Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57600 |
| ensemblid | ENSG00000052795.13 |
| hgncid | 29280 |
| symbol | FNIP2 |
| name | folliculin interacting protein 2 |
| refseq_nuc | NM_020840.3 |
| refseq_prot | NP_065891.1 |
| ensembl_nuc | ENST00000264433.11 |
| ensembl_prot | ENSP00000264433.6 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 158769026 |
| end | 158908050 |
| strand | + |
| ver | v1.2 |
| region | chr4:158769026-158908050 |
| region5000 | chr4:158764026-158913050 |
| regionname0 | FNIP2_chr4_158769026_158908050 |
| regionname5000 | FNIP2_chr4_158764026_158913050 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1114 | 195 | 62 | 40 | 58 | 7 | 26 | 39 | FNIP2_chr4_158764026_158913050 | FNIP2 | MAPTL others(1109): Show |
chr4 | 158764026 | 158913050 |
| a0002 | 0/0 | 1114 | 37 | 9 | 3 | 20 | 1 | 4 | 15 | FNIP2_chr4_158764026_158913050 | FNIP2 | MAPTL others(1109): Show |
chr4 | 158764026 | 158913050 |
| a0003 | 0/0 | 1114 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | MAPTL others(1109): Show |
chr4 | 158764026 | 158913050 |
| a0004 | 0/0 | 1114 | 5 | 0 | 4 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | MAPTL others(1109): Show |
chr4 | 158764026 | 158913050 |
| a0005 | 0/0 | 1114 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | MAPTL others(1109): Show |
chr4 | 158764026 | 158913050 |
| a0006 | 0/0 | 1114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | MAPTL others(1109): Show |
chr4 | 158764026 | 158913050 |
| a0007 | 0/0 | 1114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | MAPTL others(1109): Show |
chr4 | 158764026 | 158913050 |
| a0008 | 0/0 | 1114 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | MAPTL others(1109): Show |
chr4 | 158764026 | 158913050 |
| a0009 | 0/0 | 1114 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | MAPTL others(1109): Show |
chr4 | 158764026 | 158913050 |
| a0010 | 0/0 | 1114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | MAPTL others(1109): Show |
chr4 | 158764026 | 158913050 |
| a0011 | 0/0 | 1114 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | MAPTL others(1109): Show |
chr4 | 158764026 | 158913050 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3342 | 165 | 41 | 40 | 55 | 7 | 20 | FNIP2_chr4_158764026_158913050 | FNIP2 | ATGGC others(3337): Show |
chr4 | 158764026 | 158913050 | ||
| a0001c0003 | 0/0 | 3342 | 16 | 12 | 0 | 3 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | ATGGC others(3337): Show |
chr4 | 158764026 | 158913050 | ||
| a0001c0005 | 0/0 | 3342 | 5 | 0 | 0 | 0 | 0 | 5 | FNIP2_chr4_158764026_158913050 | FNIP2 | ATGGC others(3337): Show |
chr4 | 158764026 | 158913050 | ||
| a0001c0007 | 0/0 | 3342 | 4 | 4 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | ATGGC others(3337): Show |
chr4 | 158764026 | 158913050 | ||
| a0001c0008 | 0/0 | 3342 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | ATGGC others(3337): Show |
chr4 | 158764026 | 158913050 | ||
| a0001c0009 | 0/0 | 3342 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | ATGGC others(3337): Show |
chr4 | 158764026 | 158913050 | ||
| a0001c0014 | 0/0 | 3342 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | ATGGC others(3337): Show |
chr4 | 158764026 | 158913050 | ||
| a0002c0002 | 0/0 | 3342 | 36 | 8 | 3 | 20 | 1 | 4 | FNIP2_chr4_158764026_158913050 | FNIP2 | ATGGC others(3337): Show |
chr4 | 158764026 | 158913050 | ||
| a0002c0017 | 0/0 | 3342 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | ATGGC others(3337): Show |
chr4 | 158764026 | 158913050 | ||
| a0003c0004 | 0/0 | 3342 | 10 | 10 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | ATGGC others(3337): Show |
chr4 | 158764026 | 158913050 | ||
| a0004c0006 | 0/0 | 3342 | 5 | 0 | 4 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | ATGGC others(3337): Show |
chr4 | 158764026 | 158913050 | ||
| a0005c0011 | 0/0 | 3342 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | ATGGC others(3337): Show |
chr4 | 158764026 | 158913050 | ||
| a0006c0015 | 0/0 | 3342 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | ATGGC others(3337): Show |
chr4 | 158764026 | 158913050 | ||
| a0007c0016 | 0/0 | 3342 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | ATGGC others(3337): Show |
chr4 | 158764026 | 158913050 | ||
| a0008c0018 | 0/0 | 3342 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | ATGGC others(3337): Show |
chr4 | 158764026 | 158913050 | ||
| a0009c0010 | 0/0 | 3342 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | ATGGC others(3337): Show |
chr4 | 158764026 | 158913050 | ||
| a0010c0013 | 0/0 | 3342 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | ATGGC others(3337): Show |
chr4 | 158764026 | 158913050 | ||
| a0011c0012 | 0/0 | 3342 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | ATGGC others(3337): Show |
chr4 | 158764026 | 158913050 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 7037 | 103 | 19 | 24 | 40 | 4 | 15 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7032): Show |
chr4 | 158764026 | 158913050 |
| a0001c0001t0002 | 0/0 | 7037 | 34 | 4 | 13 | 9 | 3 | 5 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7032): Show |
chr4 | 158764026 | 158913050 |
| a0001c0001t0003 | 0/0 | 7037 | 2 | 1 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7032): Show |
chr4 | 158764026 | 158913050 |
| a0001c0001t0004 | 0/0 | 7037 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7032): Show |
chr4 | 158764026 | 158913050 |
| a0001c0001t0005 | 0/0 | 7036 | 8 | 8 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7031): Show |
chr4 | 158764026 | 158913050 |
| a0001c0001t0006 | 1/0 | 7038 | 1 | 0 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7033): Show |
chr4 | 158764026 | 158913050 |
| a0001c0001t0007 | 0/0 | 7041 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7036): Show |
chr4 | 158764026 | 158913050 |
| a0001c0001t0008 | 0/0 | 7038 | 3 | 1 | 1 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7033): Show |
chr4 | 158764026 | 158913050 |
| a0001c0001t0009 | 0/0 | 7038 | 3 | 1 | 0 | 2 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7033): Show |
chr4 | 158764026 | 158913050 |
| a0001c0001t0011 | 0/0 | 7037 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7032): Show |
chr4 | 158764026 | 158913050 |
| a0001c0001t0012 | 0/0 | 7037 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7032): Show |
chr4 | 158764026 | 158913050 |
| a0001c0001t0014 | 0/0 | 7037 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7032): Show |
chr4 | 158764026 | 158913050 |
| a0001c0001t0015 | 0/0 | 7037 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7032): Show |
chr4 | 158764026 | 158913050 |
| a0001c0001t0018 | 0/0 | 7037 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7032): Show |
chr4 | 158764026 | 158913050 |
| a0001c0001t0019 | 0/0 | 7037 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7032): Show |
chr4 | 158764026 | 158913050 |
| a0001c0003t0004 | 0/0 | 7037 | 13 | 9 | 0 | 3 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7032): Show |
chr4 | 158764026 | 158913050 |
| a0001c0003t0013 | 0/0 | 7037 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7032): Show |
chr4 | 158764026 | 158913050 |
| a0001c0003t0017 | 0/0 | 7038 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7033): Show |
chr4 | 158764026 | 158913050 |
| a0001c0005t0002 | 0/0 | 7037 | 5 | 0 | 0 | 0 | 0 | 5 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7032): Show |
chr4 | 158764026 | 158913050 |
| a0001c0007t0006 | 0/0 | 7038 | 4 | 4 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7033): Show |
chr4 | 158764026 | 158913050 |
| a0001c0008t0010 | 0/0 | 7037 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7032): Show |
chr4 | 158764026 | 158913050 |
| a0001c0009t0002 | 0/0 | 7037 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7032): Show |
chr4 | 158764026 | 158913050 |
| a0001c0014t0020 | 0/0 | 7038 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7033): Show |
chr4 | 158764026 | 158913050 |
| a0002c0002t0003 | 0/0 | 7037 | 31 | 4 | 3 | 19 | 1 | 4 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7032): Show |
chr4 | 158764026 | 158913050 |
| a0002c0002t0004 | 0/0 | 7037 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7032): Show |
chr4 | 158764026 | 158913050 |
| a0002c0002t0007 | 0/0 | 7041 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7036): Show |
chr4 | 158764026 | 158913050 |
| a0002c0002t0016 | 0/0 | 7038 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7033): Show |
chr4 | 158764026 | 158913050 |
| a0002c0017t0003 | 0/0 | 7037 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7032): Show |
chr4 | 158764026 | 158913050 |
| a0003c0004t0001 | 0/0 | 7037 | 10 | 10 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7032): Show |
chr4 | 158764026 | 158913050 |
| a0004c0006t0002 | 0/0 | 7037 | 5 | 0 | 4 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7032): Show |
chr4 | 158764026 | 158913050 |
| a0005c0011t0005 | 0/0 | 7036 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7031): Show |
chr4 | 158764026 | 158913050 |
| a0006c0015t0004 | 0/0 | 7037 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7032): Show |
chr4 | 158764026 | 158913050 |
| a0007c0016t0002 | 0/0 | 7037 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7032): Show |
chr4 | 158764026 | 158913050 |
| a0008c0018t0003 | 0/0 | 7037 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7032): Show |
chr4 | 158764026 | 158913050 |
| a0009c0010t0001 | 0/0 | 7037 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7032): Show |
chr4 | 158764026 | 158913050 |
| a0010c0013t0008 | 0/0 | 7038 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7033): Show |
chr4 | 158764026 | 158913050 |
| a0011c0012t0002 | 0/0 | 7037 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | AGTCA others(7032): Show |
chr4 | 158764026 | 158913050 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0153 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0005g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0006g0005 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0007g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0007g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0008g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0008g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0008g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0009g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0009g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0009g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0011g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0011g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0012g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0012g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0014g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0015g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0018g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0019g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0004g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0013g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0013g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0017g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0005t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0005t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0005t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0005t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0005t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0007t0006g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0007t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0007t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0007t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0008t0010g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0008t0010g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0009t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0009t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0014t0020g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0007g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0007g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0016g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0017t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0003c0004t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0003c0004t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0003c0004t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0003c0004t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0003c0004t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0003c0004t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0003c0004t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0003c0004t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0003c0004t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0003c0004t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0004c0006t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0004c0006t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0004c0006t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0004c0006t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0004c0006t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0005c0011t0005g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0006c0015t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0007c0016t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0008c0018t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0009c0010t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0010c0013t0008g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0011c0012t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0002 | c0002 | t0003 | g0198 | EUR | FIN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0207 | EUR | FIN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00423 | hp2 | a0002 | c0002 | t0003 | g0179 | EAS | CHS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00438 | hp2 | a0002 | c0002 | t0003 | g0174 | EAS | CHS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00558 | hp1 | a0002 | c0002 | t0003 | g0173 | EAS | CHS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00597 | hp2 | a0001 | c0001 | t0009 | g0244 | EAS | CHS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00609 | hp2 | a0001 | c0003 | t0004 | g0134 | EAS | CHS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0219 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00738 | hp1 | a0002 | c0002 | t0003 | g0166 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01169 | hp2 | a0002 | c0002 | t0003 | g0201 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | CLM | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01257 | hp2 | a0004 | c0006 | t0002 | g0246 | AMR | CLM | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01258 | hp1 | a0004 | c0006 | t0002 | g0247 | AMR | CLM | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01258 | hp2 | a0001 | c0001 | t0018 | g0102 | AMR | CLM | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01261 | hp1 | a0004 | c0006 | t0002 | g0212 | AMR | CLM | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | CLM | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | CLM | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | IBS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | IBS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01884 | hp2 | a0001 | c0009 | t0002 | g0234 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0239 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01891 | hp2 | a0001 | c0001 | t0012 | g0125 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01934 | hp2 | a0001 | c0001 | t0019 | g0088 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01943 | hp2 | a0002 | c0002 | t0003 | g0189 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01975 | hp2 | a0004 | c0006 | t0002 | g0222 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01978 | hp2 | a0001 | c0001 | t0008 | g0098 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01981 | hp2 | a0005 | c0011 | t0005 | g0003 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02055 | hp1 | a0001 | c0003 | t0004 | g0029 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02055 | hp2 | a0001 | c0007 | t0006 | g0163 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02080 | hp2 | a0002 | c0002 | t0016 | g0177 | EAS | KHV | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | KHV | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02129 | hp2 | a0002 | c0002 | t0003 | g0182 | EAS | KHV | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02135 | hp1 | a0001 | c0003 | t0004 | g0104 | EAS | KHV | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02145 | hp1 | a0001 | c0001 | t0012 | g0124 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02145 | hp2 | a0001 | c0007 | t0006 | g0165 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0159 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02258 | hp2 | a0002 | c0017 | t0003 | g0030 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02280 | hp2 | a0002 | c0002 | t0004 | g0037 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | KHV | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02572 | hp1 | a0001 | c0003 | t0017 | g0017 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02572 | hp2 | a0003 | c0004 | t0001 | g0054 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0202 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02615 | hp1 | a0002 | c0002 | t0003 | g0172 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02615 | hp2 | a0006 | c0015 | t0004 | g0013 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02622 | hp1 | a0003 | c0004 | t0001 | g0056 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02630 | hp2 | a0001 | c0003 | t0004 | g0027 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02647 | hp1 | a0001 | c0001 | t0011 | g0068 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02647 | hp2 | a0001 | c0001 | t0007 | g0031 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02683 | hp1 | a0001 | c0003 | t0004 | g0024 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02717 | hp1 | a0003 | c0004 | t0001 | g0055 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02717 | hp2 | a0001 | c0003 | t0004 | g0023 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02735 | hp1 | a0002 | c0002 | t0003 | g0185 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02735 | hp2 | a0001 | c0005 | t0002 | g0213 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02809 | hp1 | a0001 | c0003 | t0004 | g0020 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02818 | hp2 | a0001 | c0009 | t0002 | g0235 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02886 | hp1 | a0001 | c0007 | t0006 | g0012 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02886 | hp2 | a0002 | c0002 | t0003 | g0167 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02895 | hp1 | a0003 | c0004 | t0001 | g0117 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02896 | hp1 | a0001 | c0008 | t0010 | g0034 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02896 | hp2 | a0001 | c0003 | t0004 | g0019 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02897 | hp1 | a0001 | c0008 | t0010 | g0033 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | ESN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02922 | hp2 | a0003 | c0004 | t0001 | g0149 | AFR | ESN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | ESN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02965 | hp2 | a0001 | c0003 | t0013 | g0028 | AFR | ESN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ESN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0143 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | ESN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03139 | hp1 | a0002 | c0002 | t0003 | g0171 | AFR | ESN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03195 | hp1 | a0002 | c0002 | t0007 | g0170 | AFR | ESN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03195 | hp2 | a0001 | c0003 | t0013 | g0026 | AFR | ESN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0136 | AFR | MSL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | MSL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03239 | hp2 | a0002 | c0002 | t0003 | g0181 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03453 | hp1 | a0001 | c0003 | t0004 | g0022 | AFR | MSL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03453 | hp2 | a0003 | c0004 | t0001 | g0146 | AFR | MSL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | MSL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03491 | hp1 | a0001 | c0005 | t0002 | g0209 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03492 | hp1 | a0001 | c0005 | t0002 | g0214 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03516 | hp1 | a0003 | c0004 | t0001 | g0148 | AFR | ESN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03516 | hp2 | a0007 | c0016 | t0002 | g0236 | AFR | ESN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03579 | hp1 | a0001 | c0001 | t0011 | g0107 | AFR | MSL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03579 | hp2 | a0001 | c0003 | t0004 | g0021 | AFR | MSL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03669 | hp2 | a0001 | c0005 | t0002 | g0228 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03710 | hp2 | a0008 | c0018 | t0003 | g0183 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0210 | SAS | BEB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03942 | hp1 | a0009 | c0010 | t0001 | g0106 | SAS | BEB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03942 | hp2 | a0001 | c0005 | t0002 | g0223 | SAS | BEB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | STU | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | STU | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | STU | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG04199 | hp2 | a0002 | c0002 | t0003 | g0186 | SAS | STU | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | STU | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0227 | SAS | STU | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | STU | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | STU | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18522 | hp1 | a0010 | c0013 | t0008 | g0150 | AFR | YRI | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18522 | hp2 | a0001 | c0003 | t0004 | g0018 | AFR | YRI | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18906 | hp1 | a0003 | c0004 | t0001 | g0057 | AFR | YRI | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18906 | hp2 | a0002 | c0002 | t0003 | g0025 | AFR | YRI | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18951 | hp2 | a0002 | c0002 | t0003 | g0194 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18966 | hp1 | a0002 | c0002 | t0003 | g0191 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18966 | hp2 | a0001 | c0001 | t0014 | g0141 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18967 | hp1 | a0002 | c0002 | t0003 | g0196 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18982 | hp1 | a0002 | c0002 | t0003 | g0175 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18989 | hp1 | a0002 | c0002 | t0003 | g0199 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18998 | hp1 | a0002 | c0002 | t0003 | g0192 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19004 | hp2 | a0002 | c0002 | t0003 | g0187 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19009 | hp1 | a0001 | c0003 | t0004 | g0103 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19009 | hp2 | a0002 | c0002 | t0003 | g0190 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19011 | hp1 | a0002 | c0002 | t0003 | g0193 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19030 | hp1 | a0001 | c0014 | t0020 | g0035 | AFR | LWK | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19030 | hp2 | a0001 | c0001 | t0008 | g0048 | AFR | LWK | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19057 | hp2 | a0002 | c0002 | t0003 | g0188 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19060 | hp1 | a0001 | c0001 | t0015 | g0074 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19060 | hp2 | a0002 | c0002 | t0003 | g0178 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19067 | hp1 | a0001 | c0001 | t0009 | g0231 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19068 | hp2 | a0002 | c0002 | t0003 | g0180 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19070 | hp1 | a0002 | c0002 | t0003 | g0168 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19087 | hp1 | a0001 | c0001 | t0008 | g0069 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19087 | hp2 | a0002 | c0002 | t0003 | g0195 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19089 | hp1 | a0002 | c0002 | t0003 | g0082 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ASW | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0032 | AFR | ASW | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | TSI | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA20752 | hp2 | a0011 | c0012 | t0002 | g0208 | EUR | TSI | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | TSI | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA20805 | hp2 | a0004 | c0006 | t0002 | g0248 | EUR | TSI | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA20905 | hp1 | a0002 | c0002 | t0003 | g0197 | SAS | GIH | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0218 | SAS | GIH | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02109 | hp2 | a0003 | c0004 | t0001 | g0058 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02486 | hp1 | a0001 | c0003 | t0004 | g0016 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02486 | hp2 | a0001 | c0007 | t0006 | g0164 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02559 | hp1 | a0002 | c0002 | t0007 | g0169 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0225 | AFR | MSL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | USA | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | USA | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA21309 | hp1 | a0003 | c0004 | t0001 | g0147 | AFR | LWK | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA21309 | hp2 | a0002 | c0002 | t0004 | g0038 | AFR | LWK | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0153 | REF | REF | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0006 | g0005 | REF | REF | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:158859092 | C | G | 2 | a0002 a0008 |
38 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(35): Show |
missense_variant | MODERATE | c.893C>G | p.Thr298Ser | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 9/17 | 1080/7038 | 893/3345 | 298/1114 | chr4 | 158859092 | |||
| chr4:158859100 | T | C | 1 | a0009 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.901T>C | p.Ser301Pro | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 9/17 | 1088/7038 | 901/3345 | 301/1114 | chr4 | 158859100 | |||
| chr4:158861737 | G | T | 1 | a0004 | 5 | HG01257.hp2 HG01258.hp1 HG01261.hp1 others(2): Show |
missense_variant | MODERATE | c.1426G>T | p.Ala476Ser | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/17 | 1613/7038 | 1426/3345 | 476/1114 | chr4 | 158861737 | |||
| chr4:158868261 | G | C | 1 | a0005 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1625G>C | p.Gly542Ala | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 13/17 | 1812/7038 | 1625/3345 | 542/1114 | chr4 | 158868261 | |||
| chr4:158868666 | T | C | 1 | a0003 | 10 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(7): Show |
missense_variant | MODERATE | c.2030T>C | p.Met677Thr | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 13/17 | 2217/7038 | 2030/3345 | 677/1114 | chr4 | 158868666 | |||
| chr4:158868858 | G | A | 1 | a0011 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.2222G>A | p.Arg741Gln | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 13/17 | 2409/7038 | 2222/3345 | 741/1114 | chr4 | 158868858 | |||
| chr4:158868981 | G | A | 1 | a0007 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.2345G>A | p.Arg782Gln | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 13/17 | 2532/7038 | 2345/3345 | 782/1114 | chr4 | 158868981 | |||
| chr4:158869046 | G | A | 1 | a0010 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.2410G>A | p.Asp804Asn | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 13/17 | 2597/7038 | 2410/3345 | 804/1114 | chr4 | 158869046 | |||
| chr4:158869122 | C | T | 1 | a0006 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.2486C>T | p.Thr829Met | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 13/17 | 2673/7038 | 2486/3345 | 829/1114 | chr4 | 158869122 | |||
| chr4:158891507 | G | T | 1 | a0008 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.3011G>T | p.Trp1004Leu | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/17 | 3198/7038 | 3011/3345 | 1004/1114 | chr4 | 158891507 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:158861342 | A | G | 2 | a0001c0009 a0007c0016 |
3 | HG01884.hp2 HG02818.hp2 HG03516.hp2 |
splice_region_variant&synonymous_variant | LOW | c.1149A>G | p.Arg383Arg | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 11/17 | 1336/7038 | 1149/3345 | 383/1114 | chr4 | 158861342 | |||
| chr4:158868112 | C | T | 1 | a0001c0005 | 5 | HG02735.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
synonymous_variant | LOW | c.1476C>T | p.Tyr492Tyr | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 13/17 | 1663/7038 | 1476/3345 | 492/1114 | chr4 | 158868112 | |||
| chr4:158868403 | G | A | 1 | a0001c0007 | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
synonymous_variant | LOW | c.1767G>A | p.Glu589Glu | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 13/17 | 1954/7038 | 1767/3345 | 589/1114 | chr4 | 158868403 | |||
| chr4:158868859 | G | C | 1 | a0002c0017 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.2223G>C | p.Arg741Arg | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 13/17 | 2410/7038 | 2223/3345 | 741/1114 | chr4 | 158868859 | |||
| chr4:158869321 | C | T | 1 | a0001c0014 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.2685C>T | p.Ser895Ser | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 13/17 | 2872/7038 | 2685/3345 | 895/1114 | chr4 | 158869321 | |||
| chr4:158870367 | G | A | 1 | a0001c0003 | 16 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(13): Show |
synonymous_variant | LOW | c.2847G>A | p.Ala949Ala | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/17 | 3034/7038 | 2847/3345 | 949/1114 | chr4 | 158870367 | |||
| chr4:158904499 | T | C | 1 | a0001c0008 | 2 | HG02896.hp1 HG02897.hp1 |
synonymous_variant | LOW | c.3300T>C | p.Ala1100Ala | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 3487/7038 | 3300/3345 | 1100/1114 | chr4 | 158904499 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:158769188 | C | A | 1 | a0001c0001t0014 | 1 | NA18966.hp2 | 5_prime_UTR_variant | MODIFIER | c.-25C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/17 | 25 | chr4 | 158769188 | ||||||
| chr4:158904633 | G | A | 1 | a0001c0001t0015 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*89G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 89 | chr4 | 158904633 | ||||||
| chr4:158904924 | G | C | 1 | a0001c0008t0010 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*380G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 380 | chr4 | 158904924 | ||||||
| chr4:158904997 | C | T | 1 | a0001c0003t0013 | 2 | HG02965.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*453C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 453 | chr4 | 158904997 | ||||||
| chr4:158905227 | T | C | 7 | a0001c0001t0002 a0001c0001t0009 a0001c0005t0002 others(4): Show |
51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*683T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 683 | chr4 | 158905227 | ||||||
| chr4:158905609 | T | G | 2 | a0001c0001t0007 a0002c0002t0007 |
4 | HG02559.hp1 HG02647.hp2 HG03195.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1065T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 1065 | chr4 | 158905609 | ||||||
| chr4:158905621 | T | G | 33 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(30): Show |
245 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*1077T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 1077 | chr4 | 158905621 | ||||||
| chr4:158905694 | CA | C | 27 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(24): Show |
229 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*1166delA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 1166 | INFO_REALIGN_3_PRIME | chr4 | 158905694 | |||||
| chr4:158905709 | AAC | A | 2 | a0001c0001t0005 a0005c0011t0005 |
9 | HG01884.hp1 HG01981.hp2 HG02257.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1167_*1168delCA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 1167 | INFO_REALIGN_3_PRIME | chr4 | 158905709 | |||||
| chr4:158905715 | C | CTAAT | 2 | a0001c0001t0007 a0002c0002t0007 |
4 | HG02559.hp1 HG02647.hp2 HG03195.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1173_*1176dupAATT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 1177 | INFO_REALIGN_3_PRIME | chr4 | 158905715 | |||||
| chr4:158905756 | C | T | 1 | a0001c0014t0020 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1212C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 1212 | chr4 | 158905756 | ||||||
| chr4:158906007 | A | C | 1 | a0001c0001t0012 | 2 | HG01891.hp2 HG02145.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1463A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 1463 | chr4 | 158906007 | ||||||
| chr4:158906071 | T | G | 35 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(32): Show |
248 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*1527T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 1527 | chr4 | 158906071 | ||||||
| chr4:158906161 | T | C | 7 | a0001c0001t0002 a0001c0001t0009 a0001c0005t0002 others(4): Show |
51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1617T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 1617 | chr4 | 158906161 | ||||||
| chr4:158906501 | C | T | 1 | a0001c0001t0011 | 2 | HG02647.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1957C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 1957 | chr4 | 158906501 | ||||||
| chr4:158906655 | C | T | 1 | a0001c0001t0019 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2111C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 2111 | chr4 | 158906655 | ||||||
| chr4:158906656 | G | A | 5 | a0001c0001t0003 a0002c0002t0003 a0002c0002t0016 others(2): Show |
36 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2112G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 2112 | chr4 | 158906656 | ||||||
| chr4:158907176 | T | C | 10 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0011 others(7): Show |
123 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*2632T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 2632 | chr4 | 158907176 | ||||||
| chr4:158907537 | C | G | 1 | a0001c0001t0018 | 1 | HG01258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2993C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 2993 | chr4 | 158907537 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:158769382 | G | T | 4 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(1): Show |
4 | HG02083.hp1 NA18955.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+63G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158769382 | |||||||
| chr4:158769470 | C | T | 50 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(47): Show |
51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.107+151C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158769470 | |||||||
| chr4:158769488 | C | A | 50 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(47): Show |
51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.107+169C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158769488 | |||||||
| chr4:158769491 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.107+172C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158769491 | |||||||
| chr4:158769554 | A | T | 1 | a0001c0001t0002g0249 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.107+235A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158769554 | |||||||
| chr4:158769820 | A | G | 34 | a0001c0001t0001g0176 a0001c0001t0003g0184 a0002c0002t0003g0166 others(31): Show |
34 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.107+501A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158769820 | |||||||
| chr4:158769920 | G | T | 3 | a0001c0007t0006g0163 a0001c0007t0006g0164 a0001c0007t0006g0165 |
3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.107+601G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158769920 | |||||||
| chr4:158769921 | A | T | 3 | a0001c0007t0006g0163 a0001c0007t0006g0164 a0001c0007t0006g0165 |
3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.107+602A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158769921 | |||||||
| chr4:158769960 | G | A | 1 | a0001c0001t0001g0002 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.107+641G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158769960 | |||||||
| chr4:158770181 | A | AC | 129 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(126): Show |
129 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.107+864dupC | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158770181 | ||||||
| chr4:158770261 | ATATTGCC others(15): Show |
A | 1 | a0002c0002t0003g0166 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.107+943_107+964del others(22): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158770261 | |||||||
| chr4:158770304 | A | G | 4 | a0001c0001t0003g0036 a0001c0014t0020g0035 a0002c0002t0004g0037 others(1): Show |
4 | HG02280.hp2 HG03225.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+985A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158770304 | |||||||
| chr4:158770435 | A | G | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+1116A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158770435 | |||||||
| chr4:158770443 | A | G | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+1124A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158770443 | |||||||
| chr4:158770502 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.107+1183G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158770502 | |||||||
| chr4:158770851 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG01517.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.107+1532C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158770851 | |||||||
| chr4:158770986 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.107+1667A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158770986 | |||||||
| chr4:158770991 | A | G | 75 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0001 others(72): Show |
76 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.107+1672A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158770991 | |||||||
| chr4:158771212 | G | A | 1 | a0002c0002t0003g0167 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.107+1893G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158771212 | |||||||
| chr4:158771360 | C | A | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+2041C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158771360 | |||||||
| chr4:158771400 | C | T | 2 | a0001c0001t0007g0031 a0001c0001t0007g0032 |
2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.107+2081C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158771400 | |||||||
| chr4:158771433 | A | G | 2 | a0001c0001t0007g0031 a0001c0001t0007g0032 |
2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.107+2114A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158771433 | |||||||
| chr4:158771558 | A | G | 1 | a0002c0017t0003g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.107+2239A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158771558 | |||||||
| chr4:158772144 | C | A | 128 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(125): Show |
128 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.107+2825C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158772144 | |||||||
| chr4:158772265 | C | G | 1 | a0001c0001t0005g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.107+2946C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158772265 | |||||||
| chr4:158772425 | A | G | 1 | a0001c0001t0005g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.107+3106A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158772425 | |||||||
| chr4:158772824 | A | G | 3 | a0001c0007t0006g0163 a0001c0007t0006g0164 a0001c0007t0006g0165 |
3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.107+3505A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158772824 | |||||||
| chr4:158772879 | A | G | 6 | a0001c0001t0007g0031 a0001c0001t0007g0032 a0001c0007t0006g0163 others(3): Show |
6 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.107+3560A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158772879 | |||||||
| chr4:158773029 | C | T | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+3710C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158773029 | |||||||
| chr4:158773460 | T | C | 1 | a0001c0001t0001g0040 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.107+4141T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158773460 | |||||||
| chr4:158773464 | C | T | 3 | a0004c0006t0002g0246 a0004c0006t0002g0247 a0004c0006t0002g0248 |
3 | HG01257.hp2 HG01258.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.107+4145C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158773464 | |||||||
| chr4:158773640 | C | T | 5 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(2): Show |
5 | HG01255.hp2 HG01433.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.107+4321C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158773640 | |||||||
| chr4:158773717 | C | T | 14 | a0001c0003t0004g0016 a0001c0003t0004g0018 a0001c0003t0004g0019 others(11): Show |
14 | HG02055.hp1 HG02486.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.107+4398C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158773717 | |||||||
| chr4:158773833 | C | T | 2 | a0001c0001t0007g0031 a0001c0001t0007g0032 |
2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.107+4514C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158773833 | |||||||
| chr4:158773872 | T | A | 14 | a0001c0003t0004g0016 a0001c0003t0004g0018 a0001c0003t0004g0019 others(11): Show |
14 | HG02055.hp1 HG02486.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.107+4553T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158773872 | |||||||
| chr4:158774055 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | NA18986.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.107+4736G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158774055 | |||||||
| chr4:158774541 | C | T | 1 | a0001c0001t0002g0245 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.107+5222C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158774541 | |||||||
| chr4:158774700 | G | C | 1 | a0002c0002t0003g0168 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.107+5381G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158774700 | |||||||
| chr4:158774952 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.107+5633C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158774952 | |||||||
| chr4:158774972 | A | T | 38 | a0001c0001t0001g0176 a0001c0001t0003g0036 a0001c0001t0003g0184 others(35): Show |
38 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.107+5653A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158774972 | |||||||
| chr4:158775265 | C | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 |
3 | HG00597.hp1 NA18957.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.107+5946C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158775265 | |||||||
| chr4:158775799 | A | G | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+6480A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158775799 | |||||||
| chr4:158775822 | T | C | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+6503T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158775822 | |||||||
| chr4:158776122 | A | G | 124 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(121): Show |
124 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.107+6803A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776122 | |||||||
| chr4:158776184 | A | T | 75 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0001 others(72): Show |
76 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.107+6865A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776184 | |||||||
| chr4:158776270 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.107+6951A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776270 | |||||||
| chr4:158776320 | A | G | 1 | a0010c0013t0008g0150 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.107+7001A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776320 | |||||||
| chr4:158776332 | C | G | 4 | a0003c0004t0001g0146 a0003c0004t0001g0147 a0003c0004t0001g0148 others(1): Show |
4 | HG02922.hp2 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+7013C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776332 | |||||||
| chr4:158776407 | G | T | 75 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0001 others(72): Show |
76 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.107+7088G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776407 | |||||||
| chr4:158776427 | A | C | 8 | a0001c0001t0002g0237 a0001c0001t0002g0238 a0001c0001t0002g0239 others(5): Show |
8 | HG00597.hp2 HG01891.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.107+7108A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776427 | |||||||
| chr4:158776457 | G | A | 7 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0154 others(4): Show |
7 | HG01255.hp2 HG01433.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+7138G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776457 | |||||||
| chr4:158776458 | C | T | 7 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0154 others(4): Show |
7 | HG01255.hp2 HG01433.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+7139C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776458 | |||||||
| chr4:158776547 | A | G | 38 | a0001c0001t0001g0176 a0001c0001t0003g0036 a0001c0001t0003g0184 others(35): Show |
38 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.107+7228A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776547 | |||||||
| chr4:158776594 | T | A | 77 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0001 others(74): Show |
78 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.107+7275T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776594 | |||||||
| chr4:158776662 | GA | G | 5 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0009t0002g0234 others(2): Show |
5 | HG00735.hp2 HG01884.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+7346delA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158776662 | ||||||
| chr4:158776751 | G | T | 29 | a0001c0001t0001g0176 a0001c0001t0003g0184 a0002c0002t0003g0166 others(26): Show |
29 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.107+7432G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776751 | |||||||
| chr4:158776796 | G | A | 72 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(69): Show |
73 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.107+7477G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776796 | |||||||
| chr4:158776810 | A | C | 38 | a0001c0001t0001g0176 a0001c0001t0003g0036 a0001c0001t0003g0184 others(35): Show |
38 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.107+7491A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776810 | |||||||
| chr4:158776874 | T | C | 75 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0001 others(72): Show |
76 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.107+7555T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776874 | |||||||
| chr4:158776934 | A | G | 75 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0001 others(72): Show |
76 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.107+7615A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776934 | |||||||
| chr4:158777117 | A | C | 1 | a0001c0001t0001g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.107+7798A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158777117 | |||||||
| chr4:158777131 | G | A | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.107+7812G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158777131 | |||||||
| chr4:158777455 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.107+8136A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158777455 | |||||||
| chr4:158777560 | C | T | 38 | a0001c0001t0001g0176 a0001c0001t0003g0036 a0001c0001t0003g0184 others(35): Show |
38 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.107+8241C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158777560 | |||||||
| chr4:158777633 | C | T | 75 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0001 others(72): Show |
76 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.107+8314C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158777633 | |||||||
| chr4:158777732 | C | T | 1 | a0001c0001t0009g0143 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.107+8413C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158777732 | |||||||
| chr4:158778123 | C | T | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+8804C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158778123 | |||||||
| chr4:158778368 | C | T | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+9049C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158778368 | |||||||
| chr4:158778524 | G | A | 75 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0001 others(72): Show |
76 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.107+9205G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158778524 | |||||||
| chr4:158778534 | G | C | 1 | a0001c0001t0001g0052 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.107+9215G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158778534 | |||||||
| chr4:158778576 | C | T | 1 | a0001c0001t0009g0231 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.107+9257C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158778576 | |||||||
| chr4:158778598 | GTATAT | G | 11 | a0001c0001t0001g0053 a0001c0001t0001g0151 a0003c0004t0001g0054 others(8): Show |
11 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.107+9284_107+9288d others(7): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158778598 | ||||||
| chr4:158778654 | G | A | 1 | a0002c0002t0003g0167 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.107+9335G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158778654 | |||||||
| chr4:158778819 | A | G | 34 | a0001c0001t0001g0176 a0001c0001t0003g0184 a0002c0002t0003g0166 others(31): Show |
34 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.107+9500A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158778819 | |||||||
| chr4:158778908 | G | A | 75 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0001 others(72): Show |
76 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.107+9589G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158778908 | |||||||
| chr4:158779059 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.107+9740G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158779059 | |||||||
| chr4:158779325 | T | C | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02523.hp1 NA18956.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+10006T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158779325 | |||||||
| chr4:158779343 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0014g0141 |
2 | NA18966.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.107+10024C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158779343 | |||||||
| chr4:158779565 | G | A | 1 | a0001c0001t0003g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.107+10246G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158779565 | |||||||
| chr4:158779571 | G | GT | 6 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(3): Show |
6 | HG01884.hp1 HG02257.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.107+10269dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158779571 | ||||||
| chr4:158779571 | GT | G | 230 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(227): Show |
231 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.107+10269delT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158779571 | ||||||
| chr4:158779681 | C | T | 1 | a0001c0001t0002g0229 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.107+10362C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158779681 | |||||||
| chr4:158779737 | C | CT | 69 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0063 others(66): Show |
70 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.107+10434dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158779737 | ||||||
| chr4:158779737 | C | CTT | 5 | a0001c0001t0002g0227 a0001c0001t0002g0230 a0001c0001t0009g0231 others(2): Show |
5 | HG00597.hp2 HG03669.hp2 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+10433_107+1043 others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158779737 | ||||||
| chr4:158779767 | C | T | 1 | a0005c0011t0005g0003 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.107+10448C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158779767 | |||||||
| chr4:158779778 | T | C | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+10459T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158779778 | |||||||
| chr4:158779795 | G | A | 5 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(2): Show |
5 | HG00423.hp1 HG00609.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.107+10476G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158779795 | |||||||
| chr4:158779808 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0005g0159 |
2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.107+10489C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158779808 | |||||||
| chr4:158780043 | A | T | 1 | a0001c0001t0003g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.107+10724A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158780043 | |||||||
| chr4:158780227 | C | A | 243 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(240): Show |
244 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.107+10908C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158780227 | |||||||
| chr4:158780326 | A | G | 1 | a0001c0007t0006g0012 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.107+11007A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158780326 | |||||||
| chr4:158780543 | A | C | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+11224A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158780543 | |||||||
| chr4:158781034 | C | CA | 13 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0049 others(10): Show |
13 | HG01255.hp2 HG01433.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.107+11731dupA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158781034 | ||||||
| chr4:158781034 | CA | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0053 others(98): Show |
101 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.107+11731delA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158781034 | ||||||
| chr4:158781034 | CAA | C | 73 | a0001c0001t0001g0131 a0001c0001t0002g0001 a0001c0001t0002g0202 others(70): Show |
74 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.107+11730_107+1173 others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158781034 | ||||||
| chr4:158781035 | A | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.107+11716A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158781035 | |||||||
| chr4:158781136 | T | C | 1 | a0001c0001t0011g0068 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.107+11817T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158781136 | |||||||
| chr4:158781154 | A | C | 73 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0001 others(70): Show |
74 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.107+11835A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158781154 | |||||||
| chr4:158781213 | C | T | 1 | a0001c0003t0004g0134 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.107+11894C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158781213 | |||||||
| chr4:158781323 | G | T | 1 | a0001c0007t0006g0012 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.107+12004G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158781323 | |||||||
| chr4:158781380 | G | A | 35 | a0001c0001t0001g0176 a0001c0001t0003g0184 a0002c0002t0003g0166 others(32): Show |
35 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.107+12061G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158781380 | |||||||
| chr4:158781553 | C | T | 39 | a0001c0001t0001g0176 a0001c0001t0003g0036 a0001c0001t0003g0184 others(36): Show |
39 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.107+12234C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158781553 | |||||||
| chr4:158781758 | C | A | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+12439C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158781758 | |||||||
| chr4:158781759 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.107+12440C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158781759 | |||||||
| chr4:158781776 | G | A | 1 | a0002c0002t0003g0167 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.107+12457G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158781776 | |||||||
| chr4:158781890 | G | GT | 12 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(9): Show |
12 | HG01255.hp2 HG01433.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.107+12580dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158781890 | ||||||
| chr4:158781909 | A | T | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+12590A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158781909 | |||||||
| chr4:158781922 | G | A | 1 | a0001c0001t0008g0069 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.107+12603G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158781922 | |||||||
| chr4:158781968 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.107+12649A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158781968 | |||||||
| chr4:158781993 | G | A | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+12674G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158781993 | |||||||
| chr4:158782073 | T | A | 73 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0001 others(70): Show |
74 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.107+12754T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158782073 | |||||||
| chr4:158782376 | A | G | 1 | a0002c0017t0003g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.107+13057A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158782376 | |||||||
| chr4:158782521 | TTG | T | 10 | a0001c0001t0002g0225 a0001c0001t0002g0226 a0001c0001t0002g0237 others(7): Show |
10 | HG00597.hp2 HG01891.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.107+13204_107+1320 others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158782521 | ||||||
| chr4:158782522 | TG | T | 39 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(36): Show |
40 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.107+13204delG | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158782522 | |||||||
| chr4:158782535 | T | TCCTCAAA others(306): Show |
2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.107+13233_107+1323 others(317): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158782535 | ||||||
| chr4:158782752 | C | T | 15 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0132 others(12): Show |
15 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.107+13433C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158782752 | |||||||
| chr4:158783175 | A | C | 5 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
5 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.107+13856A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158783175 | |||||||
| chr4:158783506 | G | C | 49 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(46): Show |
50 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.107+14187G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158783506 | |||||||
| chr4:158783720 | G | T | 1 | a0002c0002t0003g0198 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.107+14401G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158783720 | |||||||
| chr4:158783751 | A | T | 1 | a0002c0017t0003g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.107+14432A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158783751 | |||||||
| chr4:158783904 | G | A | 113 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(110): Show |
113 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.107+14585G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158783904 | |||||||
| chr4:158784076 | A | C | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+14757A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784076 | |||||||
| chr4:158784092 | T | C | 1 | a0003c0004t0001g0054 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.107+14773T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784092 | |||||||
| chr4:158784302 | G | A | 1 | a0001c0001t0002g0237 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.107+14983G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784302 | |||||||
| chr4:158784337 | G | A | 1 | a0001c0001t0007g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.107+15018G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784337 | |||||||
| chr4:158784352 | T | C | 1 | a0001c0001t0009g0143 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.107+15033T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784352 | |||||||
| chr4:158784662 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.107+15343C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784662 | |||||||
| chr4:158784665 | G | A | 6 | a0001c0001t0001g0176 a0002c0002t0003g0173 a0002c0002t0003g0174 others(3): Show |
6 | HG00438.hp2 HG00558.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.107+15346G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784665 | |||||||
| chr4:158784688 | G | A | 70 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(67): Show |
71 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.107+15369G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784688 | |||||||
| chr4:158784707 | A | G | 1 | a0002c0017t0003g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.107+15388A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784707 | |||||||
| chr4:158784714 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0005g0159 |
3 | HG02258.hp1 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.107+15395C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784714 | |||||||
| chr4:158784715 | A | G | 75 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0001 others(72): Show |
76 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.107+15396A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784715 | |||||||
| chr4:158784762 | C | G | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+15443C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784762 | |||||||
| chr4:158784794 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.107+15475A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784794 | |||||||
| chr4:158784821 | G | C | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | NA18955.hp2 NA18963.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.107+15502G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784821 | |||||||
| chr4:158784834 | G | C | 73 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0001 others(70): Show |
74 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.107+15515G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784834 | |||||||
| chr4:158784904 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.107+15585T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784904 | |||||||
| chr4:158784958 | A | C | 1 | a0002c0002t0003g0197 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.107+15639A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784958 | |||||||
| chr4:158784969 | C | G | 49 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(46): Show |
50 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.107+15650C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784969 | |||||||
| chr4:158785087 | C | CT | 18 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(15): Show |
18 | HG01978.hp1 HG02109.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.107+15785dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158785087 | ||||||
| chr4:158785087 | C | CTTTTT | 59 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0001 others(56): Show |
60 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.107+15781_107+1578 others(9): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158785087 | ||||||
| chr4:158785087 | C | CTTTTTT | 9 | a0001c0001t0002g0224 a0001c0001t0002g0243 a0001c0003t0004g0027 others(6): Show |
9 | HG02145.hp2 HG02486.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.107+15780_107+1578 others(10): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158785087 | ||||||
| chr4:158785087 | C | CTTTTTTT others(3): Show |
1 | a0001c0008t0010g0034 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.107+15776_107+1578 others(14): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158785087 | ||||||
| chr4:158785087 | C | CTTTTTTT others(4): Show |
4 | a0001c0001t0003g0036 a0002c0002t0003g0180 a0002c0002t0003g0181 others(1): Show |
4 | HG02129.hp2 HG03225.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.107+15775_107+1578 others(15): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158785087 | ||||||
| chr4:158785087 | C | CTTTTTTT others(5): Show |
29 | a0001c0001t0001g0176 a0001c0001t0003g0184 a0001c0014t0020g0035 others(26): Show |
29 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.107+15774_107+1578 others(16): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158785087 | ||||||
| chr4:158785087 | C | CTTTTTTT others(6): Show |
5 | a0002c0002t0003g0178 a0002c0002t0003g0196 a0002c0002t0004g0037 others(2): Show |
5 | HG02080.hp2 HG02280.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.107+15773_107+1578 others(17): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158785087 | ||||||
| chr4:158785155 | A | G | 75 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0001 others(72): Show |
76 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.107+15836A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158785155 | |||||||
| chr4:158785303 | C | T | 1 | a0001c0007t0006g0012 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.107+15984C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158785303 | |||||||
| chr4:158785374 | G | A | 70 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0053 others(67): Show |
70 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.107+16055G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158785374 | |||||||
| chr4:158785382 | C | T | 1 | a0001c0007t0006g0012 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.107+16063C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158785382 | |||||||
| chr4:158785479 | T | C | 1 | a0001c0001t0005g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.107+16160T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158785479 | |||||||
| chr4:158785516 | A | G | 3 | a0001c0001t0004g0136 a0001c0001t0012g0124 a0001c0001t0012g0125 |
3 | HG01891.hp2 HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.107+16197A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158785516 | |||||||
| chr4:158785621 | G | A | 1 | a0005c0011t0005g0003 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.107+16302G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158785621 | |||||||
| chr4:158785710 | C | CT | 68 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0001 others(65): Show |
69 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.107+16403dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158785710 | ||||||
| chr4:158785710 | C | CTT | 5 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0009t0002g0234 others(2): Show |
5 | HG00735.hp2 HG01884.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+16402_107+1640 others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158785710 | ||||||
| chr4:158785714 | T | C | 15 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0132 others(12): Show |
15 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.107+16395T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158785714 | |||||||
| chr4:158785843 | A | G | 1 | a0009c0010t0001g0106 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.107+16524A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158785843 | |||||||
| chr4:158786006 | C | T | 3 | a0001c0014t0020g0035 a0002c0002t0004g0037 a0002c0002t0004g0038 |
3 | HG02280.hp2 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.107+16687C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158786006 | |||||||
| chr4:158786450 | T | C | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.107+17131T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158786450 | |||||||
| chr4:158786542 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.107+17223G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158786542 | |||||||
| chr4:158786545 | T | G | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG00621.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.107+17226T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158786545 | |||||||
| chr4:158786668 | T | A | 1 | a0001c0001t0011g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.107+17349T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158786668 | |||||||
| chr4:158786669 | A | T | 1 | a0001c0001t0001g0039 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.107+17350A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158786669 | |||||||
| chr4:158786688 | G | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(124): Show |
127 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.107+17369G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158786688 | |||||||
| chr4:158786823 | C | T | 3 | a0001c0007t0006g0163 a0001c0007t0006g0164 a0001c0007t0006g0165 |
3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.107+17504C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158786823 | |||||||
| chr4:158786886 | C | G | 1 | a0001c0001t0001g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.107+17567C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158786886 | |||||||
| chr4:158787008 | C | T | 75 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0119 others(72): Show |
76 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.107+17689C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158787008 | |||||||
| chr4:158787024 | G | C | 76 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(73): Show |
77 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.107+17705G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158787024 | |||||||
| chr4:158787081 | G | A | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+17762G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158787081 | |||||||
| chr4:158787132 | C | A | 15 | a0001c0001t0001g0119 a0001c0003t0004g0016 a0001c0003t0004g0018 others(12): Show |
15 | HG02055.hp1 HG02109.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.107+17813C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158787132 | |||||||
| chr4:158787226 | G | A | 14 | a0001c0003t0004g0016 a0001c0003t0004g0018 a0001c0003t0004g0019 others(11): Show |
14 | HG02055.hp1 HG02486.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.107+17907G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158787226 | |||||||
| chr4:158787379 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.107+18060G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158787379 | |||||||
| chr4:158787539 | C | T | 4 | a0001c0001t0001g0105 a0001c0003t0004g0103 a0001c0003t0004g0104 others(1): Show |
4 | HG00609.hp2 HG02135.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+18220C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158787539 | |||||||
| chr4:158787826 | C | T | 1 | a0001c0001t0018g0102 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.107+18507C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158787826 | |||||||
| chr4:158787849 | C | G | 2 | a0001c0001t0011g0068 a0001c0001t0011g0107 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.107+18530C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158787849 | |||||||
| chr4:158787852 | A | G | 3 | a0001c0007t0006g0163 a0001c0007t0006g0164 a0001c0007t0006g0165 |
3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.107+18533A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158787852 | |||||||
| chr4:158788348 | A | G | 6 | a0001c0007t0006g0163 a0001c0007t0006g0164 a0001c0007t0006g0165 others(3): Show |
6 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.107+19029A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158788348 | |||||||
| chr4:158788383 | T | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(194): Show |
198 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.107+19064T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158788383 | |||||||
| chr4:158788517 | T | C | 1 | a0001c0003t0004g0018 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.107+19198T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158788517 | |||||||
| chr4:158788779 | C | T | 5 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
5 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.107+19460C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158788779 | |||||||
| chr4:158788881 | C | T | 3 | a0001c0009t0002g0234 a0001c0009t0002g0235 a0007c0016t0002g0236 |
3 | HG01884.hp2 HG02818.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.107+19562C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158788881 | |||||||
| chr4:158788938 | A | G | 2 | a0001c0001t0001g0142 a0001c0001t0014g0141 |
2 | NA18966.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.107+19619A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158788938 | |||||||
| chr4:158789019 | C | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(195): Show |
199 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.107+19700C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158789019 | |||||||
| chr4:158789092 | G | T | 2 | a0001c0001t0007g0031 a0001c0001t0007g0032 |
2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.107+19773G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158789092 | |||||||
| chr4:158789180 | G | T | 197 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(194): Show |
198 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.107+19861G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158789180 | |||||||
| chr4:158789239 | C | T | 1 | a0001c0007t0006g0012 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.107+19920C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158789239 | |||||||
| chr4:158789315 | GTGTGTA | G | 66 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(63): Show |
67 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.107+20002_107+2000 others(10): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158789315 | ||||||
| chr4:158789321 | A | G | 130 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(127): Show |
130 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.107+20002A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158789321 | |||||||
| chr4:158789325 | G | A | 184 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(181): Show |
185 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.107+20006G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158789325 | |||||||
| chr4:158789325 | G | GTA | 11 | a0001c0001t0001g0041 a0001c0001t0001g0097 a0001c0001t0001g0099 others(8): Show |
11 | HG00735.hp1 HG01081.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.107+20007_107+2000 others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158789325 | ||||||
| chr4:158789644 | C | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.107+20325C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158789644 | |||||||
| chr4:158789677 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.107+20358C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158789677 | |||||||
| chr4:158789739 | C | T | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.107+20420C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158789739 | |||||||
| chr4:158789826 | G | GCCTATTA others(3): Show |
197 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(194): Show |
198 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.107+20510_107+2051 others(14): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158789826 | ||||||
| chr4:158790057 | A | G | 3 | a0002c0002t0003g0193 a0002c0002t0003g0194 a0002c0002t0003g0195 |
3 | NA18951.hp2 NA19011.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.107+20738A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158790057 | |||||||
| chr4:158790242 | C | T | 1 | a0001c0001t0007g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.107+20923C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158790242 | |||||||
| chr4:158790294 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.107+20975G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158790294 | |||||||
| chr4:158790738 | C | A | 36 | a0001c0001t0001g0176 a0001c0001t0003g0184 a0002c0002t0003g0166 others(33): Show |
36 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.107+21419C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158790738 | |||||||
| chr4:158790789 | G | A | 242 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(239): Show |
243 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(240): Show |
intron_variant | MODIFIER | c.107+21470G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158790789 | |||||||
| chr4:158791072 | G | A | 2 | a0002c0002t0004g0037 a0002c0002t0004g0038 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.107+21753G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158791072 | |||||||
| chr4:158791118 | GA | G | 44 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0001 others(41): Show |
45 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.107+21800delA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158791118 | |||||||
| chr4:158791266 | CT | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0041 others(103): Show |
106 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.107+21976delT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158791266 | ||||||
| chr4:158791266 | CTT | C | 9 | a0001c0001t0001g0127 a0001c0001t0001g0151 a0001c0001t0001g0154 others(6): Show |
9 | HG01192.hp2 HG01255.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.107+21975_107+2197 others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158791266 | ||||||
| chr4:158791266 | CTTT | C | 36 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0176 others(33): Show |
36 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.107+21974_107+2197 others(7): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158791266 | ||||||
| chr4:158791266 | CTTTTTTT others(6): Show |
C | 12 | a0001c0003t0004g0016 a0001c0003t0004g0018 a0001c0003t0004g0020 others(9): Show |
12 | HG02055.hp1 HG02486.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.107+21964_107+2197 others(17): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158791266 | ||||||
| chr4:158791266 | CTTTTTTT others(7): Show |
C | 1 | a0001c0003t0004g0019 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.107+21963_107+2197 others(18): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158791266 | ||||||
| chr4:158791266 | CTTTTTTT others(9): Show |
C | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+21961_107+2197 others(20): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158791266 | ||||||
| chr4:158791266 | CTTTTTTT others(11): Show |
C | 54 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(51): Show |
55 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.107+21959_107+2197 others(22): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158791266 | ||||||
| chr4:158791282 | TTTTTTTT others(7): Show |
T | 1 | a0006c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.107+21969_107+2198 others(18): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158791282 | ||||||
| chr4:158791283 | TTTTTTTT others(6): Show |
T | 2 | a0001c0001t0007g0031 a0001c0001t0007g0032 |
2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.107+21970_107+2198 others(17): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158791283 | ||||||
| chr4:158791340 | A | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.107+22021A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158791340 | |||||||
| chr4:158791441 | G | C | 1 | a0008c0018t0003g0183 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.107+22122G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158791441 | |||||||
| chr4:158791573 | C | T | 1 | a0001c0003t0004g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.107+22254C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158791573 | |||||||
| chr4:158791888 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.107+22569G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158791888 | |||||||
| chr4:158791905 | C | T | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.107+22586C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158791905 | |||||||
| chr4:158792053 | G | A | 1 | a0001c0007t0006g0012 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.107+22734G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158792053 | |||||||
| chr4:158792122 | C | T | 1 | a0001c0001t0002g0242 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.107+22803C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158792122 | |||||||
| chr4:158792203 | A | G | 1 | a0004c0006t0002g0222 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.107+22884A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158792203 | |||||||
| chr4:158792216 | C | T | 2 | a0002c0002t0003g0181 a0002c0002t0003g0182 |
2 | HG02129.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.107+22897C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158792216 | |||||||
| chr4:158792288 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.107+22969C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158792288 | |||||||
| chr4:158792359 | A | C | 4 | a0001c0001t0001g0151 a0003c0004t0001g0055 a0003c0004t0001g0056 others(1): Show |
4 | HG02109.hp2 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+23040A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158792359 | |||||||
| chr4:158792372 | C | CT | 6 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0002g0224 others(3): Show |
6 | HG00735.hp2 HG01975.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.107+23069dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158792372 | ||||||
| chr4:158792482 | A | G | 1 | a0001c0007t0006g0012 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.107+23163A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158792482 | |||||||
| chr4:158792496 | T | C | 1 | a0003c0004t0001g0055 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.107+23177T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158792496 | |||||||
| chr4:158793272 | G | A | 7 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(4): Show |
7 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.107+23953G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158793272 | |||||||
| chr4:158794328 | A | AT | 67 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0053 others(64): Show |
67 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.107+25017dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158794328 | ||||||
| chr4:158794329 | T | A | 50 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(47): Show |
51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.107+25010T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158794329 | |||||||
| chr4:158794414 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.107+25095G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158794414 | |||||||
| chr4:158794428 | C | T | 1 | a0001c0001t0011g0068 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.107+25109C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158794428 | |||||||
| chr4:158794457 | C | T | 2 | a0002c0002t0004g0037 a0002c0002t0004g0038 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.107+25138C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158794457 | |||||||
| chr4:158794505 | A | G | 3 | a0001c0001t0004g0136 a0001c0001t0012g0124 a0001c0001t0012g0125 |
3 | HG01891.hp2 HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.107+25186A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158794505 | |||||||
| chr4:158794526 | G | T | 106 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(103): Show |
106 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.107+25207G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158794526 | |||||||
| chr4:158795011 | A | G | 1 | a0001c0001t0011g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.107+25692A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158795011 | |||||||
| chr4:158795189 | C | T | 3 | a0001c0007t0006g0163 a0001c0007t0006g0164 a0001c0007t0006g0165 |
3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.107+25870C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158795189 | |||||||
| chr4:158795349 | G | A | 2 | a0001c0001t0007g0031 a0001c0001t0007g0032 |
2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.107+26030G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158795349 | |||||||
| chr4:158796253 | G | A | 1 | a0001c0001t0009g0143 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.107+26934G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158796253 | |||||||
| chr4:158796406 | CTTA | C | 50 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(47): Show |
51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.107+27090_107+2709 others(7): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158796406 | ||||||
| chr4:158796460 | T | G | 6 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0075 others(3): Show |
6 | HG00621.hp2 NA18951.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.107+27141T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158796460 | |||||||
| chr4:158797007 | T | A | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 |
3 | HG01167.hp1 HG01169.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.107+27688T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158797007 | |||||||
| chr4:158797303 | C | T | 1 | a0001c0001t0007g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.107+27984C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158797303 | |||||||
| chr4:158797362 | T | C | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+28043T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158797362 | |||||||
| chr4:158797499 | A | C | 3 | a0001c0008t0010g0033 a0001c0008t0010g0034 a0001c0014t0020g0035 |
3 | HG02896.hp1 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.107+28180A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158797499 | |||||||
| chr4:158797527 | C | T | 1 | a0002c0002t0003g0167 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.107+28208C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158797527 | |||||||
| chr4:158798010 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.108-27906T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158798010 | |||||||
| chr4:158798140 | C | G | 37 | a0001c0001t0001g0176 a0001c0001t0003g0036 a0001c0001t0003g0184 others(34): Show |
37 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.108-27776C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158798140 | |||||||
| chr4:158798165 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.108-27751A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158798165 | |||||||
| chr4:158798387 | A | C | 1 | a0001c0001t0002g0203 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.108-27529A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158798387 | |||||||
| chr4:158798792 | T | TAACACA | 6 | a0001c0001t0001g0176 a0002c0002t0003g0173 a0002c0002t0003g0174 others(3): Show |
6 | HG00438.hp2 HG00558.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.108-27123_108-2711 others(10): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158798792 | ||||||
| chr4:158798803 | A | G | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0009c0010t0001g0106 |
3 | HG01517.hp2 HG02559.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.108-27113A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158798803 | |||||||
| chr4:158799745 | CT | C | 6 | a0001c0003t0004g0016 a0001c0003t0004g0027 a0001c0003t0013g0026 others(3): Show |
6 | HG02486.hp1 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.108-26169delT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158799745 | ||||||
| chr4:158799976 | C | T | 1 | a0002c0002t0003g0171 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.108-25940C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158799976 | |||||||
| chr4:158800141 | T | G | 1 | a0006c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.108-25775T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158800141 | |||||||
| chr4:158800192 | C | G | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.108-25724C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158800192 | |||||||
| chr4:158800302 | A | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.108-25614A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158800302 | |||||||
| chr4:158800364 | T | C | 3 | a0001c0001t0004g0136 a0001c0001t0012g0124 a0001c0001t0012g0125 |
3 | HG01891.hp2 HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.108-25552T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158800364 | |||||||
| chr4:158800615 | T | C | 49 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(46): Show |
50 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.108-25301T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158800615 | |||||||
| chr4:158800723 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.108-25193T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158800723 | |||||||
| chr4:158800733 | T | A | 1 | a0001c0001t0001g0128 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.108-25183T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158800733 | |||||||
| chr4:158800824 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.108-25092A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158800824 | |||||||
| chr4:158800996 | A | G | 1 | a0006c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.108-24920A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158800996 | |||||||
| chr4:158801425 | A | C | 1 | a0001c0001t0001g0089 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.108-24491A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158801425 | |||||||
| chr4:158801565 | C | T | 2 | a0002c0002t0004g0037 a0002c0002t0004g0038 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.108-24351C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158801565 | |||||||
| chr4:158802000 | C | T | 1 | a0001c0001t0003g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.108-23916C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158802000 | |||||||
| chr4:158802009 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.108-23907A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158802009 | |||||||
| chr4:158802094 | G | T | 1 | a0001c0001t0001g0050 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.108-23822G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158802094 | |||||||
| chr4:158802417 | G | A | 1 | a0001c0001t0005g0006 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.108-23499G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158802417 | |||||||
| chr4:158802516 | G | A | 3 | a0003c0004t0001g0146 a0003c0004t0001g0147 a0003c0004t0001g0148 |
3 | HG03453.hp2 HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.108-23400G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158802516 | |||||||
| chr4:158802591 | G | T | 1 | a0002c0002t0003g0198 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.108-23325G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158802591 | |||||||
| chr4:158802905 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.108-23011G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158802905 | |||||||
| chr4:158803032 | G | C | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.108-22884G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158803032 | |||||||
| chr4:158803063 | C | T | 3 | a0001c0001t0007g0031 a0001c0001t0007g0032 a0006c0015t0004g0013 |
3 | HG02615.hp2 HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.108-22853C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158803063 | |||||||
| chr4:158803140 | T | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0093 |
2 | HG02602.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.108-22776T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158803140 | |||||||
| chr4:158803204 | A | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.108-22712A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158803204 | |||||||
| chr4:158803594 | T | A | 1 | a0001c0001t0001g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.108-22322T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158803594 | |||||||
| chr4:158803597 | C | G | 1 | a0001c0001t0002g0226 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.108-22319C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158803597 | |||||||
| chr4:158803629 | A | T | 243 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(240): Show |
244 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.108-22287A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158803629 | |||||||
| chr4:158803782 | A | G | 1 | a0001c0001t0002g0204 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.108-22134A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158803782 | |||||||
| chr4:158803817 | A | C | 1 | a0001c0001t0001g0041 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.108-22099A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158803817 | |||||||
| chr4:158804153 | G | T | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-21763G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158804153 | |||||||
| chr4:158804413 | C | CT | 220 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(217): Show |
221 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.108-21486dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158804413 | ||||||
| chr4:158804413 | C | CTT | 15 | a0001c0001t0001g0046 a0001c0001t0001g0049 a0001c0001t0001g0061 others(12): Show |
15 | HG00597.hp2 HG00735.hp1 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.108-21487_108-2148 others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158804413 | ||||||
| chr4:158804432 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.108-21484G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158804432 | |||||||
| chr4:158804613 | A | T | 17 | a0001c0003t0004g0016 a0001c0003t0004g0018 a0001c0003t0004g0019 others(14): Show |
17 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.108-21303A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158804613 | |||||||
| chr4:158804667 | C | G | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.108-21249C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158804667 | |||||||
| chr4:158804897 | A | T | 1 | a0001c0001t0019g0088 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.108-21019A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158804897 | |||||||
| chr4:158805051 | C | T | 15 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0132 others(12): Show |
15 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.108-20865C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158805051 | |||||||
| chr4:158805123 | A | G | 15 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0132 others(12): Show |
15 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.108-20793A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158805123 | |||||||
| chr4:158805132 | G | A | 50 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(47): Show |
51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.108-20784G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158805132 | |||||||
| chr4:158805147 | A | G | 2 | a0001c0001t0001g0040 a0001c0001t0008g0069 |
2 | NA18612.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.108-20769A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158805147 | |||||||
| chr4:158805193 | T | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(122): Show |
125 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.108-20723T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158805193 | |||||||
| chr4:158805390 | T | C | 1 | a0001c0003t0004g0019 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.108-20526T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158805390 | |||||||
| chr4:158805411 | A | G | 1 | a0005c0011t0005g0003 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.108-20505A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158805411 | |||||||
| chr4:158805446 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.108-20470G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158805446 | |||||||
| chr4:158805800 | C | T | 1 | a0002c0017t0003g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.108-20116C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158805800 | |||||||
| chr4:158805898 | T | G | 3 | a0001c0009t0002g0234 a0001c0009t0002g0235 a0007c0016t0002g0236 |
3 | HG01884.hp2 HG02818.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.108-20018T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158805898 | |||||||
| chr4:158805913 | A | G | 57 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(54): Show |
58 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.108-20003A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158805913 | |||||||
| chr4:158806040 | C | CT | 79 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0043 others(76): Show |
79 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.108-19863dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158806040 | ||||||
| chr4:158806292 | G | A | 1 | a0001c0001t0009g0244 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.108-19624G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158806292 | |||||||
| chr4:158806292 | G | T | 1 | a0001c0007t0006g0012 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.108-19624G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158806292 | |||||||
| chr4:158806525 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.108-19391A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158806525 | |||||||
| chr4:158806944 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.108-18972A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158806944 | |||||||
| chr4:158807147 | C | T | 1 | a0001c0001t0002g0245 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.108-18769C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158807147 | |||||||
| chr4:158807486 | G | A | 3 | a0001c0007t0006g0163 a0001c0007t0006g0164 a0001c0007t0006g0165 |
3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.108-18430G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158807486 | |||||||
| chr4:158807558 | A | G | 1 | a0001c0001t0007g0032 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.108-18358A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158807558 | |||||||
| chr4:158807994 | C | T | 5 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
5 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.108-17922C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158807994 | |||||||
| chr4:158808104 | A | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.108-17812A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158808104 | |||||||
| chr4:158808359 | A | G | 2 | a0001c0001t0001g0086 a0001c0001t0019g0088 |
2 | HG01934.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.108-17557A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158808359 | |||||||
| chr4:158808544 | G | A | 1 | a0001c0001t0002g0206 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.108-17372G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158808544 | |||||||
| chr4:158808642 | C | T | 66 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0043 others(63): Show |
66 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.108-17274C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158808642 | |||||||
| chr4:158808761 | C | T | 1 | a0001c0001t0001g0041 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.108-17155C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158808761 | |||||||
| chr4:158808801 | G | A | 78 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(75): Show |
78 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.108-17115G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158808801 | |||||||
| chr4:158808831 | T | C | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.108-17085T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158808831 | |||||||
| chr4:158808858 | A | C | 50 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(47): Show |
51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.108-17058A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158808858 | |||||||
| chr4:158809191 | G | A | 50 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(47): Show |
51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.108-16725G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158809191 | |||||||
| chr4:158809310 | T | G | 2 | a0002c0002t0007g0169 a0002c0002t0007g0170 |
2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.108-16606T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158809310 | |||||||
| chr4:158809328 | A | G | 2 | a0001c0001t0007g0031 a0001c0001t0007g0032 |
2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.108-16588A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158809328 | |||||||
| chr4:158809385 | G | C | 1 | a0002c0017t0003g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.108-16531G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158809385 | |||||||
| chr4:158809630 | T | G | 7 | a0001c0001t0001g0052 a0001c0001t0001g0109 a0001c0001t0001g0110 others(4): Show |
7 | HG00438.hp1 HG01261.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.108-16286T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158809630 | |||||||
| chr4:158809656 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0014g0141 |
2 | NA18966.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.108-16260C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158809656 | |||||||
| chr4:158810151 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.108-15765C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158810151 | |||||||
| chr4:158810667 | C | T | 3 | a0001c0001t0004g0136 a0001c0001t0012g0124 a0001c0001t0012g0125 |
3 | HG01891.hp2 HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.108-15249C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158810667 | |||||||
| chr4:158810885 | G | A | 5 | a0001c0001t0002g0237 a0001c0007t0006g0012 a0001c0007t0006g0163 others(2): Show |
5 | HG01934.hp1 HG02055.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.108-15031G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158810885 | |||||||
| chr4:158811519 | T | C | 117 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0176 others(114): Show |
118 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.108-14397T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158811519 | |||||||
| chr4:158811541 | T | C | 97 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0176 others(94): Show |
98 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.108-14375T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158811541 | |||||||
| chr4:158811551 | T | A | 242 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(239): Show |
243 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(240): Show |
intron_variant | MODIFIER | c.108-14365T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158811551 | |||||||
| chr4:158811555 | T | TTAATAA | 60 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0001 others(57): Show |
61 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.108-14353_108-1434 others(10): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158811555 | ||||||
| chr4:158811622 | G | A | 60 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0001 others(57): Show |
61 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.108-14294G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158811622 | |||||||
| chr4:158811659 | T | TAC | 54 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(51): Show |
55 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.108-14243_108-1424 others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158811659 | ||||||
| chr4:158811696 | G | T | 6 | a0001c0001t0001g0053 a0001c0001t0001g0127 a0001c0001t0001g0128 others(3): Show |
6 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-14220G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158811696 | |||||||
| chr4:158811736 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0008g0048 |
2 | HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.108-14180C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158811736 | |||||||
| chr4:158811882 | C | T | 1 | a0001c0001t0007g0032 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.108-14034C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158811882 | |||||||
| chr4:158812064 | A | G | 1 | a0002c0002t0003g0182 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.108-13852A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158812064 | |||||||
| chr4:158812089 | C | G | 51 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(48): Show |
52 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.108-13827C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158812089 | |||||||
| chr4:158812346 | C | T | 2 | a0001c0001t0002g0206 a0001c0001t0002g0224 |
2 | HG02083.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.108-13570C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158812346 | |||||||
| chr4:158812347 | G | A | 2 | a0001c0001t0007g0031 a0001c0001t0007g0032 |
2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.108-13569G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158812347 | |||||||
| chr4:158812495 | A | G | 2 | a0001c0001t0012g0124 a0001c0001t0012g0125 |
2 | HG01891.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.108-13421A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158812495 | |||||||
| chr4:158812555 | T | A | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-13361T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158812555 | |||||||
| chr4:158812589 | T | G | 3 | a0001c0001t0002g0202 a0001c0001t0002g0207 a0001c0001t0002g0249 |
3 | HG00280.hp2 HG01496.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.108-13327T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158812589 | |||||||
| chr4:158812898 | C | T | 17 | a0001c0003t0004g0016 a0001c0003t0004g0018 a0001c0003t0004g0019 others(14): Show |
17 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.108-13018C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158812898 | |||||||
| chr4:158812944 | T | C | 1 | a0001c0001t0003g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.108-12972T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158812944 | |||||||
| chr4:158813222 | C | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | NA18986.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.108-12694C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158813222 | |||||||
| chr4:158813534 | A | G | 2 | a0002c0002t0004g0037 a0002c0002t0004g0038 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.108-12382A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158813534 | |||||||
| chr4:158813840 | G | C | 1 | a0001c0003t0004g0016 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.108-12076G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158813840 | |||||||
| chr4:158814346 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.108-11570G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158814346 | |||||||
| chr4:158814348 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.108-11568G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158814348 | |||||||
| chr4:158814429 | C | G | 17 | a0001c0003t0004g0016 a0001c0003t0004g0018 a0001c0003t0004g0019 others(14): Show |
17 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.108-11487C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158814429 | |||||||
| chr4:158814891 | A | G | 1 | a0001c0007t0006g0012 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.108-11025A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158814891 | |||||||
| chr4:158815250 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.108-10666G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158815250 | |||||||
| chr4:158815384 | C | CT | 60 | a0001c0001t0001g0072 a0001c0001t0002g0001 a0001c0001t0002g0202 others(57): Show |
61 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.108-10516dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158815384 | ||||||
| chr4:158815524 | A | G | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.108-10392A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158815524 | |||||||
| chr4:158815655 | C | T | 15 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0132 others(12): Show |
15 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.108-10261C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158815655 | |||||||
| chr4:158815960 | A | G | 54 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(51): Show |
55 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.108-9956A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158815960 | |||||||
| chr4:158816071 | G | GTA | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-9831_108-9830d others(4): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158816071 | ||||||
| chr4:158816075 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.108-9841A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158816075 | |||||||
| chr4:158816145 | G | T | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.108-9771G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158816145 | |||||||
| chr4:158816585 | C | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.108-9331C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158816585 | |||||||
| chr4:158816634 | A | C | 7 | a0001c0001t0001g0044 a0001c0001t0001g0063 a0001c0001t0001g0072 others(4): Show |
7 | HG00597.hp1 HG01192.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.108-9282A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158816634 | |||||||
| chr4:158816756 | G | C | 2 | a0002c0002t0004g0037 a0002c0002t0004g0038 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.108-9160G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158816756 | |||||||
| chr4:158816784 | CA | C | 100 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0097 others(97): Show |
101 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.108-9115delA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158816784 | ||||||
| chr4:158816809 | A | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.108-9107A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158816809 | |||||||
| chr4:158816959 | T | G | 1 | a0008c0018t0003g0183 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.108-8957T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158816959 | |||||||
| chr4:158816969 | T | G | 1 | a0008c0018t0003g0183 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.108-8947T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158816969 | |||||||
| chr4:158817057 | A | G | 1 | a0001c0001t0002g0229 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.108-8859A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158817057 | |||||||
| chr4:158817586 | G | A | 1 | a0001c0003t0004g0020 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.108-8330G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158817586 | |||||||
| chr4:158817662 | T | G | 1 | a0001c0001t0001g0076 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.108-8254T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158817662 | |||||||
| chr4:158817793 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.108-8123C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158817793 | |||||||
| chr4:158817797 | G | A | 1 | a0003c0004t0001g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.108-8119G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158817797 | |||||||
| chr4:158818048 | T | C | 2 | a0001c0001t0007g0031 a0001c0001t0007g0032 |
2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.108-7868T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158818048 | |||||||
| chr4:158818542 | A | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.108-7374A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158818542 | |||||||
| chr4:158818731 | T | A | 1 | a0011c0012t0002g0208 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.108-7185T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158818731 | |||||||
| chr4:158818937 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG01517.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.108-6979G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158818937 | |||||||
| chr4:158819112 | G | A | 1 | a0002c0002t0003g0201 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.108-6804G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158819112 | |||||||
| chr4:158819142 | C | T | 1 | a0002c0002t0007g0170 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.108-6774C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158819142 | |||||||
| chr4:158819287 | G | C | 3 | a0001c0001t0001g0151 a0003c0004t0001g0055 a0003c0004t0001g0056 |
3 | HG02622.hp1 HG02717.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.108-6629G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158819287 | |||||||
| chr4:158819295 | A | G | 10 | a0001c0001t0001g0151 a0003c0004t0001g0054 a0003c0004t0001g0055 others(7): Show |
10 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.108-6621A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158819295 | |||||||
| chr4:158819398 | AATTAAT | A | 50 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(47): Show |
51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.108-6509_108-6504d others(8): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158819398 | ||||||
| chr4:158819455 | T | A | 1 | a0011c0012t0002g0208 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.108-6461T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158819455 | |||||||
| chr4:158819891 | A | G | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.108-6025A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158819891 | |||||||
| chr4:158820253 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.108-5663C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158820253 | |||||||
| chr4:158820280 | T | G | 51 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(48): Show |
52 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.108-5636T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158820280 | |||||||
| chr4:158820292 | G | A | 6 | a0002c0002t0003g0168 a0002c0002t0003g0187 a0002c0002t0003g0188 others(3): Show |
6 | NA18951.hp2 NA19004.hp2 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-5624G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158820292 | |||||||
| chr4:158820391 | G | A | 1 | a0001c0007t0006g0012 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.108-5525G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158820391 | |||||||
| chr4:158820648 | C | T | 35 | a0001c0001t0001g0176 a0001c0001t0003g0184 a0002c0002t0003g0166 others(32): Show |
35 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.108-5268C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158820648 | |||||||
| chr4:158821121 | A | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.108-4795A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158821121 | |||||||
| chr4:158821256 | G | T | 1 | a0001c0001t0014g0141 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.108-4660G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158821256 | |||||||
| chr4:158821274 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.108-4642A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158821274 | |||||||
| chr4:158821994 | A | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0123 |
2 | HG02257.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.108-3922A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158821994 | |||||||
| chr4:158822034 | A | G | 58 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(55): Show |
59 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.108-3882A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158822034 | |||||||
| chr4:158822044 | C | T | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-3872C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158822044 | |||||||
| chr4:158822174 | C | CT | 59 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0052 others(56): Show |
60 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.108-3721dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158822174 | ||||||
| chr4:158822174 | CT | C | 10 | a0001c0001t0001g0060 a0001c0001t0001g0070 a0001c0007t0006g0012 others(7): Show |
10 | HG01943.hp2 HG02055.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.108-3721delT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158822174 | ||||||
| chr4:158822273 | G | A | 1 | a0002c0002t0003g0186 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.108-3643G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158822273 | |||||||
| chr4:158822427 | G | A | 2 | a0003c0004t0001g0054 a0003c0004t0001g0057 |
2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.108-3489G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158822427 | |||||||
| chr4:158822474 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.108-3442C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158822474 | |||||||
| chr4:158822475 | G | A | 6 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(3): Show |
6 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-3441G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158822475 | |||||||
| chr4:158822481 | T | C | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.108-3435T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158822481 | |||||||
| chr4:158823316 | A | G | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-2600A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158823316 | |||||||
| chr4:158823341 | C | T | 1 | a0006c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.108-2575C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158823341 | |||||||
| chr4:158823486 | G | C | 1 | a0002c0002t0004g0038 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.108-2430G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158823486 | |||||||
| chr4:158823612 | G | C | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-2304G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158823612 | |||||||
| chr4:158824017 | C | T | 57 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(54): Show |
58 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.108-1899C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158824017 | |||||||
| chr4:158824724 | G | T | 1 | a0001c0001t0009g0244 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.108-1192G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158824724 | |||||||
| chr4:158824756 | CT | C | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-1157delT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158824756 | ||||||
| chr4:158824764 | C | T | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.108-1152C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158824764 | |||||||
| chr4:158825480 | G | C | 1 | a0001c0001t0002g0227 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.108-436G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158825480 | |||||||
| chr4:158825585 | T | C | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.108-331T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158825585 | |||||||
| chr4:158826101 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.234+59C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158826101 | |||||||
| chr4:158826197 | C | G | 1 | a0001c0001t0003g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.234+155C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158826197 | |||||||
| chr4:158826301 | C | A | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.234+259C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158826301 | |||||||
| chr4:158826462 | C | T | 1 | a0002c0002t0003g0195 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.234+420C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158826462 | |||||||
| chr4:158826616 | AGTG | A | 8 | a0001c0001t0002g0237 a0001c0001t0002g0238 a0001c0001t0002g0239 others(5): Show |
8 | HG00597.hp2 HG01891.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.234+593_234+595del others(3): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr4 | 158826616 | ||||||
| chr4:158826834 | C | T | 2 | a0002c0002t0004g0037 a0002c0002t0004g0038 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.234+792C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158826834 | |||||||
| chr4:158826880 | A | G | 1 | a0002c0002t0003g0181 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.234+838A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158826880 | |||||||
| chr4:158827001 | A | G | 6 | a0002c0002t0003g0168 a0002c0002t0003g0187 a0002c0002t0003g0188 others(3): Show |
6 | NA18951.hp2 NA19004.hp2 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.234+959A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158827001 | |||||||
| chr4:158827064 | C | T | 5 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
5 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.234+1022C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158827064 | |||||||
| chr4:158827303 | T | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.234+1261T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158827303 | |||||||
| chr4:158827458 | T | G | 15 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0132 others(12): Show |
15 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.234+1416T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158827458 | |||||||
| chr4:158827511 | G | A | 1 | a0001c0003t0004g0103 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.234+1469G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158827511 | |||||||
| chr4:158827872 | A | G | 7 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0217 others(4): Show |
7 | HG00639.hp2 HG00738.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.235-1207A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158827872 | |||||||
| chr4:158827899 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.235-1180A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158827899 | |||||||
| chr4:158827968 | A | G | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-1111A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158827968 | |||||||
| chr4:158828014 | T | C | 1 | a0001c0001t0002g0237 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.235-1065T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158828014 | |||||||
| chr4:158828344 | C | T | 1 | a0009c0010t0001g0106 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.235-735C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158828344 | |||||||
| chr4:158828345 | G | A | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.235-734G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158828345 | |||||||
| chr4:158828636 | A | C | 1 | a0001c0001t0001g0053 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.235-443A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158828636 | |||||||
| chr4:158828820 | T | C | 7 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(4): Show |
7 | HG01884.hp1 HG01981.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.235-259T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158828820 | |||||||
| chr4:158828878 | C | T | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.235-201C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158828878 | |||||||
| chr4:158829392 | G | T | 1 | a0001c0001t0002g0237 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.381+167G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158829392 | |||||||
| chr4:158829647 | G | A | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.381+422G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158829647 | |||||||
| chr4:158829711 | G | GGT | 20 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0047 others(17): Show |
20 | HG02055.hp1 HG02486.hp1 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.381+511_381+512dup others(2): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr4 | 158829711 | ||||||
| chr4:158829711 | G | GGTGT | 3 | a0001c0003t0004g0024 a0001c0003t0004g0103 a0001c0003t0004g0134 |
3 | HG00609.hp2 HG02683.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.381+509_381+512dup others(4): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr4 | 158829711 | ||||||
| chr4:158829711 | GGT | G | 33 | a0001c0001t0001g0161 a0001c0001t0003g0036 a0002c0002t0003g0166 others(30): Show |
33 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.381+511_381+512del others(2): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr4 | 158829711 | ||||||
| chr4:158829713 | T | G | 6 | a0001c0001t0001g0152 a0001c0001t0005g0006 a0001c0007t0006g0012 others(3): Show |
6 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.381+488T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158829713 | |||||||
| chr4:158829747 | G | A | 3 | a0001c0007t0006g0163 a0001c0007t0006g0164 a0001c0007t0006g0165 |
3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.381+522G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158829747 | |||||||
| chr4:158829845 | T | C | 1 | a0002c0017t0003g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.381+620T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158829845 | |||||||
| chr4:158829903 | A | G | 51 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(48): Show |
52 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.381+678A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158829903 | |||||||
| chr4:158829919 | C | T | 1 | a0006c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.381+694C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158829919 | |||||||
| chr4:158830001 | A | T | 60 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0001 others(57): Show |
61 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.381+776A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830001 | |||||||
| chr4:158830082 | T | G | 1 | a0001c0001t0018g0102 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.381+857T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830082 | |||||||
| chr4:158830116 | G | C | 2 | a0001c0001t0002g0217 a0001c0001t0002g0221 |
2 | HG02148.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.381+891G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830116 | |||||||
| chr4:158830123 | G | A | 17 | a0001c0003t0004g0016 a0001c0003t0004g0018 a0001c0003t0004g0019 others(14): Show |
17 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.381+898G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830123 | |||||||
| chr4:158830173 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.381+948A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830173 | |||||||
| chr4:158830210 | G | A | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.381+985G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830210 | |||||||
| chr4:158830235 | T | C | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.381+1010T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830235 | |||||||
| chr4:158830248 | C | CT | 9 | a0001c0001t0001g0151 a0003c0004t0001g0054 a0003c0004t0001g0055 others(6): Show |
9 | HG01981.hp2 HG02572.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.381+1048dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr4 | 158830248 | ||||||
| chr4:158830248 | CT | C | 155 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(152): Show |
156 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.381+1048delT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr4 | 158830248 | ||||||
| chr4:158830248 | CTT | C | 58 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0070 others(55): Show |
58 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.381+1047_381+1048d others(4): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr4 | 158830248 | ||||||
| chr4:158830278 | C | T | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.381+1053C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830278 | |||||||
| chr4:158830299 | A | G | 1 | a0001c0001t0001g0015 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.381+1074A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830299 | |||||||
| chr4:158830316 | G | T | 1 | a0001c0001t0001g0160 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.381+1091G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830316 | |||||||
| chr4:158830329 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.381+1104C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830329 | |||||||
| chr4:158830388 | G | A | 2 | a0001c0001t0007g0031 a0001c0001t0007g0032 |
2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.381+1163G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830388 | |||||||
| chr4:158830424 | G | A | 3 | a0001c0001t0007g0031 a0001c0001t0007g0032 a0006c0015t0004g0013 |
3 | HG02615.hp2 HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.381+1199G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830424 | |||||||
| chr4:158830551 | C | T | 3 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0242 |
3 | NA18963.hp2 NA18972.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.382-1310C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830551 | |||||||
| chr4:158830583 | G | A | 2 | a0001c0001t0007g0031 a0001c0001t0007g0032 |
2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.382-1278G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830583 | |||||||
| chr4:158830707 | T | G | 1 | a0001c0001t0001g0133 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.382-1154T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830707 | |||||||
| chr4:158830795 | A | G | 5 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(2): Show |
5 | HG01255.hp2 HG01433.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.382-1066A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830795 | |||||||
| chr4:158830855 | G | A | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.382-1006G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830855 | |||||||
| chr4:158830926 | C | T | 1 | a0001c0001t0003g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.382-935C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830926 | |||||||
| chr4:158830976 | G | C | 1 | a0002c0002t0003g0172 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.382-885G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830976 | |||||||
| chr4:158831037 | G | T | 1 | a0006c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.382-824G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158831037 | |||||||
| chr4:158831219 | A | T | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0132 others(2): Show |
5 | HG03471.hp2 HG04228.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.382-642A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158831219 | |||||||
| chr4:158831513 | A | G | 51 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(48): Show |
52 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.382-348A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158831513 | |||||||
| chr4:158831689 | G | A | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.382-172G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158831689 | |||||||
| chr4:158832192 | A | G | 2 | a0001c0001t0002g0238 a0001c0001t0009g0244 |
2 | HG00597.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.554+54A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 5/16 | chr4 | 158832192 | |||||||
| chr4:158832254 | T | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.554+116T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 5/16 | chr4 | 158832254 | |||||||
| chr4:158832423 | A | G | 8 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0063 others(5): Show |
8 | HG00597.hp1 HG01192.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.554+285A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 5/16 | chr4 | 158832423 | |||||||
| chr4:158832770 | T | G | 58 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(55): Show |
59 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.554+632T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 5/16 | chr4 | 158832770 | |||||||
| chr4:158832929 | T | C | 2 | a0001c0001t0005g0006 a0001c0001t0005g0008 |
2 | HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.555-599T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 5/16 | chr4 | 158832929 | |||||||
| chr4:158833197 | G | T | 1 | a0001c0001t0002g0243 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.555-331G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 5/16 | chr4 | 158833197 | |||||||
| chr4:158833208 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.555-320T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 5/16 | chr4 | 158833208 | |||||||
| chr4:158833432 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.555-96C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 5/16 | chr4 | 158833432 | |||||||
| chr4:158833499 | C | A | 1 | a0001c0001t0012g0125 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.555-29C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 5/16 | chr4 | 158833499 | |||||||
| chr4:158833713 | G | GT | 23 | a0001c0001t0001g0135 a0001c0001t0008g0069 a0001c0003t0004g0016 others(20): Show |
23 | HG00609.hp2 HG02055.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.655+96dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158833713 | ||||||
| chr4:158833727 | G | A | 1 | a0001c0001t0002g0242 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.655+99G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158833727 | |||||||
| chr4:158833792 | C | T | 1 | a0001c0001t0002g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.655+164C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158833792 | |||||||
| chr4:158834012 | T | C | 1 | a0002c0002t0003g0181 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.655+384T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834012 | |||||||
| chr4:158834025 | C | T | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.655+397C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834025 | |||||||
| chr4:158834084 | G | A | 1 | a0002c0002t0003g0166 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.655+456G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834084 | |||||||
| chr4:158834140 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.655+512G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834140 | |||||||
| chr4:158834246 | C | T | 1 | a0001c0001t0002g0207 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.655+618C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834246 | |||||||
| chr4:158834288 | T | TTC | 3 | a0001c0001t0001g0108 a0002c0002t0003g0175 a0005c0011t0005g0003 |
3 | HG01981.hp2 HG03491.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.655+701_655+702dup others(2): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | ||||||
| chr4:158834288 | T | TTCTC | 12 | a0001c0001t0001g0105 a0001c0001t0001g0120 a0001c0001t0002g0249 others(9): Show |
12 | HG00423.hp2 HG01496.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.655+699_655+702dup others(4): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | ||||||
| chr4:158834288 | T | TTCTCTC | 14 | a0001c0001t0002g0225 a0001c0001t0003g0184 a0002c0002t0003g0166 others(11): Show |
14 | HG00280.hp1 HG00738.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.655+697_655+702dup others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | ||||||
| chr4:158834288 | T | TTCTCTCT others(1): Show |
9 | a0001c0001t0001g0100 a0001c0001t0001g0115 a0001c0001t0001g0121 others(6): Show |
9 | HG00735.hp1 HG00738.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.655+695_655+702dup others(8): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | ||||||
| chr4:158834288 | T | TTCTCTCT others(3): Show |
29 | a0001c0001t0001g0002 a0001c0001t0001g0051 a0001c0001t0001g0070 others(26): Show |
29 | HG00609.hp1 HG00639.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.655+693_655+702dup others(10): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | ||||||
| chr4:158834288 | T | TTCTCTCT others(5): Show |
43 | a0001c0001t0001g0041 a0001c0001t0001g0046 a0001c0001t0001g0049 others(40): Show |
44 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.655+691_655+702dup others(12): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | ||||||
| chr4:158834288 | T | TTCTCTCT others(7): Show |
33 | a0001c0001t0001g0039 a0001c0001t0001g0077 a0001c0001t0001g0083 others(30): Show |
33 | HG00280.hp2 HG00642.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.655+689_655+702dup others(14): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | ||||||
| chr4:158834288 | T | TTCTCTCT others(9): Show |
28 | a0001c0001t0001g0042 a0001c0001t0001g0062 a0001c0001t0001g0065 others(25): Show |
28 | HG00423.hp1 HG00438.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.655+687_655+702dup others(16): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | ||||||
| chr4:158834288 | T | TTCTCTCT others(11): Show |
14 | a0001c0001t0001g0052 a0001c0001t0001g0066 a0001c0001t0001g0067 others(11): Show |
14 | HG01261.hp2 HG01496.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.655+685_655+702dup others(18): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | ||||||
| chr4:158834288 | T | TTCTCTCT others(13): Show |
9 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0053 others(6): Show |
9 | HG00597.hp1 HG02622.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.655+683_655+702dup others(20): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | ||||||
| chr4:158834288 | T | TTCTCTCT others(15): Show |
3 | a0001c0001t0001g0064 a0003c0004t0001g0055 a0003c0004t0001g0057 |
3 | HG02717.hp1 NA18906.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.655+681_655+702dup others(22): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | ||||||
| chr4:158834288 | T | TTCTCTCT others(17): Show |
3 | a0001c0001t0001g0043 a0001c0001t0012g0124 a0003c0004t0001g0058 |
3 | HG02109.hp2 HG02145.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.655+679_655+702dup others(24): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | ||||||
| chr4:158834288 | T | TTCTCTCT others(19): Show |
2 | a0001c0001t0001g0132 a0001c0001t0019g0088 |
2 | HG01934.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.655+677_655+702dup others(26): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | ||||||
| chr4:158834288 | T | TTCTCTCT others(23): Show |
1 | a0001c0001t0001g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.655+673_655+702dup others(30): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | ||||||
| chr4:158834288 | T | TTCTCTCT others(13): Show |
1 | a0006c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.655+677_655+678ins others(20): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | ||||||
| chr4:158834288 | TTC | T | 9 | a0001c0001t0001g0078 a0001c0001t0002g0238 a0001c0001t0005g0004 others(6): Show |
9 | HG00558.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.655+701_655+702del others(2): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | ||||||
| chr4:158834288 | TTCTCTC | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0005g0159 |
3 | HG02258.hp1 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.655+697_655+702del others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | ||||||
| chr4:158834313 | TCTCTCTC others(11): Show |
T | 3 | a0001c0007t0006g0012 a0001c0007t0006g0164 a0001c0007t0006g0165 |
3 | HG02145.hp2 HG02486.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.655+692_655+709del others(18): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834313 | ||||||
| chr4:158834317 | TCTCTCTC others(7): Show |
T | 1 | a0001c0007t0006g0163 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.655+696_655+709del others(14): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834317 | ||||||
| chr4:158834325 | T | TCTCTCTC others(11): Show |
1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.655+702_655+703ins others(18): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834325 | ||||||
| chr4:158834329 | T | TCTCTCTC others(7): Show |
2 | a0001c0003t0004g0020 a0001c0003t0004g0021 |
2 | HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.655+702_655+703ins others(14): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834329 | ||||||
| chr4:158834329 | T | TCTCTCTC others(11): Show |
1 | a0003c0004t0001g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.655+702_655+703ins others(18): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834329 | ||||||
| chr4:158834330 | C | CTCTCTCT others(2): Show |
3 | a0001c0001t0001g0116 a0001c0001t0001g0140 a0002c0002t0004g0037 |
3 | HG02280.hp2 HG03225.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.655+702_655+703ins others(9): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834330 | |||||||
| chr4:158834330 | C | CTCTCTCT others(4): Show |
7 | a0001c0001t0001g0040 a0001c0001t0001g0072 a0001c0001t0001g0079 others(4): Show |
7 | HG00642.hp2 HG01192.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.655+702_655+703ins others(11): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834330 | |||||||
| chr4:158834330 | C | CTCTCTCT others(6): Show |
3 | a0001c0001t0001g0047 a0001c0001t0001g0155 a0004c0006t0002g0247 |
3 | HG01258.hp1 HG01975.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.655+702_655+703ins others(13): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834330 | |||||||
| chr4:158834330 | C | CTCTCTCT others(8): Show |
2 | a0001c0001t0001g0094 a0001c0001t0001g0101 |
2 | HG02148.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.655+702_655+703ins others(15): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834330 | |||||||
| chr4:158834330 | C | CTCTCTCT others(10): Show |
1 | a0001c0001t0002g0211 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.655+702_655+703ins others(17): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834330 | |||||||
| chr4:158834330 | C | CTCTCTCT others(12): Show |
2 | a0001c0001t0004g0136 a0003c0004t0001g0146 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.655+702_655+703ins others(19): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834330 | |||||||
| chr4:158834330 | C | CTCTCTCT others(14): Show |
1 | a0001c0001t0001g0151 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.655+702_655+703ins others(21): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834330 | |||||||
| chr4:158834331 | C | T | 1 | a0002c0002t0003g0199 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.655+703C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834331 | |||||||
| chr4:158834342 | A | G | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.655+714A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834342 | |||||||
| chr4:158834841 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.656-564T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834841 | |||||||
| chr4:158835018 | C | T | 33 | a0002c0002t0003g0166 a0002c0002t0003g0167 a0002c0002t0003g0168 others(30): Show |
33 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.656-387C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158835018 | |||||||
| chr4:158835393 | C | G | 1 | a0001c0001t0001g0110 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.656-12C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158835393 | |||||||
| chr4:158835395 | T | G | 1 | a0001c0001t0002g0230 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.656-10T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158835395 | |||||||
| chr4:158836168 | T | G | 1 | a0001c0001t0001g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.727+692T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158836168 | |||||||
| chr4:158836423 | G | A | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.727+947G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158836423 | |||||||
| chr4:158836644 | CA | C | 58 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(55): Show |
59 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.727+1182delA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr4 | 158836644 | ||||||
| chr4:158836677 | G | A | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+1201G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158836677 | |||||||
| chr4:158836693 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.727+1217A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158836693 | |||||||
| chr4:158836811 | C | CA | 19 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0043 others(16): Show |
19 | HG00597.hp1 HG01192.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.727+1362dupA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr4 | 158836811 | ||||||
| chr4:158836811 | CA | C | 89 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0042 others(86): Show |
90 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.727+1362delA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr4 | 158836811 | ||||||
| chr4:158836811 | CAA | C | 51 | a0001c0001t0001g0121 a0001c0001t0007g0031 a0001c0001t0007g0032 others(48): Show |
51 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.727+1361_727+1362d others(4): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr4 | 158836811 | ||||||
| chr4:158836811 | CAAAAAAA others(7): Show |
C | 1 | a0002c0002t0003g0185 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.727+1349_727+1362d others(16): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr4 | 158836811 | ||||||
| chr4:158836927 | T | G | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+1451T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158836927 | |||||||
| chr4:158837441 | A | G | 7 | a0002c0002t0003g0171 a0002c0002t0003g0172 a0002c0002t0004g0037 others(4): Show |
7 | HG02258.hp2 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.727+1965A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158837441 | |||||||
| chr4:158837764 | G | A | 51 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(48): Show |
52 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.727+2288G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158837764 | |||||||
| chr4:158837928 | G | A | 3 | a0001c0001t0007g0031 a0001c0001t0007g0032 a0006c0015t0004g0013 |
3 | HG02615.hp2 HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.727+2452G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158837928 | |||||||
| chr4:158837974 | G | A | 36 | a0002c0002t0003g0166 a0002c0002t0003g0167 a0002c0002t0003g0168 others(33): Show |
36 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.727+2498G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158837974 | |||||||
| chr4:158838101 | A | AATTGTGT others(14): Show |
1 | a0001c0001t0001g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.727+2627_727+2647d others(23): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr4 | 158838101 | ||||||
| chr4:158838229 | C | CT | 113 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(110): Show |
113 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.727+2772dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr4 | 158838229 | ||||||
| chr4:158838229 | CT | C | 57 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0144 others(54): Show |
57 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.727+2772delT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr4 | 158838229 | ||||||
| chr4:158838339 | G | A | 1 | a0002c0002t0003g0167 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.727+2863G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158838339 | |||||||
| chr4:158838391 | T | A | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0132 others(1): Show |
4 | HG04228.hp1 NA18986.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+2915T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158838391 | |||||||
| chr4:158838497 | A | G | 1 | a0006c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.727+3021A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158838497 | |||||||
| chr4:158838545 | G | T | 1 | a0001c0001t0001g0039 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.727+3069G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158838545 | |||||||
| chr4:158838761 | T | A | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+3285T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158838761 | |||||||
| chr4:158839124 | C | G | 2 | a0001c0001t0001g0040 a0001c0001t0008g0069 |
2 | NA18612.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.727+3648C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158839124 | |||||||
| chr4:158839200 | C | T | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.727+3724C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158839200 | |||||||
| chr4:158839357 | A | ATTAT | 8 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0008t0010g0033 others(5): Show |
8 | HG00735.hp2 HG01884.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.727+3896_727+3899d others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr4 | 158839357 | ||||||
| chr4:158839357 | A | ATTATTTA others(1): Show |
46 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(43): Show |
47 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.727+3892_727+3899d others(10): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr4 | 158839357 | ||||||
| chr4:158839577 | C | T | 20 | a0001c0001t0007g0031 a0001c0001t0007g0032 a0001c0003t0004g0016 others(17): Show |
20 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.727+4101C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158839577 | |||||||
| chr4:158839831 | A | G | 243 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(240): Show |
244 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.727+4355A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158839831 | |||||||
| chr4:158840132 | G | A | 3 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 |
3 | HG02523.hp1 NA18956.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.727+4656G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158840132 | |||||||
| chr4:158840200 | T | C | 1 | a0001c0001t0005g0008 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.727+4724T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158840200 | |||||||
| chr4:158840240 | C | T | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+4764C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158840240 | |||||||
| chr4:158840330 | G | A | 1 | a0001c0001t0002g0205 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.727+4854G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158840330 | |||||||
| chr4:158840394 | TTTG | T | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+4927_727+4929d others(5): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr4 | 158840394 | ||||||
| chr4:158840457 | G | A | 6 | a0001c0001t0001g0043 a0001c0001t0001g0064 a0001c0001t0001g0065 others(3): Show |
6 | HG00423.hp1 HG00609.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.727+4981G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158840457 | |||||||
| chr4:158840541 | G | A | 2 | a0002c0002t0004g0037 a0002c0002t0004g0038 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.727+5065G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158840541 | |||||||
| chr4:158840756 | T | G | 1 | a0002c0002t0003g0173 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.727+5280T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158840756 | |||||||
| chr4:158840839 | A | C | 1 | a0002c0002t0007g0169 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.727+5363A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158840839 | |||||||
| chr4:158841208 | T | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.727+5732T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158841208 | |||||||
| chr4:158841280 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.727+5804G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158841280 | |||||||
| chr4:158841478 | G | A | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0132 others(1): Show |
4 | HG04228.hp1 NA18986.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+6002G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158841478 | |||||||
| chr4:158841683 | A | C | 242 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(239): Show |
243 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(240): Show |
intron_variant | MODIFIER | c.727+6207A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158841683 | |||||||
| chr4:158841777 | G | A | 1 | a0005c0011t0005g0003 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.727+6301G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158841777 | |||||||
| chr4:158841957 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.727+6481G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158841957 | |||||||
| chr4:158841978 | A | G | 2 | a0001c0001t0002g0210 a0001c0001t0002g0216 |
2 | HG01167.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.727+6502A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158841978 | |||||||
| chr4:158842044 | T | G | 1 | a0004c0006t0002g0248 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.727+6568T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158842044 | |||||||
| chr4:158842147 | T | C | 37 | a0001c0001t0003g0184 a0002c0002t0003g0166 a0002c0002t0003g0167 others(34): Show |
37 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.727+6671T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158842147 | |||||||
| chr4:158842184 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.727+6708A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158842184 | |||||||
| chr4:158842215 | A | G | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0009c0010t0001g0106 |
3 | HG01517.hp2 HG02559.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.727+6739A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158842215 | |||||||
| chr4:158842388 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.727+6912A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158842388 | |||||||
| chr4:158842483 | T | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.727+7007T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158842483 | |||||||
| chr4:158842577 | G | A | 1 | a0002c0002t0004g0038 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.727+7101G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158842577 | |||||||
| chr4:158842611 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.727+7135C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158842611 | |||||||
| chr4:158842616 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.727+7140A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158842616 | |||||||
| chr4:158842687 | A | G | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.727+7211A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158842687 | |||||||
| chr4:158843145 | C | G | 2 | a0002c0002t0004g0037 a0002c0002t0004g0038 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.727+7669C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158843145 | |||||||
| chr4:158843710 | T | C | 51 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(48): Show |
52 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.728-7611T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158843710 | |||||||
| chr4:158844044 | T | G | 1 | a0001c0001t0001g0050 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.728-7277T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158844044 | |||||||
| chr4:158844132 | G | C | 51 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(48): Show |
52 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.728-7189G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158844132 | |||||||
| chr4:158844209 | A | G | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.728-7112A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158844209 | |||||||
| chr4:158844285 | A | G | 7 | a0001c0001t0001g0052 a0001c0001t0001g0109 a0001c0001t0001g0110 others(4): Show |
7 | HG00438.hp1 HG01261.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.728-7036A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158844285 | |||||||
| chr4:158844517 | C | G | 1 | a0002c0002t0003g0082 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.728-6804C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158844517 | |||||||
| chr4:158844798 | A | C | 1 | a0001c0001t0003g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.728-6523A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158844798 | |||||||
| chr4:158845009 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.728-6312G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158845009 | |||||||
| chr4:158845081 | T | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.728-6240T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158845081 | |||||||
| chr4:158845187 | A | G | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.728-6134A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158845187 | |||||||
| chr4:158845305 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.728-6016C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158845305 | |||||||
| chr4:158845362 | C | T | 1 | a0002c0017t0003g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.728-5959C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158845362 | |||||||
| chr4:158845397 | C | T | 10 | a0003c0004t0001g0054 a0003c0004t0001g0055 a0003c0004t0001g0056 others(7): Show |
10 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.728-5924C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158845397 | |||||||
| chr4:158845445 | T | C | 51 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(48): Show |
52 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.728-5876T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158845445 | |||||||
| chr4:158845633 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.728-5688A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158845633 | |||||||
| chr4:158845834 | T | C | 1 | a0001c0001t0007g0032 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.728-5487T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158845834 | |||||||
| chr4:158845938 | G | A | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.728-5383G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158845938 | |||||||
| chr4:158846010 | A | T | 17 | a0001c0003t0004g0016 a0001c0003t0004g0018 a0001c0003t0004g0019 others(14): Show |
17 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.728-5311A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158846010 | |||||||
| chr4:158846102 | T | G | 1 | a0002c0017t0003g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.728-5219T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158846102 | |||||||
| chr4:158846161 | G | T | 1 | a0001c0001t0009g0244 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.728-5160G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158846161 | |||||||
| chr4:158846271 | T | G | 7 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(4): Show |
7 | HG01884.hp1 HG01981.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.728-5050T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158846271 | |||||||
| chr4:158846363 | G | T | 2 | a0002c0002t0004g0037 a0002c0002t0004g0038 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.728-4958G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158846363 | |||||||
| chr4:158846434 | G | T | 1 | a0001c0001t0004g0136 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.728-4887G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158846434 | |||||||
| chr4:158846786 | C | T | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.728-4535C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158846786 | |||||||
| chr4:158846962 | G | A | 1 | a0001c0001t0007g0032 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.728-4359G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158846962 | |||||||
| chr4:158847032 | G | C | 1 | a0008c0018t0003g0183 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.728-4289G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158847032 | |||||||
| chr4:158847074 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.728-4247G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158847074 | |||||||
| chr4:158847232 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.728-4089G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158847232 | |||||||
| chr4:158847458 | C | G | 1 | a0002c0002t0003g0182 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.728-3863C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158847458 | |||||||
| chr4:158847877 | C | T | 1 | a0001c0001t0005g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.728-3444C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158847877 | |||||||
| chr4:158847909 | C | T | 1 | a0002c0002t0003g0171 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.728-3412C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158847909 | |||||||
| chr4:158847943 | A | T | 1 | a0001c0001t0001g0200 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.728-3378A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158847943 | |||||||
| chr4:158848004 | G | A | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0063 |
3 | HG00597.hp1 NA18957.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.728-3317G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158848004 | |||||||
| chr4:158848038 | A | G | 10 | a0003c0004t0001g0054 a0003c0004t0001g0055 a0003c0004t0001g0056 others(7): Show |
10 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.728-3283A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158848038 | |||||||
| chr4:158848805 | C | T | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.728-2516C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158848805 | |||||||
| chr4:158848953 | G | C | 1 | a0001c0001t0005g0009 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.728-2368G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158848953 | |||||||
| chr4:158848961 | A | T | 1 | a0006c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.728-2360A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158848961 | |||||||
| chr4:158849133 | A | G | 2 | a0001c0001t0001g0047 a0001c0001t0008g0048 |
2 | HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.728-2188A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158849133 | |||||||
| chr4:158849602 | A | C | 1 | a0006c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.728-1719A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158849602 | |||||||
| chr4:158849605 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.728-1716G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158849605 | |||||||
| chr4:158849904 | T | C | 38 | a0001c0001t0003g0184 a0002c0002t0003g0025 a0002c0002t0003g0166 others(35): Show |
38 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.728-1417T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158849904 | |||||||
| chr4:158849970 | G | A | 2 | a0001c0001t0007g0031 a0001c0001t0007g0032 |
2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.728-1351G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158849970 | |||||||
| chr4:158850293 | T | C | 17 | a0001c0003t0004g0016 a0001c0003t0004g0018 a0001c0003t0004g0019 others(14): Show |
17 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.728-1028T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158850293 | |||||||
| chr4:158850317 | T | C | 1 | a0001c0001t0002g0226 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.728-1004T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158850317 | |||||||
| chr4:158850488 | T | C | 1 | a0001c0001t0009g0143 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.728-833T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158850488 | |||||||
| chr4:158850689 | A | C | 4 | a0001c0003t0004g0016 a0001c0003t0013g0026 a0001c0003t0013g0028 others(1): Show |
4 | HG02486.hp1 HG02572.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.728-632A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158850689 | |||||||
| chr4:158850822 | G | T | 1 | a0004c0006t0002g0248 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.728-499G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158850822 | |||||||
| chr4:158850921 | G | A | 1 | a0002c0017t0003g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.728-400G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158850921 | |||||||
| chr4:158850934 | C | T | 2 | a0001c0001t0007g0031 a0001c0001t0007g0032 |
2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.728-387C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158850934 | |||||||
| chr4:158851180 | G | A | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.728-141G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158851180 | |||||||
| chr4:158851201 | T | C | 1 | a0001c0003t0017g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.728-120T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158851201 | |||||||
| chr4:158851490 | G | C | 1 | a0001c0001t0019g0088 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.857+40G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158851490 | |||||||
| chr4:158851557 | C | G | 3 | a0001c0001t0002g0202 a0001c0001t0002g0207 a0001c0001t0002g0249 |
3 | HG00280.hp2 HG01496.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.857+107C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158851557 | |||||||
| chr4:158851627 | G | A | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.857+177G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158851627 | |||||||
| chr4:158851628 | C | T | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.857+178C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158851628 | |||||||
| chr4:158851688 | T | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0059 |
2 | HG01081.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.857+238T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158851688 | |||||||
| chr4:158851704 | G | A | 2 | a0001c0001t0007g0031 a0001c0001t0007g0032 |
2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.857+254G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158851704 | |||||||
| chr4:158852062 | G | A | 1 | a0001c0001t0002g0238 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.857+612G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158852062 | |||||||
| chr4:158852360 | T | A | 1 | a0001c0001t0001g0053 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.857+910T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158852360 | |||||||
| chr4:158852453 | A | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.857+1003A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158852453 | |||||||
| chr4:158852550 | G | A | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.857+1100G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158852550 | |||||||
| chr4:158853110 | CATA | C | 37 | a0002c0002t0003g0082 a0002c0002t0003g0166 a0002c0002t0003g0167 others(34): Show |
37 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.857+1664_857+1666d others(5): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr4 | 158853110 | ||||||
| chr4:158853208 | G | A | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.857+1758G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158853208 | |||||||
| chr4:158853329 | G | A | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0132 others(1): Show |
4 | HG04228.hp1 NA18986.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.857+1879G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158853329 | |||||||
| chr4:158853419 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.857+1969C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158853419 | |||||||
| chr4:158853504 | C | T | 1 | a0001c0001t0002g0245 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.857+2054C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158853504 | |||||||
| chr4:158853833 | A | G | 2 | a0001c0001t0002g0210 a0001c0001t0002g0216 |
2 | HG01167.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.857+2383A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158853833 | |||||||
| chr4:158854090 | T | G | 1 | a0001c0001t0001g0053 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.857+2640T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158854090 | |||||||
| chr4:158854286 | C | CTGGCCTC others(3): Show |
1 | a0001c0001t0002g0242 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.857+2837_857+2846d others(12): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr4 | 158854286 | ||||||
| chr4:158854449 | T | G | 117 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0001 others(114): Show |
118 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.857+2999T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158854449 | |||||||
| chr4:158854521 | G | A | 38 | a0002c0002t0003g0025 a0002c0002t0003g0082 a0002c0002t0003g0166 others(35): Show |
38 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.857+3071G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158854521 | |||||||
| chr4:158854876 | G | A | 2 | a0002c0002t0004g0037 a0002c0002t0004g0038 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.857+3426G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158854876 | |||||||
| chr4:158855000 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.857+3550C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158855000 | |||||||
| chr4:158855008 | T | A | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.857+3558T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158855008 | |||||||
| chr4:158855123 | T | C | 28 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(25): Show |
28 | HG00438.hp1 HG00597.hp1 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.857+3673T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158855123 | |||||||
| chr4:158855212 | G | A | 2 | a0001c0001t0007g0031 a0001c0001t0007g0032 |
2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.857+3762G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158855212 | |||||||
| chr4:158855446 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.858-3611G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158855446 | |||||||
| chr4:158855851 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.858-3206C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158855851 | |||||||
| chr4:158855984 | C | A | 1 | a0001c0001t0001g0064 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.858-3073C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158855984 | |||||||
| chr4:158856038 | C | T | 1 | a0002c0002t0003g0172 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.858-3019C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158856038 | |||||||
| chr4:158856371 | T | A | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.858-2686T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158856371 | |||||||
| chr4:158856438 | A | C | 98 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0001 others(95): Show |
99 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.858-2619A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158856438 | |||||||
| chr4:158856444 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.858-2613G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158856444 | |||||||
| chr4:158856612 | A | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(103): Show |
106 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.858-2445A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158856612 | |||||||
| chr4:158856718 | A | T | 16 | a0001c0003t0004g0016 a0001c0003t0004g0018 a0001c0003t0004g0019 others(13): Show |
16 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.858-2339A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158856718 | |||||||
| chr4:158856953 | T | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.858-2104T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158856953 | |||||||
| chr4:158856969 | G | A | 2 | a0001c0001t0002g0240 a0001c0001t0002g0241 |
2 | NA18963.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.858-2088G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158856969 | |||||||
| chr4:158857092 | G | A | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.858-1965G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158857092 | |||||||
| chr4:158857332 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.858-1725G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158857332 | |||||||
| chr4:158857647 | T | C | 1 | a0002c0002t0003g0082 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.858-1410T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158857647 | |||||||
| chr4:158857650 | A | T | 1 | a0002c0002t0003g0082 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.858-1407A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158857650 | |||||||
| chr4:158857663 | C | G | 1 | a0002c0002t0003g0082 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.858-1394C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158857663 | |||||||
| chr4:158857693 | A | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.858-1364A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158857693 | |||||||
| chr4:158857771 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.858-1286C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158857771 | |||||||
| chr4:158857780 | C | CA | 105 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(102): Show |
105 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.858-1260dupA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr4 | 158857780 | ||||||
| chr4:158857780 | CA | C | 55 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(52): Show |
56 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.858-1260delA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr4 | 158857780 | ||||||
| chr4:158857780 | CAAAAAAA others(1): Show |
C | 16 | a0001c0003t0004g0016 a0001c0003t0004g0018 a0001c0003t0004g0019 others(13): Show |
16 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.858-1267_858-1260d others(10): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr4 | 158857780 | ||||||
| chr4:158857785 | A | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.858-1272A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158857785 | |||||||
| chr4:158857946 | C | G | 12 | a0001c0001t0001g0039 a0001c0001t0001g0059 a0001c0001t0001g0115 others(9): Show |
12 | HG01081.hp1 HG02109.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.858-1111C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158857946 | |||||||
| chr4:158857975 | C | T | 1 | a0001c0001t0005g0004 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.858-1082C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158857975 | |||||||
| chr4:158857986 | A | G | 1 | a0001c0003t0004g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.858-1071A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158857986 | |||||||
| chr4:158858017 | T | C | 1 | a0001c0001t0015g0074 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.858-1040T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158858017 | |||||||
| chr4:158858042 | T | C | 117 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0001 others(114): Show |
118 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.858-1015T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158858042 | |||||||
| chr4:158858089 | G | A | 28 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(25): Show |
28 | HG00438.hp1 HG00597.hp1 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.858-968G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158858089 | |||||||
| chr4:158858109 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.858-948T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158858109 | |||||||
| chr4:158858112 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.858-945T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158858112 | |||||||
| chr4:158858156 | A | G | 3 | a0001c0001t0004g0136 a0001c0001t0012g0124 a0001c0001t0012g0125 |
3 | HG01891.hp2 HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.858-901A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158858156 | |||||||
| chr4:158858660 | C | T | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.858-397C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158858660 | |||||||
| chr4:158859516 | G | A | 1 | a0001c0001t0007g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1060-62G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 9/16 | chr4 | 158859516 | |||||||
| chr4:158859696 | A | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1148+30A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | chr4 | 158859696 | |||||||
| chr4:158859838 | C | T | 15 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0132 others(12): Show |
15 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1148+172C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | chr4 | 158859838 | |||||||
| chr4:158859854 | C | G | 1 | a0001c0001t0002g0210 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1148+188C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | chr4 | 158859854 | |||||||
| chr4:158860418 | C | CT | 35 | a0002c0002t0003g0025 a0002c0002t0003g0082 a0002c0002t0003g0166 others(32): Show |
35 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.1148+760dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr4 | 158860418 | ||||||
| chr4:158860470 | T | C | 1 | a0001c0001t0005g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1148+804T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | chr4 | 158860470 | |||||||
| chr4:158860549 | T | C | 3 | a0001c0007t0006g0163 a0001c0007t0006g0164 a0001c0007t0006g0165 |
3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1149-793T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | chr4 | 158860549 | |||||||
| chr4:158860654 | C | CT | 64 | a0001c0001t0001g0111 a0001c0001t0001g0253 a0001c0001t0002g0001 others(61): Show |
65 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1149-666dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr4 | 158860654 | ||||||
| chr4:158860689 | G | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1149-653G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | chr4 | 158860689 | |||||||
| chr4:158860798 | A | C | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1149-544A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | chr4 | 158860798 | |||||||
| chr4:158860799 | G | A | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1149-543G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | chr4 | 158860799 | |||||||
| chr4:158860800 | G | T | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1149-542G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | chr4 | 158860800 | |||||||
| chr4:158860801 | C | A | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1149-541C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | chr4 | 158860801 | |||||||
| chr4:158860857 | A | G | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1149-485A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | chr4 | 158860857 | |||||||
| chr4:158861001 | A | G | 3 | a0001c0007t0006g0163 a0001c0007t0006g0164 a0001c0007t0006g0165 |
3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1149-341A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | chr4 | 158861001 | |||||||
| chr4:158861128 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1149-214C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | chr4 | 158861128 | |||||||
| chr4:158861858 | C | G | 17 | a0001c0003t0004g0016 a0001c0003t0004g0018 a0001c0003t0004g0019 others(14): Show |
17 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.1465+82C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158861858 | |||||||
| chr4:158862003 | A | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1465+227A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158862003 | |||||||
| chr4:158862087 | T | C | 1 | a0001c0003t0004g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1465+311T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158862087 | |||||||
| chr4:158862497 | A | C | 60 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0001 others(57): Show |
61 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.1465+721A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158862497 | |||||||
| chr4:158862819 | T | G | 242 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(239): Show |
243 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(240): Show |
intron_variant | MODIFIER | c.1465+1043T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158862819 | |||||||
| chr4:158862956 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1465+1180T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158862956 | |||||||
| chr4:158863217 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1465+1441C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158863217 | |||||||
| chr4:158863218 | G | A | 1 | a0001c0009t0002g0234 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1465+1442G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158863218 | |||||||
| chr4:158863243 | G | A | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1465+1467G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158863243 | |||||||
| chr4:158863304 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1465+1528G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158863304 | |||||||
| chr4:158863343 | C | T | 38 | a0001c0001t0003g0184 a0002c0002t0003g0082 a0002c0002t0003g0166 others(35): Show |
38 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.1465+1567C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158863343 | |||||||
| chr4:158863376 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1465+1600A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158863376 | |||||||
| chr4:158863509 | C | T | 1 | a0006c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1465+1733C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158863509 | |||||||
| chr4:158863594 | G | A | 6 | a0002c0002t0003g0025 a0002c0002t0003g0167 a0002c0002t0003g0171 others(3): Show |
6 | HG02559.hp1 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1465+1818G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158863594 | |||||||
| chr4:158863810 | TC | T | 49 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(46): Show |
50 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1465+2036delC | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr4 | 158863810 | ||||||
| chr4:158864183 | G | A | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1465+2407G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158864183 | |||||||
| chr4:158864250 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1465+2474T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158864250 | |||||||
| chr4:158864266 | C | T | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1465+2490C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158864266 | |||||||
| chr4:158864267 | G | A | 1 | a0001c0001t0007g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1465+2491G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158864267 | |||||||
| chr4:158864361 | C | T | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1465+2585C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158864361 | |||||||
| chr4:158864365 | T | C | 2 | a0001c0001t0001g0064 a0001c0001t0001g0067 |
2 | HG02129.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1465+2589T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158864365 | |||||||
| chr4:158864377 | AATT | A | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0132 others(2): Show |
5 | HG03471.hp2 HG04228.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.1465+2603_1465+260 others(7): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr4 | 158864377 | ||||||
| chr4:158864590 | A | G | 1 | a0002c0017t0003g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1465+2814A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158864590 | |||||||
| chr4:158864786 | A | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1465+3010A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158864786 | |||||||
| chr4:158864835 | C | T | 16 | a0001c0003t0004g0018 a0001c0003t0004g0019 a0001c0003t0004g0020 others(13): Show |
16 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.1465+3059C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158864835 | |||||||
| chr4:158864955 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1466-3147C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158864955 | |||||||
| chr4:158865039 | C | T | 66 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0043 others(63): Show |
66 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1466-3063C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158865039 | |||||||
| chr4:158865105 | G | A | 4 | a0001c0003t0004g0024 a0001c0003t0004g0103 a0001c0003t0004g0104 others(1): Show |
4 | HG00609.hp2 HG02135.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1466-2997G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158865105 | |||||||
| chr4:158865458 | A | G | 1 | a0001c0001t0018g0102 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1466-2644A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158865458 | |||||||
| chr4:158865627 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1466-2475G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158865627 | |||||||
| chr4:158865686 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1466-2416C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158865686 | |||||||
| chr4:158865992 | C | T | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1466-2110C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158865992 | |||||||
| chr4:158866065 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1466-2037A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158866065 | |||||||
| chr4:158866221 | C | CTTTTTTT others(3): Show |
55 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0041 others(52): Show |
55 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1466-1875_1466-186 others(14): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr4 | 158866221 | ||||||
| chr4:158866221 | C | CTTTTTTT others(4): Show |
14 | a0001c0001t0001g0114 a0001c0001t0001g0116 a0001c0001t0001g0145 others(11): Show |
14 | HG01257.hp2 HG01891.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1466-1876_1466-186 others(15): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr4 | 158866221 | ||||||
| chr4:158866221 | C | CTTTTTTT others(5): Show |
132 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(129): Show |
133 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.1466-1877_1466-186 others(16): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr4 | 158866221 | ||||||
| chr4:158866221 | C | CTTTTTTT others(6): Show |
36 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0053 others(33): Show |
36 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.1466-1878_1466-186 others(17): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr4 | 158866221 | ||||||
| chr4:158866221 | C | CTTTTTTT others(7): Show |
3 | a0001c0001t0001g0127 a0001c0001t0002g0221 a0001c0001t0009g0231 |
3 | HG01192.hp2 HG02300.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1466-1879_1466-186 others(18): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr4 | 158866221 | ||||||
| chr4:158866221 | C | T | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1466-1881C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158866221 | |||||||
| chr4:158866305 | G | A | 1 | a0004c0006t0002g0222 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1466-1797G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158866305 | |||||||
| chr4:158866322 | G | A | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1466-1780G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158866322 | |||||||
| chr4:158866416 | C | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0132 others(1): Show |
4 | HG04228.hp1 NA18986.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.1466-1686C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158866416 | |||||||
| chr4:158866507 | C | T | 106 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(103): Show |
106 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.1466-1595C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158866507 | |||||||
| chr4:158866584 | T | A | 1 | a0001c0001t0001g0135 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1466-1518T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158866584 | |||||||
| chr4:158866736 | TGGCTAAT others(54): Show |
T | 1 | a0001c0001t0002g0211 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1466-1365_1466-130 others(65): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158866736 | |||||||
| chr4:158866877 | G | A | 15 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0132 others(12): Show |
15 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1466-1225G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158866877 | |||||||
| chr4:158866947 | C | T | 1 | a0001c0003t0004g0018 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1466-1155C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158866947 | |||||||
| chr4:158867212 | A | G | 1 | a0001c0001t0007g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1466-890A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158867212 | |||||||
| chr4:158867453 | A | G | 51 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(48): Show |
52 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1466-649A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158867453 | |||||||
| chr4:158867455 | G | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(103): Show |
106 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.1466-647G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158867455 | |||||||
| chr4:158867602 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1466-500G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158867602 | |||||||
| chr4:158867698 | A | G | 38 | a0002c0002t0003g0025 a0002c0002t0003g0082 a0002c0002t0003g0166 others(35): Show |
38 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.1466-404A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158867698 | |||||||
| chr4:158867714 | C | G | 5 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0009t0002g0234 others(2): Show |
5 | HG00735.hp2 HG01884.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1466-388C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158867714 | |||||||
| chr4:158867779 | C | T | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1466-323C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158867779 | |||||||
| chr4:158867838 | C | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | NA18986.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1466-264C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158867838 | |||||||
| chr4:158867848 | A | C | 58 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(55): Show |
59 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1466-254A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158867848 | |||||||
| chr4:158868016 | A | G | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1466-86A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158868016 | |||||||
| chr4:158868045 | A | C | 1 | a0001c0001t0002g0211 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1466-57A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158868045 | |||||||
| chr4:158868047 | C | G | 1 | a0001c0001t0002g0211 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1466-55C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158868047 | |||||||
| chr4:158869717 | G | T | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2792+289G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 13/16 | chr4 | 158869717 | |||||||
| chr4:158870737 | T | G | 1 | a0001c0001t0002g0211 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2949+268T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158870737 | |||||||
| chr4:158870828 | G | A | 1 | a0001c0001t0008g0098 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2949+359G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158870828 | |||||||
| chr4:158870880 | G | A | 1 | a0001c0001t0003g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2949+411G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158870880 | |||||||
| chr4:158870919 | C | T | 1 | a0002c0002t0003g0197 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2949+450C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158870919 | |||||||
| chr4:158871178 | G | A | 1 | a0001c0001t0009g0143 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2949+709G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158871178 | |||||||
| chr4:158871478 | C | A | 1 | a0001c0001t0002g0211 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2949+1009C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158871478 | |||||||
| chr4:158871478 | C | T | 56 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(53): Show |
57 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.2949+1009C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158871478 | |||||||
| chr4:158871557 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2949+1088A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158871557 | |||||||
| chr4:158871831 | C | T | 1 | a0006c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2949+1362C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158871831 | |||||||
| chr4:158872490 | C | T | 1 | a0011c0012t0002g0208 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2949+2021C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158872490 | |||||||
| chr4:158872734 | G | GT | 16 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0132 others(13): Show |
16 | HG01981.hp2 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2949+2282dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158872734 | ||||||
| chr4:158872736 | T | G | 51 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(48): Show |
52 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.2949+2267T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158872736 | |||||||
| chr4:158872741 | T | G | 1 | a0001c0001t0002g0221 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2949+2272T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158872741 | |||||||
| chr4:158872743 | T | TG | 16 | a0001c0003t0004g0016 a0001c0003t0004g0018 a0001c0003t0004g0019 others(13): Show |
16 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.2949+2274_2949+227 others(5): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158872743 | |||||||
| chr4:158872745 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2949+2276T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158872745 | |||||||
| chr4:158872751 | TA | T | 9 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0108 others(6): Show |
9 | HG01169.hp1 HG01257.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.2949+2288delA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158872751 | ||||||
| chr4:158872752 | A | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(234): Show |
238 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(235): Show |
intron_variant | MODIFIER | c.2949+2283A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158872752 | |||||||
| chr4:158872753 | A | T | 15 | a0001c0001t0001g0078 a0001c0001t0001g0115 a0001c0001t0001g0116 others(12): Show |
15 | HG00558.hp2 HG02083.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.2949+2284A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158872753 | |||||||
| chr4:158872983 | A | G | 6 | a0002c0002t0003g0082 a0002c0002t0003g0173 a0002c0002t0003g0174 others(3): Show |
6 | HG00438.hp2 HG00558.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.2949+2514A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158872983 | |||||||
| chr4:158873032 | C | T | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2949+2563C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158873032 | |||||||
| chr4:158873156 | AAAG | A | 10 | a0003c0004t0001g0054 a0003c0004t0001g0055 a0003c0004t0001g0056 others(7): Show |
10 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2949+2690_2949+269 others(7): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158873156 | ||||||
| chr4:158873636 | T | C | 1 | a0001c0001t0002g0001 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2949+3167T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158873636 | |||||||
| chr4:158873824 | T | A | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2949+3355T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158873824 | |||||||
| chr4:158873908 | G | A | 1 | a0003c0004t0001g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2949+3439G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158873908 | |||||||
| chr4:158873928 | G | T | 1 | a0001c0001t0002g0224 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2949+3459G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158873928 | |||||||
| chr4:158874492 | C | CAAAAAAA others(2): Show |
43 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0078 others(40): Show |
43 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.2949+4028_2949+403 others(13): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158874492 | ||||||
| chr4:158874492 | C | CAAAAAAA others(3): Show |
113 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0039 others(110): Show |
113 | HG00423.hp1 HG00609.hp1 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.2949+4027_2949+403 others(14): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158874492 | ||||||
| chr4:158874492 | C | CAAAAAAA others(4): Show |
83 | a0001c0001t0001g0002 a0001c0001t0001g0044 a0001c0001t0001g0045 others(80): Show |
84 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.2949+4026_2949+403 others(15): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158874492 | ||||||
| chr4:158874492 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0002g0211 a0001c0001t0012g0124 |
2 | HG02145.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.2949+4025_2949+403 others(16): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158874492 | ||||||
| chr4:158874492 | C | CAAAAAAA others(6): Show |
1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2949+4024_2949+403 others(17): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158874492 | ||||||
| chr4:158874579 | A | G | 58 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(55): Show |
59 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.2949+4110A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158874579 | |||||||
| chr4:158874593 | C | G | 1 | a0010c0013t0008g0150 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2949+4124C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158874593 | |||||||
| chr4:158874790 | A | G | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2949+4321A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158874790 | |||||||
| chr4:158874923 | CA | C | 248 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(245): Show |
249 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.2949+4468delA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158874923 | ||||||
| chr4:158875086 | C | CA | 8 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0065 others(5): Show |
8 | HG00423.hp1 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2949+4632dupA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875086 | ||||||
| chr4:158875091 | A | G | 51 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(48): Show |
52 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.2949+4622A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158875091 | |||||||
| chr4:158875098 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0005g0009 |
2 | HG03486.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.2949+4629A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158875098 | |||||||
| chr4:158875159 | C | G | 51 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(48): Show |
52 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.2949+4690C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158875159 | |||||||
| chr4:158875412 | C | T | 51 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(48): Show |
52 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.2949+4943C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158875412 | |||||||
| chr4:158875515 | G | GATATAT | 57 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(54): Show |
57 | HG00558.hp2 HG00621.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.2949+5067_2949+507 others(10): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | ||||||
| chr4:158875515 | G | GATATATA others(1): Show |
36 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0043 others(33): Show |
36 | HG00597.hp1 HG00621.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.2949+5065_2949+507 others(12): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | ||||||
| chr4:158875515 | G | GATATATA others(3): Show |
9 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0131 others(6): Show |
9 | HG00423.hp1 HG00609.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.2949+5063_2949+507 others(14): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | ||||||
| chr4:158875515 | G | GATATATA others(5): Show |
7 | a0001c0001t0001g0066 a0001c0001t0001g0120 a0002c0002t0007g0169 others(4): Show |
7 | HG02258.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2949+5061_2949+507 others(16): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | ||||||
| chr4:158875515 | G | GATATATA others(7): Show |
10 | a0002c0002t0003g0082 a0002c0002t0003g0174 a0002c0002t0003g0178 others(7): Show |
10 | HG00438.hp2 HG02080.hp2 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.2949+5059_2949+507 others(18): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | ||||||
| chr4:158875515 | G | GATATATA others(9): Show |
10 | a0001c0001t0003g0184 a0001c0001t0004g0136 a0001c0001t0012g0125 others(7): Show |
10 | HG01891.hp2 HG02055.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.2949+5057_2949+507 others(20): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | ||||||
| chr4:158875515 | G | GATATATA others(11): Show |
10 | a0001c0001t0012g0124 a0001c0003t0004g0019 a0001c0003t0004g0022 others(7): Show |
10 | HG00280.hp1 HG01943.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.2949+5055_2949+507 others(22): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | ||||||
| chr4:158875515 | G | GATATATA others(13): Show |
14 | a0001c0001t0001g0052 a0001c0001t0001g0109 a0001c0001t0001g0111 others(11): Show |
14 | HG00438.hp1 HG00738.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.2949+5053_2949+507 others(24): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | ||||||
| chr4:158875515 | G | GATATATA others(15): Show |
6 | a0001c0001t0001g0123 a0001c0001t0005g0007 a0001c0001t0005g0008 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2949+5051_2949+507 others(26): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | ||||||
| chr4:158875515 | G | GATATATA others(17): Show |
7 | a0001c0001t0001g0112 a0001c0001t0001g0133 a0001c0001t0005g0159 others(4): Show |
7 | HG01981.hp2 HG02135.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2949+5049_2949+507 others(28): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | ||||||
| chr4:158875515 | G | GATATATA others(19): Show |
7 | a0001c0001t0001g0053 a0001c0001t0001g0110 a0001c0001t0001g0144 others(4): Show |
7 | HG00423.hp2 HG00609.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.2949+5047_2949+507 others(30): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | ||||||
| chr4:158875515 | G | GATATATA others(21): Show |
3 | a0001c0003t0013g0028 a0002c0002t0003g0192 a0006c0015t0004g0013 |
3 | HG02615.hp2 HG02965.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.2949+5072_2949+507 others(32): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | ||||||
| chr4:158875515 | G | GATATATA others(23): Show |
3 | a0001c0001t0003g0036 a0003c0004t0001g0057 a0003c0004t0001g0146 |
3 | HG03225.hp2 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2949+5072_2949+507 others(34): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | ||||||
| chr4:158875515 | G | GATATATA others(25): Show |
3 | a0001c0001t0005g0010 a0002c0002t0003g0201 a0003c0004t0001g0055 |
3 | HG01169.hp2 HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2949+5072_2949+507 others(36): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | ||||||
| chr4:158875515 | G | GATATATA others(27): Show |
1 | a0002c0002t0004g0037 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2949+5072_2949+507 others(38): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | ||||||
| chr4:158875515 | G | GATATATA others(29): Show |
4 | a0001c0001t0001g0042 a0001c0001t0001g0132 a0001c0001t0001g0145 others(1): Show |
4 | HG02109.hp2 HG03471.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.2949+5072_2949+507 others(40): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | ||||||
| chr4:158875515 | G | GATATATA others(31): Show |
3 | a0001c0003t0017g0017 a0002c0002t0003g0173 a0003c0004t0001g0054 |
3 | HG00558.hp1 HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2949+5072_2949+507 others(42): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | ||||||
| chr4:158875515 | G | GATATATA others(33): Show |
4 | a0001c0003t0004g0016 a0002c0002t0003g0167 a0003c0004t0001g0148 others(1): Show |
4 | HG02486.hp1 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2949+5072_2949+507 others(44): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | ||||||
| chr4:158875515 | G | GATATATA others(39): Show |
1 | a0001c0003t0013g0026 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2949+5072_2949+507 others(50): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | ||||||
| chr4:158875515 | GATATATA others(1): Show |
G | 48 | a0001c0001t0001g0041 a0001c0001t0002g0001 a0001c0001t0002g0202 others(45): Show |
49 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.2949+5065_2949+507 others(12): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | ||||||
| chr4:158875515 | GATATATA others(7): Show |
G | 2 | a0001c0001t0007g0031 a0001c0001t0007g0032 |
2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2949+5059_2949+507 others(18): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | ||||||
| chr4:158875540 | A | G | 45 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(42): Show |
46 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.2949+5071A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158875540 | |||||||
| chr4:158875541 | T | C | 45 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(42): Show |
46 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.2949+5072T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158875541 | |||||||
| chr4:158875541 | T | TATATATA others(41): Show |
1 | a0007c0016t0002g0236 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2949+5072_2949+507 others(52): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158875541 | |||||||
| chr4:158875541 | T | TATATATA others(39): Show |
2 | a0001c0001t0002g0233 a0001c0009t0002g0235 |
2 | HG00735.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2949+5072_2949+507 others(50): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158875541 | |||||||
| chr4:158875541 | T | TATATATA others(25): Show |
1 | a0001c0009t0002g0234 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2949+5072_2949+507 others(36): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158875541 | |||||||
| chr4:158875541 | T | TATATATA others(23): Show |
1 | a0001c0001t0002g0232 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2949+5072_2949+507 others(34): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158875541 | |||||||
| chr4:158875542 | G | A | 38 | a0001c0001t0003g0184 a0002c0002t0003g0082 a0002c0002t0003g0166 others(35): Show |
38 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.2949+5073G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158875542 | |||||||
| chr4:158875704 | T | A | 1 | a0006c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2949+5235T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158875704 | |||||||
| chr4:158875890 | A | C | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2949+5421A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158875890 | |||||||
| chr4:158876010 | C | T | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2949+5541C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158876010 | |||||||
| chr4:158876063 | A | G | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2949+5594A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158876063 | |||||||
| chr4:158876174 | C | T | 1 | a0001c0001t0002g0215 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2949+5705C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158876174 | |||||||
| chr4:158876245 | T | A | 12 | a0001c0001t0001g0039 a0001c0001t0001g0059 a0001c0001t0001g0115 others(9): Show |
12 | HG01081.hp1 HG02109.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.2949+5776T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158876245 | |||||||
| chr4:158876463 | A | G | 10 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0089 others(7): Show |
10 | HG00621.hp1 HG02080.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2949+5994A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158876463 | |||||||
| chr4:158876507 | C | T | 1 | a0002c0002t0003g0167 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2949+6038C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158876507 | |||||||
| chr4:158876773 | A | G | 1 | a0001c0001t0007g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2949+6304A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158876773 | |||||||
| chr4:158876994 | C | T | 6 | a0002c0002t0003g0166 a0002c0002t0003g0185 a0002c0002t0003g0186 others(3): Show |
6 | HG00280.hp1 HG00738.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.2949+6525C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158876994 | |||||||
| chr4:158877010 | A | G | 3 | a0001c0001t0004g0136 a0001c0001t0012g0124 a0001c0001t0012g0125 |
3 | HG01891.hp2 HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2949+6541A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158877010 | |||||||
| chr4:158877265 | C | T | 5 | a0001c0005t0002g0209 a0001c0005t0002g0213 a0001c0005t0002g0214 others(2): Show |
5 | HG02735.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.2949+6796C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158877265 | |||||||
| chr4:158877310 | C | A | 1 | a0005c0011t0005g0003 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2949+6841C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158877310 | |||||||
| chr4:158877386 | A | C | 58 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(55): Show |
59 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.2949+6917A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158877386 | |||||||
| chr4:158877531 | G | A | 1 | a0001c0001t0002g0207 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2949+7062G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158877531 | |||||||
| chr4:158877803 | A | G | 115 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(112): Show |
116 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.2949+7334A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158877803 | |||||||
| chr4:158877883 | T | C | 1 | a0001c0001t0002g0229 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2949+7414T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158877883 | |||||||
| chr4:158877934 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2949+7465C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158877934 | |||||||
| chr4:158878191 | G | T | 1 | a0001c0001t0002g0219 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2949+7722G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158878191 | |||||||
| chr4:158878536 | A | G | 1 | a0002c0002t0003g0167 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2949+8067A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158878536 | |||||||
| chr4:158878790 | C | T | 52 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(49): Show |
53 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.2949+8321C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158878790 | |||||||
| chr4:158878862 | TGTAAGAA others(1290): Show |
T | 35 | a0001c0001t0003g0184 a0002c0002t0003g0025 a0002c0002t0003g0082 others(32): Show |
35 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.2949+8394_2949+969 others(4): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158878862 | |||||||
| chr4:158878999 | T | A | 1 | a0001c0001t0001g0043 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2949+8530T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158878999 | |||||||
| chr4:158879081 | A | G | 2 | a0003c0004t0001g0054 a0003c0004t0001g0057 |
2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2949+8612A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158879081 | |||||||
| chr4:158879640 | A | G | 1 | a0001c0001t0002g0245 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2949+9171A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158879640 | |||||||
| chr4:158879923 | A | C | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2949+9454A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158879923 | |||||||
| chr4:158880139 | C | G | 50 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(47): Show |
51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.2949+9670C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158880139 | |||||||
| chr4:158880160 | A | T | 35 | a0001c0001t0003g0184 a0002c0002t0003g0025 a0002c0002t0003g0082 others(32): Show |
35 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.2949+9691A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158880160 | |||||||
| chr4:158880166 | C | T | 35 | a0001c0001t0003g0184 a0002c0002t0003g0025 a0002c0002t0003g0082 others(32): Show |
35 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.2949+9697C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158880166 | |||||||
| chr4:158880174 | C | T | 35 | a0001c0001t0003g0184 a0002c0002t0003g0025 a0002c0002t0003g0082 others(32): Show |
35 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.2949+9705C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158880174 | |||||||
| chr4:158880193 | C | G | 35 | a0001c0001t0003g0184 a0002c0002t0003g0025 a0002c0002t0003g0082 others(32): Show |
35 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.2949+9724C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158880193 | |||||||
| chr4:158880207 | T | G | 35 | a0001c0001t0003g0184 a0002c0002t0003g0025 a0002c0002t0003g0082 others(32): Show |
35 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.2949+9738T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158880207 | |||||||
| chr4:158880208 | A | G | 35 | a0001c0001t0003g0184 a0002c0002t0003g0025 a0002c0002t0003g0082 others(32): Show |
35 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.2949+9739A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158880208 | |||||||
| chr4:158880220 | T | A | 35 | a0001c0001t0003g0184 a0002c0002t0003g0025 a0002c0002t0003g0082 others(32): Show |
35 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.2949+9751T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158880220 | |||||||
| chr4:158880332 | C | G | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0075 |
3 | HG00621.hp2 NA18951.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.2949+9863C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158880332 | |||||||
| chr4:158880813 | A | G | 1 | a0001c0007t0006g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2949+10344A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158880813 | |||||||
| chr4:158880877 | G | A | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2949+10408G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158880877 | |||||||
| chr4:158880959 | A | G | 57 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(54): Show |
58 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.2950-10487A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158880959 | |||||||
| chr4:158880996 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2950-10450C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158880996 | |||||||
| chr4:158881115 | C | T | 17 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0052 others(14): Show |
17 | HG00438.hp1 HG00597.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.2950-10331C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881115 | |||||||
| chr4:158881190 | CTCCACGG others(18): Show |
C | 7 | a0001c0001t0003g0036 a0001c0001t0007g0031 a0001c0001t0007g0032 others(4): Show |
7 | HG02258.hp2 HG02559.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2950-10199_2950-10 others(31): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158881190 | ||||||
| chr4:158881211 | C | G | 2 | a0002c0002t0004g0037 a0002c0002t0004g0038 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2950-10235C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881211 | |||||||
| chr4:158881221 | G | A | 106 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(103): Show |
106 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.2950-10225G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881221 | |||||||
| chr4:158881247 | G | T | 2 | a0002c0002t0004g0037 a0002c0002t0004g0038 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2950-10199G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881247 | |||||||
| chr4:158881272 | T | G | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0063 |
3 | HG00597.hp1 NA18957.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2950-10174T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881272 | |||||||
| chr4:158881287 | T | TCTTTCCA others(12): Show |
8 | a0001c0001t0005g0004 a0001c0001t0005g0006 a0001c0001t0005g0007 others(5): Show |
8 | HG01884.hp1 HG01981.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.2950-10156_2950-10 others(25): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158881287 | ||||||
| chr4:158881296 | GGTCTCCC others(23): Show |
G | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0063 |
3 | HG00597.hp1 NA18957.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2950-10140_2950-10 others(36): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158881296 | ||||||
| chr4:158881322 | G | A | 19 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0075 others(16): Show |
19 | HG00609.hp2 HG00621.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.2950-10124G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881322 | |||||||
| chr4:158881326 | C | CGTCTCCC others(18): Show |
2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2950-10076_2950-10 others(31): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158881326 | ||||||
| chr4:158881327 | G | A | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-10119G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881327 | |||||||
| chr4:158881327 | G | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0063 |
3 | HG00597.hp1 NA18957.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2950-10119G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881327 | |||||||
| chr4:158881361 | T | C | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0063 |
3 | HG00597.hp1 NA18957.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2950-10085T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881361 | |||||||
| chr4:158881363 | C | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0063 |
3 | HG00597.hp1 NA18957.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2950-10083C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881363 | |||||||
| chr4:158881376 | G | C | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0063 |
3 | HG00597.hp1 NA18957.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2950-10070G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881376 | |||||||
| chr4:158881380 | TC | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0063 |
3 | HG00597.hp1 NA18957.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2950-10063delC | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158881380 | ||||||
| chr4:158881383 | C | G | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0063 |
3 | HG00597.hp1 NA18957.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2950-10063C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881383 | |||||||
| chr4:158881393 | C | T | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-10053C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881393 | |||||||
| chr4:158881394 | T | C | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0063 |
3 | HG00597.hp1 NA18957.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2950-10052T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881394 | |||||||
| chr4:158881394 | TCTCTCTT others(18): Show |
T | 239 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(236): Show |
240 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.2950-9978_2950-995 others(29): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158881394 | ||||||
| chr4:158881394 | TCTCTCTT others(43): Show |
T | 1 | a0001c0001t0001g0138 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2950-10003_2950-99 others(55): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158881394 | ||||||
| chr4:158881444 | C | CCTCTCT | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0063 |
3 | HG00597.hp1 NA18957.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2950-10001_2950-99 others(11): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158881444 | ||||||
| chr4:158881481 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2950-9965C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881481 | |||||||
| chr4:158881509 | T | C | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-9937T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881509 | |||||||
| chr4:158881513 | C | T | 1 | a0001c0001t0002g0229 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2950-9933C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881513 | |||||||
| chr4:158881535 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2950-9911C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881535 | |||||||
| chr4:158881546 | CCCTGCCT others(6): Show |
C | 194 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(191): Show |
194 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.2950-9892_2950-988 others(17): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158881546 | ||||||
| chr4:158881561 | C | G | 2 | a0001c0001t0001g0040 a0001c0001t0008g0069 |
2 | NA18612.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.2950-9885C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881561 | |||||||
| chr4:158881626 | T | A | 3 | a0001c0001t0004g0136 a0001c0001t0012g0124 a0001c0001t0012g0125 |
3 | HG01891.hp2 HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2950-9820T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881626 | |||||||
| chr4:158881660 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2950-9786C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881660 | |||||||
| chr4:158881685 | G | A | 1 | a0001c0001t0019g0088 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2950-9761G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881685 | |||||||
| chr4:158881712 | C | T | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2950-9734C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881712 | |||||||
| chr4:158881783 | C | T | 7 | a0001c0001t0001g0052 a0001c0001t0001g0109 a0001c0001t0001g0110 others(4): Show |
7 | HG00438.hp1 HG01261.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2950-9663C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881783 | |||||||
| chr4:158881871 | A | AC | 9 | a0001c0001t0001g0039 a0001c0001t0001g0093 a0001c0001t0002g0211 others(6): Show |
9 | HG02145.hp2 HG02602.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2950-9571dupC | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158881871 | ||||||
| chr4:158881983 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2950-9463C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881983 | |||||||
| chr4:158882059 | T | G | 16 | a0001c0003t0004g0016 a0001c0003t0004g0018 a0001c0003t0004g0019 others(13): Show |
16 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.2950-9387T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882059 | |||||||
| chr4:158882187 | A | AGCAGCCG others(33): Show |
1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-9220_2950-918 others(44): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158882187 | ||||||
| chr4:158882187 | AGCAGCCG others(33): Show |
A | 1 | a0001c0001t0001g0155 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2950-9220_2950-918 others(44): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158882187 | ||||||
| chr4:158882193 | C | T | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0009c0010t0001g0106 |
3 | HG01517.hp2 HG02559.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.2950-9253C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882193 | |||||||
| chr4:158882197 | C | G | 50 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(47): Show |
51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.2950-9249C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882197 | |||||||
| chr4:158882226 | C | T | 17 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0041 others(14): Show |
17 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.2950-9220C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882226 | |||||||
| chr4:158882233 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2950-9213C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882233 | |||||||
| chr4:158882239 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2950-9207G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882239 | |||||||
| chr4:158882266 | T | C | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-9180T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882266 | |||||||
| chr4:158882274 | A | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-9172A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882274 | |||||||
| chr4:158882297 | G | A | 1 | a0001c0001t0002g0237 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2950-9149G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882297 | |||||||
| chr4:158882309 | C | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-9137C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882309 | |||||||
| chr4:158882365 | G | A | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-9081G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882365 | |||||||
| chr4:158882396 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2950-9050C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882396 | |||||||
| chr4:158882413 | G | A | 1 | a0002c0002t0003g0186 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2950-9033G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882413 | |||||||
| chr4:158882481 | A | AC | 69 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0050 others(66): Show |
69 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.2950-8961dupC | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158882481 | ||||||
| chr4:158882532 | C | T | 1 | a0001c0001t0018g0102 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2950-8914C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882532 | |||||||
| chr4:158882548 | G | A | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-8898G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882548 | |||||||
| chr4:158882568 | C | T | 50 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(47): Show |
51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.2950-8878C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882568 | |||||||
| chr4:158882653 | G | C | 1 | a0008c0018t0003g0183 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2950-8793G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882653 | |||||||
| chr4:158882787 | G | A | 2 | a0001c0001t0002g0206 a0001c0001t0002g0224 |
2 | HG02083.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.2950-8659G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882787 | |||||||
| chr4:158882800 | A | G | 4 | a0001c0001t0007g0031 a0001c0001t0007g0032 a0002c0002t0007g0169 others(1): Show |
4 | HG02559.hp1 HG02647.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2950-8646A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882800 | |||||||
| chr4:158882856 | C | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-8590C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882856 | |||||||
| chr4:158882859 | C | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-8587C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882859 | |||||||
| chr4:158882867 | C | T | 4 | a0001c0001t0007g0031 a0001c0001t0007g0032 a0002c0002t0007g0169 others(1): Show |
4 | HG02559.hp1 HG02647.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2950-8579C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882867 | |||||||
| chr4:158882976 | C | T | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2950-8470C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882976 | |||||||
| chr4:158883113 | A | C | 61 | a0001c0001t0001g0072 a0001c0001t0001g0083 a0001c0001t0001g0085 others(58): Show |
62 | HG00280.hp2 HG00597.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.2950-8333A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158883113 | |||||||
| chr4:158883115 | A | C | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-8331A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158883115 | |||||||
| chr4:158883146 | A | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0067 |
2 | HG02129.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.2950-8300A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158883146 | |||||||
| chr4:158883238 | T | G | 1 | a0001c0001t0001g0139 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2950-8208T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158883238 | |||||||
| chr4:158883243 | G | GT | 48 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(45): Show |
49 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.2950-8195dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158883243 | ||||||
| chr4:158883320 | C | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0123 |
2 | HG02257.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2950-8126C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158883320 | |||||||
| chr4:158883334 | T | C | 1 | a0002c0002t0003g0194 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2950-8112T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158883334 | |||||||
| chr4:158883342 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2950-8104C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158883342 | |||||||
| chr4:158883387 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2950-8059G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158883387 | |||||||
| chr4:158883429 | G | A | 1 | a0002c0002t0003g0172 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2950-8017G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158883429 | |||||||
| chr4:158883431 | C | T | 5 | a0001c0001t0002g0237 a0001c0001t0002g0240 a0001c0001t0002g0241 others(2): Show |
5 | HG01934.hp1 NA18955.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.2950-8015C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158883431 | |||||||
| chr4:158883521 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2950-7925G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158883521 | |||||||
| chr4:158883529 | T | C | 117 | a0001c0001t0001g0135 a0001c0001t0002g0001 a0001c0001t0002g0202 others(114): Show |
118 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.2950-7917T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158883529 | |||||||
| chr4:158883587 | T | C | 1 | a0001c0001t0003g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2950-7859T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158883587 | |||||||
| chr4:158883802 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2950-7644A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158883802 | |||||||
| chr4:158883949 | CT | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(199): Show |
203 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.2950-7477delT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158883949 | ||||||
| chr4:158883949 | CTT | C | 35 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(32): Show |
35 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.2950-7478_2950-747 others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158883949 | ||||||
| chr4:158884218 | T | G | 57 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(54): Show |
58 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.2950-7228T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158884218 | |||||||
| chr4:158884424 | A | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-7022A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158884424 | |||||||
| chr4:158884495 | G | T | 1 | a0001c0001t0001g0052 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2950-6951G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158884495 | |||||||
| chr4:158884723 | G | A | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-6723G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158884723 | |||||||
| chr4:158884733 | G | C | 3 | a0001c0007t0006g0163 a0001c0007t0006g0164 a0001c0007t0006g0165 |
3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2950-6713G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158884733 | |||||||
| chr4:158884762 | G | A | 2 | a0002c0002t0004g0037 a0002c0002t0004g0038 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2950-6684G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158884762 | |||||||
| chr4:158884858 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2950-6588C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158884858 | |||||||
| chr4:158884978 | T | TA | 10 | a0001c0001t0001g0072 a0001c0001t0001g0076 a0001c0001t0001g0127 others(7): Show |
10 | HG01192.hp1 HG01192.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.2950-6448dupA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158884978 | ||||||
| chr4:158884978 | TA | T | 56 | a0001c0001t0001g0066 a0001c0001t0002g0001 a0001c0001t0002g0202 others(53): Show |
57 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.2950-6448delA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158884978 | ||||||
| chr4:158885000 | A | T | 1 | a0006c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2950-6446A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158885000 | |||||||
| chr4:158885037 | T | G | 1 | a0001c0007t0006g0012 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2950-6409T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158885037 | |||||||
| chr4:158885594 | G | T | 1 | a0002c0002t0003g0178 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2950-5852G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158885594 | |||||||
| chr4:158885651 | G | A | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-5795G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158885651 | |||||||
| chr4:158885658 | C | T | 1 | a0001c0001t0002g0242 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2950-5788C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158885658 | |||||||
| chr4:158885810 | C | G | 4 | a0001c0001t0007g0031 a0001c0001t0007g0032 a0002c0002t0007g0169 others(1): Show |
4 | HG02559.hp1 HG02647.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2950-5636C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158885810 | |||||||
| chr4:158886051 | C | G | 8 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0063 others(5): Show |
8 | HG00597.hp1 HG01192.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.2950-5395C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158886051 | |||||||
| chr4:158886456 | T | G | 34 | a0001c0001t0003g0184 a0002c0002t0003g0025 a0002c0002t0003g0082 others(31): Show |
34 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.2950-4990T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158886456 | |||||||
| chr4:158886511 | C | A | 18 | a0001c0001t0003g0036 a0001c0003t0004g0016 a0001c0003t0004g0018 others(15): Show |
18 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(15): Show |
intron_variant | MODIFIER | c.2950-4935C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158886511 | |||||||
| chr4:158886526 | C | G | 34 | a0001c0001t0003g0184 a0002c0002t0003g0025 a0002c0002t0003g0082 others(31): Show |
34 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.2950-4920C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158886526 | |||||||
| chr4:158886860 | A | G | 6 | a0001c0001t0003g0036 a0001c0001t0007g0031 a0001c0001t0007g0032 others(3): Show |
6 | HG02559.hp1 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2950-4586A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158886860 | |||||||
| chr4:158887047 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2950-4399C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158887047 | |||||||
| chr4:158887064 | G | T | 8 | a0003c0004t0001g0054 a0003c0004t0001g0055 a0003c0004t0001g0056 others(5): Show |
8 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2950-4382G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158887064 | |||||||
| chr4:158887084 | A | G | 1 | a0002c0002t0007g0169 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2950-4362A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158887084 | |||||||
| chr4:158887631 | G | T | 4 | a0001c0001t0007g0031 a0001c0001t0007g0032 a0002c0002t0007g0169 others(1): Show |
4 | HG02559.hp1 HG02647.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2950-3815G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158887631 | |||||||
| chr4:158887736 | C | CA | 5 | a0001c0001t0002g0240 a0001c0001t0005g0006 a0001c0008t0010g0033 others(2): Show |
5 | HG01169.hp2 HG02257.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2950-3689dupA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158887736 | ||||||
| chr4:158887736 | C | CAA | 176 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0039 others(173): Show |
177 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.2950-3690_2950-368 others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158887736 | ||||||
| chr4:158887736 | C | CAAA | 46 | a0001c0001t0001g0015 a0001c0001t0001g0044 a0001c0001t0001g0045 others(43): Show |
46 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.2950-3691_2950-368 others(7): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158887736 | ||||||
| chr4:158887736 | C | CAAAA | 9 | a0001c0003t0004g0016 a0001c0003t0004g0018 a0001c0003t0004g0019 others(6): Show |
9 | HG00609.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2950-3692_2950-368 others(8): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158887736 | ||||||
| chr4:158887736 | C | CAAAAA | 7 | a0001c0003t0004g0020 a0001c0003t0004g0021 a0001c0003t0004g0022 others(4): Show |
7 | HG02055.hp1 HG02135.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2950-3693_2950-368 others(9): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158887736 | ||||||
| chr4:158887758 | C | A | 50 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(47): Show |
51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.2950-3688C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158887758 | |||||||
| chr4:158888228 | G | A | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2950-3218G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158888228 | |||||||
| chr4:158888288 | T | C | 10 | a0003c0004t0001g0054 a0003c0004t0001g0055 a0003c0004t0001g0056 others(7): Show |
10 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2950-3158T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158888288 | |||||||
| chr4:158888346 | A | G | 242 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(239): Show |
243 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(240): Show |
intron_variant | MODIFIER | c.2950-3100A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158888346 | |||||||
| chr4:158888404 | A | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2950-3042A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158888404 | |||||||
| chr4:158888432 | C | T | 1 | a0009c0010t0001g0106 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2950-3014C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158888432 | |||||||
| chr4:158888643 | T | G | 3 | a0001c0007t0006g0163 a0001c0007t0006g0164 a0001c0007t0006g0165 |
3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2950-2803T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158888643 | |||||||
| chr4:158888830 | C | T | 54 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(51): Show |
55 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.2950-2616C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158888830 | |||||||
| chr4:158888853 | G | A | 1 | a0001c0003t0004g0016 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2950-2593G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158888853 | |||||||
| chr4:158888875 | CAAAAAAA others(1): Show |
C | 34 | a0001c0001t0003g0184 a0002c0002t0003g0025 a0002c0002t0003g0082 others(31): Show |
34 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.2950-2561_2950-255 others(12): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158888875 | ||||||
| chr4:158889237 | AT | A | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2950-2203delT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158889237 | ||||||
| chr4:158889263 | A | G | 1 | a0001c0001t0007g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2950-2183A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158889263 | |||||||
| chr4:158889325 | T | A | 1 | a0001c0001t0007g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2950-2121T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158889325 | |||||||
| chr4:158889489 | C | A | 5 | a0002c0002t0003g0179 a0002c0002t0003g0190 a0002c0002t0003g0191 others(2): Show |
5 | HG00423.hp2 NA18966.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.2950-1957C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158889489 | |||||||
| chr4:158889566 | C | A | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-1880C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158889566 | |||||||
| chr4:158889619 | A | T | 1 | a0002c0002t0003g0182 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2950-1827A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158889619 | |||||||
| chr4:158889638 | A | G | 1 | a0001c0001t0002g0216 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2950-1808A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158889638 | |||||||
| chr4:158889805 | CT | C | 57 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(54): Show |
58 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.2950-1627delT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158889805 | ||||||
| chr4:158890633 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2950-813T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158890633 | |||||||
| chr4:158890767 | G | T | 2 | a0002c0002t0004g0037 a0002c0002t0004g0038 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2950-679G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158890767 | |||||||
| chr4:158890959 | C | T | 3 | a0001c0001t0007g0032 a0002c0002t0007g0169 a0002c0002t0007g0170 |
3 | HG02559.hp1 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2950-487C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158890959 | |||||||
| chr4:158891149 | T | C | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-297T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158891149 | |||||||
| chr4:158891158 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2950-288T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158891158 | |||||||
| chr4:158891192 | C | G | 5 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0009t0002g0234 others(2): Show |
5 | HG00735.hp2 HG01884.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2950-254C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158891192 | |||||||
| chr4:158891247 | C | A | 50 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(47): Show |
51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.2950-199C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158891247 | |||||||
| chr4:158891794 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3150+148C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158891794 | |||||||
| chr4:158891830 | G | A | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG00621.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.3150+184G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158891830 | |||||||
| chr4:158892047 | G | A | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3150+401G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158892047 | |||||||
| chr4:158892141 | C | CT | 11 | a0001c0001t0001g0083 a0001c0001t0001g0123 a0001c0001t0001g0140 others(8): Show |
11 | HG01891.hp2 HG02135.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.3150+516dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr4 | 158892141 | ||||||
| chr4:158892141 | CT | C | 52 | a0001c0001t0001g0052 a0001c0001t0001g0111 a0001c0001t0002g0001 others(49): Show |
53 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.3150+516delT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr4 | 158892141 | ||||||
| chr4:158892412 | G | A | 6 | a0001c0001t0003g0036 a0001c0001t0007g0031 a0001c0001t0007g0032 others(3): Show |
6 | HG02559.hp1 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.3150+766G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158892412 | |||||||
| chr4:158892552 | A | T | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3150+906A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158892552 | |||||||
| chr4:158892622 | C | T | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3150+976C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158892622 | |||||||
| chr4:158892624 | C | G | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3150+978C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158892624 | |||||||
| chr4:158892666 | C | G | 1 | a0006c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3150+1020C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158892666 | |||||||
| chr4:158892945 | AAG | A | 6 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0100 others(3): Show |
6 | HG00735.hp1 HG01081.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.3150+1302_3150+130 others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr4 | 158892945 | ||||||
| chr4:158893099 | A | C | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3150+1453A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158893099 | |||||||
| chr4:158893277 | T | C | 3 | a0001c0007t0006g0163 a0001c0007t0006g0164 a0001c0007t0006g0165 |
3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.3150+1631T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158893277 | |||||||
| chr4:158893481 | A | G | 2 | a0001c0001t0001g0079 a0001c0001t0001g0087 |
2 | NA18982.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.3150+1835A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158893481 | |||||||
| chr4:158893626 | T | TATGATCT others(369): Show |
1 | a0001c0001t0001g0049 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3150+1995_3150+199 others(380): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr4 | 158893626 | ||||||
| chr4:158893702 | G | A | 1 | a0002c0002t0003g0182 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3151-2048G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158893702 | |||||||
| chr4:158893891 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3151-1859A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158893891 | |||||||
| chr4:158894170 | C | CT | 17 | a0001c0001t0007g0031 a0001c0003t0004g0016 a0001c0003t0004g0019 others(14): Show |
17 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.3151-1562dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr4 | 158894170 | ||||||
| chr4:158894170 | CT | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0039 others(106): Show |
109 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.3151-1562delT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr4 | 158894170 | ||||||
| chr4:158894418 | T | C | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3151-1332T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158894418 | |||||||
| chr4:158894604 | G | A | 1 | a0002c0017t0003g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3151-1146G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158894604 | |||||||
| chr4:158894727 | G | A | 3 | a0001c0003t0004g0103 a0001c0003t0004g0104 a0001c0003t0004g0134 |
3 | HG00609.hp2 HG02135.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.3151-1023G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158894727 | |||||||
| chr4:158895344 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.3151-406T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158895344 | |||||||
| chr4:158895610 | G | T | 2 | a0001c0001t0001g0040 a0001c0001t0008g0069 |
2 | NA18612.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.3151-140G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158895610 | |||||||
| chr4:158895973 | C | T | 4 | a0001c0007t0006g0012 a0001c0007t0006g0163 a0001c0007t0006g0164 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3266+108C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158895973 | |||||||
| chr4:158896254 | GGCACATT | G | 4 | a0003c0004t0001g0055 a0003c0004t0001g0056 a0003c0004t0001g0058 others(1): Show |
4 | HG02109.hp2 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.3266+390_3266+396d others(9): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158896254 | |||||||
| chr4:158896497 | TTTGGG | T | 3 | a0001c0007t0006g0163 a0001c0007t0006g0164 a0001c0007t0006g0165 |
3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.3266+633_3266+637d others(7): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158896497 | |||||||
| chr4:158896503 | G | A | 3 | a0001c0007t0006g0163 a0001c0007t0006g0164 a0001c0007t0006g0165 |
3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.3266+638G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158896503 | |||||||
| chr4:158896777 | G | GT | 19 | a0001c0001t0001g0095 a0001c0001t0005g0159 a0001c0003t0004g0016 others(16): Show |
19 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.3266+924dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr4 | 158896777 | ||||||
| chr4:158896816 | C | A | 1 | a0001c0001t0001g0200 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3266+951C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158896816 | |||||||
| chr4:158896841 | G | GT | 43 | a0001c0001t0003g0184 a0001c0007t0006g0163 a0001c0007t0006g0164 others(40): Show |
43 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.3266+986dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr4 | 158896841 | ||||||
| chr4:158896841 | G | GTT | 50 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(47): Show |
51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.3266+985_3266+986d others(4): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr4 | 158896841 | ||||||
| chr4:158896851 | T | A | 4 | a0001c0001t0007g0032 a0002c0002t0007g0169 a0002c0002t0007g0170 others(1): Show |
4 | HG02559.hp1 HG02615.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3266+986T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158896851 | |||||||
| chr4:158897036 | C | T | 7 | a0001c0001t0001g0052 a0001c0001t0001g0109 a0001c0001t0001g0110 others(4): Show |
7 | HG00438.hp1 HG01261.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.3266+1171C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158897036 | |||||||
| chr4:158897154 | C | T | 1 | a0008c0018t0003g0183 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3266+1289C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158897154 | |||||||
| chr4:158897201 | A | C | 1 | a0001c0009t0002g0235 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3266+1336A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158897201 | |||||||
| chr4:158897205 | T | C | 1 | a0001c0001t0002g0218 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3266+1340T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158897205 | |||||||
| chr4:158897412 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0002c0017t0003g0030 |
3 | HG02258.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3266+1547G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158897412 | |||||||
| chr4:158897531 | G | A | 2 | a0002c0002t0003g0025 a0002c0002t0003g0171 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3266+1666G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158897531 | |||||||
| chr4:158897796 | C | A | 1 | a0001c0001t0002g0207 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3266+1931C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158897796 | |||||||
| chr4:158898031 | G | A | 1 | a0002c0002t0003g0172 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3266+2166G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158898031 | |||||||
| chr4:158898104 | C | T | 35 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(32): Show |
36 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.3266+2239C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158898104 | |||||||
| chr4:158898176 | A | T | 116 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(113): Show |
117 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.3266+2311A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158898176 | |||||||
| chr4:158898237 | G | A | 3 | a0002c0002t0003g0193 a0002c0002t0003g0194 a0002c0002t0003g0195 |
3 | NA18951.hp2 NA19011.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.3266+2372G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158898237 | |||||||
| chr4:158898374 | G | A | 126 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(123): Show |
126 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.3266+2509G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158898374 | |||||||
| chr4:158898600 | A | G | 1 | a0001c0007t0006g0012 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3266+2735A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158898600 | |||||||
| chr4:158898645 | T | C | 1 | a0001c0001t0001g0043 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.3266+2780T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158898645 | |||||||
| chr4:158898658 | C | T | 4 | a0001c0001t0007g0031 a0001c0001t0007g0032 a0002c0002t0007g0169 others(1): Show |
4 | HG02559.hp1 HG02647.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3266+2793C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158898658 | |||||||
| chr4:158898769 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3266+2904G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158898769 | |||||||
| chr4:158898824 | A | C | 2 | a0001c0001t0002g0206 a0001c0001t0002g0224 |
2 | HG02083.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.3266+2959A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158898824 | |||||||
| chr4:158898998 | T | C | 4 | a0001c0001t0001g0108 a0001c0001t0001g0113 a0001c0001t0001g0114 others(1): Show |
4 | HG03491.hp2 HG03704.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.3266+3133T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158898998 | |||||||
| chr4:158899109 | C | G | 1 | a0001c0003t0004g0104 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3266+3244C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158899109 | |||||||
| chr4:158899535 | A | G | 1 | a0002c0002t0003g0171 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3266+3670A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158899535 | |||||||
| chr4:158899755 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3266+3890G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158899755 | |||||||
| chr4:158899946 | C | G | 1 | a0001c0001t0001g0096 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3266+4081C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158899946 | |||||||
| chr4:158899981 | T | C | 1 | a0002c0002t0003g0082 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3266+4116T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158899981 | |||||||
| chr4:158900006 | A | T | 5 | a0001c0001t0002g0237 a0001c0001t0002g0240 a0001c0001t0002g0241 others(2): Show |
5 | HG01934.hp1 NA18955.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.3266+4141A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158900006 | |||||||
| chr4:158900216 | T | C | 1 | a0001c0001t0002g0204 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3267-4250T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158900216 | |||||||
| chr4:158900350 | A | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3267-4116A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158900350 | |||||||
| chr4:158900582 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3267-3884A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158900582 | |||||||
| chr4:158900704 | CTTTAT | C | 3 | a0002c0002t0003g0166 a0002c0002t0003g0185 a0002c0002t0003g0201 |
3 | HG00738.hp1 HG01169.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.3267-3758_3267-375 others(9): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr4 | 158900704 | ||||||
| chr4:158900826 | C | T | 2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3267-3640C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158900826 | |||||||
| chr4:158900853 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3267-3613A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158900853 | |||||||
| chr4:158900963 | T | C | 7 | a0001c0003t0004g0018 a0001c0003t0004g0019 a0001c0003t0004g0020 others(4): Show |
7 | HG02055.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.3267-3503T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158900963 | |||||||
| chr4:158900986 | C | T | 16 | a0001c0003t0004g0016 a0001c0003t0004g0018 a0001c0003t0004g0019 others(13): Show |
16 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.3267-3480C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158900986 | |||||||
| chr4:158901128 | A | AT | 47 | a0001c0001t0001g0039 a0001c0001t0001g0064 a0001c0001t0001g0067 others(44): Show |
47 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.3267-3316dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr4 | 158901128 | ||||||
| chr4:158901128 | A | ATT | 86 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0041 others(83): Show |
87 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.3267-3317_3267-331 others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr4 | 158901128 | ||||||
| chr4:158901128 | A | ATTT | 14 | a0001c0001t0002g0237 a0001c0001t0002g0238 a0001c0001t0002g0240 others(11): Show |
14 | HG00597.hp2 HG01884.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.3267-3318_3267-331 others(7): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr4 | 158901128 | ||||||
| chr4:158901128 | AT | A | 7 | a0001c0001t0001g0044 a0001c0001t0001g0059 a0001c0001t0001g0063 others(4): Show |
7 | HG00597.hp1 HG00639.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.3267-3316delT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr4 | 158901128 | ||||||
| chr4:158901128 | ATTTTTTT others(4): Show |
A | 3 | a0001c0007t0006g0163 a0001c0007t0006g0164 a0001c0007t0006g0165 |
3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.3267-3326_3267-331 others(15): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr4 | 158901128 | ||||||
| chr4:158901194 | G | A | 1 | a0003c0004t0001g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3267-3272G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158901194 | |||||||
| chr4:158901238 | A | G | 1 | a0002c0002t0003g0173 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3267-3228A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158901238 | |||||||
| chr4:158901287 | G | A | 1 | a0001c0001t0002g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3267-3179G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158901287 | |||||||
| chr4:158901502 | T | G | 4 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0219 others(1): Show |
4 | HG00639.hp2 HG00738.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.3267-2964T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158901502 | |||||||
| chr4:158901634 | G | A | 50 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(47): Show |
51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.3267-2832G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158901634 | |||||||
| chr4:158901717 | C | T | 1 | a0001c0001t0009g0244 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3267-2749C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158901717 | |||||||
| chr4:158901744 | A | G | 4 | a0001c0001t0001g0108 a0001c0001t0001g0113 a0001c0001t0001g0114 others(1): Show |
4 | HG03491.hp2 HG03704.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.3267-2722A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158901744 | |||||||
| chr4:158901901 | G | T | 16 | a0001c0003t0004g0016 a0001c0003t0004g0018 a0001c0003t0004g0019 others(13): Show |
16 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.3267-2565G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158901901 | |||||||
| chr4:158901911 | T | C | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG01517.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.3267-2555T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158901911 | |||||||
| chr4:158902130 | A | G | 1 | a0010c0013t0008g0150 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3267-2336A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158902130 | |||||||
| chr4:158902145 | C | T | 1 | a0003c0004t0001g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3267-2321C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158902145 | |||||||
| chr4:158902278 | A | G | 4 | a0002c0002t0003g0190 a0002c0002t0003g0191 a0002c0002t0003g0196 others(1): Show |
4 | NA18966.hp1 NA18967.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.3267-2188A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158902278 | |||||||
| chr4:158902296 | C | G | 3 | a0001c0007t0006g0163 a0001c0007t0006g0164 a0001c0007t0006g0165 |
3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.3267-2170C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158902296 | |||||||
| chr4:158902419 | C | T | 50 | a0001c0001t0002g0001 a0001c0001t0002g0202 a0001c0001t0002g0203 others(47): Show |
51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.3267-2047C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158902419 | |||||||
| chr4:158902521 | G | T | 78 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(75): Show |
78 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.3267-1945G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158902521 | |||||||
| chr4:158902625 | G | A | 4 | a0001c0003t0004g0024 a0001c0003t0004g0103 a0001c0003t0004g0104 others(1): Show |
4 | HG00609.hp2 HG02135.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.3267-1841G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158902625 | |||||||
| chr4:158902719 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3267-1747G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158902719 | |||||||
| chr4:158902955 | C | CGGCTCCC others(5): Show |
2 | a0001c0008t0010g0033 a0001c0008t0010g0034 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3267-1502_3267-150 others(16): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr4 | 158902955 | ||||||
| chr4:158902955 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3267-1511C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158902955 | |||||||
| chr4:158903103 | G | A | 1 | a0002c0002t0003g0198 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3267-1363G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158903103 | |||||||
| chr4:158903383 | G | A | 1 | a0001c0001t0004g0136 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3267-1083G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158903383 | |||||||
| chr4:158903426 | G | A | 1 | a0011c0012t0002g0208 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3267-1040G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158903426 | |||||||
| chr4:158903541 | C | G | 2 | a0001c0001t0003g0036 a0002c0002t0003g0172 |
2 | HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3267-925C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158903541 | |||||||
| chr4:158903619 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3267-847C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158903619 | |||||||
| chr4:158903843 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3267-623C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158903843 | |||||||
| chr4:158903909 | T | G | 1 | a0001c0001t0009g0231 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.3267-557T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158903909 | |||||||
| chr4:158904105 | A | C | 1 | a0001c0001t0005g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3267-361A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158904105 | |||||||
| chr4:158904127 | T | A | 250 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(247): Show |
251 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(248): Show |
intron_variant | MODIFIER | c.3267-339T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158904127 | |||||||
| chr4:158904148 | G | T | 10 | a0003c0004t0001g0054 a0003c0004t0001g0055 a0003c0004t0001g0056 others(7): Show |
10 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.3267-318G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158904148 | |||||||
| chr4:158904242 | C | A | 34 | a0001c0001t0003g0184 a0002c0002t0003g0025 a0002c0002t0003g0082 others(31): Show |
34 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.3267-224C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158904242 |