Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 206338 |
| ensemblid | ENSG00000172901.21 |
| hgncid | 26904 |
| symbol | LVRN |
| name | laeverin |
| refseq_nuc | NM_173800.5 |
| refseq_prot | NP_776161.3 |
| ensembl_nuc | ENST00000357872.9 |
| ensembl_prot | ENSP00000350541.4 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 115962475 |
| end | 116027606 |
| strand | + |
| ver | v1.2 |
| region | chr5:115962475-116027606 |
| region5000 | chr5:115957475-116032606 |
| regionname0 | LVRN_chr5_115962475_116027606 |
| regionname5000 | LVRN_chr5_115957475_116032606 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 990 | 243 | 51 | 46 | 110 | 10 | 25 | 85 | LVRN_chr5_115957475_116032606 | LVRN | MGPPS others(985): Show |
chr5 | 115957475 | 116032606 |
| a0002 | 1/0 | 990 | 69 | 1 | 17 | 38 | 1 | 11 | 31 | LVRN_chr5_115957475_116032606 | LVRN | MGPPS others(985): Show |
chr5 | 115957475 | 116032606 |
| a0003 | 0/0 | 990 | 35 | 11 | 4 | 18 | 0 | 2 | 16 | LVRN_chr5_115957475_116032606 | LVRN | MGPPS others(985): Show |
chr5 | 115957475 | 116032606 |
| a0004 | 0/0 | 990 | 23 | 14 | 1 | 5 | 0 | 3 | 5 | LVRN_chr5_115957475_116032606 | LVRN | MGPPS others(985): Show |
chr5 | 115957475 | 116032606 |
| a0005 | 0/0 | 990 | 12 | 5 | 0 | 7 | 0 | 0 | 5 | LVRN_chr5_115957475_116032606 | LVRN | MGPPS others(985): Show |
chr5 | 115957475 | 116032606 |
| a0006 | 0/0 | 990 | 8 | 0 | 4 | 0 | 1 | 3 | 0 | LVRN_chr5_115957475_116032606 | LVRN | MGPPS others(985): Show |
chr5 | 115957475 | 116032606 |
| a0007 | 0/0 | 990 | 8 | 0 | 0 | 8 | 0 | 0 | 2 | LVRN_chr5_115957475_116032606 | LVRN | MGPPS others(985): Show |
chr5 | 115957475 | 116032606 |
| a0008 | 0/0 | 990 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | LVRN_chr5_115957475_116032606 | LVRN | MGPPS others(985): Show |
chr5 | 115957475 | 116032606 |
| a0009 | 0/0 | 759 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | MGPPS others(754): Show |
chr5 | 115957475 | 116032606 |
| a0010 | 0/0 | 990 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | MGPPS others(985): Show |
chr5 | 115957475 | 116032606 |
| a0011 | 0/0 | 990 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | LVRN_chr5_115957475_116032606 | LVRN | MGPPS others(985): Show |
chr5 | 115957475 | 116032606 |
| a0012 | 0/0 | 990 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | MGPPS others(985): Show |
chr5 | 115957475 | 116032606 |
| a0013 | 0/0 | 990 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | MGPPS others(985): Show |
chr5 | 115957475 | 116032606 |
| a0014 | 0/0 | 990 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | MGPPS others(985): Show |
chr5 | 115957475 | 116032606 |
| a0015 | 0/0 | 990 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | MGPPS others(985): Show |
chr5 | 115957475 | 116032606 |
| a0016 | 0/0 | 990 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | MGPPS others(985): Show |
chr5 | 115957475 | 116032606 |
| a0017 | 0/0 | 990 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LVRN_chr5_115957475_116032606 | LVRN | MGPPS others(985): Show |
chr5 | 115957475 | 116032606 |
| a0018 | 0/0 | 990 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | MGPPS others(985): Show |
chr5 | 115957475 | 116032606 |
| a0019 | 0/0 | 990 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | MGPPS others(985): Show |
chr5 | 115957475 | 116032606 |
| a0020 | 0/0 | 990 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LVRN_chr5_115957475_116032606 | LVRN | MGPPS others(985): Show |
chr5 | 115957475 | 116032606 |
| a0021 | 0/0 | 990 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | MGPPS others(985): Show |
chr5 | 115957475 | 116032606 |
| a0022 | 0/0 | 990 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | MGPPS others(985): Show |
chr5 | 115957475 | 116032606 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2970 | 109 | 10 | 25 | 52 | 4 | 17 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0001c0002 | 0/0 | 2970 | 86 | 18 | 17 | 39 | 6 | 6 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0001c0004 | 0/0 | 2970 | 39 | 16 | 4 | 17 | 0 | 2 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0001c0014 | 0/0 | 2970 | 2 | 2 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0001c0015 | 0/0 | 2970 | 2 | 2 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0001c0017 | 0/0 | 2970 | 2 | 1 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0001c0025 | 0/0 | 2970 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0001c0026 | 0/0 | 2970 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0001c0036 | 0/0 | 2970 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0002c0003 | 1/0 | 2970 | 67 | 1 | 17 | 37 | 1 | 10 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0002c0021 | 0/0 | 2970 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0002c0037 | 0/0 | 2970 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0003c0005 | 0/0 | 2970 | 25 | 11 | 4 | 9 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0003c0008 | 0/0 | 2970 | 10 | 0 | 0 | 9 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0004c0007 | 0/0 | 2970 | 11 | 6 | 1 | 3 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0004c0011 | 0/0 | 2970 | 6 | 3 | 0 | 2 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0004c0012 | 0/0 | 2970 | 5 | 5 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0004c0028 | 0/0 | 2970 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0005c0006 | 0/0 | 2970 | 11 | 4 | 0 | 7 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0005c0034 | 0/0 | 2970 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0006c0009 | 0/0 | 2970 | 8 | 0 | 4 | 0 | 1 | 3 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0007c0010 | 0/0 | 2970 | 7 | 0 | 0 | 7 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0007c0022 | 0/0 | 2970 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0008c0013 | 0/0 | 2970 | 3 | 0 | 0 | 3 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0009c0016 | 0/0 | 2970 | 2 | 2 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0010c0024 | 0/0 | 2970 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0010c0032 | 0/0 | 2970 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0011c0018 | 0/0 | 2970 | 2 | 0 | 0 | 2 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0012c0035 | 0/0 | 2970 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0013c0027 | 0/0 | 2970 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0014c0030 | 0/0 | 2970 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0015c0019 | 0/0 | 2970 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0016c0039 | 0/0 | 2970 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0017c0029 | 0/0 | 2970 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0018c0020 | 0/0 | 2970 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0019c0038 | 0/0 | 2970 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0020c0033 | 0/0 | 2970 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0021c0023 | 0/0 | 2970 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 | ||
| a0022c0031 | 0/0 | 2970 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | ATGGG others(2965): Show |
chr5 | 115957475 | 116032606 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4604 | 64 | 2 | 18 | 33 | 2 | 8 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0001c0001t0002 | 0/0 | 4604 | 35 | 7 | 7 | 15 | 1 | 5 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0001c0001t0004 | 0/0 | 4604 | 9 | 0 | 0 | 4 | 1 | 4 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0001c0001t0018 | 0/0 | 4604 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0001c0002t0001 | 0/0 | 4604 | 32 | 6 | 3 | 21 | 1 | 1 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0001c0002t0002 | 0/0 | 4604 | 32 | 5 | 10 | 11 | 4 | 2 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0001c0002t0004 | 0/0 | 4604 | 9 | 0 | 2 | 4 | 0 | 3 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0001c0002t0007 | 0/0 | 4604 | 7 | 6 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0001c0002t0009 | 0/0 | 4604 | 3 | 0 | 0 | 3 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0001c0002t0012 | 0/0 | 4604 | 2 | 0 | 1 | 0 | 1 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0001c0002t0013 | 0/0 | 4604 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0001c0004t0001 | 0/0 | 4604 | 27 | 11 | 2 | 13 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0001c0004t0002 | 0/0 | 4604 | 6 | 2 | 2 | 1 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0001c0004t0004 | 0/0 | 4604 | 4 | 2 | 0 | 2 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0001c0004t0008 | 0/0 | 4604 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0001c0004t0016 | 0/0 | 4604 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0001c0014t0001 | 0/0 | 4604 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0001c0014t0004 | 0/0 | 4604 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0001c0015t0015 | 0/0 | 4604 | 2 | 2 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | GGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0001c0017t0001 | 0/0 | 4604 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0001c0017t0004 | 0/0 | 4604 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0001c0025t0001 | 0/0 | 4604 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0001c0026t0001 | 0/0 | 4604 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0001c0036t0004 | 0/0 | 4604 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0002c0003t0003 | 0/0 | 4604 | 34 | 1 | 8 | 21 | 1 | 3 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0002c0003t0005 | 1/0 | 4604 | 13 | 0 | 5 | 2 | 0 | 5 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0002c0003t0006 | 0/0 | 4604 | 16 | 0 | 1 | 13 | 0 | 2 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0002c0003t0014 | 0/0 | 4604 | 2 | 0 | 2 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0002c0003t0019 | 0/0 | 4604 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0002c0003t0021 | 0/0 | 4604 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0002c0021t0005 | 0/0 | 4604 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0002c0037t0001 | 0/0 | 4604 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0003c0005t0003 | 0/0 | 4604 | 16 | 7 | 3 | 6 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0003c0005t0005 | 0/0 | 4604 | 8 | 4 | 1 | 3 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0003c0005t0006 | 0/0 | 4604 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0003c0008t0003 | 0/0 | 4604 | 2 | 0 | 0 | 2 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0003c0008t0005 | 0/0 | 4604 | 5 | 0 | 0 | 5 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0003c0008t0006 | 0/0 | 4604 | 3 | 0 | 0 | 2 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0004c0007t0001 | 0/0 | 4604 | 4 | 1 | 1 | 2 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0004c0007t0002 | 0/0 | 4604 | 6 | 5 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0004c0007t0004 | 0/0 | 4604 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0004c0011t0001 | 0/0 | 4604 | 3 | 1 | 0 | 2 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0004c0011t0002 | 0/0 | 4604 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0004c0011t0008 | 0/0 | 4604 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0004c0011t0017 | 0/0 | 4604 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0004c0012t0002 | 0/0 | 4604 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0004c0012t0008 | 0/0 | 4604 | 3 | 3 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0004c0012t0013 | 0/0 | 4604 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0004c0028t0002 | 0/0 | 4604 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0005c0006t0004 | 0/0 | 4604 | 8 | 1 | 0 | 7 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0005c0006t0010 | 0/0 | 4604 | 3 | 3 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0005c0034t0004 | 0/0 | 4604 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0006c0009t0002 | 0/0 | 4604 | 6 | 0 | 4 | 0 | 1 | 1 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0006c0009t0011 | 0/0 | 4604 | 2 | 0 | 0 | 0 | 0 | 2 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0007c0010t0001 | 0/0 | 4604 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0007c0010t0002 | 0/0 | 4604 | 6 | 0 | 0 | 6 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0007c0022t0002 | 0/0 | 4604 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0008c0013t0003 | 0/0 | 4604 | 3 | 0 | 0 | 3 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0009c0016t0002 | 0/0 | 4604 | 2 | 2 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0010c0024t0001 | 0/0 | 4604 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0010c0032t0001 | 0/0 | 4604 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0011c0018t0001 | 0/0 | 4604 | 2 | 0 | 0 | 2 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0012c0035t0002 | 0/0 | 4604 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0013c0027t0004 | 0/0 | 4604 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0014c0030t0007 | 0/0 | 4604 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0015c0019t0020 | 0/0 | 4604 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0016c0039t0001 | 0/0 | 4604 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0017c0029t0004 | 0/0 | 4604 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0018c0020t0005 | 0/0 | 4604 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0019c0038t0001 | 0/0 | 4604 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0020c0033t0001 | 0/0 | 4604 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0021c0023t0002 | 0/0 | 4604 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| a0022c0031t0004 | 0/0 | 4604 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | AGTCC others(4599): Show |
chr5 | 115957475 | 116032606 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0208 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0004g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0001t0018g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0001g0043 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0002g0004 | 0/0 | 5 | 0 | 2 | 2 | 1 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0002g0006 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0004g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0004g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0004g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0004g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0007g0011 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0007g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0007g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0007g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0007g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0009g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0009g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0009g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0012g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0012g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0002t0013g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0002g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0008g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0004t0016g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0014t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0014t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0015t0015g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0015t0015g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0017t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0017t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0025t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0026t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0001c0036t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0003g0001 | 0/0 | 8 | 0 | 3 | 5 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0003g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0003g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0003g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0005g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0005g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0005g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0005g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0005g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0005g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0005g0075 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0005g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0005g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0006g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0006g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0006g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0006g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0006g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0006g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0006g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0006g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0006g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0006g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0006g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0006g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0014g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0019g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0003t0021g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0021t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0002c0037t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0005t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0005t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0005t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0005t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0005t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0005t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0005t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0005t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0005t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0005t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0005t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0005t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0005t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0005t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0005t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0005t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0005t0005g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0005t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0005t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0005t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0005t0005g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0005t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0005t0005g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0005t0006g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0008t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0008t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0008t0005g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0008t0005g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0008t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0008t0005g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0008t0006g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0008t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0003c0008t0006g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0004c0007t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0004c0007t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0004c0007t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0004c0007t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0004c0007t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0004c0007t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0004c0007t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0004c0007t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0004c0007t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0004c0007t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0004c0011t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0004c0011t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0004c0011t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0004c0011t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0004c0011t0008g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0004c0011t0017g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0004c0012t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0004c0012t0008g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0004c0012t0008g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0004c0012t0013g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0004c0028t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0005c0006t0004g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0005c0006t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0005c0006t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0005c0006t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0005c0006t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0005c0006t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0005c0006t0010g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0005c0006t0010g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0005c0006t0010g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0005c0034t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0006c0009t0002g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0006c0009t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0006c0009t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0006c0009t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0006c0009t0011g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0007c0010t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0007c0010t0002g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0007c0010t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0007c0010t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0007c0022t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0008c0013t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0008c0013t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0009c0016t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0009c0016t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0010c0024t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0010c0032t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0011c0018t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0012c0035t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0013c0027t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0014c0030t0007g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0015c0019t0020g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0016c0039t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0017c0029t0004g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0018c0020t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0019c0038t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0020c0033t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0021c0023t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| a0022c0031t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0315 | EUR | GBR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00099 | hp2 | a0006 | c0009 | t0002 | g0135 | EUR | GBR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00140 | hp1 | a0001 | c0002 | t0012 | g0317 | EUR | GBR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0127 | EUR | GBR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0004 | EUR | FIN | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00280 | hp2 | a0002 | c0003 | t0003 | g0074 | EUR | FIN | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00408 | hp2 | a0007 | c0010 | t0001 | g0029 | EAS | CHS | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | CHS | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00544 | hp1 | a0001 | c0004 | t0001 | g0304 | EAS | CHS | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00544 | hp2 | a0002 | c0003 | t0019 | g0108 | EAS | CHS | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00558 | hp1 | a0001 | c0004 | t0016 | g0256 | EAS | CHS | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00558 | hp2 | a0001 | c0004 | t0001 | g0257 | EAS | CHS | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | CHS | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | CHS | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00609 | hp1 | a0001 | c0004 | t0001 | g0301 | EAS | CHS | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00609 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | CHS | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | CHS | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00639 | hp2 | a0002 | c0003 | t0005 | g0016 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00642 | hp1 | a0002 | c0003 | t0003 | g0087 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00642 | hp2 | a0001 | c0004 | t0001 | g0291 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00673 | hp1 | a0002 | c0003 | t0006 | g0092 | EAS | CHS | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00733 | hp2 | a0002 | c0003 | t0005 | g0093 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0227 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0331 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0326 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00741 | hp1 | a0001 | c0002 | t0012 | g0318 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG00741 | hp2 | a0001 | c0002 | t0007 | g0011 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0252 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01070 | hp1 | a0002 | c0003 | t0003 | g0018 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0324 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01071 | hp2 | a0002 | c0003 | t0003 | g0018 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01081 | hp1 | a0012 | c0035 | t0002 | g0329 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01081 | hp2 | a0002 | c0003 | t0003 | g0085 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0332 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01167 | hp2 | a0001 | c0002 | t0004 | g0041 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01168 | hp1 | a0002 | c0003 | t0014 | g0017 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01168 | hp2 | a0003 | c0005 | t0003 | g0053 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01169 | hp1 | a0002 | c0003 | t0014 | g0017 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01169 | hp2 | a0001 | c0002 | t0004 | g0041 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01175 | hp2 | a0004 | c0007 | t0001 | g0224 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0272 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01192 | hp2 | a0002 | c0003 | t0005 | g0073 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01243 | hp1 | a0001 | c0004 | t0002 | g0042 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01243 | hp2 | a0013 | c0027 | t0004 | g0280 | AMR | PUR | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01255 | hp1 | a0006 | c0009 | t0002 | g0026 | AMR | CLM | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01255 | hp2 | a0002 | c0003 | t0005 | g0089 | AMR | CLM | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | CLM | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0320 | AMR | CLM | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01346 | hp2 | a0002 | c0003 | t0005 | g0016 | AMR | CLM | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01358 | hp1 | a0006 | c0009 | t0002 | g0173 | AMR | CLM | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0325 | AMR | CLM | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01361 | hp1 | a0006 | c0009 | t0002 | g0005 | AMR | CLM | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01361 | hp2 | a0003 | c0005 | t0003 | g0088 | AMR | CLM | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01496 | hp1 | a0003 | c0005 | t0005 | g0113 | AMR | CLM | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0043 | AMR | CLM | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0322 | EUR | IBS | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | IBS | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0043 | AFR | ACB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01884 | hp2 | a0001 | c0004 | t0001 | g0289 | AFR | ACB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0336 | AFR | ACB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01891 | hp2 | a0003 | c0005 | t0003 | g0056 | AFR | ACB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01934 | hp1 | a0002 | c0003 | t0003 | g0001 | AMR | PEL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01943 | hp1 | a0003 | c0005 | t0003 | g0097 | AMR | PEL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01952 | hp1 | a0002 | c0003 | t0003 | g0001 | AMR | PEL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01952 | hp2 | a0001 | c0004 | t0001 | g0300 | AMR | PEL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01975 | hp1 | a0002 | c0003 | t0003 | g0100 | AMR | PEL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PEL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0330 | AMR | PEL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | PEL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG01993 | hp2 | a0002 | c0003 | t0003 | g0001 | AMR | PEL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02004 | hp2 | a0002 | c0003 | t0006 | g0096 | AMR | PEL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | KHV | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02027 | hp1 | a0007 | c0010 | t0002 | g0160 | EAS | KHV | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02027 | hp2 | a0002 | c0003 | t0006 | g0064 | EAS | KHV | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02040 | hp1 | a0001 | c0004 | t0001 | g0299 | EAS | KHV | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02040 | hp2 | a0001 | c0002 | t0004 | g0264 | EAS | KHV | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02055 | hp1 | a0014 | c0030 | t0007 | g0313 | AFR | ACB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | ACB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02056 | hp1 | a0003 | c0008 | t0006 | g0086 | EAS | KHV | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02056 | hp2 | a0007 | c0010 | t0002 | g0003 | EAS | KHV | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0251 | EAS | KHV | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | KHV | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02074 | hp1 | a0007 | c0022 | t0002 | g0003 | EAS | KHV | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02074 | hp2 | a0005 | c0006 | t0004 | g0310 | EAS | KHV | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02129 | hp1 | a0003 | c0005 | t0005 | g0109 | EAS | KHV | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | KHV | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0180 | EAS | KHV | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02132 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | KHV | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02135 | hp1 | a0001 | c0004 | t0001 | g0298 | EAS | KHV | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02145 | hp1 | a0003 | c0005 | t0003 | g0049 | AFR | ACB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PEL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02165 | hp1 | a0007 | c0010 | t0002 | g0146 | EAS | CDX | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02165 | hp2 | a0002 | c0003 | t0003 | g0078 | EAS | CDX | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02257 | hp1 | a0001 | c0025 | t0001 | g0232 | AFR | ACB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02257 | hp2 | a0002 | c0003 | t0003 | g0090 | AFR | ACB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02258 | hp1 | a0001 | c0004 | t0001 | g0038 | AFR | ACB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02258 | hp2 | a0001 | c0001 | t0018 | g0198 | AFR | ACB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02273 | hp1 | a0002 | c0003 | t0021 | g0098 | AMR | PEL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | ACB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02280 | hp2 | a0005 | c0006 | t0004 | g0290 | AFR | ACB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02293 | hp2 | a0001 | c0004 | t0002 | g0303 | AMR | PEL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02300 | hp2 | a0006 | c0009 | t0002 | g0026 | AMR | PEL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02451 | hp1 | a0001 | c0004 | t0001 | g0234 | AFR | ACB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02451 | hp2 | a0001 | c0036 | t0004 | g0196 | AFR | ACB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02523 | hp1 | a0005 | c0006 | t0004 | g0308 | EAS | KHV | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02572 | hp1 | a0001 | c0002 | t0013 | g0335 | AFR | GWD | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02572 | hp2 | a0003 | c0005 | t0005 | g0055 | AFR | GWD | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02602 | hp1 | a0002 | c0003 | t0005 | g0068 | SAS | PJL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02615 | hp1 | a0004 | c0012 | t0013 | g0192 | AFR | GWD | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02622 | hp1 | a0001 | c0014 | t0004 | g0314 | AFR | GWD | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02622 | hp2 | a0001 | c0002 | t0007 | g0011 | AFR | GWD | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02630 | hp1 | a0005 | c0006 | t0010 | g0247 | AFR | GWD | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02630 | hp2 | a0004 | c0012 | t0008 | g0032 | AFR | GWD | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02647 | hp1 | a0004 | c0007 | t0002 | g0034 | AFR | GWD | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02647 | hp2 | a0005 | c0034 | t0004 | g0199 | AFR | GWD | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02683 | hp1 | a0017 | c0029 | t0004 | g0273 | SAS | PJL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02683 | hp2 | a0002 | c0003 | t0005 | g0071 | SAS | PJL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02717 | hp1 | a0001 | c0004 | t0008 | g0246 | AFR | GWD | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02717 | hp2 | a0001 | c0004 | t0001 | g0237 | AFR | GWD | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0222 | SAS | PJL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02735 | hp2 | a0003 | c0005 | t0006 | g0052 | SAS | PJL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0323 | SAS | PJL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02809 | hp1 | a0004 | c0011 | t0001 | g0279 | AFR | GWD | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02809 | hp2 | a0001 | c0015 | t0015 | g0343 | AFR | GWD | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02818 | hp1 | a0004 | c0011 | t0017 | g0240 | AFR | GWD | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02818 | hp2 | a0004 | c0012 | t0008 | g0032 | AFR | GWD | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02886 | hp1 | a0001 | c0004 | t0002 | g0131 | AFR | GWD | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02886 | hp2 | a0004 | c0007 | t0001 | g0229 | AFR | GWD | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02895 | hp1 | a0001 | c0017 | t0001 | g0200 | AFR | GWD | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02895 | hp2 | a0003 | c0005 | t0005 | g0013 | AFR | GWD | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0044 | AFR | GWD | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02896 | hp2 | a0004 | c0012 | t0002 | g0223 | AFR | GWD | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0044 | AFR | GWD | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02897 | hp2 | a0003 | c0005 | t0005 | g0013 | AFR | GWD | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0235 | AFR | ESN | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02922 | hp2 | a0001 | c0004 | t0001 | g0038 | AFR | ESN | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02965 | hp1 | a0001 | c0004 | t0004 | g0294 | AFR | ESN | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0278 | AFR | ESN | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02970 | hp1 | a0009 | c0016 | t0002 | g0243 | AFR | ESN | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02970 | hp2 | a0001 | c0004 | t0004 | g0293 | AFR | ESN | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02976 | hp1 | a0001 | c0002 | t0007 | g0011 | AFR | ESN | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02976 | hp2 | a0001 | c0004 | t0001 | g0037 | AFR | ESN | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03017 | hp1 | a0001 | c0002 | t0004 | g0268 | SAS | PJL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03041 | hp1 | a0001 | c0002 | t0007 | g0341 | AFR | GWD | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03041 | hp2 | a0003 | c0005 | t0003 | g0048 | AFR | GWD | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03098 | hp1 | a0001 | c0002 | t0007 | g0338 | AFR | MSL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03098 | hp2 | a0001 | c0002 | t0007 | g0342 | AFR | MSL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | ESN | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03130 | hp2 | a0004 | c0011 | t0008 | g0281 | AFR | ESN | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03139 | hp1 | a0018 | c0020 | t0005 | g0091 | AFR | ESN | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03139 | hp2 | a0001 | c0004 | t0002 | g0042 | AFR | ESN | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03209 | hp1 | a0001 | c0004 | t0001 | g0339 | AFR | MSL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03225 | hp1 | a0001 | c0002 | t0007 | g0239 | AFR | MSL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03225 | hp2 | a0003 | c0005 | t0003 | g0050 | AFR | MSL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0327 | SAS | PJL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03239 | hp2 | a0004 | c0011 | t0002 | g0271 | SAS | PJL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03486 | hp1 | a0001 | c0004 | t0001 | g0248 | AFR | MSL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03486 | hp2 | a0019 | c0038 | t0001 | g0220 | AFR | MSL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03490 | hp1 | a0001 | c0002 | t0004 | g0284 | SAS | PJL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03490 | hp2 | a0006 | c0009 | t0011 | g0005 | SAS | PJL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0202 | SAS | PJL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0033 | SAS | PJL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03492 | hp1 | a0006 | c0009 | t0011 | g0005 | SAS | PJL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0033 | SAS | PJL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03516 | hp1 | a0005 | c0006 | t0010 | g0245 | AFR | ESN | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03516 | hp2 | a0004 | c0007 | t0002 | g0216 | AFR | ESN | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0288 | AFR | GWD | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03540 | hp2 | a0004 | c0012 | t0008 | g0193 | AFR | GWD | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03579 | hp1 | a0010 | c0032 | t0001 | g0241 | AFR | MSL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03579 | hp2 | a0004 | c0007 | t0002 | g0034 | AFR | MSL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03654 | hp1 | a0001 | c0004 | t0001 | g0230 | SAS | PJL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03654 | hp2 | a0004 | c0028 | t0002 | g0065 | SAS | PJL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03669 | hp1 | a0003 | c0008 | t0006 | g0062 | SAS | PJL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03669 | hp2 | a0006 | c0009 | t0002 | g0005 | SAS | PJL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | STU | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03688 | hp2 | a0002 | c0003 | t0005 | g0012 | SAS | STU | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03704 | hp1 | a0020 | c0033 | t0001 | g0218 | SAS | PJL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03710 | hp2 | a0002 | c0003 | t0006 | g0076 | SAS | PJL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | BEB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0346 | SAS | BEB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03834 | hp1 | a0002 | c0003 | t0003 | g0067 | SAS | BEB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03834 | hp2 | a0002 | c0003 | t0005 | g0072 | SAS | BEB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03927 | hp1 | a0001 | c0002 | t0004 | g0249 | SAS | BEB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03927 | hp2 | a0004 | c0007 | t0002 | g0225 | SAS | BEB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03942 | hp1 | a0002 | c0003 | t0006 | g0083 | SAS | BEB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0345 | SAS | BEB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0205 | SAS | STU | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0255 | SAS | STU | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG04184 | hp1 | a0002 | c0037 | t0001 | g0081 | SAS | BEB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG04184 | hp2 | a0002 | c0003 | t0003 | g0020 | SAS | BEB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | STU | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG04199 | hp2 | a0002 | c0003 | t0005 | g0012 | SAS | STU | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG04228 | hp1 | a0002 | c0003 | t0003 | g0084 | SAS | STU | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG04228 | hp2 | a0001 | c0004 | t0002 | g0274 | SAS | STU | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18522 | hp1 | a0001 | c0015 | t0015 | g0344 | AFR | YRI | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | YRI | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18612 | hp1 | a0002 | c0003 | t0006 | g0001 | EAS | CHB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0328 | EAS | CHB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18747 | hp2 | a0007 | c0010 | t0002 | g0003 | EAS | CHB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18906 | hp1 | a0003 | c0005 | t0003 | g0057 | AFR | YRI | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18906 | hp2 | a0004 | c0007 | t0002 | g0215 | AFR | YRI | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18939 | hp2 | a0001 | c0002 | t0004 | g0259 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18940 | hp2 | a0004 | c0011 | t0001 | g0040 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18941 | hp1 | a0001 | c0004 | t0001 | g0296 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18941 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18942 | hp1 | a0002 | c0003 | t0006 | g0121 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18942 | hp2 | a0002 | c0003 | t0003 | g0015 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18943 | hp2 | a0007 | c0010 | t0002 | g0003 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18945 | hp2 | a0001 | c0002 | t0009 | g0267 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18946 | hp1 | a0005 | c0006 | t0004 | g0010 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18950 | hp1 | a0002 | c0003 | t0006 | g0082 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18950 | hp2 | a0011 | c0018 | t0001 | g0025 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18951 | hp1 | a0001 | c0004 | t0004 | g0306 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18952 | hp2 | a0003 | c0005 | t0005 | g0110 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18953 | hp1 | a0002 | c0003 | t0005 | g0107 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18954 | hp1 | a0003 | c0008 | t0006 | g0120 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0261 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18956 | hp1 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18957 | hp1 | a0001 | c0004 | t0001 | g0311 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18959 | hp2 | a0003 | c0005 | t0003 | g0104 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18961 | hp2 | a0002 | c0003 | t0006 | g0069 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18963 | hp1 | a0008 | c0013 | t0003 | g0001 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18964 | hp1 | a0002 | c0003 | t0003 | g0061 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18964 | hp2 | a0007 | c0010 | t0002 | g0003 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18966 | hp1 | a0002 | c0003 | t0003 | g0103 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18966 | hp2 | a0001 | c0026 | t0001 | g0212 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18967 | hp2 | a0002 | c0003 | t0003 | g0066 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18968 | hp1 | a0002 | c0003 | t0006 | g0019 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0282 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18972 | hp1 | a0001 | c0004 | t0001 | g0297 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18973 | hp1 | a0002 | c0003 | t0003 | g0007 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18973 | hp2 | a0001 | c0004 | t0002 | g0307 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18978 | hp2 | a0002 | c0003 | t0003 | g0007 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18979 | hp1 | a0002 | c0003 | t0003 | g0077 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18981 | hp2 | a0003 | c0005 | t0003 | g0094 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18983 | hp1 | a0002 | c0003 | t0003 | g0015 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0265 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18984 | hp1 | a0003 | c0005 | t0003 | g0114 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18984 | hp2 | a0004 | c0007 | t0004 | g0176 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18985 | hp2 | a0002 | c0003 | t0003 | g0079 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18989 | hp2 | a0001 | c0004 | t0001 | g0292 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18991 | hp1 | a0005 | c0006 | t0004 | g0010 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18993 | hp2 | a0001 | c0002 | t0004 | g0254 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18994 | hp1 | a0005 | c0006 | t0004 | g0312 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18994 | hp2 | a0011 | c0018 | t0001 | g0025 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18995 | hp1 | a0002 | c0003 | t0006 | g0014 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0136 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18998 | hp1 | a0003 | c0008 | t0005 | g0021 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18999 | hp1 | a0003 | c0008 | t0005 | g0347 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18999 | hp2 | a0003 | c0005 | t0003 | g0111 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19000 | hp1 | a0002 | c0003 | t0006 | g0014 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0286 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19001 | hp2 | a0021 | c0023 | t0002 | g0166 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19002 | hp1 | a0003 | c0008 | t0005 | g0021 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19004 | hp1 | a0002 | c0003 | t0006 | g0022 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19006 | hp2 | a0001 | c0002 | t0009 | g0277 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19009 | hp1 | a0002 | c0003 | t0003 | g0007 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19010 | hp2 | a0008 | c0013 | t0003 | g0001 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19011 | hp1 | a0001 | c0004 | t0001 | g0305 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0233 | AFR | LWK | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19030 | hp2 | a0001 | c0004 | t0001 | g0236 | AFR | LWK | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | LWK | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | LWK | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19055 | hp1 | a0003 | c0005 | t0003 | g0112 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19056 | hp2 | a0002 | c0003 | t0003 | g0020 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19058 | hp1 | a0001 | c0004 | t0001 | g0302 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19058 | hp2 | a0003 | c0005 | t0003 | g0119 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0168 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19063 | hp2 | a0002 | c0003 | t0003 | g0101 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0334 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19065 | hp1 | a0003 | c0008 | t0003 | g0117 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19065 | hp2 | a0004 | c0007 | t0001 | g0156 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19068 | hp1 | a0002 | c0003 | t0003 | g0099 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0316 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19070 | hp2 | a0003 | c0008 | t0005 | g0118 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19072 | hp1 | a0003 | c0008 | t0003 | g0116 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19072 | hp2 | a0002 | c0003 | t0006 | g0019 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19074 | hp2 | a0002 | c0003 | t0005 | g0102 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19076 | hp1 | a0001 | c0004 | t0004 | g0231 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19076 | hp2 | a0002 | c0003 | t0003 | g0063 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19077 | hp2 | a0003 | c0008 | t0005 | g0115 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19078 | hp1 | a0001 | c0017 | t0004 | g0132 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19078 | hp2 | a0002 | c0003 | t0003 | g0105 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19079 | hp2 | a0001 | c0002 | t0009 | g0276 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19080 | hp1 | a0004 | c0011 | t0001 | g0266 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19082 | hp1 | a0001 | c0004 | t0001 | g0036 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0333 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19083 | hp1 | a0001 | c0004 | t0001 | g0036 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19083 | hp2 | a0001 | c0002 | t0004 | g0287 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19085 | hp1 | a0003 | c0005 | t0005 | g0070 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19086 | hp2 | a0002 | c0021 | t0005 | g0080 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19087 | hp2 | a0005 | c0006 | t0004 | g0010 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19088 | hp1 | a0005 | c0006 | t0004 | g0309 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19088 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19090 | hp1 | a0002 | c0003 | t0006 | g0022 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19091 | hp2 | a0008 | c0013 | t0003 | g0106 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19240 | hp1 | a0003 | c0005 | t0005 | g0054 | AFR | YRI | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA19240 | hp2 | a0009 | c0016 | t0002 | g0244 | AFR | YRI | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA20129 | hp1 | a0010 | c0024 | t0001 | g0295 | AFR | ASW | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0337 | AFR | ASW | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0253 | EUR | TSI | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0149 | EUR | TSI | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | TSI | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0319 | EUR | TSI | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02486 | hp1 | a0001 | c0014 | t0001 | g0060 | AFR | ACB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02486 | hp2 | a0003 | c0005 | t0003 | g0058 | AFR | ACB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02559 | hp1 | a0015 | c0019 | t0020 | g0059 | AFR | ACB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG02559 | hp2 | a0016 | c0039 | t0001 | g0221 | AFR | ACB | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0238 | AFR | MSL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG03471 | hp2 | a0004 | c0007 | t0002 | g0228 | AFR | MSL | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG06807 | hp1 | a0003 | c0005 | t0003 | g0051 | AFR | USA | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0321 | AFR | USA | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18955 | hp1 | a0004 | c0007 | t0001 | g0164 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA18955 | hp2 | a0002 | c0003 | t0006 | g0095 | EAS | JPT | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0285 | AFR | USA | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA20300 | hp2 | a0001 | c0004 | t0001 | g0037 | AFR | USA | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA21309 | hp1 | a0022 | c0031 | t0004 | g0122 | AFR | LWK | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| NA21309 | hp2 | a0005 | c0006 | t0010 | g0242 | AFR | LWK | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0208 | REF | REF | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| homoSapiens | grch38p0 | a0002 | c0003 | t0005 | g0075 | REF | REF | LVRN_chr5_115957475_116032606 | LVRN | chr5 | 115957475 | 116032606 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:115962720 | G | T | 2 | a0016 a0019 |
2 | HG02559.hp2 HG03486.hp2 |
missense_variant | MODERATE | c.103G>T | p.Ala35Ser | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/20 | 246/4604 | 103/2973 | 35/990 | chr5 | 115962720 | |||
| chr5:115962778 | T | C | 17 | a0001 a0004 a0005 others(14): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
missense_variant | MODERATE | c.161T>C | p.Leu54Ser | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/20 | 304/4604 | 161/2973 | 54/990 | chr5 | 115962778 | |||
| chr5:115962806 | G | C | 2 | a0007 a0021 |
9 | HG00408.hp2 HG02027.hp1 HG02056.hp2 others(6): Show |
missense_variant | MODERATE | c.189G>C | p.Arg63Ser | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/20 | 332/4604 | 189/2973 | 63/990 | chr5 | 115962806 | |||
| chr5:115963029 | A | T | 1 | a0012 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.412A>T | p.Thr138Ser | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/20 | 555/4604 | 412/2973 | 138/990 | chr5 | 115963029 | |||
| chr5:115987816 | C | T | 1 | a0010 | 2 | HG03579.hp1 NA20129.hp1 |
missense_variant | MODERATE | c.982C>T | p.Arg328Cys | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/20 | 1125/4604 | 982/2973 | 328/990 | chr5 | 115987816 | |||
| chr5:115987860 | C | G | 1 | a0022 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1026C>G | p.Asp342Glu | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/20 | 1169/4604 | 1026/2973 | 342/990 | chr5 | 115987860 | |||
| chr5:115987871 | A | C | 2 | a0014 a0016 |
2 | HG02055.hp1 HG02559.hp2 |
missense_variant | MODERATE | c.1037A>C | p.Asn346Thr | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/20 | 1180/4604 | 1037/2973 | 346/990 | chr5 | 115987871 | |||
| chr5:115993832 | A | G | 1 | a0017 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.1352A>G | p.Tyr451Cys | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/20 | 1495/4604 | 1352/2973 | 451/990 | chr5 | 115993832 | |||
| chr5:115999780 | A | C | 1 | a0008 | 3 | NA18963.hp1 NA19010.hp2 NA19091.hp2 |
missense_variant | MODERATE | c.1393A>C | p.Asn465His | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 7/20 | 1536/4604 | 1393/2973 | 465/990 | chr5 | 115999780 | |||
| chr5:116001125 | G | C | 1 | a0020 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.1706G>C | p.Ser569Thr | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 10/20 | 1849/4604 | 1706/2973 | 569/990 | chr5 | 116001125 | |||
| chr5:116001196 | T | C | 1 | a0022 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1777T>C | p.Phe593Leu | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 10/20 | 1920/4604 | 1777/2973 | 593/990 | chr5 | 116001196 | |||
| chr5:116003261 | G | T | 1 | a0006 | 8 | HG00099.hp2 HG01255.hp1 HG01358.hp1 others(5): Show |
missense_variant | MODERATE | c.1918G>T | p.Val640Phe | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/20 | 2061/4604 | 1918/2973 | 640/990 | chr5 | 116003261 | |||
| chr5:116005941 | G | C | 15 | a0001 a0003 a0005 others(12): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
missense_variant | MODERATE | c.2067G>C | p.Leu689Phe | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/20 | 2210/4604 | 2067/2973 | 689/990 | chr5 | 116005941 | |||
| chr5:116005952 | C | T | 1 | a0018 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.2078C>T | p.Ala693Val | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/20 | 2221/4604 | 2078/2973 | 693/990 | chr5 | 116005952 | |||
| chr5:116012405 | G | A | 1 | a0009 | 2 | HG02970.hp1 NA19240.hp2 |
stop_gained | HIGH | c.2279G>A | p.Trp760* | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/20 | 2422/4604 | 2279/2973 | 760/990 | chr5 | 116012405 | |||
| chr5:116012422 | A | G | 1 | a0011 | 2 | NA18950.hp2 NA18994.hp2 |
missense_variant | MODERATE | c.2296A>G | p.Ile766Val | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/20 | 2439/4604 | 2296/2973 | 766/990 | chr5 | 116012422 | |||
| chr5:116022440 | G | A | 3 | a0005 a0013 a0015 |
14 | HG01243.hp2 HG02074.hp2 HG02280.hp2 others(11): Show |
missense_variant | MODERATE | c.2806G>A | p.Val936Ile | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/20 | 2949/4604 | 2806/2973 | 936/990 | chr5 | 116022440 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:115962681 | C | T | 32 | a0001c0001 a0001c0002 a0001c0004 others(29): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
synonymous_variant | LOW | c.64C>T | p.Leu22Leu | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/20 | 207/4604 | 64/2973 | 22/990 | chr5 | 115962681 | |||
| chr5:115962821 | A | G | 32 | a0001c0001 a0001c0002 a0001c0004 others(29): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
synonymous_variant | LOW | c.204A>G | p.Pro68Pro | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/20 | 347/4604 | 204/2973 | 68/990 | chr5 | 115962821 | |||
| chr5:115963007 | C | T | 1 | a0001c0036 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.390C>T | p.Arg130Arg | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/20 | 533/4604 | 390/2973 | 130/990 | chr5 | 115963007 | |||
| chr5:115963151 | C | T | 1 | a0002c0021 | 1 | NA19086.hp2 | synonymous_variant | LOW | c.534C>T | p.Asp178Asp | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/20 | 677/4604 | 534/2973 | 178/990 | chr5 | 115963151 | |||
| chr5:115963280 | C | T | 14 | a0001c0001 a0001c0017 a0001c0036 others(11): Show |
150 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(147): Show |
synonymous_variant | LOW | c.663C>T | p.Phe221Phe | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/20 | 806/4604 | 663/2973 | 221/990 | chr5 | 115963280 | |||
| chr5:115983299 | G | A | 3 | a0001c0014 a0010c0024 a0015c0019 |
4 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
synonymous_variant | LOW | c.708G>A | p.Ala236Ala | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 2/20 | 851/4604 | 708/2973 | 236/990 | chr5 | 115983299 | |||
| chr5:115993782 | C | A | 1 | a0007c0022 | 1 | HG02074.hp1 | synonymous_variant | LOW | c.1302C>A | p.Ile434Ile | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/20 | 1445/4604 | 1302/2973 | 434/990 | chr5 | 115993782 | |||
| chr5:116000438 | G | A | 2 | a0001c0015 a0001c0025 |
3 | HG02257.hp1 HG02809.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.1521G>A | p.Ala507Ala | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 8/20 | 1664/4604 | 1521/2973 | 507/990 | chr5 | 116000438 | |||
| chr5:116001165 | T | C | 10 | a0001c0002 a0001c0017 a0001c0026 others(7): Show |
115 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(112): Show |
synonymous_variant | LOW | c.1746T>C | p.Asn582Asn | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 10/20 | 1889/4604 | 1746/2973 | 582/990 | chr5 | 116001165 | |||
| chr5:116003365 | T | C | 1 | a0001c0026 | 1 | NA18966.hp2 | synonymous_variant | LOW | c.2022T>C | p.Leu674Leu | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/20 | 2165/4604 | 2022/2973 | 674/990 | chr5 | 116003365 | |||
| chr5:116005914 | G | T | 27 | a0001c0001 a0001c0002 a0001c0004 others(24): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
splice_region_variant&synonymous_variant | LOW | c.2040G>T | p.Ala680Ala | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/20 | 2183/4604 | 2040/2973 | 680/990 | chr5 | 116005914 | |||
| chr5:116005953 | C | G | 1 | a0001c0025 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.2079C>G | p.Ala693Ala | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/20 | 2222/4604 | 2079/2973 | 693/990 | chr5 | 116005953 | |||
| chr5:116015315 | G | A | 1 | a0001c0015 | 2 | HG02809.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.2514G>A | p.Glu838Glu | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 17/20 | 2657/4604 | 2514/2973 | 838/990 | chr5 | 116015315 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:115962475 | A | G | 1 | a0001c0015t0015 | 2 | HG02809.hp2 NA18522.hp1 |
5_prime_UTR_variant | MODIFIER | c.-143A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/20 | 143 | chr5 | 115962475 | ||||||
| chr5:115962506 | C | A | 2 | a0001c0002t0009 a0001c0004t0016 |
4 | HG00558.hp1 NA18945.hp2 NA19006.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-112C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/20 | 112 | chr5 | 115962506 | ||||||
| chr5:115962518 | G | A | 1 | a0004c0011t0017 | 1 | HG02818.hp1 | 5_prime_UTR_variant | MODIFIER | c.-100G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/20 | 100 | chr5 | 115962518 | ||||||
| chr5:115962535 | G | C | 57 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(54): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
5_prime_UTR_variant | MODIFIER | c.-83G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/20 | 83 | chr5 | 115962535 | ||||||
| chr5:115962578 | T | A | 1 | a0002c0003t0014 | 2 | HG01168.hp1 HG01169.hp1 |
5_prime_UTR_variant | MODIFIER | c.-40T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/20 | 40 | chr5 | 115962578 | ||||||
| chr5:116026260 | C | T | 2 | a0001c0002t0013 a0004c0012t0013 |
2 | HG02572.hp1 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*142C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 20/20 | 142 | chr5 | 116026260 | ||||||
| chr5:116026265 | A | G | 1 | a0002c0003t0021 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*147A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 20/20 | 147 | chr5 | 116026265 | ||||||
| chr5:116026294 | A | T | 2 | a0005c0006t0010 a0015c0019t0020 |
4 | HG02559.hp1 HG02630.hp1 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*176A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 20/20 | 176 | chr5 | 116026294 | ||||||
| chr5:116026346 | A | G | 1 | a0001c0001t0018 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*228A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 20/20 | 228 | chr5 | 116026346 | ||||||
| chr5:116026347 | T | C | 1 | a0006c0009t0011 | 2 | HG03490.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*229T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 20/20 | 229 | chr5 | 116026347 | ||||||
| chr5:116026451 | A | G | 50 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0018 others(47): Show |
283 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*333A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 20/20 | 333 | chr5 | 116026451 | ||||||
| chr5:116026522 | T | C | 1 | a0001c0002t0012 | 2 | HG00140.hp1 HG00741.hp1 |
3_prime_UTR_variant | MODIFIER | c.*404T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 20/20 | 404 | chr5 | 116026522 | ||||||
| chr5:116026524 | A | G | 3 | a0001c0002t0007 a0004c0011t0017 a0014c0030t0007 |
9 | HG00741.hp2 HG02055.hp1 HG02622.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*406A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 20/20 | 406 | chr5 | 116026524 | ||||||
| chr5:116026663 | C | T | 2 | a0005c0006t0010 a0015c0019t0020 |
4 | HG02559.hp1 HG02630.hp1 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*545C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 20/20 | 545 | chr5 | 116026663 | ||||||
| chr5:116027088 | G | C | 3 | a0001c0004t0008 a0004c0011t0008 a0004c0012t0008 |
5 | HG02630.hp2 HG02717.hp1 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*970G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 20/20 | 970 | chr5 | 116027088 | ||||||
| chr5:116027275 | A | T | 1 | a0002c0003t0019 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1157A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 20/20 | 1157 | chr5 | 116027275 | ||||||
| chr5:116027461 | T | C | 2 | a0005c0006t0010 a0015c0019t0020 |
4 | HG02559.hp1 HG02630.hp1 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1343T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 20/20 | 1343 | chr5 | 116027461 | ||||||
| chr5:116027584 | T | G | 17 | a0001c0001t0004 a0001c0002t0004 a0001c0004t0004 others(14): Show |
61 | HG00673.hp1 HG01167.hp2 HG01169.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1466T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 20/20 | 1466 | chr5 | 116027584 | ||||||
| chr5:116027598 | G | T | 2 | a0005c0006t0010 a0015c0019t0020 |
4 | HG02559.hp1 HG02630.hp1 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1480G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 20/20 | 1480 | chr5 | 116027598 | ||||||
| chr5:116027601 | T | C | 2 | a0005c0006t0010 a0015c0019t0020 |
4 | HG02559.hp1 HG02630.hp1 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1483T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 20/20 | 1483 | chr5 | 116027601 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:115963370 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.695+58G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115963370 | |||||||
| chr5:115963374 | C | A | 1 | a0001c0001t0001g0046 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.695+62C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115963374 | |||||||
| chr5:115963387 | C | A | 1 | a0001c0002t0001g0047 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.695+75C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115963387 | |||||||
| chr5:115963408 | C | G | 1 | a0003c0008t0005g0347 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.695+96C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115963408 | |||||||
| chr5:115963645 | A | G | 262 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(259): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.695+333A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115963645 | |||||||
| chr5:115963711 | C | G | 2 | a0001c0001t0002g0345 a0001c0001t0002g0346 |
2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.695+399C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115963711 | |||||||
| chr5:115963767 | G | A | 1 | a0022c0031t0004g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.695+455G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115963767 | |||||||
| chr5:115963876 | C | T | 2 | a0001c0015t0015g0343 a0001c0015t0015g0344 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.695+564C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115963876 | |||||||
| chr5:115963947 | A | G | 1 | a0022c0031t0004g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.695+635A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115963947 | |||||||
| chr5:115964013 | T | C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0123 a0001c0001t0001g0124 |
4 | HG01109.hp1 HG01261.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.695+701T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115964013 | |||||||
| chr5:115964039 | A | G | 5 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0007g0011 others(2): Show |
9 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.695+727A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115964039 | |||||||
| chr5:115964071 | C | T | 1 | a0001c0001t0001g0340 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.695+759C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115964071 | |||||||
| chr5:115964129 | G | C | 3 | a0002c0003t0005g0012 a0003c0005t0003g0048 a0003c0005t0003g0049 |
4 | HG02145.hp1 HG03041.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.695+817G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115964129 | |||||||
| chr5:115964254 | C | T | 1 | a0022c0031t0004g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.695+942C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115964254 | |||||||
| chr5:115964263 | A | G | 5 | a0001c0002t0001g0336 a0001c0002t0001g0337 a0001c0002t0007g0338 others(2): Show |
5 | HG01891.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.695+951A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115964263 | |||||||
| chr5:115964361 | C | T | 139 | a0001c0002t0001g0009 a0001c0002t0001g0039 a0001c0002t0001g0040 others(136): Show |
161 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.695+1049C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115964361 | |||||||
| chr5:115964379 | T | C | 1 | a0001c0004t0004g0231 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.695+1067T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115964379 | |||||||
| chr5:115964425 | C | A | 5 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0002g0127 others(2): Show |
5 | HG00140.hp2 HG01106.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.695+1113C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115964425 | |||||||
| chr5:115964462 | G | A | 2 | a0001c0002t0002g0233 a0001c0025t0001g0232 |
2 | HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.695+1150G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115964462 | |||||||
| chr5:115964567 | A | G | 54 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0001g0315 others(51): Show |
64 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.695+1255A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115964567 | |||||||
| chr5:115964584 | C | T | 135 | a0001c0002t0001g0009 a0001c0002t0001g0039 a0001c0002t0001g0040 others(132): Show |
157 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.695+1272C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115964584 | |||||||
| chr5:115964599 | CT | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(147): Show |
176 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.695+1299delT | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 115964599 | ||||||
| chr5:115964660 | G | C | 14 | a0001c0001t0001g0130 a0002c0003t0005g0012 a0003c0005t0003g0048 others(11): Show |
16 | HG00438.hp2 HG01168.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.695+1348G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115964660 | |||||||
| chr5:115964673 | G | A | 1 | a0001c0004t0001g0292 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.695+1361G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115964673 | |||||||
| chr5:115964701 | T | G | 287 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(284): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.695+1389T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115964701 | |||||||
| chr5:115964781 | T | C | 1 | a0001c0004t0004g0231 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.695+1469T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115964781 | |||||||
| chr5:115964802 | A | G | 28 | a0001c0002t0001g0238 a0001c0002t0001g0315 a0001c0002t0001g0328 others(25): Show |
32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.695+1490A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115964802 | |||||||
| chr5:115964841 | G | A | 77 | a0001c0002t0001g0009 a0001c0002t0001g0039 a0001c0002t0001g0040 others(74): Show |
89 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.695+1529G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115964841 | |||||||
| chr5:115964872 | T | A | 1 | a0002c0003t0003g0061 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.695+1560T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115964872 | |||||||
| chr5:115964941 | G | T | 1 | a0003c0005t0005g0113 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.695+1629G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115964941 | |||||||
| chr5:115965003 | G | T | 68 | a0001c0002t0001g0009 a0001c0002t0001g0039 a0001c0002t0001g0040 others(65): Show |
80 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.695+1691G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115965003 | |||||||
| chr5:115965237 | T | C | 1 | a0001c0002t0001g0315 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.695+1925T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115965237 | |||||||
| chr5:115965294 | G | A | 212 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0024 others(209): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.695+1982G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115965294 | |||||||
| chr5:115965437 | T | C | 2 | a0001c0002t0001g0043 a0001c0002t0007g0011 |
5 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.695+2125T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115965437 | |||||||
| chr5:115965537 | G | A | 23 | a0001c0002t0001g0315 a0001c0002t0001g0328 a0001c0002t0002g0004 others(20): Show |
27 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.695+2225G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115965537 | |||||||
| chr5:115965599 | C | T | 1 | a0022c0031t0004g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.695+2287C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115965599 | |||||||
| chr5:115965687 | T | A | 123 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0024 others(120): Show |
149 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.695+2375T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115965687 | |||||||
| chr5:115965687 | T | C | 2 | a0002c0003t0005g0012 a0003c0005t0003g0048 |
3 | HG03041.hp2 HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.695+2375T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115965687 | |||||||
| chr5:115965810 | T | C | 2 | a0001c0004t0004g0293 a0001c0004t0004g0294 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.695+2498T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115965810 | |||||||
| chr5:115965871 | A | T | 1 | a0001c0002t0001g0044 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.695+2559A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115965871 | |||||||
| chr5:115966020 | T | C | 2 | a0001c0004t0004g0231 a0010c0024t0001g0295 |
2 | NA19076.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.695+2708T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115966020 | |||||||
| chr5:115966046 | C | G | 1 | a0001c0001t0001g0130 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.695+2734C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115966046 | |||||||
| chr5:115966087 | A | G | 1 | a0001c0001t0002g0227 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.695+2775A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115966087 | |||||||
| chr5:115966128 | A | C | 4 | a0001c0002t0002g0006 a0001c0002t0002g0285 a0001c0002t0002g0286 others(1): Show |
7 | HG02293.hp1 NA18943.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.695+2816A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115966128 | |||||||
| chr5:115966142 | G | A | 1 | a0014c0030t0007g0313 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.695+2830G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115966142 | |||||||
| chr5:115966262 | G | A | 2 | a0001c0001t0001g0024 a0001c0017t0004g0132 |
3 | HG00408.hp1 HG00673.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.695+2950G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115966262 | |||||||
| chr5:115966330 | T | C | 26 | a0001c0002t0001g0315 a0001c0002t0001g0328 a0001c0002t0002g0004 others(23): Show |
30 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(27): Show |
intron_variant | MODIFIER | c.695+3018T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115966330 | |||||||
| chr5:115966343 | T | C | 1 | a0014c0030t0007g0313 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.695+3031T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115966343 | |||||||
| chr5:115966364 | T | C | 1 | a0001c0002t0002g0316 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.695+3052T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115966364 | |||||||
| chr5:115966369 | A | C | 26 | a0001c0002t0001g0315 a0001c0002t0001g0328 a0001c0002t0002g0004 others(23): Show |
30 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(27): Show |
intron_variant | MODIFIER | c.695+3057A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115966369 | |||||||
| chr5:115966393 | G | T | 1 | a0001c0002t0004g0284 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.695+3081G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115966393 | |||||||
| chr5:115966437 | T | C | 1 | a0001c0002t0001g0238 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.695+3125T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115966437 | |||||||
| chr5:115966496 | T | C | 2 | a0001c0002t0012g0317 a0001c0002t0012g0318 |
2 | HG00140.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.695+3184T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115966496 | |||||||
| chr5:115966510 | G | A | 4 | a0004c0012t0008g0032 a0004c0012t0008g0193 a0004c0012t0013g0192 others(1): Show |
5 | HG02280.hp2 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.695+3198G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115966510 | |||||||
| chr5:115966514 | A | T | 1 | a0004c0007t0002g0228 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.695+3202A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115966514 | |||||||
| chr5:115966602 | C | T | 1 | a0001c0001t0002g0191 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.695+3290C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115966602 | |||||||
| chr5:115966748 | C | A | 73 | a0001c0002t0001g0009 a0001c0002t0001g0039 a0001c0002t0001g0040 others(70): Show |
84 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.695+3436C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115966748 | |||||||
| chr5:115966807 | C | A | 266 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(263): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.695+3495C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115966807 | |||||||
| chr5:115966909 | T | C | 1 | a0001c0001t0002g0133 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.695+3597T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115966909 | |||||||
| chr5:115966937 | A | G | 145 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(142): Show |
170 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.695+3625A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115966937 | |||||||
| chr5:115966954 | G | A | 2 | a0001c0004t0004g0293 a0001c0004t0004g0294 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.695+3642G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115966954 | |||||||
| chr5:115966963 | C | T | 73 | a0001c0002t0001g0009 a0001c0002t0001g0039 a0001c0002t0001g0040 others(70): Show |
84 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.695+3651C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115966963 | |||||||
| chr5:115967065 | C | A | 269 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(266): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.695+3753C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115967065 | |||||||
| chr5:115967075 | C | A | 4 | a0004c0012t0008g0032 a0004c0012t0008g0193 a0004c0012t0013g0192 others(1): Show |
5 | HG02280.hp2 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.695+3763C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115967075 | |||||||
| chr5:115967213 | C | G | 25 | a0001c0002t0001g0315 a0001c0002t0001g0328 a0001c0002t0002g0004 others(22): Show |
29 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(26): Show |
intron_variant | MODIFIER | c.695+3901C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115967213 | |||||||
| chr5:115967216 | A | C | 1 | a0010c0032t0001g0241 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.695+3904A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115967216 | |||||||
| chr5:115967244 | C | A | 1 | a0001c0001t0001g0194 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.695+3932C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115967244 | |||||||
| chr5:115967253 | T | C | 16 | a0001c0004t0001g0038 a0001c0004t0001g0248 a0001c0004t0004g0231 others(13): Show |
18 | HG02258.hp1 HG02280.hp2 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.695+3941T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115967253 | |||||||
| chr5:115967353 | T | A | 1 | a0010c0024t0001g0295 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.695+4041T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115967353 | |||||||
| chr5:115967444 | C | G | 1 | a0001c0001t0002g0129 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.695+4132C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115967444 | |||||||
| chr5:115967481 | T | C | 73 | a0001c0002t0001g0009 a0001c0002t0001g0039 a0001c0002t0001g0040 others(70): Show |
84 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.695+4169T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115967481 | |||||||
| chr5:115967665 | T | G | 1 | a0022c0031t0004g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.695+4353T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115967665 | |||||||
| chr5:115967696 | C | A | 267 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(264): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.695+4384C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115967696 | |||||||
| chr5:115967793 | A | T | 3 | a0001c0002t0002g0235 a0001c0004t0001g0236 a0001c0004t0001g0237 |
3 | HG02717.hp2 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.695+4481A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115967793 | |||||||
| chr5:115967991 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.695+4679G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115967991 | |||||||
| chr5:115968034 | G | A | 23 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0007g0011 others(20): Show |
29 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.695+4722G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115968034 | |||||||
| chr5:115968200 | C | G | 4 | a0003c0005t0003g0056 a0003c0005t0005g0013 a0003c0005t0005g0054 others(1): Show |
5 | HG01891.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.695+4888C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115968200 | |||||||
| chr5:115968207 | T | C | 26 | a0001c0002t0001g0315 a0001c0002t0001g0328 a0001c0002t0002g0004 others(23): Show |
30 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(27): Show |
intron_variant | MODIFIER | c.695+4895T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115968207 | |||||||
| chr5:115968220 | A | C | 2 | a0002c0003t0006g0022 a0002c0003t0006g0121 |
3 | NA18942.hp1 NA19004.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.695+4908A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115968220 | |||||||
| chr5:115968271 | AT | A | 267 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(264): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.695+4966delT | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 115968271 | ||||||
| chr5:115968310 | A | C | 1 | a0001c0004t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.695+4998A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115968310 | |||||||
| chr5:115968433 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.695+5121C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115968433 | |||||||
| chr5:115968437 | CT | C | 10 | a0001c0002t0001g0044 a0001c0002t0007g0341 a0001c0002t0007g0342 others(7): Show |
13 | HG01175.hp2 HG02027.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.695+5142delT | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 115968437 | ||||||
| chr5:115968437 | CTT | C | 258 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(255): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.695+5141_695+5142d others(4): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 115968437 | ||||||
| chr5:115968462 | G | A | 2 | a0001c0004t0001g0288 a0001c0004t0001g0289 |
2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.695+5150G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115968462 | |||||||
| chr5:115968555 | C | T | 61 | a0001c0002t0001g0009 a0001c0002t0001g0039 a0001c0002t0001g0040 others(58): Show |
72 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.695+5243C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115968555 | |||||||
| chr5:115968645 | C | G | 2 | a0001c0004t0004g0231 a0010c0024t0001g0295 |
2 | NA19076.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.695+5333C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115968645 | |||||||
| chr5:115968697 | T | A | 73 | a0001c0002t0001g0009 a0001c0002t0001g0039 a0001c0002t0001g0040 others(70): Show |
84 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.695+5385T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115968697 | |||||||
| chr5:115968711 | G | A | 1 | a0014c0030t0007g0313 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.695+5399G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115968711 | |||||||
| chr5:115968743 | T | C | 1 | a0001c0004t0001g0296 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.695+5431T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115968743 | |||||||
| chr5:115968824 | T | A | 143 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(140): Show |
168 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(165): Show |
intron_variant | MODIFIER | c.695+5512T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115968824 | |||||||
| chr5:115968844 | G | T | 1 | a0001c0002t0001g0238 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.695+5532G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115968844 | |||||||
| chr5:115968906 | G | C | 2 | a0001c0004t0004g0293 a0001c0004t0004g0294 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.695+5594G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115968906 | |||||||
| chr5:115968998 | A | G | 17 | a0002c0003t0003g0001 a0002c0003t0003g0099 a0002c0003t0003g0100 others(14): Show |
25 | HG00544.hp2 HG00609.hp2 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.695+5686A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115968998 | |||||||
| chr5:115969033 | T | C | 1 | a0001c0004t0004g0231 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.695+5721T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115969033 | |||||||
| chr5:115969076 | C | G | 1 | a0001c0002t0013g0335 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.695+5764C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115969076 | |||||||
| chr5:115969139 | C | T | 1 | a0001c0004t0001g0237 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.695+5827C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115969139 | |||||||
| chr5:115969161 | G | A | 99 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0024 others(96): Show |
119 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.695+5849G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115969161 | |||||||
| chr5:115969192 | T | G | 20 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0007g0011 others(17): Show |
25 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.695+5880T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115969192 | |||||||
| chr5:115969287 | A | G | 26 | a0001c0002t0001g0315 a0001c0002t0001g0328 a0001c0002t0002g0004 others(23): Show |
30 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(27): Show |
intron_variant | MODIFIER | c.695+5975A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115969287 | |||||||
| chr5:115969331 | T | G | 147 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(144): Show |
172 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(169): Show |
intron_variant | MODIFIER | c.695+6019T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115969331 | |||||||
| chr5:115969429 | C | A | 98 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0024 others(95): Show |
118 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.695+6117C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115969429 | |||||||
| chr5:115969497 | T | G | 8 | a0001c0004t0001g0038 a0001c0004t0001g0248 a0001c0004t0008g0246 others(5): Show |
9 | HG02258.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.695+6185T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115969497 | |||||||
| chr5:115969507 | G | A | 1 | a0003c0005t0005g0113 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.695+6195G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115969507 | |||||||
| chr5:115969536 | G | A | 1 | a0011c0018t0001g0025 | 2 | NA18950.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.695+6224G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115969536 | |||||||
| chr5:115969561 | G | C | 1 | a0004c0028t0002g0065 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.695+6249G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115969561 | |||||||
| chr5:115969647 | A | G | 1 | a0003c0008t0006g0062 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.695+6335A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115969647 | |||||||
| chr5:115969714 | C | T | 142 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(139): Show |
167 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(164): Show |
intron_variant | MODIFIER | c.695+6402C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115969714 | |||||||
| chr5:115969799 | C | CA | 183 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(180): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.695+6505dupA | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 115969799 | ||||||
| chr5:115969799 | C | CAA | 6 | a0001c0001t0001g0195 a0001c0001t0004g0136 a0001c0004t0001g0230 others(3): Show |
6 | HG02145.hp2 HG02970.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.695+6504_695+6505d others(4): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 115969799 | ||||||
| chr5:115969799 | CA | C | 7 | a0001c0002t0001g0238 a0001c0002t0001g0282 a0001c0002t0001g0283 others(4): Show |
8 | HG02615.hp1 HG02630.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.695+6505delA | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 115969799 | ||||||
| chr5:115969799 | CAA | C | 15 | a0001c0001t0001g0130 a0001c0001t0001g0226 a0001c0001t0002g0127 others(12): Show |
17 | HG00140.hp2 HG00438.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.695+6504_695+6505d others(4): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 115969799 | ||||||
| chr5:115969822 | T | C | 1 | a0001c0036t0004g0196 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.695+6510T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115969822 | |||||||
| chr5:115969834 | T | A | 1 | a0010c0024t0001g0295 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.695+6522T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115969834 | |||||||
| chr5:115969876 | C | T | 15 | a0001c0001t0001g0130 a0001c0001t0001g0226 a0001c0001t0002g0127 others(12): Show |
17 | HG00140.hp2 HG00438.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.695+6564C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115969876 | |||||||
| chr5:115969963 | C | T | 2 | a0002c0003t0005g0012 a0003c0005t0003g0048 |
3 | HG03041.hp2 HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.695+6651C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115969963 | |||||||
| chr5:115970016 | C | G | 14 | a0001c0001t0001g0130 a0001c0001t0001g0226 a0001c0001t0002g0127 others(11): Show |
16 | HG00140.hp2 HG00438.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.695+6704C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115970016 | |||||||
| chr5:115970022 | GT | G | 12 | a0001c0002t0001g0336 a0001c0002t0001g0337 a0001c0002t0002g0233 others(9): Show |
12 | HG01891.hp1 HG02257.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.695+6712delT | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 115970022 | ||||||
| chr5:115970029 | C | T | 26 | a0001c0002t0001g0315 a0001c0002t0001g0328 a0001c0002t0002g0004 others(23): Show |
30 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(27): Show |
intron_variant | MODIFIER | c.695+6717C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115970029 | |||||||
| chr5:115970107 | C | T | 16 | a0001c0001t0001g0130 a0001c0001t0001g0226 a0001c0001t0002g0127 others(13): Show |
18 | HG00140.hp2 HG00438.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.695+6795C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115970107 | |||||||
| chr5:115970141 | T | C | 15 | a0001c0001t0001g0130 a0001c0001t0001g0226 a0001c0001t0002g0127 others(12): Show |
17 | HG00140.hp2 HG00438.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.695+6829T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115970141 | |||||||
| chr5:115970269 | A | G | 143 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(140): Show |
168 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(165): Show |
intron_variant | MODIFIER | c.695+6957A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115970269 | |||||||
| chr5:115970335 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.695+7023C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115970335 | |||||||
| chr5:115970340 | A | G | 44 | a0001c0001t0001g0023 a0001c0001t0001g0123 a0001c0001t0001g0124 others(41): Show |
49 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.695+7028A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115970340 | |||||||
| chr5:115970343 | T | A | 1 | a0001c0002t0004g0249 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.695+7031T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115970343 | |||||||
| chr5:115970350 | T | C | 1 | a0001c0002t0001g0315 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.695+7038T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115970350 | |||||||
| chr5:115970384 | C | CT | 14 | a0001c0001t0001g0187 a0001c0001t0001g0194 a0001c0001t0002g0345 others(11): Show |
14 | HG00639.hp1 HG01943.hp1 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.695+7089dupT | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 115970384 | ||||||
| chr5:115970384 | C | CTTT | 16 | a0001c0001t0001g0130 a0001c0001t0001g0226 a0001c0001t0002g0127 others(13): Show |
18 | HG00140.hp2 HG00438.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.695+7087_695+7089d others(5): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 115970384 | ||||||
| chr5:115970384 | CT | C | 47 | a0001c0001t0001g0139 a0001c0001t0002g0137 a0001c0001t0002g0138 others(44): Show |
53 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(50): Show |
intron_variant | MODIFIER | c.695+7089delT | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 115970384 | ||||||
| chr5:115970424 | C | G | 20 | a0001c0001t0001g0139 a0001c0004t0001g0292 a0001c0004t0001g0296 others(17): Show |
22 | HG00544.hp1 HG00609.hp1 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.695+7112C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115970424 | |||||||
| chr5:115970529 | C | T | 265 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(262): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.695+7217C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115970529 | |||||||
| chr5:115970596 | G | A | 256 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(253): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.695+7284G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115970596 | |||||||
| chr5:115970596 | G | C | 5 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(2): Show |
5 | HG02135.hp2 NA18940.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.695+7284G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115970596 | |||||||
| chr5:115970632 | A | G | 281 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(278): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.695+7320A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115970632 | |||||||
| chr5:115970676 | C | T | 1 | a0001c0004t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.695+7364C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115970676 | |||||||
| chr5:115970699 | TTGTA | T | 142 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(139): Show |
167 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(164): Show |
intron_variant | MODIFIER | c.695+7393_695+7396d others(6): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 115970699 | ||||||
| chr5:115970744 | T | C | 1 | a0001c0001t0002g0140 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.695+7432T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115970744 | |||||||
| chr5:115970749 | A | G | 1 | a0001c0004t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.695+7437A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115970749 | |||||||
| chr5:115970752 | A | G | 1 | a0022c0031t0004g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.695+7440A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115970752 | |||||||
| chr5:115970804 | T | G | 1 | a0002c0003t0003g0100 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.695+7492T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115970804 | |||||||
| chr5:115970835 | T | G | 1 | a0001c0004t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.695+7523T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115970835 | |||||||
| chr5:115970979 | C | T | 1 | a0001c0002t0002g0233 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.695+7667C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115970979 | |||||||
| chr5:115971017 | C | A | 4 | a0004c0011t0008g0281 a0004c0012t0008g0032 a0004c0012t0008g0193 others(1): Show |
5 | HG02615.hp1 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.695+7705C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115971017 | |||||||
| chr5:115971019 | G | T | 1 | a0003c0008t0006g0062 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.695+7707G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115971019 | |||||||
| chr5:115971104 | T | A | 1 | a0001c0001t0004g0141 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.695+7792T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115971104 | |||||||
| chr5:115971215 | A | G | 1 | a0022c0031t0004g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.695+7903A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115971215 | |||||||
| chr5:115971284 | CT | C | 265 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(262): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.695+7975delT | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 115971284 | ||||||
| chr5:115971322 | G | A | 2 | a0001c0015t0015g0343 a0001c0015t0015g0344 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.695+8010G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115971322 | |||||||
| chr5:115971353 | A | C | 5 | a0001c0002t0001g0336 a0001c0002t0001g0337 a0001c0002t0007g0338 others(2): Show |
5 | HG01891.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.695+8041A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115971353 | |||||||
| chr5:115971366 | T | C | 2 | a0003c0005t0003g0050 a0003c0005t0003g0051 |
2 | HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.695+8054T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115971366 | |||||||
| chr5:115971392 | G | A | 265 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(262): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.695+8080G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115971392 | |||||||
| chr5:115971397 | A | G | 143 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(140): Show |
168 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(165): Show |
intron_variant | MODIFIER | c.695+8085A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115971397 | |||||||
| chr5:115971398 | A | G | 5 | a0001c0002t0001g0336 a0001c0002t0001g0337 a0001c0002t0007g0338 others(2): Show |
5 | HG01891.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.695+8086A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115971398 | |||||||
| chr5:115971569 | T | C | 143 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(140): Show |
168 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(165): Show |
intron_variant | MODIFIER | c.695+8257T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115971569 | |||||||
| chr5:115971583 | A | C | 4 | a0001c0002t0002g0006 a0001c0002t0002g0285 a0001c0002t0002g0286 others(1): Show |
7 | HG02293.hp1 NA18943.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.695+8271A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115971583 | |||||||
| chr5:115971595 | C | T | 96 | a0001c0002t0001g0009 a0001c0002t0001g0039 a0001c0002t0001g0040 others(93): Show |
113 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.695+8283C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115971595 | |||||||
| chr5:115971705 | G | A | 1 | a0001c0002t0001g0250 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.695+8393G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115971705 | |||||||
| chr5:115971898 | A | G | 5 | a0002c0003t0003g0063 a0002c0003t0006g0014 a0002c0003t0006g0064 others(2): Show |
6 | HG02027.hp2 NA18955.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.695+8586A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115971898 | |||||||
| chr5:115971958 | GTA | G | 261 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(258): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.695+8652_695+8653d others(4): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 115971958 | ||||||
| chr5:115971988 | T | C | 4 | a0001c0001t0001g0226 a0001c0001t0002g0127 a0001c0001t0002g0128 others(1): Show |
4 | HG00140.hp2 HG01175.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.695+8676T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115971988 | |||||||
| chr5:115972071 | A | G | 1 | a0003c0008t0006g0120 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.695+8759A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115972071 | |||||||
| chr5:115972129 | C | T | 240 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(237): Show |
282 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(279): Show |
intron_variant | MODIFIER | c.695+8817C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115972129 | |||||||
| chr5:115972158 | T | C | 1 | a0002c0003t0003g0101 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.695+8846T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115972158 | |||||||
| chr5:115972176 | T | C | 281 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(278): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.695+8864T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115972176 | |||||||
| chr5:115972177 | G | A | 5 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0007g0011 others(2): Show |
9 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.695+8865G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115972177 | |||||||
| chr5:115972470 | C | A | 2 | a0001c0002t0001g0039 a0001c0002t0001g0251 |
3 | HG02071.hp1 NA18990.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.695+9158C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115972470 | |||||||
| chr5:115972516 | A | T | 1 | a0014c0030t0007g0313 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.695+9204A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115972516 | |||||||
| chr5:115972700 | C | A | 1 | a0014c0030t0007g0313 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.695+9388C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115972700 | |||||||
| chr5:115972731 | G | T | 13 | a0001c0001t0001g0130 a0001c0001t0001g0226 a0001c0001t0002g0127 others(10): Show |
15 | HG00140.hp2 HG00438.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.695+9419G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115972731 | |||||||
| chr5:115972732 | G | T | 1 | a0003c0005t0003g0053 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.695+9420G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115972732 | |||||||
| chr5:115972738 | T | C | 144 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(141): Show |
169 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(166): Show |
intron_variant | MODIFIER | c.695+9426T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115972738 | |||||||
| chr5:115972842 | G | A | 8 | a0001c0004t0001g0038 a0001c0004t0001g0248 a0001c0004t0008g0246 others(5): Show |
9 | HG02258.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.695+9530G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115972842 | |||||||
| chr5:115972860 | A | T | 1 | a0013c0027t0004g0280 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.695+9548A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115972860 | |||||||
| chr5:115972905 | A | T | 1 | a0005c0006t0004g0290 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.695+9593A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115972905 | |||||||
| chr5:115973024 | G | A | 99 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0024 others(96): Show |
119 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.695+9712G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115973024 | |||||||
| chr5:115973086 | G | A | 22 | a0001c0002t0001g0315 a0001c0002t0001g0328 a0001c0002t0002g0004 others(19): Show |
26 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(23): Show |
intron_variant | MODIFIER | c.695+9774G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115973086 | |||||||
| chr5:115973208 | G | A | 1 | a0001c0001t0002g0142 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.695+9896G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115973208 | |||||||
| chr5:115973273 | T | C | 26 | a0001c0002t0001g0315 a0001c0002t0001g0328 a0001c0002t0002g0004 others(23): Show |
30 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(27): Show |
intron_variant | MODIFIER | c.695+9961T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115973273 | |||||||
| chr5:115973331 | C | T | 2 | a0001c0002t0002g0333 a0001c0002t0002g0334 |
2 | NA19064.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.696-9956C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115973331 | |||||||
| chr5:115973350 | G | T | 240 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(237): Show |
282 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(279): Show |
intron_variant | MODIFIER | c.696-9937G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115973350 | |||||||
| chr5:115973420 | T | A | 1 | a0003c0005t0005g0113 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.696-9867T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115973420 | |||||||
| chr5:115973525 | C | A | 239 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(236): Show |
281 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(278): Show |
intron_variant | MODIFIER | c.696-9762C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115973525 | |||||||
| chr5:115973582 | A | G | 4 | a0001c0002t0002g0006 a0001c0002t0002g0285 a0001c0002t0002g0286 others(1): Show |
7 | HG02293.hp1 NA18943.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.696-9705A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115973582 | |||||||
| chr5:115973671 | GT | G | 5 | a0001c0001t0002g0197 a0001c0001t0002g0227 a0001c0001t0018g0198 others(2): Show |
5 | HG00735.hp1 HG01106.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.696-9614delT | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 115973671 | ||||||
| chr5:115973687 | G | A | 2 | a0001c0004t0004g0231 a0010c0024t0001g0295 |
2 | NA19076.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.696-9600G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115973687 | |||||||
| chr5:115973816 | C | T | 19 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0007g0011 others(16): Show |
24 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.696-9471C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115973816 | |||||||
| chr5:115973900 | G | A | 44 | a0001c0001t0001g0023 a0001c0001t0001g0123 a0001c0001t0001g0124 others(41): Show |
49 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.696-9387G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115973900 | |||||||
| chr5:115973986 | A | G | 2 | a0003c0005t0003g0050 a0003c0005t0003g0051 |
2 | HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.696-9301A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115973986 | |||||||
| chr5:115974105 | T | C | 20 | a0001c0001t0001g0139 a0001c0004t0001g0292 a0001c0004t0001g0296 others(17): Show |
22 | HG00544.hp1 HG00609.hp1 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.696-9182T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115974105 | |||||||
| chr5:115974196 | T | C | 1 | a0022c0031t0004g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.696-9091T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115974196 | |||||||
| chr5:115974285 | C | T | 240 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(237): Show |
282 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(279): Show |
intron_variant | MODIFIER | c.696-9002C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115974285 | |||||||
| chr5:115974301 | C | G | 13 | a0001c0004t0001g0038 a0001c0004t0001g0248 a0001c0004t0004g0231 others(10): Show |
14 | HG02258.hp1 HG02280.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.696-8986C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115974301 | |||||||
| chr5:115974350 | C | A | 240 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(237): Show |
282 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(279): Show |
intron_variant | MODIFIER | c.696-8937C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115974350 | |||||||
| chr5:115974507 | G | T | 5 | a0001c0001t0002g0197 a0001c0001t0002g0227 a0001c0001t0018g0198 others(2): Show |
5 | HG00735.hp1 HG01106.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.696-8780G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115974507 | |||||||
| chr5:115974529 | C | T | 2 | a0001c0004t0002g0042 a0004c0011t0001g0279 |
3 | HG01243.hp1 HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.696-8758C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115974529 | |||||||
| chr5:115974584 | T | G | 1 | a0002c0003t0003g0067 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.696-8703T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115974584 | |||||||
| chr5:115974596 | C | G | 4 | a0001c0002t0002g0006 a0001c0002t0002g0285 a0001c0002t0002g0286 others(1): Show |
7 | HG02293.hp1 NA18943.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.696-8691C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115974596 | |||||||
| chr5:115974678 | A | C | 2 | a0016c0039t0001g0221 a0019c0038t0001g0220 |
2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.696-8609A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115974678 | |||||||
| chr5:115974722 | C | T | 5 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0007g0011 others(2): Show |
9 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.696-8565C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115974722 | |||||||
| chr5:115974760 | T | C | 5 | a0001c0001t0001g0143 a0001c0001t0001g0145 a0001c0001t0002g0144 others(2): Show |
6 | HG01167.hp1 HG01255.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.696-8527T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115974760 | |||||||
| chr5:115974780 | A | G | 2 | a0001c0002t0007g0239 a0004c0011t0017g0240 |
2 | HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.696-8507A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115974780 | |||||||
| chr5:115974869 | C | T | 1 | a0001c0001t0002g0219 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.696-8418C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115974869 | |||||||
| chr5:115975003 | G | T | 164 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(161): Show |
194 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(191): Show |
intron_variant | MODIFIER | c.696-8284G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115975003 | |||||||
| chr5:115975063 | C | T | 14 | a0001c0001t0001g0130 a0001c0001t0001g0226 a0001c0001t0002g0127 others(11): Show |
16 | HG00140.hp2 HG00438.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.696-8224C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115975063 | |||||||
| chr5:115975196 | C | T | 2 | a0001c0004t0004g0231 a0010c0024t0001g0295 |
2 | NA19076.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.696-8091C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115975196 | |||||||
| chr5:115975346 | A | G | 1 | a0001c0004t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.696-7941A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115975346 | |||||||
| chr5:115975408 | A | G | 2 | a0001c0001t0001g0217 a0020c0033t0001g0218 |
2 | HG03017.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.696-7879A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115975408 | |||||||
| chr5:115975580 | C | T | 1 | a0003c0005t0003g0053 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.696-7707C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115975580 | |||||||
| chr5:115975616 | A | T | 5 | a0001c0002t0001g0336 a0001c0002t0001g0337 a0001c0002t0007g0338 others(2): Show |
5 | HG01891.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.696-7671A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115975616 | |||||||
| chr5:115975619 | C | T | 240 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(237): Show |
282 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(279): Show |
intron_variant | MODIFIER | c.696-7668C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115975619 | |||||||
| chr5:115975627 | C | T | 3 | a0001c0002t0002g0235 a0001c0004t0001g0236 a0001c0004t0001g0237 |
3 | HG02717.hp2 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.696-7660C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115975627 | |||||||
| chr5:115975652 | C | T | 1 | a0004c0007t0001g0229 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.696-7635C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115975652 | |||||||
| chr5:115975665 | A | G | 20 | a0001c0001t0001g0139 a0001c0004t0001g0292 a0001c0004t0001g0296 others(17): Show |
22 | HG00544.hp1 HG00609.hp1 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.696-7622A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115975665 | |||||||
| chr5:115975832 | T | C | 5 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0007g0011 others(2): Show |
9 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.696-7455T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115975832 | |||||||
| chr5:115976018 | G | A | 14 | a0001c0001t0001g0130 a0001c0001t0001g0226 a0001c0001t0002g0127 others(11): Show |
16 | HG00140.hp2 HG00438.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.696-7269G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115976018 | |||||||
| chr5:115976018 | G | T | 8 | a0001c0004t0001g0038 a0001c0004t0001g0248 a0001c0004t0008g0246 others(5): Show |
9 | HG02258.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.696-7269G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115976018 | |||||||
| chr5:115976080 | C | T | 5 | a0001c0001t0002g0197 a0001c0001t0002g0227 a0001c0001t0018g0198 others(2): Show |
5 | HG00735.hp1 HG01106.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.696-7207C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115976080 | |||||||
| chr5:115976110 | C | T | 3 | a0001c0002t0002g0235 a0001c0004t0001g0236 a0001c0004t0001g0237 |
3 | HG02717.hp2 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.696-7177C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115976110 | |||||||
| chr5:115976156 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.696-7131C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115976156 | |||||||
| chr5:115976193 | G | T | 5 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0007g0011 others(2): Show |
9 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.696-7094G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115976193 | |||||||
| chr5:115976231 | G | A | 78 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0024 others(75): Show |
96 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.696-7056G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115976231 | |||||||
| chr5:115976237 | C | T | 19 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0007g0011 others(16): Show |
24 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.696-7050C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115976237 | |||||||
| chr5:115976383 | G | C | 1 | a0022c0031t0004g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.696-6904G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115976383 | |||||||
| chr5:115976515 | G | A | 1 | a0014c0030t0007g0313 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.696-6772G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115976515 | |||||||
| chr5:115976600 | A | G | 1 | a0016c0039t0001g0221 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.696-6687A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115976600 | |||||||
| chr5:115976602 | G | T | 1 | a0014c0030t0007g0313 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.696-6685G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115976602 | |||||||
| chr5:115976605 | A | G | 14 | a0001c0001t0001g0031 a0001c0001t0001g0046 a0001c0001t0001g0175 others(11): Show |
15 | HG01069.hp1 HG01071.hp1 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.696-6682A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115976605 | |||||||
| chr5:115976669 | C | T | 1 | a0005c0006t0004g0290 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.696-6618C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115976669 | |||||||
| chr5:115976721 | T | C | 1 | a0001c0001t0001g0340 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.696-6566T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115976721 | |||||||
| chr5:115976779 | A | G | 1 | a0001c0004t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.696-6508A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115976779 | |||||||
| chr5:115976787 | G | A | 2 | a0001c0004t0004g0293 a0001c0004t0004g0294 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.696-6500G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115976787 | |||||||
| chr5:115976796 | A | G | 1 | a0003c0005t0003g0119 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.696-6491A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115976796 | |||||||
| chr5:115976854 | G | T | 1 | a0003c0005t0003g0112 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.696-6433G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115976854 | |||||||
| chr5:115976855 | T | G | 1 | a0003c0005t0003g0112 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.696-6432T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115976855 | |||||||
| chr5:115976891 | T | A | 1 | a0003c0005t0005g0113 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.696-6396T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115976891 | |||||||
| chr5:115976974 | A | G | 284 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(281): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.696-6313A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115976974 | |||||||
| chr5:115977080 | G | T | 267 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(264): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.696-6207G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115977080 | |||||||
| chr5:115977085 | C | A | 28 | a0001c0001t0001g0023 a0001c0001t0001g0123 a0001c0001t0001g0124 others(25): Show |
31 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.696-6202C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115977085 | |||||||
| chr5:115977186 | G | A | 1 | a0001c0002t0002g0319 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.696-6101G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115977186 | |||||||
| chr5:115977251 | G | A | 19 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0007g0011 others(16): Show |
24 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.696-6036G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115977251 | |||||||
| chr5:115977511 | C | T | 162 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(159): Show |
192 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(189): Show |
intron_variant | MODIFIER | c.696-5776C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115977511 | |||||||
| chr5:115977533 | G | A | 5 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0007g0011 others(2): Show |
9 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.696-5754G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115977533 | |||||||
| chr5:115977614 | A | G | 1 | a0001c0002t0004g0287 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.696-5673A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115977614 | |||||||
| chr5:115977636 | T | C | 2 | a0001c0002t0001g0252 a0001c0002t0002g0253 |
2 | HG01069.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.696-5651T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115977636 | |||||||
| chr5:115977771 | C | A | 123 | a0001c0002t0001g0009 a0001c0002t0001g0039 a0001c0002t0001g0040 others(120): Show |
144 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.696-5516C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115977771 | |||||||
| chr5:115977773 | A | G | 19 | a0001c0001t0001g0139 a0001c0004t0001g0292 a0001c0004t0001g0296 others(16): Show |
21 | HG00544.hp1 HG00609.hp1 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.696-5514A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115977773 | |||||||
| chr5:115977773 | A | T | 1 | a0001c0001t0004g0141 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.696-5514A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115977773 | |||||||
| chr5:115977821 | G | A | 20 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0007g0011 others(17): Show |
25 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.696-5466G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115977821 | |||||||
| chr5:115977996 | A | T | 1 | a0002c0003t0005g0093 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.696-5291A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115977996 | |||||||
| chr5:115978202 | G | A | 14 | a0001c0001t0001g0130 a0001c0001t0001g0226 a0001c0001t0002g0127 others(11): Show |
16 | HG00140.hp2 HG00438.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.696-5085G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115978202 | |||||||
| chr5:115978424 | C | T | 236 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(233): Show |
273 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(270): Show |
intron_variant | MODIFIER | c.696-4863C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115978424 | |||||||
| chr5:115978507 | A | G | 1 | a0003c0005t0003g0053 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.696-4780A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115978507 | |||||||
| chr5:115978678 | A | G | 5 | a0002c0003t0006g0019 a0002c0003t0006g0092 a0002c0003t0006g0096 others(2): Show |
6 | HG00673.hp1 HG01943.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.696-4609A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115978678 | |||||||
| chr5:115978705 | G | A | 16 | a0001c0004t0001g0038 a0001c0004t0001g0248 a0001c0004t0004g0231 others(13): Show |
17 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.696-4582G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115978705 | |||||||
| chr5:115978755 | G | A | 1 | a0007c0010t0002g0146 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.696-4532G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115978755 | |||||||
| chr5:115978761 | A | G | 42 | a0001c0001t0001g0023 a0001c0001t0001g0123 a0001c0001t0001g0124 others(39): Show |
46 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.696-4526A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115978761 | |||||||
| chr5:115978802 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.696-4485C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115978802 | |||||||
| chr5:115978805 | G | A | 2 | a0001c0002t0002g0320 a0001c0002t0002g0321 |
2 | HG01257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.696-4482G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115978805 | |||||||
| chr5:115978851 | T | C | 1 | a0001c0014t0004g0314 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.696-4436T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115978851 | |||||||
| chr5:115978852 | C | G | 4 | a0001c0002t0002g0006 a0001c0002t0002g0285 a0001c0002t0002g0286 others(1): Show |
7 | HG02293.hp1 NA18943.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.696-4435C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115978852 | |||||||
| chr5:115978964 | C | T | 2 | a0001c0004t0001g0037 a0018c0020t0005g0091 |
3 | HG02976.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.696-4323C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115978964 | |||||||
| chr5:115979001 | T | C | 2 | a0001c0001t0001g0201 a0001c0017t0001g0200 |
2 | HG02895.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.696-4286T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115979001 | |||||||
| chr5:115979061 | C | T | 1 | a0006c0009t0002g0173 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.696-4226C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115979061 | |||||||
| chr5:115979267 | G | A | 1 | a0001c0002t0004g0254 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.696-4020G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115979267 | |||||||
| chr5:115979334 | C | T | 2 | a0001c0001t0001g0217 a0020c0033t0001g0218 |
2 | HG03017.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.696-3953C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115979334 | |||||||
| chr5:115979361 | C | G | 2 | a0002c0003t0003g0018 a0002c0003t0003g0090 |
3 | HG01070.hp1 HG01071.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.696-3926C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115979361 | |||||||
| chr5:115979431 | G | A | 157 | a0001c0001t0001g0023 a0001c0001t0001g0123 a0001c0001t0001g0124 others(154): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.696-3856G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115979431 | |||||||
| chr5:115979467 | T | C | 3 | a0001c0004t0001g0288 a0001c0004t0001g0289 a0001c0004t0001g0339 |
3 | HG01884.hp2 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.696-3820T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115979467 | |||||||
| chr5:115979515 | C | T | 2 | a0003c0005t0003g0057 a0003c0005t0003g0058 |
2 | HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.696-3772C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115979515 | |||||||
| chr5:115979699 | C | T | 3 | a0001c0004t0001g0288 a0001c0004t0001g0289 a0001c0004t0001g0339 |
3 | HG01884.hp2 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.696-3588C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115979699 | |||||||
| chr5:115979711 | A | G | 6 | a0001c0001t0002g0035 a0004c0007t0002g0034 a0004c0007t0002g0215 others(3): Show |
8 | HG02615.hp2 HG02647.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.696-3576A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115979711 | |||||||
| chr5:115979821 | A | T | 1 | a0022c0031t0004g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.696-3466A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115979821 | |||||||
| chr5:115979979 | A | G | 26 | a0001c0002t0001g0336 a0001c0002t0001g0337 a0001c0002t0002g0233 others(23): Show |
27 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(24): Show |
intron_variant | MODIFIER | c.696-3308A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115979979 | |||||||
| chr5:115980004 | C | T | 65 | a0001c0002t0001g0009 a0001c0002t0001g0039 a0001c0002t0001g0040 others(62): Show |
77 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.696-3283C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115980004 | |||||||
| chr5:115980022 | A | G | 5 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0007g0011 others(2): Show |
9 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.696-3265A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115980022 | |||||||
| chr5:115980040 | T | C | 3 | a0001c0002t0002g0235 a0001c0004t0001g0236 a0001c0004t0001g0237 |
3 | HG02717.hp2 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.696-3247T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115980040 | |||||||
| chr5:115980057 | A | G | 2 | a0005c0006t0004g0010 a0005c0006t0004g0312 |
4 | NA18946.hp1 NA18991.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.696-3230A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115980057 | |||||||
| chr5:115980059 | G | A | 26 | a0001c0002t0001g0336 a0001c0002t0001g0337 a0001c0002t0002g0233 others(23): Show |
27 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(24): Show |
intron_variant | MODIFIER | c.696-3228G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115980059 | |||||||
| chr5:115980068 | T | C | 4 | a0001c0004t0004g0231 a0001c0014t0004g0314 a0010c0024t0001g0295 others(1): Show |
4 | HG02559.hp1 HG02622.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.696-3219T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115980068 | |||||||
| chr5:115980122 | G | T | 1 | a0001c0002t0002g0278 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.696-3165G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115980122 | |||||||
| chr5:115980123 | C | A | 1 | a0002c0003t0005g0068 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.696-3164C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115980123 | |||||||
| chr5:115980172 | G | C | 2 | a0001c0002t0001g0252 a0001c0002t0002g0253 |
2 | HG01069.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.696-3115G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115980172 | |||||||
| chr5:115980188 | G | A | 2 | a0002c0003t0006g0069 a0003c0005t0005g0070 |
2 | NA18961.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.696-3099G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115980188 | |||||||
| chr5:115980247 | A | G | 32 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0001g0336 others(29): Show |
37 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.696-3040A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115980247 | |||||||
| chr5:115980270 | A | G | 2 | a0002c0003t0006g0022 a0002c0003t0006g0121 |
3 | NA18942.hp1 NA19004.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.696-3017A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115980270 | |||||||
| chr5:115980272 | G | A | 1 | a0001c0002t0002g0320 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.696-3015G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115980272 | |||||||
| chr5:115980351 | A | G | 1 | a0001c0004t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.696-2936A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115980351 | |||||||
| chr5:115980543 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.696-2744C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115980543 | |||||||
| chr5:115980641 | C | T | 1 | a0022c0031t0004g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.696-2646C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115980641 | |||||||
| chr5:115980664 | T | G | 2 | a0001c0004t0001g0297 a0001c0004t0001g0311 |
2 | NA18957.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.696-2623T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115980664 | |||||||
| chr5:115980694 | C | T | 1 | a0001c0002t0002g0321 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.696-2593C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115980694 | |||||||
| chr5:115980884 | T | G | 1 | a0001c0004t0001g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.696-2403T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115980884 | |||||||
| chr5:115980891 | A | G | 21 | a0001c0001t0001g0139 a0001c0004t0001g0230 a0001c0004t0001g0292 others(18): Show |
23 | HG00544.hp1 HG00609.hp1 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.696-2396A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115980891 | |||||||
| chr5:115980895 | A | G | 5 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0007g0011 others(2): Show |
9 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.696-2392A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115980895 | |||||||
| chr5:115981168 | T | C | 1 | a0001c0004t0001g0298 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.696-2119T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115981168 | |||||||
| chr5:115981350 | C | A | 1 | a0001c0004t0001g0299 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.696-1937C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115981350 | |||||||
| chr5:115981374 | C | T | 194 | a0001c0001t0001g0008 a0001c0001t0001g0045 a0001c0001t0001g0125 others(191): Show |
229 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(226): Show |
intron_variant | MODIFIER | c.696-1913C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115981374 | |||||||
| chr5:115981553 | A | C | 8 | a0001c0004t0001g0038 a0001c0004t0001g0248 a0001c0004t0008g0246 others(5): Show |
9 | HG02258.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.696-1734A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115981553 | |||||||
| chr5:115981632 | A | T | 42 | a0001c0001t0001g0023 a0001c0001t0001g0123 a0001c0001t0001g0124 others(39): Show |
46 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.696-1655A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115981632 | |||||||
| chr5:115981662 | C | A | 2 | a0001c0004t0002g0042 a0004c0011t0001g0279 |
3 | HG01243.hp1 HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.696-1625C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115981662 | |||||||
| chr5:115981750 | C | T | 1 | a0001c0001t0002g0213 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.696-1537C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115981750 | |||||||
| chr5:115981795 | T | C | 1 | a0001c0036t0004g0196 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.696-1492T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115981795 | |||||||
| chr5:115981895 | A | T | 1 | a0004c0011t0017g0240 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.696-1392A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115981895 | |||||||
| chr5:115981999 | G | A | 183 | a0001c0001t0001g0023 a0001c0001t0001g0123 a0001c0001t0001g0124 others(180): Show |
218 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(215): Show |
intron_variant | MODIFIER | c.696-1288G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115981999 | |||||||
| chr5:115982105 | A | T | 2 | a0001c0002t0001g0272 a0017c0029t0004g0273 |
2 | HG01192.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.696-1182A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115982105 | |||||||
| chr5:115982160 | T | C | 4 | a0001c0001t0001g0226 a0001c0001t0002g0127 a0001c0001t0002g0128 others(1): Show |
4 | HG00140.hp2 HG01175.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.696-1127T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115982160 | |||||||
| chr5:115982173 | G | A | 20 | a0001c0001t0001g0139 a0001c0004t0001g0292 a0001c0004t0001g0296 others(17): Show |
22 | HG00544.hp1 HG00609.hp1 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.696-1114G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115982173 | |||||||
| chr5:115982191 | G | A | 156 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(153): Show |
184 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.696-1096G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115982191 | |||||||
| chr5:115982198 | T | C | 143 | a0001c0001t0001g0139 a0001c0001t0002g0219 a0001c0002t0001g0009 others(140): Show |
173 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(170): Show |
intron_variant | MODIFIER | c.696-1089T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115982198 | |||||||
| chr5:115982248 | T | G | 1 | a0001c0002t0002g0285 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.696-1039T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115982248 | |||||||
| chr5:115982272 | C | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0024 others(91): Show |
116 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.696-1015C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115982272 | |||||||
| chr5:115982297 | C | T | 11 | a0001c0004t0001g0037 a0001c0004t0001g0038 a0001c0004t0001g0248 others(8): Show |
13 | HG02258.hp1 HG02630.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.696-990C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115982297 | |||||||
| chr5:115982395 | C | T | 2 | a0001c0014t0004g0314 a0015c0019t0020g0059 |
2 | HG02559.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.696-892C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115982395 | |||||||
| chr5:115982471 | A | T | 1 | a0003c0008t0006g0120 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.696-816A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115982471 | |||||||
| chr5:115982494 | G | C | 13 | a0001c0001t0002g0197 a0001c0001t0002g0227 a0001c0001t0018g0198 others(10): Show |
15 | HG00735.hp1 HG01106.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.696-793G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115982494 | |||||||
| chr5:115982568 | A | G | 1 | a0001c0004t0001g0289 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.696-719A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115982568 | |||||||
| chr5:115982606 | G | A | 309 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(306): Show |
369 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(366): Show |
intron_variant | MODIFIER | c.696-681G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115982606 | |||||||
| chr5:115982607 | T | A | 2 | a0001c0004t0001g0236 a0001c0004t0001g0237 |
2 | HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.696-680T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115982607 | |||||||
| chr5:115982614 | G | C | 1 | a0010c0024t0001g0295 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.696-673G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115982614 | |||||||
| chr5:115982622 | G | A | 1 | a0001c0002t0001g0255 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.696-665G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115982622 | |||||||
| chr5:115982651 | G | C | 2 | a0001c0002t0001g0272 a0017c0029t0004g0273 |
2 | HG01192.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.696-636G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115982651 | |||||||
| chr5:115982721 | C | T | 297 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(294): Show |
356 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(353): Show |
intron_variant | MODIFIER | c.696-566C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115982721 | |||||||
| chr5:115982735 | C | A | 1 | a0001c0004t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.696-552C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115982735 | |||||||
| chr5:115982740 | C | A | 1 | a0022c0031t0004g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.696-547C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115982740 | |||||||
| chr5:115982866 | GA | G | 85 | a0001c0001t0001g0139 a0001c0002t0001g0009 a0001c0002t0001g0039 others(82): Show |
97 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.696-413delA | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 115982866 | ||||||
| chr5:115982887 | C | A | 12 | a0001c0002t0007g0239 a0001c0004t0001g0037 a0001c0004t0001g0038 others(9): Show |
14 | HG02258.hp1 HG02630.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.696-400C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115982887 | |||||||
| chr5:115983047 | A | C | 1 | a0001c0001t0001g0188 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.696-240A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115983047 | |||||||
| chr5:115983080 | G | A | 1 | a0001c0004t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.696-207G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115983080 | |||||||
| chr5:115983224 | T | A | 1 | a0002c0003t0005g0102 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.696-63T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 1/19 | chr5 | 115983224 | |||||||
| chr5:115983535 | T | C | 1 | a0001c0001t0002g0214 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.838+106T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 2/19 | chr5 | 115983535 | |||||||
| chr5:115983673 | C | A | 1 | a0001c0002t0001g0258 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.838+244C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 2/19 | chr5 | 115983673 | |||||||
| chr5:115984051 | A | T | 1 | a0001c0001t0001g0134 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.839-519A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 2/19 | chr5 | 115984051 | |||||||
| chr5:115984214 | C | T | 9 | a0002c0003t0003g0018 a0002c0003t0003g0084 a0002c0003t0003g0085 others(6): Show |
12 | HG00639.hp2 HG00642.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.839-356C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 2/19 | chr5 | 115984214 | |||||||
| chr5:115984285 | G | A | 4 | a0001c0014t0001g0060 a0001c0014t0004g0314 a0010c0024t0001g0295 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.839-285G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 2/19 | chr5 | 115984285 | |||||||
| chr5:115984410 | G | A | 315 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(312): Show |
376 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(373): Show |
intron_variant | MODIFIER | c.839-160G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 2/19 | chr5 | 115984410 | |||||||
| chr5:115984471 | G | A | 1 | a0004c0012t0013g0192 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.839-99G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 2/19 | chr5 | 115984471 | |||||||
| chr5:115984518 | A | T | 60 | a0001c0002t0001g0009 a0001c0002t0001g0039 a0001c0002t0001g0040 others(57): Show |
69 | HG00597.hp1 HG01069.hp2 HG01167.hp2 others(66): Show |
intron_variant | MODIFIER | c.839-52A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 2/19 | chr5 | 115984518 | |||||||
| chr5:115984801 | T | C | 2 | a0001c0002t0002g0233 a0004c0011t0017g0240 |
2 | HG02818.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.978+92T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115984801 | |||||||
| chr5:115984811 | G | A | 3 | a0001c0001t0002g0197 a0001c0001t0002g0227 a0004c0007t0001g0224 |
3 | HG00735.hp1 HG01106.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.978+102G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115984811 | |||||||
| chr5:115984911 | C | T | 100 | a0001c0001t0001g0139 a0001c0001t0002g0191 a0001c0002t0001g0009 others(97): Show |
113 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.978+202C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115984911 | |||||||
| chr5:115985020 | C | G | 1 | a0001c0002t0004g0254 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.978+311C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115985020 | |||||||
| chr5:115985206 | C | T | 5 | a0001c0001t0001g0226 a0001c0001t0002g0127 a0001c0001t0002g0128 others(2): Show |
5 | HG00140.hp2 HG01175.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.978+497C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115985206 | |||||||
| chr5:115985303 | G | T | 1 | a0002c0003t0014g0017 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.978+594G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115985303 | |||||||
| chr5:115985328 | T | G | 2 | a0001c0015t0015g0343 a0001c0015t0015g0344 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.978+619T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115985328 | |||||||
| chr5:115985415 | G | A | 1 | a0001c0036t0004g0196 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.978+706G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115985415 | |||||||
| chr5:115985427 | G | A | 124 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(121): Show |
151 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.978+718G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115985427 | |||||||
| chr5:115985428 | T | C | 2 | a0001c0004t0001g0236 a0001c0004t0001g0237 |
2 | HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.978+719T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115985428 | |||||||
| chr5:115985500 | A | G | 315 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(312): Show |
376 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(373): Show |
intron_variant | MODIFIER | c.978+791A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115985500 | |||||||
| chr5:115985561 | G | A | 1 | a0002c0003t0006g0076 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.978+852G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115985561 | |||||||
| chr5:115985577 | A | T | 1 | a0001c0001t0002g0182 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.978+868A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115985577 | |||||||
| chr5:115985606 | G | A | 3 | a0002c0003t0006g0069 a0002c0003t0006g0092 a0003c0005t0005g0070 |
3 | HG00673.hp1 NA18961.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.978+897G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115985606 | |||||||
| chr5:115985635 | A | G | 1 | a0001c0004t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.978+926A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115985635 | |||||||
| chr5:115985704 | T | C | 1 | a0001c0004t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.978+995T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115985704 | |||||||
| chr5:115985787 | G | A | 152 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(149): Show |
170 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.978+1078G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115985787 | |||||||
| chr5:115985858 | C | T | 15 | a0001c0002t0007g0239 a0001c0004t0001g0037 a0001c0004t0001g0038 others(12): Show |
17 | HG02258.hp1 HG02630.hp1 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.978+1149C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115985858 | |||||||
| chr5:115985868 | A | C | 1 | a0003c0005t0003g0111 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.978+1159A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115985868 | |||||||
| chr5:115986016 | A | C | 1 | a0001c0004t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.978+1307A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115986016 | |||||||
| chr5:115986043 | C | G | 1 | a0001c0001t0002g0140 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.978+1334C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115986043 | |||||||
| chr5:115986047 | G | A | 3 | a0001c0004t0001g0288 a0001c0004t0001g0289 a0001c0004t0001g0339 |
3 | HG01884.hp2 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.978+1338G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115986047 | |||||||
| chr5:115986051 | T | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(173): Show |
208 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(205): Show |
intron_variant | MODIFIER | c.978+1342T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115986051 | |||||||
| chr5:115986066 | G | T | 1 | a0001c0025t0001g0232 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.978+1357G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115986066 | |||||||
| chr5:115986078 | C | T | 12 | a0001c0002t0007g0239 a0001c0004t0001g0037 a0001c0004t0001g0038 others(9): Show |
14 | HG02258.hp1 HG02630.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.978+1369C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115986078 | |||||||
| chr5:115986122 | T | G | 249 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(246): Show |
301 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(298): Show |
intron_variant | MODIFIER | c.978+1413T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115986122 | |||||||
| chr5:115986136 | G | A | 310 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(307): Show |
371 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(368): Show |
intron_variant | MODIFIER | c.978+1427G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115986136 | |||||||
| chr5:115986180 | C | G | 2 | a0001c0004t0001g0236 a0001c0004t0001g0237 |
2 | HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.978+1471C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115986180 | |||||||
| chr5:115986418 | C | T | 1 | a0001c0002t0002g0233 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.979-1395C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115986418 | |||||||
| chr5:115986459 | G | T | 62 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(59): Show |
71 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.979-1354G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115986459 | |||||||
| chr5:115986464 | C | T | 62 | a0001c0002t0001g0009 a0001c0002t0001g0039 a0001c0002t0001g0040 others(59): Show |
71 | HG00597.hp1 HG01069.hp2 HG01167.hp2 others(68): Show |
intron_variant | MODIFIER | c.979-1349C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115986464 | |||||||
| chr5:115986604 | C | T | 1 | a0001c0001t0002g0181 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.979-1209C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115986604 | |||||||
| chr5:115986632 | T | A | 2 | a0014c0030t0007g0313 a0016c0039t0001g0221 |
2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.979-1181T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115986632 | |||||||
| chr5:115986750 | T | C | 92 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(89): Show |
113 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.979-1063T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115986750 | |||||||
| chr5:115986792 | C | T | 58 | a0001c0001t0002g0219 a0002c0003t0003g0001 a0002c0003t0003g0007 others(55): Show |
76 | HG00544.hp2 HG00609.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.979-1021C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115986792 | |||||||
| chr5:115986990 | T | A | 2 | a0001c0004t0004g0293 a0001c0004t0004g0294 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.979-823T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115986990 | |||||||
| chr5:115987017 | C | G | 1 | a0022c0031t0004g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.979-796C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115987017 | |||||||
| chr5:115987034 | CT | C | 14 | a0001c0001t0001g0150 a0001c0001t0001g0183 a0001c0001t0001g0188 others(11): Show |
14 | HG00140.hp2 HG00738.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.979-768delT | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 115987034 | ||||||
| chr5:115987125 | G | A | 54 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(51): Show |
59 | HG00408.hp1 HG00558.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.979-688G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115987125 | |||||||
| chr5:115987175 | G | A | 1 | a0022c0031t0004g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.979-638G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115987175 | |||||||
| chr5:115987218 | C | T | 12 | a0001c0001t0001g0130 a0001c0001t0002g0035 a0002c0003t0005g0012 others(9): Show |
15 | HG00438.hp2 HG01168.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.979-595C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115987218 | |||||||
| chr5:115987348 | T | C | 1 | a0001c0004t0001g0296 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.979-465T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115987348 | |||||||
| chr5:115987420 | C | G | 1 | a0003c0005t0005g0113 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.979-393C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115987420 | |||||||
| chr5:115987519 | C | T | 7 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0002g0235 others(4): Show |
11 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.979-294C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115987519 | |||||||
| chr5:115987537 | G | A | 57 | a0001c0001t0002g0219 a0002c0003t0003g0001 a0002c0003t0003g0007 others(54): Show |
75 | HG00544.hp2 HG00609.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.979-276G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115987537 | |||||||
| chr5:115987630 | A | C | 1 | a0002c0003t0003g0085 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.979-183A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115987630 | |||||||
| chr5:115987666 | A | G | 1 | a0001c0004t0001g0299 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.979-147A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115987666 | |||||||
| chr5:115987792 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(91): Show |
115 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.979-21T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 3/19 | chr5 | 115987792 | |||||||
| chr5:115987994 | G | A | 49 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(46): Show |
54 | HG00408.hp1 HG00558.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.1105+55G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115987994 | |||||||
| chr5:115988027 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(90): Show |
114 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.1105+88A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115988027 | |||||||
| chr5:115988079 | T | C | 1 | a0001c0002t0002g0286 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1105+140T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115988079 | |||||||
| chr5:115988087 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(90): Show |
114 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.1105+148A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115988087 | |||||||
| chr5:115988109 | T | C | 344 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(341): Show |
409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.1105+170T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115988109 | |||||||
| chr5:115988206 | C | T | 2 | a0001c0002t0002g0233 a0004c0011t0017g0240 |
2 | HG02818.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1105+267C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115988206 | |||||||
| chr5:115988219 | C | T | 1 | a0016c0039t0001g0221 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1105+280C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115988219 | |||||||
| chr5:115988252 | C | A | 4 | a0001c0001t0002g0197 a0001c0001t0002g0227 a0001c0001t0018g0198 others(1): Show |
4 | HG00735.hp1 HG01106.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.1105+313C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115988252 | |||||||
| chr5:115988296 | C | T | 1 | a0001c0002t0002g0332 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1105+357C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115988296 | |||||||
| chr5:115988332 | GT | G | 300 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(297): Show |
357 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(354): Show |
intron_variant | MODIFIER | c.1105+407delT | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr5 | 115988332 | ||||||
| chr5:115988346 | TA | T | 7 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0002g0235 others(4): Show |
11 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1105+410delA | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr5 | 115988346 | ||||||
| chr5:115988402 | T | C | 2 | a0003c0005t0005g0113 a0018c0020t0005g0091 |
2 | HG01496.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1105+463T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115988402 | |||||||
| chr5:115988425 | CAT | C | 5 | a0001c0001t0001g0226 a0001c0001t0002g0127 a0001c0001t0002g0128 others(2): Show |
5 | HG00140.hp2 HG01175.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1105+489_1105+490d others(4): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr5 | 115988425 | ||||||
| chr5:115988447 | C | G | 1 | a0016c0039t0001g0221 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1105+508C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115988447 | |||||||
| chr5:115988451 | A | G | 1 | a0001c0002t0002g0331 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1105+512A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115988451 | |||||||
| chr5:115988496 | T | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(90): Show |
114 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.1105+557T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115988496 | |||||||
| chr5:115988595 | T | G | 179 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(176): Show |
211 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(208): Show |
intron_variant | MODIFIER | c.1105+656T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115988595 | |||||||
| chr5:115988602 | A | G | 59 | a0001c0002t0001g0009 a0001c0002t0001g0039 a0001c0002t0001g0040 others(56): Show |
68 | HG00597.hp1 HG01069.hp2 HG01167.hp2 others(65): Show |
intron_variant | MODIFIER | c.1105+663A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115988602 | |||||||
| chr5:115988620 | C | T | 1 | a0003c0005t0003g0112 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1105+681C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115988620 | |||||||
| chr5:115988631 | C | G | 7 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0002g0235 others(4): Show |
11 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1105+692C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115988631 | |||||||
| chr5:115988766 | C | T | 1 | a0001c0004t0002g0042 | 2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1105+827C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115988766 | |||||||
| chr5:115988881 | G | A | 1 | a0001c0002t0001g0260 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1105+942G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115988881 | |||||||
| chr5:115989041 | G | C | 1 | a0010c0032t0001g0241 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1105+1102G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115989041 | |||||||
| chr5:115989056 | C | A | 58 | a0001c0001t0002g0219 a0002c0003t0003g0001 a0002c0003t0003g0007 others(55): Show |
76 | HG00544.hp2 HG00609.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.1105+1117C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115989056 | |||||||
| chr5:115989218 | G | A | 8 | a0001c0001t0001g0143 a0001c0001t0001g0145 a0001c0001t0001g0150 others(5): Show |
8 | HG00738.hp1 HG01167.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.1105+1279G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115989218 | |||||||
| chr5:115989230 | G | A | 206 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(203): Show |
244 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(241): Show |
intron_variant | MODIFIER | c.1105+1291G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115989230 | |||||||
| chr5:115989241 | A | G | 175 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(172): Show |
207 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(204): Show |
intron_variant | MODIFIER | c.1105+1302A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115989241 | |||||||
| chr5:115989242 | A | C | 5 | a0001c0001t0001g0226 a0001c0001t0002g0127 a0001c0001t0002g0128 others(2): Show |
5 | HG00140.hp2 HG01175.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1105+1303A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115989242 | |||||||
| chr5:115989333 | A | T | 1 | a0003c0005t0006g0052 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1105+1394A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115989333 | |||||||
| chr5:115989390 | C | T | 1 | a0002c0003t0003g0084 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1105+1451C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115989390 | |||||||
| chr5:115989582 | T | C | 211 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(208): Show |
259 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(256): Show |
intron_variant | MODIFIER | c.1105+1643T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115989582 | |||||||
| chr5:115989583 | G | C | 1 | a0001c0001t0001g0147 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1105+1644G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115989583 | |||||||
| chr5:115989607 | G | T | 1 | a0003c0005t0006g0052 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1105+1668G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115989607 | |||||||
| chr5:115989621 | AC | A | 2 | a0002c0003t0006g0014 a0002c0003t0006g0064 |
3 | HG02027.hp2 NA18995.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1105+1683delC | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115989621 | |||||||
| chr5:115989674 | G | T | 302 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(299): Show |
361 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(358): Show |
intron_variant | MODIFIER | c.1105+1735G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115989674 | |||||||
| chr5:115989733 | G | A | 3 | a0002c0003t0003g0099 a0002c0003t0003g0103 a0003c0005t0003g0104 |
3 | NA18959.hp2 NA18966.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1105+1794G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115989733 | |||||||
| chr5:115989773 | G | A | 82 | a0001c0001t0001g0139 a0001c0002t0001g0009 a0001c0002t0001g0039 others(79): Show |
93 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.1105+1834G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115989773 | |||||||
| chr5:115989884 | C | T | 9 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0134 others(6): Show |
11 | HG00408.hp1 HG00673.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.1105+1945C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115989884 | |||||||
| chr5:115989931 | T | C | 1 | a0001c0002t0002g0323 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1105+1992T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115989931 | |||||||
| chr5:115989945 | G | A | 1 | a0001c0014t0001g0060 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1105+2006G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115989945 | |||||||
| chr5:115990244 | T | A | 1 | a0001c0004t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1106-1879T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115990244 | |||||||
| chr5:115990339 | A | G | 1 | a0004c0007t0002g0216 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1106-1784A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115990339 | |||||||
| chr5:115990452 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1106-1671G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115990452 | |||||||
| chr5:115990525 | C | T | 1 | a0001c0001t0002g0219 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1106-1598C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115990525 | |||||||
| chr5:115990547 | A | G | 58 | a0001c0002t0001g0009 a0001c0002t0001g0039 a0001c0002t0001g0040 others(55): Show |
67 | HG00597.hp1 HG01069.hp2 HG01167.hp2 others(64): Show |
intron_variant | MODIFIER | c.1106-1576A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115990547 | |||||||
| chr5:115990555 | G | C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(172): Show |
207 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(204): Show |
intron_variant | MODIFIER | c.1106-1568G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115990555 | |||||||
| chr5:115990564 | T | C | 204 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(201): Show |
248 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.1106-1559T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115990564 | |||||||
| chr5:115990569 | A | G | 1 | a0001c0002t0001g0039 | 2 | NA18990.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1106-1554A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115990569 | |||||||
| chr5:115990746 | AT | A | 7 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0002g0235 others(4): Show |
11 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1106-1374delT | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr5 | 115990746 | ||||||
| chr5:115990847 | C | T | 1 | a0003c0008t0006g0086 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1106-1276C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115990847 | |||||||
| chr5:115990856 | G | A | 57 | a0001c0001t0002g0219 a0002c0003t0003g0001 a0002c0003t0003g0007 others(54): Show |
75 | HG00544.hp2 HG00609.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.1106-1267G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115990856 | |||||||
| chr5:115990896 | T | C | 1 | a0003c0008t0005g0115 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1106-1227T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115990896 | |||||||
| chr5:115990998 | A | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(90): Show |
114 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.1106-1125A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115990998 | |||||||
| chr5:115991001 | A | G | 1 | a0004c0007t0001g0224 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1106-1122A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991001 | |||||||
| chr5:115991031 | A | G | 1 | a0005c0034t0004g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1106-1092A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991031 | |||||||
| chr5:115991034 | T | G | 1 | a0003c0005t0005g0113 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1106-1089T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991034 | |||||||
| chr5:115991066 | T | C | 19 | a0001c0001t0001g0139 a0001c0004t0001g0292 a0001c0004t0001g0296 others(16): Show |
21 | HG00544.hp1 HG00609.hp1 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.1106-1057T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991066 | |||||||
| chr5:115991070 | C | T | 1 | a0001c0004t0004g0231 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1106-1053C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991070 | |||||||
| chr5:115991101 | T | C | 19 | a0001c0001t0001g0139 a0001c0004t0001g0292 a0001c0004t0001g0296 others(16): Show |
21 | HG00544.hp1 HG00609.hp1 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.1106-1022T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991101 | |||||||
| chr5:115991127 | C | T | 6 | a0001c0001t0001g0226 a0001c0001t0002g0127 a0001c0001t0002g0128 others(3): Show |
6 | HG00140.hp2 HG01175.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1106-996C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991127 | |||||||
| chr5:115991149 | C | T | 1 | a0001c0004t0001g0292 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1106-974C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991149 | |||||||
| chr5:115991180 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1106-943C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991180 | |||||||
| chr5:115991216 | C | G | 3 | a0002c0003t0005g0012 a0003c0005t0003g0048 a0003c0005t0003g0049 |
4 | HG02145.hp1 HG03041.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1106-907C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991216 | |||||||
| chr5:115991296 | T | C | 1 | a0003c0005t0005g0113 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1106-827T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991296 | |||||||
| chr5:115991343 | C | T | 4 | a0001c0001t0001g0226 a0001c0001t0002g0127 a0001c0001t0002g0128 others(1): Show |
4 | HG00140.hp2 HG01175.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1106-780C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991343 | |||||||
| chr5:115991356 | A | G | 58 | a0001c0001t0002g0219 a0002c0003t0003g0001 a0002c0003t0003g0007 others(55): Show |
76 | HG00544.hp2 HG00609.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.1106-767A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991356 | |||||||
| chr5:115991499 | A | G | 2 | a0001c0001t0002g0035 a0004c0012t0002g0223 |
3 | HG02615.hp2 HG02896.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1106-624A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991499 | |||||||
| chr5:115991609 | A | G | 1 | a0003c0005t0005g0113 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1106-514A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991609 | |||||||
| chr5:115991610 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1106-513T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991610 | |||||||
| chr5:115991612 | T | A | 1 | a0001c0001t0001g0184 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1106-511T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991612 | |||||||
| chr5:115991614 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1106-509G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991614 | |||||||
| chr5:115991624 | G | T | 1 | a0001c0001t0001g0184 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1106-499G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991624 | |||||||
| chr5:115991625 | A | C | 1 | a0001c0001t0001g0184 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1106-498A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991625 | |||||||
| chr5:115991626 | G | T | 1 | a0001c0001t0001g0184 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1106-497G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991626 | |||||||
| chr5:115991635 | G | C | 1 | a0002c0003t0003g0084 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1106-488G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991635 | |||||||
| chr5:115991727 | T | C | 2 | a0001c0004t0004g0293 a0001c0004t0004g0294 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1106-396T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991727 | |||||||
| chr5:115991745 | C | T | 54 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(51): Show |
59 | HG00408.hp1 HG00558.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1106-378C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991745 | |||||||
| chr5:115991750 | A | G | 174 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(171): Show |
206 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(203): Show |
intron_variant | MODIFIER | c.1106-373A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991750 | |||||||
| chr5:115991753 | A | G | 1 | a0003c0005t0005g0113 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1106-370A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991753 | |||||||
| chr5:115991781 | G | A | 47 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(44): Show |
52 | HG00408.hp1 HG00558.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.1106-342G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991781 | |||||||
| chr5:115991902 | A | G | 1 | a0022c0031t0004g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1106-221A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991902 | |||||||
| chr5:115991949 | T | A | 7 | a0002c0003t0003g0007 a0002c0003t0003g0061 a0002c0003t0003g0063 others(4): Show |
10 | HG02027.hp2 NA18955.hp2 NA18964.hp1 others(7): Show |
intron_variant | MODIFIER | c.1106-174T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991949 | |||||||
| chr5:115991999 | C | T | 7 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0002g0235 others(4): Show |
11 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1106-124C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115991999 | |||||||
| chr5:115992000 | G | C | 1 | a0001c0004t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1106-123G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115992000 | |||||||
| chr5:115992019 | C | T | 5 | a0001c0001t0001g0023 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
6 | HG00733.hp1 HG01109.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.1106-104C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115992019 | |||||||
| chr5:115992026 | T | G | 19 | a0001c0001t0001g0139 a0001c0004t0001g0292 a0001c0004t0001g0296 others(16): Show |
21 | HG00544.hp1 HG00609.hp1 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.1106-97T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115992026 | |||||||
| chr5:115992071 | C | G | 15 | a0001c0002t0007g0239 a0001c0004t0001g0037 a0001c0004t0001g0038 others(12): Show |
17 | HG02258.hp1 HG02630.hp1 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.1106-52C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115992071 | |||||||
| chr5:115992072 | C | A | 15 | a0001c0002t0007g0239 a0001c0004t0001g0037 a0001c0004t0001g0038 others(12): Show |
17 | HG02258.hp1 HG02630.hp1 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.1106-51C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 4/19 | chr5 | 115992072 | |||||||
| chr5:115992414 | G | A | 1 | a0014c0030t0007g0313 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1260+137G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 5/19 | chr5 | 115992414 | |||||||
| chr5:115992422 | G | C | 2 | a0001c0002t0002g0233 a0004c0011t0017g0240 |
2 | HG02818.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1260+145G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 5/19 | chr5 | 115992422 | |||||||
| chr5:115992460 | T | G | 1 | a0022c0031t0004g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1260+183T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 5/19 | chr5 | 115992460 | |||||||
| chr5:115992543 | C | T | 7 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0002g0235 others(4): Show |
11 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1260+266C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 5/19 | chr5 | 115992543 | |||||||
| chr5:115992596 | A | C | 8 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0002g0235 others(5): Show |
12 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1260+319A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 5/19 | chr5 | 115992596 | |||||||
| chr5:115992688 | T | G | 1 | a0002c0003t0003g0061 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1260+411T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 5/19 | chr5 | 115992688 | |||||||
| chr5:115992739 | T | C | 114 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(111): Show |
137 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.1260+462T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 5/19 | chr5 | 115992739 | |||||||
| chr5:115992751 | T | C | 61 | a0001c0002t0001g0009 a0001c0002t0001g0039 a0001c0002t0001g0040 others(58): Show |
70 | HG00597.hp1 HG01069.hp2 HG01167.hp2 others(67): Show |
intron_variant | MODIFIER | c.1260+474T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 5/19 | chr5 | 115992751 | |||||||
| chr5:115992889 | G | T | 1 | a0001c0014t0001g0060 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1260+612G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 5/19 | chr5 | 115992889 | |||||||
| chr5:115992928 | G | A | 93 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(90): Show |
114 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.1260+651G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 5/19 | chr5 | 115992928 | |||||||
| chr5:115992941 | A | G | 2 | a0001c0015t0015g0343 a0001c0015t0015g0344 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1260+664A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 5/19 | chr5 | 115992941 | |||||||
| chr5:115992971 | A | C | 1 | a0004c0011t0002g0271 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1260+694A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 5/19 | chr5 | 115992971 | |||||||
| chr5:115993015 | C | G | 8 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0002g0235 others(5): Show |
12 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1261-726C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 5/19 | chr5 | 115993015 | |||||||
| chr5:115993200 | G | GTTTT | 90 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(87): Show |
111 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.1261-533_1261-530d others(6): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr5 | 115993200 | ||||||
| chr5:115993200 | G | GTTTTT | 23 | a0001c0001t0001g0139 a0001c0001t0001g0185 a0001c0001t0002g0169 others(20): Show |
25 | HG00544.hp1 HG00609.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1261-534_1261-530d others(7): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr5 | 115993200 | ||||||
| chr5:115993200 | GT | G | 127 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(124): Show |
156 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.1261-530delT | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr5 | 115993200 | ||||||
| chr5:115993218 | A | G | 114 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(111): Show |
137 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.1261-523A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 5/19 | chr5 | 115993218 | |||||||
| chr5:115993237 | TA | T | 114 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(111): Show |
137 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.1261-502delA | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr5 | 115993237 | ||||||
| chr5:115993245 | G | A | 14 | a0001c0004t0001g0037 a0001c0004t0001g0038 a0001c0004t0001g0248 others(11): Show |
16 | HG02258.hp1 HG02630.hp1 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.1261-496G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 5/19 | chr5 | 115993245 | |||||||
| chr5:115993322 | C | T | 1 | a0019c0038t0001g0220 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1261-419C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 5/19 | chr5 | 115993322 | |||||||
| chr5:115993553 | G | T | 114 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(111): Show |
137 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.1261-188G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 5/19 | chr5 | 115993553 | |||||||
| chr5:115993596 | T | C | 114 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(111): Show |
137 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.1261-145T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 5/19 | chr5 | 115993596 | |||||||
| chr5:115993872 | G | C | 1 | a0005c0006t0004g0290 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1374+18G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115993872 | |||||||
| chr5:115993872 | G | T | 1 | a0001c0001t0004g0168 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1374+18G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115993872 | |||||||
| chr5:115993916 | C | T | 1 | a0001c0004t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1374+62C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115993916 | |||||||
| chr5:115994001 | G | A | 12 | a0001c0002t0007g0239 a0001c0004t0001g0037 a0001c0004t0001g0038 others(9): Show |
14 | HG02258.hp1 HG02630.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.1374+147G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115994001 | |||||||
| chr5:115994004 | AT | A | 7 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0002g0235 others(4): Show |
11 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1374+159delT | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 115994004 | ||||||
| chr5:115994006 | T | A | 1 | a0003c0008t0003g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1374+152T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115994006 | |||||||
| chr5:115994038 | A | C | 114 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(111): Show |
137 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.1374+184A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115994038 | |||||||
| chr5:115994042 | GT | G | 114 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(111): Show |
137 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.1374+193delT | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 115994042 | ||||||
| chr5:115994092 | A | G | 1 | a0001c0014t0001g0060 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1374+238A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115994092 | |||||||
| chr5:115994297 | T | C | 317 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(314): Show |
378 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(375): Show |
intron_variant | MODIFIER | c.1374+443T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115994297 | |||||||
| chr5:115994425 | AC | A | 92 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(89): Show |
113 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.1374+573delC | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 115994425 | ||||||
| chr5:115994450 | G | C | 92 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(89): Show |
113 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.1374+596G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115994450 | |||||||
| chr5:115994462 | G | A | 1 | a0006c0009t0002g0135 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1374+608G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115994462 | |||||||
| chr5:115994553 | G | T | 2 | a0001c0004t0001g0236 a0001c0004t0001g0237 |
2 | HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1374+699G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115994553 | |||||||
| chr5:115994565 | G | T | 113 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(110): Show |
136 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.1374+711G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115994565 | |||||||
| chr5:115994579 | G | A | 294 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(291): Show |
353 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(350): Show |
intron_variant | MODIFIER | c.1374+725G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115994579 | |||||||
| chr5:115994599 | C | T | 1 | a0001c0002t0001g0251 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1374+745C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115994599 | |||||||
| chr5:115994642 | TTTAA | T | 181 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(178): Show |
217 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(214): Show |
intron_variant | MODIFIER | c.1374+794_1374+797d others(6): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 115994642 | ||||||
| chr5:115994758 | T | C | 4 | a0002c0003t0003g0020 a0002c0003t0003g0078 a0002c0003t0006g0022 others(1): Show |
6 | HG02165.hp2 HG04184.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1374+904T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115994758 | |||||||
| chr5:115994797 | G | A | 119 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(116): Show |
146 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.1374+943G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115994797 | |||||||
| chr5:115994869 | C | T | 1 | a0001c0002t0007g0011 | 3 | HG00741.hp2 HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1374+1015C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115994869 | |||||||
| chr5:115994930 | T | G | 1 | a0005c0034t0004g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1374+1076T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115994930 | |||||||
| chr5:115995032 | C | T | 12 | a0001c0001t0001g0031 a0001c0001t0001g0177 a0001c0001t0001g0179 others(9): Show |
14 | HG01978.hp1 HG01981.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.1374+1178C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995032 | |||||||
| chr5:115995081 | T | A | 1 | a0001c0004t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1374+1227T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995081 | |||||||
| chr5:115995151 | A | G | 1 | a0001c0001t0002g0346 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1374+1297A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995151 | |||||||
| chr5:115995214 | G | A | 1 | a0005c0006t0004g0290 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1374+1360G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995214 | |||||||
| chr5:115995230 | T | C | 140 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(137): Show |
169 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(166): Show |
intron_variant | MODIFIER | c.1374+1376T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995230 | |||||||
| chr5:115995283 | A | G | 21 | a0001c0001t0001g0139 a0001c0004t0001g0292 a0001c0004t0001g0296 others(18): Show |
23 | HG00544.hp1 HG00609.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1374+1429A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995283 | |||||||
| chr5:115995285 | T | A | 1 | a0001c0001t0004g0202 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1374+1431T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995285 | |||||||
| chr5:115995373 | A | C | 58 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(55): Show |
63 | HG00408.hp1 HG00558.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1374+1519A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995373 | |||||||
| chr5:115995415 | A | G | 1 | a0004c0011t0017g0240 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1374+1561A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995415 | |||||||
| chr5:115995421 | T | C | 134 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(131): Show |
159 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.1374+1567T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995421 | |||||||
| chr5:115995439 | C | T | 2 | a0001c0002t0013g0335 a0001c0004t0001g0230 |
2 | HG02572.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1374+1585C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995439 | |||||||
| chr5:115995508 | G | A | 1 | a0001c0002t0001g0044 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1374+1654G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995508 | |||||||
| chr5:115995554 | T | G | 1 | a0001c0036t0004g0196 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1374+1700T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995554 | |||||||
| chr5:115995559 | A | G | 1 | a0010c0024t0001g0295 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1374+1705A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995559 | |||||||
| chr5:115995612 | T | A | 1 | a0001c0002t0001g0238 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1374+1758T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995612 | |||||||
| chr5:115995638 | A | G | 135 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(132): Show |
160 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(157): Show |
intron_variant | MODIFIER | c.1374+1784A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995638 | |||||||
| chr5:115995641 | A | C | 54 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(51): Show |
59 | HG00408.hp1 HG00558.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1374+1787A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995641 | |||||||
| chr5:115995708 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1374+1854C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995708 | |||||||
| chr5:115995718 | A | G | 58 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(55): Show |
63 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.1374+1864A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995718 | |||||||
| chr5:115995771 | A | T | 83 | a0001c0002t0001g0009 a0001c0002t0001g0039 a0001c0002t0001g0040 others(80): Show |
98 | HG00597.hp1 HG00741.hp2 HG01069.hp2 others(95): Show |
intron_variant | MODIFIER | c.1374+1917A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995771 | |||||||
| chr5:115995811 | G | A | 1 | a0022c0031t0004g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1374+1957G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995811 | |||||||
| chr5:115995811 | G | C | 1 | a0001c0002t0001g0261 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1374+1957G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995811 | |||||||
| chr5:115995814 | C | T | 1 | a0022c0031t0004g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1374+1960C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995814 | |||||||
| chr5:115995816 | A | C | 1 | a0022c0031t0004g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1374+1962A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995816 | |||||||
| chr5:115995817 | G | T | 1 | a0022c0031t0004g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1374+1963G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995817 | |||||||
| chr5:115995879 | C | G | 1 | a0001c0004t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1374+2025C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995879 | |||||||
| chr5:115995911 | A | G | 1 | a0002c0003t0005g0093 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1374+2057A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995911 | |||||||
| chr5:115995947 | CGT | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(123): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.1374+2118_1374+211 others(6): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 115995947 | ||||||
| chr5:115995947 | CGTGT | C | 36 | a0001c0001t0001g0139 a0001c0001t0001g0153 a0001c0001t0004g0202 others(33): Show |
40 | HG00544.hp1 HG00609.hp1 HG02015.hp2 others(37): Show |
intron_variant | MODIFIER | c.1374+2116_1374+211 others(8): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 115995947 | ||||||
| chr5:115995947 | CGTGTGT | C | 188 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(185): Show |
224 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(221): Show |
intron_variant | MODIFIER | c.1374+2114_1374+211 others(10): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 115995947 | ||||||
| chr5:115995981 | T | C | 61 | a0001c0002t0001g0009 a0001c0002t0001g0039 a0001c0002t0001g0040 others(58): Show |
70 | HG00597.hp1 HG01069.hp2 HG01167.hp2 others(67): Show |
intron_variant | MODIFIER | c.1374+2127T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995981 | |||||||
| chr5:115995987 | C | T | 61 | a0001c0002t0001g0009 a0001c0002t0001g0039 a0001c0002t0001g0040 others(58): Show |
70 | HG00597.hp1 HG01069.hp2 HG01167.hp2 others(67): Show |
intron_variant | MODIFIER | c.1374+2133C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115995987 | |||||||
| chr5:115996027 | T | TTC | 3 | a0001c0014t0004g0314 a0010c0024t0001g0295 a0015c0019t0020g0059 |
3 | HG02559.hp1 HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1374+2173_1374+217 others(6): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115996027 | |||||||
| chr5:115996028 | C | A | 3 | a0001c0014t0004g0314 a0010c0024t0001g0295 a0015c0019t0020g0059 |
3 | HG02559.hp1 HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1374+2174C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115996028 | |||||||
| chr5:115996106 | A | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(89): Show |
113 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.1374+2252A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115996106 | |||||||
| chr5:115996177 | A | G | 1 | a0001c0004t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1374+2323A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115996177 | |||||||
| chr5:115996182 | C | A | 2 | a0001c0004t0004g0293 a0001c0004t0004g0294 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1374+2328C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115996182 | |||||||
| chr5:115996200 | A | G | 1 | a0001c0004t0001g0248 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1374+2346A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115996200 | |||||||
| chr5:115996279 | T | A | 59 | a0001c0002t0001g0009 a0001c0002t0001g0039 a0001c0002t0001g0040 others(56): Show |
68 | HG00597.hp1 HG01069.hp2 HG01167.hp2 others(65): Show |
intron_variant | MODIFIER | c.1374+2425T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115996279 | |||||||
| chr5:115996454 | A | C | 1 | a0001c0004t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1374+2600A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115996454 | |||||||
| chr5:115996471 | C | A | 24 | a0001c0001t0001g0139 a0001c0004t0001g0230 a0001c0004t0001g0292 others(21): Show |
26 | HG00544.hp1 HG00609.hp1 HG02015.hp2 others(23): Show |
intron_variant | MODIFIER | c.1374+2617C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115996471 | |||||||
| chr5:115996472 | G | A | 7 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0002g0235 others(4): Show |
11 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1374+2618G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115996472 | |||||||
| chr5:115996478 | T | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(179): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1374+2624T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115996478 | |||||||
| chr5:115996522 | T | C | 56 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(53): Show |
61 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.1374+2668T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115996522 | |||||||
| chr5:115996529 | C | T | 1 | a0001c0014t0004g0314 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1374+2675C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115996529 | |||||||
| chr5:115996551 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1374+2697T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115996551 | |||||||
| chr5:115996764 | G | A | 148 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(145): Show |
174 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1374+2910G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115996764 | |||||||
| chr5:115996786 | G | C | 148 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(145): Show |
174 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1374+2932G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115996786 | |||||||
| chr5:115996815 | T | C | 148 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(145): Show |
174 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1375-2947T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115996815 | |||||||
| chr5:115996905 | C | A | 56 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(53): Show |
61 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.1375-2857C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115996905 | |||||||
| chr5:115996930 | T | A | 92 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(89): Show |
113 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.1375-2832T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115996930 | |||||||
| chr5:115996978 | G | A | 1 | a0022c0031t0004g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1375-2784G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115996978 | |||||||
| chr5:115996985 | G | A | 148 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(145): Show |
174 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1375-2777G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115996985 | |||||||
| chr5:115997005 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1375-2757A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115997005 | |||||||
| chr5:115997181 | T | C | 4 | a0002c0003t0003g0063 a0002c0003t0006g0014 a0002c0003t0006g0064 others(1): Show |
5 | HG02027.hp2 NA18955.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.1375-2581T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115997181 | |||||||
| chr5:115997191 | C | T | 61 | a0001c0002t0001g0009 a0001c0002t0001g0039 a0001c0002t0001g0040 others(58): Show |
70 | HG00597.hp1 HG01069.hp2 HG01167.hp2 others(67): Show |
intron_variant | MODIFIER | c.1375-2571C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115997191 | |||||||
| chr5:115997192 | G | A | 1 | a0004c0028t0002g0065 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1375-2570G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115997192 | |||||||
| chr5:115997202 | T | C | 1 | a0001c0001t0002g0133 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1375-2560T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115997202 | |||||||
| chr5:115997211 | G | A | 2 | a0003c0008t0005g0021 a0003c0008t0005g0115 |
3 | NA18998.hp1 NA19002.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1375-2551G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115997211 | |||||||
| chr5:115997432 | G | A | 21 | a0001c0001t0001g0139 a0001c0004t0001g0292 a0001c0004t0001g0296 others(18): Show |
23 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.1375-2330G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115997432 | |||||||
| chr5:115997479 | CAT | C | 3 | a0001c0001t0001g0031 a0001c0001t0001g0177 a0004c0007t0004g0176 |
4 | NA18951.hp2 NA18984.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1375-2281_1375-228 others(6): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 115997479 | ||||||
| chr5:115997493 | G | A | 2 | a0001c0002t0002g0262 a0001c0004t0001g0301 |
2 | HG00609.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1375-2269G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115997493 | |||||||
| chr5:115997518 | G | C | 28 | a0001c0002t0001g0315 a0001c0002t0001g0328 a0001c0002t0001g0336 others(25): Show |
32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1375-2244G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115997518 | |||||||
| chr5:115997523 | G | A | 3 | a0001c0015t0015g0343 a0001c0015t0015g0344 a0001c0025t0001g0232 |
3 | HG02257.hp1 HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1375-2239G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115997523 | |||||||
| chr5:115997536 | C | A | 3 | a0001c0015t0015g0343 a0001c0015t0015g0344 a0001c0025t0001g0232 |
3 | HG02257.hp1 HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1375-2226C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115997536 | |||||||
| chr5:115997566 | C | T | 148 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(145): Show |
175 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1375-2196C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115997566 | |||||||
| chr5:115997660 | C | CA | 8 | a0001c0002t0001g0047 a0001c0002t0001g0260 a0001c0002t0001g0263 others(5): Show |
8 | HG02040.hp2 NA18939.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1375-2091dupA | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 115997660 | ||||||
| chr5:115997728 | G | T | 59 | a0001c0001t0002g0144 a0001c0001t0002g0219 a0002c0003t0003g0001 others(56): Show |
77 | HG00544.hp2 HG00609.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.1375-2034G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115997728 | |||||||
| chr5:115997826 | T | G | 1 | a0001c0001t0002g0227 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1375-1936T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115997826 | |||||||
| chr5:115997860 | A | G | 1 | a0010c0024t0001g0295 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1375-1902A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115997860 | |||||||
| chr5:115997865 | A | T | 1 | a0002c0003t0003g0085 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1375-1897A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115997865 | |||||||
| chr5:115997888 | A | G | 9 | a0001c0004t0001g0037 a0001c0004t0001g0038 a0001c0004t0001g0248 others(6): Show |
11 | HG02258.hp1 HG02630.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1375-1874A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115997888 | |||||||
| chr5:115997973 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(59): Show |
78 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1375-1789T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115997973 | |||||||
| chr5:115998126 | G | A | 25 | a0001c0001t0001g0139 a0001c0004t0001g0230 a0001c0004t0001g0292 others(22): Show |
27 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.1375-1636G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115998126 | |||||||
| chr5:115998221 | A | T | 1 | a0002c0003t0003g0061 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1375-1541A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115998221 | |||||||
| chr5:115998251 | TC | T | 150 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(147): Show |
176 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1375-1510delC | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115998251 | |||||||
| chr5:115998346 | A | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(207): Show |
254 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.1375-1416A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115998346 | |||||||
| chr5:115998352 | G | T | 25 | a0001c0001t0001g0139 a0001c0004t0001g0230 a0001c0004t0001g0292 others(22): Show |
27 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.1375-1410G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115998352 | |||||||
| chr5:115998429 | T | C | 1 | a0001c0001t0002g0345 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1375-1333T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115998429 | |||||||
| chr5:115998446 | C | T | 49 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(46): Show |
54 | HG00140.hp2 HG00408.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.1375-1316C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115998446 | |||||||
| chr5:115998654 | C | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(143): Show |
172 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.1375-1108C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115998654 | |||||||
| chr5:115998709 | A | G | 1 | a0001c0014t0001g0060 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1375-1053A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115998709 | |||||||
| chr5:115998877 | T | G | 57 | a0001c0002t0001g0009 a0001c0002t0001g0039 a0001c0002t0001g0040 others(54): Show |
66 | HG00597.hp1 HG01069.hp2 HG01167.hp2 others(63): Show |
intron_variant | MODIFIER | c.1375-885T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115998877 | |||||||
| chr5:115998972 | G | A | 3 | a0005c0006t0004g0290 a0005c0034t0004g0199 a0014c0030t0007g0313 |
3 | HG02055.hp1 HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1375-790G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115998972 | |||||||
| chr5:115998990 | A | G | 1 | a0001c0001t0001g0008 | 3 | NA18970.hp2 NA19079.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1375-772A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115998990 | |||||||
| chr5:115999047 | T | C | 64 | a0001c0002t0001g0009 a0001c0002t0001g0039 a0001c0002t0001g0040 others(61): Show |
73 | HG00597.hp1 HG01069.hp2 HG01167.hp2 others(70): Show |
intron_variant | MODIFIER | c.1375-715T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115999047 | |||||||
| chr5:115999135 | C | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(89): Show |
113 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.1375-627C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115999135 | |||||||
| chr5:115999150 | G | A | 1 | a0001c0002t0012g0317 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1375-612G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115999150 | |||||||
| chr5:115999152 | T | A | 1 | a0002c0003t0003g0079 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1375-610T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115999152 | |||||||
| chr5:115999196 | G | A | 73 | a0001c0001t0001g0139 a0001c0002t0001g0043 a0001c0002t0001g0044 others(70): Show |
85 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.1375-566G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115999196 | |||||||
| chr5:115999217 | A | G | 23 | a0001c0001t0001g0139 a0001c0004t0001g0292 a0001c0004t0001g0296 others(20): Show |
25 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.1375-545A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115999217 | |||||||
| chr5:115999218 | T | C | 2 | a0001c0004t0004g0293 a0001c0004t0004g0294 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1375-544T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115999218 | |||||||
| chr5:115999256 | T | G | 1 | a0002c0003t0003g0079 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1375-506T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115999256 | |||||||
| chr5:115999397 | G | A | 1 | a0002c0003t0003g0079 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1375-365G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115999397 | |||||||
| chr5:115999501 | C | A | 1 | a0004c0007t0002g0215 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1375-261C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115999501 | |||||||
| chr5:115999516 | T | C | 3 | a0002c0003t0005g0012 a0003c0005t0003g0048 a0003c0005t0003g0049 |
4 | HG02145.hp1 HG03041.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1375-246T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115999516 | |||||||
| chr5:115999712 | T | C | 1 | a0005c0034t0004g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1375-50T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 6/19 | chr5 | 115999712 | |||||||
| chr5:116000037 | G | C | 61 | a0001c0002t0001g0009 a0001c0002t0001g0039 a0001c0002t0001g0040 others(58): Show |
70 | HG00597.hp1 HG01069.hp2 HG01167.hp2 others(67): Show |
intron_variant | MODIFIER | c.1515+135G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 7/19 | chr5 | 116000037 | |||||||
| chr5:116000105 | G | A | 61 | a0001c0002t0001g0009 a0001c0002t0001g0039 a0001c0002t0001g0040 others(58): Show |
70 | HG00597.hp1 HG01069.hp2 HG01167.hp2 others(67): Show |
intron_variant | MODIFIER | c.1515+203G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 7/19 | chr5 | 116000105 | |||||||
| chr5:116000222 | C | G | 55 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(52): Show |
60 | HG00140.hp2 HG00408.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.1516-211C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 7/19 | chr5 | 116000222 | |||||||
| chr5:116000334 | A | G | 21 | a0001c0001t0001g0139 a0001c0004t0001g0292 a0001c0004t0001g0296 others(18): Show |
23 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.1516-99A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 7/19 | chr5 | 116000334 | |||||||
| chr5:116000359 | C | T | 1 | a0001c0004t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1516-74C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 7/19 | chr5 | 116000359 | |||||||
| chr5:116000517 | C | T | 1 | a0001c0001t0018g0198 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1581+19C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 8/19 | chr5 | 116000517 | |||||||
| chr5:116000518 | G | A | 73 | a0001c0002t0001g0009 a0001c0002t0001g0039 a0001c0002t0001g0040 others(70): Show |
84 | HG00597.hp1 HG01069.hp2 HG01167.hp2 others(81): Show |
intron_variant | MODIFIER | c.1581+20G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 8/19 | chr5 | 116000518 | |||||||
| chr5:116000523 | C | A | 2 | a0001c0002t0002g0233 a0004c0011t0017g0240 |
2 | HG02818.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1581+25C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 8/19 | chr5 | 116000523 | |||||||
| chr5:116000880 | T | C | 2 | a0001c0001t0001g0183 a0001c0001t0001g0188 |
2 | NA18940.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1648-187T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 9/19 | chr5 | 116000880 | |||||||
| chr5:116000982 | G | C | 2 | a0001c0004t0004g0293 a0001c0004t0004g0294 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1648-85G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 9/19 | chr5 | 116000982 | |||||||
| chr5:116001027 | G | A | 1 | a0002c0003t0003g0066 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1648-40G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 9/19 | chr5 | 116001027 | |||||||
| chr5:116001270 | C | A | 1 | a0003c0005t0003g0112 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1820+31C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 10/19 | chr5 | 116001270 | |||||||
| chr5:116001296 | A | G | 2 | a0001c0002t0002g0233 a0004c0011t0017g0240 |
2 | HG02818.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1820+57A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 10/19 | chr5 | 116001296 | |||||||
| chr5:116001373 | G | T | 1 | a0001c0001t0001g0150 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1820+134G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 10/19 | chr5 | 116001373 | |||||||
| chr5:116001375 | G | C | 1 | a0001c0001t0001g0150 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1820+136G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 10/19 | chr5 | 116001375 | |||||||
| chr5:116001418 | T | C | 1 | a0010c0032t0001g0241 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1820+179T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 10/19 | chr5 | 116001418 | |||||||
| chr5:116001448 | G | T | 1 | a0002c0003t0003g0079 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1820+209G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 10/19 | chr5 | 116001448 | |||||||
| chr5:116001469 | G | A | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0004g0149 |
3 | HG00738.hp1 HG02273.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1820+230G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 10/19 | chr5 | 116001469 | |||||||
| chr5:116001499 | C | A | 1 | a0003c0005t0003g0048 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1820+260C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 10/19 | chr5 | 116001499 | |||||||
| chr5:116001650 | C | T | 1 | a0022c0031t0004g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1820+411C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 10/19 | chr5 | 116001650 | |||||||
| chr5:116001689 | G | A | 3 | a0001c0015t0015g0343 a0001c0015t0015g0344 a0001c0025t0001g0232 |
3 | HG02257.hp1 HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1820+450G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 10/19 | chr5 | 116001689 | |||||||
| chr5:116001724 | G | A | 1 | a0014c0030t0007g0313 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1820+485G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 10/19 | chr5 | 116001724 | |||||||
| chr5:116001889 | A | G | 2 | a0004c0007t0002g0215 a0004c0007t0002g0216 |
2 | HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1820+650A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 10/19 | chr5 | 116001889 | |||||||
| chr5:116002024 | GTAAT | G | 3 | a0001c0014t0004g0314 a0010c0024t0001g0295 a0015c0019t0020g0059 |
3 | HG02559.hp1 HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1820+791_1820+794d others(6): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr5 | 116002024 | ||||||
| chr5:116002105 | C | T | 2 | a0001c0004t0001g0230 a0006c0009t0002g0026 |
3 | HG01255.hp1 HG02300.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1821-730C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 10/19 | chr5 | 116002105 | |||||||
| chr5:116002217 | T | C | 4 | a0001c0004t0004g0293 a0001c0004t0004g0294 a0009c0016t0002g0243 others(1): Show |
4 | HG02965.hp1 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1821-618T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 10/19 | chr5 | 116002217 | |||||||
| chr5:116002257 | TGAGTAGT others(16): Show |
T | 1 | a0003c0008t0003g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1821-577_1821-555d others(25): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 10/19 | chr5 | 116002257 | |||||||
| chr5:116002407 | C | G | 1 | a0004c0011t0002g0271 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1821-428C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 10/19 | chr5 | 116002407 | |||||||
| chr5:116002445 | T | C | 4 | a0001c0004t0004g0293 a0001c0004t0004g0294 a0009c0016t0002g0243 others(1): Show |
4 | HG02965.hp1 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1821-390T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 10/19 | chr5 | 116002445 | |||||||
| chr5:116002537 | A | T | 22 | a0001c0002t0001g0315 a0001c0002t0001g0328 a0001c0002t0002g0004 others(19): Show |
26 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(23): Show |
intron_variant | MODIFIER | c.1821-298A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 10/19 | chr5 | 116002537 | |||||||
| chr5:116002749 | C | G | 1 | a0002c0003t0005g0016 | 2 | HG00639.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1821-86C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 10/19 | chr5 | 116002749 | |||||||
| chr5:116003007 | T | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(144): Show |
173 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.1897+96T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 11/19 | chr5 | 116003007 | |||||||
| chr5:116003035 | G | A | 283 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(280): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.1897+124G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 11/19 | chr5 | 116003035 | |||||||
| chr5:116003187 | A | T | 10 | a0001c0002t0007g0239 a0001c0004t0001g0037 a0001c0004t0001g0038 others(7): Show |
12 | HG02258.hp1 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1898-54A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 11/19 | chr5 | 116003187 | |||||||
| chr5:116003204 | A | T | 1 | a0003c0008t0003g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1898-37A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 11/19 | chr5 | 116003204 | |||||||
| chr5:116003205 | T | G | 1 | a0003c0008t0003g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1898-36T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 11/19 | chr5 | 116003205 | |||||||
| chr5:116003206 | G | T | 1 | a0003c0008t0003g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1898-35G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 11/19 | chr5 | 116003206 | |||||||
| chr5:116003389 | A | G | 284 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(281): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.2037+9A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116003389 | |||||||
| chr5:116003434 | G | A | 1 | a0001c0002t0001g0275 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2037+54G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116003434 | |||||||
| chr5:116003567 | G | GT | 80 | a0001c0001t0001g0190 a0001c0001t0001g0226 a0001c0001t0002g0197 others(77): Show |
91 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(88): Show |
intron_variant | MODIFIER | c.2037+187_2037+188i others(3): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116003567 | |||||||
| chr5:116003567 | G | GTT | 7 | a0001c0002t0001g0270 a0003c0008t0003g0116 a0004c0012t0008g0032 others(4): Show |
8 | HG00597.hp1 HG01243.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.2037+187_2037+188i others(4): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116003567 | |||||||
| chr5:116003568 | G | T | 284 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(281): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.2037+188G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116003568 | |||||||
| chr5:116003573 | T | G | 1 | a0001c0002t0002g0233 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2037+193T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116003573 | |||||||
| chr5:116003587 | G | T | 8 | a0001c0001t0001g0209 a0001c0001t0002g0197 a0001c0001t0002g0227 others(5): Show |
8 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.2037+207G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116003587 | |||||||
| chr5:116003587 | GT | G | 263 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(260): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.2037+219delT | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr5 | 116003587 | ||||||
| chr5:116003588 | T | G | 7 | a0001c0001t0001g0209 a0001c0001t0002g0197 a0001c0001t0002g0227 others(4): Show |
7 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.2037+208T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116003588 | |||||||
| chr5:116003590 | T | G | 1 | a0001c0001t0004g0033 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2037+210T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116003590 | |||||||
| chr5:116003641 | A | G | 3 | a0002c0003t0003g0007 a0002c0003t0003g0061 a0002c0003t0003g0077 |
5 | NA18964.hp1 NA18973.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.2037+261A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116003641 | |||||||
| chr5:116003664 | C | T | 1 | a0004c0011t0017g0240 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2037+284C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116003664 | |||||||
| chr5:116003675 | G | A | 4 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0195 others(1): Show |
4 | HG00642.hp2 HG01106.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2037+295G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116003675 | |||||||
| chr5:116003730 | T | C | 1 | a0001c0002t0001g0336 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2037+350T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116003730 | |||||||
| chr5:116003737 | A | G | 1 | a0001c0002t0001g0336 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2037+357A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116003737 | |||||||
| chr5:116003798 | A | G | 1 | a0001c0004t0001g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2037+418A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116003798 | |||||||
| chr5:116003803 | A | C | 1 | a0004c0011t0008g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2037+423A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116003803 | |||||||
| chr5:116003803 | A | G | 1 | a0001c0004t0001g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2037+423A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116003803 | |||||||
| chr5:116003916 | C | T | 1 | a0002c0003t0003g0079 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2037+536C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116003916 | |||||||
| chr5:116003926 | C | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0175 a0001c0001t0001g0189 others(1): Show |
5 | HG01069.hp1 HG01071.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.2037+546C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116003926 | |||||||
| chr5:116003934 | G | A | 4 | a0001c0014t0001g0060 a0001c0014t0004g0314 a0010c0024t0001g0295 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2037+554G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116003934 | |||||||
| chr5:116004206 | A | T | 62 | a0001c0002t0001g0009 a0001c0002t0001g0039 a0001c0002t0001g0040 others(59): Show |
71 | HG00597.hp1 HG01069.hp2 HG01167.hp2 others(68): Show |
intron_variant | MODIFIER | c.2037+826A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116004206 | |||||||
| chr5:116004327 | G | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(144): Show |
173 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.2037+947G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116004327 | |||||||
| chr5:116004329 | A | T | 1 | a0001c0026t0001g0212 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2037+949A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116004329 | |||||||
| chr5:116004336 | C | A | 1 | a0001c0004t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2037+956C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116004336 | |||||||
| chr5:116004367 | G | A | 1 | a0001c0025t0001g0232 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2037+987G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116004367 | |||||||
| chr5:116004387 | C | G | 1 | a0001c0004t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2037+1007C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116004387 | |||||||
| chr5:116004440 | A | G | 2 | a0003c0005t0003g0057 a0003c0005t0003g0058 |
2 | HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2037+1060A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116004440 | |||||||
| chr5:116004448 | C | G | 251 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(248): Show |
291 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.2037+1068C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116004448 | |||||||
| chr5:116004586 | C | T | 1 | a0001c0004t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2037+1206C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116004586 | |||||||
| chr5:116004587 | G | A | 3 | a0005c0006t0004g0290 a0005c0034t0004g0199 a0014c0030t0007g0313 |
3 | HG02055.hp1 HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2037+1207G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116004587 | |||||||
| chr5:116004619 | A | G | 3 | a0001c0004t0001g0230 a0001c0004t0001g0296 a0001c0014t0004g0314 |
3 | HG02622.hp1 HG03654.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.2037+1239A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116004619 | |||||||
| chr5:116004621 | A | T | 1 | a0001c0004t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2037+1241A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116004621 | |||||||
| chr5:116004626 | A | T | 3 | a0001c0015t0015g0343 a0001c0015t0015g0344 a0001c0025t0001g0232 |
3 | HG02257.hp1 HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2037+1246A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116004626 | |||||||
| chr5:116004692 | T | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(90): Show |
114 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.2038-1220T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116004692 | |||||||
| chr5:116004798 | G | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0175 a0001c0001t0001g0189 others(1): Show |
5 | HG01069.hp1 HG01071.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.2038-1114G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116004798 | |||||||
| chr5:116004892 | A | T | 157 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(154): Show |
185 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.2038-1020A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116004892 | |||||||
| chr5:116004982 | A | C | 20 | a0001c0001t0001g0139 a0001c0004t0001g0292 a0001c0004t0001g0296 others(17): Show |
22 | HG00544.hp1 HG00609.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.2038-930A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116004982 | |||||||
| chr5:116005046 | T | A | 2 | a0001c0002t0001g0272 a0017c0029t0004g0273 |
2 | HG01192.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2038-866T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116005046 | |||||||
| chr5:116005060 | T | C | 1 | a0001c0004t0001g0302 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2038-852T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116005060 | |||||||
| chr5:116005135 | A | G | 1 | a0003c0005t0005g0070 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2038-777A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116005135 | |||||||
| chr5:116005304 | C | A | 4 | a0001c0002t0001g0044 a0001c0002t0002g0235 a0001c0002t0007g0341 others(1): Show |
5 | HG02896.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2038-608C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116005304 | |||||||
| chr5:116005323 | A | G | 2 | a0003c0005t0003g0057 a0003c0005t0003g0058 |
2 | HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2038-589A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116005323 | |||||||
| chr5:116005331 | A | G | 146 | a0001c0001t0001g0139 a0001c0001t0001g0165 a0001c0001t0002g0148 others(143): Show |
168 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.2038-581A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116005331 | |||||||
| chr5:116005355 | G | C | 1 | a0002c0003t0003g0063 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2038-557G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116005355 | |||||||
| chr5:116005406 | C | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0177 a0004c0007t0004g0176 |
4 | NA18951.hp2 NA18984.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.2038-506C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116005406 | |||||||
| chr5:116005509 | C | T | 3 | a0001c0004t0001g0288 a0001c0004t0001g0289 a0001c0004t0001g0339 |
3 | HG01884.hp2 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2038-403C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116005509 | |||||||
| chr5:116005659 | G | A | 4 | a0001c0002t0001g0044 a0001c0002t0002g0235 a0001c0002t0007g0341 others(1): Show |
5 | HG02896.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2038-253G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116005659 | |||||||
| chr5:116005710 | A | G | 1 | a0001c0002t0002g0233 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2038-202A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116005710 | |||||||
| chr5:116005713 | G | C | 1 | a0001c0002t0001g0337 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2038-199G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116005713 | |||||||
| chr5:116005861 | C | A | 2 | a0005c0006t0004g0010 a0005c0006t0004g0312 |
4 | NA18946.hp1 NA18991.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.2038-51C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116005861 | |||||||
| chr5:116005862 | G | A | 5 | a0001c0002t0001g0238 a0001c0004t0002g0042 a0001c0014t0001g0060 others(2): Show |
6 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2038-50G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 12/19 | chr5 | 116005862 | |||||||
| chr5:116005970 | G | A | 1 | a0001c0004t0002g0042 | 2 | HG01243.hp1 HG03139.hp2 |
splice_region_variant&intron_variant | LOW | c.2093+3G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116005970 | |||||||
| chr5:116006101 | T | C | 3 | a0003c0005t0003g0048 a0003c0005t0003g0049 a0003c0005t0006g0052 |
3 | HG02145.hp1 HG02735.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2093+134T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116006101 | |||||||
| chr5:116006167 | G | A | 2 | a0014c0030t0007g0313 a0022c0031t0004g0122 |
2 | HG02055.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2093+200G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116006167 | |||||||
| chr5:116006169 | A | C | 5 | a0004c0011t0008g0281 a0004c0012t0008g0032 a0004c0012t0008g0193 others(2): Show |
6 | HG01243.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2093+202A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116006169 | |||||||
| chr5:116006195 | G | A | 6 | a0001c0001t0002g0219 a0003c0005t0003g0056 a0003c0005t0005g0013 others(3): Show |
7 | HG01257.hp1 HG01496.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.2093+228G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116006195 | |||||||
| chr5:116006264 | G | C | 1 | a0001c0001t0001g0203 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2093+297G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116006264 | |||||||
| chr5:116006286 | C | T | 5 | a0003c0005t0003g0094 a0005c0006t0004g0010 a0005c0006t0004g0308 others(2): Show |
7 | HG02074.hp2 HG02523.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.2093+319C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116006286 | |||||||
| chr5:116006341 | C | G | 69 | a0001c0001t0001g0139 a0001c0001t0001g0162 a0001c0001t0001g0163 others(66): Show |
78 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.2093+374C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116006341 | |||||||
| chr5:116006362 | G | T | 8 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0002t0001g0272 others(5): Show |
10 | HG01106.hp1 HG01192.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.2093+395G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116006362 | |||||||
| chr5:116006529 | G | T | 7 | a0001c0004t0001g0037 a0001c0004t0001g0038 a0001c0004t0001g0248 others(4): Show |
9 | HG02258.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2093+562G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116006529 | |||||||
| chr5:116006734 | A | T | 9 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0002t0001g0272 others(6): Show |
11 | HG01106.hp1 HG01192.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.2093+767A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116006734 | |||||||
| chr5:116006745 | G | A | 1 | a0001c0004t0002g0042 | 2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2093+778G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116006745 | |||||||
| chr5:116006785 | A | G | 1 | a0001c0002t0002g0233 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2093+818A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116006785 | |||||||
| chr5:116006862 | A | T | 268 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(265): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.2093+895A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116006862 | |||||||
| chr5:116007006 | T | C | 29 | a0001c0001t0002g0204 a0001c0002t0001g0315 a0001c0002t0001g0336 others(26): Show |
33 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.2093+1039T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116007006 | |||||||
| chr5:116007026 | C | G | 1 | a0001c0002t0002g0326 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2093+1059C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116007026 | |||||||
| chr5:116007045 | A | G | 4 | a0001c0002t0002g0320 a0001c0002t0002g0321 a0001c0002t0002g0330 others(1): Show |
4 | HG01109.hp2 HG01257.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.2093+1078A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116007045 | |||||||
| chr5:116007139 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2093+1172A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116007139 | |||||||
| chr5:116007151 | T | C | 1 | a0010c0032t0001g0241 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2093+1184T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116007151 | |||||||
| chr5:116007163 | T | C | 1 | a0001c0004t0001g0292 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2093+1196T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116007163 | |||||||
| chr5:116007216 | T | A | 68 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(65): Show |
80 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.2093+1249T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116007216 | |||||||
| chr5:116007273 | T | C | 2 | a0005c0006t0004g0308 a0005c0006t0004g0310 |
2 | HG02074.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.2093+1306T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116007273 | |||||||
| chr5:116007300 | T | G | 7 | a0001c0004t0001g0037 a0001c0004t0001g0038 a0001c0004t0001g0248 others(4): Show |
9 | HG02258.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2093+1333T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116007300 | |||||||
| chr5:116007359 | T | C | 1 | a0001c0002t0013g0335 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2093+1392T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116007359 | |||||||
| chr5:116007449 | A | T | 67 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(64): Show |
76 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.2093+1482A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116007449 | |||||||
| chr5:116007585 | A | G | 1 | a0001c0001t0002g0035 | 2 | HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2093+1618A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116007585 | |||||||
| chr5:116007621 | T | C | 68 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(65): Show |
80 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.2093+1654T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116007621 | |||||||
| chr5:116007638 | T | C | 68 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(65): Show |
80 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.2093+1671T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116007638 | |||||||
| chr5:116007673 | C | T | 7 | a0001c0004t0004g0293 a0001c0004t0004g0294 a0001c0014t0004g0314 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2093+1706C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116007673 | |||||||
| chr5:116007676 | C | T | 3 | a0001c0001t0002g0137 a0001c0001t0002g0138 a0001c0001t0002g0167 |
3 | HG02280.hp1 HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2093+1709C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116007676 | |||||||
| chr5:116007687 | A | G | 264 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(261): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.2093+1720A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116007687 | |||||||
| chr5:116007760 | G | A | 1 | a0003c0005t0003g0097 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2093+1793G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116007760 | |||||||
| chr5:116007773 | A | C | 3 | a0001c0001t0002g0144 a0001c0004t0002g0303 a0006c0009t0002g0026 |
4 | HG01255.hp1 HG02148.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.2093+1806A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116007773 | |||||||
| chr5:116007809 | G | C | 148 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(145): Show |
172 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.2093+1842G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116007809 | |||||||
| chr5:116007829 | A | T | 1 | a0001c0001t0001g0206 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2093+1862A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116007829 | |||||||
| chr5:116007877 | G | A | 1 | a0001c0004t0002g0042 | 2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2093+1910G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116007877 | |||||||
| chr5:116007887 | A | G | 8 | a0001c0002t0001g0336 a0001c0002t0001g0337 a0001c0002t0002g0278 others(5): Show |
8 | HG01891.hp1 HG02572.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2093+1920A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116007887 | |||||||
| chr5:116007980 | G | C | 280 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(277): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.2093+2013G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116007980 | |||||||
| chr5:116007996 | C | T | 1 | a0004c0012t0002g0223 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2093+2029C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116007996 | |||||||
| chr5:116008022 | C | T | 155 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(152): Show |
181 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.2093+2055C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116008022 | |||||||
| chr5:116008079 | T | C | 265 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(262): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.2093+2112T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116008079 | |||||||
| chr5:116008080 | G | A | 8 | a0001c0004t0001g0037 a0001c0004t0001g0038 a0001c0004t0001g0230 others(5): Show |
10 | HG02258.hp1 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.2093+2113G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116008080 | |||||||
| chr5:116008089 | C | T | 1 | a0010c0032t0001g0241 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2093+2122C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116008089 | |||||||
| chr5:116008104 | G | A | 156 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(153): Show |
182 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.2093+2137G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116008104 | |||||||
| chr5:116008236 | C | T | 155 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(152): Show |
181 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.2093+2269C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116008236 | |||||||
| chr5:116008261 | A | G | 157 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(154): Show |
183 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.2093+2294A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116008261 | |||||||
| chr5:116008270 | G | A | 3 | a0003c0005t0003g0056 a0003c0005t0005g0013 a0003c0005t0005g0054 |
4 | HG01891.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2093+2303G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116008270 | |||||||
| chr5:116008304 | G | A | 1 | a0004c0012t0002g0223 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2093+2337G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116008304 | |||||||
| chr5:116008438 | T | C | 4 | a0001c0002t0001g0044 a0001c0002t0002g0235 a0001c0002t0007g0341 others(1): Show |
5 | HG02896.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2094-2303T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116008438 | |||||||
| chr5:116008527 | C | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(154): Show |
183 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.2094-2214C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116008527 | |||||||
| chr5:116008603 | A | AATG | 155 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(152): Show |
180 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.2094-2138_2094-213 others(7): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116008603 | |||||||
| chr5:116008604 | T | A | 156 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(153): Show |
181 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.2094-2137T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116008604 | |||||||
| chr5:116008606 | A | G | 1 | a0001c0001t0002g0178 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2094-2135A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116008606 | |||||||
| chr5:116008606 | A | T | 155 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(152): Show |
180 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.2094-2135A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116008606 | |||||||
| chr5:116008699 | C | T | 9 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0002t0001g0272 others(6): Show |
11 | HG01106.hp1 HG01192.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.2094-2042C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116008699 | |||||||
| chr5:116008728 | C | T | 4 | a0001c0002t0001g0044 a0001c0002t0002g0235 a0001c0002t0007g0341 others(1): Show |
5 | HG02896.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2094-2013C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116008728 | |||||||
| chr5:116008833 | T | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(154): Show |
183 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.2094-1908T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116008833 | |||||||
| chr5:116008864 | A | G | 6 | a0001c0001t0002g0219 a0003c0005t0003g0056 a0003c0005t0005g0013 others(3): Show |
7 | HG01257.hp1 HG01496.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.2094-1877A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116008864 | |||||||
| chr5:116009111 | C | T | 1 | a0002c0003t0005g0016 | 2 | HG00639.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.2094-1630C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116009111 | |||||||
| chr5:116009129 | G | C | 70 | a0001c0001t0001g0139 a0001c0001t0001g0162 a0001c0001t0001g0163 others(67): Show |
79 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.2094-1612G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116009129 | |||||||
| chr5:116009298 | A | G | 2 | a0001c0001t0001g0134 a0003c0005t0003g0097 |
2 | HG01943.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.2094-1443A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116009298 | |||||||
| chr5:116009324 | C | A | 1 | a0010c0032t0001g0241 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2094-1417C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116009324 | |||||||
| chr5:116009337 | A | T | 2 | a0001c0002t0001g0250 a0001c0002t0001g0269 |
2 | NA18985.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.2094-1404A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116009337 | |||||||
| chr5:116009418 | G | A | 268 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(265): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.2094-1323G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116009418 | |||||||
| chr5:116009488 | A | G | 2 | a0014c0030t0007g0313 a0022c0031t0004g0122 |
2 | HG02055.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2094-1253A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116009488 | |||||||
| chr5:116009574 | G | C | 1 | a0004c0011t0017g0240 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2094-1167G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116009574 | |||||||
| chr5:116009683 | A | C | 1 | a0003c0005t0003g0057 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2094-1058A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116009683 | |||||||
| chr5:116009725 | C | T | 1 | a0001c0015t0015g0343 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2094-1016C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116009725 | |||||||
| chr5:116009831 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0002g0140 |
2 | HG00621.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.2094-910A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116009831 | |||||||
| chr5:116009842 | C | T | 151 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(148): Show |
175 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.2094-899C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116009842 | |||||||
| chr5:116009878 | A | G | 68 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(65): Show |
80 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.2094-863A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116009878 | |||||||
| chr5:116009888 | A | T | 1 | a0004c0012t0002g0223 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2094-853A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116009888 | |||||||
| chr5:116009899 | C | T | 7 | a0001c0004t0001g0037 a0001c0004t0001g0038 a0001c0004t0001g0248 others(4): Show |
9 | HG02258.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2094-842C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116009899 | |||||||
| chr5:116009905 | G | C | 1 | a0003c0008t0003g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2094-836G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116009905 | |||||||
| chr5:116009997 | T | C | 2 | a0009c0016t0002g0243 a0009c0016t0002g0244 |
2 | HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2094-744T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116009997 | |||||||
| chr5:116010092 | A | T | 7 | a0001c0004t0001g0037 a0001c0004t0001g0038 a0001c0004t0001g0248 others(4): Show |
9 | HG02258.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2094-649A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116010092 | |||||||
| chr5:116010115 | A | G | 68 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(65): Show |
80 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.2094-626A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116010115 | |||||||
| chr5:116010238 | A | G | 1 | a0001c0001t0002g0214 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2094-503A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116010238 | |||||||
| chr5:116010436 | G | A | 1 | a0001c0004t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2094-305G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116010436 | |||||||
| chr5:116010469 | C | A | 1 | a0001c0001t0001g0161 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2094-272C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116010469 | |||||||
| chr5:116010475 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2094-266C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116010475 | |||||||
| chr5:116010548 | T | G | 74 | a0001c0001t0001g0155 a0001c0002t0001g0043 a0001c0002t0001g0238 others(71): Show |
98 | HG00544.hp2 HG00609.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.2094-193T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116010548 | |||||||
| chr5:116010677 | G | A | 1 | a0001c0004t0001g0296 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2094-64G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116010677 | |||||||
| chr5:116010697 | G | A | 5 | a0001c0001t0002g0137 a0001c0001t0002g0138 a0001c0001t0002g0167 others(2): Show |
5 | HG02055.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2094-44G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 13/19 | chr5 | 116010697 | |||||||
| chr5:116010935 | C | T | 64 | a0001c0001t0001g0139 a0001c0001t0001g0163 a0001c0001t0001g0203 others(61): Show |
72 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.2247+41C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116010935 | |||||||
| chr5:116011004 | C | CAT | 3 | a0001c0002t0002g0332 a0001c0014t0001g0060 a0003c0005t0005g0055 |
3 | HG01109.hp2 HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2247+131_2247+132d others(4): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr5 | 116011004 | ||||||
| chr5:116011004 | CAT | C | 87 | a0001c0001t0001g0155 a0001c0001t0001g0162 a0001c0001t0002g0219 others(84): Show |
111 | HG00544.hp2 HG00609.hp2 HG00639.hp2 others(108): Show |
intron_variant | MODIFIER | c.2247+131_2247+132d others(4): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr5 | 116011004 | ||||||
| chr5:116011004 | CATAT | C | 65 | a0001c0001t0001g0139 a0001c0001t0001g0163 a0001c0001t0001g0203 others(62): Show |
73 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.2247+129_2247+132d others(6): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr5 | 116011004 | ||||||
| chr5:116011004 | CATATAT | C | 86 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(83): Show |
103 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.2247+127_2247+132d others(8): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr5 | 116011004 | ||||||
| chr5:116011018 | T | TATCTTTT others(132): Show |
70 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(67): Show |
79 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.2247+126_2247+127i others(141): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr5 | 116011018 | ||||||
| chr5:116011023 | A | T | 70 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(67): Show |
79 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.2247+129A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116011023 | |||||||
| chr5:116011025 | A | T | 70 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(67): Show |
79 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.2247+131A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116011025 | |||||||
| chr5:116011027 | G | C | 70 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(67): Show |
79 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.2247+133G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116011027 | |||||||
| chr5:116011028 | G | A | 70 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(67): Show |
79 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.2247+134G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116011028 | |||||||
| chr5:116011029 | A | T | 70 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(67): Show |
79 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.2247+135A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116011029 | |||||||
| chr5:116011031 | G | A | 245 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(242): Show |
297 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(294): Show |
intron_variant | MODIFIER | c.2247+137G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116011031 | |||||||
| chr5:116011034 | T | G | 70 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(67): Show |
79 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.2247+140T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116011034 | |||||||
| chr5:116011035 | A | T | 70 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(67): Show |
79 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.2247+141A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116011035 | |||||||
| chr5:116011036 | TAC | T | 70 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(67): Show |
79 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.2247+144_2247+145d others(4): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr5 | 116011036 | ||||||
| chr5:116011041 | T | G | 70 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(67): Show |
79 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.2247+147T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116011041 | |||||||
| chr5:116011155 | C | G | 67 | a0001c0001t0001g0139 a0001c0001t0001g0162 a0001c0001t0001g0163 others(64): Show |
76 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.2247+261C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116011155 | |||||||
| chr5:116011162 | A | G | 1 | a0006c0009t0002g0173 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2247+268A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116011162 | |||||||
| chr5:116011190 | G | GT | 135 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(132): Show |
158 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.2247+309dupT | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr5 | 116011190 | ||||||
| chr5:116011190 | G | GTT | 52 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(49): Show |
55 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.2247+308_2247+309d others(4): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr5 | 116011190 | ||||||
| chr5:116011190 | G | GTTT | 22 | a0001c0001t0001g0046 a0001c0001t0001g0161 a0001c0001t0002g0133 others(19): Show |
28 | HG00099.hp2 HG00621.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.2247+307_2247+309d others(5): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr5 | 116011190 | ||||||
| chr5:116011212 | G | C | 1 | a0001c0025t0001g0232 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2247+318G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116011212 | |||||||
| chr5:116011268 | A | C | 2 | a0005c0006t0004g0290 a0005c0034t0004g0199 |
2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2247+374A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116011268 | |||||||
| chr5:116011293 | T | G | 1 | a0001c0004t0002g0042 | 2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2247+399T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116011293 | |||||||
| chr5:116011296 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2247+402A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116011296 | |||||||
| chr5:116011312 | G | A | 9 | a0001c0004t0001g0037 a0001c0004t0001g0038 a0001c0004t0001g0230 others(6): Show |
11 | HG02258.hp1 HG02630.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2247+418G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116011312 | |||||||
| chr5:116011322 | T | G | 8 | a0001c0002t0001g0336 a0001c0002t0001g0337 a0001c0002t0002g0278 others(5): Show |
8 | HG01891.hp1 HG02572.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2247+428T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116011322 | |||||||
| chr5:116011487 | A | C | 6 | a0003c0005t0003g0094 a0005c0006t0004g0010 a0005c0006t0004g0308 others(3): Show |
8 | HG02074.hp2 HG02523.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.2247+593A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116011487 | |||||||
| chr5:116011507 | G | A | 1 | a0001c0002t0002g0323 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2247+613G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116011507 | |||||||
| chr5:116011600 | A | G | 301 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(298): Show |
360 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(357): Show |
intron_variant | MODIFIER | c.2247+706A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116011600 | |||||||
| chr5:116011629 | G | A | 1 | a0004c0007t0002g0215 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2247+735G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116011629 | |||||||
| chr5:116011804 | T | C | 218 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(215): Show |
251 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.2248-570T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116011804 | |||||||
| chr5:116011806 | T | C | 1 | a0001c0004t0004g0231 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2248-568T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116011806 | |||||||
| chr5:116011808 | A | T | 68 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(65): Show |
80 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.2248-566A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116011808 | |||||||
| chr5:116011819 | G | A | 2 | a0014c0030t0007g0313 a0022c0031t0004g0122 |
2 | HG02055.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2248-555G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116011819 | |||||||
| chr5:116011897 | A | G | 66 | a0001c0001t0001g0139 a0001c0001t0001g0162 a0001c0001t0001g0163 others(63): Show |
75 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.2248-477A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116011897 | |||||||
| chr5:116012105 | A | C | 5 | a0001c0001t0002g0137 a0001c0001t0002g0138 a0001c0001t0002g0167 others(2): Show |
5 | HG02055.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2248-269A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116012105 | |||||||
| chr5:116012223 | A | G | 2 | a0005c0006t0004g0290 a0005c0034t0004g0199 |
2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2248-151A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116012223 | |||||||
| chr5:116012350 | G | C | 1 | a0003c0008t0003g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2248-24G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 14/19 | chr5 | 116012350 | |||||||
| chr5:116012481 | T | C | 2 | a0005c0006t0004g0290 a0005c0034t0004g0199 |
2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2342+13T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/19 | chr5 | 116012481 | |||||||
| chr5:116012503 | A | G | 5 | a0001c0001t0002g0137 a0001c0001t0002g0138 a0001c0001t0002g0167 others(2): Show |
5 | HG02055.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2342+35A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/19 | chr5 | 116012503 | |||||||
| chr5:116012604 | C | G | 1 | a0001c0002t0004g0287 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2342+136C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/19 | chr5 | 116012604 | |||||||
| chr5:116012644 | A | G | 315 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(312): Show |
376 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(373): Show |
intron_variant | MODIFIER | c.2342+176A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/19 | chr5 | 116012644 | |||||||
| chr5:116012657 | T | TTAATTTA others(19): Show |
1 | a0001c0001t0001g0046 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2342+192_2342+217d others(28): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr5 | 116012657 | ||||||
| chr5:116012714 | C | A | 1 | a0003c0008t0003g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2342+246C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/19 | chr5 | 116012714 | |||||||
| chr5:116012800 | T | G | 1 | a0010c0032t0001g0241 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2342+332T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/19 | chr5 | 116012800 | |||||||
| chr5:116012839 | T | C | 2 | a0001c0015t0015g0343 a0001c0015t0015g0344 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2342+371T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/19 | chr5 | 116012839 | |||||||
| chr5:116012934 | A | C | 1 | a0001c0001t0001g0177 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2342+466A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/19 | chr5 | 116012934 | |||||||
| chr5:116013058 | G | T | 1 | a0002c0003t0003g0077 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2342+590G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/19 | chr5 | 116013058 | |||||||
| chr5:116013065 | G | C | 71 | a0001c0001t0001g0139 a0001c0001t0001g0163 a0001c0001t0001g0203 others(68): Show |
80 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.2342+597G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/19 | chr5 | 116013065 | |||||||
| chr5:116013119 | G | A | 65 | a0001c0001t0001g0155 a0001c0002t0001g0252 a0001c0002t0002g0253 others(62): Show |
86 | HG00544.hp2 HG00609.hp2 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.2342+651G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/19 | chr5 | 116013119 | |||||||
| chr5:116013135 | C | A | 3 | a0001c0001t0002g0219 a0003c0005t0005g0113 a0018c0020t0005g0091 |
3 | HG01257.hp1 HG01496.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2342+667C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/19 | chr5 | 116013135 | |||||||
| chr5:116013135 | C | G | 1 | a0001c0001t0004g0180 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2342+667C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/19 | chr5 | 116013135 | |||||||
| chr5:116013185 | A | G | 3 | a0001c0001t0001g0143 a0001c0001t0001g0145 a0001c0004t0001g0300 |
3 | HG01167.hp1 HG01934.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.2342+717A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/19 | chr5 | 116013185 | |||||||
| chr5:116013197 | C | G | 1 | a0001c0001t0001g0130 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2342+729C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/19 | chr5 | 116013197 | |||||||
| chr5:116013441 | C | G | 2 | a0001c0004t0001g0236 a0001c0004t0001g0237 |
2 | HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2342+973C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/19 | chr5 | 116013441 | |||||||
| chr5:116013606 | C | A | 75 | a0001c0001t0001g0139 a0001c0001t0001g0162 a0001c0001t0001g0163 others(72): Show |
84 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.2343-814C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/19 | chr5 | 116013606 | |||||||
| chr5:116013678 | C | T | 310 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(307): Show |
370 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(367): Show |
intron_variant | MODIFIER | c.2343-742C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/19 | chr5 | 116013678 | |||||||
| chr5:116013698 | G | A | 1 | a0001c0001t0002g0219 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2343-722G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/19 | chr5 | 116013698 | |||||||
| chr5:116013741 | C | G | 2 | a0001c0004t0001g0236 a0001c0004t0001g0237 |
2 | HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2343-679C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/19 | chr5 | 116013741 | |||||||
| chr5:116013825 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2343-595A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/19 | chr5 | 116013825 | |||||||
| chr5:116013845 | G | T | 2 | a0001c0036t0004g0196 a0004c0012t0002g0223 |
2 | HG02451.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2343-575G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/19 | chr5 | 116013845 | |||||||
| chr5:116013850 | C | A | 11 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0002g0127 others(8): Show |
13 | HG00140.hp2 HG01106.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.2343-570C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/19 | chr5 | 116013850 | |||||||
| chr5:116013878 | A | C | 8 | a0001c0001t0002g0137 a0001c0001t0002g0138 a0001c0001t0002g0167 others(5): Show |
8 | HG02055.hp1 HG02280.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2343-542A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/19 | chr5 | 116013878 | |||||||
| chr5:116013985 | A | G | 69 | a0001c0001t0001g0139 a0001c0001t0001g0162 a0001c0001t0001g0163 others(66): Show |
78 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.2343-435A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/19 | chr5 | 116013985 | |||||||
| chr5:116014026 | T | C | 64 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(61): Show |
73 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.2343-394T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/19 | chr5 | 116014026 | |||||||
| chr5:116014329 | C | T | 2 | a0001c0002t0007g0338 a0004c0011t0017g0240 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2343-91C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 15/19 | chr5 | 116014329 | |||||||
| chr5:116014559 | T | A | 1 | a0001c0001t0001g0046 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2450+32T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 16/19 | chr5 | 116014559 | |||||||
| chr5:116014565 | A | G | 2 | a0002c0003t0006g0069 a0002c0003t0006g0092 |
2 | HG00673.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.2450+38A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 16/19 | chr5 | 116014565 | |||||||
| chr5:116014683 | G | A | 5 | a0001c0004t0001g0038 a0001c0004t0001g0248 a0001c0004t0008g0246 others(2): Show |
6 | HG02258.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2450+156G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 16/19 | chr5 | 116014683 | |||||||
| chr5:116014729 | A | G | 4 | a0001c0002t0002g0320 a0001c0002t0002g0321 a0001c0002t0002g0330 others(1): Show |
4 | HG01109.hp2 HG01257.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.2450+202A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 16/19 | chr5 | 116014729 | |||||||
| chr5:116014801 | T | G | 1 | a0001c0001t0001g0046 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2450+274T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 16/19 | chr5 | 116014801 | |||||||
| chr5:116014810 | G | A | 2 | a0001c0036t0004g0196 a0004c0012t0002g0223 |
2 | HG02451.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2450+283G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 16/19 | chr5 | 116014810 | |||||||
| chr5:116014837 | T | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0029 others(61): Show |
76 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.2450+310T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 16/19 | chr5 | 116014837 | |||||||
| chr5:116014994 | A | G | 3 | a0001c0004t0001g0288 a0001c0004t0001g0289 a0001c0004t0001g0339 |
3 | HG01884.hp2 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2451-258A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 16/19 | chr5 | 116014994 | |||||||
| chr5:116014996 | A | C | 2 | a0001c0002t0001g0238 a0001c0014t0001g0060 |
2 | HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2451-256A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 16/19 | chr5 | 116014996 | |||||||
| chr5:116015453 | T | G | 254 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(251): Show |
305 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(302): Show |
intron_variant | MODIFIER | c.2618+34T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 17/19 | chr5 | 116015453 | |||||||
| chr5:116015500 | G | T | 1 | a0001c0017t0004g0132 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2618+81G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 17/19 | chr5 | 116015500 | |||||||
| chr5:116015527 | G | A | 100 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0155 others(97): Show |
129 | HG00140.hp2 HG00544.hp2 HG00609.hp2 others(126): Show |
intron_variant | MODIFIER | c.2619-101G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 17/19 | chr5 | 116015527 | |||||||
| chr5:116015544 | C | A | 76 | a0001c0001t0001g0139 a0001c0001t0001g0162 a0001c0001t0001g0163 others(73): Show |
87 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.2619-84C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 17/19 | chr5 | 116015544 | |||||||
| chr5:116015557 | AT | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0045 a0001c0001t0001g0171 others(1): Show |
6 | NA18952.hp1 NA18969.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2619-67delT | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr5 | 116015557 | ||||||
| chr5:116015598 | A | G | 6 | a0003c0005t0003g0094 a0005c0006t0004g0010 a0005c0006t0004g0308 others(3): Show |
8 | HG02074.hp2 HG02523.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.2619-30A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 17/19 | chr5 | 116015598 | |||||||
| chr5:116015801 | C | T | 316 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(313): Show |
377 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(374): Show |
intron_variant | MODIFIER | c.2756+36C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116015801 | |||||||
| chr5:116015819 | A | G | 1 | a0018c0020t0005g0091 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2756+54A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116015819 | |||||||
| chr5:116015821 | G | T | 1 | a0001c0001t0002g0204 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2756+56G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116015821 | |||||||
| chr5:116015834 | C | G | 1 | a0001c0002t0002g0262 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2756+69C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116015834 | |||||||
| chr5:116015958 | A | G | 2 | a0001c0015t0015g0343 a0001c0015t0015g0344 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2756+193A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116015958 | |||||||
| chr5:116016141 | G | A | 3 | a0001c0001t0002g0219 a0003c0005t0005g0113 a0018c0020t0005g0091 |
3 | HG01257.hp1 HG01496.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2756+376G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116016141 | |||||||
| chr5:116016260 | A | T | 1 | a0001c0001t0002g0172 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2756+495A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116016260 | |||||||
| chr5:116016305 | C | T | 6 | a0001c0001t0002g0137 a0001c0001t0002g0138 a0001c0001t0002g0167 others(3): Show |
6 | HG02055.hp1 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2756+540C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116016305 | |||||||
| chr5:116016326 | C | T | 3 | a0001c0004t0001g0292 a0001c0004t0002g0307 a0001c0004t0004g0306 |
3 | NA18951.hp1 NA18973.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.2756+561C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116016326 | |||||||
| chr5:116016460 | T | A | 1 | a0001c0002t0002g0278 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2756+695T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116016460 | |||||||
| chr5:116016473 | C | A | 6 | a0001c0001t0002g0137 a0001c0001t0002g0138 a0001c0001t0002g0167 others(3): Show |
6 | HG02055.hp1 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2756+708C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116016473 | |||||||
| chr5:116016519 | C | T | 25 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0002g0127 others(22): Show |
29 | HG00140.hp2 HG01106.hp1 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.2756+754C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116016519 | |||||||
| chr5:116016604 | A | G | 66 | a0001c0001t0001g0139 a0001c0001t0001g0162 a0001c0001t0001g0163 others(63): Show |
75 | HG00597.hp1 HG00609.hp1 HG01167.hp2 others(72): Show |
intron_variant | MODIFIER | c.2756+839A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116016604 | |||||||
| chr5:116016654 | A | C | 1 | a0001c0004t0001g0037 | 2 | HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2756+889A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116016654 | |||||||
| chr5:116016654 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2756+889A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116016654 | |||||||
| chr5:116016656 | A | C | 1 | a0010c0032t0001g0241 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2756+891A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116016656 | |||||||
| chr5:116016725 | G | T | 1 | a0001c0001t0001g0046 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2756+960G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116016725 | |||||||
| chr5:116016741 | ACT | A | 3 | a0001c0001t0002g0219 a0003c0005t0005g0113 a0018c0020t0005g0091 |
3 | HG01257.hp1 HG01496.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2756+978_2756+979d others(4): Show |
LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 116016741 | ||||||
| chr5:116016757 | T | C | 5 | a0001c0001t0002g0219 a0001c0015t0015g0343 a0001c0015t0015g0344 others(2): Show |
5 | HG01257.hp1 HG01496.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2756+992T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116016757 | |||||||
| chr5:116016852 | T | G | 1 | a0001c0001t0004g0222 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2756+1087T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116016852 | |||||||
| chr5:116016863 | T | A | 3 | a0001c0001t0002g0219 a0003c0005t0005g0113 a0018c0020t0005g0091 |
3 | HG01257.hp1 HG01496.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2756+1098T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116016863 | |||||||
| chr5:116016863 | TA | T | 70 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(67): Show |
81 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.2756+1107delA | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 116016863 | ||||||
| chr5:116016873 | C | A | 3 | a0001c0001t0002g0219 a0003c0005t0005g0113 a0018c0020t0005g0091 |
3 | HG01257.hp1 HG01496.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2756+1108C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116016873 | |||||||
| chr5:116016941 | G | T | 67 | a0001c0001t0001g0155 a0001c0002t0001g0043 a0001c0002t0001g0238 others(64): Show |
91 | HG00544.hp2 HG00609.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.2756+1176G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116016941 | |||||||
| chr5:116016970 | C | T | 3 | a0001c0001t0002g0219 a0003c0005t0005g0113 a0018c0020t0005g0091 |
3 | HG01257.hp1 HG01496.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2756+1205C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116016970 | |||||||
| chr5:116016986 | G | A | 9 | a0001c0001t0002g0142 a0001c0001t0002g0178 a0001c0001t0002g0181 others(6): Show |
9 | HG00735.hp1 HG00735.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.2756+1221G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116016986 | |||||||
| chr5:116017031 | A | G | 3 | a0001c0001t0002g0219 a0003c0005t0005g0113 a0018c0020t0005g0091 |
3 | HG01257.hp1 HG01496.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2756+1266A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116017031 | |||||||
| chr5:116017082 | G | A | 2 | a0003c0005t0005g0113 a0018c0020t0005g0091 |
2 | HG01496.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2756+1317G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116017082 | |||||||
| chr5:116017130 | T | C | 13 | a0001c0001t0001g0031 a0001c0001t0001g0177 a0001c0001t0001g0179 others(10): Show |
17 | HG00544.hp1 HG01978.hp1 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.2756+1365T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116017130 | |||||||
| chr5:116017138 | C | G | 1 | a0004c0012t0002g0223 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2756+1373C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116017138 | |||||||
| chr5:116017140 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2756+1375A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116017140 | |||||||
| chr5:116017158 | C | A | 1 | a0001c0001t0001g0046 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2756+1393C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116017158 | |||||||
| chr5:116017212 | C | T | 1 | a0001c0014t0004g0314 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2756+1447C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116017212 | |||||||
| chr5:116017340 | G | A | 1 | a0006c0009t0002g0173 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2756+1575G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116017340 | |||||||
| chr5:116017347 | T | A | 26 | a0001c0001t0001g0139 a0001c0001t0002g0142 a0001c0001t0002g0205 others(23): Show |
30 | HG00099.hp1 HG00609.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.2756+1582T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116017347 | |||||||
| chr5:116017383 | C | T | 14 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0134 others(11): Show |
17 | HG00408.hp1 HG00642.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.2756+1618C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116017383 | |||||||
| chr5:116017401 | A | C | 1 | a0001c0001t0001g0046 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2756+1636A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116017401 | |||||||
| chr5:116017402 | C | A | 1 | a0001c0001t0001g0046 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2756+1637C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116017402 | |||||||
| chr5:116017461 | T | G | 1 | a0001c0001t0001g0046 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2756+1696T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116017461 | |||||||
| chr5:116017506 | G | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0177 a0001c0001t0001g0179 |
4 | HG01978.hp1 NA18951.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.2756+1741G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116017506 | |||||||
| chr5:116017507 | A | G | 4 | a0001c0001t0002g0138 a0003c0005t0003g0057 a0003c0005t0003g0058 others(1): Show |
4 | HG02280.hp1 HG02486.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2756+1742A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116017507 | |||||||
| chr5:116017580 | T | C | 2 | a0001c0001t0001g0201 a0001c0004t0001g0234 |
2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2756+1815T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116017580 | |||||||
| chr5:116017672 | T | C | 80 | a0001c0001t0001g0002 a0001c0001t0001g0123 a0001c0001t0001g0155 others(77): Show |
102 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.2756+1907T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116017672 | |||||||
| chr5:116017673 | A | C | 1 | a0001c0001t0001g0046 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2756+1908A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116017673 | |||||||
| chr5:116017674 | A | C | 9 | a0001c0001t0001g0201 a0001c0002t0001g0043 a0001c0002t0001g0044 others(6): Show |
11 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2756+1909A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116017674 | |||||||
| chr5:116017700 | A | G | 1 | a0002c0003t0019g0108 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2756+1935A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116017700 | |||||||
| chr5:116017813 | T | C | 3 | a0001c0036t0004g0196 a0004c0012t0013g0192 a0022c0031t0004g0122 |
3 | HG02451.hp2 HG02615.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2756+2048T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116017813 | |||||||
| chr5:116017869 | A | G | 1 | a0001c0001t0004g0202 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2756+2104A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116017869 | |||||||
| chr5:116017971 | C | T | 38 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0029 others(35): Show |
44 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.2756+2206C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116017971 | |||||||
| chr5:116018001 | C | T | 2 | a0003c0005t0003g0056 a0010c0032t0001g0241 |
2 | HG01891.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2756+2236C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116018001 | |||||||
| chr5:116018098 | C | CA | 11 | a0001c0002t0001g0238 a0001c0002t0013g0335 a0001c0004t0008g0246 others(8): Show |
12 | HG01496.hp1 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.2756+2338dupA | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 116018098 | ||||||
| chr5:116018121 | C | T | 1 | a0001c0001t0002g0182 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2756+2356C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116018121 | |||||||
| chr5:116018122 | G | A | 2 | a0001c0001t0001g0194 a0002c0003t0003g0090 |
2 | HG00639.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.2756+2357G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116018122 | |||||||
| chr5:116018130 | A | G | 1 | a0001c0001t0002g0158 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2756+2365A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116018130 | |||||||
| chr5:116018229 | C | T | 1 | a0001c0004t0008g0246 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2756+2464C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116018229 | |||||||
| chr5:116018262 | C | G | 4 | a0001c0002t0001g0336 a0001c0002t0001g0337 a0001c0014t0001g0060 others(1): Show |
4 | HG01891.hp1 HG02486.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2756+2497C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116018262 | |||||||
| chr5:116018307 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2756+2542G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116018307 | |||||||
| chr5:116018317 | T | C | 1 | a0003c0005t0003g0053 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2756+2552T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116018317 | |||||||
| chr5:116018360 | T | G | 7 | a0005c0006t0004g0290 a0005c0006t0010g0242 a0005c0006t0010g0245 others(4): Show |
7 | HG01243.hp2 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.2756+2595T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116018360 | |||||||
| chr5:116018397 | C | T | 11 | a0001c0002t0001g0336 a0001c0002t0001g0337 a0001c0014t0001g0060 others(8): Show |
13 | HG01891.hp1 HG02074.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.2756+2632C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116018397 | |||||||
| chr5:116018435 | G | A | 1 | a0002c0003t0005g0102 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2756+2670G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116018435 | |||||||
| chr5:116018471 | G | A | 2 | a0001c0001t0002g0170 a0001c0001t0002g0181 |
2 | NA18952.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.2756+2706G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116018471 | |||||||
| chr5:116018501 | C | T | 4 | a0001c0002t0001g0336 a0001c0002t0001g0337 a0001c0014t0001g0060 others(1): Show |
4 | HG01891.hp1 HG02486.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2756+2736C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116018501 | |||||||
| chr5:116018505 | A | T | 271 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(268): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.2756+2740A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116018505 | |||||||
| chr5:116018518 | C | T | 11 | a0001c0002t0001g0336 a0001c0002t0001g0337 a0001c0014t0001g0060 others(8): Show |
13 | HG01891.hp1 HG02074.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.2756+2753C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116018518 | |||||||
| chr5:116018576 | G | T | 2 | a0003c0005t0003g0057 a0003c0005t0003g0058 |
2 | HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2756+2811G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116018576 | |||||||
| chr5:116018672 | A | G | 76 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0029 others(73): Show |
86 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.2756+2907A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116018672 | |||||||
| chr5:116018677 | C | CA | 74 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0029 others(71): Show |
84 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.2756+2918dupA | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 116018677 | ||||||
| chr5:116018684 | G | A | 76 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0029 others(73): Show |
86 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.2756+2919G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116018684 | |||||||
| chr5:116018721 | C | G | 1 | a0001c0002t0004g0287 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2756+2956C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116018721 | |||||||
| chr5:116018744 | A | T | 1 | a0001c0036t0004g0196 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2756+2979A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116018744 | |||||||
| chr5:116018791 | C | A | 81 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0029 others(78): Show |
91 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.2756+3026C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116018791 | |||||||
| chr5:116018886 | G | A | 77 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0029 others(74): Show |
87 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.2756+3121G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116018886 | |||||||
| chr5:116018901 | C | G | 2 | a0003c0005t0005g0013 a0003c0005t0005g0054 |
3 | HG02895.hp2 HG02897.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2756+3136C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116018901 | |||||||
| chr5:116018959 | C | T | 1 | a0002c0003t0006g0083 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2756+3194C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116018959 | |||||||
| chr5:116019005 | G | A | 76 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0029 others(73): Show |
86 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.2756+3240G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116019005 | |||||||
| chr5:116019066 | T | C | 1 | a0003c0005t0003g0112 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2756+3301T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116019066 | |||||||
| chr5:116019083 | A | G | 14 | a0005c0006t0004g0010 a0005c0006t0004g0290 a0005c0006t0004g0308 others(11): Show |
16 | HG01243.hp2 HG02074.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.2757-3308A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116019083 | |||||||
| chr5:116019128 | G | A | 1 | a0001c0002t0002g0316 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2757-3263G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116019128 | |||||||
| chr5:116019211 | C | T | 1 | a0001c0004t0002g0131 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2757-3180C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116019211 | |||||||
| chr5:116019212 | A | C | 1 | a0001c0004t0002g0131 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2757-3179A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116019212 | |||||||
| chr5:116019237 | T | C | 2 | a0003c0005t0003g0057 a0003c0005t0003g0058 |
2 | HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2757-3154T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116019237 | |||||||
| chr5:116019282 | C | A | 76 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0029 others(73): Show |
86 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.2757-3109C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116019282 | |||||||
| chr5:116019283 | T | C | 76 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0029 others(73): Show |
86 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.2757-3108T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116019283 | |||||||
| chr5:116019417 | T | C | 76 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0029 others(73): Show |
86 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.2757-2974T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116019417 | |||||||
| chr5:116019473 | C | T | 2 | a0001c0001t0002g0204 a0004c0007t0002g0225 |
2 | HG02698.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2757-2918C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116019473 | |||||||
| chr5:116019501 | T | C | 11 | a0001c0002t0001g0238 a0001c0002t0013g0335 a0001c0004t0008g0246 others(8): Show |
12 | HG01496.hp1 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.2757-2890T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116019501 | |||||||
| chr5:116019550 | T | C | 4 | a0001c0004t0001g0038 a0001c0004t0001g0248 a0001c0004t0001g0288 others(1): Show |
5 | HG02258.hp1 HG02922.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2757-2841T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116019550 | |||||||
| chr5:116019642 | T | C | 30 | a0001c0001t0004g0033 a0001c0001t0004g0141 a0001c0001t0004g0168 others(27): Show |
34 | HG01167.hp2 HG01169.hp2 HG02004.hp2 others(31): Show |
intron_variant | MODIFIER | c.2757-2749T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116019642 | |||||||
| chr5:116019661 | C | G | 1 | a0001c0004t0002g0131 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2757-2730C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116019661 | |||||||
| chr5:116019686 | C | T | 14 | a0005c0006t0004g0010 a0005c0006t0004g0290 a0005c0006t0004g0308 others(11): Show |
16 | HG01243.hp2 HG02074.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.2757-2705C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116019686 | |||||||
| chr5:116019692 | C | T | 2 | a0003c0005t0005g0113 a0018c0020t0005g0091 |
2 | HG01496.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2757-2699C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116019692 | |||||||
| chr5:116019856 | GC | G | 2 | a0001c0004t0001g0038 a0001c0004t0001g0248 |
3 | HG02258.hp1 HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2757-2534delC | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116019856 | |||||||
| chr5:116020103 | AC | A | 4 | a0001c0002t0001g0336 a0001c0002t0001g0337 a0001c0014t0001g0060 others(1): Show |
4 | HG01891.hp1 HG02486.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2757-2287delC | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116020103 | |||||||
| chr5:116020140 | T | C | 1 | a0002c0003t0003g0105 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2757-2251T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116020140 | |||||||
| chr5:116020229 | G | T | 5 | a0001c0004t0004g0293 a0001c0004t0004g0294 a0001c0014t0004g0314 others(2): Show |
5 | HG02622.hp1 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2757-2162G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116020229 | |||||||
| chr5:116020267 | A | G | 9 | a0001c0002t0007g0011 a0001c0002t0007g0239 a0001c0002t0007g0338 others(6): Show |
11 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2757-2124A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116020267 | |||||||
| chr5:116020320 | T | G | 79 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0029 others(76): Show |
89 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.2757-2071T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116020320 | |||||||
| chr5:116020369 | A | G | 4 | a0001c0001t0002g0137 a0001c0001t0002g0138 a0001c0001t0002g0167 others(1): Show |
5 | HG01243.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2757-2022A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116020369 | |||||||
| chr5:116020378 | T | G | 79 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0029 others(76): Show |
89 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.2757-2013T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116020378 | |||||||
| chr5:116020380 | C | T | 67 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0029 others(64): Show |
76 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.2757-2011C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116020380 | |||||||
| chr5:116020412 | A | G | 1 | a0001c0036t0004g0196 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2757-1979A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116020412 | |||||||
| chr5:116020424 | C | T | 2 | a0003c0005t0003g0057 a0003c0005t0003g0058 |
2 | HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2757-1967C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116020424 | |||||||
| chr5:116020438 | T | C | 7 | a0001c0002t0007g0011 a0001c0002t0007g0239 a0001c0002t0007g0338 others(4): Show |
9 | HG00741.hp2 HG02055.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.2757-1953T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116020438 | |||||||
| chr5:116020455 | G | C | 123 | a0001c0001t0001g0002 a0001c0001t0001g0046 a0001c0001t0001g0123 others(120): Show |
151 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.2757-1936G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116020455 | |||||||
| chr5:116020482 | A | G | 2 | a0001c0002t0002g0330 a0001c0002t0002g0332 |
2 | HG01109.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.2757-1909A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116020482 | |||||||
| chr5:116020489 | C | T | 18 | a0001c0002t0001g0336 a0001c0002t0001g0337 a0001c0014t0001g0060 others(15): Show |
20 | HG01243.hp2 HG01891.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.2757-1902C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116020489 | |||||||
| chr5:116020536 | A | T | 56 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0029 others(53): Show |
64 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2757-1855A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116020536 | |||||||
| chr5:116020540 | A | T | 18 | a0001c0002t0001g0336 a0001c0002t0001g0337 a0001c0014t0001g0060 others(15): Show |
20 | HG01243.hp2 HG01891.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.2757-1851A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116020540 | |||||||
| chr5:116020741 | G | A | 1 | a0001c0001t0002g0219 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2757-1650G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116020741 | |||||||
| chr5:116020745 | G | A | 29 | a0001c0001t0004g0033 a0001c0001t0004g0141 a0001c0001t0004g0168 others(26): Show |
33 | HG01167.hp2 HG01169.hp2 HG02004.hp2 others(30): Show |
intron_variant | MODIFIER | c.2757-1646G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116020745 | |||||||
| chr5:116020851 | T | C | 7 | a0001c0002t0001g0238 a0001c0002t0013g0335 a0001c0004t0008g0246 others(4): Show |
8 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2757-1540T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116020851 | |||||||
| chr5:116020907 | G | C | 18 | a0001c0002t0001g0336 a0001c0002t0001g0337 a0001c0014t0001g0060 others(15): Show |
20 | HG01243.hp2 HG01891.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.2757-1484G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116020907 | |||||||
| chr5:116020955 | G | A | 6 | a0001c0002t0002g0253 a0002c0003t0005g0071 a0002c0003t0005g0072 others(3): Show |
6 | HG00733.hp2 HG01255.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.2757-1436G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116020955 | |||||||
| chr5:116020975 | A | G | 56 | a0001c0001t0001g0002 a0001c0001t0001g0046 a0001c0001t0001g0123 others(53): Show |
73 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.2757-1416A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116020975 | |||||||
| chr5:116021083 | G | A | 6 | a0001c0002t0001g0336 a0001c0002t0001g0337 a0001c0014t0001g0060 others(3): Show |
6 | HG01891.hp1 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.2757-1308G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116021083 | |||||||
| chr5:116021084 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2757-1307G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116021084 | |||||||
| chr5:116021134 | T | C | 18 | a0001c0002t0001g0336 a0001c0002t0001g0337 a0001c0014t0001g0060 others(15): Show |
20 | HG01243.hp2 HG01891.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.2757-1257T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116021134 | |||||||
| chr5:116021137 | A | G | 107 | a0001c0001t0001g0002 a0001c0001t0001g0046 a0001c0001t0001g0123 others(104): Show |
131 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.2757-1254A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116021137 | |||||||
| chr5:116021187 | T | G | 108 | a0001c0001t0001g0002 a0001c0001t0001g0046 a0001c0001t0001g0123 others(105): Show |
132 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.2757-1204T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116021187 | |||||||
| chr5:116021188 | T | C | 18 | a0001c0002t0001g0336 a0001c0002t0001g0337 a0001c0014t0001g0060 others(15): Show |
20 | HG01243.hp2 HG01891.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.2757-1203T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116021188 | |||||||
| chr5:116021237 | A | C | 18 | a0001c0002t0001g0336 a0001c0002t0001g0337 a0001c0014t0001g0060 others(15): Show |
20 | HG01243.hp2 HG01891.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.2757-1154A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116021237 | |||||||
| chr5:116021326 | T | C | 1 | a0017c0029t0004g0273 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2757-1065T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116021326 | |||||||
| chr5:116021355 | T | A | 12 | a0001c0002t0001g0238 a0001c0002t0013g0335 a0001c0004t0004g0293 others(9): Show |
13 | HG02572.hp1 HG02615.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.2757-1036T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116021355 | |||||||
| chr5:116021450 | A | G | 12 | a0001c0002t0001g0238 a0001c0002t0013g0335 a0001c0004t0004g0293 others(9): Show |
13 | HG02572.hp1 HG02615.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.2757-941A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116021450 | |||||||
| chr5:116021522 | A | G | 12 | a0001c0002t0001g0238 a0001c0002t0013g0335 a0001c0004t0004g0293 others(9): Show |
13 | HG02572.hp1 HG02615.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.2757-869A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116021522 | |||||||
| chr5:116021543 | C | T | 18 | a0001c0002t0001g0336 a0001c0002t0001g0337 a0001c0014t0001g0060 others(15): Show |
20 | HG01243.hp2 HG01891.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.2757-848C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116021543 | |||||||
| chr5:116021566 | G | A | 1 | a0003c0005t0005g0013 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2757-825G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116021566 | |||||||
| chr5:116021652 | T | TG | 3 | a0001c0001t0001g0008 a0001c0001t0001g0045 a0001c0001t0001g0171 |
5 | NA18969.hp2 NA18970.hp2 NA19077.hp1 others(2): Show |
intron_variant | MODIFIER | c.2757-737dupG | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 116021652 | ||||||
| chr5:116021749 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2757-642G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116021749 | |||||||
| chr5:116021785 | T | A | 2 | a0003c0005t0005g0113 a0018c0020t0005g0091 |
2 | HG01496.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2757-606T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116021785 | |||||||
| chr5:116021856 | C | G | 6 | a0001c0002t0001g0336 a0001c0002t0001g0337 a0001c0014t0001g0060 others(3): Show |
6 | HG01891.hp1 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.2757-535C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116021856 | |||||||
| chr5:116021961 | G | T | 18 | a0001c0002t0001g0336 a0001c0002t0001g0337 a0001c0014t0001g0060 others(15): Show |
20 | HG01243.hp2 HG01891.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.2757-430G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116021961 | |||||||
| chr5:116021979 | T | A | 15 | a0001c0001t0002g0128 a0001c0001t0002g0137 a0001c0001t0002g0138 others(12): Show |
18 | HG00639.hp2 HG00733.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.2757-412T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116021979 | |||||||
| chr5:116021996 | G | C | 18 | a0001c0002t0001g0336 a0001c0002t0001g0337 a0001c0014t0001g0060 others(15): Show |
20 | HG01243.hp2 HG01891.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.2757-395G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116021996 | |||||||
| chr5:116022021 | G | A | 1 | a0001c0002t0002g0323 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2757-370G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116022021 | |||||||
| chr5:116022184 | G | T | 5 | a0001c0004t0004g0293 a0001c0004t0004g0294 a0001c0014t0004g0314 others(2): Show |
5 | HG02622.hp1 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2757-207G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 18/19 | chr5 | 116022184 | |||||||
| chr5:116022493 | C | T | 32 | a0001c0001t0002g0030 a0001c0001t0002g0144 a0001c0001t0002g0148 others(29): Show |
44 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.2832+27C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116022493 | |||||||
| chr5:116022585 | A | G | 131 | a0001c0001t0001g0002 a0001c0001t0001g0046 a0001c0001t0001g0123 others(128): Show |
157 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(154): Show |
intron_variant | MODIFIER | c.2832+119A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116022585 | |||||||
| chr5:116022620 | A | G | 32 | a0001c0001t0001g0201 a0001c0002t0001g0043 a0001c0002t0001g0044 others(29): Show |
37 | HG01243.hp2 HG01496.hp2 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.2832+154A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116022620 | |||||||
| chr5:116022658 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2832+192G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116022658 | |||||||
| chr5:116022662 | G | T | 5 | a0005c0006t0004g0010 a0005c0006t0004g0308 a0005c0006t0004g0309 others(2): Show |
7 | HG02074.hp2 HG02523.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.2832+196G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116022662 | |||||||
| chr5:116022679 | C | G | 5 | a0005c0006t0004g0010 a0005c0006t0004g0308 a0005c0006t0004g0309 others(2): Show |
7 | HG02074.hp2 HG02523.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.2832+213C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116022679 | |||||||
| chr5:116022729 | C | G | 4 | a0001c0001t0002g0142 a0001c0001t0002g0178 a0001c0001t0002g0181 others(1): Show |
4 | HG01993.hp1 NA18973.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.2832+263C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116022729 | |||||||
| chr5:116022755 | A | G | 1 | a0001c0004t0002g0274 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2832+289A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116022755 | |||||||
| chr5:116022897 | A | G | 27 | a0001c0001t0001g0201 a0001c0002t0001g0043 a0001c0002t0001g0044 others(24): Show |
30 | HG01243.hp2 HG01496.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.2832+431A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116022897 | |||||||
| chr5:116022966 | A | G | 56 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0029 others(53): Show |
64 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2832+500A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116022966 | |||||||
| chr5:116023091 | A | C | 2 | a0001c0001t0001g0126 a0002c0003t0003g0074 |
2 | HG00280.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.2832+625A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116023091 | |||||||
| chr5:116023152 | C | T | 9 | a0001c0002t0013g0335 a0004c0012t0013g0192 a0005c0006t0004g0290 others(6): Show |
9 | HG01243.hp2 HG02280.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.2832+686C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116023152 | |||||||
| chr5:116023182 | T | A | 1 | a0001c0004t0004g0306 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2832+716T>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116023182 | |||||||
| chr5:116023219 | C | T | 7 | a0001c0002t0001g0238 a0001c0002t0013g0335 a0001c0004t0008g0246 others(4): Show |
8 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2832+753C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116023219 | |||||||
| chr5:116023233 | T | C | 1 | a0008c0013t0003g0106 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2832+767T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116023233 | |||||||
| chr5:116023304 | C | T | 241 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(238): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.2832+838C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116023304 | |||||||
| chr5:116023391 | A | G | 1 | a0001c0002t0002g0320 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2832+925A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116023391 | |||||||
| chr5:116023393 | A | G | 3 | a0001c0001t0001g0201 a0001c0002t0001g0043 a0001c0004t0001g0234 |
4 | HG01496.hp2 HG01884.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.2832+927A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116023393 | |||||||
| chr5:116023535 | A | G | 12 | a0001c0002t0001g0238 a0001c0002t0013g0335 a0001c0004t0004g0293 others(9): Show |
13 | HG02572.hp1 HG02615.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.2832+1069A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116023535 | |||||||
| chr5:116023576 | C | T | 2 | a0003c0005t0003g0057 a0003c0005t0003g0058 |
2 | HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2832+1110C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116023576 | |||||||
| chr5:116023619 | T | C | 7 | a0001c0002t0001g0238 a0001c0002t0013g0335 a0001c0004t0008g0246 others(4): Show |
8 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2832+1153T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116023619 | |||||||
| chr5:116023640 | C | T | 6 | a0001c0002t0001g0336 a0001c0002t0001g0337 a0001c0014t0001g0060 others(3): Show |
6 | HG01891.hp1 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.2832+1174C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116023640 | |||||||
| chr5:116023670 | A | T | 1 | a0004c0012t0013g0192 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2832+1204A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116023670 | |||||||
| chr5:116023674 | C | G | 14 | a0001c0001t0001g0201 a0001c0002t0001g0043 a0001c0002t0001g0044 others(11): Show |
17 | HG01496.hp2 HG01884.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.2832+1208C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116023674 | |||||||
| chr5:116023793 | G | T | 39 | a0001c0001t0001g0201 a0001c0002t0001g0043 a0001c0002t0001g0044 others(36): Show |
45 | HG01243.hp2 HG01496.hp1 HG01496.hp2 others(42): Show |
intron_variant | MODIFIER | c.2832+1327G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116023793 | |||||||
| chr5:116023843 | A | G | 37 | a0001c0001t0002g0127 a0001c0001t0002g0128 a0001c0001t0002g0129 others(34): Show |
40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.2832+1377A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116023843 | |||||||
| chr5:116023862 | C | G | 7 | a0001c0002t0001g0238 a0001c0002t0013g0335 a0001c0004t0008g0246 others(4): Show |
8 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2832+1396C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116023862 | |||||||
| chr5:116023915 | A | T | 7 | a0001c0002t0001g0238 a0001c0002t0013g0335 a0001c0004t0008g0246 others(4): Show |
8 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2832+1449A>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116023915 | |||||||
| chr5:116024056 | A | G | 2 | a0003c0005t0003g0057 a0003c0005t0003g0058 |
2 | HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2832+1590A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116024056 | |||||||
| chr5:116024077 | G | C | 7 | a0001c0002t0001g0238 a0001c0002t0013g0335 a0001c0004t0008g0246 others(4): Show |
8 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2832+1611G>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116024077 | |||||||
| chr5:116024116 | C | G | 1 | a0001c0001t0001g0186 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2832+1650C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116024116 | |||||||
| chr5:116024130 | A | G | 1 | a0001c0001t0002g0035 | 2 | HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2832+1664A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116024130 | |||||||
| chr5:116024185 | C | A | 6 | a0001c0002t0007g0011 a0001c0002t0007g0338 a0001c0002t0007g0341 others(3): Show |
8 | HG00741.hp2 HG02055.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2832+1719C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116024185 | |||||||
| chr5:116024582 | C | T | 2 | a0003c0005t0005g0113 a0018c0020t0005g0091 |
2 | HG01496.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2833-1396C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116024582 | |||||||
| chr5:116024589 | C | G | 2 | a0003c0005t0005g0113 a0018c0020t0005g0091 |
2 | HG01496.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2833-1389C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116024589 | |||||||
| chr5:116024628 | G | T | 57 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0134 others(54): Show |
64 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.2833-1350G>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116024628 | |||||||
| chr5:116024645 | A | C | 68 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0029 others(65): Show |
80 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.2833-1333A>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116024645 | |||||||
| chr5:116024927 | T | C | 115 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(112): Show |
141 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.2833-1051T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116024927 | |||||||
| chr5:116025025 | C | T | 4 | a0001c0001t0002g0133 a0001c0001t0002g0170 a0001c0001t0002g0172 others(1): Show |
4 | NA18945.hp1 NA18952.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.2833-953C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116025025 | |||||||
| chr5:116025142 | C | G | 11 | a0001c0002t0001g0336 a0001c0002t0001g0337 a0001c0014t0001g0060 others(8): Show |
13 | HG01891.hp1 HG02074.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.2833-836C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116025142 | |||||||
| chr5:116025217 | T | G | 1 | a0017c0029t0004g0273 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2833-761T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116025217 | |||||||
| chr5:116025267 | G | A | 1 | a0001c0014t0004g0314 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2833-711G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116025267 | |||||||
| chr5:116025338 | G | A | 49 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0134 others(46): Show |
53 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.2833-640G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116025338 | |||||||
| chr5:116025351 | A | G | 2 | a0003c0005t0003g0056 a0010c0032t0001g0241 |
2 | HG01891.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2833-627A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116025351 | |||||||
| chr5:116025394 | T | G | 1 | a0007c0010t0002g0160 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2833-584T>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116025394 | |||||||
| chr5:116025491 | G | A | 235 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(232): Show |
274 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(271): Show |
intron_variant | MODIFIER | c.2833-487G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116025491 | |||||||
| chr5:116025532 | T | C | 7 | a0001c0002t0007g0011 a0001c0002t0007g0239 a0001c0002t0007g0338 others(4): Show |
9 | HG00741.hp2 HG02055.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.2833-446T>C | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116025532 | |||||||
| chr5:116025549 | A | G | 4 | a0005c0006t0010g0242 a0005c0006t0010g0245 a0005c0006t0010g0247 others(1): Show |
4 | HG02559.hp1 HG02630.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2833-429A>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116025549 | |||||||
| chr5:116025573 | G | A | 2 | a0001c0002t0001g0047 a0001c0002t0001g0275 |
2 | NA18967.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.2833-405G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116025573 | |||||||
| chr5:116025641 | G | A | 2 | a0001c0002t0002g0235 a0004c0012t0002g0223 |
2 | HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2833-337G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116025641 | |||||||
| chr5:116025690 | G | A | 1 | a0003c0005t0003g0053 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2833-288G>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116025690 | |||||||
| chr5:116025778 | C | T | 1 | a0002c0003t0003g0018 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2833-200C>T | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116025778 | |||||||
| chr5:116025822 | C | G | 1 | a0017c0029t0004g0273 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2833-156C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116025822 | |||||||
| chr5:116025870 | C | A | 1 | a0003c0005t0005g0113 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2833-108C>A | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116025870 | |||||||
| chr5:116025879 | C | G | 4 | a0001c0004t0008g0246 a0004c0011t0008g0281 a0004c0012t0008g0032 others(1): Show |
5 | HG02630.hp2 HG02717.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2833-99C>G | LVRN | ENSG00000172901.21 | transcript | ENST00000357872.9 | protein_coding | 19/19 | chr5 | 116025879 |