2589C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59947333 | |||||||
| chr14:59947334 | G | A | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.882+2590G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59947334 | |||||||
| chr14:59947431 | C | T | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+2687C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59947431 | |||||||
| chr14:59947432 | A | G | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+2688A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59947432 | |||||||
| chr14:59947471 | A | G | 209 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(206): Show |
211 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.882+2727A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59947471 | |||||||
| chr14:59947768 | C | T | 2 | a0001c0001t0035g0156 a0001c0002t0024g0157 |
2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.882+3024C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59947768 | |||||||
| chr14:59947948 | T | G | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.882+3204T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59947948 | |||||||
| chr14:59947983 | C | T | 2 | a0001c0001t0016g0023 a0001c0002t0002g0136 |
2 | HG01074.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.882+3239C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59947983 | |||||||
| chr14:59948039 | G | A | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0016g0206 |
3 | HG00609.hp2 HG00621.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.882+3295G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59948039 | |||||||
| chr14:59948073 | T | C | 209 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(206): Show |
211 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.882+3329T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59948073 | |||||||
| chr14:59948130 | C | A | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.882+3386C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59948130 | |||||||
| chr14:59948268 | C | A | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.882+3524C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59948268 | |||||||
| chr14:59948268 | C | T | 44 | a0001c0002t0002g0003 a0001c0002t0002g0215 a0001c0002t0002g0296 others(41): Show |
45 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+3524C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59948268 | |||||||
| chr14:59948392 | C | G | 2 | a0001c0002t0004g0015 a0001c0002t0029g0017 |
2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.882+3648C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59948392 | |||||||
| chr14:59948446 | A | G | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+3702A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59948446 | |||||||
| chr14:59948461 | C | A | 5 | a0001c0006t0002g0108 a0001c0006t0002g0109 a0001c0006t0002g0114 others(2): Show |
5 | HG02074.hp1 HG02080.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+3717C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59948461 | |||||||
| chr14:59948503 | T | C | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+3759T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59948503 | |||||||
| chr14:59948594 | A | C | 3 | a0001c0005t0013g0179 a0001c0005t0013g0180 a0001c0005t0013g0181 |
3 | HG02055.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.882+3850A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59948594 | |||||||
| chr14:59948673 | A | G | 7 | a0001c0005t0013g0151 a0001c0005t0013g0171 a0001c0005t0013g0172 others(4): Show |
7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.882+3929A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59948673 | |||||||
| chr14:59948720 | G | C | 1 | a0001c0001t0001g0224 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.882+3976G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59948720 | |||||||
| chr14:59948823 | G | A | 4 | a0001c0001t0001g0225 a0001c0001t0001g0257 a0001c0001t0003g0037 others(1): Show |
4 | HG00642.hp2 HG01361.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+4079G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59948823 | |||||||
| chr14:59949066 | A | T | 8 | a0001c0005t0013g0151 a0001c0005t0013g0171 a0001c0005t0013g0172 others(5): Show |
8 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.882+4322A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59949066 | |||||||
| chr14:59949325 | G | A | 2 | a0001c0002t0004g0015 a0001c0002t0029g0017 |
2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.882+4581G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59949325 | |||||||
| chr14:59949424 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.882+4680G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59949424 | |||||||
| chr14:59949572 | G | GCTTTTCT others(4): Show |
24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+4833_882+4834i others(13): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr14 | 59949572 | ||||||
| chr14:59949590 | AG | A | 60 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(57): Show |
60 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.882+4849delG | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr14 | 59949590 | ||||||
| chr14:59949673 | G | A | 3 | a0001c0001t0001g0213 a0001c0002t0002g0005 a0001c0002t0004g0004 |
3 | HG01081.hp1 HG01243.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.882+4929G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59949673 | |||||||
| chr14:59949683 | T | G | 1 | a0001c0002t0004g0300 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.882+4939T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59949683 | |||||||
| chr14:59949708 | C | T | 1 | a0001c0002t0025g0135 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.882+4964C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59949708 | |||||||
| chr14:59949759 | G | A | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.882+5015G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59949759 | |||||||
| chr14:59949793 | A | G | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+5049A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59949793 | |||||||
| chr14:59950014 | C | T | 100 | a0001c0001t0030g0160 a0001c0002t0002g0003 a0001c0002t0002g0107 others(97): Show |
101 | HG00558.hp2 HG00609.hp1 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.882+5270C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950014 | |||||||
| chr14:59950079 | C | G | 2 | a0001c0002t0004g0015 a0001c0002t0029g0017 |
2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.882+5335C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950079 | |||||||
| chr14:59950119 | T | C | 3 | a0002c0003t0005g0001 a0002c0003t0005g0187 a0002c0003t0005g0188 |
4 | NA18939.hp2 NA18960.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+5375T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950119 | |||||||
| chr14:59950122 | G | T | 32 | a0001c0001t0030g0160 a0001c0002t0002g0107 a0001c0002t0002g0118 others(29): Show |
32 | HG00639.hp1 HG01109.hp1 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.882+5378G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950122 | |||||||
| chr14:59950178 | T | C | 209 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(206): Show |
211 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.882+5434T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950178 | |||||||
| chr14:59950439 | G | A | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.882+5695G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950439 | |||||||
| chr14:59950481 | A | C | 2 | a0001c0001t0001g0263 a0001c0001t0003g0262 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.882+5737A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950481 | |||||||
| chr14:59950482 | A | G | 7 | a0001c0005t0013g0151 a0001c0005t0013g0171 a0001c0005t0013g0172 others(4): Show |
7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.882+5738A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950482 | |||||||
| chr14:59950491 | A | G | 185 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(182): Show |
186 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.882+5747A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950491 | |||||||
| chr14:59950501 | A | G | 1 | a0001c0001t0003g0255 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.882+5757A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950501 | |||||||
| chr14:59950565 | G | A | 187 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(184): Show |
188 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.882+5821G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950565 | |||||||
| chr14:59950627 | G | A | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+5883G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950627 | |||||||
| chr14:59950679 | T | G | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.882+5935T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950679 | |||||||
| chr14:59950738 | A | C | 1 | a0001c0001t0001g0251 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.882+5994A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950738 | |||||||
| chr14:59950833 | T | C | 5 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0304 others(2): Show |
5 | HG00323.hp2 NA18946.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+6089T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950833 | |||||||
| chr14:59950866 | T | C | 1 | a0001c0004t0009g0304 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.882+6122T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950866 | |||||||
| chr14:59950907 | C | A | 1 | a0001c0001t0008g0013 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.882+6163C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950907 | |||||||
| chr14:59950913 | C | T | 1 | a0001c0001t0008g0155 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.882+6169C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950913 | |||||||
| chr14:59950937 | C | T | 2 | a0001c0001t0035g0156 a0001c0002t0024g0157 |
2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.882+6193C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950937 | |||||||
| chr14:59950990 | C | A | 1 | a0001c0002t0002g0005 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.882+6246C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950990 | |||||||
| chr14:59951053 | G | A | 209 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(206): Show |
211 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.882+6309G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951053 | |||||||
| chr14:59951080 | T | C | 1 | a0001c0002t0002g0137 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.882+6336T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951080 | |||||||
| chr14:59951116 | G | C | 2 | a0001c0001t0035g0156 a0001c0002t0024g0157 |
2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.882+6372G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951116 | |||||||
| chr14:59951231 | A | G | 1 | a0001c0002t0004g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.882+6487A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951231 | |||||||
| chr14:59951326 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.882+6582C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951326 | |||||||
| chr14:59951377 | G | A | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.882+6633G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951377 | |||||||
| chr14:59951414 | A | G | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+6670A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951414 | |||||||
| chr14:59951430 | G | T | 1 | a0001c0001t0001g0080 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.882+6686G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951430 | |||||||
| chr14:59951431 | A | C | 140 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(137): Show |
142 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.882+6687A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951431 | |||||||
| chr14:59951548 | C | T | 2 | a0001c0001t0035g0156 a0001c0002t0024g0157 |
2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.882+6804C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951548 | |||||||
| chr14:59951578 | G | A | 1 | a0002c0003t0005g0189 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.882+6834G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951578 | |||||||
| chr14:59951582 | T | C | 1 | a0001c0002t0017g0141 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.882+6838T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951582 | |||||||
| chr14:59951619 | C | A | 1 | a0001c0002t0002g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.882+6875C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951619 | |||||||
| chr14:59951659 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.882+6915T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951659 | |||||||
| chr14:59951675 | C | T | 27 | a0001c0001t0035g0156 a0001c0002t0004g0015 a0001c0002t0021g0161 others(24): Show |
28 | HG01496.hp2 HG02257.hp1 HG03453.hp1 others(25): Show |
intron_variant | MODIFIER | c.882+6931C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951675 | |||||||
| chr14:59951756 | T | C | 27 | a0001c0001t0035g0156 a0001c0002t0004g0015 a0001c0002t0021g0161 others(24): Show |
28 | HG01496.hp2 HG02257.hp1 HG03453.hp1 others(25): Show |
intron_variant | MODIFIER | c.882+7012T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951756 | |||||||
| chr14:59951832 | C | T | 2 | a0001c0004t0009g0302 a0001c0004t0009g0309 |
2 | HG00642.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.882+7088C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951832 | |||||||
| chr14:59951854 | C | T | 1 | a0001c0001t0006g0169 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.882+7110C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951854 | |||||||
| chr14:59951855 | G | A | 1 | a0001c0002t0002g0126 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.882+7111G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951855 | |||||||
| chr14:59951877 | T | G | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.882+7133T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951877 | |||||||
| chr14:59951945 | G | C | 1 | a0001c0002t0002g0127 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.882+7201G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951945 | |||||||
| chr14:59951959 | C | G | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.882+7215C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951959 | |||||||
| chr14:59951970 | C | T | 1 | a0001c0001t0011g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.882+7226C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951970 | |||||||
| chr14:59952005 | C | T | 25 | a0001c0002t0004g0015 a0001c0002t0021g0161 a0001c0002t0029g0017 others(22): Show |
26 | HG02257.hp1 HG03453.hp1 NA18939.hp2 others(23): Show |
intron_variant | MODIFIER | c.882+7261C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952005 | |||||||
| chr14:59952034 | C | T | 60 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(57): Show |
60 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.882+7290C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952034 | |||||||
| chr14:59952043 | C | T | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.882+7299C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952043 | |||||||
| chr14:59952044 | G | A | 1 | a0001c0002t0017g0117 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.882+7300G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952044 | |||||||
| chr14:59952056 | T | C | 2 | a0001c0001t0001g0263 a0001c0001t0003g0262 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.882+7312T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952056 | |||||||
| chr14:59952081 | A | G | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.882+7337A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952081 | |||||||
| chr14:59952188 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.882+7444G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952188 | |||||||
| chr14:59952242 | G | T | 27 | a0001c0001t0035g0156 a0001c0002t0004g0015 a0001c0002t0021g0161 others(24): Show |
28 | HG01496.hp2 HG02257.hp1 HG03453.hp1 others(25): Show |
intron_variant | MODIFIER | c.882+7498G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952242 | |||||||
| chr14:59952389 | G | A | 44 | a0001c0002t0002g0003 a0001c0002t0002g0215 a0001c0002t0002g0296 others(41): Show |
45 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.883-7429G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952389 | |||||||
| chr14:59952423 | G | A | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.883-7395G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952423 | |||||||
| chr14:59952423 | G | C | 1 | a0001c0002t0002g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.883-7395G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952423 | |||||||
| chr14:59952483 | G | T | 1 | a0001c0001t0006g0024 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.883-7335G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952483 | |||||||
| chr14:59952774 | C | T | 1 | a0001c0002t0002g0134 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.883-7044C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952774 | |||||||
| chr14:59952879 | G | A | 209 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(206): Show |
211 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.883-6939G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952879 | |||||||
| chr14:59952943 | G | A | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.883-6875G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952943 | |||||||
| chr14:59953061 | A | C | 1 | a0001c0001t0001g0250 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.883-6757A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59953061 | |||||||
| chr14:59953262 | T | C | 2 | a0001c0001t0035g0156 a0001c0002t0024g0157 |
2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.883-6556T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59953262 | |||||||
| chr14:59953270 | C | T | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.883-6548C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59953270 | |||||||
| chr14:59953286 | C | G | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.883-6532C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59953286 | |||||||
| chr14:59953529 | TG | T | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.883-6288delG | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59953529 | |||||||
| chr14:59953645 | G | A | 3 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0041 |
3 | HG00280.hp1 HG01175.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.883-6173G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59953645 | |||||||
| chr14:59953811 | T | C | 2 | a0001c0001t0003g0064 a0009c0017t0003g0065 |
2 | HG01169.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.883-6007T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59953811 | |||||||
| chr14:59953842 | G | C | 1 | a0001c0002t0002g0183 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.883-5976G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59953842 | |||||||
| chr14:59953879 | G | A | 1 | a0001c0002t0002g0005 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.883-5939G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59953879 | |||||||
| chr14:59953985 | A | G | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.883-5833A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59953985 | |||||||
| chr14:59954073 | A | G | 2 | a0002c0003t0005g0199 a0002c0003t0005g0204 |
2 | NA18964.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.883-5745A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59954073 | |||||||
| chr14:59954218 | T | C | 1 | a0001c0001t0010g0067 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.883-5600T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59954218 | |||||||
| chr14:59954303 | G | T | 1 | a0002c0003t0005g0188 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.883-5515G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59954303 | |||||||
| chr14:59954304 | T | G | 1 | a0001c0002t0029g0017 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.883-5514T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59954304 | |||||||
| chr14:59954321 | T | C | 2 | a0001c0002t0002g0138 a0001c0002t0002g0139 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.883-5497T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59954321 | |||||||
| chr14:59954361 | G | A | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.883-5457G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59954361 | |||||||
| chr14:59954416 | C | A | 1 | a0014c0019t0005g0042 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.883-5402C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59954416 | |||||||
| chr14:59954728 | A | G | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.883-5090A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59954728 | |||||||
| chr14:59954970 | G | A | 16 | a0001c0002t0002g0005 a0001c0002t0002g0112 a0001c0002t0002g0173 others(13): Show |
16 | HG01081.hp1 HG01243.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.883-4848G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59954970 | |||||||
| chr14:59955155 | C | T | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.883-4663C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59955155 | |||||||
| chr14:59955171 | G | A | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.883-4647G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59955171 | |||||||
| chr14:59955583 | A | C | 1 | a0001c0001t0003g0037 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.883-4235A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59955583 | |||||||
| chr14:59955608 | A | AT | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.883-4203dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr14 | 59955608 | ||||||
| chr14:59955700 | CTT | C | 45 | a0001c0002t0002g0003 a0001c0002t0002g0215 a0001c0002t0002g0296 others(42): Show |
46 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.883-4117_883-4116d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59955700 | |||||||
| chr14:59955987 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.883-3831C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59955987 | |||||||
| chr14:59956040 | A | T | 2 | a0001c0001t0035g0156 a0001c0002t0024g0157 |
2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.883-3778A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956040 | |||||||
| chr14:59956151 | GT | G | 3 | a0001c0001t0003g0022 a0001c0001t0006g0163 a0011c0014t0006g0162 |
3 | HG02735.hp1 HG03654.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.883-3666delT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956151 | |||||||
| chr14:59956231 | T | C | 1 | a0001c0001t0001g0227 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.883-3587T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956231 | |||||||
| chr14:59956244 | T | C | 1 | a0001c0001t0011g0097 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.883-3574T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956244 | |||||||
| chr14:59956279 | T | C | 1 | a0001c0002t0004g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.883-3539T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956279 | |||||||
| chr14:59956285 | A | G | 2 | a0001c0002t0002g0005 a0001c0002t0004g0004 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.883-3533A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956285 | |||||||
| chr14:59956311 | T | G | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.883-3507T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956311 | |||||||
| chr14:59956523 | A | G | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.883-3295A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956523 | |||||||
| chr14:59956538 | C | T | 45 | a0001c0002t0002g0003 a0001c0002t0002g0215 a0001c0002t0002g0296 others(42): Show |
46 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.883-3280C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956538 | |||||||
| chr14:59956548 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.883-3270G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956548 | |||||||
| chr14:59956684 | T | C | 1 | a0001c0002t0022g0269 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.883-3134T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956684 | |||||||
| chr14:59956685 | G | A | 1 | a0001c0001t0003g0228 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.883-3133G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956685 | |||||||
| chr14:59956760 | T | G | 1 | a0001c0001t0014g0040 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.883-3058T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956760 | |||||||
| chr14:59956761 | T | C | 1 | a0001c0001t0014g0040 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.883-3057T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956761 | |||||||
| chr14:59956762 | G | T | 1 | a0001c0001t0014g0040 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.883-3056G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956762 | |||||||
| chr14:59956763 | C | G | 1 | a0001c0001t0014g0040 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.883-3055C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956763 | |||||||
| chr14:59956793 | A | G | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.883-3025A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956793 | |||||||
| chr14:59956853 | G | A | 1 | a0001c0004t0009g0307 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.883-2965G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956853 | |||||||
| chr14:59956897 | T | C | 185 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(182): Show |
186 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.883-2921T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956897 | |||||||
| chr14:59957108 | G | T | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.883-2710G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59957108 | |||||||
| chr14:59957219 | G | A | 45 | a0001c0002t0002g0003 a0001c0002t0002g0215 a0001c0002t0002g0296 others(42): Show |
46 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.883-2599G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59957219 | |||||||
| chr14:59957733 | G | C | 3 | a0001c0001t0003g0070 a0001c0001t0006g0071 a0001c0001t0006g0072 |
3 | HG00423.hp2 NA18998.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.883-2085G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59957733 | |||||||
| chr14:59957739 | G | T | 3 | a0001c0001t0003g0070 a0001c0001t0006g0071 a0001c0001t0006g0072 |
3 | HG00423.hp2 NA18998.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.883-2079G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59957739 | |||||||
| chr14:59957761 | A | T | 185 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(182): Show |
186 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.883-2057A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59957761 | |||||||
| chr14:59957780 | A | T | 1 | a0001c0001t0014g0103 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.883-2038A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59957780 | |||||||
| chr14:59957843 | C | T | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.883-1975C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59957843 | |||||||
| chr14:59958022 | G | A | 1 | a0001c0002t0002g0183 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.883-1796G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59958022 | |||||||
| chr14:59958165 | G | A | 66 | a0001c0001t0030g0160 a0001c0002t0002g0005 a0001c0002t0002g0107 others(63): Show |
66 | HG00639.hp1 HG01081.hp1 HG01109.hp1 others(63): Show |
intron_variant | MODIFIER | c.883-1653G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59958165 | |||||||
| chr14:59958286 | T | G | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.883-1532T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59958286 | |||||||
| chr14:59958367 | A | T | 1 | a0001c0001t0014g0040 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.883-1451A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59958367 | |||||||
| chr14:59958524 | C | T | 1 | a0001c0001t0003g0014 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.883-1294C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59958524 | |||||||
| chr14:59958684 | C | A | 56 | a0001c0001t0030g0160 a0001c0002t0002g0107 a0001c0002t0002g0112 others(53): Show |
56 | HG00639.hp1 HG01109.hp1 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.883-1134C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59958684 | |||||||
| chr14:59958722 | G | A | 22 | a0001c0001t0001g0016 a0001c0001t0001g0080 a0001c0001t0001g0081 others(19): Show |
22 | HG01433.hp1 HG01884.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.883-1096G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59958722 | |||||||
| chr14:59958796 | C | T | 2 | a0001c0001t0035g0156 a0001c0002t0024g0157 |
2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.883-1022C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59958796 | |||||||
| chr14:59958860 | G | A | 1 | a0001c0001t0014g0040 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.883-958G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59958860 | |||||||
| chr14:59958861 | A | G | 1 | a0001c0001t0014g0040 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.883-957A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59958861 | |||||||
| chr14:59958881 | C | T | 46 | a0001c0002t0002g0003 a0001c0002t0002g0207 a0001c0002t0002g0215 others(43): Show |
47 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.883-937C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59958881 | |||||||
| chr14:59958965 | T | C | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.883-853T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59958965 | |||||||
| chr14:59959197 | C | A | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.883-621C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59959197 | |||||||
| chr14:59959210 | T | A | 2 | a0001c0001t0035g0156 a0001c0002t0024g0157 |
2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.883-608T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59959210 | |||||||
| chr14:59959391 | G | GTGGTGAA others(3): Show |
1 | a0001c0001t0014g0040 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.883-425_883-416dup others(10): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr14 | 59959391 | ||||||
| chr14:59959510 | G | A | 69 | a0001c0001t0030g0160 a0001c0002t0002g0005 a0001c0002t0002g0107 others(66): Show |
69 | HG00639.hp1 HG01081.hp1 HG01109.hp1 others(66): Show |
intron_variant | MODIFIER | c.883-308G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59959510 | |||||||
| chr14:59960044 | G | C | 3 | a0001c0002t0002g0112 a0001c0002t0002g0173 a0001c0002t0025g0113 |
3 | HG01884.hp2 HG02145.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1079+30G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 9/32 | chr14 | 59960044 | |||||||
| chr14:59960053 | T | C | 209 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(206): Show |
211 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.1079+39T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 9/32 | chr14 | 59960053 | |||||||
| chr14:59960088 | C | A | 2 | a0001c0001t0035g0156 a0001c0002t0024g0157 |
2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1079+74C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 9/32 | chr14 | 59960088 | |||||||
| chr14:59960185 | G | C | 60 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(57): Show |
60 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.1079+171G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 9/32 | chr14 | 59960185 | |||||||
| chr14:59960328 | C | G | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.1079+314C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 9/32 | chr14 | 59960328 | |||||||
| chr14:59960406 | A | G | 2 | a0001c0001t0035g0156 a0001c0002t0024g0157 |
2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1079+392A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 9/32 | chr14 | 59960406 | |||||||
| chr14:59960432 | T | G | 43 | a0001c0002t0002g0003 a0001c0002t0002g0215 a0001c0002t0002g0296 others(40): Show |
44 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.1079+418T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 9/32 | chr14 | 59960432 | |||||||
| chr14:59960533 | G | T | 209 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(206): Show |
211 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.1080-381G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 9/32 | chr14 | 59960533 | |||||||
| chr14:59960621 | A | T | 69 | a0001c0001t0030g0160 a0001c0002t0002g0005 a0001c0002t0002g0107 others(66): Show |
69 | HG00639.hp1 HG01081.hp1 HG01109.hp1 others(66): Show |
intron_variant | MODIFIER | c.1080-293A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 9/32 | chr14 | 59960621 | |||||||
| chr14:59961418 | C | T | 2 | a0001c0002t0002g0176 a0001c0002t0002g0177 |
2 | HG01255.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1211+373C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59961418 | |||||||
| chr14:59961443 | G | C | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.1211+398G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59961443 | |||||||
| chr14:59962086 | T | A | 1 | a0001c0002t0002g0176 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1211+1041T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59962086 | |||||||
| chr14:59962401 | T | C | 2 | a0001c0001t0035g0156 a0001c0002t0024g0157 |
2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1211+1356T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59962401 | |||||||
| chr14:59962409 | A | AT | 43 | a0001c0002t0002g0003 a0001c0002t0002g0215 a0001c0002t0002g0296 others(40): Show |
44 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.1211+1376dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59962409 | ||||||
| chr14:59962410 | T | C | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1211+1365T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59962410 | |||||||
| chr14:59962446 | G | A | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1211+1401G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59962446 | |||||||
| chr14:59962464 | C | T | 2 | a0001c0002t0004g0015 a0001c0002t0029g0017 |
2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1211+1419C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59962464 | |||||||
| chr14:59962528 | C | T | 1 | a0001c0002t0007g0275 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1211+1483C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59962528 | |||||||
| chr14:59962616 | T | C | 2 | a0001c0012t0002g0106 a0001c0012t0002g0140 |
2 | HG02602.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1211+1571T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59962616 | |||||||
| chr14:59962717 | T | A | 2 | a0003c0007t0004g0276 a0003c0007t0004g0277 |
2 | NA18961.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.1211+1672T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59962717 | |||||||
| chr14:59962780 | G | GA | 68 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(65): Show |
68 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1211+1748dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59962780 | ||||||
| chr14:59962780 | GA | G | 53 | a0001c0001t0035g0156 a0001c0001t0043g0012 a0001c0002t0002g0003 others(50): Show |
54 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.1211+1748delA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59962780 | ||||||
| chr14:59963414 | T | C | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1211+2369T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59963414 | |||||||
| chr14:59963511 | T | TA | 21 | a0001c0001t0001g0082 a0001c0001t0035g0156 a0001c0002t0024g0157 others(18): Show |
22 | HG01496.hp2 HG01884.hp1 HG03516.hp2 others(19): Show |
intron_variant | MODIFIER | c.1211+2479dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59963511 | ||||||
| chr14:59963544 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1211+2499A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59963544 | |||||||
| chr14:59964171 | G | A | 1 | a0002c0003t0005g0205 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1212-2418G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59964171 | |||||||
| chr14:59964366 | A | G | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.1212-2223A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59964366 | |||||||
| chr14:59964511 | A | G | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.1212-2078A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59964511 | |||||||
| chr14:59964665 | T | C | 1 | a0001c0001t0010g0043 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1212-1924T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59964665 | |||||||
| chr14:59964802 | A | ACTATTCA others(7): Show |
116 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0217 others(113): Show |
117 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1212-1776_1212-177 others(18): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59964802 | ||||||
| chr14:59965150 | A | G | 1 | a0001c0002t0004g0265 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1212-1439A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59965150 | |||||||
| chr14:59965362 | C | T | 1 | a0001c0001t0006g0024 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1212-1227C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59965362 | |||||||
| chr14:59965401 | G | T | 1 | a0001c0001t0001g0250 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1212-1188G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59965401 | |||||||
| chr14:59965434 | A | G | 1 | a0001c0002t0002g0134 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1212-1155A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59965434 | |||||||
| chr14:59965457 | A | G | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.1212-1132A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59965457 | |||||||
| chr14:59965469 | T | C | 20 | a0001c0002t0004g0265 a0001c0002t0004g0268 a0001c0002t0004g0271 others(17): Show |
20 | HG00558.hp2 HG02165.hp2 NA18942.hp2 others(17): Show |
intron_variant | MODIFIER | c.1212-1120T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59965469 | |||||||
| chr14:59965580 | A | G | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.1212-1009A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59965580 | |||||||
| chr14:59965634 | C | T | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.1212-955C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59965634 | |||||||
| chr14:59965640 | C | CTT | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.1212-948_1212-947i others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965640 | ||||||
| chr14:59965661 | A | T | 1 | a0001c0001t0003g0095 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1212-928A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59965661 | |||||||
| chr14:59965840 | G | A | 1 | a0002c0003t0005g0185 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1212-749G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59965840 | |||||||
| chr14:59965882 | C | CA | 7 | a0001c0001t0003g0100 a0001c0002t0002g0112 a0001c0002t0002g0126 others(4): Show |
7 | HG01361.hp2 HG01884.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.1212-669dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | ||||||
| chr14:59965882 | C | CAAA | 17 | a0001c0001t0001g0061 a0001c0001t0001g0069 a0001c0001t0001g0077 others(14): Show |
17 | HG00642.hp1 HG00735.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.1212-671_1212-669d others(5): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | ||||||
| chr14:59965882 | C | CAAAA | 25 | a0001c0001t0001g0027 a0001c0001t0001g0058 a0001c0001t0001g0087 others(22): Show |
25 | HG00099.hp2 HG00621.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.1212-672_1212-669d others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | ||||||
| chr14:59965882 | C | CAAAAA | 17 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0003g0022 others(14): Show |
17 | HG00423.hp1 HG00423.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1212-673_1212-669d others(7): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | ||||||
| chr14:59965882 | C | CAAAAAA | 9 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0003g0168 others(6): Show |
9 | HG01175.hp2 HG01361.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.1212-674_1212-669d others(8): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | ||||||
| chr14:59965882 | C | CAAAAAAA others(3): Show |
3 | a0001c0001t0008g0007 a0001c0001t0008g0010 a0001c0002t0004g0015 |
3 | HG01081.hp2 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1212-678_1212-669d others(12): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | ||||||
| chr14:59965882 | C | CAAAAAAA others(4): Show |
3 | a0001c0001t0008g0154 a0001c0001t0011g0097 a0001c0001t0014g0066 |
3 | HG02559.hp2 HG03579.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1212-679_1212-669d others(13): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | ||||||
| chr14:59965882 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0043g0012 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1212-680_1212-669d others(14): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | ||||||
| chr14:59965882 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0003g0095 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1212-681_1212-669d others(15): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | ||||||
| chr14:59965882 | C | CAAAAAAA others(7): Show |
3 | a0001c0001t0001g0084 a0001c0001t0008g0009 a0001c0001t0044g0008 |
3 | HG01433.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1212-682_1212-669d others(16): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | ||||||
| chr14:59965882 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0093 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1212-683_1212-669d others(17): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | ||||||
| chr14:59965882 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0008g0013 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1212-684_1212-669d others(18): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | ||||||
| chr14:59965882 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0081 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1212-689_1212-669d others(23): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | ||||||
| chr14:59965882 | C | CAAAAAAA others(15): Show |
1 | a0001c0001t0019g0083 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1212-690_1212-669d others(24): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | ||||||
| chr14:59965882 | CA | C | 23 | a0001c0002t0002g0107 a0001c0002t0002g0118 a0001c0002t0002g0145 others(20): Show |
23 | HG00323.hp2 HG01175.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1212-669delA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | ||||||
| chr14:59965882 | CAA | C | 13 | a0001c0001t0030g0160 a0001c0002t0002g0133 a0001c0002t0002g0136 others(10): Show |
13 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1212-670_1212-669d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | ||||||
| chr14:59965882 | CAAAAAAA | C | 19 | a0001c0001t0001g0089 a0001c0001t0003g0254 a0001c0001t0006g0024 others(16): Show |
20 | HG00621.hp2 HG00735.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.1212-675_1212-669d others(9): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | ||||||
| chr14:59965882 | CAAAAAAA others(1): Show |
C | 42 | a0001c0001t0001g0080 a0001c0001t0001g0208 a0001c0001t0001g0223 others(39): Show |
42 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.1212-676_1212-669d others(10): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | ||||||
| chr14:59965882 | CAAAAAAA others(2): Show |
C | 43 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0213 others(40): Show |
43 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.1212-677_1212-669d others(11): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | ||||||
| chr14:59965882 | CAAAAAAA others(3): Show |
C | 6 | a0001c0001t0001g0016 a0001c0001t0001g0092 a0001c0001t0003g0228 others(3): Show |
6 | HG00673.hp2 HG01934.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.1212-678_1212-669d others(12): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | ||||||
| chr14:59965882 | CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0008g0011 a0001c0001t0011g0075 a0001c0002t0002g0119 |
3 | HG00639.hp2 HG01192.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1212-679_1212-669d others(13): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | ||||||
| chr14:59965882 | CAAAAAAA others(5): Show |
C | 6 | a0001c0002t0002g0137 a0001c0002t0002g0149 a0001c0002t0002g0174 others(3): Show |
6 | HG00639.hp1 HG01346.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1212-680_1212-669d others(14): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | ||||||
| chr14:59965882 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0082 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1212-681_1212-669d others(15): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | ||||||
| chr14:59965882 | CAAAAAAA others(7): Show |
C | 21 | a0002c0003t0005g0001 a0002c0003t0005g0186 a0002c0003t0005g0187 others(18): Show |
22 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(19): Show |
intron_variant | MODIFIER | c.1212-682_1212-669d others(16): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | ||||||
| chr14:59965882 | CAAAAAAA others(8): Show |
C | 1 | a0002c0003t0005g0185 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1212-683_1212-669d others(17): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | ||||||
| chr14:59965882 | CAAAAAAA others(10): Show |
C | 1 | a0001c0006t0002g0116 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1212-685_1212-669d others(19): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | ||||||
| chr14:59965882 | CAAAAAAA others(13): Show |
C | 2 | a0001c0001t0003g0102 a0001c0001t0015g0096 |
2 | HG01993.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1212-688_1212-669d others(22): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | ||||||
| chr14:59966135 | T | G | 3 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0041 |
3 | HG00280.hp1 HG01175.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1212-454T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59966135 | |||||||
| chr14:59966271 | T | G | 4 | a0001c0002t0004g0271 a0001c0002t0004g0278 a0001c0002t0004g0281 others(1): Show |
4 | HG00558.hp2 NA18950.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.1212-318T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59966271 | |||||||
| chr14:59967318 | T | C | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.1506+105T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59967318 | |||||||
| chr14:59967757 | C | T | 1 | a0001c0002t0004g0287 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1506+544C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59967757 | |||||||
| chr14:59967808 | A | G | 1 | a0001c0002t0004g0310 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1506+595A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59967808 | |||||||
| chr14:59967886 | G | A | 1 | a0001c0002t0002g0134 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1506+673G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59967886 | |||||||
| chr14:59968350 | G | A | 2 | a0001c0001t0035g0156 a0001c0002t0024g0157 |
2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1506+1137G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59968350 | |||||||
| chr14:59968426 | C | T | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1506+1213C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59968426 | |||||||
| chr14:59968427 | A | C | 109 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(106): Show |
109 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.1506+1214A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59968427 | |||||||
| chr14:59968507 | T | C | 2 | a0001c0001t0003g0029 a0001c0001t0003g0047 |
2 | NA18984.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1506+1294T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59968507 | |||||||
| chr14:59968770 | G | GC | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.1506+1560dupC | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | INFO_REALIGN_3_PRIME | chr14 | 59968770 | ||||||
| chr14:59968972 | G | GA | 110 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(107): Show |
110 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.1506+1767dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | INFO_REALIGN_3_PRIME | chr14 | 59968972 | ||||||
| chr14:59969327 | G | A | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.1506+2114G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59969327 | |||||||
| chr14:59969345 | G | A | 1 | a0001c0002t0004g0289 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1506+2132G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59969345 | |||||||
| chr14:59969413 | A | G | 24 | a0001c0001t0035g0156 a0001c0002t0024g0157 a0002c0003t0005g0001 others(21): Show |
25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.1506+2200A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59969413 | |||||||
| chr14:59969484 | G | A | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1506+2271G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59969484 | |||||||
| chr14:59969546 | C | T | 25 | a0001c0001t0035g0156 a0001c0002t0002g0207 a0001c0002t0024g0157 others(22): Show |
26 | HG01496.hp2 HG02922.hp1 HG03516.hp2 others(23): Show |
intron_variant | MODIFIER | c.1506+2333C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59969546 | |||||||
| chr14:59969760 | A | G | 1 | a0001c0001t0008g0006 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1506+2547A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59969760 | |||||||
| chr14:59969775 | T | C | 1 | a0001c0002t0004g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1506+2562T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59969775 | |||||||
| chr14:59969930 | A | G | 39 | a0001c0001t0036g0314 a0001c0001t0037g0247 a0001c0002t0002g0003 others(36): Show |
40 | HG00609.hp1 HG00673.hp1 HG02015.hp2 others(37): Show |
intron_variant | MODIFIER | c.1506+2717A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59969930 | |||||||
| chr14:59970041 | G | C | 1 | a0001c0002t0017g0117 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1506+2828G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59970041 | |||||||
| chr14:59970112 | T | C | 3 | a0001c0002t0002g0005 a0001c0002t0004g0015 a0001c0002t0029g0017 |
3 | HG01081.hp1 HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1506+2899T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59970112 | |||||||
| chr14:59970155 | C | T | 9 | a0001c0001t0011g0021 a0001c0002t0004g0004 a0001c0005t0013g0151 others(6): Show |
9 | HG01243.hp2 HG01358.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1506+2942C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59970155 | |||||||
| chr14:59970208 | T | A | 3 | a0001c0001t0003g0048 a0001c0001t0014g0040 a0001c0002t0002g0136 |
3 | HG03654.hp1 NA19059.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1506+2995T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59970208 | |||||||
| chr14:59970851 | A | C | 2 | a0007c0013t0018g0110 a0007c0013t0018g0111 |
2 | HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1506+3638A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59970851 | |||||||
| chr14:59970877 | G | C | 1 | a0001c0002t0004g0310 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1506+3664G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59970877 | |||||||
| chr14:59970889 | T | C | 1 | a0001c0002t0017g0117 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1506+3676T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59970889 | |||||||
| chr14:59971054 | G | T | 1 | a0009c0017t0003g0065 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1507-3522G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59971054 | |||||||
| chr14:59971056 | TTTACATT others(7): Show |
T | 1 | a0001c0002t0004g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1507-3509_1507-349 others(18): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | INFO_REALIGN_3_PRIME | chr14 | 59971056 | ||||||
| chr14:59971193 | C | A | 7 | a0001c0005t0013g0151 a0001c0005t0013g0171 a0001c0005t0013g0172 others(4): Show |
7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1507-3383C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59971193 | |||||||
| chr14:59971311 | C | T | 3 | a0001c0002t0002g0173 a0001c0002t0002g0215 a0001c0002t0025g0113 |
3 | HG02145.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1507-3265C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59971311 | |||||||
| chr14:59971317 | C | T | 2 | a0001c0002t0002g0005 a0001c0002t0004g0004 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1507-3259C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59971317 | |||||||
| chr14:59971375 | C | T | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1507-3201C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59971375 | |||||||
| chr14:59971513 | G | A | 2 | a0001c0001t0003g0038 a0001c0001t0003g0039 |
2 | HG00099.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.1507-3063G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59971513 | |||||||
| chr14:59971524 | A | G | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.1507-3052A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59971524 | |||||||
| chr14:59971628 | C | T | 164 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(161): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.1507-2948C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59971628 | |||||||
| chr14:59972094 | A | C | 189 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(186): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1507-2482A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59972094 | |||||||
| chr14:59972401 | G | A | 42 | a0001c0002t0004g0153 a0001c0002t0004g0214 a0001c0002t0004g0265 others(39): Show |
43 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.1507-2175G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59972401 | |||||||
| chr14:59972457 | G | A | 258 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(255): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.1507-2119G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59972457 | |||||||
| chr14:59972681 | C | T | 1 | a0001c0001t0003g0014 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1507-1895C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59972681 | |||||||
| chr14:59973038 | G | A | 1 | a0001c0002t0002g0136 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1507-1538G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59973038 | |||||||
| chr14:59973323 | A | G | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.1507-1253A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59973323 | |||||||
| chr14:59973346 | G | A | 165 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.1507-1230G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59973346 | |||||||
| chr14:59973349 | C | A | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.1507-1227C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59973349 | |||||||
| chr14:59973486 | A | G | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1507-1090A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59973486 | |||||||
| chr14:59973536 | T | C | 6 | a0001c0001t0001g0044 a0001c0001t0001g0077 a0001c0001t0011g0050 others(3): Show |
6 | HG00621.hp1 HG02074.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.1507-1040T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59973536 | |||||||
| chr14:59973598 | TCTAGA | T | 4 | a0001c0001t0001g0208 a0001c0001t0001g0225 a0001c0001t0001g0257 others(1): Show |
4 | NA18944.hp1 NA18968.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.1507-974_1507-970d others(7): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | INFO_REALIGN_3_PRIME | chr14 | 59973598 | ||||||
| chr14:59973604 | C | G | 1 | a0001c0002t0012g0148 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1507-972C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59973604 | |||||||
| chr14:59973919 | G | A | 1 | a0001c0002t0007g0266 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1507-657G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59973919 | |||||||
| chr14:59973929 | C | T | 2 | a0001c0002t0002g0145 a0001c0002t0002g0146 |
2 | HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1507-647C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59973929 | |||||||
| chr14:59973930 | G | A | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1507-646G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59973930 | |||||||
| chr14:59973950 | T | C | 1 | a0001c0001t0011g0097 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1507-626T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59973950 | |||||||
| chr14:59973969 | A | G | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1507-607A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59973969 | |||||||
| chr14:59974067 | C | T | 7 | a0001c0005t0013g0151 a0001c0005t0013g0171 a0001c0005t0013g0172 others(4): Show |
7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1507-509C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59974067 | |||||||
| chr14:59974139 | T | C | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.1507-437T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59974139 | |||||||
| chr14:59974874 | A | G | 4 | a0001c0002t0002g0112 a0001c0002t0002g0173 a0001c0002t0002g0215 others(1): Show |
4 | HG01884.hp2 HG02145.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1639+166A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59974874 | |||||||
| chr14:59974944 | C | T | 1 | a0001c0002t0017g0117 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1639+236C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59974944 | |||||||
| chr14:59975033 | G | A | 1 | a0001c0002t0002g0005 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1639+325G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975033 | |||||||
| chr14:59975034 | C | CATATAT | 9 | a0001c0001t0001g0016 a0001c0001t0001g0087 a0001c0001t0001g0094 others(6): Show |
9 | HG01169.hp2 HG02572.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1639+339_1639+344d others(8): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975034 | ||||||
| chr14:59975034 | C | CATATATA others(1): Show |
49 | a0001c0001t0001g0058 a0001c0001t0001g0077 a0001c0001t0001g0084 others(46): Show |
49 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.1639+337_1639+344d others(10): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975034 | ||||||
| chr14:59975034 | C | CATATATA others(3): Show |
29 | a0001c0001t0001g0061 a0001c0001t0001g0080 a0001c0001t0001g0081 others(26): Show |
29 | HG00099.hp1 HG00280.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.1639+335_1639+344d others(12): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975034 | ||||||
| chr14:59975034 | C | CATATATA others(5): Show |
50 | a0001c0001t0001g0027 a0001c0001t0001g0044 a0001c0001t0001g0045 others(47): Show |
50 | HG00323.hp1 HG00558.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1639+333_1639+344d others(14): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975034 | ||||||
| chr14:59975034 | C | CATATATA others(7): Show |
23 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0237 others(20): Show |
23 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.1639+331_1639+344d others(16): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975034 | ||||||
| chr14:59975034 | C | CATATATA others(9): Show |
1 | a0001c0001t0028g0030 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1639+329_1639+344d others(18): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975034 | ||||||
| chr14:59975034 | C | T | 1 | a0001c0002t0002g0005 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1639+326C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975034 | |||||||
| chr14:59975034 | CAT | C | 16 | a0001c0002t0002g0159 a0001c0002t0004g0214 a0001c0002t0004g0273 others(13): Show |
16 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.1639+343_1639+344d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975034 | ||||||
| chr14:59975034 | CATAT | C | 15 | a0001c0002t0004g0004 a0001c0002t0004g0015 a0001c0002t0021g0161 others(12): Show |
15 | HG01243.hp2 HG01358.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1639+341_1639+344d others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975034 | ||||||
| chr14:59975038 | T | TGTGTCAC others(3): Show |
1 | a0001c0002t0002g0005 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1639+330_1639+331i others(12): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975038 | |||||||
| chr14:59975047 | ATATATGC others(35): Show |
A | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+345_1639+386d others(44): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975047 | ||||||
| chr14:59975063 | ACTATGTG | A | 162 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(159): Show |
162 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.1639+356_1639+362d others(9): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975063 | |||||||
| chr14:59975063 | ACTATGTG others(4): Show |
A | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1639+356_1639+366d others(13): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975063 | |||||||
| chr14:59975066 | A | G | 41 | a0001c0002t0004g0153 a0001c0002t0004g0265 a0001c0002t0004g0268 others(38): Show |
42 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(39): Show |
intron_variant | MODIFIER | c.1639+358A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975066 | |||||||
| chr14:59975066 | ATG | A | 4 | a0001c0002t0002g0136 a0001c0002t0002g0144 a0001c0002t0004g0015 others(1): Show |
4 | HG03453.hp1 HG03654.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1639+376_1639+377d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975066 | ||||||
| chr14:59975087 | G | GTGTATAT others(31): Show |
3 | a0001c0001t0030g0160 a0001c0002t0025g0135 a0001c0002t0026g0132 |
3 | HG02683.hp1 HG03942.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1639+434_1639+471d others(40): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975087 | ||||||
| chr14:59975087 | GTGTATAT others(31): Show |
G | 1 | a0001c0002t0002g0127 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1639+434_1639+471d others(40): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975087 | ||||||
| chr14:59975090 | TATATATA others(43): Show |
T | 1 | a0002c0003t0005g0197 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1639+393_1639+442d others(52): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975090 | ||||||
| chr14:59975091 | ATATATAT others(53): Show |
A | 2 | a0001c0001t0001g0094 a0012c0018t0003g0230 |
2 | HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1639+394_1639+453d others(62): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975091 | ||||||
| chr14:59975092 | TATATATA others(41): Show |
T | 4 | a0001c0001t0001g0088 a0001c0001t0001g0092 a0001c0001t0014g0066 others(1): Show |
4 | HG02818.hp2 HG03579.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1639+394_1639+441d others(50): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975092 | ||||||
| chr14:59975093 | ATATATAT others(51): Show |
A | 82 | a0001c0001t0001g0027 a0001c0001t0001g0045 a0001c0001t0001g0058 others(79): Show |
82 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1639+394_1639+451d others(60): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975093 | ||||||
| chr14:59975095 | ATATATAC others(49): Show |
A | 49 | a0001c0001t0001g0044 a0001c0001t0001g0085 a0001c0001t0001g0224 others(46): Show |
49 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1639+394_1639+449d others(58): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975095 | ||||||
| chr14:59975097 | ATATACAT others(47): Show |
A | 18 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(15): Show |
18 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.1639+394_1639+447d others(56): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975097 | ||||||
| chr14:59975099 | ATACATAT others(45): Show |
A | 9 | a0001c0001t0001g0077 a0001c0001t0001g0234 a0001c0001t0001g0299 others(6): Show |
9 | HG01952.hp1 HG02559.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.1639+394_1639+445d others(54): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975099 | ||||||
| chr14:59975101 | ACATATAT others(43): Show |
A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0091 |
2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1639+394_1639+443d others(52): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975101 | |||||||
| chr14:59975102 | C | T | 2 | a0001c0002t0002g0112 a0004c0008t0015g0167 |
2 | HG01884.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1639+394C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975102 | |||||||
| chr14:59975102 | CAT | C | 3 | a0001c0002t0002g0138 a0001c0002t0002g0139 a0001c0002t0002g0215 |
3 | HG01257.hp2 HG01258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1639+403_1639+404d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975102 | ||||||
| chr14:59975102 | CATATATA others(45): Show |
C | 2 | a0001c0002t0002g0145 a0001c0002t0017g0175 |
2 | HG01243.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1639+418_1639+469d others(54): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975102 | ||||||
| chr14:59975104 | T | C | 1 | a0001c0002t0002g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1639+396T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975104 | |||||||
| chr14:59975111 | A | G | 29 | a0001c0002t0021g0161 a0001c0005t0013g0151 a0001c0005t0013g0171 others(26): Show |
30 | HG01358.hp2 HG02145.hp1 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.1639+403A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975111 | |||||||
| chr14:59975112 | TGTATATA others(21): Show |
T | 22 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(19): Show |
23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.1639+405_1639+432d others(30): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975112 | |||||||
| chr14:59975113 | G | A | 7 | a0001c0002t0021g0161 a0001c0005t0013g0151 a0001c0005t0013g0171 others(4): Show |
7 | HG01358.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1639+405G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975113 | |||||||
| chr14:59975113 | G | GTA | 39 | a0001c0002t0004g0015 a0001c0002t0004g0153 a0001c0002t0004g0265 others(36): Show |
40 | HG00558.hp2 HG02015.hp2 HG02080.hp2 others(37): Show |
intron_variant | MODIFIER | c.1639+417_1639+418d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975113 | ||||||
| chr14:59975113 | G | GTATATAT others(35): Show |
1 | a0001c0002t0004g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1639+418_1639+419i others(44): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975113 | ||||||
| chr14:59975113 | G | GTATATAT others(47): Show |
1 | a0001c0002t0004g0289 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1639+418_1639+419i others(56): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975113 | ||||||
| chr14:59975113 | G | GTATATAT others(47): Show |
1 | a0001c0002t0004g0273 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1639+416_1639+469d others(56): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975113 | ||||||
| chr14:59975114 | T | C | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+406T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975114 | |||||||
| chr14:59975115 | A | ATATATAT others(61): Show |
9 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(6): Show |
9 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.1639+416_1639+417i others(70): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975115 | ||||||
| chr14:59975115 | A | ATATATAT others(61): Show |
1 | a0001c0004t0009g0303 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1639+416_1639+417i others(70): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975115 | ||||||
| chr14:59975115 | A | G | 8 | a0001c0002t0012g0120 a0001c0002t0012g0121 a0001c0002t0012g0122 others(5): Show |
8 | HG02486.hp1 HG02622.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1639+407A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975115 | |||||||
| chr14:59975115 | A | T | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+407A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975115 | |||||||
| chr14:59975116 | T | C | 2 | a0001c0005t0013g0180 a0001c0005t0013g0181 |
2 | HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1639+408T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975116 | |||||||
| chr14:59975116 | T | G | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+408T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975116 | |||||||
| chr14:59975116 | T | TAC | 3 | a0001c0002t0002g0005 a0001c0002t0004g0004 a0001c0005t0013g0179 |
3 | HG01081.hp1 HG01243.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1639+409_1639+410i others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975116 | ||||||
| chr14:59975117 | A | ATATATAT others(23): Show |
2 | a0001c0002t0002g0143 a0001c0002t0002g0144 |
2 | NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1639+418_1639+419i others(32): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975117 | ||||||
| chr14:59975118 | T | A | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+410T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975118 | |||||||
| chr14:59975118 | T | C | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1639+410T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975118 | |||||||
| chr14:59975119 | A | C | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+411A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975119 | |||||||
| chr14:59975122 | T | A | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+414T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975122 | |||||||
| chr14:59975125 | A | G | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+417A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975125 | |||||||
| chr14:59975127 | G | A | 2 | a0001c0002t0002g0143 a0001c0002t0002g0144 |
2 | NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1639+419G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975127 | |||||||
| chr14:59975129 | A | G | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+421A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975129 | |||||||
| chr14:59975131 | A | G | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+423A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975131 | |||||||
| chr14:59975133 | A | G | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+425A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975133 | |||||||
| chr14:59975135 | A | G | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+427A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975135 | |||||||
| chr14:59975137 | A | G | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+429A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975137 | |||||||
| chr14:59975140 | C | CAT | 5 | a0001c0002t0002g0005 a0001c0002t0004g0004 a0001c0002t0021g0161 others(2): Show |
5 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1639+441_1639+442d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975140 | ||||||
| chr14:59975140 | CAT | C | 8 | a0001c0002t0002g0107 a0001c0002t0002g0138 a0001c0002t0002g0139 others(5): Show |
8 | HG01175.hp1 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1639+441_1639+442d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975140 | ||||||
| chr14:59975143 | A | G | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+435A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975143 | |||||||
| chr14:59975145 | A | G | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+437A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975145 | |||||||
| chr14:59975147 | A | ATG | 7 | a0001c0005t0013g0151 a0001c0005t0013g0171 a0001c0005t0013g0172 others(4): Show |
7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1639+440_1639+441i others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975147 | ||||||
| chr14:59975148 | T | TAC | 4 | a0001c0004t0009g0302 a0001c0004t0009g0307 a0001c0004t0009g0308 others(1): Show |
4 | HG00642.hp1 HG00735.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1639+441_1639+442i others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975148 | ||||||
| chr14:59975150 | T | C | 6 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0303 others(3): Show |
6 | HG00323.hp2 HG01361.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.1639+442T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975150 | |||||||
| chr14:59975151 | G | A | 15 | a0001c0001t0001g0088 a0001c0001t0001g0092 a0001c0001t0014g0066 others(12): Show |
15 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.1639+443G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975151 | |||||||
| chr14:59975152 | T | C | 1 | a0001c0002t0004g0300 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1639+444T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975152 | |||||||
| chr14:59975154 | T | TAC | 17 | a0001c0002t0002g0005 a0001c0002t0002g0207 a0001c0002t0004g0004 others(14): Show |
17 | HG01081.hp1 HG01243.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.1639+447_1639+448i others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975154 | ||||||
| chr14:59975165 | G | A | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1639+457G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975165 | |||||||
| chr14:59975190 | G | A | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1639+482G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975190 | |||||||
| chr14:59975228 | C | T | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1639+520C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975228 | |||||||
| chr14:59975336 | A | G | 16 | a0001c0002t0002g0005 a0001c0002t0004g0004 a0001c0002t0004g0015 others(13): Show |
16 | HG01081.hp1 HG01243.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.1639+628A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975336 | |||||||
| chr14:59975725 | G | A | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1639+1017G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975725 | |||||||
| chr14:59976006 | C | A | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1640-1219C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59976006 | |||||||
| chr14:59976063 | G | T | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1640-1162G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59976063 | |||||||
| chr14:59976067 | G | A | 5 | a0001c0002t0021g0161 a0006c0010t0018g0166 a0006c0010t0021g0033 others(2): Show |
5 | HG02257.hp1 HG02486.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1640-1158G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59976067 | |||||||
| chr14:59976083 | G | T | 1 | a0001c0002t0002g0003 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1640-1142G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59976083 | |||||||
| chr14:59976253 | G | C | 58 | a0001c0001t0001g0044 a0001c0001t0001g0058 a0001c0001t0001g0069 others(55): Show |
58 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1640-972G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59976253 | |||||||
| chr14:59976356 | G | A | 1 | a0001c0001t0001g0238 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1640-869G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59976356 | |||||||
| chr14:59976472 | C | T | 207 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(204): Show |
208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.1640-753C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59976472 | |||||||
| chr14:59976630 | G | C | 1 | a0001c0002t0002g0005 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1640-595G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59976630 | |||||||
| chr14:59976691 | C | T | 1 | a0001c0001t0019g0311 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1640-534C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59976691 | |||||||
| chr14:59976706 | C | T | 42 | a0001c0002t0004g0153 a0001c0002t0004g0214 a0001c0002t0004g0265 others(39): Show |
43 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.1640-519C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59976706 | |||||||
| chr14:59976749 | G | A | 2 | a0001c0002t0004g0015 a0001c0002t0029g0017 |
2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1640-476G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59976749 | |||||||
| chr14:59976785 | C | A | 42 | a0001c0002t0004g0153 a0001c0002t0004g0214 a0001c0002t0004g0265 others(39): Show |
43 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.1640-440C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59976785 | |||||||
| chr14:59976945 | G | A | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1640-280G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59976945 | |||||||
| chr14:59976951 | A | G | 165 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.1640-274A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59976951 | |||||||
| chr14:59977088 | A | G | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.1640-137A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59977088 | |||||||
| chr14:59977412 | C | T | 1 | a0001c0001t0003g0245 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1762+65C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 14/32 | chr14 | 59977412 | |||||||
| chr14:59977495 | T | C | 1 | a0001c0005t0013g0182 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1762+148T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 14/32 | chr14 | 59977495 | |||||||
| chr14:59977568 | T | TTG | 86 | a0001c0001t0001g0044 a0001c0001t0001g0058 a0001c0001t0001g0077 others(83): Show |
87 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1762+255_1762+256d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 14/32 | INFO_REALIGN_3_PRIME | chr14 | 59977568 | ||||||
| chr14:59977568 | T | TTGTG | 9 | a0001c0001t0001g0165 a0001c0001t0003g0018 a0001c0001t0003g0019 others(6): Show |
9 | HG01496.hp2 HG02257.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.1762+253_1762+256d others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 14/32 | INFO_REALIGN_3_PRIME | chr14 | 59977568 | ||||||
| chr14:59977568 | T | TTGTGTGT others(1): Show |
3 | a0001c0001t0003g0029 a0001c0001t0003g0047 a0001c0005t0038g0150 |
3 | NA18984.hp2 NA19082.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1762+249_1762+256d others(10): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 14/32 | INFO_REALIGN_3_PRIME | chr14 | 59977568 | ||||||
| chr14:59977568 | TTG | T | 20 | a0001c0001t0001g0082 a0001c0001t0003g0037 a0001c0001t0003g0260 others(17): Show |
20 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.1762+255_1762+256d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 14/32 | INFO_REALIGN_3_PRIME | chr14 | 59977568 | ||||||
| chr14:59977632 | G | A | 1 | a0001c0004t0009g0209 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1762+285G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 14/32 | chr14 | 59977632 | |||||||
| chr14:59977707 | G | C | 1 | a0001c0002t0002g0176 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1763-310G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 14/32 | chr14 | 59977707 | |||||||
| chr14:59977840 | T | A | 1 | a0001c0001t0001g0218 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1763-177T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 14/32 | chr14 | 59977840 | |||||||
| chr14:59977934 | A | T | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1763-83A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 14/32 | chr14 | 59977934 | |||||||
| chr14:59978245 | A | G | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1878+113A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59978245 | |||||||
| chr14:59978251 | G | A | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1878+119G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59978251 | |||||||
| chr14:59978492 | C | T | 2 | a0001c0005t0013g0171 a0001c0005t0013g0172 |
2 | HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1878+360C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59978492 | |||||||
| chr14:59978502 | A | G | 189 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(186): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1878+370A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59978502 | |||||||
| chr14:59979291 | A | G | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1878+1159A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59979291 | |||||||
| chr14:59979344 | T | C | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1878+1212T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59979344 | |||||||
| chr14:59979372 | A | G | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1878+1240A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59979372 | |||||||
| chr14:59979484 | C | T | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1878+1352C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59979484 | |||||||
| chr14:59979536 | CGGGAGGC others(10): Show |
C | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.1878+1406_1878+142 others(21): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr14 | 59979536 | ||||||
| chr14:59979640 | C | T | 2 | a0001c0002t0002g0005 a0001c0002t0004g0004 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1878+1508C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59979640 | |||||||
| chr14:59979658 | T | G | 1 | a0001c0002t0012g0120 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1878+1526T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59979658 | |||||||
| chr14:59979716 | G | A | 6 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(3): Show |
6 | HG00609.hp2 HG00621.hp2 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.1878+1584G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59979716 | |||||||
| chr14:59979947 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1878+1815C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59979947 | |||||||
| chr14:59979979 | TA | T | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.1878+1855delA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr14 | 59979979 | ||||||
| chr14:59979988 | G | T | 1 | a0007c0013t0018g0111 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1878+1856G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59979988 | |||||||
| chr14:59980018 | C | A | 1 | a0001c0002t0004g0319 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1879-1830C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59980018 | |||||||
| chr14:59980040 | G | GCT | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.1879-1798_1879-179 others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr14 | 59980040 | ||||||
| chr14:59980189 | T | C | 1 | a0001c0001t0008g0013 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1879-1659T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59980189 | |||||||
| chr14:59980212 | T | C | 1 | a0009c0017t0003g0065 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1879-1636T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59980212 | |||||||
| chr14:59980248 | C | A | 1 | a0001c0001t0003g0070 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1879-1600C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59980248 | |||||||
| chr14:59980825 | C | G | 1 | a0001c0002t0002g0176 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1879-1023C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59980825 | |||||||
| chr14:59980964 | G | T | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1879-884G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59980964 | |||||||
| chr14:59981036 | T | C | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1879-812T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59981036 | |||||||
| chr14:59981725 | T | C | 1 | a0001c0002t0007g0290 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1879-123T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59981725 | |||||||
| chr14:59982061 | G | A | 2 | a0005c0011t0003g0211 a0005c0011t0006g0212 |
2 | HG00099.hp1 HG00280.hp2 |
splice_donor_variant&intron_variant | HIGH | c.2091+1G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59982061 | |||||||
| chr14:59982297 | T | C | 1 | a0001c0002t0004g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2091+237T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59982297 | |||||||
| chr14:59982300 | A | G | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2091+240A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59982300 | |||||||
| chr14:59982450 | G | T | 165 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.2091+390G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59982450 | |||||||
| chr14:59982549 | T | C | 2 | a0001c0001t0001g0227 a0001c0001t0001g0240 |
2 | NA18975.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.2091+489T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59982549 | |||||||
| chr14:59982632 | GT | G | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.2091+575delT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | INFO_REALIGN_3_PRIME | chr14 | 59982632 | ||||||
| chr14:59982965 | A | G | 42 | a0001c0002t0004g0153 a0001c0002t0004g0214 a0001c0002t0004g0265 others(39): Show |
43 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.2091+905A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59982965 | |||||||
| chr14:59983110 | G | A | 7 | a0001c0002t0004g0015 a0001c0002t0021g0161 a0001c0002t0029g0017 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.2091+1050G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59983110 | |||||||
| chr14:59983228 | T | C | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.2091+1168T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59983228 | |||||||
| chr14:59983238 | A | G | 2 | a0001c0001t0003g0260 a0001c0001t0003g0261 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2091+1178A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59983238 | |||||||
| chr14:59983325 | T | G | 2 | a0001c0001t0003g0048 a0001c0001t0014g0040 |
2 | NA19059.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2091+1265T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59983325 | |||||||
| chr14:59983454 | C | G | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.2091+1394C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59983454 | |||||||
| chr14:59983460 | T | G | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.2091+1400T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59983460 | |||||||
| chr14:59983963 | C | T | 165 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.2092-1142C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59983963 | |||||||
| chr14:59984067 | A | G | 1 | a0001c0002t0004g0286 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2092-1038A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59984067 | |||||||
| chr14:59984427 | T | C | 165 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.2092-678T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59984427 | |||||||
| chr14:59984716 | T | C | 1 | a0001c0001t0031g0219 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2092-389T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59984716 | |||||||
| chr14:59984755 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2092-350T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59984755 | |||||||
| chr14:59984861 | T | A | 1 | a0001c0002t0004g0287 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2092-244T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59984861 | |||||||
| chr14:59984862 | A | G | 257 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(254): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.2092-243A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59984862 | |||||||
| chr14:59985052 | G | A | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.2092-53G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59985052 | |||||||
| chr14:59985098 | G | A | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
splice_region_variant&intron_variant | LOW | c.2092-7G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59985098 | |||||||
| chr14:59985314 | T | C | 42 | a0001c0002t0004g0153 a0001c0002t0004g0214 a0001c0002t0004g0265 others(39): Show |
43 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.2211+90T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59985314 | |||||||
| chr14:59985434 | A | G | 189 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(186): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.2211+210A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59985434 | |||||||
| chr14:59985718 | C | T | 1 | a0001c0002t0002g0136 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2211+494C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59985718 | |||||||
| chr14:59985770 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2211+546C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59985770 | |||||||
| chr14:59985808 | T | C | 1 | a0001c0002t0004g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2211+584T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59985808 | |||||||
| chr14:59985972 | T | C | 189 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(186): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.2211+748T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59985972 | |||||||
| chr14:59986101 | A | G | 7 | a0001c0001t0003g0100 a0001c0001t0003g0102 a0001c0001t0003g0168 others(4): Show |
7 | HG01358.hp1 HG01361.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.2211+877A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59986101 | |||||||
| chr14:59986182 | T | C | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2211+958T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59986182 | |||||||
| chr14:59986401 | T | A | 1 | a0001c0004t0009g0209 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2211+1177T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59986401 | |||||||
| chr14:59986523 | T | G | 6 | a0001c0001t0001g0044 a0001c0001t0001g0077 a0001c0001t0011g0050 others(3): Show |
6 | HG00621.hp1 HG02074.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.2211+1299T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59986523 | |||||||
| chr14:59986650 | T | G | 2 | a0001c0002t0002g0119 a0001c0002t0002g0174 |
2 | HG01192.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.2211+1426T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59986650 | |||||||
| chr14:59986767 | A | G | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2211+1543A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59986767 | |||||||
| chr14:59987174 | C | T | 1 | a0001c0001t0003g0245 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2211+1950C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59987174 | |||||||
| chr14:59987179 | C | G | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2211+1955C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59987179 | |||||||
| chr14:59987223 | T | A | 1 | a0001c0001t0014g0040 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.2211+1999T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59987223 | |||||||
| chr14:59987245 | A | C | 257 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(254): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.2211+2021A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59987245 | |||||||
| chr14:59987330 | A | G | 3 | a0001c0002t0017g0141 a0001c0002t0017g0142 a0001c0002t0024g0157 |
3 | HG01109.hp2 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2211+2106A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59987330 | |||||||
| chr14:59987356 | G | A | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.2211+2132G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59987356 | |||||||
| chr14:59987406 | C | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2211+2182C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59987406 | |||||||
| chr14:59987437 | T | TCAACCTT others(322): Show |
7 | a0001c0001t0001g0044 a0001c0001t0001g0086 a0001c0001t0001g0087 others(4): Show |
7 | HG00738.hp1 HG01517.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2211+2229_2211+223 others(333): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr14 | 59987437 | ||||||
| chr14:59987437 | T | TCAACCTT others(323): Show |
113 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0045 others(110): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.2211+2229_2211+223 others(334): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr14 | 59987437 | ||||||
| chr14:59987437 | T | TCAACCTT others(324): Show |
1 | a0001c0001t0014g0040 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.2211+2229_2211+223 others(335): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr14 | 59987437 | ||||||
| chr14:59987437 | T | TCAACCTT others(324): Show |
38 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0227 others(35): Show |
38 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.2211+2229_2211+223 others(335): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr14 | 59987437 | ||||||
| chr14:59987437 | T | TCAACCTT others(325): Show |
3 | a0001c0001t0001g0252 a0001c0001t0014g0035 a0001c0001t0028g0030 |
3 | HG02015.hp1 HG02040.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.2211+2229_2211+223 others(336): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr14 | 59987437 | ||||||
| chr14:59987437 | T | TCAACCTT others(326): Show |
2 | a0001c0001t0001g0238 a0001c0001t0031g0219 |
2 | NA18995.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.2211+2229_2211+223 others(337): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr14 | 59987437 | ||||||
| chr14:59987555 | G | A | 3 | a0001c0001t0001g0218 a0001c0001t0001g0231 a0001c0001t0001g0313 |
3 | NA18961.hp1 NA18999.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.2211+2331G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59987555 | |||||||
| chr14:59987600 | C | A | 1 | a0001c0001t0001g0252 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2211+2376C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59987600 | |||||||
| chr14:59987954 | G | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0091 |
2 | HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2211+2730G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59987954 | |||||||
| chr14:59987955 | T | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0091 |
2 | HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2211+2731T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59987955 | |||||||
| chr14:59987999 | C | T | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2211+2775C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59987999 | |||||||
| chr14:59988047 | C | T | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.2211+2823C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59988047 | |||||||
| chr14:59988367 | G | C | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.2211+3143G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59988367 | |||||||
| chr14:59988550 | T | C | 189 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(186): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.2211+3326T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59988550 | |||||||
| chr14:59988556 | C | T | 2 | a0001c0001t0003g0064 a0009c0017t0003g0065 |
2 | HG01169.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.2211+3332C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59988556 | |||||||
| chr14:59988612 | G | T | 41 | a0001c0002t0004g0153 a0001c0002t0004g0265 a0001c0002t0004g0268 others(38): Show |
42 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(39): Show |
intron_variant | MODIFIER | c.2211+3388G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59988612 | |||||||
| chr14:59988697 | C | T | 165 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.2211+3473C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59988697 | |||||||
| chr14:59988700 | C | T | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2211+3476C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59988700 | |||||||
| chr14:59988705 | G | A | 1 | a0001c0002t0002g0296 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2211+3481G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59988705 | |||||||
| chr14:59988946 | C | T | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.2211+3722C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59988946 | |||||||
| chr14:59989149 | T | C | 1 | a0001c0002t0002g0107 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2211+3925T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59989149 | |||||||
| chr14:59989176 | T | C | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2211+3952T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59989176 | |||||||
| chr14:59989222 | T | C | 1 | a0012c0018t0003g0230 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2211+3998T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59989222 | |||||||
| chr14:59989283 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2211+4059T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59989283 | |||||||
| chr14:59989484 | C | G | 1 | a0001c0001t0001g0218 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2211+4260C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59989484 | |||||||
| chr14:59989927 | C | CT | 42 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(39): Show |
43 | HG00099.hp1 HG00280.hp2 HG01346.hp2 others(40): Show |
intron_variant | MODIFIER | c.2211+4720dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr14 | 59989927 | ||||||
| chr14:59989927 | CT | C | 7 | a0001c0001t0003g0254 a0001c0001t0011g0073 a0001c0002t0002g0138 others(4): Show |
7 | HG01257.hp2 HG01515.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2211+4720delT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr14 | 59989927 | ||||||
| chr14:59989949 | C | T | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2211+4725C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59989949 | |||||||
| chr14:59989965 | T | C | 5 | a0001c0001t0001g0226 a0001c0001t0003g0254 a0001c0001t0003g0255 others(2): Show |
5 | HG00735.hp2 HG00738.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.2211+4741T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59989965 | |||||||
| chr14:59989989 | G | A | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2211+4765G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59989989 | |||||||
| chr14:59989996 | C | T | 2 | a0007c0013t0018g0110 a0007c0013t0018g0111 |
2 | HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2211+4772C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59989996 | |||||||
| chr14:59990127 | G | A | 257 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(254): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.2211+4903G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59990127 | |||||||
| chr14:59990154 | C | T | 7 | a0001c0005t0013g0151 a0001c0005t0013g0171 a0001c0005t0013g0172 others(4): Show |
7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2211+4930C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59990154 | |||||||
| chr14:59990174 | G | A | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.2211+4950G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59990174 | |||||||
| chr14:59990213 | C | T | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2211+4989C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59990213 | |||||||
| chr14:59990253 | G | T | 257 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(254): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.2211+5029G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59990253 | |||||||
| chr14:59990328 | T | C | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.2211+5104T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59990328 | |||||||
| chr14:59990331 | T | C | 8 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0009 others(5): Show |
8 | HG00639.hp2 HG00741.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.2211+5107T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59990331 | |||||||
| chr14:59990810 | G | A | 189 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(186): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.2211+5586G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59990810 | |||||||
| chr14:59990997 | T | A | 1 | a0001c0001t0001g0016 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2211+5773T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59990997 | |||||||
| chr14:59991211 | C | T | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2211+5987C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59991211 | |||||||
| chr14:59991440 | A | G | 2 | a0001c0001t0003g0038 a0001c0001t0003g0039 |
2 | HG00099.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.2211+6216A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59991440 | |||||||
| chr14:59991587 | C | T | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2212-6069C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59991587 | |||||||
| chr14:59991678 | A | G | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2212-5978A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59991678 | |||||||
| chr14:59991758 | A | G | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.2212-5898A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59991758 | |||||||
| chr14:59991779 | GCCATTGC | G | 80 | a0001c0001t0001g0016 a0001c0001t0001g0044 a0001c0001t0001g0058 others(77): Show |
80 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.2212-5873_2212-586 others(11): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr14 | 59991779 | ||||||
| chr14:59991795 | C | G | 80 | a0001c0001t0001g0016 a0001c0001t0001g0044 a0001c0001t0001g0058 others(77): Show |
80 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.2212-5861C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59991795 | |||||||
| chr14:59991802 | T | TAAAC | 167 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.2212-5851_2212-585 others(8): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr14 | 59991802 | ||||||
| chr14:59991928 | C | T | 20 | a0002c0003t0005g0185 a0002c0003t0005g0186 a0002c0003t0005g0189 others(17): Show |
20 | NA18941.hp2 NA18945.hp2 NA18964.hp2 others(17): Show |
intron_variant | MODIFIER | c.2212-5728C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59991928 | |||||||
| chr14:59991959 | G | C | 8 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0084 others(5): Show |
8 | HG01433.hp1 HG01884.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2212-5697G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59991959 | |||||||
| chr14:59991992 | C | G | 2 | a0006c0010t0018g0166 a0006c0010t0021g0033 |
2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2212-5664C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59991992 | |||||||
| chr14:59992099 | T | C | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.2212-5557T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59992099 | |||||||
| chr14:59992197 | A | G | 2 | a0001c0001t0010g0034 a0001c0001t0015g0062 |
2 | NA18994.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.2212-5459A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59992197 | |||||||
| chr14:59992255 | A | T | 1 | a0001c0002t0004g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2212-5401A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59992255 | |||||||
| chr14:59992314 | G | A | 2 | a0001c0002t0002g0215 a0001c0002t0025g0113 |
2 | HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2212-5342G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59992314 | |||||||
| chr14:59992402 | C | T | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2212-5254C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59992402 | |||||||
| chr14:59992458 | C | T | 3 | a0001c0001t0003g0029 a0001c0001t0003g0047 a0001c0001t0016g0023 |
3 | HG01074.hp2 NA18984.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2212-5198C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59992458 | |||||||
| chr14:59992484 | G | A | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2212-5172G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59992484 | |||||||
| chr14:59992573 | C | G | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.2212-5083C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59992573 | |||||||
| chr14:59992653 | G | A | 44 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0006g0020 others(41): Show |
45 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(42): Show |
intron_variant | MODIFIER | c.2212-5003G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59992653 | |||||||
| chr14:59992738 | C | T | 165 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.2212-4918C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59992738 | |||||||
| chr14:59992739 | G | A | 7 | a0001c0005t0013g0151 a0001c0005t0013g0171 a0001c0005t0013g0172 others(4): Show |
7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2212-4917G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59992739 | |||||||
| chr14:59992959 | C | T | 2 | a0001c0001t0001g0226 a0012c0018t0003g0230 |
2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2212-4697C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59992959 | |||||||
| chr14:59993100 | A | G | 2 | a0006c0010t0018g0166 a0006c0010t0021g0033 |
2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2212-4556A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59993100 | |||||||
| chr14:59993227 | G | A | 2 | a0001c0002t0002g0233 a0001c0002t0002g0256 |
2 | HG03669.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2212-4429G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59993227 | |||||||
| chr14:59993246 | C | T | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.2212-4410C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59993246 | |||||||
| chr14:59993362 | A | G | 5 | a0001c0002t0004g0268 a0001c0002t0004g0285 a0001c0002t0004g0288 others(2): Show |
5 | NA18966.hp1 NA18968.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.2212-4294A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59993362 | |||||||
| chr14:59993389 | A | C | 7 | a0001c0002t0004g0015 a0001c0002t0021g0161 a0001c0002t0029g0017 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.2212-4267A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59993389 | |||||||
| chr14:59993553 | G | A | 3 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0306 |
3 | NA18946.hp2 NA18962.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.2212-4103G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59993553 | |||||||
| chr14:59993572 | C | G | 190 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.2212-4084C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59993572 | |||||||
| chr14:59993575 | G | C | 190 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.2212-4081G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59993575 | |||||||
| chr14:59993727 | G | C | 190 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.2212-3929G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59993727 | |||||||
| chr14:59993979 | G | C | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2212-3677G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59993979 | |||||||
| chr14:59994193 | G | A | 1 | a0001c0001t0001g0299 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2212-3463G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59994193 | |||||||
| chr14:59994242 | C | T | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2212-3414C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59994242 | |||||||
| chr14:59994318 | C | G | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2212-3338C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59994318 | |||||||
| chr14:59994327 | G | C | 1 | a0001c0001t0030g0160 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2212-3329G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59994327 | |||||||
| chr14:59994554 | A | T | 1 | a0007c0013t0018g0111 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2212-3102A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59994554 | |||||||
| chr14:59994626 | C | G | 190 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.2212-3030C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59994626 | |||||||
| chr14:59994947 | A | T | 4 | a0001c0006t0002g0108 a0001c0006t0002g0109 a0001c0006t0002g0114 others(1): Show |
4 | HG02074.hp1 HG02080.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.2212-2709A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59994947 | |||||||
| chr14:59995008 | T | TAA | 181 | a0001c0001t0001g0027 a0001c0001t0001g0044 a0001c0001t0001g0045 others(178): Show |
182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.2212-2639_2212-263 others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr14 | 59995008 | ||||||
| chr14:59995009 | A | AAT | 5 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2212-2646_2212-264 others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr14 | 59995009 | ||||||
| chr14:59995025 | A | G | 1 | a0001c0001t0003g0014 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2212-2631A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59995025 | |||||||
| chr14:59995258 | T | G | 1 | a0001c0002t0004g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2212-2398T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59995258 | |||||||
| chr14:59995362 | T | A | 190 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.2212-2294T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59995362 | |||||||
| chr14:59995376 | C | A | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2212-2280C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59995376 | |||||||
| chr14:59995466 | G | C | 190 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.2212-2190G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59995466 | |||||||
| chr14:59995710 | G | A | 1 | a0002c0003t0005g0185 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2212-1946G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59995710 | |||||||
| chr14:59995725 | G | GT | 190 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.2212-1921dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr14 | 59995725 | ||||||
| chr14:59995853 | C | A | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2212-1803C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59995853 | |||||||
| chr14:59995986 | C | T | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2212-1670C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59995986 | |||||||
| chr14:59996093 | A | T | 2 | a0001c0001t0001g0213 a0001c0001t0016g0105 |
2 | HG01074.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.2212-1563A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59996093 | |||||||
| chr14:59996581 | C | T | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2212-1075C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59996581 | |||||||
| chr14:59996875 | C | T | 1 | a0001c0001t0014g0035 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2212-781C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59996875 | |||||||
| chr14:59997197 | T | C | 1 | a0002c0003t0005g0194 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2212-459T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59997197 | |||||||
| chr14:59997276 | T | C | 3 | a0001c0002t0017g0141 a0001c0002t0017g0142 a0001c0002t0024g0157 |
3 | HG01109.hp2 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2212-380T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59997276 | |||||||
| chr14:59997393 | G | A | 190 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.2212-263G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59997393 | |||||||
| chr14:59997427 | G | T | 167 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.2212-229G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59997427 | |||||||
| chr14:59997973 | T | G | 190 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.2403+126T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 18/32 | chr14 | 59997973 | |||||||
| chr14:59998020 | G | T | 2 | a0001c0001t0010g0026 a0001c0001t0010g0028 |
2 | HG00423.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.2403+173G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 18/32 | chr14 | 59998020 | |||||||
| chr14:59998138 | T | G | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2403+291T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 18/32 | chr14 | 59998138 | |||||||
| chr14:59998798 | T | A | 2 | a0001c0002t0004g0289 a0001c0002t0004g0300 |
2 | HG02040.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.2404-303T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 18/32 | chr14 | 59998798 | |||||||
| chr14:59998803 | A | G | 42 | a0001c0002t0004g0153 a0001c0002t0004g0214 a0001c0002t0004g0265 others(39): Show |
43 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.2404-298A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 18/32 | chr14 | 59998803 | |||||||
| chr14:59999078 | A | T | 1 | a0001c0005t0013g0151 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2404-23A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 18/32 | chr14 | 59999078 | |||||||
| chr14:59999079 | T | A | 2 | a0001c0001t0031g0219 a0001c0001t0035g0156 |
2 | HG01496.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.2404-22T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 18/32 | chr14 | 59999079 | |||||||
| chr14:59999350 | G | A | 1 | a0001c0002t0012g0123 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2529+124G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 59999350 | |||||||
| chr14:59999424 | C | CATACATG others(7): Show |
1 | a0001c0001t0041g0229 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2529+198_2529+199i others(16): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 59999424 | |||||||
| chr14:59999841 | A | G | 167 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.2529+615A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 59999841 | |||||||
| chr14:59999862 | C | A | 1 | a0001c0002t0012g0123 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2529+636C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 59999862 | |||||||
| chr14:60000016 | A | T | 1 | a0001c0001t0003g0168 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2529+790A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60000016 | |||||||
| chr14:60000290 | G | A | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.2529+1064G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60000290 | |||||||
| chr14:60000301 | G | C | 1 | a0001c0002t0004g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2529+1075G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60000301 | |||||||
| chr14:60000503 | T | C | 2 | a0001c0005t0013g0171 a0001c0005t0013g0172 |
2 | HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.2529+1277T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60000503 | |||||||
| chr14:60000565 | C | T | 1 | a0001c0002t0029g0017 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2529+1339C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60000565 | |||||||
| chr14:60000747 | C | A | 1 | a0001c0001t0019g0311 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2530-1219C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60000747 | |||||||
| chr14:60001027 | A | G | 2 | a0001c0002t0004g0015 a0001c0002t0029g0017 |
2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2530-939A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60001027 | |||||||
| chr14:60001116 | G | A | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2530-850G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60001116 | |||||||
| chr14:60001188 | T | TTGTG | 16 | a0001c0001t0014g0035 a0001c0002t0002g0005 a0001c0002t0002g0112 others(13): Show |
16 | HG01081.hp1 HG01358.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.2530-758_2530-755d others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | INFO_REALIGN_3_PRIME | chr14 | 60001188 | ||||||
| chr14:60001309 | T | C | 317 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(314): Show |
319 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.2530-657T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60001309 | |||||||
| chr14:60001444 | T | A | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.2530-522T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60001444 | |||||||
| chr14:60001502 | T | G | 200 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(197): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.2530-464T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60001502 | |||||||
| chr14:60001517 | A | C | 167 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.2530-449A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60001517 | |||||||
| chr14:60001640 | G | A | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2530-326G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60001640 | |||||||
| chr14:60001722 | TTATAG | T | 42 | a0001c0002t0004g0153 a0001c0002t0004g0214 a0001c0002t0004g0265 others(39): Show |
43 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.2530-241_2530-237d others(7): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | INFO_REALIGN_3_PRIME | chr14 | 60001722 | ||||||
| chr14:60001762 | A | T | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2530-204A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60001762 | |||||||
| chr14:60001943 | C | T | 167 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.2530-23C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60001943 | |||||||
| chr14:60001944 | T | A | 1 | a0001c0001t0016g0023 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2530-22T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60001944 | |||||||
| chr14:60001945 | G | A | 1 | a0001c0001t0016g0023 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2530-21G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60001945 | |||||||
| chr14:60001946 | T | A | 1 | a0001c0001t0016g0023 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2530-20T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60001946 | |||||||
| chr14:60002145 | T | C | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.2664+45T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 20/32 | chr14 | 60002145 | |||||||
| chr14:60002577 | A | G | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.2664+477A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 20/32 | chr14 | 60002577 | |||||||
| chr14:60002599 | A | C | 165 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.2664+499A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 20/32 | chr14 | 60002599 | |||||||
| chr14:60002614 | A | G | 1 | a0001c0001t0011g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2664+514A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 20/32 | chr14 | 60002614 | |||||||
| chr14:60002842 | A | G | 1 | a0001c0012t0002g0106 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2664+742A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 20/32 | chr14 | 60002842 | |||||||
| chr14:60002863 | A | T | 1 | a0001c0002t0002g0003 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2665-758A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 20/32 | chr14 | 60002863 | |||||||
| chr14:60003075 | G | T | 1 | a0001c0001t0014g0066 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2665-546G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 20/32 | chr14 | 60003075 | |||||||
| chr14:60003310 | T | A | 1 | a0001c0002t0004g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2665-311T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 20/32 | chr14 | 60003310 | |||||||
| chr14:60003396 | C | T | 1 | a0002c0003t0005g0197 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2665-225C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 20/32 | chr14 | 60003396 | |||||||
| chr14:60003854 | C | CA | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.2842+62dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr14 | 60003854 | ||||||
| chr14:60003893 | A | T | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.2842+95A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60003893 | |||||||
| chr14:60004083 | A | G | 1 | a0001c0001t0006g0024 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2842+285A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60004083 | |||||||
| chr14:60004085 | C | T | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2842+287C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60004085 | |||||||
| chr14:60004140 | G | A | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.2842+342G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60004140 | |||||||
| chr14:60004420 | T | C | 2 | a0001c0004t0009g0210 a0001c0004t0009g0306 |
2 | NA18946.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.2842+622T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60004420 | |||||||
| chr14:60004836 | A | G | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.2842+1038A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60004836 | |||||||
| chr14:60004857 | A | C | 2 | a0001c0002t0002g0233 a0001c0002t0002g0256 |
2 | HG03669.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2842+1059A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60004857 | |||||||
| chr14:60004881 | T | TAC | 15 | a0001c0002t0004g0004 a0001c0002t0004g0214 a0001c0002t0017g0117 others(12): Show |
15 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.2842+1106_2842+110 others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr14 | 60004881 | ||||||
| chr14:60004881 | T | TACAC | 27 | a0001c0002t0002g0005 a0001c0002t0002g0112 a0001c0002t0002g0207 others(24): Show |
28 | HG01081.hp1 HG01884.hp2 HG02559.hp1 others(25): Show |
intron_variant | MODIFIER | c.2842+1104_2842+110 others(8): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr14 | 60004881 | ||||||
| chr14:60004881 | T | TACACAC | 37 | a0001c0002t0004g0265 a0001c0002t0004g0268 a0001c0002t0004g0271 others(34): Show |
38 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(35): Show |
intron_variant | MODIFIER | c.2842+1102_2842+110 others(10): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr14 | 60004881 | ||||||
| chr14:60004881 | T | TACACACA others(1): Show |
9 | a0001c0002t0004g0310 a0001c0002t0007g0274 a0001c0005t0013g0151 others(6): Show |
9 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2842+1100_2842+110 others(12): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr14 | 60004881 | ||||||
| chr14:60004881 | T | TACACACA others(3): Show |
3 | a0001c0002t0007g0317 a0001c0002t0021g0161 a0001c0005t0013g0171 |
3 | HG02257.hp1 HG03942.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.2842+1098_2842+110 others(14): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr14 | 60004881 | ||||||
| chr14:60004881 | T | TACACACA others(5): Show |
1 | a0001c0005t0013g0172 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2842+1096_2842+110 others(16): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr14 | 60004881 | ||||||
| chr14:60004881 | TAC | T | 163 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(160): Show |
163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.2842+1106_2842+110 others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr14 | 60004881 | ||||||
| chr14:60004911 | T | C | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.2842+1113T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60004911 | |||||||
| chr14:60004991 | C | T | 39 | a0001c0002t0004g0265 a0001c0002t0004g0268 a0001c0002t0004g0271 others(36): Show |
40 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(37): Show |
intron_variant | MODIFIER | c.2842+1193C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60004991 | |||||||
| chr14:60005030 | T | C | 1 | a0001c0001t0001g0253 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2842+1232T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60005030 | |||||||
| chr14:60005060 | C | T | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2842+1262C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60005060 | |||||||
| chr14:60005284 | G | A | 1 | a0001c0001t0030g0160 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2843-1113G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60005284 | |||||||
| chr14:60005769 | A | C | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.2843-628A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60005769 | |||||||
| chr14:60005976 | G | A | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2843-421G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60005976 | |||||||
| chr14:60005981 | A | C | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2843-416A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60005981 | |||||||
| chr14:60006035 | T | C | 1 | a0002c0003t0005g0204 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2843-362T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60006035 | |||||||
| chr14:60006099 | T | C | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2843-298T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60006099 | |||||||
| chr14:60006144 | C | T | 3 | a0001c0002t0002g0173 a0001c0002t0002g0215 a0001c0002t0025g0113 |
3 | HG02145.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2843-253C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60006144 | |||||||
| chr14:60006623 | C | T | 1 | a0002c0003t0005g0190 | 1 | NA18975.hp2 | splice_region_variant&intron_variant | LOW | c.3063+6C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 22/32 | chr14 | 60006623 | |||||||
| chr14:60006959 | C | T | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3063+342C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 22/32 | chr14 | 60006959 | |||||||
| chr14:60007016 | A | G | 1 | a0001c0004t0009g0303 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3063+399A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 22/32 | chr14 | 60007016 | |||||||
| chr14:60007083 | G | A | 6 | a0001c0002t0002g0143 a0001c0002t0002g0144 a0001c0002t0002g0145 others(3): Show |
6 | HG01243.hp1 HG02258.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.3063+466G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 22/32 | chr14 | 60007083 | |||||||
| chr14:60007248 | C | T | 1 | a0002c0003t0005g0204 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.3063+631C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 22/32 | chr14 | 60007248 | |||||||
| chr14:60007443 | C | A | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3064-649C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 22/32 | chr14 | 60007443 | |||||||
| chr14:60007764 | G | A | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3064-328G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 22/32 | chr14 | 60007764 | |||||||
| chr14:60007926 | C | T | 1 | a0001c0001t0003g0057 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3064-166C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 22/32 | chr14 | 60007926 | |||||||
| chr14:60007940 | TA | T | 55 | a0001c0001t0001g0250 a0001c0002t0002g0003 a0001c0002t0002g0107 others(52): Show |
55 | HG00639.hp1 HG00673.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.3064-130delA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr14 | 60007940 | ||||||
| chr14:60007940 | TAA | T | 155 | a0001c0001t0001g0027 a0001c0001t0001g0045 a0001c0001t0001g0061 others(152): Show |
157 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.3064-131_3064-130d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr14 | 60007940 | ||||||
| chr14:60007940 | TAAA | T | 103 | a0001c0001t0001g0016 a0001c0001t0001g0044 a0001c0001t0001g0058 others(100): Show |
103 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.3064-132_3064-130d others(5): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr14 | 60007940 | ||||||
| chr14:60008527 | G | C | 167 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.3186+313G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60008527 | |||||||
| chr14:60008625 | T | C | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3186+411T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60008625 | |||||||
| chr14:60008886 | T | A | 1 | a0001c0002t0004g0298 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.3186+672T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60008886 | |||||||
| chr14:60009038 | T | C | 2 | a0001c0002t0004g0015 a0001c0002t0029g0017 |
2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3186+824T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60009038 | |||||||
| chr14:60009120 | T | C | 196 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(193): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.3186+906T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60009120 | |||||||
| chr14:60009232 | C | A | 173 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.3186+1018C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60009232 | |||||||
| chr14:60009459 | G | A | 2 | a0001c0001t0001g0226 a0012c0018t0003g0230 |
2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3186+1245G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60009459 | |||||||
| chr14:60009473 | T | C | 190 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.3186+1259T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60009473 | |||||||
| chr14:60009614 | TTCAAAAC others(3): Show |
T | 1 | a0001c0001t0001g0086 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3186+1404_3186+141 others(14): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | INFO_REALIGN_3_PRIME | chr14 | 60009614 | ||||||
| chr14:60009689 | G | A | 1 | a0001c0002t0002g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3186+1475G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60009689 | |||||||
| chr14:60009714 | T | C | 167 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.3186+1500T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60009714 | |||||||
| chr14:60009769 | G | C | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.3186+1555G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60009769 | |||||||
| chr14:60009779 | C | T | 1 | a0001c0001t0010g0067 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3186+1565C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60009779 | |||||||
| chr14:60009835 | C | A | 1 | a0001c0002t0002g0005 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3186+1621C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60009835 | |||||||
| chr14:60009841 | G | A | 1 | a0001c0001t0006g0169 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3186+1627G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60009841 | |||||||
| chr14:60010226 | C | T | 190 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.3186+2012C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60010226 | |||||||
| chr14:60010241 | A | T | 259 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(256): Show |
261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.3186+2027A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60010241 | |||||||
| chr14:60010287 | T | C | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3186+2073T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60010287 | |||||||
| chr14:60010448 | G | A | 2 | a0001c0002t0002g0005 a0001c0002t0004g0004 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.3186+2234G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60010448 | |||||||
| chr14:60010449 | A | G | 1 | a0001c0002t0004g0295 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.3186+2235A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60010449 | |||||||
| chr14:60010450 | C | A | 1 | a0001c0002t0004g0295 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.3186+2236C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60010450 | |||||||
| chr14:60010462 | AC | A | 165 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.3186+2250delC | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | INFO_REALIGN_3_PRIME | chr14 | 60010462 | ||||||
| chr14:60010480 | G | A | 165 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.3186+2266G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60010480 | |||||||
| chr14:60010844 | G | C | 1 | a0001c0001t0037g0247 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3186+2630G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60010844 | |||||||
| chr14:60010861 | C | T | 167 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.3186+2647C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60010861 | |||||||
| chr14:60011211 | A | G | 190 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.3186+2997A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60011211 | |||||||
| chr14:60011409 | G | A | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3186+3195G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60011409 | |||||||
| chr14:60011493 | T | A | 167 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.3186+3279T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60011493 | |||||||
| chr14:60011550 | C | T | 1 | a0001c0002t0004g0298 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.3186+3336C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60011550 | |||||||
| chr14:60011591 | T | C | 2 | a0001c0001t0003g0038 a0001c0001t0003g0039 |
2 | HG00099.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.3186+3377T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60011591 | |||||||
| chr14:60011633 | A | G | 317 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(314): Show |
319 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.3186+3419A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60011633 | |||||||
| chr14:60011883 | A | C | 3 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0094 |
3 | HG02615.hp2 HG02896.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3186+3669A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60011883 | |||||||
| chr14:60012077 | T | A | 24 | a0001c0005t0038g0150 a0002c0003t0005g0001 a0002c0003t0005g0185 others(21): Show |
25 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(22): Show |
intron_variant | MODIFIER | c.3186+3863T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60012077 | |||||||
| chr14:60012117 | G | T | 2 | a0006c0010t0018g0166 a0006c0010t0021g0033 |
2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3186+3903G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60012117 | |||||||
| chr14:60012325 | T | C | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.3186+4111T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60012325 | |||||||
| chr14:60012335 | T | C | 81 | a0001c0001t0001g0027 a0001c0001t0001g0045 a0001c0001t0001g0061 others(78): Show |
81 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.3186+4121T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60012335 | |||||||
| chr14:60012378 | A | G | 1 | a0001c0002t0004g0272 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.3186+4164A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60012378 | |||||||
| chr14:60012695 | A | G | 1 | a0001c0001t0003g0014 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3187-3965A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60012695 | |||||||
| chr14:60012818 | C | T | 1 | a0001c0001t0006g0099 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3187-3842C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60012818 | |||||||
| chr14:60012936 | TTTTA | T | 188 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(185): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.3187-3708_3187-370 others(8): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | INFO_REALIGN_3_PRIME | chr14 | 60012936 | ||||||
| chr14:60012952 | A | T | 7 | a0001c0004t0009g0209 a0001c0004t0009g0302 a0001c0004t0009g0303 others(4): Show |
7 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.3187-3708A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60012952 | |||||||
| chr14:60013016 | C | T | 167 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.3187-3644C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60013016 | |||||||
| chr14:60013041 | G | A | 1 | a0005c0011t0003g0211 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3187-3619G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60013041 | |||||||
| chr14:60013083 | A | G | 2 | a0001c0002t0002g0005 a0001c0002t0004g0004 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.3187-3577A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60013083 | |||||||
| chr14:60013086 | T | G | 41 | a0001c0002t0004g0153 a0001c0002t0004g0265 a0001c0002t0004g0268 others(38): Show |
42 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(39): Show |
intron_variant | MODIFIER | c.3187-3574T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60013086 | |||||||
| chr14:60013246 | G | T | 1 | a0001c0001t0001g0234 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3187-3414G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60013246 | |||||||
| chr14:60013268 | C | T | 1 | a0001c0002t0002g0145 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3187-3392C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60013268 | |||||||
| chr14:60013335 | C | G | 167 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.3187-3325C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60013335 | |||||||
| chr14:60013622 | T | C | 10 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0009 others(7): Show |
10 | HG00639.hp2 HG00741.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.3187-3038T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60013622 | |||||||
| chr14:60013641 | C | T | 8 | a0001c0002t0012g0120 a0001c0002t0012g0121 a0001c0002t0012g0122 others(5): Show |
8 | HG02486.hp1 HG02622.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.3187-3019C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60013641 | |||||||
| chr14:60013643 | G | A | 16 | a0001c0002t0002g0005 a0001c0002t0004g0004 a0001c0002t0004g0015 others(13): Show |
16 | HG01081.hp1 HG01243.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.3187-3017G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60013643 | |||||||
| chr14:60013665 | T | C | 1 | a0001c0001t0016g0023 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3187-2995T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60013665 | |||||||
| chr14:60013677 | G | T | 83 | a0001c0001t0001g0016 a0001c0001t0001g0044 a0001c0001t0001g0058 others(80): Show |
83 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.3187-2983G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60013677 | |||||||
| chr14:60013756 | T | C | 2 | a0001c0001t0003g0260 a0001c0001t0003g0261 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.3187-2904T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60013756 | |||||||
| chr14:60014003 | C | G | 1 | a0001c0002t0012g0147 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3187-2657C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60014003 | |||||||
| chr14:60014054 | A | G | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3187-2606A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60014054 | |||||||
| chr14:60014199 | A | G | 2 | a0001c0002t0004g0015 a0001c0002t0029g0017 |
2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3187-2461A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60014199 | |||||||
| chr14:60014386 | T | C | 3 | a0002c0003t0005g0001 a0002c0003t0005g0187 a0002c0003t0005g0188 |
4 | NA18939.hp2 NA18960.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.3187-2274T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60014386 | |||||||
| chr14:60014389 | T | A | 1 | a0006c0010t0018g0166 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3187-2271T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60014389 | |||||||
| chr14:60014485 | G | T | 3 | a0001c0001t0001g0236 a0001c0001t0001g0251 a0001c0001t0027g0235 |
3 | NA18956.hp1 NA18986.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.3187-2175G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60014485 | |||||||
| chr14:60014776 | T | C | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3187-1884T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60014776 | |||||||
| chr14:60014998 | AC | A | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3187-1661delC | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60014998 | |||||||
| chr14:60015046 | C | T | 3 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0006g0020 |
3 | NA18945.hp1 NA19007.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.3187-1614C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60015046 | |||||||
| chr14:60015193 | A | T | 2 | a0001c0002t0002g0005 a0001c0002t0004g0004 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.3187-1467A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60015193 | |||||||
| chr14:60015259 | TA | T | 258 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(255): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.3187-1395delA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | INFO_REALIGN_3_PRIME | chr14 | 60015259 | ||||||
| chr14:60015421 | G | A | 1 | a0001c0001t0003g0057 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3187-1239G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60015421 | |||||||
| chr14:60015714 | G | A | 1 | a0002c0003t0005g0205 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.3187-946G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60015714 | |||||||
| chr14:60015949 | T | C | 1 | a0001c0001t0032g0320 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3187-711T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60015949 | |||||||
| chr14:60015969 | T | C | 2 | a0001c0005t0013g0171 a0001c0005t0013g0172 |
2 | HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.3187-691T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60015969 | |||||||
| chr14:60016010 | A | G | 1 | a0001c0002t0020g0282 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3187-650A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60016010 | |||||||
| chr14:60016017 | G | T | 1 | a0001c0001t0042g0184 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3187-643G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60016017 | |||||||
| chr14:60016033 | G | T | 2 | a0001c0001t0001g0263 a0001c0001t0003g0262 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.3187-627G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60016033 | |||||||
| chr14:60016255 | G | T | 1 | a0001c0001t0006g0241 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3187-405G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60016255 | |||||||
| chr14:60016272 | C | A | 1 | a0001c0001t0006g0241 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3187-388C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60016272 | |||||||
| chr14:60016277 | C | T | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3187-383C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60016277 | |||||||
| chr14:60016837 | G | A | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3317+47G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60016837 | |||||||
| chr14:60016880 | C | T | 167 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.3317+90C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60016880 | |||||||
| chr14:60016960 | G | A | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3317+170G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60016960 | |||||||
| chr14:60017058 | A | G | 1 | a0001c0004t0009g0303 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3317+268A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60017058 | |||||||
| chr14:60017273 | T | C | 165 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.3317+483T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60017273 | |||||||
| chr14:60017373 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3317+583G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60017373 | |||||||
| chr14:60017605 | C | T | 1 | a0001c0001t0006g0244 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3318-766C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60017605 | |||||||
| chr14:60017700 | T | C | 1 | a0001c0002t0002g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3318-671T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60017700 | |||||||
| chr14:60017745 | T | C | 2 | a0001c0002t0002g0176 a0001c0002t0002g0177 |
2 | HG01255.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.3318-626T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60017745 | |||||||
| chr14:60017772 | C | T | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3318-599C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60017772 | |||||||
| chr14:60018106 | T | C | 7 | a0001c0005t0013g0151 a0001c0005t0013g0171 a0001c0005t0013g0172 others(4): Show |
7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3318-265T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60018106 | |||||||
| chr14:60018147 | G | T | 165 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.3318-224G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60018147 | |||||||
| chr14:60018197 | T | C | 4 | a0001c0001t0011g0021 a0001c0001t0011g0078 a0001c0001t0011g0079 others(1): Show |
4 | HG02559.hp2 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3318-174T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60018197 | |||||||
| chr14:60018210 | G | A | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3318-161G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60018210 | |||||||
| chr14:60018213 | C | T | 167 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.3318-158C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60018213 | |||||||
| chr14:60018308 | AC | A | 42 | a0001c0002t0004g0153 a0001c0002t0004g0214 a0001c0002t0004g0265 others(39): Show |
43 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.3318-61delC | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | INFO_REALIGN_3_PRIME | chr14 | 60018308 | ||||||
| chr14:60018522 | G | A | 165 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.3426+43G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 25/32 | chr14 | 60018522 | |||||||
| chr14:60018550 | G | A | 1 | a0001c0002t0002g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3426+71G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 25/32 | chr14 | 60018550 | |||||||
| chr14:60018600 | G | GT | 160 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(157): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.3426+130dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 25/32 | INFO_REALIGN_3_PRIME | chr14 | 60018600 | ||||||
| chr14:60018600 | G | T | 1 | a0001c0001t0015g0060 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.3426+121G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 25/32 | chr14 | 60018600 | |||||||
| chr14:60018659 | T | G | 46 | a0001c0001t0001g0044 a0001c0001t0001g0058 a0001c0001t0001g0077 others(43): Show |
46 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.3426+180T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 25/32 | chr14 | 60018659 | |||||||
| chr14:60018854 | T | A | 1 | a0001c0002t0004g0286 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.3427-267T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 25/32 | chr14 | 60018854 | |||||||
| chr14:60018862 | T | A | 2 | a0001c0002t0004g0015 a0001c0002t0029g0017 |
2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3427-259T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 25/32 | chr14 | 60018862 | |||||||
| chr14:60019046 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3427-75G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 25/32 | chr14 | 60019046 | |||||||
| chr14:60019325 | C | T | 1 | a0001c0002t0007g0294 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.3566+65C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60019325 | |||||||
| chr14:60019499 | G | A | 1 | a0001c0002t0004g0286 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.3566+239G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60019499 | |||||||
| chr14:60019513 | A | G | 2 | a0001c0001t0008g0032 a0001c0001t0008g0041 |
2 | HG00280.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.3566+253A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60019513 | |||||||
| chr14:60019585 | T | C | 1 | a0001c0002t0002g0127 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3566+325T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60019585 | |||||||
| chr14:60019594 | A | G | 1 | a0001c0002t0004g0289 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3566+334A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60019594 | |||||||
| chr14:60019699 | C | CT | 8 | a0001c0001t0003g0100 a0001c0001t0003g0102 a0001c0001t0003g0168 others(5): Show |
8 | HG01358.hp1 HG01361.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.3566+447dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | INFO_REALIGN_3_PRIME | chr14 | 60019699 | ||||||
| chr14:60019708 | C | T | 167 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.3566+448C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60019708 | |||||||
| chr14:60019799 | A | G | 190 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.3566+539A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60019799 | |||||||
| chr14:60019860 | CAT | C | 167 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.3566+603_3566+604d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | INFO_REALIGN_3_PRIME | chr14 | 60019860 | ||||||
| chr14:60019892 | C | T | 258 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(255): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.3566+632C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60019892 | |||||||
| chr14:60020282 | G | A | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3566+1022G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60020282 | |||||||
| chr14:60020719 | A | C | 1 | a0001c0001t0008g0006 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3566+1459A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60020719 | |||||||
| chr14:60020725 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0003g0262 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.3566+1465C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60020725 | |||||||
| chr14:60021067 | A | C | 4 | a0001c0001t0011g0021 a0001c0001t0011g0078 a0001c0001t0011g0079 others(1): Show |
4 | HG02559.hp2 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3567-1667A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60021067 | |||||||
| chr14:60021112 | A | G | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3567-1622A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60021112 | |||||||
| chr14:60021284 | T | C | 2 | a0001c0001t0010g0034 a0001c0001t0015g0062 |
2 | NA18994.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.3567-1450T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60021284 | |||||||
| chr14:60021311 | C | T | 1 | a0001c0001t0010g0054 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.3567-1423C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60021311 | |||||||
| chr14:60021387 | G | T | 6 | a0001c0001t0001g0080 a0001c0001t0001g0082 a0001c0001t0001g0088 others(3): Show |
6 | HG01884.hp1 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.3567-1347G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60021387 | |||||||
| chr14:60021625 | G | A | 7 | a0001c0005t0013g0151 a0001c0005t0013g0171 a0001c0005t0013g0172 others(4): Show |
7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3567-1109G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60021625 | |||||||
| chr14:60021678 | G | A | 1 | a0001c0002t0002g0136 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3567-1056G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60021678 | |||||||
| chr14:60021861 | C | T | 1 | a0001c0002t0002g0127 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3567-873C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60021861 | |||||||
| chr14:60022018 | T | G | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3567-716T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60022018 | |||||||
| chr14:60022186 | T | A | 42 | a0001c0002t0004g0153 a0001c0002t0004g0214 a0001c0002t0004g0265 others(39): Show |
43 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.3567-548T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60022186 | |||||||
| chr14:60022900 | C | G | 1 | a0001c0001t0016g0051 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3703+30C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60022900 | |||||||
| chr14:60022947 | A | C | 1 | a0001c0002t0002g0131 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3703+77A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60022947 | |||||||
| chr14:60023089 | A | G | 190 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.3703+219A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60023089 | |||||||
| chr14:60023096 | T | C | 1 | a0001c0002t0004g0310 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3703+226T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60023096 | |||||||
| chr14:60023326 | T | C | 1 | a0001c0004t0009g0307 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3703+456T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60023326 | |||||||
| chr14:60023393 | T | A | 1 | a0001c0001t0003g0037 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3703+523T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60023393 | |||||||
| chr14:60023541 | A | AAG | 190 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.3703+674_3703+675d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr14 | 60023541 | ||||||
| chr14:60023649 | T | G | 16 | a0001c0002t0002g0005 a0001c0002t0004g0004 a0001c0002t0004g0015 others(13): Show |
16 | HG01081.hp1 HG01243.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.3703+779T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60023649 | |||||||
| chr14:60023762 | A | C | 1 | a0001c0001t0001g0069 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3703+892A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60023762 | |||||||
| chr14:60023945 | C | CT | 259 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(256): Show |
261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.3703+1076dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr14 | 60023945 | ||||||
| chr14:60024398 | TTA | T | 165 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.3703+1529_3703+153 others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60024398 | |||||||
| chr14:60024415 | G | A | 14 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0009 others(11): Show |
14 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.3703+1545G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60024415 | |||||||
| chr14:60024466 | G | C | 1 | a0001c0001t0003g0170 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3703+1596G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60024466 | |||||||
| chr14:60024495 | A | C | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3703+1625A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60024495 | |||||||
| chr14:60024734 | T | A | 1 | a0001c0002t0002g0297 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.3703+1864T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60024734 | |||||||
| chr14:60024826 | CATTCTCC others(4): Show |
C | 1 | a0001c0001t0001g0231 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.3703+1957_3703+196 others(15): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60024826 | |||||||
| chr14:60024840 | T | A | 7 | a0001c0005t0013g0151 a0001c0005t0013g0171 a0001c0005t0013g0172 others(4): Show |
7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3703+1970T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60024840 | |||||||
| chr14:60025069 | G | T | 1 | a0001c0002t0002g0136 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3703+2199G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60025069 | |||||||
| chr14:60025088 | T | G | 1 | a0001c0001t0027g0246 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.3703+2218T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60025088 | |||||||
| chr14:60025156 | T | C | 1 | a0012c0018t0003g0230 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3703+2286T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60025156 | |||||||
| chr14:60025244 | C | A | 1 | a0001c0001t0015g0060 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.3703+2374C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60025244 | |||||||
| chr14:60025250 | C | T | 2 | a0001c0002t0004g0015 a0001c0002t0029g0017 |
2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3703+2380C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60025250 | |||||||
| chr14:60025290 | A | C | 259 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(256): Show |
261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.3703+2420A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60025290 | |||||||
| chr14:60025317 | G | T | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3703+2447G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60025317 | |||||||
| chr14:60025382 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3704-2502G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60025382 | |||||||
| chr14:60025384 | G | A | 1 | a0001c0002t0004g0319 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3704-2500G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60025384 | |||||||
| chr14:60025455 | T | G | 257 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(254): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.3704-2429T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60025455 | |||||||
| chr14:60025597 | A | G | 1 | a0001c0002t0002g0134 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.3704-2287A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60025597 | |||||||
| chr14:60025611 | T | C | 1 | a0003c0007t0004g0277 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3704-2273T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60025611 | |||||||
| chr14:60025679 | CA | C | 80 | a0001c0001t0014g0040 a0001c0001t0035g0156 a0001c0002t0002g0207 others(77): Show |
82 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.3704-2190delA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr14 | 60025679 | ||||||
| chr14:60025679 | CAAA | C | 13 | a0001c0002t0004g0004 a0001c0002t0004g0015 a0001c0002t0021g0161 others(10): Show |
13 | HG01243.hp2 HG01358.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.3704-2192_3704-219 others(7): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr14 | 60025679 | ||||||
| chr14:60026229 | A | G | 2 | a0007c0013t0018g0110 a0007c0013t0018g0111 |
2 | HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3704-1655A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60026229 | |||||||
| chr14:60026337 | G | T | 1 | a0001c0002t0004g0310 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3704-1547G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60026337 | |||||||
| chr14:60026485 | T | G | 190 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.3704-1399T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60026485 | |||||||
| chr14:60026529 | C | G | 15 | a0001c0002t0004g0004 a0001c0002t0004g0015 a0001c0002t0021g0161 others(12): Show |
15 | HG01243.hp2 HG01358.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.3704-1355C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60026529 | |||||||
| chr14:60026779 | T | C | 167 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.3704-1105T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60026779 | |||||||
| chr14:60026956 | A | C | 257 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(254): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.3704-928A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60026956 | |||||||
| chr14:60026973 | T | C | 4 | a0001c0002t0004g0271 a0001c0002t0004g0278 a0001c0002t0004g0281 others(1): Show |
4 | HG00558.hp2 NA18950.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.3704-911T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60026973 | |||||||
| chr14:60027567 | C | T | 257 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(254): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.3704-317C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60027567 | |||||||
| chr14:60027663 | G | C | 2 | a0006c0010t0018g0166 a0006c0010t0021g0033 |
2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3704-221G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60027663 | |||||||
| chr14:60028344 | T | C | 3 | a0001c0002t0017g0141 a0001c0002t0017g0142 a0001c0002t0024g0157 |
3 | HG01109.hp2 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3921+243T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60028344 | |||||||
| chr14:60028401 | G | C | 1 | a0001c0001t0016g0105 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3921+300G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60028401 | |||||||
| chr14:60028424 | G | A | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3921+323G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60028424 | |||||||
| chr14:60028638 | T | C | 1 | a0001c0006t0002g0114 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3921+537T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60028638 | |||||||
| chr14:60028712 | G | A | 3 | a0001c0001t0001g0218 a0001c0001t0001g0231 a0001c0001t0001g0313 |
3 | NA18961.hp1 NA18999.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.3921+611G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60028712 | |||||||
| chr14:60028802 | C | T | 2 | a0006c0010t0018g0166 a0006c0010t0021g0033 |
2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3921+701C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60028802 | |||||||
| chr14:60029329 | G | A | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3921+1228G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60029329 | |||||||
| chr14:60029436 | C | T | 167 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.3921+1335C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60029436 | |||||||
| chr14:60029526 | G | A | 165 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.3921+1425G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60029526 | |||||||
| chr14:60029652 | C | A | 3 | a0001c0002t0002g0003 a0001c0002t0002g0296 a0001c0002t0002g0297 |
3 | HG00673.hp1 NA18978.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.3921+1551C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60029652 | |||||||
| chr14:60029724 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3921+1623T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60029724 | |||||||
| chr14:60029758 | A | C | 257 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(254): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.3921+1657A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60029758 | |||||||
| chr14:60029864 | C | T | 165 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.3921+1763C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60029864 | |||||||
| chr14:60029951 | GA | G | 190 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.3921+1859delA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr14 | 60029951 | ||||||
| chr14:60030040 | C | G | 1 | a0001c0001t0001g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3921+1939C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60030040 | |||||||
| chr14:60030109 | A | G | 1 | a0001c0001t0003g0239 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3922-1886A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60030109 | |||||||
| chr14:60030257 | C | A | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3922-1738C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60030257 | |||||||
| chr14:60030263 | G | A | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3922-1732G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60030263 | |||||||
| chr14:60030341 | A | G | 7 | a0001c0005t0013g0151 a0001c0005t0013g0171 a0001c0005t0013g0172 others(4): Show |
7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3922-1654A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60030341 | |||||||
| chr14:60030367 | A | G | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3922-1628A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60030367 | |||||||
| chr14:60030587 | A | G | 5 | a0001c0001t0001g0226 a0001c0001t0003g0254 a0001c0001t0003g0255 others(2): Show |
5 | HG00735.hp2 HG00738.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.3922-1408A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60030587 | |||||||
| chr14:60030691 | A | G | 1 | a0001c0001t0003g0057 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3922-1304A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60030691 | |||||||
| chr14:60030794 | A | G | 2 | a0001c0001t0010g0053 a0001c0001t0010g0054 |
2 | NA18612.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.3922-1201A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60030794 | |||||||
| chr14:60030928 | C | T | 5 | a0001c0002t0021g0161 a0006c0010t0018g0166 a0006c0010t0021g0033 others(2): Show |
5 | HG02257.hp1 HG02486.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3922-1067C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60030928 | |||||||
| chr14:60031183 | C | G | 1 | a0002c0003t0005g0187 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3922-812C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60031183 | |||||||
| chr14:60031244 | C | T | 2 | a0006c0010t0018g0166 a0006c0010t0021g0033 |
2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3922-751C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60031244 | |||||||
| chr14:60031291 | A | G | 2 | a0001c0002t0004g0015 a0001c0002t0029g0017 |
2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3922-704A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60031291 | |||||||
| chr14:60031367 | T | C | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.3922-628T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60031367 | |||||||
| chr14:60031407 | T | C | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3922-588T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60031407 | |||||||
| chr14:60031556 | T | C | 1 | a0001c0002t0002g0127 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3922-439T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60031556 | |||||||
| chr14:60031563 | G | A | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3922-432G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60031563 | |||||||
| chr14:60031681 | T | C | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3922-314T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60031681 | |||||||
| chr14:60031861 | C | A | 14 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0009 others(11): Show |
14 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.3922-134C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60031861 | |||||||
| chr14:60031976 | C | T | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3922-19C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60031976 | |||||||
| chr14:60032155 | A | G | 1 | a0006c0010t0021g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3990+92A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60032155 | |||||||
| chr14:60032158 | C | T | 258 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(255): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.3990+95C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60032158 | |||||||
| chr14:60032330 | T | C | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3990+267T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60032330 | |||||||
| chr14:60032567 | A | G | 1 | a0001c0002t0004g0289 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3990+504A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60032567 | |||||||
| chr14:60032620 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3990+557C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60032620 | |||||||
| chr14:60032646 | T | C | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3990+583T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60032646 | |||||||
| chr14:60032791 | T | C | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3990+728T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60032791 | |||||||
| chr14:60032859 | CT | C | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3990+797delT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60032859 | |||||||
| chr14:60032942 | A | G | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3990+879A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60032942 | |||||||
| chr14:60032978 | C | T | 165 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.3990+915C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60032978 | |||||||
| chr14:60033240 | T | C | 1 | a0001c0001t0008g0041 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3990+1177T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60033240 | |||||||
| chr14:60033589 | A | G | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3990+1526A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60033589 | |||||||
| chr14:60033713 | T | A | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3990+1650T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60033713 | |||||||
| chr14:60034015 | C | CT | 43 | a0001c0002t0002g0003 a0001c0002t0002g0137 a0001c0002t0002g0215 others(40): Show |
44 | HG00558.hp2 HG00609.hp1 HG01346.hp1 others(41): Show |
intron_variant | MODIFIER | c.3990+1975dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60034015 | ||||||
| chr14:60034015 | C | CTT | 14 | a0001c0002t0004g0004 a0001c0002t0004g0015 a0001c0002t0004g0272 others(11): Show |
14 | HG01243.hp2 HG02015.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.3990+1974_3990+197 others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60034015 | ||||||
| chr14:60034015 | CT | C | 10 | a0001c0002t0002g0112 a0001c0002t0002g0207 a0001c0004t0009g0209 others(7): Show |
10 | HG00642.hp1 HG00735.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.3990+1975delT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60034015 | ||||||
| chr14:60034017 | T | TTC | 9 | a0001c0001t0001g0080 a0001c0001t0001g0091 a0001c0001t0003g0025 others(6): Show |
9 | HG00099.hp2 HG00280.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.3990+1955_3990+195 others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60034017 | ||||||
| chr14:60034018 | T | TC | 152 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(149): Show |
152 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.3990+1955_3990+195 others(5): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60034018 | |||||||
| chr14:60034019 | T | C | 6 | a0001c0001t0006g0020 a0001c0001t0008g0013 a0001c0001t0010g0034 others(3): Show |
6 | HG00323.hp2 HG01168.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.3990+1956T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60034019 | |||||||
| chr14:60034020 | T | C | 8 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(5): Show |
8 | HG00642.hp1 HG00735.hp1 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.3990+1957T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60034020 | |||||||
| chr14:60034021 | T | C | 1 | a0001c0001t0023g0049 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3990+1958T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60034021 | |||||||
| chr14:60034084 | A | G | 257 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(254): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.3990+2021A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60034084 | |||||||
| chr14:60034103 | C | T | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3990+2040C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60034103 | |||||||
| chr14:60034142 | C | T | 2 | a0001c0002t0004g0015 a0001c0002t0029g0017 |
2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3990+2079C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60034142 | |||||||
| chr14:60034195 | T | C | 2 | a0001c0001t0003g0228 a0001c0001t0003g0245 |
2 | HG01981.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.3990+2132T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60034195 | |||||||
| chr14:60034503 | C | A | 3 | a0001c0002t0021g0161 a0006c0010t0018g0166 a0006c0010t0021g0033 |
3 | HG02257.hp1 HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3990+2440C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60034503 | |||||||
| chr14:60034562 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3990+2499T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60034562 | |||||||
| chr14:60034613 | C | T | 1 | a0001c0001t0001g0313 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3990+2550C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60034613 | |||||||
| chr14:60034857 | A | G | 3 | a0001c0001t0001g0044 a0001c0001t0011g0050 a0001c0001t0023g0049 |
3 | HG02074.hp2 NA18955.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3990+2794A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60034857 | |||||||
| chr14:60034990 | C | T | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3990+2927C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60034990 | |||||||
| chr14:60035103 | AT | A | 170 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(167): Show |
170 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.3990+3053delT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60035103 | ||||||
| chr14:60035128 | G | A | 1 | a0001c0001t0003g0014 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3990+3065G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60035128 | |||||||
| chr14:60035638 | T | C | 1 | a0001c0002t0002g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3990+3575T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60035638 | |||||||
| chr14:60035728 | G | A | 1 | a0001c0002t0002g0003 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.3990+3665G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60035728 | |||||||
| chr14:60035834 | G | A | 41 | a0001c0002t0004g0153 a0001c0002t0004g0265 a0001c0002t0004g0268 others(38): Show |
42 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(39): Show |
intron_variant | MODIFIER | c.3990+3771G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60035834 | |||||||
| chr14:60035897 | T | C | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3990+3834T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60035897 | |||||||
| chr14:60035956 | A | G | 190 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.3990+3893A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60035956 | |||||||
| chr14:60035960 | T | TG | 190 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.3990+3898dupG | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60035960 | ||||||
| chr14:60036033 | T | C | 1 | a0001c0001t0003g0100 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3990+3970T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60036033 | |||||||
| chr14:60036042 | T | TA | 7 | a0001c0002t0007g0002 a0001c0002t0007g0275 a0001c0002t0007g0290 others(4): Show |
8 | HG02015.hp2 NA18989.hp1 NA18998.hp1 others(5): Show |
intron_variant | MODIFIER | c.3990+3980dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60036042 | ||||||
| chr14:60036074 | G | A | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3990+4011G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60036074 | |||||||
| chr14:60036152 | C | T | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3990+4089C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60036152 | |||||||
| chr14:60036400 | C | T | 1 | a0001c0002t0002g0159 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3990+4337C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60036400 | |||||||
| chr14:60036432 | T | G | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3990+4369T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60036432 | |||||||
| chr14:60036512 | G | A | 1 | a0001c0001t0006g0072 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.3990+4449G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60036512 | |||||||
| chr14:60036567 | T | A | 2 | a0007c0013t0018g0110 a0007c0013t0018g0111 |
2 | HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3990+4504T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60036567 | |||||||
| chr14:60036728 | CT | C | 280 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(277): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.3990+4676delT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60036728 | ||||||
| chr14:60036728 | CTT | C | 7 | a0001c0002t0002g0143 a0001c0002t0002g0144 a0001c0002t0002g0145 others(4): Show |
7 | HG01243.hp1 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.3990+4675_3990+467 others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60036728 | ||||||
| chr14:60036829 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3990+4766A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60036829 | |||||||
| chr14:60036843 | G | A | 1 | a0001c0001t0016g0206 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3990+4780G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60036843 | |||||||
| chr14:60036880 | A | G | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3990+4817A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60036880 | |||||||
| chr14:60036887 | G | T | 1 | a0001c0002t0002g0118 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.3990+4824G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60036887 | |||||||
| chr14:60037304 | C | T | 4 | a0001c0001t0011g0021 a0001c0001t0011g0078 a0001c0001t0011g0079 others(1): Show |
4 | HG02559.hp2 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3990+5241C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60037304 | |||||||
| chr14:60037326 | T | C | 8 | a0001c0002t0002g0126 a0001c0002t0002g0128 a0001c0002t0002g0129 others(5): Show |
8 | HG02074.hp1 HG02080.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.3990+5263T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60037326 | |||||||
| chr14:60037357 | G | A | 11 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0009 others(8): Show |
11 | HG00639.hp2 HG00741.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.3990+5294G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60037357 | |||||||
| chr14:60037548 | G | C | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3990+5485G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60037548 | |||||||
| chr14:60037677 | G | A | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3990+5614G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60037677 | |||||||
| chr14:60037883 | G | A | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3990+5820G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60037883 | |||||||
| chr14:60037978 | C | G | 2 | a0001c0002t0002g0143 a0001c0002t0002g0144 |
2 | NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3990+5915C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60037978 | |||||||
| chr14:60037991 | C | T | 2 | a0002c0003t0005g0202 a0002c0003t0005g0205 |
2 | NA18941.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.3990+5928C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60037991 | |||||||
| chr14:60038069 | T | C | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3990+6006T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60038069 | |||||||
| chr14:60038120 | T | C | 1 | a0001c0006t0002g0116 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3990+6057T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60038120 | |||||||
| chr14:60038247 | G | A | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3990+6184G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60038247 | |||||||
| chr14:60038353 | G | A | 1 | a0001c0002t0025g0135 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3990+6290G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60038353 | |||||||
| chr14:60038380 | G | C | 1 | a0001c0002t0012g0120 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3990+6317G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60038380 | |||||||
| chr14:60038450 | G | A | 1 | a0001c0002t0002g0146 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3990+6387G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60038450 | |||||||
| chr14:60038463 | C | T | 1 | a0001c0002t0004g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3990+6400C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60038463 | |||||||
| chr14:60038476 | C | G | 4 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0090 others(1): Show |
4 | HG01433.hp1 HG02280.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.3990+6413C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60038476 | |||||||
| chr14:60038505 | G | T | 2 | a0006c0010t0018g0166 a0006c0010t0021g0033 |
2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3990+6442G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60038505 | |||||||
| chr14:60038625 | C | A | 8 | a0001c0002t0002g0126 a0001c0002t0002g0128 a0001c0002t0002g0129 others(5): Show |
8 | HG02074.hp1 HG02080.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.3990+6562C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60038625 | |||||||
| chr14:60038666 | G | T | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.3990+6603G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60038666 | |||||||
| chr14:60038899 | G | T | 3 | a0001c0004t0009g0302 a0001c0004t0009g0307 a0001c0004t0009g0309 |
3 | HG00642.hp1 HG00735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.3990+6836G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60038899 | |||||||
| chr14:60039018 | T | C | 1 | a0001c0001t0011g0021 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3990+6955T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60039018 | |||||||
| chr14:60039096 | G | A | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3990+7033G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60039096 | |||||||
| chr14:60039159 | G | A | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3990+7096G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60039159 | |||||||
| chr14:60039243 | G | T | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.3990+7180G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60039243 | |||||||
| chr14:60039259 | G | A | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3990+7196G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60039259 | |||||||
| chr14:60039278 | A | G | 165 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.3990+7215A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60039278 | |||||||
| chr14:60039365 | A | T | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3990+7302A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60039365 | |||||||
| chr14:60039741 | G | A | 1 | a0001c0002t0002g0136 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3990+7678G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60039741 | |||||||
| chr14:60039772 | G | C | 2 | a0001c0002t0002g0233 a0001c0002t0002g0256 |
2 | HG03669.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.3990+7709G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60039772 | |||||||
| chr14:60039779 | T | C | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3990+7716T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60039779 | |||||||
| chr14:60039811 | G | GA | 5 | a0001c0002t0002g0005 a0001c0002t0002g0112 a0001c0002t0002g0173 others(2): Show |
5 | HG01081.hp1 HG01884.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.3990+7750dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60039811 | ||||||
| chr14:60039828 | C | T | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3990+7765C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60039828 | |||||||
| chr14:60039890 | T | C | 8 | a0001c0002t0012g0120 a0001c0002t0012g0121 a0001c0002t0012g0122 others(5): Show |
8 | HG02486.hp1 HG02622.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.3990+7827T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60039890 | |||||||
| chr14:60039897 | ATTTAGTG others(1226): Show |
A | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3990+7841_3990+907 others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60039897 | ||||||
| chr14:60040176 | C | T | 1 | a0001c0002t0004g0284 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.3990+8113C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60040176 | |||||||
| chr14:60040201 | A | G | 6 | a0001c0001t0001g0027 a0001c0001t0001g0045 a0001c0001t0001g0061 others(3): Show |
6 | NA18946.hp1 NA18979.hp1 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.3990+8138A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60040201 | |||||||
| chr14:60040206 | C | T | 1 | a0001c0001t0001g0045 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.3990+8143C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60040206 | |||||||
| chr14:60040210 | G | A | 167 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.3990+8147G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60040210 | |||||||
| chr14:60040387 | A | G | 190 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.3990+8324A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60040387 | |||||||
| chr14:60040408 | C | T | 1 | a0001c0001t0045g0232 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3990+8345C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60040408 | |||||||
| chr14:60040448 | A | G | 5 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0304 others(2): Show |
5 | HG00323.hp2 NA18946.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.3990+8385A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60040448 | |||||||
| chr14:60040465 | G | T | 1 | a0004c0008t0010g0055 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.3990+8402G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60040465 | |||||||
| chr14:60040468 | G | A | 1 | a0004c0008t0010g0055 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.3990+8405G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60040468 | |||||||
| chr14:60040499 | C | T | 1 | a0002c0003t0005g0205 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.3990+8436C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60040499 | |||||||
| chr14:60040594 | T | C | 81 | a0001c0001t0001g0027 a0001c0001t0001g0045 a0001c0001t0001g0061 others(78): Show |
81 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.3990+8531T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60040594 | |||||||
| chr14:60040607 | C | G | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3990+8544C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60040607 | |||||||
| chr14:60040690 | C | T | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3990+8627C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60040690 | |||||||
| chr14:60040691 | A | G | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3990+8628A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60040691 | |||||||
| chr14:60041126 | C | G | 165 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.3990+9063C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60041126 | |||||||
| chr14:60041137 | C | T | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3990+9074C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60041137 | |||||||
| chr14:60041178 | C | G | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3990+9115C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60041178 | |||||||
| chr14:60041179 | A | G | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3990+9116A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60041179 | |||||||
| chr14:60041182 | A | G | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3990+9119A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60041182 | |||||||
| chr14:60041229 | T | G | 3 | a0001c0002t0002g0107 a0001c0002t0002g0138 a0001c0002t0002g0139 |
3 | HG01175.hp1 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.3990+9166T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60041229 | |||||||
| chr14:60041230 | A | T | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3990+9167A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60041230 | |||||||
| chr14:60041481 | T | C | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3990+9418T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60041481 | |||||||
| chr14:60041677 | T | C | 12 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(9): Show |
12 | HG01433.hp1 HG01884.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.3990+9614T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60041677 | |||||||
| chr14:60041791 | G | A | 7 | a0001c0002t0004g0015 a0001c0002t0021g0161 a0001c0002t0029g0017 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.3990+9728G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60041791 | |||||||
| chr14:60041797 | C | A | 1 | a0001c0002t0002g0233 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3990+9734C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60041797 | |||||||
| chr14:60041817 | A | T | 39 | a0001c0002t0004g0265 a0001c0002t0004g0268 a0001c0002t0004g0271 others(36): Show |
40 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(37): Show |
intron_variant | MODIFIER | c.3990+9754A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60041817 | |||||||
| chr14:60042081 | A | C | 165 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.3990+10018A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042081 | |||||||
| chr14:60042225 | C | T | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.3990+10162C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042225 | |||||||
| chr14:60042252 | G | T | 165 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.3990+10189G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042252 | |||||||
| chr14:60042306 | A | G | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3990+10243A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042306 | |||||||
| chr14:60042308 | T | A | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3990+10245T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042308 | |||||||
| chr14:60042320 | G | T | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3990+10257G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042320 | |||||||
| chr14:60042326 | C | T | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3990+10263C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042326 | |||||||
| chr14:60042327 | A | G | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3990+10264A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042327 | |||||||
| chr14:60042330 | T | A | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3990+10267T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042330 | |||||||
| chr14:60042355 | C | T | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3990+10292C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042355 | |||||||
| chr14:60042471 | C | T | 2 | a0001c0005t0013g0171 a0001c0005t0013g0172 |
2 | HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.3990+10408C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042471 | |||||||
| chr14:60042551 | T | C | 1 | a0001c0001t0033g0063 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3990+10488T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042551 | |||||||
| chr14:60042560 | T | C | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3990+10497T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042560 | |||||||
| chr14:60042579 | G | A | 2 | a0001c0001t0001g0263 a0001c0001t0003g0262 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.3991-10486G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042579 | |||||||
| chr14:60042647 | T | C | 1 | a0001c0002t0007g0290 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3991-10418T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042647 | |||||||
| chr14:60042648 | C | T | 1 | a0002c0003t0005g0199 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.3991-10417C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042648 | |||||||
| chr14:60042698 | C | T | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3991-10367C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042698 | |||||||
| chr14:60042744 | T | C | 2 | a0001c0002t0002g0145 a0001c0002t0002g0146 |
2 | HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.3991-10321T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042744 | |||||||
| chr14:60042757 | C | T | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3991-10308C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042757 | |||||||
| chr14:60043284 | C | A | 295 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(292): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.3991-9781C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60043284 | |||||||
| chr14:60043735 | G | A | 1 | a0001c0002t0002g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3991-9330G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60043735 | |||||||
| chr14:60043745 | GTTTTC | G | 12 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(9): Show |
12 | HG01433.hp1 HG01884.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.3991-9314_3991-931 others(9): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60043745 | ||||||
| chr14:60043756 | C | CT | 81 | a0001c0001t0001g0087 a0001c0001t0001g0243 a0001c0001t0001g0252 others(78): Show |
83 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.3991-9287dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60043756 | ||||||
| chr14:60043756 | C | CTT | 11 | a0001c0001t0015g0060 a0001c0002t0004g0004 a0001c0002t0004g0265 others(8): Show |
11 | HG01243.hp2 HG01358.hp2 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.3991-9288_3991-928 others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60043756 | ||||||
| chr14:60043756 | CT | C | 13 | a0001c0001t0001g0085 a0001c0001t0035g0156 a0001c0002t0002g0233 others(10): Show |
13 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.3991-9287delT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60043756 | ||||||
| chr14:60044030 | T | C | 4 | a0001c0002t0004g0273 a0001c0002t0004g0289 a0001c0002t0004g0298 others(1): Show |
4 | HG02040.hp1 HG02071.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.3991-9035T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60044030 | |||||||
| chr14:60044355 | A | G | 190 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.3991-8710A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60044355 | |||||||
| chr14:60044875 | G | A | 7 | a0001c0005t0013g0151 a0001c0005t0013g0171 a0001c0005t0013g0172 others(4): Show |
7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3991-8190G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60044875 | |||||||
| chr14:60044940 | A | G | 1 | a0001c0001t0039g0068 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3991-8125A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60044940 | |||||||
| chr14:60045006 | C | T | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3991-8059C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60045006 | |||||||
| chr14:60045051 | C | CT | 12 | a0001c0002t0002g0134 a0001c0002t0002g0233 a0001c0002t0012g0120 others(9): Show |
12 | HG01109.hp2 HG02486.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.3991-7997dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60045051 | ||||||
| chr14:60045051 | C | CTT | 13 | a0001c0001t0035g0156 a0001c0002t0004g0004 a0001c0002t0021g0161 others(10): Show |
13 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.3991-7998_3991-799 others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60045051 | ||||||
| chr14:60045051 | C | CTTT | 36 | a0001c0002t0004g0015 a0001c0002t0004g0214 a0001c0002t0004g0272 others(33): Show |
37 | HG02165.hp2 HG02486.hp2 HG03139.hp1 others(34): Show |
intron_variant | MODIFIER | c.3991-7999_3991-799 others(7): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60045051 | ||||||
| chr14:60045051 | C | CTTTT | 32 | a0001c0002t0004g0153 a0001c0002t0004g0265 a0001c0002t0004g0268 others(29): Show |
33 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(30): Show |
intron_variant | MODIFIER | c.3991-8000_3991-799 others(8): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60045051 | ||||||
| chr14:60045051 | CT | C | 26 | a0001c0001t0001g0087 a0001c0001t0001g0221 a0001c0001t0001g0222 others(23): Show |
26 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.3991-7997delT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60045051 | ||||||
| chr14:60045051 | CTT | C | 146 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(143): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.3991-7998_3991-799 others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60045051 | ||||||
| chr14:60045101 | A | G | 2 | a0005c0011t0003g0211 a0005c0011t0006g0212 |
2 | HG00099.hp1 HG00280.hp2 |
intron_variant | MODIFIER | c.3991-7964A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60045101 | |||||||
| chr14:60045299 | T | C | 1 | a0001c0002t0002g0107 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3991-7766T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60045299 | |||||||
| chr14:60045393 | C | T | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3991-7672C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60045393 | |||||||
| chr14:60045426 | C | T | 30 | a0001c0001t0003g0100 a0001c0001t0003g0102 a0001c0001t0003g0168 others(27): Show |
31 | HG01358.hp1 HG01361.hp1 HG01928.hp2 others(28): Show |
intron_variant | MODIFIER | c.3991-7639C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60045426 | |||||||
| chr14:60045477 | G | A | 190 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.3991-7588G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60045477 | |||||||
| chr14:60045738 | C | T | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3991-7327C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60045738 | |||||||
| chr14:60045758 | A | G | 2 | a0001c0002t0004g0015 a0001c0002t0029g0017 |
2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3991-7307A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60045758 | |||||||
| chr14:60046145 | A | G | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3991-6920A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60046145 | |||||||
| chr14:60046250 | C | T | 4 | a0001c0001t0001g0058 a0001c0001t0001g0165 a0001c0001t0016g0023 others(1): Show |
4 | HG01074.hp2 HG02257.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.3991-6815C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60046250 | |||||||
| chr14:60046364 | G | T | 1 | a0001c0001t0001g0086 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3991-6701G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60046364 | |||||||
| chr14:60046428 | C | T | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3991-6637C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60046428 | |||||||
| chr14:60046445 | T | G | 5 | a0001c0002t0021g0161 a0006c0010t0018g0166 a0006c0010t0021g0033 others(2): Show |
5 | HG02257.hp1 HG02486.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3991-6620T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60046445 | |||||||
| chr14:60046591 | G | A | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3991-6474G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60046591 | |||||||
| chr14:60046647 | C | T | 2 | a0001c0001t0010g0034 a0001c0001t0015g0062 |
2 | NA18994.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.3991-6418C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60046647 | |||||||
| chr14:60046682 | G | A | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3991-6383G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60046682 | |||||||
| chr14:60046701 | T | C | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3991-6364T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60046701 | |||||||
| chr14:60046785 | A | T | 189 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(186): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.3991-6280A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60046785 | |||||||
| chr14:60046788 | T | C | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3991-6277T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60046788 | |||||||
| chr14:60046804 | G | C | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3991-6261G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60046804 | |||||||
| chr14:60046855 | G | A | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3991-6210G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60046855 | |||||||
| chr14:60046934 | C | T | 258 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(255): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.3991-6131C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60046934 | |||||||
| chr14:60047248 | C | A | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.3991-5817C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60047248 | |||||||
| chr14:60047307 | T | C | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.3991-5758T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60047307 | |||||||
| chr14:60047353 | C | T | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3991-5712C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60047353 | |||||||
| chr14:60047414 | C | T | 1 | a0001c0001t0006g0169 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3991-5651C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60047414 | |||||||
| chr14:60047418 | T | C | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3991-5647T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60047418 | |||||||
| chr14:60047569 | T | C | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3991-5496T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60047569 | |||||||
| chr14:60047580 | T | C | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3991-5485T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60047580 | |||||||
| chr14:60047644 | T | C | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.3991-5421T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60047644 | |||||||
| chr14:60047794 | A | T | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3991-5271A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60047794 | |||||||
| chr14:60047825 | C | T | 1 | a0001c0002t0002g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3991-5240C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60047825 | |||||||
| chr14:60047854 | C | T | 2 | a0001c0002t0004g0015 a0001c0002t0029g0017 |
2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3991-5211C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60047854 | |||||||
| chr14:60048085 | T | C | 1 | a0007c0013t0018g0111 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3991-4980T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60048085 | |||||||
| chr14:60048128 | A | G | 189 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(186): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.3991-4937A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60048128 | |||||||
| chr14:60048227 | G | T | 1 | a0001c0002t0017g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3991-4838G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60048227 | |||||||
| chr14:60048237 | C | G | 2 | a0006c0010t0018g0166 a0006c0010t0021g0033 |
2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3991-4828C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60048237 | |||||||
| chr14:60048386 | C | T | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3991-4679C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60048386 | |||||||
| chr14:60048527 | C | T | 7 | a0001c0002t0004g0015 a0001c0002t0021g0161 a0001c0002t0029g0017 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.3991-4538C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60048527 | |||||||
| chr14:60048564 | G | T | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3991-4501G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60048564 | |||||||
| chr14:60048713 | G | A | 189 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(186): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.3991-4352G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60048713 | |||||||
| chr14:60048744 | T | G | 1 | a0001c0002t0002g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3991-4321T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60048744 | |||||||
| chr14:60048791 | G | A | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3991-4274G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60048791 | |||||||
| chr14:60049321 | G | A | 3 | a0001c0001t0003g0025 a0001c0001t0003g0048 a0001c0001t0014g0040 |
3 | NA18990.hp1 NA19059.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.3991-3744G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60049321 | |||||||
| chr14:60049766 | G | C | 3 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0006g0020 |
3 | NA18945.hp1 NA19007.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.3991-3299G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60049766 | |||||||
| chr14:60049974 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3991-3091A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60049974 | |||||||
| chr14:60049990 | C | CATTTT | 3 | a0001c0002t0021g0161 a0006c0010t0018g0166 a0006c0010t0021g0033 |
3 | HG02257.hp1 HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3991-3055_3991-305 others(9): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60049990 | ||||||
| chr14:60050046 | G | C | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3991-3019G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050046 | |||||||
| chr14:60050065 | C | T | 4 | a0001c0002t0017g0117 a0001c0002t0017g0141 a0001c0002t0017g0142 others(1): Show |
4 | HG01109.hp2 HG02818.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3991-3000C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050065 | |||||||
| chr14:60050094 | T | G | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3991-2971T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050094 | |||||||
| chr14:60050097 | A | AC | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3991-2968_3991-296 others(5): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050097 | |||||||
| chr14:60050098 | G | C | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3991-2967G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050098 | |||||||
| chr14:60050100 | G | C | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3991-2965G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050100 | |||||||
| chr14:60050101 | A | C | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3991-2964A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050101 | |||||||
| chr14:60050102 | T | A | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3991-2963T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050102 | |||||||
| chr14:60050103 | T | C | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3991-2962T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050103 | |||||||
| chr14:60050155 | C | T | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3991-2910C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050155 | |||||||
| chr14:60050174 | T | G | 1 | a0001c0001t0019g0315 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3991-2891T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050174 | |||||||
| chr14:60050192 | C | T | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3991-2873C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050192 | |||||||
| chr14:60050292 | G | A | 2 | a0001c0001t0006g0099 a0001c0001t0006g0169 |
2 | HG01928.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.3991-2773G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050292 | |||||||
| chr14:60050318 | C | T | 257 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(254): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.3991-2747C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050318 | |||||||
| chr14:60050362 | T | C | 1 | a0001c0002t0002g0137 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3991-2703T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050362 | |||||||
| chr14:60050426 | C | T | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3991-2639C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050426 | |||||||
| chr14:60050427 | G | A | 2 | a0001c0001t0006g0241 a0001c0001t0006g0244 |
2 | HG00741.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.3991-2638G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050427 | |||||||
| chr14:60050481 | T | C | 42 | a0001c0002t0004g0153 a0001c0002t0004g0214 a0001c0002t0004g0265 others(39): Show |
43 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.3991-2584T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050481 | |||||||
| chr14:60050487 | A | G | 1 | a0001c0006t0002g0116 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3991-2578A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050487 | |||||||
| chr14:60050701 | T | C | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3991-2364T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050701 | |||||||
| chr14:60050839 | T | G | 1 | a0001c0002t0004g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3991-2226T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050839 | |||||||
| chr14:60050953 | G | T | 3 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0006g0020 |
3 | NA18945.hp1 NA19007.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.3991-2112G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050953 | |||||||
| chr14:60051045 | G | A | 1 | a0001c0001t0010g0067 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3991-2020G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60051045 | |||||||
| chr14:60051071 | A | G | 165 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.3991-1994A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60051071 | |||||||
| chr14:60051118 | T | C | 2 | a0006c0010t0018g0166 a0006c0010t0021g0033 |
2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3991-1947T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60051118 | |||||||
| chr14:60051288 | G | A | 8 | a0001c0002t0012g0120 a0001c0002t0012g0121 a0001c0002t0012g0122 others(5): Show |
8 | HG02486.hp1 HG02622.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.3991-1777G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60051288 | |||||||
| chr14:60051308 | G | A | 3 | a0001c0001t0003g0064 a0001c0001t0003g0239 a0009c0017t0003g0065 |
3 | HG01169.hp2 HG01952.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.3991-1757G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60051308 | |||||||
| chr14:60051467 | A | T | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3991-1598A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60051467 | |||||||
| chr14:60051640 | C | G | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3991-1425C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60051640 | |||||||
| chr14:60051718 | G | A | 1 | a0004c0008t0010g0055 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.3991-1347G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60051718 | |||||||
| chr14:60051720 | C | T | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3991-1345C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60051720 | |||||||
| chr14:60051835 | C | T | 1 | a0003c0007t0004g0280 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3991-1230C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60051835 | |||||||
| chr14:60051891 | T | C | 3 | a0001c0001t0001g0077 a0001c0001t0001g0236 a0001c0001t0027g0235 |
3 | NA18956.hp2 NA18986.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.3991-1174T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60051891 | |||||||
| chr14:60051971 | C | T | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3991-1094C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60051971 | |||||||
| chr14:60051975 | C | T | 1 | a0001c0002t0002g0177 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3991-1090C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60051975 | |||||||
| chr14:60051997 | C | A | 1 | a0001c0001t0008g0011 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3991-1068C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60051997 | |||||||
| chr14:60052315 | G | A | 1 | a0001c0002t0004g0268 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3991-750G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60052315 | |||||||
| chr14:60052398 | T | C | 1 | a0002c0003t0005g0204 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.3991-667T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60052398 | |||||||
| chr14:60052403 | T | A | 1 | a0001c0001t0001g0090 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3991-662T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60052403 | |||||||
| chr14:60052506 | C | T | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3991-559C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60052506 | |||||||
| chr14:60052827 | C | A | 168 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.3991-238C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60052827 | |||||||
| chr14:60053247 | TAATG | T | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4131+43_4131+46del others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60053247 | |||||||
| chr14:60053301 | C | A | 7 | a0001c0005t0013g0151 a0001c0005t0013g0171 a0001c0005t0013g0172 others(4): Show |
7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.4131+96C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60053301 | |||||||
| chr14:60053381 | GCTCA | G | 20 | a0002c0003t0005g0185 a0002c0003t0005g0186 a0002c0003t0005g0189 others(17): Show |
20 | NA18941.hp2 NA18945.hp2 NA18964.hp2 others(17): Show |
intron_variant | MODIFIER | c.4131+178_4131+181d others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60053381 | ||||||
| chr14:60053381 | GCTCACA | G | 3 | a0002c0003t0005g0001 a0002c0003t0005g0187 a0002c0003t0005g0188 |
4 | NA18939.hp2 NA18960.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.4131+178_4131+183d others(8): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60053381 | ||||||
| chr14:60053383 | T | TCA | 35 | a0001c0002t0002g0129 a0001c0002t0002g0146 a0001c0002t0002g0176 others(32): Show |
35 | HG00558.hp2 HG00609.hp1 HG02040.hp1 others(32): Show |
intron_variant | MODIFIER | c.4131+215_4131+216d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60053383 | ||||||
| chr14:60053383 | T | TCACA | 42 | a0001c0002t0002g0003 a0001c0002t0002g0107 a0001c0002t0002g0118 others(39): Show |
43 | HG00673.hp1 HG01109.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.4131+213_4131+216d others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60053383 | ||||||
| chr14:60053383 | T | TCACACA | 17 | a0001c0002t0002g0127 a0001c0002t0002g0133 a0001c0002t0002g0143 others(14): Show |
17 | HG00639.hp1 HG01243.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.4131+211_4131+216d others(8): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60053383 | ||||||
| chr14:60053383 | T | TCACACAC others(1): Show |
7 | a0001c0002t0012g0124 a0001c0005t0013g0172 a0001c0006t0002g0109 others(4): Show |
7 | HG02080.hp1 HG02486.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.4131+209_4131+216d others(10): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60053383 | ||||||
| chr14:60053383 | T | TCACACAC others(3): Show |
1 | a0001c0005t0013g0171 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4131+207_4131+216d others(12): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60053383 | ||||||
| chr14:60053383 | TCA | T | 7 | a0001c0002t0002g0005 a0001c0002t0002g0112 a0001c0002t0002g0173 others(4): Show |
7 | HG01081.hp1 HG01361.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.4131+215_4131+216d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60053383 | ||||||
| chr14:60053383 | TCACA | T | 9 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(6): Show |
9 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.4131+213_4131+216d others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60053383 | ||||||
| chr14:60053412 | CACACACA others(3): Show |
C | 71 | a0001c0001t0001g0027 a0001c0001t0001g0045 a0001c0001t0001g0061 others(68): Show |
71 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.4131+209_4131+218d others(12): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60053412 | ||||||
| chr14:60053414 | CACACACA others(1): Show |
C | 6 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0057 others(3): Show |
6 | HG00099.hp2 HG01081.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.4131+211_4131+218d others(10): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60053414 | ||||||
| chr14:60053416 | CACACAT | C | 84 | a0001c0001t0001g0016 a0001c0001t0001g0044 a0001c0001t0001g0058 others(81): Show |
84 | HG00280.hp1 HG00423.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.4131+213_4131+218d others(8): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60053416 | ||||||
| chr14:60053418 | C | T | 20 | a0002c0003t0005g0185 a0002c0003t0005g0186 a0002c0003t0005g0189 others(17): Show |
20 | NA18941.hp2 NA18945.hp2 NA18964.hp2 others(17): Show |
intron_variant | MODIFIER | c.4131+213C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60053418 | |||||||
| chr14:60053418 | CACAT | C | 4 | a0001c0001t0001g0085 a0001c0001t0001g0094 a0001c0001t0003g0018 others(1): Show |
4 | HG01516.hp1 HG02896.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.4131+215_4131+218d others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60053418 | ||||||
| chr14:60053420 | C | T | 33 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(30): Show |
34 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.4131+215C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60053420 | |||||||
| chr14:60053422 | T | C | 6 | a0001c0005t0013g0151 a0001c0005t0013g0171 a0001c0005t0013g0172 others(3): Show |
6 | HG01358.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.4131+217T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60053422 | |||||||
| chr14:60053429 | G | A | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4131+224G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60053429 | |||||||
| chr14:60053493 | A | G | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4131+288A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60053493 | |||||||
| chr14:60053532 | T | C | 42 | a0001c0002t0004g0153 a0001c0002t0004g0214 a0001c0002t0004g0265 others(39): Show |
43 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.4131+327T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60053532 | |||||||
| chr14:60053535 | G | A | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4131+330G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60053535 | |||||||
| chr14:60053861 | T | C | 8 | a0001c0002t0002g0126 a0001c0002t0002g0128 a0001c0002t0002g0129 others(5): Show |
8 | HG02074.hp1 HG02080.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.4131+656T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60053861 | |||||||
| chr14:60053940 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.4131+735G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60053940 | |||||||
| chr14:60054082 | T | G | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.4131+877T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60054082 | |||||||
| chr14:60054084 | A | C | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4131+879A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60054084 | |||||||
| chr14:60054304 | A | T | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4131+1099A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60054304 | |||||||
| chr14:60054444 | G | T | 1 | a0001c0002t0017g0117 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4131+1239G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60054444 | |||||||
| chr14:60054527 | A | G | 2 | a0001c0002t0004g0289 a0001c0002t0004g0300 |
2 | HG02040.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.4131+1322A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60054527 | |||||||
| chr14:60054545 | C | T | 2 | a0001c0001t0003g0254 a0001c0001t0003g0255 |
2 | HG00738.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.4131+1340C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60054545 | |||||||
| chr14:60054620 | T | C | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4131+1415T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60054620 | |||||||
| chr14:60054622 | C | T | 40 | a0001c0002t0004g0153 a0001c0002t0004g0265 a0001c0002t0004g0268 others(37): Show |
41 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(38): Show |
intron_variant | MODIFIER | c.4131+1417C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60054622 | |||||||
| chr14:60054669 | G | GA | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4131+1465dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60054669 | ||||||
| chr14:60054736 | G | A | 15 | a0001c0002t0004g0004 a0001c0002t0004g0015 a0001c0002t0021g0161 others(12): Show |
15 | HG01243.hp2 HG01358.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.4131+1531G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60054736 | |||||||
| chr14:60054767 | C | T | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4131+1562C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60054767 | |||||||
| chr14:60055006 | C | T | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4131+1801C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055006 | |||||||
| chr14:60055205 | A | T | 1 | a0001c0001t0011g0021 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4131+2000A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055205 | |||||||
| chr14:60055401 | C | T | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4131+2196C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055401 | |||||||
| chr14:60055410 | AT | A | 42 | a0001c0002t0004g0153 a0001c0002t0004g0214 a0001c0002t0004g0265 others(39): Show |
43 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.4131+2208delT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60055410 | ||||||
| chr14:60055488 | T | A | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.4131+2283T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055488 | |||||||
| chr14:60055531 | T | G | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.4131+2326T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055531 | |||||||
| chr14:60055595 | C | A | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4132-2283C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055595 | |||||||
| chr14:60055701 | T | C | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4132-2177T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055701 | |||||||
| chr14:60055731 | T | TA | 9 | a0001c0001t0001g0044 a0001c0001t0001g0085 a0001c0001t0001g0090 others(6): Show |
9 | HG00621.hp1 HG01074.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.4132-2132dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60055731 | ||||||
| chr14:60055739 | A | C | 2 | a0001c0012t0002g0106 a0001c0012t0002g0140 |
2 | HG02602.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.4132-2139A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055739 | |||||||
| chr14:60055740 | A | T | 2 | a0001c0004t0009g0210 a0001c0004t0009g0306 |
2 | NA18946.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.4132-2138A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055740 | |||||||
| chr14:60055744 | A | AC | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4132-2134_4132-213 others(5): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055744 | |||||||
| chr14:60055744 | A | C | 1 | a0001c0001t0001g0257 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.4132-2134A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055744 | |||||||
| chr14:60055745 | A | C | 78 | a0001c0001t0001g0027 a0001c0001t0001g0045 a0001c0001t0001g0061 others(75): Show |
78 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.4132-2133A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055745 | |||||||
| chr14:60055746 | AC | A | 6 | a0001c0001t0001g0058 a0001c0001t0001g0257 a0001c0001t0011g0021 others(3): Show |
6 | HG02559.hp2 HG02922.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.4132-2131delC | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055746 | |||||||
| chr14:60055747 | C | A | 158 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(155): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.4132-2131C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055747 | |||||||
| chr14:60055747 | C | T | 2 | a0001c0004t0009g0210 a0001c0004t0009g0306 |
2 | NA18946.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.4132-2131C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055747 | |||||||
| chr14:60055860 | G | A | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.4132-2018G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055860 | |||||||
| chr14:60055902 | C | T | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4132-1976C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055902 | |||||||
| chr14:60055906 | G | GA | 177 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0045 others(174): Show |
177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.4132-1957dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60055906 | ||||||
| chr14:60055907 | A | G | 2 | a0001c0002t0002g0233 a0001c0002t0002g0256 |
2 | HG03669.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.4132-1971A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055907 | |||||||
| chr14:60056058 | C | T | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4132-1820C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60056058 | |||||||
| chr14:60056073 | T | C | 2 | a0001c0001t0001g0263 a0001c0001t0003g0262 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.4132-1805T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60056073 | |||||||
| chr14:60056483 | A | G | 1 | a0001c0002t0004g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4132-1395A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60056483 | |||||||
| chr14:60056696 | A | G | 1 | a0001c0002t0002g0146 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4132-1182A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60056696 | |||||||
| chr14:60056889 | G | C | 1 | a0001c0002t0002g0174 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.4132-989G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60056889 | |||||||
| chr14:60056952 | A | C | 165 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.4132-926A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60056952 | |||||||
| chr14:60057008 | C | T | 15 | a0001c0002t0004g0004 a0001c0002t0004g0015 a0001c0002t0021g0161 others(12): Show |
15 | HG01243.hp2 HG01358.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.4132-870C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60057008 | |||||||
| chr14:60057014 | G | A | 2 | a0007c0013t0018g0110 a0007c0013t0018g0111 |
2 | HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.4132-864G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60057014 | |||||||
| chr14:60057029 | G | C | 189 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(186): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.4132-849G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60057029 | |||||||
| chr14:60057164 | A | G | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4132-714A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60057164 | |||||||
| chr14:60057237 | A | C | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4132-641A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60057237 | |||||||
| chr14:60057274 | T | C | 1 | a0001c0002t0002g0136 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4132-604T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60057274 | |||||||
| chr14:60057569 | T | G | 190 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.4132-309T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60057569 | |||||||
| chr14:60057653 | G | GA | 224 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(221): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.4132-209dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60057653 | ||||||
| chr14:60057653 | G | GAA | 27 | a0001c0001t0011g0021 a0001c0001t0011g0078 a0001c0001t0011g0079 others(24): Show |
28 | HG02559.hp2 HG02922.hp2 HG03139.hp2 others(25): Show |
intron_variant | MODIFIER | c.4132-210_4132-209d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60057653 | ||||||
| chr14:60057771 | G | C | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4132-107G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60057771 | |||||||
| chr14:60057796 | C | T | 3 | a0001c0002t0002g0143 a0001c0002t0002g0144 a0001c0002t0002g0152 |
3 | HG02615.hp1 NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4132-82C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60057796 | |||||||
| chr14:60058032 | C | CAAAT | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4276+12_4276+13ins others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | INFO_REALIGN_3_PRIME | chr14 | 60058032 | ||||||
| chr14:60058037 | T | G | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4276+15T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60058037 | |||||||
| chr14:60058063 | A | C | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4276+41A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60058063 | |||||||
| chr14:60058080 | T | G | 1 | a0001c0001t0001g0223 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.4276+58T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60058080 | |||||||
| chr14:60058234 | C | A | 2 | a0006c0010t0018g0166 a0006c0010t0021g0033 |
2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.4276+212C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60058234 | |||||||
| chr14:60058338 | G | A | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4276+316G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60058338 | |||||||
| chr14:60058506 | G | A | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.4276+484G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60058506 | |||||||
| chr14:60058611 | A | C | 15 | a0001c0002t0004g0004 a0001c0002t0004g0015 a0001c0002t0021g0161 others(12): Show |
15 | HG01243.hp2 HG01358.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.4276+589A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60058611 | |||||||
| chr14:60058790 | TA | T | 14 | a0001c0001t0008g0006 a0001c0001t0008g0007 a0001c0001t0008g0009 others(11): Show |
14 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.4276+776delA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | INFO_REALIGN_3_PRIME | chr14 | 60058790 | ||||||
| chr14:60058872 | A | G | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4276+850A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60058872 | |||||||
| chr14:60058897 | A | G | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.4276+875A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60058897 | |||||||
| chr14:60059029 | A | G | 166 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.4276+1007A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60059029 | |||||||
| chr14:60059153 | T | C | 81 | a0001c0001t0001g0027 a0001c0001t0001g0045 a0001c0001t0001g0061 others(78): Show |
81 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.4276+1131T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60059153 | |||||||
| chr14:60059245 | T | C | 1 | a0001c0002t0007g0266 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.4276+1223T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60059245 | |||||||
| chr14:60059282 | C | T | 1 | a0001c0002t0004g0310 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4276+1260C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60059282 | |||||||
| chr14:60059534 | G | A | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4276+1512G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60059534 | |||||||
| chr14:60059609 | G | A | 1 | a0001c0002t0002g0005 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4276+1587G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60059609 | |||||||
| chr14:60059613 | G | A | 1 | a0002c0003t0005g0188 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.4276+1591G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60059613 | |||||||
| chr14:60059620 | A | G | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4276+1598A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60059620 | |||||||
| chr14:60059638 | A | T | 48 | a0001c0001t0001g0044 a0001c0001t0001g0058 a0001c0001t0001g0069 others(45): Show |
48 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.4276+1616A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60059638 | |||||||
| chr14:60059773 | C | T | 200 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(197): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.4276+1751C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60059773 | |||||||
| chr14:60060016 | T | C | 1 | a0001c0002t0002g0131 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4276+1994T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60060016 | |||||||
| chr14:60060274 | T | C | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4277-1737T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60060274 | |||||||
| chr14:60060463 | G | A | 42 | a0001c0002t0004g0153 a0001c0002t0004g0214 a0001c0002t0004g0265 others(39): Show |
43 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.4277-1548G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60060463 | |||||||
| chr14:60060609 | C | T | 7 | a0001c0005t0013g0151 a0001c0005t0013g0171 a0001c0005t0013g0172 others(4): Show |
7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.4277-1402C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60060609 | |||||||
| chr14:60060762 | T | TTAGA | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4277-1246_4277-124 others(8): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | INFO_REALIGN_3_PRIME | chr14 | 60060762 | ||||||
| chr14:60061194 | A | G | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.4277-817A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60061194 | |||||||
| chr14:60061265 | A | T | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4277-746A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60061265 | |||||||
| chr14:60061321 | G | A | 257 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(254): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.4277-690G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60061321 | |||||||
| chr14:60061404 | G | A | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.4277-607G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60061404 | |||||||
| chr14:60061444 | A | G | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4277-567A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60061444 | |||||||
| chr14:60061469 | A | T | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.4277-542A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60061469 | |||||||
| chr14:60061523 | T | C | 1 | a0001c0001t0003g0037 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.4277-488T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60061523 | |||||||
| chr14:60061699 | C | A | 168 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.4277-312C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60061699 | |||||||
| chr14:60061730 | A | T | 1 | a0001c0002t0002g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4277-281A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60061730 | |||||||
| chr14:60061770 | A | G | 5 | a0001c0005t0013g0151 a0001c0005t0013g0179 a0001c0005t0013g0180 others(2): Show |
5 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.4277-241A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60061770 | |||||||
| chr14:60061772 | C | T | 167 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.4277-239C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60061772 | |||||||
| chr14:60061790 | A | G | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4277-221A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60061790 | |||||||
| chr14:60061909 | C | A | 258 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(255): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.4277-102C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60061909 | |||||||
| chr14:60062255 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4445+76A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 32/32 | chr14 | 60062255 | |||||||
| chr14:60062310 | A | G | 42 | a0001c0002t0004g0153 a0001c0002t0004g0214 a0001c0002t0004g0265 others(39): Show |
43 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.4445+131A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 32/32 | chr14 | 60062310 | |||||||
| chr14:60062577 | C | T | 39 | a0001c0002t0004g0265 a0001c0002t0004g0268 a0001c0002t0004g0271 others(36): Show |
40 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(37): Show |
intron_variant | MODIFIER | c.4445+398C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 32/32 | chr14 | 60062577 | |||||||
| chr14:60062749 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4445+570A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 32/32 | chr14 | 60062749 | |||||||
| chr14:60062824 | A | G | 23 | a0002c0003t0005g0001 a0002c0003t0005g0185 a0002c0003t0005g0186 others(20): Show |
24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4446-499A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 32/32 | chr14 | 60062824 | |||||||
| chr14:60062894 | A | AT | 192 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0044 others(189): Show |
193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.4446-415dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 32/32 | INFO_REALIGN_3_PRIME | chr14 | 60062894 | ||||||
| chr14:60063231 | G | C | 10 | a0001c0004t0009g0209 a0001c0004t0009g0210 a0001c0004t0009g0302 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.4446-92G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 32/32 | chr14 | 60063231 | |||||||
| chr14:60063269 | C | A | 1 | a0007c0013t0018g0111 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4446-54C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 32/32 | chr14 | 60063269 |