Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 90249 |
| ensemblid | ENSG00000113763.12 |
| hgncid | 12567 |
| symbol | UNC5A |
| name | unc-5 netrin receptor A |
| refseq_nuc | NM_133369.3 |
| refseq_prot | NP_588610.2 |
| ensembl_nuc | ENST00000329542.9 |
| ensembl_prot | ENSP00000332737.4 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 176810559 |
| end | 176880898 |
| strand | + |
| ver | v1.2 |
| region | chr5:176810559-176880898 |
| region5000 | chr5:176805559-176885898 |
| regionname0 | UNC5A_chr5_176810559_176880898 |
| regionname5000 | UNC5A_chr5_176805559_176885898 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 842 | 249 | 81 | 52 | 72 | 8 | 34 | 45 | UNC5A_chr5_176805559_176885898 | UNC5A | MAVRP others(837): Show |
chr5 | 176805559 | 176885898 |
| a0002 | 0/0 | 842 | 9 | 4 | 2 | 3 | 0 | 0 | 2 | UNC5A_chr5_176805559_176885898 | UNC5A | MAVRP others(837): Show |
chr5 | 176805559 | 176885898 |
| a0003 | 0/0 | 842 | 7 | 5 | 2 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | MAVRP others(837): Show |
chr5 | 176805559 | 176885898 |
| a0004 | 0/0 | 842 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | MAVRP others(837): Show |
chr5 | 176805559 | 176885898 |
| a0005 | 0/0 | 842 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | MAVRP others(837): Show |
chr5 | 176805559 | 176885898 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2526 | 242 | 76 | 51 | 72 | 8 | 33 | UNC5A_chr5_176805559_176885898 | UNC5A | ATGGC others(2521): Show |
chr5 | 176805559 | 176885898 | ||
| a0001c0004 | 0/0 | 2526 | 3 | 3 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | ATGGC others(2521): Show |
chr5 | 176805559 | 176885898 | ||
| a0001c0005 | 0/0 | 2526 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | ATGGC others(2521): Show |
chr5 | 176805559 | 176885898 | ||
| a0001c0007 | 0/0 | 2526 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | ATGGC others(2521): Show |
chr5 | 176805559 | 176885898 | ||
| a0001c0009 | 0/0 | 2526 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | ATGGC others(2521): Show |
chr5 | 176805559 | 176885898 | ||
| a0002c0002 | 0/0 | 2526 | 9 | 4 | 2 | 3 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | ATGGC others(2521): Show |
chr5 | 176805559 | 176885898 | ||
| a0003c0003 | 0/0 | 2526 | 7 | 5 | 2 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | ATGGC others(2521): Show |
chr5 | 176805559 | 176885898 | ||
| a0004c0006 | 0/0 | 2526 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | ATGGC others(2521): Show |
chr5 | 176805559 | 176885898 | ||
| a0005c0008 | 0/0 | 2526 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | ATGGC others(2521): Show |
chr5 | 176805559 | 176885898 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3733 | 136 | 25 | 30 | 48 | 7 | 25 | UNC5A_chr5_176805559_176885898 | UNC5A | GCATT others(3728): Show |
chr5 | 176805559 | 176885898 |
| a0001c0001t0002 | 1/0 | 3733 | 64 | 14 | 19 | 22 | 1 | 7 | UNC5A_chr5_176805559_176885898 | UNC5A | GCATT others(3728): Show |
chr5 | 176805559 | 176885898 |
| a0001c0001t0003 | 0/0 | 3733 | 20 | 20 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | GCATT others(3728): Show |
chr5 | 176805559 | 176885898 |
| a0001c0001t0005 | 0/0 | 3733 | 5 | 5 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | GCATT others(3728): Show |
chr5 | 176805559 | 176885898 |
| a0001c0001t0006 | 0/0 | 3733 | 3 | 3 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | GCATT others(3728): Show |
chr5 | 176805559 | 176885898 |
| a0001c0001t0007 | 0/0 | 3733 | 3 | 3 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | GCATT others(3728): Show |
chr5 | 176805559 | 176885898 |
| a0001c0001t0008 | 0/0 | 3733 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | GCATT others(3728): Show |
chr5 | 176805559 | 176885898 |
| a0001c0001t0009 | 0/0 | 3733 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | GCATT others(3728): Show |
chr5 | 176805559 | 176885898 |
| a0001c0001t0010 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | GCATT others(3728): Show |
chr5 | 176805559 | 176885898 |
| a0001c0001t0011 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | GCATT others(3728): Show |
chr5 | 176805559 | 176885898 |
| a0001c0001t0012 | 0/0 | 3733 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | GCATT others(3728): Show |
chr5 | 176805559 | 176885898 |
| a0001c0001t0013 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | GCATT others(3728): Show |
chr5 | 176805559 | 176885898 |
| a0001c0001t0014 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | GCATT others(3728): Show |
chr5 | 176805559 | 176885898 |
| a0001c0001t0015 | 0/0 | 3733 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | GCATT others(3728): Show |
chr5 | 176805559 | 176885898 |
| a0001c0001t0016 | 0/0 | 3733 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | GCATT others(3728): Show |
chr5 | 176805559 | 176885898 |
| a0001c0001t0017 | 0/0 | 3733 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | GCATT others(3728): Show |
chr5 | 176805559 | 176885898 |
| a0001c0004t0002 | 0/0 | 3733 | 3 | 3 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | GCATT others(3728): Show |
chr5 | 176805559 | 176885898 |
| a0001c0005t0002 | 0/0 | 3733 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | GCATT others(3728): Show |
chr5 | 176805559 | 176885898 |
| a0001c0007t0001 | 0/0 | 3733 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | GCATT others(3728): Show |
chr5 | 176805559 | 176885898 |
| a0001c0009t0001 | 0/0 | 3733 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | GCATT others(3728): Show |
chr5 | 176805559 | 176885898 |
| a0002c0002t0001 | 0/0 | 3733 | 3 | 2 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | GCATT others(3728): Show |
chr5 | 176805559 | 176885898 |
| a0002c0002t0004 | 0/0 | 3733 | 6 | 2 | 1 | 3 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | GCATT others(3728): Show |
chr5 | 176805559 | 176885898 |
| a0003c0003t0001 | 0/0 | 3733 | 3 | 2 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | GCATT others(3728): Show |
chr5 | 176805559 | 176885898 |
| a0003c0003t0002 | 0/0 | 3733 | 4 | 3 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | GCATT others(3728): Show |
chr5 | 176805559 | 176885898 |
| a0004c0006t0002 | 0/0 | 3733 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | GCATT others(3728): Show |
chr5 | 176805559 | 176885898 |
| a0005c0008t0002 | 0/0 | 3733 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | GCATT others(3728): Show |
chr5 | 176805559 | 176885898 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0218 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0237 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0006g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0007g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0007g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0007g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0008g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0008g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0009g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0010g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0011g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0012g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0013g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0014g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0015g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0016g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0001t0017g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0004t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0004t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0004t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0005t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0005t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0007t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0001c0009t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0002c0002t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0002c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0002c0002t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0002c0002t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0002c0002t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0002c0002t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0002c0002t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0002c0002t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0003c0003t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0003c0003t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0003c0003t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0003c0003t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0003c0003t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0003c0003t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0003c0003t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0004c0006t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| a0005c0008t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0206 | EUR | GBR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | GBR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | CHS | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG00642 | hp1 | a0001 | c0009 | t0001 | g0177 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG00733 | hp1 | a0003 | c0003 | t0001 | g0084 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG00741 | hp2 | a0001 | c0001 | t0009 | g0043 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01109 | hp1 | a0002 | c0002 | t0004 | g0048 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | CLM | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | CLM | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | CLM | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | CLM | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | CLM | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01361 | hp1 | a0003 | c0003 | t0002 | g0107 | AMR | CLM | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0101 | AMR | CLM | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01496 | hp2 | a0001 | c0001 | t0017 | g0007 | AMR | CLM | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | IBS | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | IBS | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | IBS | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0059 | EUR | IBS | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0247 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01891 | hp1 | a0003 | c0003 | t0002 | g0073 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0080 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | PEL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | PEL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02074 | hp2 | a0002 | c0002 | t0004 | g0126 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0083 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02257 | hp1 | a0003 | c0003 | t0002 | g0017 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0214 | AMR | PEL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0256 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PEL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02451 | hp1 | a0001 | c0004 | t0002 | g0233 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0092 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0112 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0168 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0250 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0252 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02630 | hp1 | a0001 | c0001 | t0014 | g0061 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0243 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0242 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0238 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0171 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0261 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02723 | hp1 | a0003 | c0003 | t0001 | g0082 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0254 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02809 | hp2 | a0001 | c0005 | t0002 | g0235 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02818 | hp1 | a0001 | c0005 | t0002 | g0241 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0245 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02970 | hp1 | a0001 | c0001 | t0008 | g0113 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03017 | hp2 | a0001 | c0001 | t0012 | g0132 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | MSL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03098 | hp2 | a0004 | c0006 | t0002 | g0005 | AFR | MSL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03139 | hp2 | a0001 | c0001 | t0010 | g0022 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0257 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03195 | hp2 | a0001 | c0004 | t0002 | g0232 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03209 | hp1 | a0002 | c0002 | t0004 | g0066 | AFR | MSL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | MSL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | MSL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03453 | hp1 | a0004 | c0006 | t0002 | g0005 | AFR | MSL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | MSL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03516 | hp1 | a0001 | c0001 | t0011 | g0015 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03540 | hp1 | a0003 | c0003 | t0001 | g0188 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | STU | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | BEB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0163 | SAS | BEB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | STU | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | STU | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | STU | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG04199 | hp2 | a0001 | c0007 | t0001 | g0138 | SAS | STU | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | STU | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | STU | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0065 | AFR | YRI | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0249 | AFR | YRI | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | CHB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0259 | AFR | YRI | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | YRI | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18963 | hp1 | a0005 | c0008 | t0002 | g0128 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18975 | hp2 | a0002 | c0002 | t0004 | g0165 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18982 | hp1 | a0001 | c0001 | t0016 | g0161 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA19030 | hp1 | a0001 | c0004 | t0002 | g0078 | AFR | LWK | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0093 | AFR | LWK | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | LWK | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | LWK | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA19063 | hp1 | a0001 | c0001 | t0015 | g0041 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA19085 | hp2 | a0002 | c0002 | t0004 | g0166 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | YRI | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | YRI | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ASW | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0246 | AFR | ASW | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | GIH | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | GIH | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02109 | hp1 | a0003 | c0003 | t0002 | g0240 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0239 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG02559 | hp2 | a0001 | c0001 | t0008 | g0046 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03471 | hp1 | a0002 | c0002 | t0004 | g0021 | AFR | MSL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0253 | AFR | MSL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | USA | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0081 | AFR | USA | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | USA | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | USA | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| NA21309 | hp2 | a0001 | c0001 | t0013 | g0095 | AFR | LWK | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0218 | REF | REF | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0237 | REF | REF | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:176877669 | G | A | 1 | a0002 | 9 | HG01109.hp1 HG01243.hp2 HG02074.hp2 others(6): Show |
missense_variant | MODERATE | c.1601G>A | p.Arg534His | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 10/15 | 1793/3733 | 1601/2529 | 534/842 | chr5 | 176877669 | |||
| chr5:176877954 | A | G | 1 | a0004 | 2 | HG03098.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.1696A>G | p.Ser566Gly | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 11/15 | 1888/3733 | 1696/2529 | 566/842 | chr5 | 176877954 | |||
| chr5:176877966 | G | A | 1 | a0003 | 7 | HG00733.hp1 HG01361.hp1 HG01891.hp1 others(4): Show |
missense_variant | MODERATE | c.1708G>A | p.Val570Ile | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 11/15 | 1900/3733 | 1708/2529 | 570/842 | chr5 | 176877966 | |||
| chr5:176879851 | G | T | 1 | a0005 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.2494G>T | p.Ala832Ser | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 15/15 | 2686/3733 | 2494/2529 | 832/842 | chr5 | 176879851 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:176868176 | C | G | 2 | a0001c0005 a0004c0006 |
4 | HG02809.hp2 HG02818.hp1 HG03098.hp2 others(1): Show |
synonymous_variant | LOW | c.339C>G | p.Val113Val | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 3/15 | 531/3733 | 339/2529 | 113/842 | chr5 | 176868176 | |||
| chr5:176868577 | C | T | 1 | a0001c0004 | 3 | HG02451.hp1 HG03195.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.453C>T | p.Phe151Phe | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 4/15 | 645/3733 | 453/2529 | 151/842 | chr5 | 176868577 | |||
| chr5:176874454 | C | T | 1 | a0001c0009 | 1 | HG00642.hp1 | synonymous_variant | LOW | c.1266C>T | p.Phe422Phe | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/15 | 1458/3733 | 1266/2529 | 422/842 | chr5 | 176874454 | |||
| chr5:176878058 | G | A | 1 | a0001c0007 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.1800G>A | p.Pro600Pro | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 11/15 | 1992/3733 | 1800/2529 | 600/842 | chr5 | 176878058 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:176810575 | G | T | 1 | a0001c0001t0017 | 1 | HG01496.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-176G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/15 | chr5 | 176810575 | |||||||
| chr5:176810578 | C | T | 1 | a0001c0001t0016 | 1 | NA18982.hp1 | 5_prime_UTR_variant | MODIFIER | c.-173C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/15 | 173 | chr5 | 176810578 | ||||||
| chr5:176810690 | A | G | 1 | a0001c0001t0015 | 1 | NA19063.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-61A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/15 | chr5 | 176810690 | |||||||
| chr5:176810728 | C | G | 1 | a0001c0001t0014 | 1 | HG02630.hp1 | 5_prime_UTR_variant | MODIFIER | c.-23C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/15 | 23 | chr5 | 176810728 | ||||||
| chr5:176880009 | G | A | 1 | a0002c0002t0004 | 6 | HG01109.hp1 HG02074.hp2 HG03209.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*123G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 15/15 | 123 | chr5 | 176880009 | ||||||
| chr5:176880272 | G | T | 1 | a0001c0001t0007 | 3 | HG01884.hp1 HG02145.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*386G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 15/15 | 386 | chr5 | 176880272 | ||||||
| chr5:176880454 | C | T | 1 | a0001c0001t0013 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*568C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 15/15 | 568 | chr5 | 176880454 | ||||||
| chr5:176880457 | C | T | 1 | a0001c0001t0005 | 5 | HG02280.hp2 HG02976.hp1 HG03098.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*571C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 15/15 | 571 | chr5 | 176880457 | ||||||
| chr5:176880463 | C | T | 1 | a0001c0001t0008 | 2 | HG02559.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*577C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 15/15 | 577 | chr5 | 176880463 | ||||||
| chr5:176880503 | T | C | 14 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(11): Show |
162 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*617T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 15/15 | 617 | chr5 | 176880503 | ||||||
| chr5:176880705 | C | T | 1 | a0001c0001t0012 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*819C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 15/15 | 819 | chr5 | 176880705 | ||||||
| chr5:176880725 | G | A | 1 | a0001c0001t0009 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*839G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 15/15 | 839 | chr5 | 176880725 | ||||||
| chr5:176880744 | C | T | 1 | a0001c0001t0011 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*858C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 15/15 | 858 | chr5 | 176880744 | ||||||
| chr5:176880756 | T | C | 5 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(2): Show |
30 | HG01891.hp2 HG02280.hp2 HG02451.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*870T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 15/15 | 870 | chr5 | 176880756 | ||||||
| chr5:176880765 | C | T | 1 | a0001c0001t0010 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*879C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 15/15 | 879 | chr5 | 176880765 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:176810894 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.70+74C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176810894 | |||||||
| chr5:176810913 | A | T | 1 | a0001c0001t0003g0261 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.70+93A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176810913 | |||||||
| chr5:176810971 | T | A | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+151T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176810971 | |||||||
| chr5:176811002 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.70+182C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811002 | |||||||
| chr5:176811030 | G | A | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(225): Show |
232 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(229): Show |
intron_variant | MODIFIER | c.70+210G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811030 | |||||||
| chr5:176811040 | C | G | 151 | a0001c0001t0001g0004 a0001c0001t0001g0086 a0001c0001t0001g0088 others(148): Show |
153 | HG00099.hp1 HG00558.hp1 HG00621.hp2 others(150): Show |
intron_variant | MODIFIER | c.70+220C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811040 | |||||||
| chr5:176811347 | T | C | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+527T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811347 | |||||||
| chr5:176811351 | A | C | 1 | a0001c0001t0001g0262 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.70+531A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811351 | |||||||
| chr5:176811407 | ACAGT | A | 3 | a0001c0001t0001g0229 a0001c0001t0002g0230 a0001c0001t0002g0231 |
3 | HG01167.hp1 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.70+590_70+593delGT others(2): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176811407 | ||||||
| chr5:176811419 | C | T | 11 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0224 others(8): Show |
11 | HG01496.hp1 HG01891.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.70+599C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811419 | |||||||
| chr5:176811547 | C | T | 31 | a0001c0001t0001g0004 a0001c0001t0001g0076 a0001c0001t0001g0195 others(28): Show |
32 | HG00099.hp1 HG00558.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.70+727C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811547 | |||||||
| chr5:176811563 | A | C | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+743A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811563 | |||||||
| chr5:176811606 | A | AG | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(221): Show |
intron_variant | MODIFIER | c.70+790dupG | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176811606 | ||||||
| chr5:176811611 | C | G | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+791C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811611 | |||||||
| chr5:176811612 | T | C | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+792T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811612 | |||||||
| chr5:176811613 | T | TG | 19 | a0001c0001t0001g0072 a0001c0001t0001g0192 a0001c0001t0001g0227 others(16): Show |
20 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.70+799dupG | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176811613 | ||||||
| chr5:176811614 | G | T | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+794G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811614 | |||||||
| chr5:176811616 | G | A | 1 | a0001c0001t0006g0243 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.70+796G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811616 | |||||||
| chr5:176811619 | G | A | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.70+799G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811619 | |||||||
| chr5:176811712 | A | C | 7 | a0001c0001t0001g0185 a0001c0001t0001g0219 a0001c0001t0001g0220 others(4): Show |
7 | HG00741.hp1 HG01516.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.70+892A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811712 | |||||||
| chr5:176811720 | T | C | 22 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(19): Show |
22 | HG01167.hp1 HG01884.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.70+900T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811720 | |||||||
| chr5:176811721 | G | A | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+901G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811721 | |||||||
| chr5:176811722 | A | G | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+902A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811722 | |||||||
| chr5:176811725 | G | A | 1 | a0001c0001t0003g0245 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.70+905G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811725 | |||||||
| chr5:176811794 | A | G | 66 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0067 others(63): Show |
69 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.70+974A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811794 | |||||||
| chr5:176811875 | G | A | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+1055G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811875 | |||||||
| chr5:176811877 | A | G | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+1057A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811877 | |||||||
| chr5:176811880 | G | A | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+1060G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811880 | |||||||
| chr5:176811922 | A | T | 3 | a0001c0001t0002g0096 a0001c0001t0003g0065 a0002c0002t0004g0066 |
3 | HG02922.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.70+1102A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811922 | |||||||
| chr5:176812113 | C | T | 1 | a0001c0001t0010g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.70+1293C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812113 | |||||||
| chr5:176812212 | CAGCTCCG others(6): Show |
C | 1 | a0001c0001t0001g0262 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.70+1396_70+1408del others(13): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176812212 | ||||||
| chr5:176812232 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.70+1412C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812232 | |||||||
| chr5:176812468 | G | C | 35 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0025 others(32): Show |
36 | HG00099.hp2 HG00609.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.70+1648G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812468 | |||||||
| chr5:176812543 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0064 a0001c0001t0001g0094 others(5): Show |
8 | HG01106.hp1 HG01243.hp1 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.70+1723C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812543 | |||||||
| chr5:176812599 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.70+1779G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812599 | |||||||
| chr5:176812679 | C | G | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+1859C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812679 | |||||||
| chr5:176812705 | G | A | 3 | a0001c0001t0001g0064 a0001c0001t0002g0062 a0001c0001t0002g0063 |
3 | HG01106.hp1 HG02300.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.70+1885G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812705 | |||||||
| chr5:176812720 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.70+1900G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812720 | |||||||
| chr5:176812745 | T | C | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+1925T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812745 | |||||||
| chr5:176812746 | G | C | 1 | a0001c0001t0001g0260 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.70+1926G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812746 | |||||||
| chr5:176812746 | G | T | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+1926G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812746 | |||||||
| chr5:176812747 | C | G | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+1927C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812747 | |||||||
| chr5:176812765 | G | A | 34 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0025 others(31): Show |
35 | HG00099.hp2 HG00609.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.70+1945G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812765 | |||||||
| chr5:176812881 | C | T | 1 | a0001c0001t0002g0184 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.70+2061C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812881 | |||||||
| chr5:176812909 | G | T | 4 | a0001c0001t0002g0096 a0001c0001t0003g0065 a0001c0001t0011g0015 others(1): Show |
4 | HG02922.hp1 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+2089G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812909 | |||||||
| chr5:176812917 | C | G | 1 | a0001c0001t0001g0001 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.70+2097C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812917 | |||||||
| chr5:176812935 | C | T | 5 | a0001c0001t0001g0045 a0001c0001t0001g0094 a0001c0001t0003g0092 others(2): Show |
5 | HG02451.hp2 HG03130.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+2115C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812935 | |||||||
| chr5:176812952 | G | A | 4 | a0001c0001t0001g0047 a0001c0001t0001g0099 a0001c0001t0001g0229 others(1): Show |
4 | HG02559.hp2 HG02622.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+2132G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812952 | |||||||
| chr5:176812973 | C | T | 2 | a0001c0001t0007g0242 a0001c0001t0007g0247 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.70+2153C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812973 | |||||||
| chr5:176813184 | C | T | 1 | a0001c0001t0007g0247 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.70+2364C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176813184 | |||||||
| chr5:176813464 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.70+2644C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176813464 | |||||||
| chr5:176813675 | G | A | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.70+2855G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176813675 | |||||||
| chr5:176813738 | T | C | 6 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(3): Show |
6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+2918T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176813738 | |||||||
| chr5:176813773 | G | A | 11 | a0001c0001t0001g0045 a0001c0001t0001g0064 a0001c0001t0001g0094 others(8): Show |
11 | HG01106.hp1 HG01109.hp1 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.70+2953G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176813773 | |||||||
| chr5:176813786 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.70+2966C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176813786 | |||||||
| chr5:176813797 | C | G | 11 | a0001c0001t0001g0045 a0001c0001t0001g0064 a0001c0001t0001g0094 others(8): Show |
11 | HG01106.hp1 HG01109.hp1 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.70+2977C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176813797 | |||||||
| chr5:176813836 | C | T | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+3016C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176813836 | |||||||
| chr5:176813837 | T | G | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+3017T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176813837 | |||||||
| chr5:176813838 | G | C | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+3018G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176813838 | |||||||
| chr5:176813850 | G | A | 1 | a0003c0003t0001g0082 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.70+3030G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176813850 | |||||||
| chr5:176813929 | T | C | 1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.70+3109T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176813929 | |||||||
| chr5:176813955 | G | A | 1 | a0001c0001t0016g0161 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.70+3135G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176813955 | |||||||
| chr5:176813999 | G | A | 5 | a0001c0001t0001g0106 a0001c0001t0001g0162 a0001c0001t0002g0003 others(2): Show |
6 | HG01069.hp2 HG01074.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+3179G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176813999 | |||||||
| chr5:176814112 | C | T | 4 | a0001c0001t0001g0047 a0001c0001t0001g0099 a0001c0001t0001g0229 others(1): Show |
4 | HG02559.hp2 HG02622.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+3292C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176814112 | |||||||
| chr5:176814259 | C | T | 11 | a0001c0001t0001g0045 a0001c0001t0001g0064 a0001c0001t0001g0094 others(8): Show |
11 | HG01106.hp1 HG01109.hp1 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.70+3439C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176814259 | |||||||
| chr5:176814383 | A | T | 1 | a0001c0001t0003g0254 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.70+3563A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176814383 | |||||||
| chr5:176814417 | T | G | 1 | a0001c0001t0003g0261 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.70+3597T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176814417 | |||||||
| chr5:176814542 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.70+3722A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176814542 | |||||||
| chr5:176814667 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.70+3847G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176814667 | |||||||
| chr5:176814716 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.70+3896C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176814716 | |||||||
| chr5:176814854 | G | T | 1 | a0001c0001t0014g0061 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.70+4034G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176814854 | |||||||
| chr5:176814867 | A | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(157): Show |
164 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(161): Show |
intron_variant | MODIFIER | c.70+4047A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176814867 | |||||||
| chr5:176815077 | C | G | 9 | a0001c0001t0001g0045 a0001c0001t0001g0094 a0001c0001t0001g0219 others(6): Show |
9 | HG01109.hp1 HG02451.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.70+4257C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176815077 | |||||||
| chr5:176815110 | A | G | 1 | a0001c0001t0001g0260 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.70+4290A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176815110 | |||||||
| chr5:176815324 | C | T | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(201): Show |
209 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(206): Show |
intron_variant | MODIFIER | c.70+4504C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176815324 | |||||||
| chr5:176815342 | G | C | 1 | a0001c0001t0002g0070 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.70+4522G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176815342 | |||||||
| chr5:176815390 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.70+4570C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176815390 | |||||||
| chr5:176815466 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.70+4646C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176815466 | |||||||
| chr5:176815490 | A | T | 11 | a0001c0001t0001g0045 a0001c0001t0001g0064 a0001c0001t0001g0094 others(8): Show |
11 | HG01106.hp1 HG01109.hp1 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.70+4670A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176815490 | |||||||
| chr5:176815602 | A | T | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+4782A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176815602 | |||||||
| chr5:176815723 | A | G | 1 | a0001c0001t0009g0043 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.70+4903A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176815723 | |||||||
| chr5:176815894 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(168): Show |
175 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(172): Show |
intron_variant | MODIFIER | c.70+5074A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176815894 | |||||||
| chr5:176815922 | T | C | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.70+5102T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176815922 | |||||||
| chr5:176816374 | A | C | 1 | a0001c0001t0001g0001 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.70+5554A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176816374 | |||||||
| chr5:176816394 | T | C | 6 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(3): Show |
6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+5574T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176816394 | |||||||
| chr5:176816453 | G | T | 43 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0071 others(40): Show |
44 | HG00609.hp1 HG00733.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.70+5633G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176816453 | |||||||
| chr5:176816511 | G | C | 4 | a0001c0001t0001g0047 a0001c0001t0001g0099 a0001c0001t0001g0229 others(1): Show |
4 | HG02559.hp2 HG02622.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+5691G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176816511 | |||||||
| chr5:176816542 | T | A | 1 | a0001c0001t0002g0051 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.70+5722T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176816542 | |||||||
| chr5:176816715 | G | C | 3 | a0001c0001t0001g0064 a0001c0001t0002g0062 a0001c0001t0002g0063 |
3 | HG01106.hp1 HG02300.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.70+5895G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176816715 | |||||||
| chr5:176816750 | T | C | 2 | a0001c0004t0002g0232 a0001c0004t0002g0233 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.70+5930T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176816750 | |||||||
| chr5:176816809 | C | A | 3 | a0001c0001t0005g0008 a0001c0001t0005g0023 a0001c0001t0014g0061 |
3 | HG02630.hp1 HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.70+5989C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176816809 | |||||||
| chr5:176816814 | C | G | 2 | a0001c0001t0007g0242 a0001c0001t0007g0247 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.70+5994C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176816814 | |||||||
| chr5:176817063 | A | G | 7 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(4): Show |
7 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.70+6243A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176817063 | |||||||
| chr5:176817070 | G | T | 1 | a0001c0001t0001g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.70+6250G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176817070 | |||||||
| chr5:176817189 | G | GGCCT | 4 | a0001c0001t0001g0162 a0001c0001t0002g0003 a0001c0001t0002g0163 others(1): Show |
5 | HG01069.hp2 HG01074.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+6370_70+6373dup others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176817189 | ||||||
| chr5:176817281 | G | C | 1 | a0001c0001t0001g0202 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.70+6461G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176817281 | |||||||
| chr5:176817305 | A | G | 6 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(3): Show |
6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+6485A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176817305 | |||||||
| chr5:176817344 | G | A | 6 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(3): Show |
6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+6524G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176817344 | |||||||
| chr5:176817362 | T | C | 5 | a0001c0001t0001g0047 a0001c0001t0001g0099 a0001c0001t0001g0229 others(2): Show |
5 | HG02559.hp2 HG02622.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+6542T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176817362 | |||||||
| chr5:176817377 | A | G | 1 | a0001c0001t0001g0042 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.70+6557A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176817377 | |||||||
| chr5:176817419 | A | G | 6 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(3): Show |
6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+6599A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176817419 | |||||||
| chr5:176817522 | G | A | 1 | a0001c0001t0005g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.70+6702G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176817522 | |||||||
| chr5:176817577 | T | TCCCCACC others(8): Show |
4 | a0001c0001t0002g0010 a0001c0001t0002g0062 a0001c0001t0003g0009 others(1): Show |
4 | HG01106.hp1 HG01891.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+6767_70+6768ins others(15): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176817577 | ||||||
| chr5:176817577 | T | TCCCCACC others(9): Show |
2 | a0001c0001t0002g0012 a0001c0001t0003g0011 |
2 | HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.70+6767_70+6768ins others(16): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176817577 | ||||||
| chr5:176817577 | T | TCCCCACC others(9): Show |
1 | a0001c0001t0002g0063 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.70+6767_70+6768ins others(16): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176817577 | ||||||
| chr5:176817577 | T | TCCCCACC others(10): Show |
2 | a0001c0001t0001g0064 a0001c0001t0003g0081 |
2 | HG04184.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.70+6767_70+6768ins others(17): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176817577 | ||||||
| chr5:176817598 | A | T | 5 | a0001c0001t0001g0047 a0001c0001t0001g0099 a0001c0001t0001g0229 others(2): Show |
5 | HG02559.hp2 HG02622.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+6778A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176817598 | |||||||
| chr5:176817606 | G | T | 1 | a0001c0001t0007g0083 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.70+6786G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176817606 | |||||||
| chr5:176817904 | G | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(161): Show |
168 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(165): Show |
intron_variant | MODIFIER | c.70+7084G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176817904 | |||||||
| chr5:176818257 | G | T | 4 | a0001c0001t0001g0047 a0001c0001t0001g0099 a0001c0001t0001g0229 others(1): Show |
4 | HG02559.hp2 HG02622.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+7437G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176818257 | |||||||
| chr5:176818598 | G | A | 1 | a0001c0001t0001g0002 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.70+7778G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176818598 | |||||||
| chr5:176818638 | A | G | 17 | a0001c0001t0001g0045 a0001c0001t0001g0064 a0001c0001t0001g0094 others(14): Show |
17 | HG01106.hp1 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.70+7818A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176818638 | |||||||
| chr5:176818711 | G | C | 1 | a0001c0001t0001g0115 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.70+7891G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176818711 | |||||||
| chr5:176818934 | A | T | 11 | a0001c0001t0001g0045 a0001c0001t0001g0064 a0001c0001t0001g0094 others(8): Show |
11 | HG01106.hp1 HG01109.hp1 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.70+8114A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176818934 | |||||||
| chr5:176819017 | G | T | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.70+8197G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176819017 | |||||||
| chr5:176819194 | T | C | 17 | a0001c0001t0001g0045 a0001c0001t0001g0064 a0001c0001t0001g0094 others(14): Show |
17 | HG01106.hp1 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.70+8374T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176819194 | |||||||
| chr5:176819284 | T | A | 6 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(3): Show |
6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+8464T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176819284 | |||||||
| chr5:176819289 | C | T | 5 | a0001c0001t0001g0047 a0001c0001t0001g0099 a0001c0001t0001g0229 others(2): Show |
5 | HG02559.hp2 HG02622.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+8469C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176819289 | |||||||
| chr5:176819313 | G | A | 6 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(3): Show |
6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+8493G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176819313 | |||||||
| chr5:176819373 | AAAAGGAA others(3): Show |
A | 6 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(3): Show |
6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+8554_70+8563del others(10): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176819373 | |||||||
| chr5:176819384 | G | A | 2 | a0001c0004t0002g0232 a0001c0004t0002g0233 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.70+8564G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176819384 | |||||||
| chr5:176819423 | CA | C | 6 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(3): Show |
6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+8604delA | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176819423 | |||||||
| chr5:176819425 | G | A | 1 | a0001c0001t0002g0116 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.70+8605G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176819425 | |||||||
| chr5:176819466 | C | T | 6 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(3): Show |
6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+8646C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176819466 | |||||||
| chr5:176819575 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.70+8755A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176819575 | |||||||
| chr5:176819678 | C | T | 1 | a0001c0001t0003g0245 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.70+8858C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176819678 | |||||||
| chr5:176820041 | T | C | 3 | a0001c0001t0001g0064 a0001c0001t0002g0062 a0001c0001t0002g0063 |
3 | HG01106.hp1 HG02300.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.70+9221T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176820041 | |||||||
| chr5:176820115 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.70+9295G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176820115 | |||||||
| chr5:176820120 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.70+9300G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176820120 | |||||||
| chr5:176820173 | G | A | 2 | a0001c0001t0007g0242 a0001c0001t0007g0247 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.70+9353G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176820173 | |||||||
| chr5:176820179 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.70+9359C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176820179 | |||||||
| chr5:176820225 | G | A | 1 | a0001c0001t0001g0024 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.70+9405G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176820225 | |||||||
| chr5:176820354 | A | G | 6 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(3): Show |
6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+9534A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176820354 | |||||||
| chr5:176820392 | G | A | 2 | a0001c0001t0002g0230 a0001c0001t0002g0231 |
2 | HG01167.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.70+9572G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176820392 | |||||||
| chr5:176820733 | T | C | 1 | a0001c0001t0001g0255 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.70+9913T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176820733 | |||||||
| chr5:176820851 | C | G | 1 | a0001c0001t0001g0183 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.70+10031C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176820851 | |||||||
| chr5:176820989 | C | T | 6 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(3): Show |
6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+10169C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176820989 | |||||||
| chr5:176821035 | G | T | 20 | a0001c0001t0001g0045 a0001c0001t0001g0064 a0001c0001t0001g0094 others(17): Show |
20 | HG01106.hp1 HG01109.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.70+10215G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176821035 | |||||||
| chr5:176821080 | A | G | 20 | a0001c0001t0001g0045 a0001c0001t0001g0064 a0001c0001t0001g0094 others(17): Show |
20 | HG01106.hp1 HG01109.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.70+10260A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176821080 | |||||||
| chr5:176821191 | G | A | 2 | a0001c0001t0002g0230 a0001c0001t0002g0231 |
2 | HG01167.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.70+10371G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176821191 | |||||||
| chr5:176821230 | C | T | 6 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(3): Show |
6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+10410C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176821230 | |||||||
| chr5:176821377 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.70+10557A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176821377 | |||||||
| chr5:176821718 | C | T | 3 | a0001c0001t0005g0008 a0001c0001t0005g0023 a0001c0001t0014g0061 |
3 | HG02630.hp1 HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.70+10898C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176821718 | |||||||
| chr5:176821727 | C | T | 62 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0045 others(59): Show |
63 | HG00558.hp1 HG00609.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.70+10907C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176821727 | |||||||
| chr5:176821849 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.70+11029A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176821849 | |||||||
| chr5:176821943 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.70+11123G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176821943 | |||||||
| chr5:176822108 | C | A | 6 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(3): Show |
6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+11288C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176822108 | |||||||
| chr5:176822134 | C | T | 6 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(3): Show |
6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+11314C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176822134 | |||||||
| chr5:176822253 | C | T | 5 | a0001c0001t0001g0047 a0001c0001t0001g0099 a0001c0001t0001g0229 others(2): Show |
5 | HG02559.hp2 HG02622.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+11433C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176822253 | |||||||
| chr5:176822297 | G | A | 5 | a0001c0001t0001g0047 a0001c0001t0001g0099 a0001c0001t0001g0229 others(2): Show |
5 | HG02559.hp2 HG02622.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+11477G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176822297 | |||||||
| chr5:176822311 | G | T | 2 | a0001c0001t0001g0098 a0001c0001t0001g0153 |
2 | HG02300.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.70+11491G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176822311 | |||||||
| chr5:176822493 | G | C | 13 | a0001c0001t0001g0045 a0001c0001t0001g0064 a0001c0001t0001g0094 others(10): Show |
13 | HG01106.hp1 HG01109.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.70+11673G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176822493 | |||||||
| chr5:176822620 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.70+11800G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176822620 | |||||||
| chr5:176822863 | G | A | 6 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(3): Show |
6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+12043G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176822863 | |||||||
| chr5:176822870 | C | T | 3 | a0001c0001t0001g0064 a0001c0001t0002g0062 a0001c0001t0002g0063 |
3 | HG01106.hp1 HG02300.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.70+12050C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176822870 | |||||||
| chr5:176822928 | C | T | 2 | a0001c0001t0007g0242 a0001c0001t0007g0247 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.70+12108C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176822928 | |||||||
| chr5:176822946 | C | T | 1 | a0001c0001t0009g0043 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.70+12126C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176822946 | |||||||
| chr5:176823001 | A | G | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(231): Show |
239 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(236): Show |
intron_variant | MODIFIER | c.70+12181A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823001 | |||||||
| chr5:176823029 | G | A | 3 | a0001c0001t0001g0219 a0001c0001t0003g0049 a0002c0002t0004g0048 |
3 | HG01109.hp1 HG02738.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.70+12209G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823029 | |||||||
| chr5:176823125 | G | T | 3 | a0001c0001t0001g0219 a0001c0001t0003g0049 a0002c0002t0004g0048 |
3 | HG01109.hp1 HG02738.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.70+12305G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823125 | |||||||
| chr5:176823136 | C | T | 42 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0071 others(39): Show |
43 | HG00558.hp1 HG00609.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.70+12316C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823136 | |||||||
| chr5:176823137 | G | A | 6 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(3): Show |
6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+12317G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823137 | |||||||
| chr5:176823148 | G | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0170 |
3 | HG01081.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.70+12328G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823148 | |||||||
| chr5:176823419 | G | C | 2 | a0001c0001t0002g0100 a0001c0001t0002g0118 |
2 | HG02145.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.70+12599G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823419 | |||||||
| chr5:176823427 | A | G | 5 | a0001c0001t0001g0047 a0001c0001t0001g0099 a0001c0001t0001g0229 others(2): Show |
5 | HG02559.hp2 HG02622.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+12607A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823427 | |||||||
| chr5:176823482 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.70+12662C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823482 | |||||||
| chr5:176823537 | G | A | 1 | a0001c0001t0001g0251 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.70+12717G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823537 | |||||||
| chr5:176823835 | G | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(168): Show |
175 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(172): Show |
intron_variant | MODIFIER | c.70+13015G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823835 | |||||||
| chr5:176823868 | G | C | 3 | a0001c0001t0003g0252 a0001c0001t0003g0259 a0001c0001t0003g0261 |
3 | HG02615.hp2 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.70+13048G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823868 | |||||||
| chr5:176823893 | G | A | 1 | a0001c0001t0002g0189 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.70+13073G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823893 | |||||||
| chr5:176823931 | T | C | 3 | a0001c0001t0001g0119 a0001c0001t0001g0172 a0001c0001t0002g0171 |
3 | HG01361.hp2 HG02135.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.70+13111T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823931 | |||||||
| chr5:176823985 | T | C | 40 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0071 others(37): Show |
41 | HG00558.hp1 HG00609.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.70+13165T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823985 | |||||||
| chr5:176823993 | C | G | 2 | a0001c0001t0007g0242 a0001c0001t0007g0247 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.70+13173C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823993 | |||||||
| chr5:176824046 | C | G | 3 | a0001c0001t0001g0064 a0001c0001t0002g0062 a0001c0001t0002g0063 |
3 | HG01106.hp1 HG02300.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.70+13226C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176824046 | |||||||
| chr5:176824132 | G | A | 19 | a0001c0001t0001g0045 a0001c0001t0001g0064 a0001c0001t0001g0094 others(16): Show |
19 | HG01106.hp1 HG01109.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.70+13312G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176824132 | |||||||
| chr5:176824277 | G | A | 3 | a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0190 |
3 | HG01106.hp1 HG02083.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.70+13457G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176824277 | |||||||
| chr5:176824297 | G | A | 19 | a0001c0001t0001g0045 a0001c0001t0001g0064 a0001c0001t0001g0094 others(16): Show |
19 | HG01106.hp1 HG01109.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.70+13477G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176824297 | |||||||
| chr5:176824344 | C | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(163): Show |
170 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(167): Show |
intron_variant | MODIFIER | c.70+13524C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176824344 | |||||||
| chr5:176824364 | C | G | 1 | a0002c0002t0004g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.70+13544C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176824364 | |||||||
| chr5:176824385 | A | G | 19 | a0001c0001t0001g0045 a0001c0001t0001g0064 a0001c0001t0001g0094 others(16): Show |
19 | HG01106.hp1 HG01109.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.70+13565A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176824385 | |||||||
| chr5:176824630 | A | G | 1 | a0001c0001t0001g0001 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.70+13810A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176824630 | |||||||
| chr5:176824824 | C | G | 1 | a0001c0001t0001g0042 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.70+14004C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176824824 | |||||||
| chr5:176824935 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.70+14115C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176824935 | |||||||
| chr5:176825070 | A | T | 1 | a0001c0001t0001g0195 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.70+14250A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176825070 | |||||||
| chr5:176825073 | G | A | 3 | a0001c0001t0001g0064 a0001c0001t0002g0062 a0001c0001t0002g0063 |
3 | HG01106.hp1 HG02300.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.70+14253G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176825073 | |||||||
| chr5:176825221 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.70+14401G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176825221 | |||||||
| chr5:176825302 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.70+14482G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176825302 | |||||||
| chr5:176825390 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.70+14570C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176825390 | |||||||
| chr5:176825391 | G | A | 8 | a0001c0001t0001g0014 a0001c0001t0002g0186 a0001c0001t0002g0187 others(5): Show |
8 | HG01361.hp1 HG02055.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.70+14571G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176825391 | |||||||
| chr5:176825527 | G | A | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(208): Show |
216 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(213): Show |
intron_variant | MODIFIER | c.70+14707G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176825527 | |||||||
| chr5:176825573 | G | C | 10 | a0001c0001t0001g0045 a0001c0001t0001g0094 a0001c0001t0001g0219 others(7): Show |
10 | HG01109.hp1 HG02451.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.70+14753G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176825573 | |||||||
| chr5:176825599 | G | T | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.70+14779G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176825599 | |||||||
| chr5:176825755 | G | C | 1 | a0001c0001t0001g0052 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.70+14935G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176825755 | |||||||
| chr5:176825850 | CATTT | C | 3 | a0001c0001t0001g0064 a0001c0001t0002g0062 a0001c0001t0002g0063 |
3 | HG01106.hp1 HG02300.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.70+15034_70+15037d others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176825850 | ||||||
| chr5:176825872 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.70+15052G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176825872 | |||||||
| chr5:176825913 | G | A | 2 | a0001c0001t0005g0008 a0001c0001t0005g0023 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.70+15093G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176825913 | |||||||
| chr5:176825942 | G | T | 5 | a0001c0001t0001g0045 a0001c0001t0001g0094 a0001c0001t0003g0092 others(2): Show |
5 | HG02451.hp2 HG03130.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+15122G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176825942 | |||||||
| chr5:176826026 | C | T | 19 | a0001c0001t0001g0045 a0001c0001t0001g0064 a0001c0001t0001g0094 others(16): Show |
19 | HG01106.hp1 HG01109.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.70+15206C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176826026 | |||||||
| chr5:176826087 | G | A | 6 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(3): Show |
6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+15267G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176826087 | |||||||
| chr5:176826165 | G | C | 1 | a0001c0001t0001g0255 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.70+15345G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176826165 | |||||||
| chr5:176826284 | A | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
167 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(164): Show |
intron_variant | MODIFIER | c.70+15464A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176826284 | |||||||
| chr5:176826434 | G | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(156): Show |
163 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(160): Show |
intron_variant | MODIFIER | c.70+15614G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176826434 | |||||||
| chr5:176826636 | C | CT | 5 | a0001c0001t0001g0047 a0001c0001t0001g0099 a0001c0001t0002g0075 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+15840dupT | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176826636 | ||||||
| chr5:176826636 | CT | C | 18 | a0001c0001t0001g0014 a0001c0001t0001g0110 a0001c0001t0001g0150 others(15): Show |
18 | HG00733.hp1 HG01361.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.70+15840delT | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176826636 | ||||||
| chr5:176826636 | CTT | C | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(188): Show |
196 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(193): Show |
intron_variant | MODIFIER | c.70+15839_70+15840d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176826636 | ||||||
| chr5:176826636 | CTTT | C | 5 | a0001c0001t0001g0120 a0001c0001t0002g0096 a0001c0001t0002g0189 others(2): Show |
5 | HG02615.hp2 HG02698.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+15838_70+15840d others(5): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176826636 | ||||||
| chr5:176826636 | CTTTT | C | 8 | a0001c0001t0001g0045 a0001c0001t0001g0094 a0001c0001t0001g0219 others(5): Show |
8 | HG01109.hp1 HG02451.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.70+15837_70+15840d others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176826636 | ||||||
| chr5:176826636 | CTTTTT | C | 5 | a0001c0001t0001g0064 a0001c0001t0002g0062 a0001c0001t0002g0063 others(2): Show |
5 | HG01106.hp1 HG02300.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+15836_70+15840d others(7): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176826636 | ||||||
| chr5:176826697 | G | A | 1 | a0001c0001t0001g0027 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.70+15877G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176826697 | |||||||
| chr5:176826782 | A | T | 2 | a0001c0001t0002g0148 a0001c0001t0002g0149 |
2 | NA18971.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.70+15962A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176826782 | |||||||
| chr5:176826789 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.70+15969C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176826789 | |||||||
| chr5:176826864 | C | A | 1 | a0001c0001t0001g0086 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.70+16044C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176826864 | |||||||
| chr5:176826941 | A | C | 1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.70+16121A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176826941 | |||||||
| chr5:176827051 | A | G | 14 | a0001c0001t0001g0045 a0001c0001t0001g0064 a0001c0001t0001g0094 others(11): Show |
14 | HG01106.hp1 HG01109.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.70+16231A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176827051 | |||||||
| chr5:176827179 | C | CT | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(154): Show |
161 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.70+16380dupT | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176827179 | ||||||
| chr5:176827179 | C | CTT | 18 | a0001c0001t0001g0024 a0001c0001t0001g0047 a0001c0001t0001g0059 others(15): Show |
18 | HG00735.hp1 HG01517.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.70+16379_70+16380d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176827179 | ||||||
| chr5:176827179 | CT | C | 45 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0114 others(42): Show |
46 | HG00558.hp1 HG00733.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.70+16380delT | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176827179 | ||||||
| chr5:176827207 | G | T | 1 | a0001c0001t0007g0083 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.70+16387G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176827207 | |||||||
| chr5:176827221 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.70+16401C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176827221 | |||||||
| chr5:176827371 | C | T | 6 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(3): Show |
6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+16551C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176827371 | |||||||
| chr5:176827443 | A | G | 3 | a0001c0001t0001g0064 a0001c0001t0002g0062 a0001c0001t0002g0063 |
3 | HG01106.hp1 HG02300.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.70+16623A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176827443 | |||||||
| chr5:176827487 | T | C | 1 | a0001c0001t0003g0009 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.70+16667T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176827487 | |||||||
| chr5:176827553 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.70+16733A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176827553 | |||||||
| chr5:176827571 | C | T | 1 | a0001c0001t0001g0192 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.70+16751C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176827571 | |||||||
| chr5:176827628 | G | A | 1 | a0001c0001t0001g0028 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.70+16808G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176827628 | |||||||
| chr5:176827684 | G | A | 18 | a0001c0001t0001g0071 a0001c0001t0001g0108 a0001c0001t0001g0109 others(15): Show |
18 | HG00558.hp1 HG00609.hp1 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.70+16864G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176827684 | |||||||
| chr5:176827710 | C | T | 6 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(3): Show |
6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+16890C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176827710 | |||||||
| chr5:176827785 | T | C | 2 | a0001c0001t0007g0242 a0001c0001t0007g0247 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.70+16965T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176827785 | |||||||
| chr5:176827807 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.70+16987T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176827807 | |||||||
| chr5:176828002 | G | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
167 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(164): Show |
intron_variant | MODIFIER | c.70+17182G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828002 | |||||||
| chr5:176828045 | T | G | 1 | a0002c0002t0004g0165 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.70+17225T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828045 | |||||||
| chr5:176828111 | C | A | 1 | a0001c0001t0001g0154 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.70+17291C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828111 | |||||||
| chr5:176828152 | T | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(234): Show |
242 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(239): Show |
intron_variant | MODIFIER | c.70+17332T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828152 | |||||||
| chr5:176828352 | G | A | 1 | a0001c0001t0002g0123 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.70+17532G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828352 | |||||||
| chr5:176828484 | C | T | 1 | a0003c0003t0001g0188 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.70+17664C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828484 | |||||||
| chr5:176828516 | C | A | 5 | a0001c0001t0001g0108 a0001c0001t0001g0196 a0001c0001t0001g0197 others(2): Show |
5 | HG02132.hp1 HG02273.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+17696C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828516 | |||||||
| chr5:176828564 | A | G | 5 | a0001c0001t0001g0047 a0001c0001t0001g0099 a0001c0001t0001g0229 others(2): Show |
5 | HG02559.hp2 HG02622.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+17744A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828564 | |||||||
| chr5:176828567 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.70+17747G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828567 | |||||||
| chr5:176828609 | G | A | 3 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0003c0003t0001g0188 |
3 | HG02922.hp2 HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.70+17789G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828609 | |||||||
| chr5:176828645 | G | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
167 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(164): Show |
intron_variant | MODIFIER | c.70+17825G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828645 | |||||||
| chr5:176828656 | T | C | 44 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0071 others(41): Show |
45 | HG00558.hp1 HG00609.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.70+17836T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828656 | |||||||
| chr5:176828747 | T | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0030 |
2 | HG02080.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.70+17927T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828747 | |||||||
| chr5:176828814 | T | C | 6 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(3): Show |
6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+17994T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828814 | |||||||
| chr5:176828873 | G | A | 3 | a0001c0001t0005g0008 a0001c0001t0005g0023 a0001c0001t0014g0061 |
3 | HG02630.hp1 HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.70+18053G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828873 | |||||||
| chr5:176828925 | T | G | 2 | a0001c0001t0005g0249 a0003c0003t0001g0084 |
2 | HG00733.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.70+18105T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828925 | |||||||
| chr5:176829080 | G | A | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(188): Show |
195 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(192): Show |
intron_variant | MODIFIER | c.70+18260G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829080 | |||||||
| chr5:176829131 | C | CA | 10 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(7): Show |
10 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.70+18328dupA | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829131 | ||||||
| chr5:176829131 | CA | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(166): Show |
173 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(170): Show |
intron_variant | MODIFIER | c.70+18328delA | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829131 | ||||||
| chr5:176829145 | A | AG | 44 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0071 others(41): Show |
45 | HG00558.hp1 HG00609.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.70+18325_70+18326i others(3): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829145 | |||||||
| chr5:176829156 | AGATG | A | 25 | a0001c0001t0001g0047 a0001c0001t0001g0077 a0001c0001t0001g0079 others(22): Show |
26 | HG01243.hp2 HG01496.hp1 HG01943.hp2 others(23): Show |
intron_variant | MODIFIER | c.70+18382_70+18385d others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829156 | ||||||
| chr5:176829156 | AGATGGAT others(1): Show |
A | 17 | a0001c0001t0001g0014 a0001c0001t0001g0064 a0001c0001t0001g0258 others(14): Show |
17 | HG01106.hp1 HG01891.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.70+18378_70+18385d others(10): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829156 | ||||||
| chr5:176829156 | AGATGGAT others(5): Show |
A | 38 | a0001c0001t0001g0016 a0001c0001t0001g0071 a0001c0001t0001g0108 others(35): Show |
39 | HG00558.hp1 HG00609.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.70+18374_70+18385d others(14): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829156 | ||||||
| chr5:176829156 | AGATGGAT others(9): Show |
A | 7 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(4): Show |
7 | HG01884.hp2 HG02622.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.70+18370_70+18385d others(18): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829156 | ||||||
| chr5:176829159 | T | A | 4 | a0001c0001t0001g0045 a0001c0001t0003g0009 a0001c0001t0007g0242 others(1): Show |
4 | HG01884.hp1 HG02647.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+18339T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829159 | |||||||
| chr5:176829159 | TGGATGGA others(18): Show |
T | 1 | a0001c0001t0002g0087 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.70+18341_70+18365d others(27): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829159 | ||||||
| chr5:176829160 | G | A | 4 | a0001c0001t0001g0045 a0001c0001t0003g0009 a0001c0001t0007g0242 others(1): Show |
4 | HG01884.hp1 HG02647.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+18340G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829160 | |||||||
| chr5:176829174 | ATGGATGG others(25): Show |
A | 2 | a0001c0001t0002g0058 a0001c0001t0002g0194 |
2 | HG01081.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.70+18366_70+18397d others(34): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829174 | ||||||
| chr5:176829178 | ATGGATGG others(21): Show |
A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(153): Show |
intron_variant | MODIFIER | c.70+18370_70+18397d others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829178 | ||||||
| chr5:176829182 | ATGGATGG others(17): Show |
A | 7 | a0001c0001t0001g0027 a0001c0001t0001g0162 a0001c0001t0001g0216 others(4): Show |
8 | HG01069.hp2 HG01074.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.70+18374_70+18397d others(26): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829182 | ||||||
| chr5:176829186 | ATGGATGG others(13): Show |
A | 2 | a0001c0001t0003g0049 a0002c0002t0004g0048 |
2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.70+18378_70+18397d others(22): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829186 | ||||||
| chr5:176829190 | ATGGATGG others(9): Show |
A | 1 | a0001c0001t0001g0219 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.70+18382_70+18397d others(18): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829190 | ||||||
| chr5:176829206 | T | A | 1 | a0001c0001t0002g0087 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.70+18386T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829206 | |||||||
| chr5:176829231 | A | AGATG | 6 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(3): Show |
6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+18429_70+18432d others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829231 | ||||||
| chr5:176829269 | C | CTGGA | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
167 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(164): Show |
intron_variant | MODIFIER | c.70+18463_70+18466d others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829269 | ||||||
| chr5:176829305 | GATGGATG others(1): Show |
G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(175): Show |
182 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(179): Show |
intron_variant | MODIFIER | c.70+18493_70+18500d others(10): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829305 | ||||||
| chr5:176829313 | A | T | 14 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(11): Show |
14 | HG01071.hp2 HG01255.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.70+18493A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829313 | |||||||
| chr5:176829315 | TG | T | 11 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0102 others(8): Show |
11 | HG01071.hp2 HG01255.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.70+18497delG | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829315 | ||||||
| chr5:176829316 | GGATGTAT others(2): Show |
G | 3 | a0001c0001t0001g0033 a0001c0001t0001g0127 a0001c0001t0002g0116 |
3 | NA18979.hp2 NA19060.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.70+18497_70+18505d others(11): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829316 | |||||||
| chr5:176829319 | T | A | 11 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0102 others(8): Show |
11 | HG01071.hp2 HG01255.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.70+18499T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829319 | |||||||
| chr5:176829320 | G | A | 11 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0102 others(8): Show |
11 | HG01071.hp2 HG01255.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.70+18500G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829320 | |||||||
| chr5:176829324 | GAAA | G | 10 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0102 others(7): Show |
10 | HG01071.hp2 HG01255.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.70+18505_70+18507d others(5): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829324 | |||||||
| chr5:176829326 | A | T | 1 | a0001c0001t0002g0171 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.70+18506A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829326 | |||||||
| chr5:176829327 | A | G | 1 | a0001c0001t0002g0171 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.70+18507A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829327 | |||||||
| chr5:176829328 | T | G | 11 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0102 others(8): Show |
11 | HG01071.hp2 HG01255.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.70+18508T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829328 | |||||||
| chr5:176829328 | T | TATGG | 39 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0071 others(36): Show |
41 | HG00558.hp1 HG00609.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.70+18547_70+18550d others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829328 | ||||||
| chr5:176829328 | T | TATGGATG others(1): Show |
4 | a0001c0001t0001g0108 a0001c0001t0003g0050 a0001c0001t0003g0111 others(1): Show |
4 | HG02132.hp1 HG02572.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+18543_70+18550d others(10): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829328 | ||||||
| chr5:176829328 | TATGG | T | 29 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(26): Show |
30 | HG00621.hp2 HG00735.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.70+18547_70+18550d others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829328 | ||||||
| chr5:176829328 | TATGGATG others(1): Show |
T | 11 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0002g0062 others(8): Show |
11 | HG01106.hp1 HG01106.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.70+18543_70+18550d others(10): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829328 | ||||||
| chr5:176829328 | TATGGATG others(5): Show |
T | 1 | a0001c0001t0001g0064 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.70+18539_70+18550d others(14): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829328 | ||||||
| chr5:176829416 | A | AATGG | 14 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(11): Show |
14 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.70+18623_70+18626d others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829416 | ||||||
| chr5:176829416 | A | AATGGATG others(1): Show |
6 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(3): Show |
6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+18619_70+18626d others(10): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829416 | ||||||
| chr5:176829416 | A | AATGGATG others(5): Show |
3 | a0001c0001t0001g0219 a0001c0001t0003g0049 a0002c0002t0004g0048 |
3 | HG01109.hp1 HG02738.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.70+18615_70+18626d others(14): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829416 | ||||||
| chr5:176829416 | A | G | 1 | a0002c0002t0004g0165 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.70+18596A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829416 | |||||||
| chr5:176829416 | AATGG | A | 2 | a0001c0001t0003g0250 a0001c0001t0003g0254 |
2 | HG02615.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.70+18623_70+18626d others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829416 | ||||||
| chr5:176829485 | GGTGGGTG others(14): Show |
G | 1 | a0001c0001t0002g0051 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.70+18678_70+18698d others(23): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829485 | ||||||
| chr5:176829560 | A | AGATG | 5 | a0001c0001t0001g0045 a0001c0001t0001g0094 a0001c0001t0003g0092 others(2): Show |
5 | HG02451.hp2 HG03130.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+18760_70+18763d others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829560 | ||||||
| chr5:176829698 | G | C | 1 | a0001c0001t0001g0119 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.70+18878G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829698 | |||||||
| chr5:176829715 | C | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0056 others(40): Show |
44 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.70+18895C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829715 | |||||||
| chr5:176829793 | T | C | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | NA19002.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.70+18973T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829793 | |||||||
| chr5:176829830 | G | T | 1 | a0001c0001t0001g0201 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.70+19010G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829830 | |||||||
| chr5:176829881 | C | CTTTTTTT others(4): Show |
3 | a0001c0001t0001g0219 a0001c0001t0003g0049 a0002c0002t0004g0048 |
3 | HG01109.hp1 HG02738.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.70+19062_70+19072d others(13): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829881 | ||||||
| chr5:176829881 | C | CTTTTTTT others(5): Show |
12 | a0001c0001t0001g0045 a0001c0001t0001g0094 a0001c0001t0003g0009 others(9): Show |
12 | HG01891.hp2 HG02451.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.70+19072_70+19073i others(14): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829881 | ||||||
| chr5:176829881 | C | CTTTTTTT others(6): Show |
2 | a0001c0001t0002g0010 a0001c0001t0002g0012 |
2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.70+19072_70+19073i others(15): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829881 | ||||||
| chr5:176829881 | C | CTTTTTTT others(7): Show |
7 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0105 others(4): Show |
7 | HG00099.hp1 HG00621.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.70+19072_70+19073i others(16): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829881 | ||||||
| chr5:176829881 | C | CTTTTTTT others(8): Show |
131 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0024 others(128): Show |
134 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(131): Show |
intron_variant | MODIFIER | c.70+19072_70+19073i others(17): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829881 | ||||||
| chr5:176829881 | C | CTTTTTTT others(9): Show |
31 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0047 others(28): Show |
32 | HG00558.hp2 HG00609.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.70+19072_70+19073i others(18): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829881 | ||||||
| chr5:176829881 | C | CTTTTTTT others(10): Show |
2 | a0001c0001t0001g0102 a0001c0001t0001g0251 |
2 | HG02040.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.70+19072_70+19073i others(19): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829881 | ||||||
| chr5:176829881 | C | CTTTTTTT others(13): Show |
2 | a0001c0001t0001g0018 a0002c0002t0004g0021 |
2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.70+19072_70+19073i others(22): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829881 | ||||||
| chr5:176829881 | C | CTTTTTTT others(17): Show |
2 | a0001c0001t0001g0019 a0001c0001t0001g0020 |
2 | HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.70+19072_70+19073i others(26): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829881 | ||||||
| chr5:176829912 | T | C | 2 | a0001c0004t0002g0232 a0001c0004t0002g0233 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.70+19092T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829912 | |||||||
| chr5:176830018 | G | A | 4 | a0001c0001t0001g0094 a0001c0001t0003g0092 a0001c0001t0003g0093 others(1): Show |
4 | HG02451.hp2 HG03130.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+19198G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830018 | |||||||
| chr5:176830074 | C | T | 1 | a0001c0001t0010g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.70+19254C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830074 | |||||||
| chr5:176830195 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.70+19375G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830195 | |||||||
| chr5:176830273 | C | T | 1 | a0001c0001t0002g0040 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.70+19453C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830273 | |||||||
| chr5:176830366 | ATGTGTGT others(68): Show |
A | 3 | a0001c0001t0001g0064 a0001c0001t0002g0062 a0001c0001t0002g0063 |
3 | HG01106.hp1 HG02300.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.70+19574_70+19648d others(77): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176830366 | ||||||
| chr5:176830418 | T | G | 5 | a0001c0001t0001g0045 a0001c0001t0001g0094 a0001c0001t0003g0092 others(2): Show |
5 | HG02451.hp2 HG03130.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+19598T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830418 | |||||||
| chr5:176830438 | CAT | C | 4 | a0001c0001t0001g0094 a0001c0001t0003g0092 a0001c0001t0003g0093 others(1): Show |
4 | HG02451.hp2 HG03130.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+19619_70+19620d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830438 | |||||||
| chr5:176830439 | ATG | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(171): Show |
178 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(175): Show |
intron_variant | MODIFIER | c.70+19633_70+19634d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176830439 | ||||||
| chr5:176830459 | C | T | 6 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(3): Show |
6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+19639C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830459 | |||||||
| chr5:176830561 | GGT | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(228): Show |
236 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(233): Show |
intron_variant | MODIFIER | c.70+19759_70+19760d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176830561 | ||||||
| chr5:176830561 | GGTGTGTG others(3): Show |
G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0169 |
2 | HG00609.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.70+19751_70+19760d others(12): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176830561 | ||||||
| chr5:176830571 | T | TGTGTGTG others(41): Show |
3 | a0001c0001t0005g0008 a0001c0001t0005g0023 a0001c0001t0014g0061 |
3 | HG02630.hp1 HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.70+19758_70+19759i others(50): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176830571 | ||||||
| chr5:176830579 | T | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(166): Show |
173 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(170): Show |
intron_variant | MODIFIER | c.70+19759T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830579 | |||||||
| chr5:176830598 | A | G | 1 | a0002c0002t0001g0112 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.70+19778A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830598 | |||||||
| chr5:176830633 | TGC | T | 6 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(3): Show |
6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+19816_70+19817d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176830633 | ||||||
| chr5:176830635 | C | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(185): Show |
192 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(189): Show |
intron_variant | MODIFIER | c.70+19815C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830635 | |||||||
| chr5:176830650 | T | TTG | 5 | a0001c0001t0003g0065 a0001c0001t0007g0242 a0001c0001t0007g0247 others(2): Show |
5 | HG01884.hp1 HG02647.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+19841_70+19842d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176830650 | ||||||
| chr5:176830651 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(191): Show |
198 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(195): Show |
intron_variant | MODIFIER | c.70+19831T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830651 | |||||||
| chr5:176830706 | G | A | 1 | a0001c0001t0001g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.70+19886G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830706 | |||||||
| chr5:176830726 | A | G | 42 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0071 others(39): Show |
43 | HG00609.hp1 HG00733.hp1 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.70+19906A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830726 | |||||||
| chr5:176830727 | T | TGTGTGG | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(190): Show |
197 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(194): Show |
intron_variant | MODIFIER | c.70+19913_70+19918d others(8): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176830727 | ||||||
| chr5:176830739 | C | G | 2 | a0001c0004t0002g0232 a0001c0004t0002g0233 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.70+19919C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830739 | |||||||
| chr5:176830740 | T | G | 2 | a0001c0004t0002g0232 a0001c0004t0002g0233 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.70+19920T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830740 | |||||||
| chr5:176830741 | G | T | 2 | a0001c0004t0002g0232 a0001c0004t0002g0233 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.70+19921G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830741 | |||||||
| chr5:176830784 | G | A | 1 | a0001c0001t0005g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.70+19964G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830784 | |||||||
| chr5:176830897 | CGTGT | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
181 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(178): Show |
intron_variant | MODIFIER | c.70+20082_70+20085d others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176830897 | ||||||
| chr5:176830915 | CGTGTGTG others(3): Show |
C | 18 | a0001c0001t0001g0045 a0001c0001t0001g0094 a0001c0001t0001g0219 others(15): Show |
18 | HG01109.hp1 HG01891.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.70+20105_70+20114d others(12): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176830915 | ||||||
| chr5:176830973 | G | GGT | 21 | a0001c0001t0001g0045 a0001c0001t0001g0064 a0001c0001t0001g0094 others(18): Show |
21 | HG01106.hp1 HG01109.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.70+20167_70+20168d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176830973 | ||||||
| chr5:176831028 | C | G | 6 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(3): Show |
6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+20208C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176831028 | |||||||
| chr5:176831157 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.70+20337C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176831157 | |||||||
| chr5:176831210 | G | A | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0002g0104 |
3 | HG02040.hp2 NA19074.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.70+20390G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176831210 | |||||||
| chr5:176831361 | C | T | 1 | a0001c0001t0010g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.70+20541C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176831361 | |||||||
| chr5:176831400 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(192): Show |
199 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.70+20580A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176831400 | |||||||
| chr5:176831588 | C | T | 1 | a0001c0001t0010g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.70+20768C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176831588 | |||||||
| chr5:176831685 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.70+20865C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176831685 | |||||||
| chr5:176831727 | G | A | 42 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0071 others(39): Show |
43 | HG00609.hp1 HG00733.hp1 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.70+20907G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176831727 | |||||||
| chr5:176831767 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0033 |
2 | NA18944.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.70+20947C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176831767 | |||||||
| chr5:176831792 | C | T | 3 | a0001c0001t0001g0064 a0001c0001t0002g0062 a0001c0001t0002g0063 |
3 | HG01106.hp1 HG02300.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.70+20972C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176831792 | |||||||
| chr5:176831871 | C | G | 1 | a0001c0001t0001g0260 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.70+21051C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176831871 | |||||||
| chr5:176831883 | C | CT | 5 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(2): Show |
5 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+21064dupT | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176831883 | ||||||
| chr5:176831883 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0003g0049 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.70+21064_70+21065i others(12): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176831883 | ||||||
| chr5:176831883 | C | CTTTTTTT others(4): Show |
1 | a0002c0002t0004g0048 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.70+21064_70+21065i others(13): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176831883 | ||||||
| chr5:176831883 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0219 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.70+21064_70+21065i others(14): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176831883 | ||||||
| chr5:176831883 | C | T | 3 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0013g0095 |
3 | HG02451.hp2 NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.70+21063C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176831883 | |||||||
| chr5:176831883 | CTCT | C | 5 | a0001c0001t0001g0045 a0001c0001t0001g0064 a0001c0001t0002g0062 others(2): Show |
5 | HG01106.hp1 HG02300.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+21065_70+21067d others(5): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176831883 | ||||||
| chr5:176831883 | CTCTTTTT others(2): Show |
C | 5 | a0001c0001t0001g0047 a0001c0001t0001g0099 a0001c0001t0001g0229 others(2): Show |
5 | HG02559.hp2 HG02622.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+21065_70+21073d others(11): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176831883 | ||||||
| chr5:176831883 | CTCTTTTT others(3): Show |
C | 11 | a0001c0001t0001g0002 a0001c0001t0001g0154 a0001c0001t0001g0170 others(8): Show |
12 | HG01081.hp1 HG01256.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.70+21065_70+21074d others(12): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176831883 | ||||||
| chr5:176831883 | CTCTTTTT others(4): Show |
C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0024 others(142): Show |
148 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.70+21065_70+21075d others(13): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176831883 | ||||||
| chr5:176831883 | CTCTTTTT others(5): Show |
C | 8 | a0001c0001t0001g0067 a0001c0001t0001g0125 a0001c0001t0001g0162 others(5): Show |
8 | HG02040.hp1 HG02602.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.70+21065_70+21076d others(14): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176831883 | ||||||
| chr5:176831885 | C | T | 13 | a0001c0001t0001g0094 a0001c0001t0001g0219 a0001c0001t0002g0010 others(10): Show |
13 | HG01109.hp1 HG01891.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.70+21065C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176831885 | |||||||
| chr5:176831885 | CT | C | 12 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0224 others(9): Show |
13 | HG01243.hp2 HG01496.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.70+21094delT | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176831885 | ||||||
| chr5:176831885 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.70+21084_70+21094d others(13): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176831885 | ||||||
| chr5:176831885 | CTTTTTTT others(5): Show |
C | 40 | a0001c0001t0001g0014 a0001c0001t0001g0071 a0001c0001t0001g0108 others(37): Show |
41 | HG00609.hp1 HG00733.hp1 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.70+21083_70+21094d others(14): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176831885 | ||||||
| chr5:176831885 | CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0003g0050 a0001c0001t0005g0249 |
2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.70+21082_70+21094d others(15): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176831885 | ||||||
| chr5:176832120 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0172 |
2 | HG01361.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.70+21300C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176832120 | |||||||
| chr5:176832144 | A | G | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(234): Show |
242 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(239): Show |
intron_variant | MODIFIER | c.70+21324A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176832144 | |||||||
| chr5:176832181 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.70+21361G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176832181 | |||||||
| chr5:176832188 | T | C | 1 | a0001c0001t0010g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.70+21368T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176832188 | |||||||
| chr5:176832243 | C | G | 1 | a0001c0001t0002g0215 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.70+21423C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176832243 | |||||||
| chr5:176832309 | A | G | 2 | a0001c0001t0007g0242 a0001c0001t0007g0247 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.70+21489A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176832309 | |||||||
| chr5:176832392 | C | T | 2 | a0001c0001t0007g0242 a0001c0001t0007g0247 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.70+21572C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176832392 | |||||||
| chr5:176832406 | T | C | 1 | a0001c0001t0003g0245 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.70+21586T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176832406 | |||||||
| chr5:176832644 | G | C | 1 | a0001c0001t0001g0086 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.70+21824G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176832644 | |||||||
| chr5:176832813 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.70+21993G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176832813 | |||||||
| chr5:176832885 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.70+22065G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176832885 | |||||||
| chr5:176833072 | A | C | 38 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0071 others(35): Show |
39 | HG00609.hp1 HG01243.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.70+22252A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833072 | |||||||
| chr5:176833103 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.70+22283C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833103 | |||||||
| chr5:176833184 | G | A | 1 | a0001c0001t0002g0040 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.70+22364G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833184 | |||||||
| chr5:176833288 | G | A | 1 | a0001c0001t0002g0257 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.70+22468G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833288 | |||||||
| chr5:176833325 | C | T | 43 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0071 others(40): Show |
44 | HG00609.hp1 HG00733.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.70+22505C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833325 | |||||||
| chr5:176833328 | T | TG | 43 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0071 others(40): Show |
44 | HG00609.hp1 HG00733.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.70+22509dupG | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176833328 | ||||||
| chr5:176833473 | A | T | 1 | a0001c0001t0002g0171 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.70+22653A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833473 | |||||||
| chr5:176833491 | T | G | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(233): Show |
241 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(238): Show |
intron_variant | MODIFIER | c.70+22671T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833491 | |||||||
| chr5:176833580 | G | T | 2 | a0001c0001t0007g0242 a0001c0001t0007g0247 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.70+22760G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833580 | |||||||
| chr5:176833670 | C | T | 3 | a0001c0001t0003g0065 a0001c0001t0011g0015 a0002c0002t0004g0066 |
3 | HG03209.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.70+22850C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833670 | |||||||
| chr5:176833699 | T | C | 2 | a0001c0004t0002g0232 a0001c0004t0002g0233 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.70+22879T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833699 | |||||||
| chr5:176833713 | C | CT | 28 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0018 others(25): Show |
29 | HG00733.hp1 HG01109.hp1 HG01516.hp1 others(26): Show |
intron_variant | MODIFIER | c.70+22907dupT | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176833713 | ||||||
| chr5:176833732 | C | T | 9 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0028 others(6): Show |
9 | HG02027.hp2 HG02080.hp2 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.70+22912C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833732 | |||||||
| chr5:176833770 | G | A | 3 | a0001c0001t0003g0050 a0001c0001t0003g0111 a0002c0002t0001g0112 |
3 | HG02572.hp2 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.70+22950G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833770 | |||||||
| chr5:176833858 | A | G | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(256): Show |
265 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(262): Show |
intron_variant | MODIFIER | c.70+23038A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833858 | |||||||
| chr5:176833865 | C | T | 5 | a0001c0001t0001g0045 a0001c0001t0001g0094 a0001c0001t0003g0092 others(2): Show |
5 | HG02451.hp2 HG03130.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+23045C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833865 | |||||||
| chr5:176833917 | G | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(190): Show |
197 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(194): Show |
intron_variant | MODIFIER | c.70+23097G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833917 | |||||||
| chr5:176834037 | A | G | 1 | a0001c0001t0002g0038 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.70+23217A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176834037 | |||||||
| chr5:176834115 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.70+23295G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176834115 | |||||||
| chr5:176834210 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0002g0193 |
2 | NA18945.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.70+23390G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176834210 | |||||||
| chr5:176834488 | G | A | 1 | a0001c0001t0002g0038 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.70+23668G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176834488 | |||||||
| chr5:176834665 | T | TTC | 27 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0129 others(24): Show |
29 | HG00099.hp1 HG00733.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.70+23883_70+23884d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176834665 | ||||||
| chr5:176834665 | T | TTCTC | 28 | a0001c0001t0001g0071 a0001c0001t0001g0076 a0001c0001t0001g0106 others(25): Show |
28 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.70+23881_70+23884d others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176834665 | ||||||
| chr5:176834665 | T | TTCTCTC | 54 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0042 others(51): Show |
56 | HG00609.hp2 HG00642.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.70+23879_70+23884d others(8): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176834665 | ||||||
| chr5:176834665 | T | TTCTCTCT others(1): Show |
47 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0028 others(44): Show |
47 | HG00621.hp2 HG00735.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.70+23877_70+23884d others(10): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176834665 | ||||||
| chr5:176834665 | T | TTCTCTCT others(3): Show |
27 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0035 others(24): Show |
28 | HG01081.hp1 HG01255.hp1 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.70+23875_70+23884d others(12): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176834665 | ||||||
| chr5:176834665 | T | TTCTCTCT others(5): Show |
17 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0141 others(14): Show |
17 | HG00099.hp2 HG00639.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.70+23873_70+23884d others(14): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176834665 | ||||||
| chr5:176834665 | T | TTCTCTCT others(7): Show |
6 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0094 others(3): Show |
6 | HG02055.hp1 HG02451.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.70+23871_70+23884d others(16): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176834665 | ||||||
| chr5:176834665 | T | TTCTCTCT others(9): Show |
2 | a0001c0001t0001g0045 a0001c0001t0013g0095 |
2 | NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.70+23869_70+23884d others(18): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176834665 | ||||||
| chr5:176834665 | T | TTCTCTCT others(11): Show |
3 | a0001c0001t0002g0143 a0001c0001t0002g0230 a0001c0001t0003g0093 |
3 | HG01167.hp1 NA18945.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.70+23867_70+23884d others(20): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176834665 | ||||||
| chr5:176834665 | T | TTCTCTCT others(15): Show |
1 | a0001c0001t0001g0018 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.70+23863_70+23884d others(24): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176834665 | ||||||
| chr5:176834665 | TTC | T | 9 | a0001c0001t0001g0145 a0001c0001t0001g0251 a0001c0001t0002g0090 others(6): Show |
10 | HG01243.hp2 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.70+23883_70+23884d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176834665 | ||||||
| chr5:176834665 | TTCTCTC | T | 4 | a0001c0001t0001g0047 a0001c0001t0001g0099 a0001c0001t0001g0229 others(1): Show |
4 | HG02559.hp2 HG02622.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+23879_70+23884d others(8): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176834665 | ||||||
| chr5:176834665 | TTCTCTCT others(3): Show |
T | 2 | a0001c0001t0003g0074 a0003c0003t0002g0073 |
2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.70+23875_70+23884d others(12): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176834665 | ||||||
| chr5:176834711 | C | G | 4 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+23891C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176834711 | |||||||
| chr5:176834751 | T | C | 2 | a0001c0004t0002g0232 a0001c0004t0002g0233 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.70+23931T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176834751 | |||||||
| chr5:176835031 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.70+24211C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176835031 | |||||||
| chr5:176835180 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.70+24360C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176835180 | |||||||
| chr5:176835223 | T | G | 2 | a0002c0002t0001g0006 a0003c0003t0002g0017 |
3 | HG01243.hp2 HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.70+24403T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176835223 | |||||||
| chr5:176835242 | T | C | 2 | a0001c0004t0002g0232 a0001c0004t0002g0233 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.70+24422T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176835242 | |||||||
| chr5:176835324 | T | A | 1 | a0001c0001t0002g0087 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.70+24504T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176835324 | |||||||
| chr5:176835374 | C | G | 3 | a0001c0001t0002g0060 a0001c0001t0002g0147 a0001c0001t0002g0181 |
3 | NA18944.hp1 NA18977.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.70+24554C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176835374 | |||||||
| chr5:176835426 | G | A | 11 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0057 others(8): Show |
12 | HG00642.hp2 HG00735.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.70+24606G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176835426 | |||||||
| chr5:176835512 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.70+24692C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176835512 | |||||||
| chr5:176835520 | G | A | 2 | a0001c0001t0002g0230 a0001c0001t0002g0231 |
2 | HG01167.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.70+24700G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176835520 | |||||||
| chr5:176835651 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.70+24831G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176835651 | |||||||
| chr5:176835729 | A | ATG | 10 | a0001c0001t0001g0077 a0001c0001t0001g0091 a0001c0001t0001g0125 others(7): Show |
10 | HG02015.hp1 HG02074.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.70+24941_70+24942d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176835729 | ||||||
| chr5:176835729 | A | ATGTG | 131 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0024 others(128): Show |
134 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.70+24939_70+24942d others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176835729 | ||||||
| chr5:176835729 | A | ATGTGTG | 14 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0079 others(11): Show |
15 | HG00558.hp1 HG01243.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.70+24937_70+24942d others(8): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176835729 | ||||||
| chr5:176835729 | A | ATGTGTGT others(1): Show |
5 | a0001c0001t0001g0178 a0001c0001t0002g0123 a0001c0001t0002g0189 others(2): Show |
5 | HG02080.hp1 HG02129.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+24935_70+24942d others(10): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176835729 | ||||||
| chr5:176835729 | A | ATGTGTGT others(3): Show |
2 | a0001c0001t0007g0242 a0001c0001t0010g0022 |
2 | HG02647.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.70+24933_70+24942d others(12): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176835729 | ||||||
| chr5:176835729 | A | ATGTGTGT others(5): Show |
2 | a0001c0001t0002g0038 a0001c0001t0007g0247 |
2 | HG01884.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.70+24931_70+24942d others(14): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176835729 | ||||||
| chr5:176835729 | ATG | A | 38 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0071 others(35): Show |
38 | HG00609.hp1 HG00733.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.70+24941_70+24942d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176835729 | ||||||
| chr5:176835753 | G | A | 44 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0071 others(41): Show |
45 | HG00609.hp1 HG00733.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.70+24933G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176835753 | |||||||
| chr5:176835753 | G | GTA | 7 | a0001c0001t0001g0219 a0001c0001t0001g0255 a0001c0001t0003g0011 others(4): Show |
7 | HG01109.hp1 HG02451.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.70+24934_70+24935i others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176835753 | ||||||
| chr5:176835753 | G | GTGTA | 10 | a0001c0001t0001g0047 a0001c0001t0001g0094 a0001c0001t0002g0010 others(7): Show |
10 | HG01891.hp2 HG02451.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.70+24936_70+24937i others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176835753 | ||||||
| chr5:176835753 | G | GTGTGTA | 10 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(7): Show |
10 | HG01106.hp1 HG01884.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.70+24938_70+24939i others(8): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176835753 | ||||||
| chr5:176836145 | A | T | 1 | a0001c0001t0001g0260 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.70+25325A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176836145 | |||||||
| chr5:176836148 | C | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(184): Show |
191 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(188): Show |
intron_variant | MODIFIER | c.70+25328C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176836148 | |||||||
| chr5:176836496 | C | T | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.70+25676C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176836496 | |||||||
| chr5:176836549 | A | G | 41 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0071 others(38): Show |
41 | HG00609.hp1 HG00733.hp1 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.70+25729A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176836549 | |||||||
| chr5:176836566 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.70+25746G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176836566 | |||||||
| chr5:176836660 | AG | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 |
3 | HG01884.hp2 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.70+25843delG | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176836660 | ||||||
| chr5:176836985 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.71-25639C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176836985 | |||||||
| chr5:176837014 | A | T | 1 | a0002c0002t0004g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.71-25610A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176837014 | |||||||
| chr5:176837049 | G | A | 3 | a0001c0001t0001g0219 a0001c0001t0003g0049 a0002c0002t0004g0048 |
3 | HG01109.hp1 HG02738.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.71-25575G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176837049 | |||||||
| chr5:176837596 | G | C | 1 | a0001c0001t0002g0085 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.71-25028G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176837596 | |||||||
| chr5:176837799 | T | G | 6 | a0001c0001t0001g0224 a0001c0001t0001g0226 a0001c0001t0003g0074 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-24825T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176837799 | |||||||
| chr5:176837821 | G | T | 1 | a0001c0001t0002g0058 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.71-24803G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176837821 | |||||||
| chr5:176837828 | G | T | 1 | a0001c0001t0012g0132 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.71-24796G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176837828 | |||||||
| chr5:176837983 | A | G | 3 | a0001c0001t0001g0064 a0001c0001t0002g0062 a0001c0001t0002g0063 |
3 | HG01106.hp1 HG02300.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.71-24641A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176837983 | |||||||
| chr5:176837998 | C | T | 1 | a0001c0001t0002g0187 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.71-24626C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176837998 | |||||||
| chr5:176838181 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 |
3 | HG01884.hp2 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.71-24443C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176838181 | |||||||
| chr5:176838224 | T | C | 3 | a0001c0001t0001g0064 a0001c0001t0002g0062 a0001c0001t0002g0063 |
3 | HG01106.hp1 HG02300.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.71-24400T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176838224 | |||||||
| chr5:176838281 | C | T | 2 | a0001c0001t0003g0245 a0001c0001t0003g0246 |
2 | HG02895.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.71-24343C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176838281 | |||||||
| chr5:176838282 | T | G | 2 | a0001c0001t0003g0245 a0001c0001t0003g0246 |
2 | HG02895.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.71-24342T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176838282 | |||||||
| chr5:176838296 | T | C | 2 | a0001c0004t0002g0232 a0001c0004t0002g0233 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.71-24328T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176838296 | |||||||
| chr5:176838543 | A | G | 5 | a0001c0001t0001g0047 a0001c0001t0001g0099 a0001c0001t0001g0229 others(2): Show |
5 | HG02559.hp2 HG02622.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-24081A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176838543 | |||||||
| chr5:176838710 | A | T | 5 | a0001c0001t0001g0047 a0001c0001t0001g0099 a0001c0001t0001g0229 others(2): Show |
5 | HG02559.hp2 HG02622.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-23914A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176838710 | |||||||
| chr5:176838830 | A | G | 13 | a0001c0001t0001g0045 a0001c0001t0001g0094 a0001c0001t0002g0010 others(10): Show |
13 | HG01891.hp2 HG02451.hp2 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.71-23794A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176838830 | |||||||
| chr5:176838900 | A | G | 5 | a0001c0001t0001g0047 a0001c0001t0001g0099 a0001c0001t0001g0229 others(2): Show |
5 | HG02559.hp2 HG02622.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-23724A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176838900 | |||||||
| chr5:176838981 | T | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(208): Show |
216 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(213): Show |
intron_variant | MODIFIER | c.71-23643T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176838981 | |||||||
| chr5:176839083 | T | A | 2 | a0001c0001t0005g0008 a0001c0001t0005g0023 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.71-23541T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839083 | |||||||
| chr5:176839368 | C | G | 2 | a0002c0002t0001g0006 a0003c0003t0002g0017 |
3 | HG01243.hp2 HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.71-23256C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839368 | |||||||
| chr5:176839462 | G | C | 1 | a0001c0001t0001g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.71-23162G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839462 | |||||||
| chr5:176839472 | T | A | 29 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0019 others(26): Show |
30 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.71-23152T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839472 | |||||||
| chr5:176839481 | T | C | 3 | a0001c0001t0005g0008 a0001c0001t0005g0023 a0001c0001t0014g0061 |
3 | HG02630.hp1 HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.71-23143T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839481 | |||||||
| chr5:176839590 | T | G | 3 | a0001c0001t0001g0064 a0001c0001t0002g0062 a0001c0001t0002g0063 |
3 | HG01106.hp1 HG02300.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.71-23034T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839590 | |||||||
| chr5:176839601 | G | T | 2 | a0001c0001t0003g0080 a0001c0001t0003g0081 |
2 | HG01891.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.71-23023G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839601 | |||||||
| chr5:176839673 | G | A | 1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.71-22951G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839673 | |||||||
| chr5:176839717 | C | A | 23 | a0001c0001t0001g0036 a0001c0001t0001g0071 a0001c0001t0001g0108 others(20): Show |
23 | HG00558.hp1 HG00609.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.71-22907C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839717 | |||||||
| chr5:176839721 | G | A | 23 | a0001c0001t0001g0036 a0001c0001t0001g0071 a0001c0001t0001g0108 others(20): Show |
23 | HG00558.hp1 HG00609.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.71-22903G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839721 | |||||||
| chr5:176839740 | A | G | 11 | a0001c0001t0001g0045 a0001c0001t0002g0038 a0001c0001t0002g0097 others(8): Show |
11 | HG01109.hp1 HG02486.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.71-22884A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839740 | |||||||
| chr5:176839797 | C | T | 5 | a0001c0001t0003g0049 a0001c0001t0003g0065 a0001c0001t0007g0242 others(2): Show |
5 | HG01109.hp1 HG02647.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-22827C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839797 | |||||||
| chr5:176839807 | C | CT | 16 | a0001c0001t0001g0034 a0001c0001t0001g0072 a0001c0001t0001g0110 others(13): Show |
16 | HG00621.hp1 HG00735.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.71-22791dupT | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176839807 | ||||||
| chr5:176839807 | CT | C | 23 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0019 others(20): Show |
23 | HG01081.hp1 HG01168.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.71-22791delT | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176839807 | ||||||
| chr5:176839833 | T | C | 8 | a0001c0001t0001g0094 a0001c0001t0001g0255 a0001c0001t0003g0092 others(5): Show |
8 | HG02451.hp2 HG02647.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-22791T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839833 | |||||||
| chr5:176839873 | G | C | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | HG02257.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.71-22751G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839873 | |||||||
| chr5:176839911 | G | T | 2 | a0001c0001t0003g0080 a0001c0001t0003g0081 |
2 | HG01891.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.71-22713G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839911 | |||||||
| chr5:176839947 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.71-22677G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839947 | |||||||
| chr5:176839972 | A | G | 12 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(9): Show |
12 | HG01884.hp2 HG02055.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.71-22652A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839972 | |||||||
| chr5:176839980 | G | A | 8 | a0001c0001t0001g0219 a0001c0001t0002g0186 a0001c0001t0002g0187 others(5): Show |
8 | HG01361.hp1 HG02572.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.71-22644G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839980 | |||||||
| chr5:176840147 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.71-22477G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176840147 | |||||||
| chr5:176840286 | A | G | 1 | a0001c0001t0001g0236 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.71-22338A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176840286 | |||||||
| chr5:176840331 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.71-22293C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176840331 | |||||||
| chr5:176840368 | G | A | 4 | a0001c0001t0001g0036 a0001c0001t0001g0064 a0001c0001t0002g0062 others(1): Show |
4 | HG01106.hp1 HG02300.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-22256G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176840368 | |||||||
| chr5:176840414 | G | A | 2 | a0001c0004t0002g0232 a0001c0004t0002g0233 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.71-22210G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176840414 | |||||||
| chr5:176840465 | T | C | 1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.71-22159T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176840465 | |||||||
| chr5:176840508 | A | T | 1 | a0001c0001t0001g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.71-22116A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176840508 | |||||||
| chr5:176840574 | G | A | 1 | a0001c0001t0001g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.71-22050G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176840574 | |||||||
| chr5:176840629 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.71-21995G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176840629 | |||||||
| chr5:176840685 | C | A | 2 | a0001c0001t0002g0097 a0001c0001t0003g0261 |
2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.71-21939C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176840685 | |||||||
| chr5:176840827 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.71-21797C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176840827 | |||||||
| chr5:176840828 | G | A | 4 | a0001c0001t0001g0236 a0001c0001t0005g0008 a0001c0001t0005g0023 others(1): Show |
4 | HG02630.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-21796G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176840828 | |||||||
| chr5:176840845 | G | A | 3 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0167 |
3 | NA19000.hp1 NA19002.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.71-21779G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176840845 | |||||||
| chr5:176840924 | G | A | 4 | a0001c0001t0001g0236 a0001c0001t0005g0008 a0001c0001t0005g0023 others(1): Show |
4 | HG02630.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-21700G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176840924 | |||||||
| chr5:176841016 | G | A | 6 | a0001c0001t0003g0250 a0001c0001t0003g0254 a0001c0005t0002g0235 others(3): Show |
7 | HG02109.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-21608G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176841016 | |||||||
| chr5:176841039 | G | A | 1 | a0001c0001t0010g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.71-21585G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176841039 | |||||||
| chr5:176841040 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0229 |
2 | HG02622.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.71-21584C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176841040 | |||||||
| chr5:176841134 | G | A | 6 | a0001c0001t0003g0250 a0001c0001t0003g0254 a0001c0005t0002g0235 others(3): Show |
7 | HG02109.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-21490G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176841134 | |||||||
| chr5:176841201 | C | G | 8 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(5): Show |
8 | HG01891.hp2 HG02280.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-21423C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176841201 | |||||||
| chr5:176841367 | C | G | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.71-21257C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176841367 | |||||||
| chr5:176841442 | G | A | 9 | a0001c0001t0001g0016 a0001c0001t0003g0250 a0001c0001t0003g0254 others(6): Show |
10 | HG01243.hp1 HG02109.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.71-21182G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176841442 | |||||||
| chr5:176841499 | T | C | 41 | a0001c0001t0001g0036 a0001c0001t0001g0064 a0001c0001t0001g0236 others(38): Show |
41 | HG00733.hp1 HG01106.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.71-21125T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176841499 | |||||||
| chr5:176841822 | G | T | 32 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0064 others(29): Show |
34 | HG01106.hp1 HG01243.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.71-20802G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176841822 | |||||||
| chr5:176841868 | T | C | 8 | a0001c0001t0003g0049 a0001c0001t0003g0065 a0001c0001t0011g0015 others(5): Show |
8 | HG01109.hp1 HG03209.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.71-20756T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176841868 | |||||||
| chr5:176841922 | G | T | 1 | a0002c0002t0004g0165 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.71-20702G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176841922 | |||||||
| chr5:176841925 | C | T | 8 | a0001c0001t0003g0250 a0001c0001t0003g0254 a0001c0004t0002g0232 others(5): Show |
9 | HG02109.hp1 HG02451.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.71-20699C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176841925 | |||||||
| chr5:176841939 | G | T | 35 | a0001c0001t0001g0016 a0001c0001t0001g0219 a0001c0001t0001g0236 others(32): Show |
37 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.71-20685G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176841939 | |||||||
| chr5:176842013 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.71-20611T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176842013 | |||||||
| chr5:176842014 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.71-20610G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176842014 | |||||||
| chr5:176842070 | G | A | 1 | a0001c0001t0010g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.71-20554G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176842070 | |||||||
| chr5:176842192 | G | A | 3 | a0001c0001t0007g0083 a0001c0001t0007g0242 a0001c0001t0007g0247 |
3 | HG01884.hp1 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.71-20432G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176842192 | |||||||
| chr5:176842443 | G | A | 35 | a0001c0001t0001g0016 a0001c0001t0001g0219 a0001c0001t0001g0236 others(32): Show |
37 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.71-20181G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176842443 | |||||||
| chr5:176842446 | G | A | 8 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(5): Show |
8 | HG01891.hp2 HG02280.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-20178G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176842446 | |||||||
| chr5:176842492 | G | GAT | 5 | a0001c0001t0001g0036 a0001c0001t0001g0064 a0001c0001t0001g0091 others(2): Show |
5 | HG01106.hp1 HG02300.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-20115_71-20114d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176842492 | ||||||
| chr5:176842492 | G | GATATATA others(3): Show |
5 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0011 others(2): Show |
5 | HG02280.hp2 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-20123_71-20114d others(12): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176842492 | ||||||
| chr5:176842492 | G | GATATATA others(5): Show |
3 | a0001c0001t0003g0009 a0001c0001t0003g0080 a0001c0001t0003g0081 |
3 | HG01891.hp2 HG03041.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.71-20125_71-20114d others(14): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176842492 | ||||||
| chr5:176842492 | G | GATATATA others(7): Show |
2 | a0001c0001t0005g0013 a0003c0003t0001g0084 |
2 | HG00733.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.71-20127_71-20114d others(16): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176842492 | ||||||
| chr5:176842492 | G | GATATATA others(11): Show |
1 | a0001c0001t0003g0261 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.71-20131_71-20114d others(20): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176842492 | ||||||
| chr5:176842492 | G | GATATATA others(13): Show |
4 | a0001c0001t0002g0097 a0001c0001t0002g0100 a0001c0001t0002g0118 others(1): Show |
4 | HG02145.hp1 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-20114_71-20113i others(22): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176842492 | ||||||
| chr5:176842492 | G | GATATATA others(15): Show |
1 | a0001c0001t0002g0096 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.71-20114_71-20113i others(24): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176842492 | ||||||
| chr5:176842492 | G | GATATATA others(17): Show |
3 | a0001c0001t0001g0251 a0001c0001t0002g0090 a0001c0001t0003g0259 |
3 | HG02896.hp1 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.71-20114_71-20113i others(26): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176842492 | ||||||
| chr5:176842492 | G | GATATATA others(19): Show |
1 | a0001c0001t0010g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.71-20114_71-20113i others(28): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176842492 | ||||||
| chr5:176842492 | G | GATATATA others(21): Show |
2 | a0001c0001t0002g0184 a0001c0001t0002g0231 |
2 | HG02572.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.71-20114_71-20113i others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176842492 | ||||||
| chr5:176842492 | G | GATATATA others(23): Show |
1 | a0001c0001t0002g0230 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.71-20114_71-20113i others(32): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176842492 | ||||||
| chr5:176842492 | GAT | G | 35 | a0001c0001t0001g0016 a0001c0001t0001g0219 a0001c0001t0001g0236 others(32): Show |
37 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.71-20115_71-20114d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176842492 | ||||||
| chr5:176842834 | C | T | 8 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(5): Show |
8 | HG01891.hp2 HG02280.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-19790C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176842834 | |||||||
| chr5:176843068 | G | A | 1 | a0003c0003t0001g0084 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.71-19556G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843068 | |||||||
| chr5:176843172 | AAAAG | A | 15 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0236 others(12): Show |
16 | HG00733.hp1 HG01167.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.71-19432_71-19429d others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176843172 | ||||||
| chr5:176843173 | AAAG | A | 27 | a0001c0001t0001g0219 a0001c0001t0001g0224 a0001c0001t0001g0226 others(24): Show |
28 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.71-19448_71-19446d others(5): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176843173 | ||||||
| chr5:176843209 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.71-19415A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843209 | |||||||
| chr5:176843242 | G | A | 2 | a0001c0004t0002g0232 a0001c0004t0002g0233 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.71-19382G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843242 | |||||||
| chr5:176843295 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.71-19329C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843295 | |||||||
| chr5:176843355 | C | T | 18 | a0001c0001t0001g0016 a0001c0001t0001g0219 a0001c0001t0002g0186 others(15): Show |
20 | HG01243.hp1 HG01243.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.71-19269C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843355 | |||||||
| chr5:176843359 | A | T | 15 | a0001c0001t0001g0236 a0001c0001t0003g0049 a0001c0001t0003g0065 others(12): Show |
15 | HG01109.hp1 HG01884.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.71-19265A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843359 | |||||||
| chr5:176843392 | C | T | 11 | a0001c0001t0001g0219 a0001c0001t0002g0186 a0001c0001t0002g0187 others(8): Show |
12 | HG01243.hp2 HG01361.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.71-19232C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843392 | |||||||
| chr5:176843461 | G | T | 4 | a0001c0001t0001g0236 a0001c0001t0005g0008 a0001c0001t0005g0023 others(1): Show |
4 | HG02630.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-19163G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843461 | |||||||
| chr5:176843643 | G | A | 2 | a0001c0001t0002g0121 a0001c0001t0002g0143 |
2 | NA18945.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.71-18981G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843643 | |||||||
| chr5:176843687 | A | G | 1 | a0001c0001t0001g0251 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.71-18937A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843687 | |||||||
| chr5:176843803 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.71-18821C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843803 | |||||||
| chr5:176843844 | C | T | 5 | a0001c0001t0001g0236 a0001c0001t0005g0008 a0001c0001t0005g0023 others(2): Show |
5 | HG02630.hp1 HG02976.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-18780C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843844 | |||||||
| chr5:176843864 | G | A | 2 | a0001c0004t0002g0232 a0001c0004t0002g0233 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.71-18760G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843864 | |||||||
| chr5:176843887 | G | A | 11 | a0001c0001t0003g0049 a0001c0001t0003g0065 a0001c0001t0007g0083 others(8): Show |
11 | HG01109.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.71-18737G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843887 | |||||||
| chr5:176843888 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.71-18736G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843888 | |||||||
| chr5:176844075 | C | G | 63 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0064 others(60): Show |
65 | HG00733.hp1 HG01106.hp1 HG01109.hp1 others(62): Show |
intron_variant | MODIFIER | c.71-18549C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176844075 | |||||||
| chr5:176844270 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.71-18354G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176844270 | |||||||
| chr5:176844529 | T | C | 53 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0064 others(50): Show |
54 | HG00733.hp1 HG01106.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.71-18095T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176844529 | |||||||
| chr5:176844730 | C | T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0064 a0001c0001t0002g0062 others(1): Show |
4 | HG01106.hp1 HG02300.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-17894C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176844730 | |||||||
| chr5:176844790 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.71-17834G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176844790 | |||||||
| chr5:176844796 | C | T | 1 | a0002c0002t0001g0112 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.71-17828C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176844796 | |||||||
| chr5:176844817 | C | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0002g0090 others(17): Show |
20 | HG00733.hp1 HG01167.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.71-17807C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176844817 | |||||||
| chr5:176844944 | G | A | 11 | a0001c0001t0003g0049 a0001c0001t0003g0065 a0001c0001t0007g0083 others(8): Show |
11 | HG01109.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.71-17680G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176844944 | |||||||
| chr5:176845167 | C | T | 1 | a0001c0001t0002g0063 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.71-17457C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845167 | |||||||
| chr5:176845180 | T | C | 35 | a0001c0001t0001g0094 a0001c0001t0001g0251 a0001c0001t0002g0010 others(32): Show |
35 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.71-17444T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845180 | |||||||
| chr5:176845216 | G | A | 3 | a0001c0001t0001g0099 a0001c0001t0001g0229 a0001c0001t0002g0257 |
3 | HG02622.hp1 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.71-17408G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845216 | |||||||
| chr5:176845287 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.71-17337C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845287 | |||||||
| chr5:176845310 | C | T | 2 | a0001c0001t0002g0100 a0001c0001t0002g0118 |
2 | HG02145.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.71-17314C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845310 | |||||||
| chr5:176845314 | C | G | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.71-17310C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845314 | |||||||
| chr5:176845392 | C | T | 1 | a0003c0003t0001g0084 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.71-17232C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845392 | |||||||
| chr5:176845459 | G | A | 1 | a0001c0001t0011g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.71-17165G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845459 | |||||||
| chr5:176845641 | A | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0234 |
2 | HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.71-16983A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845641 | |||||||
| chr5:176845696 | C | A | 1 | a0001c0001t0010g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.71-16928C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845696 | |||||||
| chr5:176845853 | C | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0153 |
2 | HG02300.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.71-16771C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845853 | |||||||
| chr5:176845924 | C | T | 11 | a0001c0001t0003g0049 a0001c0001t0003g0065 a0001c0001t0007g0083 others(8): Show |
11 | HG01109.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.71-16700C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845924 | |||||||
| chr5:176845948 | T | G | 1 | a0001c0001t0001g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.71-16676T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845948 | |||||||
| chr5:176845950 | C | G | 1 | a0001c0001t0001g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.71-16674C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845950 | |||||||
| chr5:176845952 | G | T | 1 | a0001c0001t0001g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.71-16672G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845952 | |||||||
| chr5:176845954 | A | C | 1 | a0001c0001t0001g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.71-16670A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845954 | |||||||
| chr5:176846007 | G | A | 1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.71-16617G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176846007 | |||||||
| chr5:176846069 | G | A | 7 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(4): Show |
7 | HG01891.hp2 HG02280.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-16555G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176846069 | |||||||
| chr5:176846369 | G | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(185): Show |
193 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(190): Show |
intron_variant | MODIFIER | c.71-16255G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176846369 | |||||||
| chr5:176846384 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.71-16240G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176846384 | |||||||
| chr5:176846460 | T | C | 40 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(37): Show |
40 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.71-16164T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176846460 | |||||||
| chr5:176846641 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.71-15983C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176846641 | |||||||
| chr5:176846807 | C | T | 3 | a0001c0001t0007g0083 a0001c0001t0007g0242 a0001c0001t0007g0247 |
3 | HG01884.hp1 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.71-15817C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176846807 | |||||||
| chr5:176846808 | G | A | 2 | a0001c0001t0002g0147 a0001c0001t0002g0181 |
2 | NA18944.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.71-15816G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176846808 | |||||||
| chr5:176846828 | G | A | 5 | a0001c0001t0001g0162 a0001c0001t0002g0003 a0001c0001t0002g0070 others(2): Show |
6 | HG01069.hp2 HG01074.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-15796G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176846828 | |||||||
| chr5:176846829 | G | A | 25 | a0001c0001t0001g0219 a0001c0001t0001g0236 a0001c0001t0002g0186 others(22): Show |
26 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.71-15795G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176846829 | |||||||
| chr5:176846898 | G | C | 1 | a0001c0001t0001g0156 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.71-15726G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176846898 | |||||||
| chr5:176846919 | T | A | 1 | a0001c0001t0001g0176 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.71-15705T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176846919 | |||||||
| chr5:176846951 | A | G | 25 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0175 others(22): Show |
25 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.71-15673A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176846951 | |||||||
| chr5:176847004 | G | T | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.71-15620G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176847004 | |||||||
| chr5:176847044 | C | T | 2 | a0001c0001t0002g0230 a0001c0001t0002g0231 |
2 | HG01167.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.71-15580C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176847044 | |||||||
| chr5:176847138 | G | A | 5 | a0001c0001t0002g0051 a0001c0001t0002g0137 a0001c0001t0002g0140 others(2): Show |
5 | HG00621.hp1 HG02523.hp2 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-15486G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176847138 | |||||||
| chr5:176847729 | G | T | 5 | a0001c0001t0001g0064 a0001c0001t0002g0058 a0001c0001t0002g0062 others(2): Show |
5 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-14895G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176847729 | |||||||
| chr5:176847730 | AT | A | 6 | a0001c0001t0011g0015 a0002c0002t0004g0021 a0002c0002t0004g0048 others(3): Show |
6 | HG01109.hp1 HG03209.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-14891delT | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176847730 | ||||||
| chr5:176847746 | A | C | 3 | a0001c0001t0001g0106 a0001c0001t0001g0135 a0001c0001t0001g0136 |
3 | HG03704.hp1 HG03834.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.71-14878A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176847746 | |||||||
| chr5:176847752 | T | A | 2 | a0001c0001t0002g0090 a0001c0001t0002g0184 |
2 | HG02572.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.71-14872T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176847752 | |||||||
| chr5:176847901 | G | C | 11 | a0001c0001t0002g0230 a0001c0001t0002g0231 a0001c0001t0007g0083 others(8): Show |
11 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.71-14723G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176847901 | |||||||
| chr5:176848086 | A | ACTGACCA others(1): Show |
16 | a0001c0001t0001g0175 a0001c0001t0002g0090 a0001c0001t0002g0097 others(13): Show |
16 | HG00099.hp1 HG00639.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.71-14528_71-14521d others(10): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176848086 | ||||||
| chr5:176848139 | C | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0002g0075 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-14485C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176848139 | |||||||
| chr5:176848188 | G | A | 6 | a0001c0001t0001g0036 a0001c0001t0001g0224 a0001c0001t0001g0226 others(3): Show |
6 | HG01496.hp1 HG01891.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-14436G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176848188 | |||||||
| chr5:176848276 | A | T | 1 | a0001c0001t0002g0194 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.71-14348A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176848276 | |||||||
| chr5:176848283 | A | G | 6 | a0001c0001t0002g0248 a0001c0001t0003g0250 a0001c0001t0003g0254 others(3): Show |
7 | HG02615.hp1 HG02723.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-14341A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176848283 | |||||||
| chr5:176848529 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.71-14095C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176848529 | |||||||
| chr5:176848716 | G | A | 22 | a0001c0001t0001g0219 a0001c0001t0002g0186 a0001c0001t0002g0187 others(19): Show |
23 | HG01109.hp1 HG01167.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.71-13908G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176848716 | |||||||
| chr5:176848803 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.71-13821G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176848803 | |||||||
| chr5:176848817 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.71-13807G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176848817 | |||||||
| chr5:176848921 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.71-13703C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176848921 | |||||||
| chr5:176848936 | G | A | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.71-13688G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176848936 | |||||||
| chr5:176849184 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.71-13440C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176849184 | |||||||
| chr5:176849445 | T | C | 44 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0064 others(41): Show |
45 | HG01081.hp2 HG01106.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.71-13179T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176849445 | |||||||
| chr5:176849451 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.71-13173G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176849451 | |||||||
| chr5:176849510 | G | T | 1 | a0001c0001t0002g0040 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.71-13114G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176849510 | |||||||
| chr5:176849541 | C | T | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.71-13083C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176849541 | |||||||
| chr5:176849570 | G | A | 1 | a0001c0001t0001g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.71-13054G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176849570 | |||||||
| chr5:176849583 | A | T | 1 | a0001c0001t0002g0200 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.71-13041A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176849583 | |||||||
| chr5:176849744 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0156 |
2 | HG00733.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.71-12880C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176849744 | |||||||
| chr5:176849986 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0030 |
2 | HG02080.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.71-12638C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176849986 | |||||||
| chr5:176850103 | G | A | 6 | a0001c0001t0002g0248 a0001c0001t0003g0250 a0001c0001t0003g0254 others(3): Show |
7 | HG02615.hp1 HG02723.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-12521G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176850103 | |||||||
| chr5:176850116 | T | C | 53 | a0001c0001t0001g0064 a0001c0001t0001g0144 a0001c0001t0001g0219 others(50): Show |
55 | HG01081.hp2 HG01106.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.71-12508T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176850116 | |||||||
| chr5:176850186 | T | G | 1 | a0001c0001t0002g0168 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.71-12438T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176850186 | |||||||
| chr5:176850206 | G | A | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.71-12418G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176850206 | |||||||
| chr5:176850281 | C | G | 3 | a0001c0001t0005g0008 a0001c0001t0005g0023 a0001c0001t0014g0061 |
3 | HG02630.hp1 HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.71-12343C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176850281 | |||||||
| chr5:176850327 | G | T | 11 | a0001c0001t0001g0219 a0001c0001t0001g0234 a0001c0001t0002g0186 others(8): Show |
12 | HG01243.hp2 HG01361.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.71-12297G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176850327 | |||||||
| chr5:176850434 | G | A | 3 | a0001c0001t0010g0022 a0001c0004t0002g0232 a0001c0004t0002g0233 |
3 | HG02451.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.71-12190G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176850434 | |||||||
| chr5:176850453 | G | A | 1 | a0001c0001t0002g0257 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.71-12171G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176850453 | |||||||
| chr5:176850494 | T | G | 2 | a0001c0001t0001g0077 a0001c0004t0002g0078 |
2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.71-12130T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176850494 | |||||||
| chr5:176850503 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.71-12121T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176850503 | |||||||
| chr5:176850574 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0045 |
3 | HG01243.hp1 HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.71-12050G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176850574 | |||||||
| chr5:176850599 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.71-12025G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176850599 | |||||||
| chr5:176850628 | G | A | 4 | a0001c0001t0010g0022 a0002c0002t0004g0021 a0002c0002t0004g0048 others(1): Show |
4 | HG01109.hp1 HG03139.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-11996G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176850628 | |||||||
| chr5:176850932 | C | T | 10 | a0001c0001t0002g0230 a0001c0001t0002g0231 a0001c0001t0003g0244 others(7): Show |
10 | HG01167.hp1 HG01884.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.71-11692C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176850932 | |||||||
| chr5:176850950 | TCCAGTGC others(12): Show |
T | 2 | a0001c0001t0002g0096 a0001c0001t0008g0113 |
2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.71-11648_71-11630d others(21): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176850950 | ||||||
| chr5:176851060 | G | A | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.71-11564G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176851060 | |||||||
| chr5:176851096 | C | G | 1 | a0001c0001t0002g0116 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.71-11528C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176851096 | |||||||
| chr5:176851189 | T | G | 2 | a0001c0001t0001g0192 a0001c0001t0002g0191 |
2 | HG02132.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.71-11435T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176851189 | |||||||
| chr5:176851453 | A | G | 1 | a0001c0001t0001g0258 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.71-11171A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176851453 | |||||||
| chr5:176851524 | A | T | 28 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0031 others(25): Show |
29 | HG00558.hp1 HG00609.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.71-11100A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176851524 | |||||||
| chr5:176851565 | G | A | 7 | a0001c0001t0011g0015 a0002c0002t0001g0006 a0002c0002t0004g0021 others(4): Show |
8 | HG01109.hp1 HG01243.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.71-11059G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176851565 | |||||||
| chr5:176851657 | C | T | 6 | a0001c0001t0002g0051 a0001c0001t0002g0137 a0001c0001t0002g0140 others(3): Show |
6 | HG00621.hp1 HG02135.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-10967C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176851657 | |||||||
| chr5:176851695 | G | A | 1 | a0001c0001t0005g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.71-10929G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176851695 | |||||||
| chr5:176851824 | C | T | 5 | a0001c0001t0001g0064 a0001c0001t0002g0058 a0001c0001t0002g0062 others(2): Show |
5 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-10800C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176851824 | |||||||
| chr5:176851853 | A | G | 102 | a0001c0001t0001g0064 a0001c0001t0001g0094 a0001c0001t0001g0127 others(99): Show |
105 | HG00099.hp1 HG00621.hp1 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.71-10771A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176851853 | |||||||
| chr5:176851857 | C | T | 12 | a0001c0001t0003g0244 a0001c0001t0005g0013 a0001c0001t0007g0083 others(9): Show |
13 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.71-10767C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176851857 | |||||||
| chr5:176851858 | G | A | 19 | a0001c0001t0001g0094 a0001c0001t0001g0219 a0001c0001t0001g0234 others(16): Show |
19 | HG01361.hp1 HG01891.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.71-10766G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176851858 | |||||||
| chr5:176851997 | C | T | 1 | a0001c0001t0001g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.71-10627C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176851997 | |||||||
| chr5:176852213 | C | T | 1 | a0001c0001t0005g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.71-10411C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176852213 | |||||||
| chr5:176852325 | TCACACAC others(5): Show |
T | 1 | a0001c0001t0002g0168 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.71-10282_71-10271d others(14): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176852325 | ||||||
| chr5:176852374 | G | GCA | 11 | a0001c0001t0003g0244 a0001c0001t0007g0083 a0001c0001t0007g0242 others(8): Show |
12 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.71-10234_71-10233d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176852374 | ||||||
| chr5:176852441 | C | T | 36 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0139 others(33): Show |
37 | HG00621.hp1 HG01069.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.71-10183C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176852441 | |||||||
| chr5:176852465 | G | A | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.71-10159G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176852465 | |||||||
| chr5:176852649 | G | A | 3 | a0001c0001t0010g0022 a0001c0004t0002g0232 a0001c0004t0002g0233 |
3 | HG02451.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.71-9975G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176852649 | |||||||
| chr5:176852696 | G | A | 1 | a0003c0003t0002g0240 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.71-9928G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176852696 | |||||||
| chr5:176852703 | C | T | 4 | a0001c0001t0002g0090 a0001c0001t0002g0100 a0001c0001t0002g0118 others(1): Show |
4 | HG02145.hp1 HG02572.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-9921C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176852703 | |||||||
| chr5:176852720 | C | T | 2 | a0001c0004t0002g0232 a0001c0004t0002g0233 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.71-9904C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176852720 | |||||||
| chr5:176852743 | C | T | 1 | a0001c0001t0002g0257 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.71-9881C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176852743 | |||||||
| chr5:176852762 | G | C | 1 | a0001c0001t0002g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.71-9862G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176852762 | |||||||
| chr5:176852764 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0120 |
2 | HG02698.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.71-9860G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176852764 | |||||||
| chr5:176852786 | G | A | 1 | a0001c0001t0002g0038 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.71-9838G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176852786 | |||||||
| chr5:176852877 | C | T | 2 | a0001c0001t0016g0161 a0002c0002t0004g0126 |
2 | HG02074.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.71-9747C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176852877 | |||||||
| chr5:176852878 | G | A | 1 | a0003c0003t0002g0107 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.71-9746G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176852878 | |||||||
| chr5:176853052 | G | A | 1 | a0001c0001t0003g0252 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.71-9572G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853052 | |||||||
| chr5:176853071 | G | A | 9 | a0001c0001t0007g0083 a0001c0001t0007g0242 a0001c0001t0007g0247 others(6): Show |
10 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.71-9553G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853071 | |||||||
| chr5:176853260 | C | T | 1 | a0001c0001t0003g0050 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.71-9364C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853260 | |||||||
| chr5:176853310 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0059 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.71-9314G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853310 | |||||||
| chr5:176853318 | C | T | 1 | a0001c0001t0005g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.71-9306C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853318 | |||||||
| chr5:176853348 | C | T | 1 | a0001c0001t0002g0143 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.71-9276C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853348 | |||||||
| chr5:176853480 | G | C | 1 | a0001c0001t0002g0257 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.71-9144G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853480 | |||||||
| chr5:176853584 | T | C | 29 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0094 others(26): Show |
30 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.71-9040T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853584 | |||||||
| chr5:176853598 | T | C | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.71-9026T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853598 | |||||||
| chr5:176853602 | G | A | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | NA19002.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.71-9022G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853602 | |||||||
| chr5:176853628 | C | T | 2 | a0001c0001t0001g0228 a0001c0001t0002g0055 |
2 | HG01257.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.71-8996C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853628 | |||||||
| chr5:176853801 | G | C | 27 | a0001c0001t0001g0175 a0001c0001t0002g0040 a0001c0001t0002g0090 others(24): Show |
28 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.71-8823G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853801 | |||||||
| chr5:176853898 | A | G | 8 | a0001c0001t0001g0094 a0001c0001t0011g0015 a0002c0002t0001g0006 others(5): Show |
9 | HG01109.hp1 HG01243.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.71-8726A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853898 | |||||||
| chr5:176853922 | G | A | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.71-8702G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853922 | |||||||
| chr5:176853924 | A | G | 33 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0031 others(30): Show |
34 | HG00558.hp1 HG00609.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.71-8700A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853924 | |||||||
| chr5:176854047 | A | G | 1 | a0002c0002t0004g0126 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.71-8577A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176854047 | |||||||
| chr5:176854086 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.71-8538C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176854086 | |||||||
| chr5:176854144 | C | A | 3 | a0001c0001t0001g0133 a0001c0001t0001g0203 a0001c0001t0001g0212 |
3 | HG01069.hp1 HG01071.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.71-8480C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176854144 | |||||||
| chr5:176854168 | C | G | 30 | a0001c0001t0001g0175 a0001c0001t0002g0040 a0001c0001t0002g0090 others(27): Show |
31 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.71-8456C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176854168 | |||||||
| chr5:176854286 | GTCTCTGT others(3): Show |
G | 20 | a0001c0001t0002g0040 a0001c0001t0003g0111 a0001c0001t0003g0244 others(17): Show |
21 | HG00735.hp1 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.71-8324_71-8315del others(10): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176854286 | ||||||
| chr5:176854319 | T | C | 35 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0139 others(32): Show |
36 | HG00621.hp1 HG01069.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.71-8305T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176854319 | |||||||
| chr5:176854322 | G | A | 1 | a0001c0001t0005g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.71-8302G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176854322 | |||||||
| chr5:176854327 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.71-8297G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176854327 | |||||||
| chr5:176854529 | C | T | 1 | a0001c0001t0003g0254 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.71-8095C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176854529 | |||||||
| chr5:176854670 | C | G | 4 | a0001c0001t0002g0090 a0001c0001t0002g0184 a0001c0001t0002g0186 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-7954C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176854670 | |||||||
| chr5:176854850 | A | G | 21 | a0001c0001t0001g0094 a0001c0001t0001g0234 a0001c0001t0002g0058 others(18): Show |
21 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(18): Show |
intron_variant | MODIFIER | c.71-7774A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176854850 | |||||||
| chr5:176855064 | A | G | 2 | a0001c0001t0005g0008 a0001c0001t0005g0023 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.71-7560A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176855064 | |||||||
| chr5:176855086 | G | A | 1 | a0001c0001t0005g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.71-7538G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176855086 | |||||||
| chr5:176855149 | C | T | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.71-7475C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176855149 | |||||||
| chr5:176855356 | G | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | HG02015.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.71-7268G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176855356 | |||||||
| chr5:176855362 | C | T | 5 | a0001c0001t0003g0111 a0003c0003t0001g0188 a0003c0003t0002g0017 others(2): Show |
5 | HG01361.hp1 HG02109.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-7262C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176855362 | |||||||
| chr5:176855379 | G | A | 12 | a0001c0001t0007g0083 a0001c0001t0007g0242 a0001c0001t0007g0247 others(9): Show |
13 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.71-7245G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176855379 | |||||||
| chr5:176855425 | G | A | 8 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(5): Show |
8 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.71-7199G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176855425 | |||||||
| chr5:176855615 | G | A | 1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.71-7009G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176855615 | |||||||
| chr5:176855731 | C | T | 4 | a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(1): Show |
4 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-6893C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176855731 | |||||||
| chr5:176855750 | T | C | 42 | a0001c0001t0001g0064 a0001c0001t0001g0127 a0001c0001t0001g0130 others(39): Show |
43 | HG00621.hp1 HG01069.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.71-6874T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176855750 | |||||||
| chr5:176855812 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0139 |
2 | NA19060.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.71-6812G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176855812 | |||||||
| chr5:176855980 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.71-6644C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176855980 | |||||||
| chr5:176855995 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.71-6629C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176855995 | |||||||
| chr5:176856018 | C | T | 4 | a0001c0001t0003g0244 a0001c0001t0010g0022 a0001c0004t0002g0232 others(1): Show |
4 | HG02451.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-6606C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176856018 | |||||||
| chr5:176856019 | G | A | 4 | a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(1): Show |
4 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-6605G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176856019 | |||||||
| chr5:176856052 | C | G | 13 | a0001c0001t0001g0094 a0001c0001t0003g0092 a0001c0001t0003g0093 others(10): Show |
13 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.71-6572C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176856052 | |||||||
| chr5:176856235 | G | A | 2 | a0001c0001t0002g0230 a0001c0001t0002g0231 |
2 | HG01167.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.71-6389G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176856235 | |||||||
| chr5:176856323 | G | A | 10 | a0001c0001t0002g0038 a0001c0001t0002g0051 a0001c0001t0002g0123 others(7): Show |
10 | HG00621.hp1 HG02080.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.71-6301G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176856323 | |||||||
| chr5:176856353 | C | T | 42 | a0001c0001t0001g0064 a0001c0001t0001g0127 a0001c0001t0001g0130 others(39): Show |
43 | HG00621.hp1 HG01069.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.71-6271C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176856353 | |||||||
| chr5:176856465 | C | T | 22 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0002g0248 others(19): Show |
23 | HG01891.hp1 HG01891.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.71-6159C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176856465 | |||||||
| chr5:176856484 | G | A | 3 | a0001c0001t0001g0057 a0001c0001t0001g0213 a0001c0001t0001g0216 |
3 | HG01928.hp2 HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.71-6140G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176856484 | |||||||
| chr5:176856645 | C | T | 2 | a0001c0001t0002g0230 a0001c0001t0002g0231 |
2 | HG01167.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.71-5979C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176856645 | |||||||
| chr5:176856716 | A | G | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.71-5908A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176856716 | |||||||
| chr5:176856770 | C | T | 3 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0167 |
3 | NA19000.hp1 NA19002.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.71-5854C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176856770 | |||||||
| chr5:176856789 | C | T | 1 | a0001c0001t0005g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.71-5835C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176856789 | |||||||
| chr5:176857045 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.71-5579C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176857045 | |||||||
| chr5:176857187 | C | G | 1 | a0001c0001t0002g0123 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.71-5437C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176857187 | |||||||
| chr5:176857239 | G | A | 4 | a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(1): Show |
4 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-5385G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176857239 | |||||||
| chr5:176857314 | T | G | 43 | a0001c0001t0001g0064 a0001c0001t0001g0127 a0001c0001t0001g0130 others(40): Show |
44 | HG00621.hp1 HG01069.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.71-5310T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176857314 | |||||||
| chr5:176857534 | C | T | 1 | a0002c0002t0004g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.71-5090C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176857534 | |||||||
| chr5:176857548 | C | T | 2 | a0001c0001t0002g0058 a0001c0001t0002g0087 |
2 | HG01081.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.71-5076C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176857548 | |||||||
| chr5:176857655 | G | C | 1 | a0001c0001t0001g0167 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.71-4969G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176857655 | |||||||
| chr5:176857712 | C | T | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
222 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(219): Show |
intron_variant | MODIFIER | c.71-4912C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176857712 | |||||||
| chr5:176857797 | C | T | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.71-4827C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176857797 | |||||||
| chr5:176857798 | G | A | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.71-4826G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176857798 | |||||||
| chr5:176857847 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 |
3 | HG01884.hp2 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.71-4777C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176857847 | |||||||
| chr5:176857895 | A | G | 1 | a0001c0001t0002g0168 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.71-4729A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176857895 | |||||||
| chr5:176857900 | A | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
222 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(219): Show |
intron_variant | MODIFIER | c.71-4724A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176857900 | |||||||
| chr5:176858046 | G | A | 6 | a0001c0001t0003g0111 a0003c0003t0001g0188 a0003c0003t0002g0017 others(3): Show |
6 | HG01361.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-4578G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858046 | |||||||
| chr5:176858053 | C | T | 4 | a0001c0001t0002g0248 a0001c0005t0002g0235 a0001c0005t0002g0241 others(1): Show |
5 | HG02809.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-4571C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858053 | |||||||
| chr5:176858060 | G | C | 23 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0002g0230 others(20): Show |
24 | HG01167.hp1 HG01891.hp2 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.71-4564G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858060 | |||||||
| chr5:176858117 | G | A | 17 | a0001c0001t0001g0094 a0001c0001t0001g0234 a0001c0001t0003g0092 others(14): Show |
17 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.71-4507G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858117 | |||||||
| chr5:176858223 | C | T | 23 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0002g0230 others(20): Show |
24 | HG01167.hp1 HG01891.hp2 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.71-4401C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858223 | |||||||
| chr5:176858597 | C | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(139): Show |
145 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(142): Show |
intron_variant | MODIFIER | c.71-4027C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858597 | |||||||
| chr5:176858609 | C | T | 8 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(5): Show |
8 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.71-4015C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858609 | |||||||
| chr5:176858700 | C | T | 17 | a0001c0001t0001g0094 a0001c0001t0003g0092 a0001c0001t0003g0093 others(14): Show |
17 | HG01884.hp1 HG02451.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.71-3924C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858700 | |||||||
| chr5:176858711 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(137): Show |
143 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.71-3913A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858711 | |||||||
| chr5:176858714 | A | C | 2 | a0001c0001t0001g0098 a0001c0001t0001g0153 |
2 | HG02300.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.71-3910A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858714 | |||||||
| chr5:176858720 | A | AAGGAAGG others(7): Show |
1 | a0001c0001t0001g0146 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.71-3904_71-3903ins others(14): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858720 | |||||||
| chr5:176858721 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
141 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.71-3903G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858721 | |||||||
| chr5:176858722 | A | AAG | 11 | a0001c0001t0001g0146 a0001c0001t0002g0257 a0001c0001t0003g0093 others(8): Show |
11 | HG02647.hp2 HG02895.hp2 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.71-3902_71-3901ins others(2): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858722 | |||||||
| chr5:176858722 | A | AAGGAAG | 5 | a0001c0001t0001g0094 a0001c0001t0003g0092 a0001c0001t0003g0246 others(2): Show |
5 | HG02451.hp2 HG02615.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-3902_71-3901ins others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858722 | |||||||
| chr5:176858722 | A | AGAAG | 4 | a0001c0001t0002g0055 a0001c0001t0002g0075 a0001c0001t0002g0190 others(1): Show |
4 | HG01257.hp1 HG02055.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-3852_71-3849dup others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858722 | ||||||
| chr5:176858722 | A | AGAAGGAA others(1): Show |
13 | a0001c0001t0002g0003 a0001c0001t0002g0060 a0001c0001t0002g0137 others(10): Show |
14 | HG01069.hp2 HG01074.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.71-3856_71-3849dup others(8): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858722 | ||||||
| chr5:176858722 | A | AGAAGGAA others(5): Show |
12 | a0001c0001t0001g0127 a0001c0001t0001g0139 a0001c0001t0002g0012 others(9): Show |
12 | HG01891.hp1 HG01891.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.71-3860_71-3849dup others(12): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858722 | ||||||
| chr5:176858722 | A | AGAAGGAA others(9): Show |
11 | a0001c0001t0002g0010 a0001c0001t0002g0085 a0001c0001t0002g0123 others(8): Show |
11 | HG01106.hp2 HG01361.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.71-3864_71-3849dup others(16): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858722 | ||||||
| chr5:176858722 | A | AGAAGGAA others(13): Show |
6 | a0001c0001t0001g0130 a0001c0001t0002g0070 a0001c0001t0002g0104 others(3): Show |
6 | HG02970.hp1 HG04228.hp1 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-3868_71-3849dup others(20): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858722 | ||||||
| chr5:176858722 | A | AGAAGGAA others(17): Show |
3 | a0001c0001t0001g0234 a0001c0001t0002g0096 a0003c0003t0002g0017 |
3 | HG02257.hp1 HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.71-3872_71-3849dup others(24): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858722 | ||||||
| chr5:176858722 | A | AGAAGGAA others(37): Show |
1 | a0001c0001t0002g0038 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.71-3892_71-3849dup others(44): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858722 | ||||||
| chr5:176858722 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
141 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.71-3902A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858722 | |||||||
| chr5:176858764 | A | C | 5 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0253 others(2): Show |
5 | HG02451.hp2 HG03471.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-3860A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858764 | |||||||
| chr5:176858768 | A | AAGGCAGG others(1): Show |
2 | a0001c0001t0005g0008 a0001c0001t0005g0023 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.71-3853_71-3852ins others(8): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858768 | ||||||
| chr5:176858768 | A | C | 11 | a0001c0001t0001g0094 a0001c0001t0003g0092 a0001c0001t0003g0093 others(8): Show |
11 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.71-3856A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858768 | |||||||
| chr5:176858772 | A | AAGGAAGG others(21): Show |
1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.71-3849_71-3848ins others(28): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858772 | ||||||
| chr5:176858772 | A | AAGGCAGG others(1): Show |
2 | a0001c0001t0003g0245 a0001c0001t0003g0246 |
2 | HG02895.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.71-3847_71-3846ins others(8): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858772 | ||||||
| chr5:176858772 | A | C | 13 | a0001c0001t0001g0094 a0001c0001t0003g0092 a0001c0001t0003g0093 others(10): Show |
13 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.71-3852A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858772 | |||||||
| chr5:176858774 | G | A | 6 | a0001c0001t0001g0076 a0001c0001t0001g0174 a0001c0001t0001g0202 others(3): Show |
6 | HG00558.hp2 HG01433.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-3850G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858774 | |||||||
| chr5:176858774 | G | GGAAA | 10 | a0001c0001t0001g0002 a0001c0001t0001g0069 a0001c0001t0001g0141 others(7): Show |
11 | HG00609.hp2 HG01081.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.71-3849_71-3848ins others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | ||||||
| chr5:176858774 | G | GGAAGGAA others(1): Show |
26 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0056 others(23): Show |
26 | HG00733.hp1 HG00733.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.71-3849_71-3848ins others(8): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | ||||||
| chr5:176858774 | G | GGAAGGAA others(4): Show |
1 | a0001c0001t0009g0043 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.71-3849_71-3848ins others(11): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | ||||||
| chr5:176858774 | G | GGAAGGAA others(5): Show |
50 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0025 others(47): Show |
51 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.71-3849_71-3848ins others(12): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | ||||||
| chr5:176858774 | G | GGAAGGAA others(9): Show |
32 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0018 others(29): Show |
33 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.71-3849_71-3848ins others(16): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | ||||||
| chr5:176858774 | G | GGAAGGAA others(12): Show |
1 | a0001c0001t0001g0136 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.71-3849_71-3848ins others(19): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | ||||||
| chr5:176858774 | G | GGAAGGAA others(13): Show |
28 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0026 others(25): Show |
29 | HG00099.hp1 HG00099.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.71-3849_71-3848ins others(20): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | ||||||
| chr5:176858774 | G | GGAAGGAA others(17): Show |
11 | a0001c0001t0001g0020 a0001c0001t0001g0110 a0001c0001t0001g0133 others(8): Show |
11 | HG00639.hp2 HG01109.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.71-3849_71-3848ins others(24): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | ||||||
| chr5:176858774 | G | GGAAGGAA others(21): Show |
8 | a0001c0001t0001g0086 a0001c0001t0002g0118 a0001c0001t0002g0204 others(5): Show |
8 | HG01257.hp2 HG01258.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.71-3849_71-3848ins others(28): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | ||||||
| chr5:176858774 | G | GGAAGGAA others(25): Show |
2 | a0001c0001t0001g0175 a0001c0001t0002g0097 |
2 | HG02818.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.71-3849_71-3848ins others(32): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | ||||||
| chr5:176858774 | G | GGAAGGAA others(29): Show |
1 | a0001c0001t0002g0100 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.71-3849_71-3848ins others(36): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | ||||||
| chr5:176858774 | G | GGAAGGAA others(21): Show |
2 | a0002c0002t0004g0021 a0002c0002t0004g0166 |
2 | HG03471.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.71-3849_71-3848ins others(28): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | ||||||
| chr5:176858774 | G | GGAAGGAA others(13): Show |
2 | a0001c0001t0007g0242 a0001c0001t0007g0247 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.71-3849_71-3848ins others(20): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | ||||||
| chr5:176858774 | G | GGAAGGAA others(9): Show |
1 | a0001c0001t0007g0083 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.71-3849_71-3848ins others(16): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | ||||||
| chr5:176858774 | G | GGAAGGAA others(13): Show |
3 | a0002c0002t0001g0006 a0002c0002t0001g0112 a0002c0002t0004g0066 |
4 | HG01243.hp2 HG02572.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-3849_71-3848ins others(20): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | ||||||
| chr5:176858774 | G | GGAAGGAA others(21): Show |
1 | a0001c0001t0011g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.71-3849_71-3848ins others(28): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | ||||||
| chr5:176858774 | G | GGAAGGAA others(9): Show |
1 | a0002c0002t0004g0048 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.71-3849_71-3848ins others(16): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | ||||||
| chr5:176858774 | G | GGAAGGCA others(5): Show |
2 | a0002c0002t0004g0126 a0002c0002t0004g0165 |
2 | HG02074.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.71-3849_71-3848ins others(12): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | ||||||
| chr5:176858776 | C | A | 8 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(5): Show |
8 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.71-3848C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858776 | |||||||
| chr5:176858778 | A | G | 21 | a0001c0001t0001g0094 a0001c0001t0001g0234 a0001c0001t0002g0058 others(18): Show |
21 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(18): Show |
intron_variant | MODIFIER | c.71-3846A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858778 | |||||||
| chr5:176858782 | A | AGCAG | 3 | a0001c0001t0001g0144 a0001c0001t0001g0146 a0001c0001t0002g0257 |
3 | HG03195.hp1 HG03688.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.71-3836_71-3833dup others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858782 | ||||||
| chr5:176858782 | A | G | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(202): Show |
210 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(207): Show |
intron_variant | MODIFIER | c.71-3842A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858782 | |||||||
| chr5:176858806 | A | G | 6 | a0001c0001t0003g0111 a0003c0003t0001g0188 a0003c0003t0002g0017 others(3): Show |
6 | HG01361.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-3818A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858806 | |||||||
| chr5:176858918 | G | C | 1 | a0001c0001t0002g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.71-3706G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858918 | |||||||
| chr5:176858920 | G | C | 4 | a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(1): Show |
4 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-3704G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858920 | |||||||
| chr5:176858920 | G | T | 42 | a0001c0001t0001g0175 a0001c0001t0002g0010 a0001c0001t0002g0012 others(39): Show |
43 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.71-3704G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858920 | |||||||
| chr5:176859070 | C | CATGCCCT others(83): Show |
1 | a0001c0001t0001g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.71-3504_71-3503ins others(90): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859070 | ||||||
| chr5:176859074 | C | CCCTTGCT others(23): Show |
6 | a0001c0001t0002g0075 a0001c0001t0002g0137 a0001c0001t0002g0140 others(3): Show |
6 | HG02055.hp1 HG02135.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-3533_71-3504dup others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859074 | ||||||
| chr5:176859083 | G | A | 9 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0002g0097 others(6): Show |
9 | HG01891.hp2 HG02818.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.71-3541G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859083 | |||||||
| chr5:176859091 | AGCTGCTA others(23): Show |
A | 5 | a0001c0001t0002g0010 a0001c0001t0003g0009 a0001c0001t0003g0011 others(2): Show |
5 | HG01891.hp2 HG03041.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-3520_71-3491del others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859091 | ||||||
| chr5:176859091 | AGCTGCTA others(83): Show |
A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.71-3520_71-3431del others(90): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859091 | ||||||
| chr5:176859099 | G | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0255 |
2 | HG02559.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.71-3525G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859099 | |||||||
| chr5:176859099 | GAATGTCC others(53): Show |
G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(100): Show |
106 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.71-3465_71-3406del others(60): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859099 | ||||||
| chr5:176859104 | T | C | 53 | a0001c0001t0001g0094 a0001c0001t0001g0175 a0001c0001t0002g0040 others(50): Show |
54 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.71-3520T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859104 | |||||||
| chr5:176859104 | TCCTTGCT others(23): Show |
T | 22 | a0001c0001t0001g0014 a0001c0001t0001g0026 a0001c0001t0001g0039 others(19): Show |
22 | HG00099.hp2 HG01109.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.71-3503_71-3474del others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859104 | ||||||
| chr5:176859104 | TCCTTGCT others(83): Show |
T | 5 | a0001c0001t0001g0045 a0001c0001t0003g0244 a0001c0001t0010g0022 others(2): Show |
5 | HG02451.hp1 HG03139.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-3503_71-3414del others(90): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859104 | ||||||
| chr5:176859121 | G | A | 78 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0056 others(75): Show |
80 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.71-3503G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859121 | |||||||
| chr5:176859121 | G | GGCTGCTA others(113): Show |
1 | a0003c0003t0002g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.71-3496_71-3495ins others(120): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859121 | ||||||
| chr5:176859121 | GGCTGCTA others(23): Show |
G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0020 |
2 | HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.71-3495_71-3466del others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859121 | ||||||
| chr5:176859129 | G | C | 16 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0036 others(13): Show |
16 | HG01069.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.71-3495G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859129 | |||||||
| chr5:176859129 | GAATGCCC others(23): Show |
G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0255 |
2 | HG02559.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.71-3490_71-3461del others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859129 | ||||||
| chr5:176859133 | GCCCTTGC others(50): Show |
G | 1 | a0004c0006t0002g0005 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.71-3490_71-3434del others(57): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859133 | |||||||
| chr5:176859133 | GCCCTTGC others(80): Show |
G | 3 | a0001c0001t0007g0083 a0001c0001t0007g0242 a0001c0001t0007g0247 |
3 | HG01884.hp1 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.71-3490_71-3404del others(87): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859133 | |||||||
| chr5:176859133 | GCCCTTGC others(230): Show |
G | 16 | a0001c0001t0001g0094 a0001c0001t0003g0092 a0001c0001t0003g0093 others(13): Show |
16 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.71-3490_71-3254del | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859133 | |||||||
| chr5:176859134 | C | CCCTTGCT others(113): Show |
4 | a0001c0001t0003g0111 a0003c0003t0002g0073 a0003c0003t0002g0107 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-3371_71-3370ins others(120): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859134 | ||||||
| chr5:176859134 | C | CCCTTGCT others(53): Show |
1 | a0003c0003t0001g0188 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.71-3466_71-3465ins others(60): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859134 | ||||||
| chr5:176859134 | C | CCCTTGCT others(23): Show |
1 | a0001c0001t0005g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.71-3474_71-3473ins others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859134 | ||||||
| chr5:176859134 | C | T | 30 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0036 others(27): Show |
31 | HG01069.hp1 HG01081.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.71-3490C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859134 | |||||||
| chr5:176859151 | A | G | 14 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0036 others(11): Show |
14 | HG01069.hp1 HG01243.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.71-3473A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859151 | |||||||
| chr5:176859159 | C | G | 33 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0036 others(30): Show |
34 | HG01069.hp1 HG01109.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.71-3465C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859159 | |||||||
| chr5:176859160 | A | AATGATGT others(704): Show |
1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.71-3461_71-3460ins others(711): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859160 | ||||||
| chr5:176859163 | GTCCTTGC others(80): Show |
G | 2 | a0001c0005t0002g0235 a0001c0005t0002g0241 |
2 | HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.71-3460_71-3374del others(87): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859163 | |||||||
| chr5:176859164 | T | C | 5 | a0001c0001t0002g0012 a0001c0001t0002g0230 a0001c0001t0002g0231 others(2): Show |
5 | HG01167.hp1 HG02965.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-3460T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859164 | |||||||
| chr5:176859164 | TCCTTGCT others(173): Show |
T | 4 | a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(1): Show |
4 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-3370_71-3191del | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859164 | ||||||
| chr5:176859181 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(117): Show |
124 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.71-3443G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859181 | |||||||
| chr5:176859181 | GGCTGCTA others(143): Show |
G | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | NA19002.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.71-3413_71-3264del | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859181 | ||||||
| chr5:176859189 | G | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(97): Show |
103 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.71-3435G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859189 | |||||||
| chr5:176859190 | A | AATG | 11 | a0001c0001t0002g0230 a0001c0001t0002g0231 a0001c0001t0011g0015 others(8): Show |
12 | HG01109.hp1 HG01167.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.71-3433_71-3431dup others(3): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859190 | ||||||
| chr5:176859194 | C | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(156): Show |
164 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(161): Show |
intron_variant | MODIFIER | c.71-3430C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859194 | |||||||
| chr5:176859211 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(137): Show |
143 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.71-3413A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859211 | |||||||
| chr5:176859219 | G | C | 23 | a0001c0001t0001g0175 a0001c0001t0002g0040 a0001c0001t0002g0090 others(20): Show |
23 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.71-3405G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859219 | |||||||
| chr5:176859219 | GAATGTCC others(53): Show |
G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0056 a0001c0001t0001g0059 others(2): Show |
5 | HG01069.hp1 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-3383_71-3324del others(60): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859219 | ||||||
| chr5:176859224 | T | C | 24 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0020 others(21): Show |
24 | HG00099.hp2 HG01109.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.71-3400T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859224 | |||||||
| chr5:176859224 | TCCTTGCT others(83): Show |
T | 15 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0001c0001t0001g0036 others(12): Show |
15 | HG01243.hp1 HG01496.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.71-3353_71-3264del others(90): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859224 | ||||||
| chr5:176859226 | C | A | 1 | a0004c0006t0002g0005 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.71-3398C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859226 | |||||||
| chr5:176859241 | A | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(124): Show |
130 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.71-3383A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859241 | |||||||
| chr5:176859249 | G | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.71-3375G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859249 | |||||||
| chr5:176859250 | AATGCCCT others(176): Show |
A | 1 | a0001c0001t0014g0061 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.71-3370_71-3188del | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859250 | ||||||
| chr5:176859253 | GCCCTTGC others(50): Show |
G | 1 | a0001c0001t0002g0248 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.71-3370_71-3314del others(57): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859253 | |||||||
| chr5:176859254 | C | CCCTTGCT others(23): Show |
4 | a0001c0001t0011g0015 a0002c0002t0004g0126 a0002c0002t0004g0165 others(1): Show |
4 | HG02074.hp2 HG03516.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-3346_71-3345ins others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859254 | ||||||
| chr5:176859254 | C | CCCTTGCT others(23): Show |
5 | a0002c0002t0001g0006 a0002c0002t0001g0112 a0002c0002t0004g0021 others(2): Show |
6 | HG01109.hp1 HG01243.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-3346_71-3345ins others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859254 | ||||||
| chr5:176859254 | C | T | 38 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0020 others(35): Show |
38 | HG00099.hp2 HG01109.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.71-3370C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859254 | |||||||
| chr5:176859271 | A | G | 4 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0002g0164 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-3353A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859271 | |||||||
| chr5:176859271 | AGCTGCTA others(23): Show |
A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(97): Show |
103 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.71-3345_71-3316del others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859271 | ||||||
| chr5:176859279 | C | G | 50 | a0001c0001t0001g0045 a0001c0001t0001g0053 a0001c0001t0001g0054 others(47): Show |
52 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.71-3345C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859279 | |||||||
| chr5:176859284 | T | C | 3 | a0001c0001t0007g0083 a0001c0001t0007g0242 a0001c0001t0007g0247 |
3 | HG01884.hp1 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.71-3340T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859284 | |||||||
| chr5:176859284 | T | TCCTTGCT others(113): Show |
5 | a0001c0001t0001g0234 a0001c0001t0003g0111 a0003c0003t0002g0073 others(2): Show |
5 | HG01361.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-3324_71-3323ins others(120): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859284 | ||||||
| chr5:176859284 | TCCTTGCT others(23): Show |
T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0056 a0001c0001t0001g0059 others(2): Show |
5 | HG01069.hp1 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-3323_71-3294del others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859284 | ||||||
| chr5:176859284 | TCCTTGCT others(53): Show |
T | 23 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0020 others(20): Show |
23 | HG00099.hp2 HG01109.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.71-3280_71-3221del others(60): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859284 | ||||||
| chr5:176859286 | C | A | 3 | a0001c0001t0005g0256 a0001c0005t0002g0235 a0001c0005t0002g0241 |
3 | HG02280.hp2 HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.71-3338C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859286 | |||||||
| chr5:176859301 | G | A | 38 | a0001c0001t0001g0045 a0001c0001t0001g0175 a0001c0001t0001g0234 others(35): Show |
39 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.71-3323G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859301 | |||||||
| chr5:176859301 | G | GGCTGCTA others(233): Show |
1 | a0003c0003t0002g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.71-3281_71-3280ins others(240): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859301 | ||||||
| chr5:176859301 | G | GGCTGCTA others(353): Show |
1 | a0003c0003t0001g0188 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.71-3281_71-3280ins others(360): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859301 | ||||||
| chr5:176859309 | G | C | 2 | a0001c0001t0001g0045 a0001c0001t0008g0113 |
2 | HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.71-3315G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859309 | |||||||
| chr5:176859313 | GCCCTTGC others(50): Show |
G | 23 | a0001c0001t0001g0175 a0001c0001t0002g0040 a0001c0001t0002g0090 others(20): Show |
23 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.71-3310_71-3254del others(57): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859313 | |||||||
| chr5:176859314 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(115): Show |
123 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.71-3310C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859314 | |||||||
| chr5:176859331 | A | G | 14 | a0001c0001t0001g0045 a0001c0001t0002g0230 a0001c0001t0002g0231 others(11): Show |
16 | HG01109.hp1 HG01167.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.71-3293A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859331 | |||||||
| chr5:176859339 | G | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(129): Show |
136 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(133): Show |
intron_variant | MODIFIER | c.71-3285G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859339 | |||||||
| chr5:176859340 | AATGCCCT others(86): Show |
A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.71-3280_71-3188del others(93): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859340 | ||||||
| chr5:176859344 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(143): Show |
151 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(148): Show |
intron_variant | MODIFIER | c.71-3280C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859344 | |||||||
| chr5:176859346 | C | A | 1 | a0001c0001t0002g0248 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.71-3278C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859346 | |||||||
| chr5:176859361 | G | A | 8 | a0001c0001t0002g0248 a0001c0001t0003g0244 a0001c0001t0008g0113 others(5): Show |
8 | HG02451.hp1 HG02809.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.71-3263G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859361 | |||||||
| chr5:176859369 | G | C | 1 | a0004c0006t0002g0005 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.71-3255G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859369 | |||||||
| chr5:176859370 | A | AATG | 4 | a0001c0001t0003g0244 a0001c0001t0010g0022 a0001c0004t0002g0232 others(1): Show |
4 | HG02451.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-3253_71-3251dup others(3): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859370 | ||||||
| chr5:176859374 | C | T | 50 | a0001c0001t0001g0094 a0001c0001t0001g0175 a0001c0001t0002g0040 others(47): Show |
51 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.71-3250C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859374 | |||||||
| chr5:176859391 | A | G | 6 | a0001c0001t0007g0083 a0001c0001t0007g0242 a0001c0001t0007g0247 others(3): Show |
7 | HG01884.hp1 HG02145.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.71-3233A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859391 | |||||||
| chr5:176859399 | G | C | 3 | a0001c0001t0007g0083 a0001c0001t0007g0242 a0001c0001t0007g0247 |
3 | HG01884.hp1 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.71-3225G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859399 | |||||||
| chr5:176859406 | C | A | 4 | a0001c0001t0003g0074 a0001c0001t0003g0252 a0001c0001t0003g0259 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-3218C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859406 | |||||||
| chr5:176859421 | A | G | 5 | a0001c0001t0007g0083 a0001c0001t0007g0242 a0001c0001t0007g0247 others(2): Show |
5 | HG01884.hp1 HG02145.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-3203A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859421 | |||||||
| chr5:176859429 | G | C | 5 | a0001c0001t0001g0045 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | HG02809.hp2 HG02818.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-3195G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859429 | |||||||
| chr5:176859430 | AATG | A | 53 | a0001c0001t0001g0045 a0001c0001t0001g0094 a0001c0001t0001g0141 others(50): Show |
54 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.71-3190_71-3188del others(3): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859430 | ||||||
| chr5:176859437 | T | C | 30 | a0001c0001t0001g0175 a0001c0001t0002g0040 a0001c0001t0002g0090 others(27): Show |
30 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.71-3187T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859437 | |||||||
| chr5:176859454 | A | G | 6 | a0001c0001t0001g0045 a0001c0001t0001g0141 a0001c0001t0001g0142 others(3): Show |
6 | HG02809.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-3170A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859454 | |||||||
| chr5:176859462 | G | C | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0014g0061 |
3 | HG01167.hp2 HG01169.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.71-3162G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859462 | |||||||
| chr5:176859466 | GTCCTTGC others(80): Show |
G | 1 | a0004c0006t0002g0005 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.71-3157_71-3071del others(87): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859466 | |||||||
| chr5:176859467 | T | C | 3 | a0001c0001t0001g0045 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | NA19002.hp1 NA19043.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.71-3157T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859467 | |||||||
| chr5:176859469 | C | A | 9 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0009 others(6): Show |
9 | HG01891.hp2 HG02280.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.71-3155C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859469 | |||||||
| chr5:176859484 | A | G | 4 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0002g0248 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-3140A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859484 | |||||||
| chr5:176859484 | AGCTGCTA others(143): Show |
A | 16 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0018 others(13): Show |
16 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.71-3050_71-2901del | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859484 | ||||||
| chr5:176859492 | G | C | 1 | a0001c0001t0002g0248 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.71-3132G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859492 | |||||||
| chr5:176859496 | GCCCTTGC others(140): Show |
G | 3 | a0001c0001t0007g0083 a0001c0001t0007g0242 a0001c0001t0007g0247 |
3 | HG01884.hp1 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.71-3127_71-2981del | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859496 | |||||||
| chr5:176859496 | GCCCTTGC others(170): Show |
G | 4 | a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(1): Show |
4 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-3127_71-2951del | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859496 | |||||||
| chr5:176859497 | C | T | 33 | a0001c0001t0001g0045 a0001c0001t0001g0141 a0001c0001t0001g0142 others(30): Show |
33 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.71-3127C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859497 | |||||||
| chr5:176859497 | CCCTTGCT others(23): Show |
C | 16 | a0001c0001t0001g0094 a0001c0001t0003g0092 a0001c0001t0003g0093 others(13): Show |
16 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.71-3080_71-3051del others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859497 | ||||||
| chr5:176859514 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(149): Show |
155 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(152): Show |
intron_variant | MODIFIER | c.71-3110A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859514 | |||||||
| chr5:176859526 | GTCCTTGC others(50): Show |
G | 4 | a0001c0001t0001g0045 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | HG02630.hp1 NA19002.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-3097_71-3041del others(57): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859526 | |||||||
| chr5:176859526 | GTCCTTGC others(110): Show |
G | 2 | a0001c0005t0002g0235 a0001c0005t0002g0241 |
2 | HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.71-3097_71-2981del | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859526 | |||||||
| chr5:176859544 | A | G | 35 | a0001c0001t0001g0175 a0001c0001t0002g0010 a0001c0001t0002g0012 others(32): Show |
35 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.71-3080A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859544 | |||||||
| chr5:176859552 | G | C | 38 | a0001c0001t0001g0036 a0001c0001t0001g0175 a0001c0001t0001g0224 others(35): Show |
38 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.71-3072G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859552 | |||||||
| chr5:176859556 | GTCCTTGC others(20): Show |
G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.71-3067_71-3041del others(27): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859556 | |||||||
| chr5:176859557 | TCCTTGCT others(83): Show |
T | 1 | a0004c0006t0002g0005 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.71-3050_71-2961del others(90): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859557 | ||||||
| chr5:176859574 | G | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(114): Show |
120 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.71-3050G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859574 | |||||||
| chr5:176859582 | G | C | 2 | a0001c0001t0002g0230 a0001c0001t0002g0231 |
2 | HG01167.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.71-3042G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859582 | |||||||
| chr5:176859586 | GTCCTTGC others(50): Show |
G | 1 | a0001c0001t0002g0248 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.71-3037_71-2981del others(57): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859586 | |||||||
| chr5:176859586 | GTCCTTGC others(203): Show |
G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): Show |
119 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.71-3037_71-2828del | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859586 | |||||||
| chr5:176859587 | T | C | 22 | a0001c0001t0001g0036 a0001c0001t0001g0175 a0001c0001t0001g0224 others(19): Show |
22 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.71-3037T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859587 | |||||||
| chr5:176859604 | G | A | 36 | a0001c0001t0001g0036 a0001c0001t0001g0045 a0001c0001t0001g0053 others(33): Show |
36 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.71-3020G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859604 | |||||||
| chr5:176859612 | C | G | 44 | a0001c0001t0001g0036 a0001c0001t0001g0045 a0001c0001t0001g0053 others(41): Show |
44 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.71-3012C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859612 | |||||||
| chr5:176859634 | G | A | 44 | a0001c0001t0001g0036 a0001c0001t0001g0045 a0001c0001t0001g0053 others(41): Show |
44 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.71-2990G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859634 | |||||||
| chr5:176859643 | A | AATG | 38 | a0001c0001t0001g0036 a0001c0001t0001g0175 a0001c0001t0001g0224 others(35): Show |
38 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.71-2980_71-2978dup others(3): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859643 | ||||||
| chr5:176859647 | C | CCCTTGCT others(56): Show |
12 | a0001c0001t0002g0230 a0001c0001t0002g0231 a0001c0001t0008g0113 others(9): Show |
13 | HG01109.hp1 HG01167.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.71-2918_71-2917ins others(63): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859647 | ||||||
| chr5:176859647 | C | T | 45 | a0001c0001t0001g0036 a0001c0001t0001g0175 a0001c0001t0001g0224 others(42): Show |
45 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.71-2977C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859647 | |||||||
| chr5:176859647 | CCCTTGCT others(23): Show |
C | 16 | a0001c0001t0001g0094 a0001c0001t0003g0092 a0001c0001t0003g0093 others(13): Show |
16 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.71-2917_71-2888del others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859647 | ||||||
| chr5:176859664 | A | G | 22 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0018 others(19): Show |
22 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.71-2960A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859664 | |||||||
| chr5:176859707 | T | C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0224 a0001c0001t0001g0226 |
3 | HG01496.hp1 HG01943.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.71-2917T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859707 | |||||||
| chr5:176859724 | A | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0224 a0001c0001t0001g0226 |
3 | HG01496.hp1 HG01943.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.71-2900A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859724 | |||||||
| chr5:176859733 | AATG | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0224 a0001c0001t0001g0226 |
3 | HG01496.hp1 HG01943.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.71-2887_71-2885del others(3): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859733 | ||||||
| chr5:176859736 | G | GTCCTTGC others(20): Show |
1 | a0001c0001t0005g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.71-2888_71-2887ins others(27): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859736 | |||||||
| chr5:176859753 | GCATAGCT others(53): Show |
G | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0014g0061 |
3 | HG02630.hp1 NA19002.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.71-2831_71-2772del others(60): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859753 | ||||||
| chr5:176859796 | A | AATG | 3 | a0001c0001t0001g0036 a0001c0001t0001g0224 a0001c0001t0001g0226 |
3 | HG01496.hp1 HG01943.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.71-2827_71-2825dup others(3): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859796 | ||||||
| chr5:176859800 | T | C | 4 | a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(1): Show |
4 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-2824T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859800 | |||||||
| chr5:176859813 | T | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(121): Show |
127 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.71-2811T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859813 | |||||||
| chr5:176860025 | C | T | 2 | a0001c0001t0002g0230 a0001c0001t0002g0231 |
2 | HG01167.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.71-2599C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860025 | |||||||
| chr5:176860028 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(213): Show |
221 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(218): Show |
intron_variant | MODIFIER | c.71-2596A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860028 | |||||||
| chr5:176860127 | C | T | 28 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0031 others(25): Show |
29 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.71-2497C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860127 | |||||||
| chr5:176860145 | A | G | 1 | a0002c0002t0004g0165 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.71-2479A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860145 | |||||||
| chr5:176860194 | G | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(220): Show |
228 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(225): Show |
intron_variant | MODIFIER | c.71-2430G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860194 | |||||||
| chr5:176860195 | G | A | 1 | a0001c0001t0002g0143 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.71-2429G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860195 | |||||||
| chr5:176860197 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.71-2427A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860197 | |||||||
| chr5:176860208 | G | T | 1 | a0001c0001t0001g0203 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.71-2416G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860208 | |||||||
| chr5:176860210 | G | T | 17 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0002g0248 others(14): Show |
18 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.71-2414G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860210 | |||||||
| chr5:176860346 | G | A | 7 | a0001c0001t0001g0234 a0001c0001t0003g0111 a0003c0003t0001g0188 others(4): Show |
7 | HG01361.hp1 HG01891.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.71-2278G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860346 | |||||||
| chr5:176860517 | C | T | 1 | a0001c0001t0003g0009 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.71-2107C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860517 | |||||||
| chr5:176860591 | C | T | 1 | a0001c0001t0010g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.71-2033C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860591 | |||||||
| chr5:176860629 | G | A | 4 | a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(1): Show |
4 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-1995G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860629 | |||||||
| chr5:176860638 | GT | G | 4 | a0001c0001t0003g0244 a0001c0001t0010g0022 a0001c0004t0002g0232 others(1): Show |
4 | HG02451.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-1985delT | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860638 | |||||||
| chr5:176860652 | C | A | 1 | a0001c0001t0001g0203 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.71-1972C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860652 | |||||||
| chr5:176860821 | G | A | 2 | a0003c0003t0001g0188 a0003c0003t0002g0017 |
2 | HG02257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.71-1803G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860821 | |||||||
| chr5:176860949 | G | A | 3 | a0001c0001t0001g0099 a0001c0001t0001g0229 a0001c0001t0002g0096 |
3 | HG02622.hp1 HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.71-1675G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860949 | |||||||
| chr5:176860965 | C | T | 1 | a0001c0001t0002g0257 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.71-1659C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860965 | |||||||
| chr5:176860966 | G | A | 3 | a0001c0001t0007g0083 a0001c0001t0007g0242 a0001c0001t0007g0247 |
3 | HG01884.hp1 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.71-1658G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860966 | |||||||
| chr5:176861163 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(137): Show |
143 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.71-1461G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861163 | |||||||
| chr5:176861330 | C | G | 1 | a0001c0001t0001g0155 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.71-1294C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861330 | |||||||
| chr5:176861424 | G | A | 19 | a0001c0001t0001g0175 a0001c0001t0002g0040 a0001c0001t0002g0090 others(16): Show |
19 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.71-1200G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861424 | |||||||
| chr5:176861442 | G | A | 1 | a0001c0001t0003g0065 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.71-1182G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861442 | |||||||
| chr5:176861450 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(162): Show |
168 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(165): Show |
intron_variant | MODIFIER | c.71-1174A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861450 | |||||||
| chr5:176861541 | C | T | 4 | a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(1): Show |
4 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-1083C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861541 | |||||||
| chr5:176861550 | T | A | 16 | a0001c0001t0001g0094 a0001c0001t0003g0092 a0001c0001t0003g0093 others(13): Show |
16 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.71-1074T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861550 | |||||||
| chr5:176861581 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.71-1043C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861581 | |||||||
| chr5:176861728 | A | G | 3 | a0001c0001t0002g0230 a0001c0001t0002g0231 a0001c0001t0008g0113 |
3 | HG01167.hp1 HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.71-896A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861728 | |||||||
| chr5:176861824 | G | GGAGGCCA others(3): Show |
223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(220): Show |
228 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(225): Show |
intron_variant | MODIFIER | c.71-800_71-799insGA others(8): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861824 | |||||||
| chr5:176861825 | A | T | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(220): Show |
228 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(225): Show |
intron_variant | MODIFIER | c.71-799A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861825 | |||||||
| chr5:176861848 | C | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0224 a0001c0001t0001g0226 |
3 | HG01496.hp1 HG01943.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.71-776C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861848 | |||||||
| chr5:176861849 | A | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(138): Show |
144 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.71-775A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861849 | |||||||
| chr5:176861854 | G | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(115): Show |
121 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.71-770G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861854 | |||||||
| chr5:176861860 | G | A | 2 | a0001c0001t0002g0123 a0001c0001t0002g0191 |
2 | HG02080.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.71-764G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861860 | |||||||
| chr5:176861891 | T | A | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.71-733T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861891 | |||||||
| chr5:176861892 | C | T | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.71-732C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861892 | |||||||
| chr5:176862254 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.71-370G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176862254 | |||||||
| chr5:176862459 | T | G | 16 | a0001c0001t0001g0094 a0001c0001t0003g0092 a0001c0001t0003g0093 others(13): Show |
16 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.71-165T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176862459 | |||||||
| chr5:176862860 | G | T | 1 | a0001c0001t0002g0096 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.292+15G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176862860 | |||||||
| chr5:176862865 | A | G | 3 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0214 |
3 | HG01256.hp1 HG01934.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.292+20A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176862865 | |||||||
| chr5:176862866 | G | C | 2 | a0001c0001t0002g0010 a0001c0001t0002g0012 |
2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.292+21G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176862866 | |||||||
| chr5:176862896 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.292+51G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176862896 | |||||||
| chr5:176862903 | C | G | 1 | a0001c0001t0001g0172 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.292+58C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176862903 | |||||||
| chr5:176863060 | C | A | 1 | a0001c0007t0001g0138 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.292+215C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176863060 | |||||||
| chr5:176863218 | G | A | 1 | a0001c0001t0002g0200 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.292+373G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176863218 | |||||||
| chr5:176863279 | A | C | 1 | a0001c0001t0001g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.292+434A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176863279 | |||||||
| chr5:176863420 | T | A | 2 | a0001c0001t0002g0010 a0001c0001t0002g0012 |
2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.292+575T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176863420 | |||||||
| chr5:176863497 | G | C | 3 | a0001c0001t0007g0083 a0001c0001t0007g0242 a0001c0001t0007g0247 |
3 | HG01884.hp1 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.292+652G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176863497 | |||||||
| chr5:176863626 | C | T | 1 | a0001c0001t0005g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.292+781C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176863626 | |||||||
| chr5:176863629 | G | A | 1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.292+784G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176863629 | |||||||
| chr5:176863674 | C | A | 3 | a0002c0002t0004g0126 a0002c0002t0004g0165 a0002c0002t0004g0166 |
3 | HG02074.hp2 NA18975.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.292+829C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176863674 | |||||||
| chr5:176863734 | T | TC | 6 | a0001c0001t0001g0053 a0001c0001t0001g0110 a0001c0001t0001g0127 others(3): Show |
6 | HG00735.hp1 HG01167.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.292+894dupC | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 176863734 | ||||||
| chr5:176863746 | TCCTCCTC others(54): Show |
T | 3 | a0001c0001t0010g0022 a0001c0004t0002g0232 a0001c0004t0002g0233 |
3 | HG02451.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.292+911_292+971del others(61): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 176863746 | ||||||
| chr5:176863805 | T | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(137): Show |
143 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.292+960T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176863805 | |||||||
| chr5:176863807 | C | CCCTCCT | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(124): Show |
129 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.292+965_292+970dup others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 176863807 | ||||||
| chr5:176863807 | C | CCCTCCTC others(8): Show |
82 | a0001c0001t0001g0064 a0001c0001t0001g0127 a0001c0001t0001g0139 others(79): Show |
84 | HG00099.hp1 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.292+983_292+997dup others(15): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 176863807 | ||||||
| chr5:176863807 | C | CCCTCCTC others(23): Show |
1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.292+968_292+997dup others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 176863807 | ||||||
| chr5:176863807 | C | CCCTCCTC others(14): Show |
1 | a0001c0001t0002g0257 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.292+970_292+971ins others(21): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 176863807 | ||||||
| chr5:176863808 | C | CCTCCTCC others(8): Show |
3 | a0001c0001t0005g0008 a0001c0001t0005g0013 a0001c0001t0005g0023 |
3 | HG02976.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.292+977_292+978ins others(15): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 176863808 | ||||||
| chr5:176863811 | C | T | 1 | a0001c0001t0010g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.292+966C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176863811 | |||||||
| chr5:176863813 | T | TCCCCCTC others(9): Show |
1 | a0001c0001t0002g0186 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.292+973_292+988dup others(16): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 176863813 | ||||||
| chr5:176863816 | C | T | 10 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0057 others(7): Show |
11 | HG00642.hp2 HG00735.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.292+971C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176863816 | |||||||
| chr5:176863819 | T | TCCC | 9 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0057 others(6): Show |
10 | HG00642.hp2 HG00735.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.292+976_292+977ins others(3): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 176863819 | ||||||
| chr5:176863822 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.292+977T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176863822 | |||||||
| chr5:176863828 | T | TCCCCCTC others(9): Show |
1 | a0001c0001t0005g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.292+997_292+998ins others(16): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 176863828 | ||||||
| chr5:176863898 | T | C | 2 | a0001c0001t0002g0230 a0001c0001t0002g0231 |
2 | HG01167.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.292+1053T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176863898 | |||||||
| chr5:176864129 | C | T | 1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.292+1284C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176864129 | |||||||
| chr5:176864196 | G | A | 1 | a0001c0001t0003g0050 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.292+1351G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176864196 | |||||||
| chr5:176864289 | G | A | 1 | a0001c0001t0002g0116 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.292+1444G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176864289 | |||||||
| chr5:176864330 | C | A | 4 | a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(1): Show |
4 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+1485C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176864330 | |||||||
| chr5:176864386 | T | C | 16 | a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(13): Show |
17 | HG01081.hp2 HG01106.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.292+1541T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176864386 | |||||||
| chr5:176864449 | G | A | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0202 |
3 | HG01934.hp2 HG01943.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.292+1604G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176864449 | |||||||
| chr5:176864510 | A | G | 1 | a0001c0001t0002g0121 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.292+1665A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176864510 | |||||||
| chr5:176864540 | C | T | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.292+1695C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176864540 | |||||||
| chr5:176864727 | G | A | 12 | a0001c0001t0007g0083 a0001c0001t0007g0242 a0001c0001t0007g0247 others(9): Show |
13 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.292+1882G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176864727 | |||||||
| chr5:176865055 | G | C | 1 | a0001c0001t0001g0102 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.292+2210G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176865055 | |||||||
| chr5:176865098 | C | T | 4 | a0001c0001t0003g0111 a0003c0003t0002g0073 a0003c0003t0002g0107 others(1): Show |
4 | HG01361.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+2253C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176865098 | |||||||
| chr5:176865155 | A | G | 12 | a0001c0001t0007g0083 a0001c0001t0007g0242 a0001c0001t0007g0247 others(9): Show |
13 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.292+2310A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176865155 | |||||||
| chr5:176865263 | T | A | 16 | a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(13): Show |
17 | HG01081.hp2 HG01106.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.292+2418T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176865263 | |||||||
| chr5:176865392 | G | A | 2 | a0001c0001t0002g0230 a0001c0001t0002g0231 |
2 | HG01167.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.292+2547G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176865392 | |||||||
| chr5:176865409 | G | A | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.292+2564G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176865409 | |||||||
| chr5:176865569 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.293-2561G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176865569 | |||||||
| chr5:176865606 | C | T | 2 | a0001c0004t0002g0232 a0001c0004t0002g0233 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.293-2524C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176865606 | |||||||
| chr5:176865664 | G | A | 1 | a0003c0003t0002g0240 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.293-2466G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176865664 | |||||||
| chr5:176865845 | C | G | 4 | a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(1): Show |
4 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-2285C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176865845 | |||||||
| chr5:176865975 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.293-2155A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176865975 | |||||||
| chr5:176866016 | C | T | 2 | a0001c0001t0003g0080 a0001c0001t0003g0081 |
2 | HG01891.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.293-2114C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176866016 | |||||||
| chr5:176866071 | C | G | 3 | a0001c0001t0005g0008 a0001c0001t0005g0013 a0001c0001t0005g0023 |
3 | HG02976.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.293-2059C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176866071 | |||||||
| chr5:176866073 | G | A | 2 | a0001c0001t0002g0010 a0001c0001t0002g0012 |
2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.293-2057G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176866073 | |||||||
| chr5:176866099 | C | A | 1 | a0001c0001t0001g0195 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.293-2031C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176866099 | |||||||
| chr5:176866106 | G | T | 2 | a0001c0001t0002g0062 a0001c0001t0002g0063 |
2 | HG01106.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.293-2024G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176866106 | |||||||
| chr5:176866266 | G | A | 2 | a0001c0001t0001g0224 a0001c0001t0001g0226 |
2 | HG01496.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.293-1864G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176866266 | |||||||
| chr5:176866339 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.293-1791C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176866339 | |||||||
| chr5:176866692 | C | T | 1 | a0001c0001t0001g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.293-1438C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176866692 | |||||||
| chr5:176866702 | C | T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(207): Show |
215 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(212): Show |
intron_variant | MODIFIER | c.293-1428C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176866702 | |||||||
| chr5:176866812 | G | A | 1 | a0001c0001t0001g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.293-1318G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176866812 | |||||||
| chr5:176866938 | A | C | 29 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0031 others(26): Show |
30 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.293-1192A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176866938 | |||||||
| chr5:176867064 | G | A | 1 | a0002c0002t0004g0166 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.293-1066G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176867064 | |||||||
| chr5:176867172 | A | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0020 |
2 | HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.293-958A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176867172 | |||||||
| chr5:176867250 | G | A | 1 | a0001c0001t0011g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.293-880G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176867250 | |||||||
| chr5:176867296 | T | C | 2 | a0001c0001t0003g0111 a0003c0003t0002g0073 |
2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.293-834T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176867296 | |||||||
| chr5:176867483 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.293-647G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176867483 | |||||||
| chr5:176867599 | C | T | 3 | a0001c0001t0007g0083 a0001c0001t0007g0242 a0001c0001t0007g0247 |
3 | HG01884.hp1 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.293-531C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176867599 | |||||||
| chr5:176867686 | G | A | 1 | a0001c0001t0010g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.293-444G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176867686 | |||||||
| chr5:176867894 | G | T | 21 | a0001c0001t0001g0175 a0001c0001t0002g0010 a0001c0001t0002g0012 others(18): Show |
21 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.293-236G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176867894 | |||||||
| chr5:176867911 | A | C | 3 | a0001c0004t0002g0078 a0001c0004t0002g0232 a0001c0004t0002g0233 |
3 | HG02451.hp1 HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.293-219A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176867911 | |||||||
| chr5:176867964 | A | G | 1 | a0001c0001t0002g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.293-166A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176867964 | |||||||
| chr5:176868003 | T | A | 7 | a0001c0001t0001g0183 a0001c0001t0003g0009 a0001c0001t0003g0011 others(4): Show |
7 | HG01891.hp2 HG02015.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-127T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176868003 | |||||||
| chr5:176868003 | T | TA | 17 | a0001c0001t0001g0094 a0001c0001t0001g0236 a0001c0001t0002g0123 others(14): Show |
18 | HG02080.hp1 HG02135.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-114dupA | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 176868003 | ||||||
| chr5:176868004 | A | T | 5 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0120 others(2): Show |
5 | HG01515.hp2 HG01517.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-126A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176868004 | |||||||
| chr5:176868305 | G | A | 1 | a0001c0001t0010g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.436+32G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 3/14 | chr5 | 176868305 | |||||||
| chr5:176868311 | C | T | 21 | a0001c0001t0003g0009 a0001c0001t0003g0011 a0001c0001t0003g0049 others(18): Show |
21 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.436+38C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 3/14 | chr5 | 176868311 | |||||||
| chr5:176868328 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0059 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.436+55G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 3/14 | chr5 | 176868328 | |||||||
| chr5:176868363 | C | A | 3 | a0001c0001t0001g0133 a0001c0001t0001g0203 a0001c0001t0001g0212 |
3 | HG01069.hp1 HG01071.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.436+90C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 3/14 | chr5 | 176868363 | |||||||
| chr5:176868363 | C | T | 1 | a0001c0001t0011g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.436+90C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 3/14 | chr5 | 176868363 | |||||||
| chr5:176868492 | G | A | 1 | a0003c0003t0001g0084 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.437-69G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 3/14 | chr5 | 176868492 | |||||||
| chr5:176868720 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.540+56G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 4/14 | chr5 | 176868720 | |||||||
| chr5:176868977 | A | G | 67 | a0001c0001t0001g0175 a0001c0001t0002g0010 a0001c0001t0002g0012 others(64): Show |
69 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.721+13A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 5/14 | chr5 | 176868977 | |||||||
| chr5:176868981 | C | T | 1 | a0001c0001t0002g0190 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.721+17C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 5/14 | chr5 | 176868981 | |||||||
| chr5:176869138 | T | C | 3 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0160 |
3 | HG02027.hp2 HG02523.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.721+174T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 5/14 | chr5 | 176869138 | |||||||
| chr5:176869203 | G | T | 15 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(12): Show |
15 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.721+239G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 5/14 | chr5 | 176869203 | |||||||
| chr5:176869358 | G | T | 1 | a0001c0001t0001g0155 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.721+394G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 5/14 | chr5 | 176869358 | |||||||
| chr5:176869396 | G | A | 3 | a0001c0001t0006g0238 a0001c0001t0006g0239 a0001c0001t0006g0243 |
3 | HG02486.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.721+432G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 5/14 | chr5 | 176869396 | |||||||
| chr5:176869925 | G | A | 3 | a0001c0001t0007g0083 a0001c0001t0007g0242 a0001c0001t0007g0247 |
3 | HG01884.hp1 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.722-445G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 5/14 | chr5 | 176869925 | |||||||
| chr5:176870225 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.722-145C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 5/14 | chr5 | 176870225 | |||||||
| chr5:176870367 | T | C | 1 | a0001c0001t0005g0249 | 1 | NA18522.hp2 | splice_region_variant&intron_variant | LOW | c.722-3T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 5/14 | chr5 | 176870367 | |||||||
| chr5:176870544 | C | T | 1 | a0001c0001t0002g0200 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.886+10C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870544 | |||||||
| chr5:176870603 | G | C | 22 | a0001c0001t0003g0009 a0001c0001t0003g0011 a0001c0001t0003g0049 others(19): Show |
22 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.886+69G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870603 | |||||||
| chr5:176870628 | C | A | 22 | a0001c0001t0003g0009 a0001c0001t0003g0011 a0001c0001t0003g0049 others(19): Show |
22 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.886+94C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870628 | |||||||
| chr5:176870673 | C | T | 2 | a0001c0001t0002g0010 a0001c0001t0002g0012 |
2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.886+139C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870673 | |||||||
| chr5:176870691 | G | A | 3 | a0001c0001t0003g0244 a0001c0001t0008g0113 a0001c0001t0011g0015 |
3 | HG02970.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.886+157G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870691 | |||||||
| chr5:176870737 | C | T | 21 | a0001c0001t0001g0175 a0001c0001t0002g0010 a0001c0001t0002g0012 others(18): Show |
21 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.886+203C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870737 | |||||||
| chr5:176870840 | C | T | 1 | a0001c0001t0005g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.886+306C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870840 | |||||||
| chr5:176870842 | G | T | 7 | a0001c0001t0003g0245 a0001c0001t0003g0246 a0001c0001t0003g0250 others(4): Show |
7 | HG02486.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.886+308G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870842 | |||||||
| chr5:176870888 | CCCACACC others(14): Show |
C | 1 | a0001c0001t0001g0031 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.886+355_886+375del others(21): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870888 | |||||||
| chr5:176870920 | ACCCCACA others(197): Show |
A | 19 | a0001c0001t0001g0175 a0001c0001t0002g0040 a0001c0001t0002g0090 others(16): Show |
19 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.886+416_886+619del | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176870920 | ||||||
| chr5:176870950 | A | G | 14 | a0001c0001t0001g0077 a0001c0001t0001g0227 a0001c0001t0003g0050 others(11): Show |
15 | HG01109.hp1 HG01243.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.886+416A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870950 | |||||||
| chr5:176870954 | G | A | 4 | a0001c0001t0001g0077 a0001c0001t0003g0244 a0001c0001t0008g0113 others(1): Show |
4 | HG02970.hp1 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+420G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870954 | |||||||
| chr5:176870958 | A | AACACCAC others(61): Show |
1 | a0001c0001t0002g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.886+450_886+517dup others(68): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176870958 | ||||||
| chr5:176870958 | A | C | 4 | a0001c0001t0001g0077 a0001c0001t0003g0244 a0001c0001t0008g0113 others(1): Show |
4 | HG02970.hp1 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+424A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870958 | |||||||
| chr5:176870984 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.886+450G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870984 | |||||||
| chr5:176870984 | G | GCTCGCCC others(27): Show |
1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.886+586_886+619dup others(34): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176870984 | ||||||
| chr5:176870984 | GCTCGCCC others(27): Show |
G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(159): Show |
167 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(164): Show |
intron_variant | MODIFIER | c.886+586_886+619del others(34): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176870984 | ||||||
| chr5:176870988 | G | A | 5 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0003g0244 others(2): Show |
5 | HG02970.hp1 HG03225.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.886+454G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870988 | |||||||
| chr5:176870990 | CCCACACC others(25): Show |
C | 1 | a0001c0001t0001g0031 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.886+459_886+490del others(32): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176870990 | ||||||
| chr5:176870992 | C | A | 1 | a0001c0001t0001g0077 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.886+458C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870992 | |||||||
| chr5:176871018 | A | G | 15 | a0001c0001t0001g0077 a0001c0001t0001g0135 a0001c0001t0001g0136 others(12): Show |
15 | HG01081.hp2 HG01106.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.886+484A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871018 | |||||||
| chr5:176871022 | G | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.886+488G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871022 | |||||||
| chr5:176871026 | C | A | 3 | a0001c0001t0003g0244 a0001c0001t0008g0113 a0001c0001t0011g0015 |
3 | HG02970.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.886+492C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871026 | |||||||
| chr5:176871026 | CACACCAC others(264): Show |
C | 2 | a0001c0004t0002g0078 a0001c0004t0002g0233 |
2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.886+620_886+890del | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871026 | ||||||
| chr5:176871052 | A | G | 36 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0037 others(33): Show |
38 | HG01109.hp1 HG01243.hp2 HG01928.hp1 others(35): Show |
intron_variant | MODIFIER | c.886+518A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871052 | |||||||
| chr5:176871056 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.886+522G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871056 | |||||||
| chr5:176871056 | GCCCCACA others(230): Show |
G | 1 | a0001c0001t0001g0135 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.886+526_886+762del | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871056 | ||||||
| chr5:176871060 | C | A | 1 | a0001c0001t0001g0136 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.886+526C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871060 | |||||||
| chr5:176871060 | C | CACACCAC others(196): Show |
18 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(15): Show |
18 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.886+585_886+586ins others(203): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871060 | ||||||
| chr5:176871086 | A | G | 4 | a0001c0001t0001g0136 a0001c0001t0003g0244 a0001c0001t0008g0113 others(1): Show |
4 | HG02970.hp1 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.886+552A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871086 | |||||||
| chr5:176871094 | C | CACACCAC others(26): Show |
1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+585_886+586ins others(33): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871094 | ||||||
| chr5:176871098 | C | A | 2 | a0001c0001t0002g0003 a0001c0001t0002g0163 |
3 | HG01069.hp2 HG01074.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.886+564C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871098 | |||||||
| chr5:176871120 | A | G | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.886+586A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871120 | |||||||
| chr5:176871128 | CACACCAC others(26): Show |
C | 3 | a0001c0001t0003g0244 a0001c0001t0011g0015 a0002c0002t0004g0126 |
3 | HG02074.hp2 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.886+620_886+652del others(33): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871128 | ||||||
| chr5:176871128 | CACACCAC others(162): Show |
C | 1 | a0001c0001t0001g0136 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.886+620_886+788del | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871128 | ||||||
| chr5:176871154 | G | A | 18 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(15): Show |
18 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.886+620G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871154 | |||||||
| chr5:176871154 | GCTCACCA others(26): Show |
G | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.886+624_886+656del others(33): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871154 | ||||||
| chr5:176871158 | A | ACCAACAC others(61): Show |
1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+640_886+641ins others(68): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871158 | ||||||
| chr5:176871158 | A | C | 1 | a0001c0001t0001g0031 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.886+624A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871158 | |||||||
| chr5:176871175 | C | A | 18 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(15): Show |
18 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.886+641C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871175 | |||||||
| chr5:176871189 | T | C | 18 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(15): Show |
18 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.886+655T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871189 | |||||||
| chr5:176871190 | C | T | 18 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(15): Show |
18 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.886+656C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871190 | |||||||
| chr5:176871195 | CA | C | 5 | a0001c0001t0001g0157 a0001c0001t0003g0244 a0001c0001t0008g0113 others(2): Show |
5 | HG02074.hp2 HG02970.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.886+663delA | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871195 | ||||||
| chr5:176871222 | G | A | 19 | a0001c0001t0001g0157 a0001c0001t0003g0092 a0001c0001t0003g0093 others(16): Show |
19 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.886+688G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871222 | |||||||
| chr5:176871222 | GCTCACCA others(776): Show |
G | 4 | a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(1): Show |
4 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+709_886+1491de others(1): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871222 | ||||||
| chr5:176871225 | C | CG | 19 | a0001c0001t0001g0157 a0001c0001t0003g0092 a0001c0001t0003g0093 others(16): Show |
19 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.886+691_886+692ins others(1): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871225 | |||||||
| chr5:176871226 | A | C | 19 | a0001c0001t0001g0157 a0001c0001t0003g0092 a0001c0001t0003g0093 others(16): Show |
19 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.886+692A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871226 | |||||||
| chr5:176871229 | A | C | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+695A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871229 | |||||||
| chr5:176871243 | A | C | 17 | a0001c0001t0001g0157 a0001c0001t0003g0092 a0001c0001t0003g0093 others(14): Show |
17 | HG02074.hp2 HG02451.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.886+709A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871243 | |||||||
| chr5:176871256 | CTCACCAA others(128): Show |
C | 7 | a0001c0001t0003g0009 a0001c0001t0003g0011 a0001c0001t0003g0049 others(4): Show |
7 | HG01891.hp2 HG03041.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.886+723_886+857del | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871256 | |||||||
| chr5:176871257 | T | TCG | 4 | a0001c0001t0003g0244 a0001c0001t0008g0113 a0001c0001t0011g0015 others(1): Show |
4 | HG02074.hp2 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+724_886+725ins others(2): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871257 | ||||||
| chr5:176871259 | A | C | 4 | a0001c0001t0003g0244 a0001c0001t0008g0113 a0001c0001t0011g0015 others(1): Show |
4 | HG02074.hp2 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+725A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871259 | |||||||
| chr5:176871276 | C | A | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+742C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871276 | |||||||
| chr5:176871288 | A | G | 4 | a0001c0001t0003g0244 a0001c0001t0008g0113 a0001c0001t0011g0015 others(1): Show |
4 | HG02074.hp2 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+754A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871288 | |||||||
| chr5:176871289 | CCT | C | 4 | a0001c0001t0003g0244 a0001c0001t0008g0113 a0001c0001t0011g0015 others(1): Show |
4 | HG02074.hp2 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+756_886+757del others(2): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871289 | |||||||
| chr5:176871290 | C | T | 18 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(15): Show |
18 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.886+756C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871290 | |||||||
| chr5:176871291 | T | C | 18 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(15): Show |
18 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.886+757T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871291 | |||||||
| chr5:176871292 | G | T | 4 | a0001c0001t0003g0244 a0001c0001t0008g0113 a0001c0001t0011g0015 others(1): Show |
4 | HG02074.hp2 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+758G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871292 | |||||||
| chr5:176871294 | C | A | 4 | a0001c0001t0003g0244 a0001c0001t0008g0113 a0001c0001t0011g0015 others(1): Show |
4 | HG02074.hp2 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+760C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871294 | |||||||
| chr5:176871297 | AACACCAC others(27): Show |
A | 1 | a0001c0001t0001g0105 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.886+891_886+924del others(34): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871297 | ||||||
| chr5:176871297 | AACACCAC others(61): Show |
A | 7 | a0001c0001t0001g0175 a0001c0001t0002g0040 a0001c0001t0002g0118 others(4): Show |
7 | HG00099.hp1 HG00735.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.886+857_886+924del others(68): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871297 | ||||||
| chr5:176871311 | C | A | 4 | a0001c0001t0003g0244 a0001c0001t0008g0113 a0001c0001t0011g0015 others(1): Show |
4 | HG02074.hp2 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+777C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871311 | |||||||
| chr5:176871323 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.886+789A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871323 | |||||||
| chr5:176871326 | CG | C | 4 | a0001c0001t0003g0244 a0001c0001t0008g0113 a0001c0001t0011g0015 others(1): Show |
4 | HG02074.hp2 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+793delG | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871326 | |||||||
| chr5:176871328 | C | A | 4 | a0001c0001t0003g0244 a0001c0001t0008g0113 a0001c0001t0011g0015 others(1): Show |
4 | HG02074.hp2 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+794C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871328 | |||||||
| chr5:176871331 | C | A | 23 | a0001c0001t0001g0157 a0001c0001t0003g0092 a0001c0001t0003g0093 others(20): Show |
23 | HG01884.hp1 HG02074.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.886+797C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871331 | |||||||
| chr5:176871345 | C | A | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+811C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871345 | |||||||
| chr5:176871359 | T | C | 4 | a0001c0001t0003g0244 a0001c0001t0008g0113 a0001c0001t0011g0015 others(1): Show |
4 | HG02074.hp2 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+825T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871359 | |||||||
| chr5:176871360 | C | T | 4 | a0001c0001t0003g0244 a0001c0001t0008g0113 a0001c0001t0011g0015 others(1): Show |
4 | HG02074.hp2 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+826C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871360 | |||||||
| chr5:176871360 | CG | C | 3 | a0001c0001t0001g0099 a0001c0001t0001g0157 a0001c0001t0001g0229 |
3 | HG02622.hp1 NA19005.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.886+827delG | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871360 | |||||||
| chr5:176871362 | C | A | 3 | a0001c0001t0001g0099 a0001c0001t0001g0157 a0001c0001t0001g0229 |
3 | HG02622.hp1 NA19005.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.886+828C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871362 | |||||||
| chr5:176871365 | C | A | 3 | a0001c0001t0001g0099 a0001c0001t0001g0157 a0001c0001t0001g0229 |
3 | HG02622.hp1 NA19005.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.886+831C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871365 | |||||||
| chr5:176871365 | C | CA | 19 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0244 others(16): Show |
19 | HG02074.hp2 HG02451.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.886+832dupA | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871365 | ||||||
| chr5:176871365 | C | CAACACCA others(29): Show |
3 | a0001c0001t0007g0083 a0001c0001t0007g0242 a0001c0001t0007g0247 |
3 | HG01884.hp1 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.886+832_886+833ins others(36): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871365 | ||||||
| chr5:176871379 | C | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0229 |
2 | HG02622.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.886+845C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871379 | |||||||
| chr5:176871379 | CCATCTGC others(162): Show |
C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(130): Show |
136 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.886+861_886+1029de others(1): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871379 | ||||||
| chr5:176871391 | ACTCGCCC others(61): Show |
A | 31 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0002g0090 others(28): Show |
33 | HG00639.hp2 HG01074.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.886+861_886+928del others(68): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871391 | ||||||
| chr5:176871393 | T | C | 2 | a0001c0001t0001g0099 a0001c0001t0001g0229 |
2 | HG02622.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.886+859T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871393 | |||||||
| chr5:176871394 | C | CACCAACA others(26): Show |
1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.886+860_886+861ins others(33): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871394 | |||||||
| chr5:176871394 | C | G | 7 | a0001c0001t0003g0009 a0001c0001t0003g0011 a0001c0001t0003g0049 others(4): Show |
7 | HG01891.hp2 HG03041.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.886+860C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871394 | |||||||
| chr5:176871394 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0229 |
2 | HG02622.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.886+860C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871394 | |||||||
| chr5:176871395 | G | C | 7 | a0001c0001t0003g0009 a0001c0001t0003g0011 a0001c0001t0003g0049 others(4): Show |
7 | HG01891.hp2 HG03041.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.886+861G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871395 | |||||||
| chr5:176871396 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.886+862C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871396 | |||||||
| chr5:176871399 | C | A | 8 | a0001c0001t0001g0120 a0001c0001t0003g0009 a0001c0001t0003g0011 others(5): Show |
8 | HG01891.hp2 HG02698.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.886+865C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871399 | |||||||
| chr5:176871399 | C | CA | 22 | a0001c0001t0001g0099 a0001c0001t0001g0157 a0001c0001t0001g0229 others(19): Show |
22 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.886+866dupA | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871399 | ||||||
| chr5:176871399 | C | CACACCAC others(196): Show |
2 | a0001c0001t0002g0230 a0001c0001t0002g0231 |
2 | HG01167.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.886+925_886+1127du others(204): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871399 | ||||||
| chr5:176871413 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.886+879C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871413 | |||||||
| chr5:176871417 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.886+883C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871417 | |||||||
| chr5:176871427 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.886+893T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871427 | |||||||
| chr5:176871428 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.886+894C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871428 | |||||||
| chr5:176871433 | C | A | 3 | a0001c0001t0001g0099 a0001c0001t0001g0229 a0001c0004t0002g0232 |
3 | HG02622.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.886+899C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871433 | |||||||
| chr5:176871433 | C | CA | 20 | a0001c0001t0001g0120 a0001c0001t0001g0157 a0001c0001t0003g0092 others(17): Show |
20 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.886+900dupA | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871433 | ||||||
| chr5:176871447 | C | A | 3 | a0001c0001t0001g0099 a0001c0001t0001g0229 a0001c0004t0002g0232 |
3 | HG02622.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.886+913C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871447 | |||||||
| chr5:176871459 | G | A | 42 | a0001c0001t0001g0031 a0001c0001t0001g0099 a0001c0001t0001g0120 others(39): Show |
42 | HG00099.hp1 HG00735.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.886+925G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871459 | |||||||
| chr5:176871459 | G | GCTCACCA others(196): Show |
1 | a0001c0001t0002g0051 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.886+992_886+993ins others(203): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871459 | ||||||
| chr5:176871463 | A | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0157 |
2 | HG02698.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.886+929A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871463 | |||||||
| chr5:176871463 | A | G | 1 | a0001c0001t0001g0031 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.886+929A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871463 | |||||||
| chr5:176871464 | CCAACACC others(60): Show |
C | 1 | a0001c0001t0001g0031 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.886+932_886+998del others(67): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871464 | ||||||
| chr5:176871470 | C | T | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.886+936C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871470 | |||||||
| chr5:176871480 | C | A | 48 | a0001c0001t0001g0120 a0001c0001t0001g0175 a0001c0001t0002g0040 others(45): Show |
50 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.886+946C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871480 | |||||||
| chr5:176871494 | T | C | 49 | a0001c0001t0001g0175 a0001c0001t0002g0010 a0001c0001t0002g0012 others(46): Show |
51 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.886+960T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871494 | |||||||
| chr5:176871495 | C | T | 49 | a0001c0001t0001g0175 a0001c0001t0002g0010 a0001c0001t0002g0012 others(46): Show |
51 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.886+961C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871495 | |||||||
| chr5:176871498 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.886+964C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871498 | |||||||
| chr5:176871498 | CCCAACAC others(297): Show |
C | 2 | a0001c0001t0001g0099 a0001c0001t0001g0229 |
2 | HG02622.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.886+993_886+1296de others(1): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871498 | ||||||
| chr5:176871522 | C | T | 20 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(17): Show |
20 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.886+988C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871522 | |||||||
| chr5:176871527 | G | A | 50 | a0001c0001t0001g0120 a0001c0001t0001g0157 a0001c0001t0001g0175 others(47): Show |
52 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.886+993G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871527 | |||||||
| chr5:176871530 | C | CG | 48 | a0001c0001t0001g0175 a0001c0001t0002g0040 a0001c0001t0002g0090 others(45): Show |
50 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.886+996_886+997ins others(1): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871530 | |||||||
| chr5:176871531 | A | C | 49 | a0001c0001t0001g0120 a0001c0001t0001g0175 a0001c0001t0002g0040 others(46): Show |
51 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.886+997A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871531 | |||||||
| chr5:176871548 | A | C | 23 | a0001c0001t0001g0031 a0001c0001t0001g0120 a0001c0001t0001g0157 others(20): Show |
23 | HG01255.hp2 HG01884.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.886+1014A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871548 | |||||||
| chr5:176871562 | T | TCG | 3 | a0001c0001t0001g0120 a0001c0001t0001g0157 a0001c0004t0002g0232 |
3 | HG02698.hp2 HG03195.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.886+1029_886+1030i others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871562 | ||||||
| chr5:176871564 | A | C | 3 | a0001c0001t0001g0120 a0001c0001t0001g0157 a0001c0004t0002g0232 |
3 | HG02698.hp2 HG03195.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.886+1030A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871564 | |||||||
| chr5:176871567 | A | AACACCAC others(27): Show |
1 | a0001c0001t0006g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.886+1046_886+1047i others(36): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871567 | ||||||
| chr5:176871581 | C | A | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(147): Show |
153 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(150): Show |
intron_variant | MODIFIER | c.886+1047C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871581 | |||||||
| chr5:176871581 | CCATCTGC others(129): Show |
C | 1 | a0001c0001t0002g0116 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.886+1102_886+1237d others(2): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871581 | ||||||
| chr5:176871588 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+1054C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871588 | |||||||
| chr5:176871593 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+1059A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871593 | |||||||
| chr5:176871594 | C | CTCACCCC others(26): Show |
17 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(14): Show |
17 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.886+1060_886+1061i others(35): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871594 | |||||||
| chr5:176871595 | C | T | 50 | a0001c0001t0001g0031 a0001c0001t0001g0120 a0001c0001t0001g0175 others(47): Show |
52 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.886+1061C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871595 | |||||||
| chr5:176871596 | T | C | 50 | a0001c0001t0001g0031 a0001c0001t0001g0120 a0001c0001t0001g0175 others(47): Show |
52 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.886+1062T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871596 | |||||||
| chr5:176871597 | G | C | 18 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(15): Show |
18 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.886+1063G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871597 | |||||||
| chr5:176871597 | G | T | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+1063G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871597 | |||||||
| chr5:176871598 | C | A | 18 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(15): Show |
18 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.886+1064C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871598 | |||||||
| chr5:176871599 | C | A | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+1065C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871599 | |||||||
| chr5:176871602 | A | C | 18 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(15): Show |
18 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.886+1068A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871602 | |||||||
| chr5:176871613 | T | C | 18 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(15): Show |
18 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.886+1079T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871613 | |||||||
| chr5:176871616 | C | A | 18 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(15): Show |
18 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.886+1082C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871616 | |||||||
| chr5:176871633 | C | A | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+1099C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871633 | |||||||
| chr5:176871636 | C | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(179): Show |
187 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(184): Show |
intron_variant | MODIFIER | c.886+1102C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871636 | |||||||
| chr5:176871638 | C | T | 13 | a0001c0001t0002g0248 a0001c0001t0003g0074 a0001c0001t0003g0244 others(10): Show |
14 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.886+1104C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871638 | |||||||
| chr5:176871650 | C | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(131): Show |
137 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.886+1116C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871650 | |||||||
| chr5:176871657 | C | T | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.886+1123C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871657 | |||||||
| chr5:176871665 | CG | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(131): Show |
137 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.886+1132delG | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871665 | |||||||
| chr5:176871665 | CGCCCCAC others(60): Show |
C | 3 | a0001c0001t0005g0256 a0001c0001t0008g0113 a0001c0001t0010g0022 |
3 | HG02280.hp2 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.886+1138_886+1204d others(69): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871665 | ||||||
| chr5:176871666 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+1132G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871666 | |||||||
| chr5:176871667 | C | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(131): Show |
137 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.886+1133C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871667 | |||||||
| chr5:176871668 | CCCACACC others(127): Show |
C | 34 | a0001c0001t0001g0031 a0001c0001t0002g0040 a0001c0001t0002g0090 others(31): Show |
36 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.886+1138_886+1271d others(2): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871668 | ||||||
| chr5:176871670 | C | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(131): Show |
137 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.886+1136C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871670 | |||||||
| chr5:176871670 | C | CA | 11 | a0001c0001t0001g0175 a0001c0001t0003g0009 a0001c0001t0003g0011 others(8): Show |
11 | HG01891.hp2 HG02717.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.886+1137dupA | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871670 | ||||||
| chr5:176871691 | C | G | 2 | a0001c0001t0001g0134 a0001c0001t0001g0156 |
2 | HG00733.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.886+1157C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871691 | |||||||
| chr5:176871700 | A | C | 1 | a0001c0001t0003g0259 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.886+1166A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871700 | |||||||
| chr5:176871700 | A | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(140): Show |
146 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.886+1166A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871700 | |||||||
| chr5:176871702 | CAACACCA others(93): Show |
C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(140): Show |
146 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.886+1169_886+1268d others(102): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871702 | |||||||
| chr5:176871703 | A | C | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+1169A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871703 | |||||||
| chr5:176871714 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+1180T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871714 | |||||||
| chr5:176871717 | A | C | 1 | a0001c0001t0003g0259 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.886+1183A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871717 | |||||||
| chr5:176871722 | T | C | 1 | a0001c0001t0002g0121 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.886+1188T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871722 | |||||||
| chr5:176871731 | C | T | 2 | a0001c0001t0001g0157 a0001c0001t0003g0259 |
2 | NA18906.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.886+1197C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871731 | |||||||
| chr5:176871732 | T | C | 2 | a0001c0001t0001g0157 a0001c0001t0003g0259 |
2 | NA18906.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.886+1198T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871732 | |||||||
| chr5:176871733 | G | C | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.886+1199G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871733 | |||||||
| chr5:176871734 | C | A | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.886+1200C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871734 | |||||||
| chr5:176871735 | C | CCCAACAC others(60): Show |
3 | a0001c0001t0007g0083 a0001c0001t0007g0242 a0001c0001t0007g0247 |
3 | HG01884.hp1 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.886+1238_886+1304d others(69): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871735 | ||||||
| chr5:176871738 | A | C | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.886+1204A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871738 | |||||||
| chr5:176871768 | G | A | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.886+1234G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871768 | |||||||
| chr5:176871768 | G | GC | 4 | a0001c0001t0003g0259 a0001c0001t0005g0256 a0001c0001t0008g0113 others(1): Show |
4 | HG02280.hp2 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+1237dupC | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871768 | ||||||
| chr5:176871772 | A | C | 2 | a0001c0001t0001g0157 a0001c0004t0002g0232 |
2 | HG03195.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.886+1238A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871772 | |||||||
| chr5:176871783 | T | C | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.886+1249T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871783 | |||||||
| chr5:176871786 | A | C | 5 | a0001c0001t0001g0157 a0001c0001t0003g0259 a0001c0001t0005g0256 others(2): Show |
5 | HG02280.hp2 HG02970.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.886+1252A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871786 | |||||||
| chr5:176871800 | T | TCG | 3 | a0001c0001t0005g0256 a0001c0001t0008g0113 a0001c0001t0010g0022 |
3 | HG02280.hp2 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.886+1267_886+1268i others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871800 | ||||||
| chr5:176871802 | A | C | 4 | a0001c0001t0005g0256 a0001c0001t0008g0113 a0001c0001t0010g0022 others(1): Show |
4 | HG02280.hp2 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+1268A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871802 | |||||||
| chr5:176871805 | A | C | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.886+1271A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871805 | |||||||
| chr5:176871809 | C | T | 4 | a0001c0001t0002g0230 a0001c0001t0002g0231 a0001c0004t0002g0078 others(1): Show |
4 | HG01167.hp1 HG02451.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.886+1275C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871809 | |||||||
| chr5:176871819 | C | A | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+1285C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871819 | |||||||
| chr5:176871819 | C | CCATCTGC others(60): Show |
1 | a0001c0001t0006g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.886+1304_886+1305i others(69): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871819 | ||||||
| chr5:176871833 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+1299T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871833 | |||||||
| chr5:176871834 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+1300C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871834 | |||||||
| chr5:176871835 | GC | G | 15 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(12): Show |
15 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.886+1305delC | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871835 | ||||||
| chr5:176871836 | CCCCAACA others(27): Show |
C | 4 | a0001c0001t0001g0120 a0001c0001t0001g0175 a0001c0001t0003g0244 others(1): Show |
4 | HG02698.hp2 HG02717.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+1340_886+1373d others(36): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871836 | ||||||
| chr5:176871842 | C | T | 1 | a0001c0001t0003g0259 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.886+1308C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871842 | |||||||
| chr5:176871854 | C | A | 14 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(11): Show |
14 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.886+1320C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871854 | |||||||
| chr5:176871868 | TCGCCCAA others(64): Show |
T | 10 | a0001c0001t0003g0009 a0001c0001t0003g0011 a0001c0001t0003g0049 others(7): Show |
10 | HG01891.hp2 HG02280.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.886+1336_886+1406d others(73): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871868 | ||||||
| chr5:176871869 | CG | C | 16 | a0001c0001t0001g0031 a0001c0001t0003g0092 a0001c0001t0003g0093 others(13): Show |
16 | HG01255.hp2 HG02451.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.886+1336delG | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871869 | |||||||
| chr5:176871870 | G | GC | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(168): Show |
176 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(173): Show |
intron_variant | MODIFIER | c.886+1339dupC | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871870 | ||||||
| chr5:176871871 | C | A | 16 | a0001c0001t0001g0031 a0001c0001t0003g0092 a0001c0001t0003g0093 others(13): Show |
16 | HG01255.hp2 HG02451.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.886+1337C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871871 | |||||||
| chr5:176871888 | C | A | 2 | a0001c0001t0001g0157 a0001c0004t0002g0232 |
2 | HG03195.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.886+1354C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871888 | |||||||
| chr5:176871899 | C | T | 14 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(11): Show |
14 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.886+1365C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871899 | |||||||
| chr5:176871902 | T | C | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.886+1368T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871902 | |||||||
| chr5:176871903 | C | T | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.886+1369C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871903 | |||||||
| chr5:176871906 | C | A | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+1372C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871906 | |||||||
| chr5:176871937 | TCG | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(184): Show |
192 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(189): Show |
intron_variant | MODIFIER | c.886+1405_886+1406d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871937 | ||||||
| chr5:176871938 | C | CACCAACA others(26): Show |
1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.886+1404_886+1405i others(35): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871938 | |||||||
| chr5:176871940 | C | A | 1 | a0001c0001t0001g0031 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.886+1406C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871940 | |||||||
| chr5:176871941 | C | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
202 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(199): Show |
intron_variant | MODIFIER | c.886+1407C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871941 | |||||||
| chr5:176871941 | C | CCAACACC others(25): Show |
1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+1408_886+1409i others(34): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871941 | ||||||
| chr5:176871941 | C | CCCAACAC others(26): Show |
1 | a0001c0001t0001g0105 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.886+1439_886+1440i others(35): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871941 | ||||||
| chr5:176871941 | C | CCCAACAC others(61): Show |
1 | a0001c0001t0006g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.886+1445_886+1446i others(70): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871941 | ||||||
| chr5:176871958 | C | A | 14 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(11): Show |
14 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.886+1424C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871958 | |||||||
| chr5:176871971 | CTCGCCCC others(60): Show |
C | 1 | a0001c0001t0001g0031 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.886+1438_886+1504d others(69): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871971 | |||||||
| chr5:176871972 | T | C | 13 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(10): Show |
13 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.886+1438T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871972 | |||||||
| chr5:176871972 | TCG | T | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0004t0002g0232 |
3 | HG03195.hp2 HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.886+1440_886+1441d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871972 | ||||||
| chr5:176871973 | C | T | 13 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(10): Show |
13 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.886+1439C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871973 | |||||||
| chr5:176871976 | C | A | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0004t0002g0232 |
3 | HG03195.hp2 HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.886+1442C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871976 | |||||||
| chr5:176871980 | G | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(205): Show |
213 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(210): Show |
intron_variant | MODIFIER | c.886+1446G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871980 | |||||||
| chr5:176871993 | C | A | 1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.886+1459C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871993 | |||||||
| chr5:176872000 | T | C | 18 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0010 others(15): Show |
18 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.886+1466T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872000 | |||||||
| chr5:176872005 | A | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(189): Show |
197 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(194): Show |
intron_variant | MODIFIER | c.886+1471A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872005 | |||||||
| chr5:176872007 | T | TCG | 4 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0010 others(1): Show |
4 | HG02965.hp2 HG03704.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.886+1474_886+1475i others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872007 | ||||||
| chr5:176872008 | C | CG | 13 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(10): Show |
13 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.886+1474_886+1475i others(3): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872008 | |||||||
| chr5:176872009 | A | C | 17 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0010 others(14): Show |
17 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.886+1475A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872009 | |||||||
| chr5:176872020 | A | T | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.886+1486A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872020 | |||||||
| chr5:176872026 | C | A | 14 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(11): Show |
14 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.886+1492C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872026 | |||||||
| chr5:176872033 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.886+1499C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872033 | |||||||
| chr5:176872038 | A | G | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.886+1504A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872038 | |||||||
| chr5:176872040 | T | G | 1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.886+1506T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872040 | |||||||
| chr5:176872042 | A | C | 1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.886+1508A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872042 | |||||||
| chr5:176872059 | A | C | 19 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0010 others(16): Show |
19 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.886+1525A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872059 | |||||||
| chr5:176872075 | A | G | 17 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0092 others(14): Show |
17 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.886+1541A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872075 | |||||||
| chr5:176872075 | ACCCCACA others(61): Show |
A | 19 | a0001c0001t0001g0175 a0001c0001t0002g0040 a0001c0001t0002g0090 others(16): Show |
19 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.886+1575_886+1642d others(70): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872075 | ||||||
| chr5:176872079 | C | A | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0005g0013 |
3 | HG03540.hp2 HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.886+1545C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872079 | |||||||
| chr5:176872079 | C | CA | 16 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0092 others(13): Show |
16 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.886+1546dupA | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872079 | ||||||
| chr5:176872093 | C | A | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0005g0013 |
3 | HG03540.hp2 HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.886+1559C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872093 | |||||||
| chr5:176872100 | C | T | 2 | a0001c0001t0002g0010 a0001c0001t0002g0012 |
2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.886+1566C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872100 | |||||||
| chr5:176872101 | C | A | 1 | a0003c0003t0002g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.886+1567C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872101 | |||||||
| chr5:176872105 | A | G | 2 | a0001c0001t0002g0010 a0001c0001t0002g0012 |
2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.886+1571A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872105 | |||||||
| chr5:176872109 | A | G | 14 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(11): Show |
14 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.886+1575A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872109 | |||||||
| chr5:176872109 | ACCCCACA others(62): Show |
A | 2 | a0001c0001t0002g0010 a0001c0001t0002g0012 |
2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.886+1579_886+1647d others(71): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872109 | ||||||
| chr5:176872113 | C | A | 15 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(12): Show |
15 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.886+1579C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872113 | |||||||
| chr5:176872120 | C | T | 1 | a0003c0003t0001g0188 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.886+1586C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872120 | |||||||
| chr5:176872124 | C | T | 17 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0003g0092 others(14): Show |
17 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.886+1590C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872124 | |||||||
| chr5:176872127 | A | C | 17 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0003g0092 others(14): Show |
17 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.886+1593A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872127 | |||||||
| chr5:176872143 | G | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.886+1609G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872143 | |||||||
| chr5:176872147 | C | A | 2 | a0001c0001t0001g0031 a0001c0004t0002g0232 |
2 | HG01255.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.886+1613C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872147 | |||||||
| chr5:176872147 | C | CA | 14 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(11): Show |
14 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.886+1614dupA | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872147 | ||||||
| chr5:176872149 | C | T | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.886+1615C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872149 | |||||||
| chr5:176872158 | T | C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.886+1624T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872158 | |||||||
| chr5:176872161 | C | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.886+1627C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872161 | |||||||
| chr5:176872181 | C | A | 3 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0005g0013 |
3 | HG02965.hp2 HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.886+1647C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872181 | |||||||
| chr5:176872181 | C | CA | 14 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(11): Show |
14 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.886+1648dupA | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872181 | ||||||
| chr5:176872209 | T | TCG | 14 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(11): Show |
14 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.886+1676_886+1677i others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872209 | ||||||
| chr5:176872211 | A | C | 15 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(12): Show |
15 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.886+1677A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872211 | |||||||
| chr5:176872211 | A | G | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.886+1677A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872211 | |||||||
| chr5:176872212 | CCAACACC others(127): Show |
C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.886+1680_887-1621d others(2): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872212 | ||||||
| chr5:176872228 | A | C | 15 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(12): Show |
15 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.886+1694A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872228 | |||||||
| chr5:176872241 | CCT | C | 13 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(10): Show |
13 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.886+1708_886+1709d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872241 | |||||||
| chr5:176872242 | C | T | 2 | a0001c0001t0005g0013 a0001c0004t0002g0232 |
2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.886+1708C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872242 | |||||||
| chr5:176872243 | T | C | 2 | a0001c0001t0005g0013 a0001c0004t0002g0232 |
2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.886+1709T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872243 | |||||||
| chr5:176872243 | TGCCCCAA others(161): Show |
T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0026 others(74): Show |
79 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.887-1671_887-1504d others(2): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872243 | ||||||
| chr5:176872244 | G | C | 2 | a0001c0001t0002g0010 a0001c0001t0002g0012 |
2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.886+1710G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872244 | |||||||
| chr5:176872244 | G | T | 13 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(10): Show |
13 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.886+1710G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872244 | |||||||
| chr5:176872245 | C | A | 2 | a0001c0001t0002g0010 a0001c0001t0002g0012 |
2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.886+1711C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872245 | |||||||
| chr5:176872246 | C | A | 13 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(10): Show |
13 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.886+1712C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872246 | |||||||
| chr5:176872249 | A | C | 2 | a0001c0001t0002g0010 a0001c0001t0002g0012 |
2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.886+1715A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872249 | |||||||
| chr5:176872263 | C | A | 12 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0028 others(9): Show |
12 | HG01928.hp1 HG02027.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.887-1705C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872263 | |||||||
| chr5:176872270 | C | T | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.887-1698C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872270 | |||||||
| chr5:176872275 | A | G | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.887-1693A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872275 | |||||||
| chr5:176872276 | CTCGCCCA others(125): Show |
C | 12 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0028 others(9): Show |
12 | HG01928.hp1 HG02027.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.887-1691_887-1560d others(2): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872276 | |||||||
| chr5:176872279 | G | GC | 14 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(11): Show |
14 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.887-1686dupC | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872279 | ||||||
| chr5:176872280 | C | A | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.887-1688C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872280 | |||||||
| chr5:176872283 | A | C | 2 | a0001c0001t0002g0010 a0001c0001t0002g0012 |
2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.887-1685A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872283 | |||||||
| chr5:176872287 | C | A | 1 | a0001c0001t0002g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.887-1681C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872287 | |||||||
| chr5:176872297 | A | C | 17 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0003g0092 others(14): Show |
17 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.887-1671A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872297 | |||||||
| chr5:176872304 | C | T | 13 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(10): Show |
13 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.887-1664C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872304 | |||||||
| chr5:176872309 | A | G | 13 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(10): Show |
13 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.887-1659A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872309 | |||||||
| chr5:176872313 | A | ACCAACAC others(28): Show |
1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.887-1632_887-1631i others(37): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872313 | ||||||
| chr5:176872313 | ACCAACAC others(94): Show |
A | 13 | a0001c0001t0002g0040 a0001c0001t0002g0118 a0001c0001t0002g0184 others(10): Show |
13 | HG00099.hp1 HG00735.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.887-1631_887-1531d others(2): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872313 | ||||||
| chr5:176872321 | C | A | 1 | a0001c0001t0001g0031 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.887-1647C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872321 | |||||||
| chr5:176872322 | A | C | 1 | a0001c0001t0001g0031 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.887-1646A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872322 | |||||||
| chr5:176872323 | C | A | 1 | a0001c0001t0001g0031 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.887-1645C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872323 | |||||||
| chr5:176872330 | C | A | 3 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0004t0002g0232 |
3 | HG02965.hp2 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.887-1638C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872330 | |||||||
| chr5:176872337 | T | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(101): Show |
107 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(104): Show |
intron_variant | MODIFIER | c.887-1631T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872337 | |||||||
| chr5:176872342 | G | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(101): Show |
107 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(104): Show |
intron_variant | MODIFIER | c.887-1626G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872342 | |||||||
| chr5:176872344 | T | G | 2 | a0001c0001t0002g0010 a0001c0001t0002g0012 |
2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.887-1624T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872344 | |||||||
| chr5:176872345 | C | CG | 87 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(84): Show |
90 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.887-1623_887-1622i others(3): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872345 | |||||||
| chr5:176872345 | C | CGCCCAAC others(164): Show |
1 | a0001c0001t0006g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.887-1623_887-1622i others(173): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872345 | |||||||
| chr5:176872346 | A | ACCCCACA others(131): Show |
1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.887-1620_887-1619i others(140): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872346 | ||||||
| chr5:176872346 | A | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(87): Show |
93 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.887-1622A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872346 | |||||||
| chr5:176872349 | A | C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.887-1619A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872349 | |||||||
| chr5:176872357 | A | T | 1 | a0001c0004t0002g0233 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.887-1611A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872357 | |||||||
| chr5:176872363 | A | C | 7 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0251 others(4): Show |
7 | HG02965.hp2 HG03195.hp2 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.887-1605A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872363 | |||||||
| chr5:176872363 | ACATCTGC others(26): Show |
A | 1 | a0001c0001t0001g0064 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.887-1589_887-1557d others(35): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872363 | ||||||
| chr5:176872378 | C | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0169 |
2 | HG00609.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.887-1590C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872378 | |||||||
| chr5:176872379 | A | AC | 13 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(10): Show |
13 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.887-1587dupC | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872379 | ||||||
| chr5:176872379 | A | C | 2 | a0001c0001t0002g0010 a0001c0001t0002g0012 |
2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.887-1589A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872379 | |||||||
| chr5:176872379 | ACCAACAC others(96): Show |
A | 13 | a0001c0001t0001g0175 a0001c0001t0002g0090 a0001c0001t0002g0097 others(10): Show |
13 | HG00639.hp2 HG01074.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.887-1483_887-1381d others(2): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872379 | ||||||
| chr5:176872382 | A | C | 13 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(10): Show |
13 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.887-1586A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872382 | |||||||
| chr5:176872396 | C | A | 5 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0010 others(2): Show |
5 | HG02965.hp2 HG03540.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.887-1572C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872396 | |||||||
| chr5:176872410 | T | C | 5 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0010 others(2): Show |
5 | HG02965.hp2 HG03195.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.887-1558T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872410 | |||||||
| chr5:176872410 | TC | T | 12 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0028 others(9): Show |
12 | HG01928.hp1 HG02027.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.887-1557delC | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872410 | |||||||
| chr5:176872411 | C | T | 5 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0010 others(2): Show |
5 | HG02965.hp2 HG03195.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.887-1557C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872411 | |||||||
| chr5:176872412 | G | A | 14 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(11): Show |
14 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.887-1556G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872412 | |||||||
| chr5:176872413 | CCCCAACA others(27): Show |
C | 24 | a0001c0001t0002g0248 a0001c0001t0003g0074 a0001c0001t0003g0244 others(21): Show |
26 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.887-1483_887-1450d others(36): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872413 | ||||||
| chr5:176872414 | C | CCCACACC others(195): Show |
13 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0245 others(10): Show |
13 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.887-1551_887-1550i others(204): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872414 | ||||||
| chr5:176872414 | C | CCCACACC others(229): Show |
1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.887-1551_887-1550i others(238): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872414 | ||||||
| chr5:176872447 | G | A | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.887-1521G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872447 | |||||||
| chr5:176872465 | C | A | 16 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0002g0040 others(13): Show |
16 | HG00099.hp1 HG00735.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.887-1503C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872465 | |||||||
| chr5:176872480 | CG | C | 29 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0002g0040 others(26): Show |
29 | HG00099.hp1 HG00735.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.887-1487delG | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872480 | |||||||
| chr5:176872481 | G | A | 2 | a0001c0001t0001g0183 a0001c0004t0002g0232 |
2 | HG02015.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.887-1487G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872481 | |||||||
| chr5:176872482 | C | A | 29 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0002g0040 others(26): Show |
29 | HG00099.hp1 HG00735.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.887-1486C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872482 | |||||||
| chr5:176872482 | C | CCCCAACA others(536): Show |
1 | a0001c0001t0006g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.887-1484_887-1483i others(545): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872482 | ||||||
| chr5:176872497 | T | G | 1 | a0001c0001t0001g0223 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.887-1471T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872497 | |||||||
| chr5:176872513 | T | C | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.887-1455T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872513 | |||||||
| chr5:176872514 | C | T | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.887-1454C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872514 | |||||||
| chr5:176872530 | C | T | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.887-1438C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872530 | |||||||
| chr5:176872549 | CG | C | 24 | a0001c0001t0002g0248 a0001c0001t0003g0074 a0001c0001t0003g0244 others(21): Show |
26 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.887-1418delG | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872549 | |||||||
| chr5:176872550 | G | A | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.887-1418G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872550 | |||||||
| chr5:176872550 | G | C | 1 | a0001c0001t0001g0031 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.887-1418G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872550 | |||||||
| chr5:176872551 | C | A | 24 | a0001c0001t0002g0248 a0001c0001t0003g0074 a0001c0001t0003g0244 others(21): Show |
26 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.887-1417C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872551 | |||||||
| chr5:176872551 | C | G | 1 | a0001c0001t0001g0031 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.887-1417C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872551 | |||||||
| chr5:176872584 | G | A | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.887-1384G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872584 | |||||||
| chr5:176872585 | C | CCAACACC others(25): Show |
1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.887-1382_887-1381i others(34): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872585 | ||||||
| chr5:176872586 | CCCAACAC others(59): Show |
C | 2 | a0001c0001t0002g0010 a0001c0001t0002g0012 |
2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.887-1365_887-1300d others(68): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872586 | ||||||
| chr5:176872589 | A | C | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.887-1379A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872589 | |||||||
| chr5:176872610 | T | C | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.887-1358T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872610 | |||||||
| chr5:176872615 | G | A | 2 | a0001c0001t0002g0257 a0001c0004t0002g0232 |
2 | HG03195.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.887-1353G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872615 | |||||||
| chr5:176872648 | A | G | 2 | a0001c0001t0001g0255 a0001c0001t0008g0046 |
2 | HG02559.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.887-1320A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872648 | |||||||
| chr5:176872669 | A | C | 2 | a0001c0001t0002g0101 a0001c0004t0002g0232 |
2 | HG01433.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.887-1299A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872669 | |||||||
| chr5:176872681 | A | G | 1 | a0001c0001t0002g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.887-1287A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872681 | |||||||
| chr5:176872698 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.887-1270G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872698 | |||||||
| chr5:176872803 | T | C | 1 | a0001c0001t0003g0050 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.887-1165T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872803 | |||||||
| chr5:176872855 | CACCAACA others(26): Show |
C | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.887-1112_887-1080d others(35): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872855 | |||||||
| chr5:176872873 | C | A | 3 | a0001c0001t0007g0083 a0001c0001t0007g0242 a0001c0001t0007g0247 |
3 | HG01884.hp1 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.887-1095C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872873 | |||||||
| chr5:176872893 | CAACACCA others(28): Show |
C | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.887-1073_887-1039d others(37): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872893 | ||||||
| chr5:176872903 | G | A | 5 | a0001c0001t0003g0009 a0001c0001t0003g0011 a0001c0001t0003g0049 others(2): Show |
5 | HG03041.hp1 HG03139.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.887-1065G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872903 | |||||||
| chr5:176872988 | AC | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
181 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(178): Show |
intron_variant | MODIFIER | c.887-978delC | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872988 | ||||||
| chr5:176872992 | G | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
181 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(178): Show |
intron_variant | MODIFIER | c.887-976G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872992 | |||||||
| chr5:176872992 | G | T | 1 | a0001c0001t0001g0031 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.887-976G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872992 | |||||||
| chr5:176872993 | C | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
181 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(178): Show |
intron_variant | MODIFIER | c.887-975C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872993 | |||||||
| chr5:176872994 | C | A | 1 | a0001c0001t0001g0031 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.887-974C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872994 | |||||||
| chr5:176872997 | A | C | 1 | a0001c0001t0001g0031 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.887-971A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872997 | |||||||
| chr5:176873007 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(210): Show |
218 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(215): Show |
intron_variant | MODIFIER | c.887-961T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176873007 | |||||||
| chr5:176873027 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.887-941A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176873027 | |||||||
| chr5:176873051 | G | T | 5 | a0001c0001t0003g0009 a0001c0001t0003g0011 a0001c0001t0003g0049 others(2): Show |
5 | HG03041.hp1 HG03139.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.887-917G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176873051 | |||||||
| chr5:176873129 | C | CCCAACAC others(26): Show |
2 | a0001c0001t0002g0010 a0001c0001t0002g0012 |
2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.887-806_887-774dup others(33): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176873129 | ||||||
| chr5:176873164 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.887-804C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176873164 | |||||||
| chr5:176873186 | C | T | 15 | a0001c0001t0002g0051 a0001c0001t0002g0116 a0001c0001t0002g0137 others(12): Show |
16 | HG00621.hp1 HG01109.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.887-782C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176873186 | |||||||
| chr5:176873199 | A | AACACCAC others(27): Show |
1 | a0001c0001t0001g0125 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.887-747_887-746ins others(34): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176873199 | ||||||
| chr5:176873319 | AT | A | 7 | a0001c0001t0001g0031 a0001c0001t0002g0248 a0001c0001t0003g0093 others(4): Show |
8 | HG01255.hp2 HG02809.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.887-638delT | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176873319 | ||||||
| chr5:176873522 | A | G | 2 | a0001c0004t0002g0232 a0001c0004t0002g0233 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.887-446A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176873522 | |||||||
| chr5:176873611 | C | G | 1 | a0001c0001t0002g0097 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.887-357C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176873611 | |||||||
| chr5:176873746 | C | T | 2 | a0003c0003t0002g0107 a0003c0003t0002g0240 |
2 | HG01361.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.887-222C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176873746 | |||||||
| chr5:176873838 | A | G | 1 | a0001c0001t0001g0192 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.887-130A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176873838 | |||||||
| chr5:176874587 | C | T | 11 | a0001c0001t0007g0083 a0001c0001t0007g0242 a0001c0001t0007g0247 others(8): Show |
12 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1378+21C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176874587 | |||||||
| chr5:176874721 | G | A | 1 | a0001c0004t0002g0078 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1378+155G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176874721 | |||||||
| chr5:176874849 | A | C | 22 | a0001c0001t0003g0009 a0001c0001t0003g0011 a0001c0001t0003g0049 others(19): Show |
22 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.1378+283A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176874849 | |||||||
| chr5:176874870 | G | A | 1 | a0001c0001t0002g0189 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1378+304G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176874870 | |||||||
| chr5:176874912 | G | A | 1 | a0001c0001t0011g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1378+346G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176874912 | |||||||
| chr5:176874932 | C | T | 11 | a0001c0001t0007g0083 a0001c0001t0007g0242 a0001c0001t0007g0247 others(8): Show |
12 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1378+366C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176874932 | |||||||
| chr5:176875092 | G | C | 11 | a0001c0001t0007g0083 a0001c0001t0007g0242 a0001c0001t0007g0247 others(8): Show |
12 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1378+526G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176875092 | |||||||
| chr5:176875409 | G | A | 4 | a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(1): Show |
4 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1378+843G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176875409 | |||||||
| chr5:176875555 | C | T | 1 | a0001c0001t0002g0248 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1378+989C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176875555 | |||||||
| chr5:176875634 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1378+1068G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176875634 | |||||||
| chr5:176875767 | C | T | 1 | a0003c0003t0001g0082 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1378+1201C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176875767 | |||||||
| chr5:176875826 | C | T | 2 | a0001c0001t0001g0175 a0001c0001t0010g0022 |
2 | HG03139.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1378+1260C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176875826 | |||||||
| chr5:176875832 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0020 |
2 | HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1378+1266C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176875832 | |||||||
| chr5:176875895 | G | T | 2 | a0001c0001t0002g0010 a0001c0001t0002g0012 |
2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1379-1297G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176875895 | |||||||
| chr5:176876029 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1379-1163G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176876029 | |||||||
| chr5:176876345 | C | T | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1379-847C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176876345 | |||||||
| chr5:176876455 | G | C | 1 | a0001c0001t0001g0018 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1379-737G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176876455 | |||||||
| chr5:176876523 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1379-669A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176876523 | |||||||
| chr5:176876580 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0030 |
2 | HG02080.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1379-612C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176876580 | |||||||
| chr5:176876670 | A | G | 37 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0002g0040 others(34): Show |
38 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.1379-522A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176876670 | |||||||
| chr5:176876809 | G | A | 1 | a0001c0009t0001g0177 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1379-383G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176876809 | |||||||
| chr5:176877302 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1466+23C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 9/14 | chr5 | 176877302 | |||||||
| chr5:176877398 | A | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(222): Show |
230 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(227): Show |
intron_variant | MODIFIER | c.1466+119A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 9/14 | chr5 | 176877398 | |||||||
| chr5:176877755 | G | A | 18 | a0001c0001t0002g0040 a0001c0001t0002g0090 a0001c0001t0002g0097 others(15): Show |
18 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.1635+52G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 10/14 | chr5 | 176877755 | |||||||
| chr5:176877792 | C | T | 2 | a0001c0001t0001g0201 a0002c0002t0004g0166 |
2 | NA18971.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1635+89C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 10/14 | chr5 | 176877792 | |||||||
| chr5:176877817 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1636-77C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 10/14 | chr5 | 176877817 | |||||||
| chr5:176878136 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1869+9C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 11/14 | chr5 | 176878136 | |||||||
| chr5:176878137 | G | A | 1 | a0001c0001t0002g0181 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1869+10G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 11/14 | chr5 | 176878137 | |||||||
| chr5:176878164 | C | T | 13 | a0001c0001t0003g0050 a0001c0001t0003g0092 a0001c0001t0003g0093 others(10): Show |
13 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1869+37C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 11/14 | chr5 | 176878164 | |||||||
| chr5:176878465 | T | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(136): Show |
142 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.2020-10T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 12/14 | chr5 | 176878465 | |||||||
| chr5:176878677 | C | T | 40 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0026 others(37): Show |
41 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.2184+38C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 13/14 | chr5 | 176878677 | |||||||
| chr5:176878694 | A | T | 1 | a0001c0001t0001g0044 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2184+55A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 13/14 | chr5 | 176878694 | |||||||
| chr5:176878862 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0009g0043 |
2 | HG00741.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.2184+223G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 13/14 | chr5 | 176878862 | |||||||
| chr5:176878867 | A | G | 3 | a0001c0001t0001g0018 a0001c0001t0002g0010 a0001c0001t0002g0012 |
3 | HG01884.hp2 HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2184+228A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 13/14 | chr5 | 176878867 | |||||||
| chr5:176878889 | G | A | 7 | a0003c0003t0001g0082 a0003c0003t0001g0084 a0003c0003t0001g0188 others(4): Show |
7 | HG00733.hp1 HG01361.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.2184+250G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 13/14 | chr5 | 176878889 | |||||||
| chr5:176878918 | G | A | 2 | a0001c0001t0002g0230 a0001c0001t0002g0231 |
2 | HG01167.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2184+279G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 13/14 | chr5 | 176878918 | |||||||
| chr5:176878952 | A | G | 35 | a0001c0001t0001g0018 a0001c0001t0002g0010 a0001c0001t0002g0012 others(32): Show |
35 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.2184+313A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 13/14 | chr5 | 176878952 | |||||||
| chr5:176878973 | G | A | 42 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0002g0040 others(39): Show |
42 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.2184+334G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 13/14 | chr5 | 176878973 | |||||||
| chr5:176879019 | G | C | 1 | a0001c0001t0002g0151 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2185-291G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 13/14 | chr5 | 176879019 | |||||||
| chr5:176879107 | C | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0160 |
3 | HG02027.hp2 HG02523.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.2185-203C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 13/14 | chr5 | 176879107 | |||||||
| chr5:176879129 | G | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0160 |
3 | HG02027.hp2 HG02523.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.2185-181G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 13/14 | chr5 | 176879129 | |||||||
| chr5:176879250 | G | T | 1 | a0001c0001t0003g0074 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2185-60G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 13/14 | chr5 | 176879250 | |||||||
| chr5:176879655 | CA | C | 3 | a0002c0002t0004g0021 a0002c0002t0004g0048 a0002c0002t0004g0066 |
3 | HG01109.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2364-65delA | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 14/14 | chr5 | 176879655 | |||||||
| chr5:176879658 | G | A | 3 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0030 |
3 | HG02080.hp2 HG03834.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.2364-63G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 14/14 | chr5 | 176879658 | |||||||
| chr5:176879675 | G | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(121): Show |
128 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.2364-46G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 14/14 | chr5 | 176879675 |