Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79815 |
| ensemblid | ENSG00000104361.10 |
| hgncid | 25854 |
| symbol | NIPAL2 |
| name | NIPA like domain containing 2 |
| refseq_nuc | NM_001321635.2 |
| refseq_prot | NP_001308564.1 |
| ensembl_nuc | ENST00000430223.7 |
| ensembl_prot | ENSP00000407087.2 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 98189826 |
| end | 98294235 |
| strand | - |
| ver | v1.2 |
| region | chr8:98189826-98294235 |
| region5000 | chr8:98184826-98299235 |
| regionname0 | NIPAL2_chr8_98189826_98294235 |
| regionname5000 | NIPAL2_chr8_98184826_98299235 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 383 | 305 | 81 | 66 | 111 | 13 | 32 | 82 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | MAAVA others(378): Show |
chr8 | 98184826 | 98299235 |
| a0002 | 0/0 | 383 | 24 | 0 | 1 | 23 | 0 | 0 | 12 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | MAAVA others(378): Show |
chr8 | 98184826 | 98299235 |
| a0003 | 0/0 | 383 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | MAAVA others(378): Show |
chr8 | 98184826 | 98299235 |
| a0004 | 0/0 | 383 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | MAAVA others(378): Show |
chr8 | 98184826 | 98299235 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1149 | 187 | 53 | 41 | 65 | 7 | 19 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | ATGGC others(1144): Show |
chr8 | 98184826 | 98299235 | ||
| a0001c0002 | 0/0 | 1149 | 111 | 21 | 25 | 46 | 6 | 13 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | ATGGC others(1144): Show |
chr8 | 98184826 | 98299235 | ||
| a0001c0005 | 0/0 | 1149 | 5 | 5 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | ATGGC others(1144): Show |
chr8 | 98184826 | 98299235 | ||
| a0001c0006 | 0/0 | 1149 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | ATGGC others(1144): Show |
chr8 | 98184826 | 98299235 | ||
| a0002c0003 | 0/0 | 1149 | 15 | 0 | 0 | 15 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | ATGGC others(1144): Show |
chr8 | 98184826 | 98299235 | ||
| a0002c0004 | 0/0 | 1149 | 9 | 0 | 1 | 8 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | ATGGC others(1144): Show |
chr8 | 98184826 | 98299235 | ||
| a0003c0007 | 0/0 | 1149 | 2 | 0 | 1 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | ATGGC others(1144): Show |
chr8 | 98184826 | 98299235 | ||
| a0004c0008 | 0/0 | 1149 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | ATGGC others(1144): Show |
chr8 | 98184826 | 98299235 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4403 | 48 | 19 | 5 | 17 | 3 | 4 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4398): Show |
chr8 | 98184826 | 98299235 |
| a0001c0001t0002 | 1/0 | 4402 | 61 | 17 | 11 | 29 | 1 | 2 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4397): Show |
chr8 | 98184826 | 98299235 |
| a0001c0001t0003 | 0/1 | 4402 | 44 | 9 | 14 | 10 | 3 | 7 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4397): Show |
chr8 | 98184826 | 98299235 |
| a0001c0001t0005 | 0/0 | 4402 | 11 | 1 | 4 | 1 | 0 | 5 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4397): Show |
chr8 | 98184826 | 98299235 |
| a0001c0001t0007 | 0/0 | 4398 | 4 | 2 | 2 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4393): Show |
chr8 | 98184826 | 98299235 |
| a0001c0001t0008 | 0/0 | 4402 | 4 | 0 | 0 | 4 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4397): Show |
chr8 | 98184826 | 98299235 |
| a0001c0001t0009 | 0/0 | 4402 | 3 | 3 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4397): Show |
chr8 | 98184826 | 98299235 |
| a0001c0001t0010 | 0/0 | 4402 | 3 | 0 | 3 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4397): Show |
chr8 | 98184826 | 98299235 |
| a0001c0001t0011 | 0/0 | 4402 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4397): Show |
chr8 | 98184826 | 98299235 |
| a0001c0001t0014 | 0/0 | 4402 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4397): Show |
chr8 | 98184826 | 98299235 |
| a0001c0001t0015 | 0/0 | 4402 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4397): Show |
chr8 | 98184826 | 98299235 |
| a0001c0001t0016 | 0/0 | 4402 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4397): Show |
chr8 | 98184826 | 98299235 |
| a0001c0001t0018 | 0/0 | 4402 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4397): Show |
chr8 | 98184826 | 98299235 |
| a0001c0001t0021 | 0/0 | 4402 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4397): Show |
chr8 | 98184826 | 98299235 |
| a0001c0001t0024 | 0/0 | 4403 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4398): Show |
chr8 | 98184826 | 98299235 |
| a0001c0002t0001 | 0/0 | 4403 | 82 | 3 | 20 | 42 | 6 | 11 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4398): Show |
chr8 | 98184826 | 98299235 |
| a0001c0002t0004 | 0/0 | 4402 | 18 | 16 | 2 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4397): Show |
chr8 | 98184826 | 98299235 |
| a0001c0002t0006 | 0/0 | 4402 | 4 | 0 | 0 | 4 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4397): Show |
chr8 | 98184826 | 98299235 |
| a0001c0002t0013 | 0/0 | 4403 | 2 | 0 | 2 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4398): Show |
chr8 | 98184826 | 98299235 |
| a0001c0002t0019 | 0/0 | 4403 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4398): Show |
chr8 | 98184826 | 98299235 |
| a0001c0002t0020 | 0/0 | 4402 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4397): Show |
chr8 | 98184826 | 98299235 |
| a0001c0002t0022 | 0/0 | 4403 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4398): Show |
chr8 | 98184826 | 98299235 |
| a0001c0002t0023 | 0/0 | 4403 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4398): Show |
chr8 | 98184826 | 98299235 |
| a0001c0002t0025 | 0/0 | 4403 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4398): Show |
chr8 | 98184826 | 98299235 |
| a0001c0005t0001 | 0/0 | 4403 | 3 | 3 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4398): Show |
chr8 | 98184826 | 98299235 |
| a0001c0005t0004 | 0/0 | 4402 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4397): Show |
chr8 | 98184826 | 98299235 |
| a0001c0006t0002 | 0/0 | 4402 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4397): Show |
chr8 | 98184826 | 98299235 |
| a0002c0003t0001 | 0/0 | 4403 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4398): Show |
chr8 | 98184826 | 98299235 |
| a0002c0003t0002 | 0/0 | 4402 | 10 | 0 | 0 | 10 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4397): Show |
chr8 | 98184826 | 98299235 |
| a0002c0003t0012 | 0/0 | 4402 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4397): Show |
chr8 | 98184826 | 98299235 |
| a0002c0003t0017 | 0/0 | 4402 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4397): Show |
chr8 | 98184826 | 98299235 |
| a0002c0004t0001 | 0/0 | 4403 | 9 | 0 | 1 | 8 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4398): Show |
chr8 | 98184826 | 98299235 |
| a0003c0007t0002 | 0/0 | 4402 | 2 | 0 | 1 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4397): Show |
chr8 | 98184826 | 98299235 |
| a0004c0008t0003 | 0/0 | 4402 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | GAGCA others(4397): Show |
chr8 | 98184826 | 98299235 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0212 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0275 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0005g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0005g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0005g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0005g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0005g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0005g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0005g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0007g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0007g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0007g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0007g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0008g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0008g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0008g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0008g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0009g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0009g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0009g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0010g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0010g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0010g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0011g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0011g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0014g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0014g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0015g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0016g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0018g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0021g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0024g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0004g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0006g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0006g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0006g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0006g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0013g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0013g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0019g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0020g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0022g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0023g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0025g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0005t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0005t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0005t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0005t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0005t0004g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0006t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0006t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0012g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0012g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0017g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0004t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0004t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0004t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0004t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0004t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0004t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0004t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0004t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0003c0007t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0003c0007t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0004c0008t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0007 | t0002 | g0236 | EUR | GBR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0060 | EUR | GBR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0105 | EUR | FIN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0152 | EUR | FIN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0144 | EUR | FIN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | FIN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00438 | hp2 | a0002 | c0004 | t0001 | g0271 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0207 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00609 | hp2 | a0002 | c0004 | t0001 | g0222 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00621 | hp1 | a0002 | c0003 | t0001 | g0273 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00642 | hp1 | a0001 | c0001 | t0010 | g0137 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0230 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00733 | hp1 | a0001 | c0001 | t0007 | g0291 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00733 | hp2 | a0001 | c0001 | t0024 | g0150 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0164 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0319 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00738 | hp2 | a0001 | c0001 | t0007 | g0292 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0277 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01069 | hp2 | a0001 | c0001 | t0010 | g0140 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0045 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01071 | hp2 | a0001 | c0001 | t0010 | g0139 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0143 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0266 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01099 | hp2 | a0001 | c0001 | t0018 | g0163 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01106 | hp2 | a0003 | c0007 | t0002 | g0066 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0063 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0183 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0276 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0020 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01175 | hp2 | a0001 | c0002 | t0025 | g0318 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0062 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01243 | hp1 | a0001 | c0002 | t0004 | g0325 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01243 | hp2 | a0001 | c0002 | t0004 | g0084 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0244 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0101 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01257 | hp2 | a0001 | c0002 | t0013 | g0058 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01258 | hp1 | a0001 | c0002 | t0013 | g0057 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0076 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01346 | hp2 | a0001 | c0001 | t0005 | g0136 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0119 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0248 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0181 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0056 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0142 | EUR | IBS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0003 | EUR | IBS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0141 | EUR | IBS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0003 | EUR | IBS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01884 | hp1 | a0001 | c0002 | t0004 | g0310 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0326 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0043 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01975 | hp2 | a0002 | c0004 | t0001 | g0053 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0282 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0097 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0327 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0104 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0256 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0052 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02015 | hp2 | a0002 | c0004 | t0001 | g0287 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02055 | hp1 | a0001 | c0002 | t0004 | g0295 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02055 | hp2 | a0001 | c0002 | t0004 | g0017 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02056 | hp1 | a0001 | c0001 | t0005 | g0196 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02080 | hp1 | a0002 | c0003 | t0002 | g0065 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02080 | hp2 | a0002 | c0003 | t0002 | g0201 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02129 | hp2 | a0002 | c0003 | t0002 | g0167 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02132 | hp1 | a0002 | c0004 | t0001 | g0206 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02145 | hp1 | a0001 | c0005 | t0001 | g0035 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | CDX | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02155 | hp2 | a0001 | c0001 | t0008 | g0161 | EAS | CDX | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | CDX | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CDX | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0116 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0284 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0132 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0046 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0059 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0051 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0263 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0208 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02523 | hp1 | a0002 | c0003 | t0002 | g0068 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0191 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02572 | hp1 | a0001 | c0001 | t0016 | g0293 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0021 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0134 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0316 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02630 | hp2 | a0001 | c0002 | t0004 | g0015 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0127 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0321 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0006 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02723 | hp2 | a0001 | c0002 | t0020 | g0086 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0096 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0296 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02809 | hp2 | a0001 | c0001 | t0009 | g0013 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02818 | hp1 | a0001 | c0005 | t0004 | g0029 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02886 | hp2 | a0001 | c0002 | t0004 | g0257 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02895 | hp1 | a0001 | c0002 | t0004 | g0083 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02897 | hp2 | a0001 | c0002 | t0004 | g0082 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | ESN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02922 | hp2 | a0001 | c0002 | t0004 | g0081 | AFR | ESN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0283 | AFR | ESN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02965 | hp2 | a0001 | c0002 | t0004 | g0114 | AFR | ESN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | ESN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0131 | AFR | ESN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02976 | hp1 | a0001 | c0006 | t0002 | g0117 | AFR | ESN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02976 | hp2 | a0001 | c0002 | t0004 | g0304 | AFR | ESN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03017 | hp2 | a0001 | c0002 | t0023 | g0231 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0324 | AFR | MSL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0185 | AFR | MSL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03130 | hp1 | a0001 | c0006 | t0002 | g0019 | AFR | ESN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03209 | hp1 | a0001 | c0005 | t0004 | g0312 | AFR | MSL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03209 | hp2 | a0001 | c0002 | t0004 | g0037 | AFR | MSL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | MSL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03225 | hp2 | a0001 | c0002 | t0004 | g0294 | AFR | MSL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0155 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0260 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03453 | hp1 | a0001 | c0002 | t0004 | g0011 | AFR | MSL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | MSL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0009 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03491 | hp2 | a0001 | c0002 | t0019 | g0320 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0158 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0007 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03516 | hp1 | a0004 | c0008 | t0003 | g0262 | AFR | ESN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03516 | hp2 | a0001 | c0001 | t0021 | g0285 | AFR | ESN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03540 | hp2 | a0001 | c0001 | t0009 | g0012 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03579 | hp1 | a0001 | c0005 | t0001 | g0026 | AFR | MSL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0038 | AFR | MSL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0122 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0203 | SAS | STU | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03688 | hp2 | a0001 | c0001 | t0015 | g0195 | SAS | STU | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0313 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0135 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0149 | SAS | BEB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0128 | SAS | BEB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0036 | SAS | BEB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03942 | hp2 | a0001 | c0001 | t0005 | g0233 | SAS | BEB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0281 | SAS | STU | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0255 | SAS | STU | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | STU | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0064 | SAS | STU | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG04228 | hp1 | a0001 | c0001 | t0005 | g0008 | SAS | STU | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | STU | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18612 | hp1 | a0002 | c0004 | t0001 | g0078 | EAS | CHB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18747 | hp1 | a0002 | c0003 | t0017 | g0217 | EAS | CHB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | CHB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0307 | AFR | YRI | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0322 | AFR | YRI | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18941 | hp1 | a0002 | c0004 | t0001 | g0225 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18942 | hp1 | a0001 | c0001 | t0011 | g0005 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18944 | hp2 | a0002 | c0004 | t0001 | g0253 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0298 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18947 | hp2 | a0002 | c0003 | t0002 | g0077 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18960 | hp2 | a0002 | c0003 | t0012 | g0216 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18963 | hp1 | a0002 | c0003 | t0012 | g0213 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18966 | hp1 | a0001 | c0001 | t0014 | g0069 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18970 | hp2 | a0002 | c0003 | t0002 | g0194 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18979 | hp2 | a0002 | c0003 | t0002 | g0250 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18980 | hp1 | a0002 | c0003 | t0001 | g0223 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18983 | hp2 | a0002 | c0003 | t0002 | g0224 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0299 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18990 | hp2 | a0002 | c0003 | t0002 | g0192 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18992 | hp1 | a0001 | c0001 | t0011 | g0004 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18993 | hp2 | a0002 | c0003 | t0002 | g0075 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18997 | hp1 | a0001 | c0002 | t0006 | g0079 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0315 | AFR | LWK | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0309 | AFR | LWK | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0130 | AFR | LWK | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0071 | AFR | LWK | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19062 | hp1 | a0001 | c0001 | t0008 | g0034 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19063 | hp2 | a0001 | c0001 | t0014 | g0187 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19064 | hp1 | a0001 | c0001 | t0008 | g0032 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19066 | hp2 | a0001 | c0002 | t0006 | g0264 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19082 | hp1 | a0001 | c0002 | t0006 | g0061 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19084 | hp1 | a0001 | c0002 | t0006 | g0246 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19088 | hp2 | a0001 | c0001 | t0008 | g0031 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19091 | hp2 | a0002 | c0004 | t0001 | g0297 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0323 | AFR | YRI | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA20129 | hp1 | a0001 | c0002 | t0004 | g0305 | AFR | ASW | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0138 | AFR | ASW | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0317 | EUR | TSI | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0129 | EUR | TSI | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0237 | EUR | TSI | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0209 | EUR | TSI | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0145 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0301 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0115 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02486 | hp1 | a0001 | c0002 | t0022 | g0303 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02486 | hp2 | a0001 | c0005 | t0001 | g0030 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02559 | hp2 | a0001 | c0002 | t0004 | g0306 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | MSL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | MSL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | USA | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0311 | AFR | USA | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0328 | AFR | USA | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA20300 | hp2 | a0001 | c0002 | t0004 | g0087 | AFR | USA | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0275 | REF | REF | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0212 | REF | REF | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:98205163 | T | C | 1 | a0003 | 2 | HG00099.hp1 HG01106.hp2 |
missense_variant | MODERATE | c.739A>G | p.Ile247Val | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/11 | 837/4402 | 739/1152 | 247/383 | chr8 | 98205163 | |||
| chr8:98222544 | T | G | 1 | a0002 | 24 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(21): Show |
missense_variant | MODERATE | c.493A>C | p.Thr165Pro | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/11 | 591/4402 | 493/1152 | 165/383 | chr8 | 98222544 | |||
| chr8:98252527 | G | T | 1 | a0004 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.312C>A | p.Asn104Lys | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/11 | 410/4402 | 312/1152 | 104/383 | chr8 | 98252527 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:98195962 | A | C | 3 | a0001c0002 a0001c0005 a0002c0004 |
125 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(122): Show |
synonymous_variant | LOW | c.924T>G | p.Thr308Thr | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/11 | 1022/4402 | 924/1152 | 308/383 | chr8 | 98195962 | |||
| chr8:98254043 | C | T | 2 | a0001c0005 a0001c0006 |
7 | HG02145.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
synonymous_variant | LOW | c.180G>A | p.Val60Val | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 2/11 | 278/4402 | 180/1152 | 60/383 | chr8 | 98254043 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:98189921 | A | G | 1 | a0002c0003t0017 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3057T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 3057 | chr8 | 98189921 | ||||||
| chr8:98190029 | C | T | 1 | a0001c0002t0025 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2949G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 2949 | chr8 | 98190029 | ||||||
| chr8:98190116 | T | C | 1 | a0001c0001t0009 | 3 | HG02809.hp2 HG03098.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2862A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 2862 | chr8 | 98190116 | ||||||
| chr8:98190132 | T | C | 1 | a0001c0001t0018 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2846A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 2846 | chr8 | 98190132 | ||||||
| chr8:98190237 | G | A | 1 | a0001c0002t0013 | 2 | HG01257.hp2 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2741C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 2741 | chr8 | 98190237 | ||||||
| chr8:98190313 | TTTTG | T | 1 | a0001c0001t0007 | 4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2661_*2664delCAAA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 2661 | chr8 | 98190313 | ||||||
| chr8:98190314 | T | G | 2 | a0001c0001t0001 a0002c0003t0001 |
49 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*2664A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 2664 | chr8 | 98190314 | ||||||
| chr8:98190316 | T | A | 1 | a0001c0002t0004 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2662A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 2662 | chr8 | 98190316 | ||||||
| chr8:98190359 | G | A | 15 | a0001c0001t0001 a0001c0001t0021 a0001c0002t0001 others(12): Show |
176 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*2619C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 2619 | chr8 | 98190359 | ||||||
| chr8:98190362 | G | A | 1 | a0001c0001t0021 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2616C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 2616 | chr8 | 98190362 | ||||||
| chr8:98190665 | T | C | 1 | a0001c0001t0008 | 4 | HG02155.hp2 NA19062.hp1 NA19064.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2313A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 2313 | chr8 | 98190665 | ||||||
| chr8:98190760 | C | T | 1 | a0001c0002t0023 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2218G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 2218 | chr8 | 98190760 | ||||||
| chr8:98191079 | C | T | 1 | a0001c0002t0022 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1899G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 1899 | chr8 | 98191079 | ||||||
| chr8:98191156 | G | A | 1 | a0001c0001t0021 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1822C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 1822 | chr8 | 98191156 | ||||||
| chr8:98191178 | A | G | 1 | a0001c0001t0021 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1800T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 1800 | chr8 | 98191178 | ||||||
| chr8:98191280 | C | T | 5 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0015 others(2): Show |
49 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1698G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 1698 | chr8 | 98191280 | ||||||
| chr8:98191330 | C | T | 3 | a0001c0002t0004 a0001c0002t0020 a0001c0005t0004 |
21 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1648G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 1648 | chr8 | 98191330 | ||||||
| chr8:98191481 | G | GC | 12 | a0001c0001t0001 a0001c0001t0024 a0001c0002t0001 others(9): Show |
155 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*1496dupG | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 1496 | chr8 | 98191481 | ||||||
| chr8:98191564 | C | T | 1 | a0001c0001t0016 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1414G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 1414 | chr8 | 98191564 | ||||||
| chr8:98191700 | C | T | 1 | a0001c0002t0020 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1278G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 1278 | chr8 | 98191700 | ||||||
| chr8:98191710 | T | C | 16 | a0001c0001t0001 a0001c0001t0021 a0001c0001t0024 others(13): Show |
177 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*1268A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 1268 | chr8 | 98191710 | ||||||
| chr8:98192160 | C | T | 1 | a0001c0001t0015 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*818G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 818 | chr8 | 98192160 | ||||||
| chr8:98192315 | A | G | 1 | a0002c0003t0012 | 2 | NA18960.hp2 NA18963.hp1 |
3_prime_UTR_variant | MODIFIER | c.*663T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 663 | chr8 | 98192315 | ||||||
| chr8:98192490 | C | T | 16 | a0001c0001t0001 a0001c0001t0021 a0001c0001t0024 others(13): Show |
177 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*488G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 488 | chr8 | 98192490 | ||||||
| chr8:98192495 | T | G | 12 | a0001c0001t0001 a0001c0001t0024 a0001c0002t0001 others(9): Show |
155 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*483A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 483 | chr8 | 98192495 | ||||||
| chr8:98192538 | T | A | 12 | a0001c0001t0001 a0001c0001t0024 a0001c0002t0001 others(9): Show |
155 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*440A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 440 | chr8 | 98192538 | ||||||
| chr8:98192543 | GA | G | 1 | a0001c0002t0006 | 4 | NA18997.hp1 NA19066.hp2 NA19082.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*434delT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 434 | chr8 | 98192543 | ||||||
| chr8:98192652 | C | T | 1 | a0001c0002t0019 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*326G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 326 | chr8 | 98192652 | ||||||
| chr8:98192818 | G | A | 1 | a0001c0001t0010 | 3 | HG00642.hp1 HG01069.hp2 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*160C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 160 | chr8 | 98192818 | ||||||
| chr8:98192883 | T | C | 20 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(17): Show |
199 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*95A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 95 | chr8 | 98192883 | ||||||
| chr8:98192921 | G | C | 1 | a0001c0001t0014 | 2 | NA18966.hp1 NA19063.hp2 |
3_prime_UTR_variant | MODIFIER | c.*57C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 57 | chr8 | 98192921 | ||||||
| chr8:98294139 | A | G | 1 | a0001c0001t0011 | 2 | NA18942.hp1 NA18992.hp1 |
5_prime_UTR_variant | MODIFIER | c.-2T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/11 | 2 | chr8 | 98294139 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:98193113 | G | A | 4 | a0001c0001t0002g0106 a0001c0001t0002g0108 a0001c0001t0002g0111 others(1): Show |
4 | HG02109.hp1 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1040-23C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98193113 | |||||||
| chr8:98193195 | C | G | 3 | a0001c0002t0001g0200 a0001c0002t0001g0204 a0001c0002t0001g0205 |
3 | HG00558.hp1 NA18991.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1040-105G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98193195 | |||||||
| chr8:98193201 | G | A | 4 | a0001c0001t0007g0291 a0001c0001t0007g0292 a0001c0001t0007g0307 others(1): Show |
4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1040-111C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98193201 | |||||||
| chr8:98193293 | C | G | 1 | a0001c0001t0002g0133 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1040-203G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98193293 | |||||||
| chr8:98193384 | C | T | 195 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(192): Show |
197 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.1040-294G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98193384 | |||||||
| chr8:98193386 | T | G | 5 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(2): Show |
5 | HG01109.hp1 HG02280.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1040-296A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98193386 | |||||||
| chr8:98193616 | C | T | 6 | a0001c0001t0002g0309 a0001c0001t0002g0311 a0001c0001t0002g0322 others(3): Show |
6 | HG02976.hp1 HG03098.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1040-526G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98193616 | |||||||
| chr8:98193732 | G | A | 3 | a0001c0001t0001g0109 a0001c0001t0001g0184 a0001c0001t0001g0290 |
3 | HG02572.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1040-642C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98193732 | |||||||
| chr8:98193746 | T | G | 128 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(125): Show |
129 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.1040-656A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98193746 | |||||||
| chr8:98193802 | C | CA | 117 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(114): Show |
118 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.1040-713dupT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98193802 | |||||||
| chr8:98193802 | CA | C | 38 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(35): Show |
38 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.1040-713delT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98193802 | |||||||
| chr8:98193855 | T | C | 19 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(16): Show |
19 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1040-765A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98193855 | |||||||
| chr8:98194070 | G | A | 103 | a0001c0002t0001g0003 a0001c0002t0001g0020 a0001c0002t0001g0021 others(100): Show |
104 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.1039+658C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98194070 | |||||||
| chr8:98194082 | A | G | 1 | a0001c0001t0003g0018 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1039+646T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98194082 | |||||||
| chr8:98194112 | GAGAGTGC others(3): Show |
G | 1 | a0001c0002t0004g0310 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1039+606_1039+615d others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98194112 | |||||||
| chr8:98194125 | G | A | 1 | a0001c0002t0004g0310 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1039+603C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98194125 | |||||||
| chr8:98194126 | C | T | 1 | a0001c0002t0004g0310 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1039+602G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98194126 | |||||||
| chr8:98194140 | A | G | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039+588T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98194140 | |||||||
| chr8:98194205 | C | T | 1 | a0001c0001t0005g0196 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1039+523G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98194205 | |||||||
| chr8:98194233 | G | A | 4 | a0001c0001t0002g0322 a0001c0001t0002g0323 a0001c0001t0002g0324 others(1): Show |
4 | HG02976.hp1 HG03098.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039+495C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98194233 | |||||||
| chr8:98194359 | G | C | 2 | a0002c0003t0002g0167 a0002c0003t0002g0250 |
2 | HG02129.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1039+369C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98194359 | |||||||
| chr8:98194646 | T | C | 12 | a0001c0002t0001g0199 a0001c0002t0001g0211 a0001c0002t0001g0214 others(9): Show |
12 | NA18953.hp2 NA18962.hp2 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.1039+82A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98194646 | |||||||
| chr8:98194874 | G | A | 1 | a0001c0002t0001g0072 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.945-52C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98194874 | |||||||
| chr8:98194889 | G | A | 1 | a0001c0001t0021g0285 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.945-67C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98194889 | |||||||
| chr8:98194900 | T | C | 3 | a0001c0002t0001g0003 a0001c0002t0001g0127 a0001c0002t0001g0128 |
4 | HG01515.hp2 HG01517.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.945-78A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98194900 | |||||||
| chr8:98194978 | A | G | 23 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(20): Show |
23 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.945-156T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98194978 | |||||||
| chr8:98195116 | A | G | 13 | a0001c0001t0005g0002 a0001c0001t0005g0136 a0001c0001t0005g0138 others(10): Show |
14 | HG00642.hp1 HG00733.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.945-294T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98195116 | |||||||
| chr8:98195150 | A | G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(1): Show |
4 | HG01109.hp1 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.945-328T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98195150 | |||||||
| chr8:98195168 | T | C | 1 | a0002c0004t0001g0078 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.945-346A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98195168 | |||||||
| chr8:98195572 | T | A | 1 | a0001c0002t0001g0145 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.944+370A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98195572 | |||||||
| chr8:98195633 | C | T | 4 | a0001c0001t0009g0012 a0001c0001t0009g0013 a0001c0001t0009g0185 others(1): Show |
4 | HG02572.hp1 HG02809.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.944+309G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98195633 | |||||||
| chr8:98195699 | T | C | 1 | a0001c0002t0001g0021 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.944+243A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98195699 | |||||||
| chr8:98195721 | C | T | 124 | a0001c0002t0001g0003 a0001c0002t0001g0020 a0001c0002t0001g0021 others(121): Show |
125 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.944+221G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98195721 | |||||||
| chr8:98195780 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.944+162G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98195780 | |||||||
| chr8:98195837 | T | C | 171 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(168): Show |
173 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.944+105A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98195837 | |||||||
| chr8:98195882 | G | A | 19 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(16): Show |
19 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.944+60C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98195882 | |||||||
| chr8:98195892 | C | T | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.944+50G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98195892 | |||||||
| chr8:98195896 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.944+46T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98195896 | |||||||
| chr8:98195914 | A | C | 19 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(16): Show |
19 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.944+28T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98195914 | |||||||
| chr8:98196016 | G | T | 41 | a0001c0001t0001g0177 a0001c0001t0003g0001 a0001c0001t0003g0043 others(38): Show |
43 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.881-11C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98196016 | |||||||
| chr8:98196362 | GC | G | 3 | a0001c0002t0001g0003 a0001c0002t0001g0127 a0001c0002t0001g0128 |
4 | HG01515.hp2 HG01517.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.881-358delG | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98196362 | |||||||
| chr8:98196366 | G | T | 2 | a0001c0001t0001g0239 a0001c0001t0001g0241 |
2 | HG02683.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.881-361C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98196366 | |||||||
| chr8:98196466 | G | T | 1 | a0001c0001t0005g0006 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.881-461C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98196466 | |||||||
| chr8:98196630 | T | G | 17 | a0001c0001t0005g0002 a0001c0001t0005g0136 a0001c0001t0005g0138 others(14): Show |
18 | HG00642.hp1 HG00733.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.881-625A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98196630 | |||||||
| chr8:98196659 | G | T | 2 | a0001c0002t0004g0017 a0001c0005t0004g0312 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.881-654C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98196659 | |||||||
| chr8:98196793 | G | A | 1 | a0001c0002t0004g0011 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.881-788C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98196793 | |||||||
| chr8:98196809 | G | A | 1 | a0001c0001t0002g0169 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.881-804C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98196809 | |||||||
| chr8:98196834 | G | A | 157 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(154): Show |
158 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.881-829C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98196834 | |||||||
| chr8:98196858 | A | G | 1 | a0001c0002t0004g0304 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.881-853T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98196858 | |||||||
| chr8:98196891 | A | C | 3 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0002c0003t0002g0068 |
3 | HG02523.hp1 NA18942.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.881-886T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98196891 | |||||||
| chr8:98196976 | C | A | 101 | a0001c0002t0001g0003 a0001c0002t0001g0020 a0001c0002t0001g0021 others(98): Show |
102 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.881-971G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98196976 | |||||||
| chr8:98197004 | T | C | 2 | a0001c0002t0001g0319 a0001c0002t0019g0320 |
2 | HG00738.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.881-999A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98197004 | |||||||
| chr8:98197020 | C | T | 121 | a0001c0002t0001g0003 a0001c0002t0001g0020 a0001c0002t0001g0021 others(118): Show |
122 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.881-1015G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98197020 | |||||||
| chr8:98197081 | CT | C | 30 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(27): Show |
30 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.881-1077delA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98197081 | |||||||
| chr8:98197311 | C | T | 3 | a0001c0001t0003g0043 a0001c0001t0003g0052 a0001c0001t0003g0055 |
3 | HG01975.hp1 HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.881-1306G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98197311 | |||||||
| chr8:98197437 | T | C | 24 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(21): Show |
24 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.881-1432A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98197437 | |||||||
| chr8:98197505 | T | C | 19 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(16): Show |
19 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.881-1500A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98197505 | |||||||
| chr8:98197545 | G | A | 24 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(21): Show |
24 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.881-1540C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98197545 | |||||||
| chr8:98197580 | C | T | 1 | a0001c0001t0005g0143 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.881-1575G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98197580 | |||||||
| chr8:98197735 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.881-1730T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98197735 | |||||||
| chr8:98197751 | T | C | 14 | a0001c0002t0004g0011 a0001c0002t0004g0015 a0001c0002t0004g0037 others(11): Show |
14 | HG01243.hp1 HG01243.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.881-1746A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98197751 | |||||||
| chr8:98197871 | A | C | 4 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0034 others(1): Show |
4 | HG02155.hp2 NA19062.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.881-1866T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98197871 | |||||||
| chr8:98197923 | T | G | 24 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(21): Show |
24 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.881-1918A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98197923 | |||||||
| chr8:98197947 | C | T | 41 | a0001c0001t0001g0177 a0001c0001t0003g0001 a0001c0001t0003g0043 others(38): Show |
43 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.881-1942G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98197947 | |||||||
| chr8:98198021 | G | A | 1 | a0001c0001t0002g0178 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.881-2016C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98198021 | |||||||
| chr8:98198146 | AAAC | A | 6 | a0001c0001t0003g0001 a0001c0001t0003g0050 a0001c0001t0003g0060 others(3): Show |
8 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.881-2144_881-2142d others(5): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98198146 | |||||||
| chr8:98198378 | T | C | 179 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(176): Show |
180 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.881-2373A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98198378 | |||||||
| chr8:98198572 | G | C | 125 | a0001c0001t0024g0150 a0001c0002t0001g0003 a0001c0002t0001g0020 others(122): Show |
126 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.881-2567C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98198572 | |||||||
| chr8:98198843 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.881-2838G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98198843 | |||||||
| chr8:98199071 | C | T | 19 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(16): Show |
19 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.881-3066G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98199071 | |||||||
| chr8:98199175 | C | T | 1 | a0001c0001t0021g0285 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.881-3170G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98199175 | |||||||
| chr8:98199203 | G | A | 2 | a0001c0001t0003g0183 a0001c0001t0003g0276 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.881-3198C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98199203 | |||||||
| chr8:98199460 | T | C | 196 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(193): Show |
198 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.881-3455A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98199460 | |||||||
| chr8:98199484 | C | T | 1 | a0001c0001t0002g0279 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.881-3479G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98199484 | |||||||
| chr8:98199863 | T | G | 1 | a0001c0001t0021g0285 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.880+3245A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98199863 | |||||||
| chr8:98199978 | A | G | 182 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(179): Show |
183 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.880+3130T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98199978 | |||||||
| chr8:98200568 | T | C | 131 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(128): Show |
132 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.880+2540A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98200568 | |||||||
| chr8:98200576 | A | G | 2 | a0001c0002t0004g0017 a0001c0005t0004g0312 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.880+2532T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98200576 | |||||||
| chr8:98200644 | G | A | 30 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(27): Show |
30 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.880+2464C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98200644 | |||||||
| chr8:98200732 | C | A | 3 | a0001c0001t0009g0012 a0001c0001t0009g0013 a0001c0001t0009g0185 |
3 | HG02809.hp2 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.880+2376G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98200732 | |||||||
| chr8:98200735 | C | T | 2 | a0001c0001t0003g0183 a0001c0001t0003g0276 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.880+2373G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98200735 | |||||||
| chr8:98201020 | G | T | 2 | a0001c0002t0004g0017 a0001c0005t0004g0312 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.880+2088C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98201020 | |||||||
| chr8:98201160 | G | T | 1 | a0001c0001t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.880+1948C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98201160 | |||||||
| chr8:98201170 | G | A | 1 | a0001c0001t0003g0315 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.880+1938C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98201170 | |||||||
| chr8:98201241 | C | T | 1 | a0001c0001t0003g0018 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.880+1867G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98201241 | |||||||
| chr8:98201414 | C | T | 5 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0034 others(2): Show |
5 | HG01243.hp1 HG02155.hp2 NA19062.hp1 others(2): Show |
intron_variant | MODIFIER | c.880+1694G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98201414 | |||||||
| chr8:98201415 | G | A | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.880+1693C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98201415 | |||||||
| chr8:98201722 | T | C | 2 | a0001c0001t0001g0239 a0001c0001t0001g0241 |
2 | HG02683.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.880+1386A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98201722 | |||||||
| chr8:98201744 | T | C | 14 | a0001c0002t0004g0011 a0001c0002t0004g0015 a0001c0002t0004g0037 others(11): Show |
14 | HG01243.hp1 HG01243.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.880+1364A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98201744 | |||||||
| chr8:98201801 | T | G | 1 | a0001c0001t0005g0008 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.880+1307A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98201801 | |||||||
| chr8:98202020 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.880+1088T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98202020 | |||||||
| chr8:98202028 | C | A | 1 | a0001c0001t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.880+1080G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98202028 | |||||||
| chr8:98202238 | C | G | 1 | a0001c0001t0021g0285 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.880+870G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98202238 | |||||||
| chr8:98202251 | T | C | 1 | a0001c0001t0021g0285 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.880+857A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98202251 | |||||||
| chr8:98202252 | T | C | 1 | a0001c0001t0021g0285 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.880+856A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98202252 | |||||||
| chr8:98202315 | A | G | 1 | a0001c0002t0001g0020 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.880+793T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98202315 | |||||||
| chr8:98202323 | C | G | 1 | a0001c0001t0003g0282 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.880+785G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98202323 | |||||||
| chr8:98202481 | C | T | 30 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(27): Show |
30 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.880+627G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98202481 | |||||||
| chr8:98202515 | T | C | 1 | a0001c0002t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.880+593A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98202515 | |||||||
| chr8:98202531 | C | A | 1 | a0001c0001t0003g0296 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.880+577G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98202531 | |||||||
| chr8:98202591 | G | A | 2 | a0001c0001t0007g0307 a0001c0001t0007g0316 |
2 | HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.880+517C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98202591 | |||||||
| chr8:98202842 | A | G | 4 | a0002c0003t0002g0075 a0002c0003t0002g0192 a0002c0003t0002g0194 others(1): Show |
4 | NA18970.hp2 NA18983.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.880+266T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98202842 | |||||||
| chr8:98202874 | A | G | 19 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(16): Show |
19 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.880+234T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98202874 | |||||||
| chr8:98203228 | CTTTAGGA others(4): Show |
C | 2 | a0001c0001t0003g0134 a0001c0001t0003g0135 |
2 | HG02602.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.792-43_792-33delTG others(9): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203228 | |||||||
| chr8:98203283 | T | C | 2 | a0001c0001t0014g0069 a0001c0001t0014g0187 |
2 | NA18966.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.792-87A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203283 | |||||||
| chr8:98203338 | G | A | 1 | a0001c0002t0001g0191 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.792-142C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203338 | |||||||
| chr8:98203383 | C | T | 17 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(14): Show |
17 | HG01109.hp1 HG02145.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.792-187G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203383 | |||||||
| chr8:98203570 | T | C | 1 | a0001c0001t0005g0196 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.792-374A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203570 | |||||||
| chr8:98203576 | G | A | 6 | a0001c0001t0002g0144 a0001c0001t0002g0165 a0001c0001t0002g0286 others(3): Show |
6 | HG00099.hp1 HG00323.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.792-380C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203576 | |||||||
| chr8:98203695 | T | C | 4 | a0001c0002t0004g0257 a0001c0002t0004g0294 a0001c0002t0004g0295 others(1): Show |
4 | HG02055.hp1 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.792-499A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203695 | |||||||
| chr8:98203831 | C | T | 1 | a0001c0001t0003g0203 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.792-635G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203831 | |||||||
| chr8:98203846 | C | CTG | 93 | a0001c0001t0001g0123 a0001c0001t0002g0094 a0001c0001t0021g0285 others(90): Show |
94 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.792-652_792-651dup others(2): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203846 | |||||||
| chr8:98203846 | C | CTGTG | 30 | a0001c0002t0001g0021 a0001c0002t0001g0038 a0001c0002t0001g0080 others(27): Show |
30 | HG00438.hp2 HG01243.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.792-654_792-651dup others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203846 | |||||||
| chr8:98203846 | C | CTGTGTG | 26 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0146 others(23): Show |
26 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.792-656_792-651dup others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203846 | |||||||
| chr8:98203846 | C | CTGTGTGT others(3): Show |
4 | a0001c0001t0001g0027 a0001c0001t0008g0031 a0001c0001t0008g0034 others(1): Show |
4 | HG02155.hp2 NA19062.hp1 NA19088.hp2 others(1): Show |
intron_variant | MODIFIER | c.792-660_792-651dup others(10): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203846 | |||||||
| chr8:98203846 | C | CTGTGTGT others(5): Show |
8 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0028 others(5): Show |
8 | HG01109.hp1 HG02280.hp1 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.792-662_792-651dup others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203846 | |||||||
| chr8:98203846 | C | CTGTGTGT others(9): Show |
4 | a0001c0001t0001g0184 a0001c0001t0001g0193 a0001c0001t0001g0308 others(1): Show |
4 | HG02145.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.792-666_792-651dup others(16): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203846 | |||||||
| chr8:98203846 | C | CTGTGTGT others(11): Show |
8 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0041 others(5): Show |
8 | HG01884.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.792-668_792-651dup others(18): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203846 | |||||||
| chr8:98203846 | C | CTGTGTGT others(13): Show |
3 | a0001c0001t0001g0016 a0001c0001t0001g0109 a0001c0001t0001g0120 |
3 | HG02451.hp1 HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.792-670_792-651dup others(20): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203846 | |||||||
| chr8:98203846 | CTG | C | 14 | a0001c0001t0002g0110 a0001c0001t0003g0018 a0001c0001t0003g0281 others(11): Show |
15 | HG00642.hp1 HG00733.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.792-652_792-651del others(2): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203846 | |||||||
| chr8:98204042 | G | T | 15 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0040 others(12): Show |
15 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.792-846C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98204042 | |||||||
| chr8:98204315 | C | G | 15 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0040 others(12): Show |
15 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.791+796G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98204315 | |||||||
| chr8:98204523 | G | A | 3 | a0001c0001t0003g0207 a0001c0001t0003g0268 a0001c0001t0003g0269 |
3 | HG00558.hp2 NA18948.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.791+588C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98204523 | |||||||
| chr8:98204569 | T | A | 19 | a0001c0002t0001g0003 a0001c0002t0001g0062 a0001c0002t0001g0072 others(16): Show |
20 | HG00408.hp1 HG00609.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.791+542A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98204569 | |||||||
| chr8:98204890 | C | T | 1 | a0001c0002t0001g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.791+221G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98204890 | |||||||
| chr8:98204891 | G | A | 12 | a0001c0002t0004g0011 a0001c0002t0004g0015 a0001c0002t0004g0037 others(9): Show |
12 | HG01243.hp1 HG01243.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.791+220C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98204891 | |||||||
| chr8:98205424 | G | A | 8 | a0001c0002t0001g0051 a0001c0002t0001g0056 a0001c0002t0001g0063 others(5): Show |
8 | HG01109.hp2 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.656-178C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98205424 | |||||||
| chr8:98205435 | C | T | 1 | a0001c0002t0001g0020 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.656-189G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98205435 | |||||||
| chr8:98205478 | G | GT | 25 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(22): Show |
25 | HG01074.hp1 HG01109.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.656-233dupA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98205478 | |||||||
| chr8:98205478 | G | T | 100 | a0001c0002t0001g0003 a0001c0002t0001g0020 a0001c0002t0001g0021 others(97): Show |
101 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.656-232C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98205478 | |||||||
| chr8:98205480 | T | G | 2 | a0001c0002t0004g0017 a0001c0005t0004g0312 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.656-234A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98205480 | |||||||
| chr8:98205490 | T | A | 4 | a0001c0001t0007g0291 a0001c0001t0007g0292 a0001c0001t0007g0307 others(1): Show |
4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-244A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98205490 | |||||||
| chr8:98205582 | A | C | 4 | a0001c0001t0003g0001 a0001c0001t0003g0050 a0001c0001t0003g0281 others(1): Show |
6 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.656-336T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98205582 | |||||||
| chr8:98205661 | T | G | 1 | a0001c0001t0003g0203 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.656-415A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98205661 | |||||||
| chr8:98205677 | T | A | 148 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(145): Show |
149 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.656-431A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98205677 | |||||||
| chr8:98205941 | A | G | 1 | a0001c0001t0003g0315 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.656-695T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98205941 | |||||||
| chr8:98206048 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0001g0308 |
2 | HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.656-802C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206048 | |||||||
| chr8:98206214 | G | A | 2 | a0001c0002t0004g0017 a0001c0005t0004g0312 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.656-968C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206214 | |||||||
| chr8:98206316 | G | GTA | 14 | a0001c0001t0001g0098 a0001c0001t0001g0146 a0001c0001t0001g0147 others(11): Show |
14 | HG00544.hp1 HG00673.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.656-1072_656-1071d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206316 | |||||||
| chr8:98206316 | G | GTGTATA | 27 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(24): Show |
27 | HG00733.hp1 HG00738.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.656-1071_656-1070i others(8): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206316 | |||||||
| chr8:98206316 | G | GTGTATAT others(3): Show |
2 | a0001c0001t0005g0006 a0001c0001t0005g0008 |
2 | HG02698.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.656-1071_656-1070i others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206316 | |||||||
| chr8:98206316 | G | GTGTATAT others(5): Show |
13 | a0001c0001t0003g0018 a0001c0001t0003g0115 a0001c0001t0003g0116 others(10): Show |
13 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.656-1071_656-1070i others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206316 | |||||||
| chr8:98206316 | G | GTGTATAT others(9): Show |
1 | a0001c0001t0005g0002 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.656-1071_656-1070i others(18): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206316 | |||||||
| chr8:98206326 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.656-1081_656-1080i others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206326 | |||||||
| chr8:98206326 | A | G | 21 | a0001c0001t0003g0018 a0001c0001t0003g0115 a0001c0001t0003g0116 others(18): Show |
22 | HG00642.hp1 HG00733.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.656-1080T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206326 | |||||||
| chr8:98206354 | A | AAT | 22 | a0001c0001t0001g0118 a0001c0001t0003g0018 a0001c0001t0003g0115 others(19): Show |
23 | HG00642.hp1 HG00733.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.656-1110_656-1109d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206354 | |||||||
| chr8:98206513 | G | A | 2 | a0001c0001t0003g0134 a0001c0001t0003g0135 |
2 | HG02602.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.656-1267C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206513 | |||||||
| chr8:98206561 | C | T | 121 | a0001c0001t0003g0001 a0001c0001t0003g0050 a0001c0001t0003g0281 others(118): Show |
124 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.656-1315G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206561 | |||||||
| chr8:98206705 | G | A | 1 | a0001c0001t0021g0285 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.656-1459C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206705 | |||||||
| chr8:98206718 | G | T | 201 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(198): Show |
202 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.656-1472C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206718 | |||||||
| chr8:98206726 | C | T | 29 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(26): Show |
29 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.656-1480G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206726 | |||||||
| chr8:98206763 | C | T | 1 | a0001c0002t0001g0064 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.656-1517G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206763 | |||||||
| chr8:98206776 | C | CA | 27 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(24): Show |
27 | HG01074.hp1 HG01109.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-1531dupT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206776 | |||||||
| chr8:98206776 | CA | C | 119 | a0001c0001t0001g0300 a0001c0001t0002g0095 a0001c0001t0002g0110 others(116): Show |
120 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.656-1531delT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206776 | |||||||
| chr8:98206849 | C | T | 10 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0040 others(7): Show |
10 | HG01884.hp2 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.656-1603G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206849 | |||||||
| chr8:98206851 | C | T | 1 | a0001c0002t0001g0155 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.656-1605G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206851 | |||||||
| chr8:98207191 | G | A | 1 | a0001c0001t0003g0164 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.656-1945C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98207191 | |||||||
| chr8:98207193 | C | T | 4 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0034 others(1): Show |
4 | HG02155.hp2 NA19062.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-1947G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98207193 | |||||||
| chr8:98207268 | TTC | T | 3 | a0001c0001t0002g0091 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | NA18747.hp2 NA18953.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.656-2024_656-2023d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98207268 | |||||||
| chr8:98207316 | G | A | 4 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(1): Show |
4 | HG01884.hp2 HG02258.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.656-2070C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98207316 | |||||||
| chr8:98207477 | T | C | 17 | a0001c0002t0001g0071 a0001c0002t0004g0011 a0001c0002t0004g0015 others(14): Show |
17 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.656-2231A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98207477 | |||||||
| chr8:98207479 | C | T | 27 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(24): Show |
27 | HG00733.hp1 HG00738.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.656-2233G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98207479 | |||||||
| chr8:98207594 | T | TA | 7 | a0001c0001t0002g0106 a0001c0001t0002g0108 a0001c0001t0002g0111 others(4): Show |
7 | HG02109.hp1 HG02723.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.656-2349dupT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98207594 | |||||||
| chr8:98207749 | G | A | 1 | a0001c0002t0001g0260 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.656-2503C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98207749 | |||||||
| chr8:98207809 | A | T | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.656-2563T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98207809 | |||||||
| chr8:98207962 | G | T | 1 | a0001c0002t0001g0191 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.656-2716C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98207962 | |||||||
| chr8:98207979 | A | G | 1 | a0001c0001t0003g0209 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.656-2733T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98207979 | |||||||
| chr8:98207981 | G | A | 1 | a0001c0001t0003g0122 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.656-2735C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98207981 | |||||||
| chr8:98208057 | A | T | 1 | a0001c0001t0002g0279 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.656-2811T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98208057 | |||||||
| chr8:98208172 | G | T | 146 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(143): Show |
147 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.656-2926C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98208172 | |||||||
| chr8:98208196 | T | C | 1 | a0001c0001t0005g0008 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.656-2950A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98208196 | |||||||
| chr8:98208288 | C | T | 1 | a0001c0001t0003g0055 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.656-3042G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98208288 | |||||||
| chr8:98208313 | T | C | 190 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(187): Show |
192 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.656-3067A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98208313 | |||||||
| chr8:98208416 | C | A | 2 | a0001c0002t0004g0017 a0001c0005t0004g0312 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.656-3170G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98208416 | |||||||
| chr8:98208540 | G | A | 1 | a0001c0001t0002g0085 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.656-3294C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98208540 | |||||||
| chr8:98208920 | C | T | 9 | a0001c0001t0007g0291 a0001c0001t0007g0292 a0001c0001t0007g0307 others(6): Show |
9 | HG00733.hp1 HG00738.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.655+3485G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98208920 | |||||||
| chr8:98208942 | A | G | 1 | a0002c0004t0001g0253 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.655+3463T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98208942 | |||||||
| chr8:98209100 | T | C | 1 | a0001c0002t0001g0072 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.655+3305A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209100 | |||||||
| chr8:98209192 | A | G | 2 | a0001c0002t0004g0017 a0001c0005t0004g0312 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.655+3213T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209192 | |||||||
| chr8:98209401 | G | A | 10 | a0001c0001t0001g0118 a0001c0001t0007g0291 a0001c0001t0007g0292 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.655+3004C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209401 | |||||||
| chr8:98209418 | G | A | 36 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(33): Show |
37 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.655+2987C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209418 | |||||||
| chr8:98209427 | G | A | 36 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(33): Show |
37 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.655+2978C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209427 | |||||||
| chr8:98209445 | C | CA | 26 | a0001c0001t0001g0177 a0001c0001t0001g0314 a0001c0001t0002g0095 others(23): Show |
26 | HG00438.hp1 HG01192.hp2 HG02056.hp1 others(23): Show |
intron_variant | MODIFIER | c.655+2959dupT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209445 | |||||||
| chr8:98209445 | C | CAAAA | 8 | a0001c0001t0007g0291 a0001c0001t0007g0292 a0001c0001t0007g0307 others(5): Show |
8 | HG00733.hp1 HG00738.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.655+2956_655+2959d others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209445 | |||||||
| chr8:98209445 | C | CAAAAAA | 13 | a0001c0001t0001g0118 a0001c0002t0001g0093 a0001c0002t0004g0011 others(10): Show |
13 | HG01243.hp1 HG01243.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.655+2954_655+2959d others(8): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209445 | |||||||
| chr8:98209445 | C | CAAAAAAA | 89 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0040 others(86): Show |
90 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.655+2953_655+2959d others(9): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209445 | |||||||
| chr8:98209445 | C | CAAAAAAA others(1): Show |
34 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0028 others(31): Show |
34 | HG00280.hp1 HG00438.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.655+2952_655+2959d others(10): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209445 | |||||||
| chr8:98209445 | C | CAAAAAAA others(2): Show |
6 | a0001c0001t0001g0025 a0001c0001t0001g0308 a0001c0001t0005g0006 others(3): Show |
6 | HG02698.hp2 HG03471.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.655+2951_655+2959d others(11): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209445 | |||||||
| chr8:98209445 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0021g0285 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.655+2937_655+2959d others(25): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209445 | |||||||
| chr8:98209445 | CA | C | 34 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0146 others(31): Show |
35 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.655+2959delT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209445 | |||||||
| chr8:98209457 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.655+2948T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209457 | |||||||
| chr8:98209488 | C | T | 18 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(15): Show |
18 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.655+2917G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209488 | |||||||
| chr8:98209512 | G | A | 37 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(34): Show |
38 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.655+2893C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209512 | |||||||
| chr8:98209557 | G | A | 3 | a0001c0002t0001g0255 a0001c0002t0022g0303 a0001c0005t0001g0026 |
3 | HG02486.hp1 HG03579.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.655+2848C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209557 | |||||||
| chr8:98209582 | T | C | 151 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(148): Show |
152 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.655+2823A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209582 | |||||||
| chr8:98209622 | C | G | 141 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(138): Show |
142 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.655+2783G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209622 | |||||||
| chr8:98209675 | A | AT | 16 | a0001c0001t0001g0118 a0001c0001t0001g0176 a0001c0001t0001g0179 others(13): Show |
16 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.655+2729dupA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209675 | |||||||
| chr8:98210048 | T | C | 37 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(34): Show |
38 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.655+2357A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98210048 | |||||||
| chr8:98210231 | G | T | 1 | a0001c0002t0004g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.655+2174C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98210231 | |||||||
| chr8:98210267 | G | A | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.655+2138C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98210267 | |||||||
| chr8:98210275 | C | T | 1 | a0001c0001t0002g0095 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.655+2130G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98210275 | |||||||
| chr8:98210310 | ATAAT | A | 36 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(33): Show |
37 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.655+2091_655+2094d others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98210310 | |||||||
| chr8:98210928 | C | T | 126 | a0001c0001t0007g0291 a0001c0001t0007g0292 a0001c0001t0007g0307 others(123): Show |
127 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.655+1477G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98210928 | |||||||
| chr8:98211049 | G | A | 2 | a0001c0001t0003g0283 a0001c0001t0021g0285 |
2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.655+1356C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211049 | |||||||
| chr8:98211138 | A | G | 1 | a0001c0006t0002g0019 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.655+1267T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211138 | |||||||
| chr8:98211530 | G | A | 288 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(285): Show |
292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.655+875C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211530 | |||||||
| chr8:98211561 | G | T | 117 | a0001c0002t0001g0003 a0001c0002t0001g0020 a0001c0002t0001g0021 others(114): Show |
118 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.655+844C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211561 | |||||||
| chr8:98211711 | T | TGA | 8 | a0001c0001t0001g0014 a0001c0001t0001g0044 a0001c0001t0001g0099 others(5): Show |
8 | HG02630.hp1 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.655+692_655+693dup others(2): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211711 | |||||||
| chr8:98211732 | A | G | 142 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(139): Show |
143 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.655+673T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211732 | |||||||
| chr8:98211733 | A | AAAGT | 10 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0041 others(7): Show |
10 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.655+671_655+672ins others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | |||||||
| chr8:98211733 | A | AAAGTGT | 57 | a0001c0001t0001g0109 a0001c0001t0001g0118 a0001c0001t0001g0290 others(54): Show |
57 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.655+671_655+672ins others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | |||||||
| chr8:98211733 | A | AAAGTGTG others(1): Show |
29 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(26): Show |
30 | HG00438.hp2 HG01109.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.655+671_655+672ins others(8): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | |||||||
| chr8:98211733 | A | AAAGTGTG others(3): Show |
20 | a0001c0001t0003g0283 a0001c0001t0008g0031 a0001c0001t0008g0032 others(17): Show |
20 | HG00738.hp1 HG01123.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.655+671_655+672ins others(10): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | |||||||
| chr8:98211733 | A | AAAGTGTG others(5): Show |
12 | a0001c0002t0001g0072 a0001c0002t0001g0090 a0001c0002t0001g0093 others(9): Show |
12 | HG00408.hp1 HG02015.hp1 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.655+671_655+672ins others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | |||||||
| chr8:98211733 | A | AAAGTGTG others(7): Show |
2 | a0001c0001t0021g0285 a0001c0002t0022g0303 |
2 | HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.655+671_655+672ins others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | |||||||
| chr8:98211733 | A | AAAGTGTG others(9): Show |
5 | a0001c0002t0004g0017 a0001c0002t0004g0037 a0001c0002t0004g0304 others(2): Show |
5 | HG02055.hp2 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.655+671_655+672ins others(16): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | |||||||
| chr8:98211733 | A | AAAGTGTG others(11): Show |
1 | a0001c0002t0004g0310 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.655+671_655+672ins others(18): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | |||||||
| chr8:98211733 | A | AGAAAGTG others(3): Show |
6 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(3): Show |
6 | HG02683.hp2 HG02698.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.655+671_655+672ins others(10): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | |||||||
| chr8:98211733 | A | AGT | 3 | a0001c0001t0002g0248 a0001c0001t0002g0301 a0001c0001t0005g0143 |
3 | HG01074.hp1 HG01123.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.655+670_655+671dup others(2): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | |||||||
| chr8:98211733 | A | AGTGT | 29 | a0001c0001t0001g0179 a0001c0001t0002g0022 a0001c0001t0002g0023 others(26): Show |
29 | HG00323.hp1 HG00609.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.655+668_655+671dup others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | |||||||
| chr8:98211733 | A | AGTGTGT | 14 | a0001c0001t0001g0121 a0001c0001t0001g0242 a0001c0001t0002g0113 others(11): Show |
14 | HG00099.hp1 HG00621.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.655+666_655+671dup others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | |||||||
| chr8:98211733 | A | AGTGTGTG others(1): Show |
28 | a0001c0001t0001g0123 a0001c0001t0001g0160 a0001c0001t0001g0302 others(25): Show |
31 | HG00099.hp2 HG00323.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.655+664_655+671dup others(8): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | |||||||
| chr8:98211733 | A | AGTGTGTG others(3): Show |
47 | a0001c0001t0001g0098 a0001c0001t0001g0146 a0001c0001t0001g0147 others(44): Show |
47 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.655+662_655+671dup others(10): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | |||||||
| chr8:98211733 | A | AGTGTGTG others(5): Show |
13 | a0001c0001t0003g0052 a0001c0001t0003g0115 a0001c0001t0003g0116 others(10): Show |
13 | HG00438.hp1 HG01255.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.655+660_655+671dup others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | |||||||
| chr8:98211733 | A | AGTGTGTG others(7): Show |
1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.655+658_655+671dup others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | |||||||
| chr8:98211787 | A | C | 1 | a0001c0005t0001g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.655+618T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211787 | |||||||
| chr8:98211929 | T | C | 1 | a0001c0006t0002g0019 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.655+476A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211929 | |||||||
| chr8:98212153 | A | C | 1 | a0001c0002t0001g0155 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.655+252T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98212153 | |||||||
| chr8:98212281 | T | C | 2 | a0001c0001t0005g0007 a0001c0001t0005g0009 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.655+124A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98212281 | |||||||
| chr8:98212304 | A | G | 2 | a0001c0002t0013g0057 a0001c0002t0013g0058 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.655+101T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98212304 | |||||||
| chr8:98212306 | C | A | 140 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0040 others(137): Show |
141 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.655+99G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98212306 | |||||||
| chr8:98212708 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.559-207A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98212708 | |||||||
| chr8:98212795 | C | T | 1 | a0001c0001t0021g0285 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.559-294G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98212795 | |||||||
| chr8:98212851 | C | A | 2 | a0001c0001t0001g0239 a0001c0001t0001g0241 |
2 | HG02683.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.559-350G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98212851 | |||||||
| chr8:98212852 | C | A | 4 | a0001c0002t0001g0119 a0001c0002t0001g0141 a0001c0002t0001g0142 others(1): Show |
4 | HG01358.hp1 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.559-351G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98212852 | |||||||
| chr8:98212955 | A | G | 3 | a0001c0001t0001g0118 a0001c0001t0003g0283 a0001c0001t0021g0285 |
3 | HG02965.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.559-454T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98212955 | |||||||
| chr8:98212992 | C | T | 3 | a0001c0001t0001g0118 a0001c0001t0003g0283 a0001c0001t0021g0285 |
3 | HG02965.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.559-491G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98212992 | |||||||
| chr8:98213109 | T | C | 138 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(135): Show |
139 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.559-608A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98213109 | |||||||
| chr8:98213118 | C | A | 3 | a0001c0001t0001g0118 a0001c0001t0003g0283 a0001c0001t0021g0285 |
3 | HG02965.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.559-617G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98213118 | |||||||
| chr8:98213126 | G | C | 7 | a0001c0001t0001g0118 a0001c0001t0003g0283 a0001c0001t0005g0006 others(4): Show |
7 | HG02698.hp2 HG02965.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.559-625C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98213126 | |||||||
| chr8:98213442 | T | A | 1 | a0001c0001t0021g0285 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.559-941A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98213442 | |||||||
| chr8:98213620 | C | T | 1 | a0001c0002t0001g0092 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.559-1119G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98213620 | |||||||
| chr8:98213757 | C | T | 12 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(9): Show |
12 | HG01109.hp1 HG02280.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.559-1256G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98213757 | |||||||
| chr8:98214167 | CTT | C | 140 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(137): Show |
141 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.559-1668_559-1667d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214167 | |||||||
| chr8:98214167 | CTTT | C | 10 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0109 others(7): Show |
10 | HG02451.hp1 HG02572.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.559-1669_559-1667d others(5): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214167 | |||||||
| chr8:98214209 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.559-1708C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214209 | |||||||
| chr8:98214283 | A | C | 151 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(148): Show |
152 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.559-1782T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214283 | |||||||
| chr8:98214291 | G | A | 105 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(102): Show |
106 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.559-1790C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214291 | |||||||
| chr8:98214337 | T | C | 4 | a0001c0001t0001g0123 a0001c0001t0001g0180 a0001c0001t0001g0240 others(1): Show |
4 | HG00609.hp1 HG00735.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.559-1836A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214337 | |||||||
| chr8:98214382 | T | G | 122 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(119): Show |
123 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.559-1881A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214382 | |||||||
| chr8:98214428 | T | G | 41 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(38): Show |
42 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.559-1927A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214428 | |||||||
| chr8:98214490 | A | G | 151 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(148): Show |
152 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.559-1989T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214490 | |||||||
| chr8:98214513 | A | G | 1 | a0001c0002t0001g0071 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.559-2012T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214513 | |||||||
| chr8:98214545 | C | T | 1 | a0002c0003t0001g0273 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.559-2044G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214545 | |||||||
| chr8:98214554 | A | AT | 6 | a0001c0001t0001g0314 a0001c0001t0002g0324 a0001c0001t0009g0012 others(3): Show |
6 | HG02145.hp2 HG02572.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.559-2054dupA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214554 | |||||||
| chr8:98214563 | C | CT | 41 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(38): Show |
42 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.559-2063dupA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214563 | |||||||
| chr8:98214593 | C | T | 150 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(147): Show |
151 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.559-2092G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214593 | |||||||
| chr8:98214841 | T | C | 2 | a0001c0002t0004g0017 a0001c0005t0004g0312 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.559-2340A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214841 | |||||||
| chr8:98214929 | T | C | 39 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(36): Show |
40 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.559-2428A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214929 | |||||||
| chr8:98215039 | C | T | 39 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(36): Show |
40 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.559-2538G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98215039 | |||||||
| chr8:98215061 | C | T | 4 | a0002c0003t0002g0065 a0002c0003t0002g0167 a0002c0003t0002g0201 others(1): Show |
4 | HG02080.hp1 HG02080.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.559-2560G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98215061 | |||||||
| chr8:98215062 | G | A | 1 | a0001c0001t0002g0173 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.559-2561C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98215062 | |||||||
| chr8:98215121 | G | T | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.559-2620C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98215121 | |||||||
| chr8:98215503 | C | T | 1 | a0001c0002t0001g0270 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.559-3002G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98215503 | |||||||
| chr8:98215714 | C | T | 1 | a0002c0003t0012g0216 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.559-3213G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98215714 | |||||||
| chr8:98215995 | G | A | 2 | a0001c0001t0001g0289 a0001c0001t0001g0300 |
2 | NA18997.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.559-3494C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98215995 | |||||||
| chr8:98216245 | A | G | 229 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(226): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.559-3744T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98216245 | |||||||
| chr8:98216344 | G | A | 2 | a0001c0001t0001g0290 a0001c0002t0022g0303 |
2 | HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.559-3843C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98216344 | |||||||
| chr8:98216356 | C | T | 1 | a0001c0002t0001g0260 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.559-3855G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98216356 | |||||||
| chr8:98216526 | G | C | 1 | a0001c0002t0001g0313 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.559-4025C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98216526 | |||||||
| chr8:98216563 | T | C | 57 | a0001c0001t0001g0177 a0001c0001t0001g0314 a0001c0001t0002g0110 others(54): Show |
59 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.559-4062A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98216563 | |||||||
| chr8:98216660 | A | AT | 27 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(24): Show |
27 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.559-4160dupA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98216660 | |||||||
| chr8:98216760 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.559-4259C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98216760 | |||||||
| chr8:98217080 | C | T | 10 | a0001c0002t0001g0051 a0001c0002t0001g0056 a0001c0002t0001g0063 others(7): Show |
10 | HG01109.hp2 HG01257.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.559-4579G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98217080 | |||||||
| chr8:98217339 | G | T | 161 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(158): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.559-4838C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98217339 | |||||||
| chr8:98217340 | CA | C | 161 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(158): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.559-4840delT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98217340 | |||||||
| chr8:98217344 | A | T | 161 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(158): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.559-4843T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98217344 | |||||||
| chr8:98217346 | T | TGTGA | 161 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(158): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.559-4846_559-4845i others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98217346 | |||||||
| chr8:98217347 | A | G | 161 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(158): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.559-4846T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98217347 | |||||||
| chr8:98217646 | T | C | 3 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0034 |
3 | NA19062.hp1 NA19064.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.558+4833A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98217646 | |||||||
| chr8:98217903 | T | A | 6 | a0001c0001t0003g0001 a0001c0001t0003g0050 a0001c0001t0003g0060 others(3): Show |
8 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.558+4576A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98217903 | |||||||
| chr8:98217945 | C | T | 2 | a0001c0002t0004g0017 a0001c0005t0004g0312 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.558+4534G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98217945 | |||||||
| chr8:98217959 | C | T | 13 | a0001c0001t0002g0175 a0001c0001t0002g0182 a0001c0001t0002g0301 others(10): Show |
14 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.558+4520G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98217959 | |||||||
| chr8:98217988 | G | C | 2 | a0001c0001t0003g0174 a0001c0001t0003g0235 |
2 | HG00673.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.558+4491C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98217988 | |||||||
| chr8:98218256 | G | A | 1 | a0001c0001t0003g0283 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.558+4223C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218256 | |||||||
| chr8:98218341 | A | C | 2 | a0001c0002t0001g0089 a0001c0002t0001g0263 |
2 | HG02300.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.558+4138T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218341 | |||||||
| chr8:98218368 | G | A | 5 | a0001c0001t0001g0290 a0001c0002t0004g0257 a0001c0002t0004g0294 others(2): Show |
5 | HG02055.hp1 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.558+4111C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218368 | |||||||
| chr8:98218502 | C | G | 290 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(287): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.558+3977G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218502 | |||||||
| chr8:98218556 | G | T | 13 | a0001c0002t0001g0071 a0001c0002t0004g0011 a0001c0002t0004g0037 others(10): Show |
13 | HG01243.hp1 HG01243.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.558+3923C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218556 | |||||||
| chr8:98218584 | G | A | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.558+3895C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218584 | |||||||
| chr8:98218594 | A | G | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.558+3885T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218594 | |||||||
| chr8:98218667 | C | T | 2 | a0001c0002t0004g0017 a0001c0005t0004g0312 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.558+3812G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218667 | |||||||
| chr8:98218694 | G | A | 1 | a0001c0005t0001g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.558+3785C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218694 | |||||||
| chr8:98218723 | A | C | 1 | a0001c0001t0021g0285 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.558+3756T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218723 | |||||||
| chr8:98218731 | A | G | 28 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(25): Show |
28 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.558+3748T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218731 | |||||||
| chr8:98218750 | C | T | 1 | a0001c0001t0002g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.558+3729G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218750 | |||||||
| chr8:98218755 | G | A | 102 | a0001c0001t0002g0091 a0001c0001t0002g0124 a0001c0001t0002g0125 others(99): Show |
103 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.558+3724C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218755 | |||||||
| chr8:98218789 | G | T | 1 | a0001c0001t0021g0285 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.558+3690C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218789 | |||||||
| chr8:98218926 | G | C | 1 | a0001c0002t0001g0154 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.558+3553C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218926 | |||||||
| chr8:98219084 | T | A | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.558+3395A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98219084 | |||||||
| chr8:98219484 | C | T | 1 | a0001c0002t0001g0299 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.558+2995G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98219484 | |||||||
| chr8:98219598 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.558+2881C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98219598 | |||||||
| chr8:98219609 | C | T | 12 | a0001c0001t0002g0175 a0001c0001t0002g0182 a0001c0001t0002g0301 others(9): Show |
13 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.558+2870G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98219609 | |||||||
| chr8:98219788 | A | C | 1 | a0001c0001t0024g0150 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.558+2691T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98219788 | |||||||
| chr8:98219798 | C | T | 3 | a0001c0002t0001g0003 a0001c0002t0001g0127 a0001c0002t0001g0128 |
4 | HG01515.hp2 HG01517.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.558+2681G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98219798 | |||||||
| chr8:98219799 | C | T | 14 | a0001c0002t0001g0071 a0001c0002t0004g0011 a0001c0002t0004g0037 others(11): Show |
14 | HG01243.hp1 HG01243.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.558+2680G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98219799 | |||||||
| chr8:98219825 | G | A | 1 | a0001c0002t0006g0061 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.558+2654C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98219825 | |||||||
| chr8:98219983 | G | A | 3 | a0001c0001t0002g0166 a0001c0001t0002g0238 a0001c0001t0002g0248 |
3 | HG00741.hp1 HG01257.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.558+2496C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98219983 | |||||||
| chr8:98220041 | A | AT | 6 | a0001c0001t0001g0290 a0001c0002t0004g0257 a0001c0002t0004g0294 others(3): Show |
6 | HG02055.hp1 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.558+2437dupA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220041 | |||||||
| chr8:98220041 | AT | A | 9 | a0001c0001t0001g0186 a0001c0001t0002g0023 a0001c0001t0002g0110 others(6): Show |
9 | HG00558.hp1 HG01069.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.558+2437delA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220041 | |||||||
| chr8:98220055 | A | T | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.558+2424T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220055 | |||||||
| chr8:98220188 | A | G | 2 | a0001c0001t0001g0290 a0001c0002t0022g0303 |
2 | HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.558+2291T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220188 | |||||||
| chr8:98220408 | A | AT | 54 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(51): Show |
55 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.558+2070dupA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220408 | |||||||
| chr8:98220408 | A | ATT | 9 | a0001c0001t0001g0179 a0001c0001t0001g0290 a0001c0001t0002g0175 others(6): Show |
9 | HG01192.hp2 HG02055.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.558+2069_558+2070d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220408 | |||||||
| chr8:98220624 | G | T | 4 | a0001c0002t0001g0080 a0001c0002t0001g0228 a0001c0002t0001g0278 others(1): Show |
4 | HG03017.hp2 NA18978.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.558+1855C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220624 | |||||||
| chr8:98220660 | T | C | 1 | a0001c0002t0001g0204 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.558+1819A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220660 | |||||||
| chr8:98220727 | C | T | 1 | a0002c0004t0001g0053 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.558+1752G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220727 | |||||||
| chr8:98220728 | G | A | 14 | a0001c0001t0002g0175 a0001c0001t0002g0182 a0001c0001t0002g0301 others(11): Show |
15 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.558+1751C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220728 | |||||||
| chr8:98220848 | A | C | 4 | a0001c0001t0007g0291 a0001c0001t0007g0292 a0001c0001t0007g0307 others(1): Show |
4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.558+1631T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220848 | |||||||
| chr8:98220853 | G | A | 33 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(30): Show |
33 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.558+1626C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220853 | |||||||
| chr8:98220868 | C | T | 14 | a0001c0001t0002g0175 a0001c0001t0002g0182 a0001c0001t0002g0301 others(11): Show |
15 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.558+1611G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220868 | |||||||
| chr8:98220889 | C | G | 2 | a0001c0001t0002g0309 a0001c0001t0002g0311 |
2 | HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.558+1590G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220889 | |||||||
| chr8:98220930 | ACACCTTC others(12): Show |
A | 1 | a0001c0002t0001g0105 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.558+1530_558+1548d others(21): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220930 | |||||||
| chr8:98220964 | C | CT | 50 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(47): Show |
50 | HG00544.hp2 HG00597.hp2 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.558+1514dupA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220964 | |||||||
| chr8:98220964 | C | CTT | 10 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0120 others(7): Show |
10 | HG01433.hp1 HG02280.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.558+1513_558+1514d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220964 | |||||||
| chr8:98220964 | CT | C | 26 | a0001c0001t0001g0186 a0001c0001t0002g0144 a0001c0001t0002g0165 others(23): Show |
26 | HG00323.hp1 HG00738.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.558+1514delA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220964 | |||||||
| chr8:98220964 | CTT | C | 16 | a0001c0001t0002g0286 a0001c0002t0001g0021 a0001c0002t0001g0071 others(13): Show |
16 | HG00099.hp1 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.558+1513_558+1514d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220964 | |||||||
| chr8:98220964 | CTTT | C | 6 | a0001c0001t0001g0290 a0001c0002t0001g0038 a0001c0002t0004g0257 others(3): Show |
6 | HG02055.hp1 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.558+1512_558+1514d others(5): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220964 | |||||||
| chr8:98220964 | CTTTT | C | 7 | a0001c0001t0003g0101 a0001c0001t0003g0174 a0001c0001t0003g0183 others(4): Show |
7 | HG00673.hp2 HG01167.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.558+1511_558+1514d others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220964 | |||||||
| chr8:98220964 | CTTTTT | C | 66 | a0001c0001t0001g0177 a0001c0001t0001g0314 a0001c0001t0002g0110 others(63): Show |
69 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.558+1510_558+1514d others(7): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220964 | |||||||
| chr8:98220964 | CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0007g0291 a0001c0001t0007g0292 a0001c0001t0007g0307 others(1): Show |
4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.558+1505_558+1514d others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220964 | |||||||
| chr8:98220964 | CTTTTTTT others(4): Show |
C | 6 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0002g0102 others(3): Show |
6 | HG01167.hp2 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.558+1504_558+1514d others(13): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220964 | |||||||
| chr8:98220964 | CTTTTTTT others(7): Show |
C | 8 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0036 others(5): Show |
8 | HG00733.hp2 HG00741.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.558+1501_558+1514d others(16): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220964 | |||||||
| chr8:98220964 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0021g0285 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.558+1499_558+1514d others(18): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220964 | |||||||
| chr8:98220964 | CTTTTTTT others(12): Show |
C | 1 | a0001c0002t0001g0145 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.558+1496_558+1514d others(21): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220964 | |||||||
| chr8:98221201 | C | A | 1 | a0001c0005t0001g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.558+1278G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221201 | |||||||
| chr8:98221252 | G | A | 154 | a0001c0001t0001g0177 a0001c0001t0001g0314 a0001c0001t0002g0091 others(151): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.558+1227C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221252 | |||||||
| chr8:98221255 | C | T | 2 | a0001c0001t0002g0039 a0001c0001t0018g0163 |
2 | HG01099.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.558+1224G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221255 | |||||||
| chr8:98221274 | C | G | 2 | a0001c0001t0003g0115 a0001c0001t0003g0116 |
2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.558+1205G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221274 | |||||||
| chr8:98221292 | T | G | 2 | a0001c0001t0003g0115 a0001c0001t0003g0116 |
2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.558+1187A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221292 | |||||||
| chr8:98221343 | G | A | 4 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0034 others(1): Show |
4 | HG02155.hp2 NA19062.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.558+1136C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221343 | |||||||
| chr8:98221363 | C | CT | 114 | a0001c0001t0002g0091 a0001c0001t0002g0144 a0001c0001t0002g0165 others(111): Show |
116 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.558+1115dupA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221363 | |||||||
| chr8:98221474 | G | T | 5 | a0001c0001t0001g0290 a0001c0002t0004g0257 a0001c0002t0004g0294 others(2): Show |
5 | HG02055.hp1 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.558+1005C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221474 | |||||||
| chr8:98221529 | G | T | 1 | a0001c0005t0001g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.558+950C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221529 | |||||||
| chr8:98221554 | A | T | 14 | a0001c0001t0002g0175 a0001c0001t0002g0182 a0001c0001t0002g0301 others(11): Show |
15 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.558+925T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221554 | |||||||
| chr8:98221575 | T | C | 13 | a0001c0002t0001g0071 a0001c0002t0004g0011 a0001c0002t0004g0037 others(10): Show |
13 | HG01243.hp1 HG01243.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.558+904A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221575 | |||||||
| chr8:98221580 | T | C | 2 | a0001c0002t0001g0021 a0001c0002t0001g0158 |
2 | HG02602.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.558+899A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221580 | |||||||
| chr8:98221585 | G | A | 28 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(25): Show |
28 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.558+894C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221585 | |||||||
| chr8:98221793 | C | A | 1 | a0001c0005t0001g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.558+686G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221793 | |||||||
| chr8:98221857 | G | A | 53 | a0001c0001t0001g0177 a0001c0001t0001g0314 a0001c0001t0002g0110 others(50): Show |
55 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.558+622C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221857 | |||||||
| chr8:98221876 | C | T | 28 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(25): Show |
28 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.558+603G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221876 | |||||||
| chr8:98222234 | C | T | 1 | a0001c0002t0001g0003 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.558+245G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98222234 | |||||||
| chr8:98222253 | G | C | 55 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(52): Show |
56 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.558+226C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98222253 | |||||||
| chr8:98222613 | T | C | 2 | a0001c0001t0011g0004 a0001c0001t0011g0005 |
2 | NA18942.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.437-13A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98222613 | |||||||
| chr8:98222658 | C | T | 1 | a0001c0001t0003g0043 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.437-58G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98222658 | |||||||
| chr8:98222659 | G | A | 1 | a0002c0003t0012g0213 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.437-59C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98222659 | |||||||
| chr8:98222704 | C | T | 13 | a0001c0002t0001g0071 a0001c0002t0004g0011 a0001c0002t0004g0037 others(10): Show |
13 | HG01243.hp1 HG01243.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.437-104G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98222704 | |||||||
| chr8:98222825 | C | T | 54 | a0001c0001t0001g0177 a0001c0001t0001g0314 a0001c0001t0002g0110 others(51): Show |
56 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.437-225G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98222825 | |||||||
| chr8:98222849 | A | G | 247 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(244): Show |
251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.437-249T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98222849 | |||||||
| chr8:98222951 | G | A | 14 | a0001c0001t0002g0175 a0001c0001t0002g0182 a0001c0001t0002g0301 others(11): Show |
15 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.437-351C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98222951 | |||||||
| chr8:98222961 | T | G | 4 | a0001c0002t0004g0037 a0001c0002t0004g0304 a0001c0002t0004g0305 others(1): Show |
4 | HG01884.hp1 HG02976.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.437-361A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98222961 | |||||||
| chr8:98223073 | T | C | 3 | a0001c0002t0001g0326 a0001c0002t0001g0327 a0001c0002t0001g0328 |
3 | HG01943.hp2 HG01993.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.437-473A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98223073 | |||||||
| chr8:98223219 | T | A | 5 | a0001c0001t0001g0290 a0001c0002t0004g0257 a0001c0002t0004g0294 others(2): Show |
5 | HG02055.hp1 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.437-619A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98223219 | |||||||
| chr8:98223490 | AAACTTGC others(3): Show |
A | 1 | a0001c0001t0002g0173 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.437-900_437-891del others(10): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98223490 | |||||||
| chr8:98223600 | A | G | 12 | a0001c0001t0002g0175 a0001c0001t0002g0182 a0001c0001t0002g0301 others(9): Show |
13 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.437-1000T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98223600 | |||||||
| chr8:98223682 | A | T | 1 | a0001c0001t0002g0010 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.437-1082T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98223682 | |||||||
| chr8:98223688 | C | T | 1 | a0001c0001t0002g0168 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.437-1088G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98223688 | |||||||
| chr8:98223720 | C | T | 209 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(206): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.437-1120G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98223720 | |||||||
| chr8:98223753 | C | A | 5 | a0001c0001t0001g0290 a0001c0002t0004g0257 a0001c0002t0004g0294 others(2): Show |
5 | HG02055.hp1 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.437-1153G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98223753 | |||||||
| chr8:98224071 | T | C | 12 | a0001c0001t0002g0175 a0001c0001t0002g0182 a0001c0001t0002g0301 others(9): Show |
13 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.437-1471A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224071 | |||||||
| chr8:98224139 | A | G | 3 | a0001c0005t0001g0030 a0001c0005t0001g0035 a0001c0005t0004g0029 |
3 | HG02145.hp1 HG02486.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.437-1539T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224139 | |||||||
| chr8:98224341 | T | G | 2 | a0001c0001t0007g0307 a0001c0001t0007g0316 |
2 | HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.437-1741A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224341 | |||||||
| chr8:98224373 | T | A | 56 | a0001c0001t0001g0177 a0001c0001t0001g0314 a0001c0001t0002g0110 others(53): Show |
58 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.437-1773A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224373 | |||||||
| chr8:98224392 | T | G | 1 | a0001c0001t0002g0284 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.437-1792A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224392 | |||||||
| chr8:98224461 | A | G | 4 | a0001c0001t0007g0291 a0001c0001t0007g0292 a0001c0001t0007g0307 others(1): Show |
4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.437-1861T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224461 | |||||||
| chr8:98224489 | A | G | 4 | a0001c0001t0007g0291 a0001c0001t0007g0292 a0001c0001t0007g0307 others(1): Show |
4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.437-1889T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224489 | |||||||
| chr8:98224572 | A | C | 2 | a0001c0001t0002g0102 a0001c0001t0002g0284 |
2 | HG01167.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.437-1972T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224572 | |||||||
| chr8:98224616 | G | A | 5 | a0001c0001t0001g0290 a0001c0002t0004g0257 a0001c0002t0004g0294 others(2): Show |
5 | HG02055.hp1 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.437-2016C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224616 | |||||||
| chr8:98224671 | A | G | 248 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(245): Show |
252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.437-2071T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224671 | |||||||
| chr8:98224755 | C | CT | 6 | a0001c0001t0001g0179 a0001c0001t0001g0290 a0001c0001t0003g0281 others(3): Show |
6 | HG02486.hp1 HG02630.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.437-2156dupA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224755 | |||||||
| chr8:98224755 | C | CTT | 144 | a0001c0001t0001g0177 a0001c0001t0001g0314 a0001c0001t0002g0091 others(141): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.437-2157_437-2156d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224755 | |||||||
| chr8:98224755 | C | CTTT | 23 | a0001c0001t0002g0175 a0001c0001t0002g0182 a0001c0001t0002g0301 others(20): Show |
24 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.437-2158_437-2156d others(5): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224755 | |||||||
| chr8:98224755 | CTTTTTTT | C | 16 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0040 others(13): Show |
16 | HG00733.hp1 HG00738.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.437-2162_437-2156d others(9): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224755 | |||||||
| chr8:98224760 | T | C | 13 | a0001c0002t0001g0071 a0001c0002t0004g0011 a0001c0002t0004g0037 others(10): Show |
13 | HG01243.hp1 HG01243.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.437-2160A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224760 | |||||||
| chr8:98224911 | C | T | 2 | a0001c0001t0003g0134 a0001c0001t0003g0135 |
2 | HG02602.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.437-2311G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224911 | |||||||
| chr8:98225018 | A | C | 197 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(194): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.437-2418T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98225018 | |||||||
| chr8:98225037 | G | T | 197 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(194): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.437-2437C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98225037 | |||||||
| chr8:98225185 | A | G | 3 | a0001c0001t0002g0166 a0001c0001t0002g0238 a0001c0001t0002g0248 |
3 | HG00741.hp1 HG01257.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.437-2585T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98225185 | |||||||
| chr8:98225414 | G | T | 4 | a0001c0001t0007g0291 a0001c0001t0007g0292 a0001c0001t0007g0307 others(1): Show |
4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.437-2814C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98225414 | |||||||
| chr8:98225462 | G | A | 2 | a0001c0001t0001g0290 a0001c0002t0022g0303 |
2 | HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.437-2862C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98225462 | |||||||
| chr8:98225586 | A | G | 1 | a0001c0002t0004g0011 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.437-2986T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98225586 | |||||||
| chr8:98225675 | G | GT | 239 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(236): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.437-3076_437-3075i others(3): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98225675 | |||||||
| chr8:98225699 | G | A | 167 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(164): Show |
170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.437-3099C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98225699 | |||||||
| chr8:98225785 | T | C | 231 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(228): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.437-3185A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98225785 | |||||||
| chr8:98225888 | G | A | 1 | a0001c0001t0015g0195 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.437-3288C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98225888 | |||||||
| chr8:98225922 | T | A | 2 | a0001c0002t0004g0017 a0001c0005t0004g0312 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.437-3322A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98225922 | |||||||
| chr8:98225979 | A | G | 5 | a0001c0001t0001g0290 a0001c0002t0004g0257 a0001c0002t0004g0294 others(2): Show |
5 | HG02055.hp1 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.437-3379T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98225979 | |||||||
| chr8:98226151 | G | A | 1 | a0001c0002t0001g0313 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.437-3551C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226151 | |||||||
| chr8:98226219 | G | A | 1 | a0001c0005t0001g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.437-3619C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226219 | |||||||
| chr8:98226240 | G | A | 10 | a0001c0002t0001g0071 a0001c0002t0004g0011 a0001c0002t0004g0081 others(7): Show |
10 | HG01243.hp1 HG01243.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-3640C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226240 | |||||||
| chr8:98226285 | T | C | 14 | a0001c0001t0002g0175 a0001c0001t0002g0182 a0001c0001t0002g0301 others(11): Show |
15 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.437-3685A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226285 | |||||||
| chr8:98226303 | G | A | 10 | a0001c0002t0001g0071 a0001c0002t0004g0011 a0001c0002t0004g0081 others(7): Show |
10 | HG01243.hp1 HG01243.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-3703C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226303 | |||||||
| chr8:98226328 | G | A | 3 | a0001c0002t0004g0257 a0001c0002t0004g0294 a0001c0002t0004g0295 |
3 | HG02055.hp1 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.437-3728C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226328 | |||||||
| chr8:98226329 | C | G | 3 | a0001c0002t0004g0257 a0001c0002t0004g0294 a0001c0002t0004g0295 |
3 | HG02055.hp1 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.437-3729G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226329 | |||||||
| chr8:98226450 | A | G | 109 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(106): Show |
110 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.437-3850T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226450 | |||||||
| chr8:98226495 | T | C | 1 | a0001c0001t0014g0187 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.437-3895A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226495 | |||||||
| chr8:98226552 | G | T | 10 | a0001c0002t0001g0071 a0001c0002t0004g0011 a0001c0002t0004g0081 others(7): Show |
10 | HG01243.hp1 HG01243.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-3952C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226552 | |||||||
| chr8:98226582 | C | T | 1 | a0001c0002t0001g0321 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.437-3982G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226582 | |||||||
| chr8:98226624 | G | C | 1 | a0001c0001t0003g0244 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.437-4024C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226624 | |||||||
| chr8:98226625 | T | C | 27 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(24): Show |
27 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.437-4025A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226625 | |||||||
| chr8:98226873 | T | C | 288 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(285): Show |
292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.437-4273A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226873 | |||||||
| chr8:98226978 | A | C | 2 | a0001c0002t0004g0017 a0001c0005t0004g0312 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.437-4378T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226978 | |||||||
| chr8:98227334 | T | C | 8 | a0001c0002t0001g0089 a0001c0002t0001g0092 a0001c0002t0001g0154 others(5): Show |
8 | HG00597.hp2 HG02300.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.437-4734A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98227334 | |||||||
| chr8:98227365 | CACCTGAA others(6): Show |
C | 1 | a0001c0002t0001g0219 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.437-4778_437-4766d others(15): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98227365 | |||||||
| chr8:98227377 | A | G | 2 | a0001c0002t0004g0017 a0001c0005t0004g0312 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.437-4777T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98227377 | |||||||
| chr8:98227390 | T | C | 1 | a0001c0002t0001g0219 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.437-4790A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98227390 | |||||||
| chr8:98227466 | G | A | 100 | a0001c0001t0002g0091 a0001c0001t0002g0144 a0001c0001t0002g0165 others(97): Show |
101 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.437-4866C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98227466 | |||||||
| chr8:98227523 | G | A | 2 | a0001c0002t0004g0017 a0001c0005t0004g0312 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.437-4923C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98227523 | |||||||
| chr8:98227537 | G | A | 1 | a0001c0001t0002g0261 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.437-4937C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98227537 | |||||||
| chr8:98227604 | A | C | 1 | a0001c0002t0001g0219 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.437-5004T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98227604 | |||||||
| chr8:98227605 | T | A | 1 | a0001c0002t0001g0219 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.437-5005A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98227605 | |||||||
| chr8:98227735 | C | T | 156 | a0001c0001t0001g0177 a0001c0001t0001g0314 a0001c0001t0002g0091 others(153): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.437-5135G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98227735 | |||||||
| chr8:98227852 | A | G | 1 | a0001c0001t0005g0002 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.437-5252T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98227852 | |||||||
| chr8:98227865 | A | G | 4 | a0001c0001t0007g0291 a0001c0001t0007g0292 a0001c0001t0007g0307 others(1): Show |
4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.437-5265T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98227865 | |||||||
| chr8:98227932 | C | T | 4 | a0001c0002t0001g0090 a0001c0002t0001g0249 a0001c0002t0001g0265 others(1): Show |
4 | HG00408.hp1 HG02015.hp1 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.437-5332G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98227932 | |||||||
| chr8:98228006 | G | C | 194 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(191): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.437-5406C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98228006 | |||||||
| chr8:98228052 | C | T | 1 | a0001c0001t0003g0018 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.437-5452G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98228052 | |||||||
| chr8:98228381 | G | A | 190 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(187): Show |
193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.437-5781C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98228381 | |||||||
| chr8:98228486 | A | G | 4 | a0001c0001t0007g0291 a0001c0001t0007g0292 a0001c0001t0007g0307 others(1): Show |
4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.437-5886T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98228486 | |||||||
| chr8:98228655 | G | GATCCATC others(9): Show |
24 | a0001c0001t0002g0175 a0001c0001t0002g0182 a0001c0001t0002g0301 others(21): Show |
25 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.437-6071_437-6056d others(18): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98228655 | |||||||
| chr8:98228807 | C | A | 1 | a0001c0001t0005g0143 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.437-6207G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98228807 | |||||||
| chr8:98228835 | G | A | 56 | a0001c0001t0001g0177 a0001c0001t0001g0314 a0001c0001t0002g0110 others(53): Show |
58 | HG00099.hp2 HG00558.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.437-6235C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98228835 | |||||||
| chr8:98229507 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.436+6648C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98229507 | |||||||
| chr8:98229510 | C | T | 27 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(24): Show |
27 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.436+6645G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98229510 | |||||||
| chr8:98229580 | G | A | 2 | a0001c0001t0001g0118 a0001c0002t0004g0015 |
2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.436+6575C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98229580 | |||||||
| chr8:98229718 | G | A | 5 | a0001c0001t0001g0290 a0001c0002t0004g0257 a0001c0002t0004g0294 others(2): Show |
5 | HG02055.hp1 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.436+6437C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98229718 | |||||||
| chr8:98229844 | A | G | 1 | a0001c0001t0002g0106 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.436+6311T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98229844 | |||||||
| chr8:98229934 | T | C | 1 | a0001c0005t0001g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.436+6221A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98229934 | |||||||
| chr8:98230169 | C | T | 1 | a0001c0001t0021g0285 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.436+5986G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98230169 | |||||||
| chr8:98230171 | G | A | 10 | a0001c0002t0001g0071 a0001c0002t0004g0011 a0001c0002t0004g0081 others(7): Show |
10 | HG01243.hp1 HG01243.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.436+5984C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98230171 | |||||||
| chr8:98230442 | T | C | 17 | a0001c0001t0001g0290 a0001c0001t0002g0175 a0001c0001t0002g0182 others(14): Show |
18 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.436+5713A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98230442 | |||||||
| chr8:98230643 | G | A | 3 | a0001c0001t0002g0106 a0001c0001t0002g0108 a0001c0001t0002g0111 |
3 | HG02109.hp1 HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.436+5512C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98230643 | |||||||
| chr8:98230687 | T | G | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+5468A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98230687 | |||||||
| chr8:98230950 | G | A | 159 | a0001c0001t0001g0177 a0001c0001t0001g0314 a0001c0001t0002g0091 others(156): Show |
162 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.436+5205C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98230950 | |||||||
| chr8:98230951 | G | A | 1 | a0001c0001t0010g0137 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.436+5204C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98230951 | |||||||
| chr8:98231350 | T | C | 1 | a0001c0001t0002g0309 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.436+4805A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98231350 | |||||||
| chr8:98231457 | C | G | 4 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(1): Show |
4 | HG01884.hp2 HG02258.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+4698G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98231457 | |||||||
| chr8:98231654 | A | T | 1 | a0001c0001t0002g0148 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.436+4501T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98231654 | |||||||
| chr8:98231689 | A | AAT | 162 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(159): Show |
163 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.436+4465_436+4466i others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98231689 | |||||||
| chr8:98231952 | T | C | 3 | a0001c0001t0003g0018 a0001c0001t0003g0115 a0001c0001t0003g0116 |
3 | HG02109.hp2 HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.436+4203A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98231952 | |||||||
| chr8:98231996 | G | A | 1 | a0001c0001t0021g0285 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.436+4159C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98231996 | |||||||
| chr8:98231997 | CT | C | 29 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(26): Show |
29 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.436+4157delA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98231997 | |||||||
| chr8:98232004 | T | A | 6 | a0001c0001t0001g0290 a0001c0001t0002g0125 a0001c0002t0004g0017 others(3): Show |
6 | HG02055.hp1 HG02055.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.436+4151A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98232004 | |||||||
| chr8:98232011 | T | A | 233 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(230): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.436+4144A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98232011 | |||||||
| chr8:98232016 | T | G | 205 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(202): Show |
208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.436+4139A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98232016 | |||||||
| chr8:98232057 | C | T | 3 | a0001c0002t0004g0017 a0001c0005t0001g0026 a0001c0005t0004g0312 |
3 | HG02055.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.436+4098G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98232057 | |||||||
| chr8:98232058 | G | A | 1 | a0001c0002t0001g0181 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.436+4097C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98232058 | |||||||
| chr8:98232138 | C | T | 2 | a0001c0001t0003g0134 a0001c0001t0003g0135 |
2 | HG02602.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.436+4017G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98232138 | |||||||
| chr8:98232139 | G | T | 3 | a0001c0002t0004g0017 a0001c0005t0001g0026 a0001c0005t0004g0312 |
3 | HG02055.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.436+4016C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98232139 | |||||||
| chr8:98232171 | G | A | 3 | a0001c0002t0004g0017 a0001c0005t0001g0026 a0001c0005t0004g0312 |
3 | HG02055.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.436+3984C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98232171 | |||||||
| chr8:98232275 | C | T | 9 | a0001c0002t0001g0071 a0001c0002t0004g0011 a0001c0002t0004g0081 others(6): Show |
9 | HG01243.hp2 HG02559.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.436+3880G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98232275 | |||||||
| chr8:98232308 | T | C | 12 | a0001c0002t0001g0071 a0001c0002t0004g0011 a0001c0002t0004g0037 others(9): Show |
12 | HG01243.hp2 HG02559.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.436+3847A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98232308 | |||||||
| chr8:98232556 | T | C | 2 | a0001c0002t0004g0257 a0001c0002t0004g0295 |
2 | HG02055.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.436+3599A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98232556 | |||||||
| chr8:98232747 | T | TA | 58 | a0001c0001t0001g0177 a0001c0001t0001g0314 a0001c0001t0002g0110 others(55): Show |
60 | HG00099.hp2 HG00558.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.436+3407dupT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98232747 | |||||||
| chr8:98232780 | T | C | 108 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(105): Show |
109 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.436+3375A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98232780 | |||||||
| chr8:98232833 | T | C | 185 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(182): Show |
188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.436+3322A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98232833 | |||||||
| chr8:98233033 | G | A | 11 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(8): Show |
11 | HG01109.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.436+3122C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233033 | |||||||
| chr8:98233058 | G | A | 12 | a0001c0002t0001g0071 a0001c0002t0004g0011 a0001c0002t0004g0037 others(9): Show |
12 | HG01243.hp2 HG02559.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.436+3097C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233058 | |||||||
| chr8:98233059 | A | G | 12 | a0001c0002t0001g0071 a0001c0002t0004g0011 a0001c0002t0004g0037 others(9): Show |
12 | HG01243.hp2 HG02559.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.436+3096T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233059 | |||||||
| chr8:98233082 | G | A | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+3073C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233082 | |||||||
| chr8:98233115 | G | A | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+3040C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233115 | |||||||
| chr8:98233214 | C | T | 2 | a0002c0003t0002g0167 a0002c0003t0002g0250 |
2 | HG02129.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.436+2941G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233214 | |||||||
| chr8:98233215 | G | A | 12 | a0001c0002t0001g0071 a0001c0002t0004g0011 a0001c0002t0004g0037 others(9): Show |
12 | HG01243.hp2 HG02559.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.436+2940C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233215 | |||||||
| chr8:98233262 | GA | G | 6 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.436+2892delT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233262 | |||||||
| chr8:98233263 | A | T | 2 | a0001c0001t0002g0309 a0001c0001t0002g0311 |
2 | HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.436+2892T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233263 | |||||||
| chr8:98233340 | A | ATG | 138 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(135): Show |
139 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.436+2813_436+2814d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233340 | |||||||
| chr8:98233340 | A | ATGTG | 7 | a0001c0002t0001g0020 a0001c0002t0001g0088 a0001c0002t0001g0155 others(4): Show |
7 | HG01099.hp1 HG01175.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.436+2811_436+2814d others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233340 | |||||||
| chr8:98233340 | ATG | A | 72 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(69): Show |
74 | HG00099.hp2 HG00558.hp2 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.436+2813_436+2814d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233340 | |||||||
| chr8:98233445 | G | A | 5 | a0001c0001t0003g0252 a0002c0003t0002g0068 a0002c0004t0001g0222 others(2): Show |
5 | HG00438.hp1 HG00609.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.436+2710C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233445 | |||||||
| chr8:98233636 | A | G | 1 | a0001c0001t0002g0277 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.436+2519T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233636 | |||||||
| chr8:98233838 | T | G | 4 | a0001c0001t0007g0291 a0001c0001t0007g0292 a0001c0001t0007g0307 others(1): Show |
4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+2317A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233838 | |||||||
| chr8:98233882 | C | T | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+2273G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233882 | |||||||
| chr8:98233934 | A | T | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+2221T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233934 | |||||||
| chr8:98234020 | TC | T | 27 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(24): Show |
27 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.436+2134delG | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234020 | |||||||
| chr8:98234037 | T | C | 5 | a0001c0001t0001g0290 a0001c0002t0004g0114 a0001c0002t0004g0257 others(2): Show |
5 | HG02055.hp1 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.436+2118A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234037 | |||||||
| chr8:98234039 | G | A | 2 | a0001c0001t0001g0290 a0001c0002t0022g0303 |
2 | HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.436+2116C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234039 | |||||||
| chr8:98234219 | C | T | 4 | a0001c0001t0007g0291 a0001c0001t0007g0292 a0001c0001t0007g0307 others(1): Show |
4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+1936G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234219 | |||||||
| chr8:98234308 | C | T | 2 | a0001c0002t0004g0017 a0001c0005t0004g0312 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.436+1847G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234308 | |||||||
| chr8:98234526 | T | A | 6 | a0001c0002t0004g0017 a0001c0002t0004g0037 a0001c0002t0004g0304 others(3): Show |
6 | HG01884.hp1 HG02055.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.436+1629A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234526 | |||||||
| chr8:98234546 | G | C | 58 | a0001c0001t0001g0177 a0001c0001t0001g0314 a0001c0001t0002g0110 others(55): Show |
60 | HG00099.hp2 HG00558.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.436+1609C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234546 | |||||||
| chr8:98234587 | G | T | 1 | a0001c0002t0001g0119 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.436+1568C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234587 | |||||||
| chr8:98234623 | C | T | 4 | a0001c0001t0007g0291 a0001c0001t0007g0292 a0001c0001t0007g0307 others(1): Show |
4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+1532G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234623 | |||||||
| chr8:98234670 | C | T | 17 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(14): Show |
17 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.436+1485G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234670 | |||||||
| chr8:98234713 | AT | A | 52 | a0001c0001t0001g0109 a0001c0001t0001g0118 a0001c0001t0001g0193 others(49): Show |
52 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.436+1441delA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234713 | |||||||
| chr8:98234713 | ATT | A | 177 | a0001c0001t0001g0177 a0001c0001t0001g0314 a0001c0001t0002g0091 others(174): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.436+1440_436+1441d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234713 | |||||||
| chr8:98234771 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.436+1384G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234771 | |||||||
| chr8:98234795 | G | A | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+1360C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234795 | |||||||
| chr8:98234825 | T | A | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+1330A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234825 | |||||||
| chr8:98235022 | C | G | 33 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(30): Show |
33 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.436+1133G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98235022 | |||||||
| chr8:98235176 | C | T | 2 | a0001c0002t0004g0017 a0001c0005t0004g0312 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.436+979G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98235176 | |||||||
| chr8:98235239 | T | C | 58 | a0001c0001t0001g0177 a0001c0001t0001g0314 a0001c0001t0002g0110 others(55): Show |
60 | HG00099.hp2 HG00558.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.436+916A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98235239 | |||||||
| chr8:98235260 | T | C | 1 | a0001c0002t0004g0310 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.436+895A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98235260 | |||||||
| chr8:98235498 | A | T | 4 | a0001c0001t0007g0291 a0001c0001t0007g0292 a0001c0001t0007g0307 others(1): Show |
4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+657T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98235498 | |||||||
| chr8:98235537 | C | T | 6 | a0001c0002t0004g0082 a0001c0002t0004g0083 a0001c0002t0004g0084 others(3): Show |
6 | HG01243.hp2 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.436+618G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98235537 | |||||||
| chr8:98235538 | G | A | 1 | a0001c0001t0003g0244 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.436+617C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98235538 | |||||||
| chr8:98235641 | ATAT | A | 22 | a0001c0001t0003g0252 a0002c0003t0001g0223 a0002c0003t0002g0065 others(19): Show |
22 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(19): Show |
intron_variant | MODIFIER | c.436+511_436+513del others(3): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98235641 | |||||||
| chr8:98235669 | A | G | 12 | a0001c0002t0001g0071 a0001c0002t0004g0011 a0001c0002t0004g0037 others(9): Show |
12 | HG01243.hp2 HG02559.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.436+486T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98235669 | |||||||
| chr8:98235718 | T | C | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+437A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98235718 | |||||||
| chr8:98235735 | C | A | 1 | a0001c0001t0003g0122 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.436+420G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98235735 | |||||||
| chr8:98235987 | C | T | 33 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(30): Show |
33 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.436+168G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98235987 | |||||||
| chr8:98235995 | G | A | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+160C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98235995 | |||||||
| chr8:98236113 | A | T | 1 | a0001c0001t0016g0293 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.436+42T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98236113 | |||||||
| chr8:98236354 | T | C | 1 | a0001c0002t0004g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.377-140A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98236354 | |||||||
| chr8:98236478 | A | T | 13 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(10): Show |
13 | HG01243.hp2 HG02559.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.377-264T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98236478 | |||||||
| chr8:98236563 | G | A | 1 | a0001c0002t0001g0205 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.377-349C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98236563 | |||||||
| chr8:98236851 | C | CA | 63 | a0001c0001t0001g0118 a0001c0001t0001g0177 a0001c0001t0002g0033 others(60): Show |
65 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.377-638dupT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98236851 | |||||||
| chr8:98236851 | C | CAA | 16 | a0001c0001t0001g0314 a0001c0001t0002g0175 a0001c0001t0002g0182 others(13): Show |
17 | HG00642.hp1 HG00642.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.377-639_377-638dup others(2): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98236851 | |||||||
| chr8:98236851 | C | CAAAAAAA | 20 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0146 others(17): Show |
20 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.377-644_377-638dup others(7): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98236851 | |||||||
| chr8:98236851 | C | CAAAAAAA others(1): Show |
7 | a0001c0001t0001g0123 a0001c0001t0001g0153 a0001c0001t0001g0157 others(4): Show |
7 | HG00609.hp1 HG02074.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.377-645_377-638dup others(8): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98236851 | |||||||
| chr8:98236851 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0005g0006 a0001c0001t0005g0008 |
2 | HG02698.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.377-647_377-638dup others(10): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98236851 | |||||||
| chr8:98236851 | CA | C | 90 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0044 others(87): Show |
91 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.377-638delT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98236851 | |||||||
| chr8:98236851 | CAA | C | 6 | a0001c0001t0001g0040 a0001c0001t0002g0144 a0001c0002t0001g0045 others(3): Show |
6 | HG00323.hp1 HG01070.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.377-639_377-638del others(2): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98236851 | |||||||
| chr8:98236851 | CAAAAAAA others(2): Show |
C | 19 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(16): Show |
19 | HG01109.hp1 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.377-646_377-638del others(9): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98236851 | |||||||
| chr8:98237060 | C | T | 1 | a0001c0002t0001g0155 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.377-846G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237060 | |||||||
| chr8:98237093 | C | T | 106 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(103): Show |
107 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.377-879G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237093 | |||||||
| chr8:98237131 | A | T | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.377-917T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237131 | |||||||
| chr8:98237137 | T | C | 8 | a0001c0002t0001g0051 a0001c0002t0001g0056 a0001c0002t0001g0063 others(5): Show |
8 | HG01109.hp2 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.377-923A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237137 | |||||||
| chr8:98237173 | G | A | 12 | a0001c0001t0002g0175 a0001c0001t0002g0182 a0001c0001t0002g0301 others(9): Show |
13 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.377-959C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237173 | |||||||
| chr8:98237209 | A | G | 8 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(5): Show |
8 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.377-995T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237209 | |||||||
| chr8:98237216 | T | TA | 20 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(17): Show |
20 | HG00733.hp1 HG00738.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.377-1003dupT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237216 | |||||||
| chr8:98237222 | T | G | 37 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(34): Show |
37 | HG00733.hp1 HG00738.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.377-1008A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237222 | |||||||
| chr8:98237253 | T | C | 2 | a0001c0002t0004g0017 a0001c0005t0004g0312 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.377-1039A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237253 | |||||||
| chr8:98237287 | A | G | 17 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(14): Show |
17 | HG01109.hp1 HG02055.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.377-1073T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237287 | |||||||
| chr8:98237474 | C | A | 17 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(14): Show |
17 | HG01109.hp1 HG02055.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.377-1260G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237474 | |||||||
| chr8:98237512 | C | T | 12 | a0001c0001t0002g0175 a0001c0001t0002g0182 a0001c0001t0002g0301 others(9): Show |
13 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.377-1298G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237512 | |||||||
| chr8:98237576 | C | T | 2 | a0002c0003t0002g0192 a0002c0003t0002g0194 |
2 | NA18970.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.377-1362G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237576 | |||||||
| chr8:98237629 | T | G | 1 | a0001c0001t0002g0259 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.377-1415A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237629 | |||||||
| chr8:98237630 | G | A | 4 | a0001c0001t0007g0291 a0001c0001t0007g0292 a0001c0001t0007g0307 others(1): Show |
4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-1416C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237630 | |||||||
| chr8:98237892 | G | A | 27 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(24): Show |
27 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.377-1678C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237892 | |||||||
| chr8:98237949 | C | T | 1 | a0001c0001t0003g0298 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.377-1735G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237949 | |||||||
| chr8:98238016 | A | G | 12 | a0001c0001t0002g0175 a0001c0001t0002g0182 a0001c0001t0002g0301 others(9): Show |
13 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.377-1802T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98238016 | |||||||
| chr8:98238492 | G | A | 1 | a0002c0003t0002g0068 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.377-2278C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98238492 | |||||||
| chr8:98238608 | C | CT | 37 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(34): Show |
37 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.377-2395dupA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98238608 | |||||||
| chr8:98238616 | T | A | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.377-2402A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98238616 | |||||||
| chr8:98238621 | T | C | 31 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(28): Show |
31 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.377-2407A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98238621 | |||||||
| chr8:98238622 | C | T | 34 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(31): Show |
34 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.377-2408G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98238622 | |||||||
| chr8:98238676 | C | T | 60 | a0001c0001t0001g0177 a0001c0001t0001g0314 a0001c0001t0002g0110 others(57): Show |
62 | HG00099.hp2 HG00558.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.377-2462G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98238676 | |||||||
| chr8:98238726 | T | C | 2 | a0002c0003t0002g0167 a0002c0003t0002g0250 |
2 | HG02129.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.377-2512A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98238726 | |||||||
| chr8:98238873 | C | T | 1 | a0002c0004t0001g0253 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.377-2659G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98238873 | |||||||
| chr8:98238903 | G | A | 1 | a0001c0002t0001g0228 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.377-2689C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98238903 | |||||||
| chr8:98238904 | G | A | 1 | a0001c0001t0024g0150 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.377-2690C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98238904 | |||||||
| chr8:98238937 | G | T | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.377-2723C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98238937 | |||||||
| chr8:98239130 | G | A | 12 | a0001c0001t0002g0175 a0001c0001t0002g0182 a0001c0001t0002g0301 others(9): Show |
13 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.377-2916C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98239130 | |||||||
| chr8:98239215 | T | C | 1 | a0001c0005t0001g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.377-3001A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98239215 | |||||||
| chr8:98239316 | C | T | 1 | a0001c0002t0004g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.377-3102G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98239316 | |||||||
| chr8:98239761 | C | T | 8 | a0001c0002t0001g0051 a0001c0002t0001g0056 a0001c0002t0001g0063 others(5): Show |
8 | HG01109.hp2 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.377-3547G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98239761 | |||||||
| chr8:98239777 | A | G | 1 | a0002c0003t0002g0224 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.377-3563T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98239777 | |||||||
| chr8:98239887 | G | A | 242 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(239): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.377-3673C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98239887 | |||||||
| chr8:98240109 | A | G | 4 | a0001c0001t0007g0291 a0001c0001t0007g0292 a0001c0001t0007g0307 others(1): Show |
4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-3895T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98240109 | |||||||
| chr8:98240144 | T | C | 1 | a0002c0003t0002g0075 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.377-3930A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98240144 | |||||||
| chr8:98240217 | T | C | 1 | a0001c0001t0002g0210 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.377-4003A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98240217 | |||||||
| chr8:98240272 | A | G | 1 | a0002c0004t0001g0053 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.377-4058T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98240272 | |||||||
| chr8:98240334 | T | C | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.377-4120A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98240334 | |||||||
| chr8:98240619 | C | T | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.377-4405G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98240619 | |||||||
| chr8:98240638 | T | C | 3 | a0001c0005t0001g0030 a0001c0005t0001g0035 a0001c0005t0004g0029 |
3 | HG02145.hp1 HG02486.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.377-4424A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98240638 | |||||||
| chr8:98240864 | G | A | 100 | a0001c0001t0002g0091 a0001c0001t0002g0144 a0001c0001t0002g0165 others(97): Show |
101 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.377-4650C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98240864 | |||||||
| chr8:98240883 | C | T | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.377-4669G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98240883 | |||||||
| chr8:98240898 | G | A | 8 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(5): Show |
8 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.377-4684C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98240898 | |||||||
| chr8:98241139 | A | T | 22 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(19): Show |
22 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.377-4925T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98241139 | |||||||
| chr8:98241411 | C | T | 241 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(238): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.377-5197G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98241411 | |||||||
| chr8:98241649 | G | A | 241 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(238): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.377-5435C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98241649 | |||||||
| chr8:98241781 | G | C | 241 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(238): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.377-5567C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98241781 | |||||||
| chr8:98241817 | C | T | 241 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(238): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.377-5603G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98241817 | |||||||
| chr8:98241831 | CT | C | 49 | a0001c0001t0001g0177 a0001c0001t0001g0314 a0001c0001t0003g0001 others(46): Show |
51 | HG00099.hp2 HG00558.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.377-5618delA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98241831 | |||||||
| chr8:98241835 | C | T | 1 | a0001c0001t0003g0283 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.377-5621G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98241835 | |||||||
| chr8:98241847 | C | T | 1 | a0001c0006t0002g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.377-5633G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98241847 | |||||||
| chr8:98241904 | C | T | 8 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(5): Show |
8 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.377-5690G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98241904 | |||||||
| chr8:98242037 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.377-5823C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242037 | |||||||
| chr8:98242093 | G | C | 240 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(237): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.377-5879C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242093 | |||||||
| chr8:98242264 | C | G | 4 | a0001c0001t0007g0291 a0001c0001t0007g0292 a0001c0001t0007g0307 others(1): Show |
4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-6050G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242264 | |||||||
| chr8:98242300 | C | A | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.377-6086G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242300 | |||||||
| chr8:98242315 | G | T | 239 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(236): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.377-6101C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242315 | |||||||
| chr8:98242402 | G | T | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.377-6188C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242402 | |||||||
| chr8:98242488 | A | ATTT | 25 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(22): Show |
25 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.377-6277_377-6275d others(5): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | |||||||
| chr8:98242488 | A | ATTTTTTG others(4): Show |
1 | a0001c0002t0001g0327 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.377-6275_377-6274i others(13): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | |||||||
| chr8:98242488 | A | ATTTTTTG others(5): Show |
1 | a0001c0002t0001g0229 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.377-6275_377-6274i others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | |||||||
| chr8:98242488 | A | ATTTTTTG others(5): Show |
50 | a0001c0001t0002g0091 a0001c0001t0002g0144 a0001c0001t0002g0165 others(47): Show |
50 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.377-6275_377-6274i others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | |||||||
| chr8:98242488 | A | ATTTTTTG others(6): Show |
37 | a0001c0001t0003g0149 a0001c0001t0003g0170 a0001c0002t0001g0003 others(34): Show |
38 | HG00408.hp1 HG00558.hp1 HG01175.hp1 others(35): Show |
intron_variant | MODIFIER | c.377-6275_377-6274i others(15): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | |||||||
| chr8:98242488 | A | ATTTTTTG others(7): Show |
8 | a0001c0001t0003g0252 a0001c0002t0001g0062 a0001c0002t0001g0063 others(5): Show |
8 | HG00438.hp1 HG01109.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.377-6275_377-6274i others(16): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | |||||||
| chr8:98242488 | A | ATTTTTTG others(8): Show |
1 | a0002c0004t0001g0222 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.377-6275_377-6274i others(17): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | |||||||
| chr8:98242488 | A | ATTTTTTT others(2): Show |
7 | a0001c0001t0002g0182 a0001c0001t0007g0307 a0001c0001t0007g0316 others(4): Show |
7 | HG01255.hp2 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.377-6283_377-6275d others(11): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | |||||||
| chr8:98242488 | A | ATTTTTTT others(3): Show |
9 | a0001c0001t0002g0175 a0001c0001t0002g0301 a0001c0001t0005g0002 others(6): Show |
10 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.377-6284_377-6275d others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | |||||||
| chr8:98242488 | A | ATTTTTTT others(4): Show |
16 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0040 others(13): Show |
16 | HG01346.hp2 HG01884.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.377-6285_377-6275d others(13): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | |||||||
| chr8:98242488 | A | ATTTTTTT others(5): Show |
3 | a0001c0001t0001g0120 a0001c0002t0006g0246 a0001c0006t0002g0019 |
3 | HG02818.hp2 HG03130.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.377-6286_377-6275d others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | |||||||
| chr8:98242488 | A | ATTTTTTT others(6): Show |
2 | a0001c0002t0006g0061 a0001c0002t0006g0264 |
2 | NA19066.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.377-6287_377-6275d others(15): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | |||||||
| chr8:98242488 | A | ATTTTTTT others(7): Show |
6 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(3): Show |
6 | HG02280.hp1 HG03130.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.377-6288_377-6275d others(16): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | |||||||
| chr8:98242488 | A | ATTTTTTT others(9): Show |
1 | a0001c0001t0001g0028 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.377-6290_377-6275d others(18): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | |||||||
| chr8:98242488 | AT | A | 53 | a0001c0001t0001g0177 a0001c0001t0001g0314 a0001c0001t0002g0067 others(50): Show |
55 | HG00099.hp2 HG00558.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.377-6275delA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | |||||||
| chr8:98242489 | T | TTTTTTGT others(7): Show |
1 | a0001c0002t0004g0310 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.377-6276_377-6275i others(16): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242489 | |||||||
| chr8:98242494 | T | TGTTTTTT others(5): Show |
1 | a0001c0002t0001g0097 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.377-6281_377-6280i others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242494 | |||||||
| chr8:98242585 | G | A | 237 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(234): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.377-6371C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242585 | |||||||
| chr8:98242635 | A | G | 33 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.377-6421T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242635 | |||||||
| chr8:98242652 | A | G | 22 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0040 others(19): Show |
23 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.377-6438T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242652 | |||||||
| chr8:98242779 | C | T | 1 | a0001c0001t0003g0132 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.377-6565G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242779 | |||||||
| chr8:98242780 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.377-6566C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242780 | |||||||
| chr8:98242839 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.377-6625A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242839 | |||||||
| chr8:98242857 | A | G | 1 | a0001c0002t0001g0190 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.377-6643T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242857 | |||||||
| chr8:98242942 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.377-6728T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242942 | |||||||
| chr8:98243197 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.377-6983G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98243197 | |||||||
| chr8:98243318 | G | A | 2 | a0001c0001t0001g0289 a0002c0004t0001g0078 |
2 | NA18612.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.377-7104C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98243318 | |||||||
| chr8:98243486 | G | A | 21 | a0001c0001t0002g0284 a0001c0001t0002g0322 a0001c0001t0002g0323 others(18): Show |
21 | HG00558.hp2 HG00673.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.377-7272C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98243486 | |||||||
| chr8:98243550 | G | A | 7 | a0001c0001t0001g0016 a0001c0001t0001g0314 a0001c0001t0009g0012 others(4): Show |
7 | HG01884.hp1 HG02145.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.377-7336C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98243550 | |||||||
| chr8:98243691 | T | C | 14 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
14 | HG01884.hp2 HG02258.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.377-7477A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98243691 | |||||||
| chr8:98243772 | A | G | 5 | a0001c0001t0001g0290 a0001c0002t0004g0015 a0001c0002t0022g0303 others(2): Show |
5 | HG02486.hp1 HG02630.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.377-7558T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98243772 | |||||||
| chr8:98243793 | AC | A | 74 | a0001c0001t0001g0109 a0001c0001t0001g0118 a0001c0001t0001g0176 others(71): Show |
77 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.377-7580delG | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98243793 | |||||||
| chr8:98243870 | T | A | 2 | a0001c0002t0001g0313 a0001c0002t0001g0317 |
2 | HG03710.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.377-7656A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98243870 | |||||||
| chr8:98243893 | A | T | 1 | a0001c0002t0001g0204 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.377-7679T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98243893 | |||||||
| chr8:98243926 | T | G | 10 | a0001c0001t0001g0290 a0001c0001t0002g0175 a0001c0001t0002g0182 others(7): Show |
10 | HG01123.hp2 HG01192.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.377-7712A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98243926 | |||||||
| chr8:98244081 | A | G | 3 | a0001c0001t0001g0290 a0001c0002t0022g0303 a0004c0008t0003g0262 |
3 | HG02486.hp1 HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.377-7867T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244081 | |||||||
| chr8:98244202 | C | CA | 66 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0001g0123 others(63): Show |
67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.377-7989dupT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244202 | |||||||
| chr8:98244266 | C | CGGTGGGC others(33): Show |
2 | a0001c0001t0003g0115 a0001c0001t0003g0116 |
2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.377-8092_377-8053d others(42): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244266 | |||||||
| chr8:98244266 | C | CGGTGGGC others(73): Show |
2 | a0001c0002t0004g0015 a0001c0005t0001g0026 |
2 | HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.377-8053_377-8052i others(82): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244266 | |||||||
| chr8:98244267 | G | T | 8 | a0001c0001t0003g0130 a0001c0001t0003g0131 a0001c0002t0004g0082 others(5): Show |
8 | HG01243.hp2 HG02559.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.377-8053C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244267 | |||||||
| chr8:98244285 | A | AGGTAGTC others(33): Show |
1 | a0001c0001t0015g0195 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.377-8111_377-8072d others(42): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244285 | |||||||
| chr8:98244285 | AGGTAGTC others(33): Show |
A | 9 | a0001c0001t0001g0118 a0001c0001t0002g0284 a0001c0001t0003g0283 others(6): Show |
9 | HG02004.hp1 HG02155.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.377-8111_377-8072d others(42): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244285 | |||||||
| chr8:98244285 | AGGTAGTC others(73): Show |
A | 184 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(181): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.376+8098_377-8072d others(82): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244285 | |||||||
| chr8:98244287 | G | GTAGTCTG others(33): Show |
66 | a0001c0001t0001g0109 a0001c0001t0001g0176 a0001c0001t0001g0179 others(63): Show |
69 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.377-8074_377-8073i others(42): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244287 | |||||||
| chr8:98244325 | G | A | 70 | a0001c0001t0001g0109 a0001c0001t0001g0176 a0001c0001t0001g0179 others(67): Show |
73 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.377-8111C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244325 | |||||||
| chr8:98244327 | G | A | 2 | a0001c0002t0004g0015 a0001c0005t0001g0026 |
2 | HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.377-8113C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244327 | |||||||
| chr8:98244365 | G | A | 71 | a0001c0001t0001g0109 a0001c0001t0001g0118 a0001c0001t0001g0176 others(68): Show |
74 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.376+8098C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244365 | |||||||
| chr8:98244405 | G | C | 16 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(13): Show |
16 | HG00733.hp1 HG00738.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.376+8058C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244405 | |||||||
| chr8:98244500 | T | C | 1 | a0001c0002t0001g0260 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.376+7963A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244500 | |||||||
| chr8:98244572 | C | CGCTGTGG others(14): Show |
59 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(56): Show |
60 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.376+7870_376+7890d others(23): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244572 | |||||||
| chr8:98244572 | CGCTGTGG others(14): Show |
C | 96 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(93): Show |
96 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.376+7870_376+7890d others(23): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244572 | |||||||
| chr8:98244579 | G | A | 5 | a0001c0001t0002g0175 a0001c0001t0002g0182 a0001c0001t0002g0301 others(2): Show |
5 | HG01123.hp2 HG01192.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.376+7884C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244579 | |||||||
| chr8:98244581 | G | A | 5 | a0001c0001t0002g0175 a0001c0001t0002g0182 a0001c0001t0002g0301 others(2): Show |
5 | HG01123.hp2 HG01192.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.376+7882C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244581 | |||||||
| chr8:98244582 | ATG | A | 5 | a0001c0001t0002g0175 a0001c0001t0002g0182 a0001c0001t0002g0301 others(2): Show |
5 | HG01123.hp2 HG01192.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.376+7879_376+7880d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244582 | |||||||
| chr8:98244585 | A | G | 5 | a0001c0001t0002g0175 a0001c0001t0002g0182 a0001c0001t0002g0301 others(2): Show |
5 | HG01123.hp2 HG01192.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.376+7878T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244585 | |||||||
| chr8:98244587 | A | G | 5 | a0001c0001t0002g0175 a0001c0001t0002g0182 a0001c0001t0002g0301 others(2): Show |
5 | HG01123.hp2 HG01192.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.376+7876T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244587 | |||||||
| chr8:98244593 | G | C | 5 | a0001c0001t0002g0175 a0001c0001t0002g0182 a0001c0001t0002g0301 others(2): Show |
5 | HG01123.hp2 HG01192.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.376+7870C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244593 | |||||||
| chr8:98244635 | T | C | 5 | a0001c0001t0002g0175 a0001c0001t0002g0182 a0001c0001t0002g0301 others(2): Show |
5 | HG01123.hp2 HG01192.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.376+7828A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244635 | |||||||
| chr8:98244645 | G | A | 2 | a0001c0002t0004g0257 a0001c0002t0004g0295 |
2 | HG02055.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.376+7818C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244645 | |||||||
| chr8:98244870 | C | T | 1 | a0001c0002t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.376+7593G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244870 | |||||||
| chr8:98244949 | C | T | 2 | a0001c0002t0001g0313 a0001c0002t0001g0317 |
2 | HG03710.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.376+7514G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244949 | |||||||
| chr8:98245163 | C | T | 58 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0123 others(55): Show |
59 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.376+7300G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98245163 | |||||||
| chr8:98245211 | C | T | 5 | a0001c0001t0001g0118 a0001c0001t0001g0290 a0001c0002t0004g0114 others(2): Show |
5 | HG02486.hp1 HG02965.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.376+7252G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98245211 | |||||||
| chr8:98245224 | C | A | 4 | a0001c0001t0003g0122 a0001c0001t0003g0134 a0001c0001t0003g0135 others(1): Show |
4 | HG02602.hp2 HG03239.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.376+7239G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98245224 | |||||||
| chr8:98245232 | G | A | 3 | a0001c0001t0002g0322 a0001c0001t0002g0323 a0001c0001t0002g0324 |
3 | HG03098.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.376+7231C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98245232 | |||||||
| chr8:98245289 | A | T | 6 | a0001c0001t0007g0291 a0001c0001t0007g0292 a0001c0001t0007g0307 others(3): Show |
6 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.376+7174T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98245289 | |||||||
| chr8:98245680 | T | C | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.376+6783A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98245680 | |||||||
| chr8:98245808 | A | G | 1 | a0001c0001t0003g0101 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.376+6655T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98245808 | |||||||
| chr8:98245959 | G | A | 74 | a0001c0001t0001g0098 a0001c0001t0001g0118 a0001c0001t0001g0123 others(71): Show |
75 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.376+6504C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98245959 | |||||||
| chr8:98245975 | TC | T | 5 | a0001c0001t0001g0239 a0001c0001t0001g0241 a0001c0005t0001g0030 others(2): Show |
5 | HG02145.hp1 HG02486.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.376+6487delG | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98245975 | |||||||
| chr8:98246006 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.376+6457C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98246006 | |||||||
| chr8:98246261 | A | C | 7 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(4): Show |
7 | HG01109.hp1 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.376+6202T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98246261 | |||||||
| chr8:98246388 | C | T | 5 | a0001c0001t0002g0284 a0001c0001t0002g0322 a0001c0001t0002g0323 others(2): Show |
5 | HG02257.hp2 HG03098.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.376+6075G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98246388 | |||||||
| chr8:98246420 | A | T | 3 | a0001c0001t0002g0322 a0001c0001t0002g0323 a0001c0001t0002g0324 |
3 | HG03098.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.376+6043T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98246420 | |||||||
| chr8:98246451 | G | A | 3 | a0001c0001t0002g0169 a0001c0001t0002g0171 a0001c0001t0002g0172 |
3 | NA18944.hp1 NA18957.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.376+6012C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98246451 | |||||||
| chr8:98246628 | G | T | 2 | a0001c0001t0007g0291 a0001c0001t0007g0292 |
2 | HG00733.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.376+5835C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98246628 | |||||||
| chr8:98246785 | G | C | 1 | a0001c0001t0001g0197 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.376+5678C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98246785 | |||||||
| chr8:98246945 | A | T | 1 | a0002c0004t0001g0287 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.376+5518T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98246945 | |||||||
| chr8:98246956 | C | A | 1 | a0001c0002t0001g0059 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.376+5507G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98246956 | |||||||
| chr8:98247120 | C | G | 1 | a0001c0001t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.376+5343G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98247120 | |||||||
| chr8:98247346 | A | C | 1 | a0001c0002t0004g0325 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.376+5117T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98247346 | |||||||
| chr8:98247413 | C | A | 83 | a0001c0001t0001g0197 a0001c0001t0001g0290 a0001c0001t0002g0033 others(80): Show |
84 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.376+5050G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98247413 | |||||||
| chr8:98247454 | T | C | 222 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(219): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.376+5009A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98247454 | |||||||
| chr8:98247564 | C | T | 12 | a0001c0001t0003g0134 a0001c0001t0003g0135 a0001c0001t0003g0296 others(9): Show |
12 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.376+4899G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98247564 | |||||||
| chr8:98247723 | G | A | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.376+4740C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98247723 | |||||||
| chr8:98247736 | A | C | 2 | a0001c0001t0002g0277 a0001c0002t0001g0020 |
2 | HG00741.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.376+4727T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98247736 | |||||||
| chr8:98248084 | A | G | 1 | a0001c0002t0004g0017 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.376+4379T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98248084 | |||||||
| chr8:98248088 | C | T | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.376+4375G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98248088 | |||||||
| chr8:98248137 | T | C | 3 | a0001c0001t0001g0118 a0001c0001t0003g0018 a0001c0002t0004g0081 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.376+4326A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98248137 | |||||||
| chr8:98248216 | C | T | 1 | a0001c0002t0001g0089 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.376+4247G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98248216 | |||||||
| chr8:98248976 | C | A | 7 | a0001c0001t0002g0085 a0001c0002t0004g0082 a0001c0002t0004g0083 others(4): Show |
7 | HG01243.hp1 HG01243.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.376+3487G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98248976 | |||||||
| chr8:98248985 | T | C | 1 | a0001c0001t0001g0237 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.376+3478A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98248985 | |||||||
| chr8:98249097 | T | A | 3 | a0001c0005t0001g0030 a0001c0005t0001g0035 a0001c0005t0004g0029 |
3 | HG02145.hp1 HG02486.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.376+3366A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98249097 | |||||||
| chr8:98249102 | G | A | 1 | a0001c0002t0025g0318 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.376+3361C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98249102 | |||||||
| chr8:98249154 | T | G | 81 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(78): Show |
81 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.376+3309A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98249154 | |||||||
| chr8:98249220 | G | C | 1 | a0001c0002t0001g0107 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.376+3243C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98249220 | |||||||
| chr8:98249490 | A | G | 8 | a0001c0001t0002g0036 a0001c0001t0003g0050 a0001c0001t0003g0244 others(5): Show |
9 | HG00280.hp1 HG01106.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.376+2973T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98249490 | |||||||
| chr8:98249517 | G | A | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.376+2946C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98249517 | |||||||
| chr8:98249598 | A | G | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.376+2865T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98249598 | |||||||
| chr8:98249739 | C | T | 10 | a0001c0001t0001g0118 a0001c0002t0004g0081 a0001c0002t0004g0306 others(7): Show |
10 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.376+2724G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98249739 | |||||||
| chr8:98249802 | G | A | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.376+2661C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98249802 | |||||||
| chr8:98249936 | A | C | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.376+2527T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98249936 | |||||||
| chr8:98250003 | C | T | 5 | a0001c0001t0002g0085 a0001c0002t0004g0082 a0001c0002t0004g0083 others(2): Show |
5 | HG02723.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.376+2460G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98250003 | |||||||
| chr8:98250217 | A | G | 131 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(128): Show |
132 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.376+2246T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98250217 | |||||||
| chr8:98250289 | G | C | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.376+2174C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98250289 | |||||||
| chr8:98250324 | TAA | T | 5 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(2): Show |
5 | HG01109.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.376+2137_376+2138d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98250324 | |||||||
| chr8:98250336 | G | A | 31 | a0001c0001t0001g0176 a0001c0001t0001g0179 a0001c0001t0001g0240 others(28): Show |
31 | HG00408.hp2 HG00597.hp1 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.376+2127C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98250336 | |||||||
| chr8:98250411 | G | T | 2 | a0001c0001t0009g0185 a0001c0002t0004g0257 |
2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.376+2052C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98250411 | |||||||
| chr8:98250498 | C | T | 3 | a0001c0001t0001g0240 a0001c0001t0003g0174 a0001c0002t0001g0191 |
3 | HG00673.hp2 HG02523.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.376+1965G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98250498 | |||||||
| chr8:98250510 | A | G | 5 | a0001c0001t0001g0120 a0001c0001t0003g0115 a0001c0001t0003g0116 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.376+1953T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98250510 | |||||||
| chr8:98250659 | A | C | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.376+1804T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98250659 | |||||||
| chr8:98250837 | C | G | 1 | a0001c0002t0004g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.376+1626G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98250837 | |||||||
| chr8:98250944 | C | T | 1 | a0001c0001t0016g0293 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.376+1519G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98250944 | |||||||
| chr8:98251164 | A | G | 2 | a0001c0002t0004g0017 a0001c0002t0022g0303 |
2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.376+1299T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98251164 | |||||||
| chr8:98251190 | C | T | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.376+1273G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98251190 | |||||||
| chr8:98251191 | G | A | 1 | a0001c0001t0009g0013 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.376+1272C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98251191 | |||||||
| chr8:98251449 | T | C | 7 | a0001c0001t0001g0109 a0001c0001t0002g0108 a0001c0001t0002g0110 others(4): Show |
7 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.376+1014A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98251449 | |||||||
| chr8:98251489 | G | C | 1 | a0001c0001t0001g0314 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.376+974C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98251489 | |||||||
| chr8:98251497 | A | C | 2 | a0001c0001t0001g0239 a0001c0001t0001g0241 |
2 | HG02683.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.376+966T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98251497 | |||||||
| chr8:98251586 | A | G | 9 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(6): Show |
9 | HG01884.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.376+877T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98251586 | |||||||
| chr8:98251631 | A | G | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.376+832T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98251631 | |||||||
| chr8:98252178 | T | C | 7 | a0001c0005t0001g0026 a0001c0005t0001g0030 a0001c0005t0001g0035 others(4): Show |
7 | HG02145.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.376+285A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98252178 | |||||||
| chr8:98252230 | C | G | 1 | a0001c0001t0009g0012 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.376+233G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98252230 | |||||||
| chr8:98252260 | C | T | 2 | a0001c0001t0003g0183 a0001c0001t0003g0276 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.376+203G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98252260 | |||||||
| chr8:98252417 | A | T | 1 | a0001c0001t0003g0243 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.376+46T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98252417 | |||||||
| chr8:98252733 | G | A | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.205-99C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 2/10 | chr8 | 98252733 | |||||||
| chr8:98253020 | T | C | 1 | a0001c0001t0005g0233 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.205-386A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 2/10 | chr8 | 98253020 | |||||||
| chr8:98253393 | A | G | 2 | a0001c0001t0003g0183 a0001c0001t0003g0276 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.204+626T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 2/10 | chr8 | 98253393 | |||||||
| chr8:98253743 | A | G | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.204+276T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 2/10 | chr8 | 98253743 | |||||||
| chr8:98253750 | C | T | 1 | a0001c0002t0001g0062 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.204+269G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 2/10 | chr8 | 98253750 | |||||||
| chr8:98253876 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.204+143A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 2/10 | chr8 | 98253876 | |||||||
| chr8:98254511 | A | T | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-424T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98254511 | |||||||
| chr8:98254559 | A | G | 12 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0002g0309 others(9): Show |
12 | HG01884.hp1 HG02451.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.136-472T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98254559 | |||||||
| chr8:98254854 | G | C | 2 | a0001c0001t0001g0024 a0001c0002t0004g0114 |
2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.136-767C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98254854 | |||||||
| chr8:98254854 | G | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG01109.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.136-767C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98254854 | |||||||
| chr8:98255045 | ATGCTTCT others(15): Show |
A | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-980_136-959del others(22): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98255045 | |||||||
| chr8:98255417 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.136-1330G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98255417 | |||||||
| chr8:98255520 | T | C | 3 | a0001c0001t0001g0118 a0001c0001t0003g0018 a0001c0002t0004g0081 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136-1433A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98255520 | |||||||
| chr8:98255913 | G | T | 1 | a0001c0002t0001g0080 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.136-1826C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98255913 | |||||||
| chr8:98255968 | G | A | 1 | a0001c0001t0003g0001 | 3 | HG01070.hp2 HG01071.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.136-1881C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98255968 | |||||||
| chr8:98256213 | G | A | 7 | a0001c0005t0001g0026 a0001c0005t0001g0030 a0001c0005t0001g0035 others(4): Show |
7 | HG02145.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-2126C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98256213 | |||||||
| chr8:98256221 | G | A | 127 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(124): Show |
128 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.136-2134C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98256221 | |||||||
| chr8:98256469 | T | G | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-2382A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98256469 | |||||||
| chr8:98256472 | T | C | 9 | a0001c0001t0001g0197 a0001c0001t0003g0126 a0001c0001t0005g0196 others(6): Show |
9 | HG00558.hp1 HG02056.hp1 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.136-2385A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98256472 | |||||||
| chr8:98256621 | T | C | 1 | a0001c0005t0004g0029 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.136-2534A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98256621 | |||||||
| chr8:98256631 | T | TA | 203 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(200): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.136-2545dupT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98256631 | |||||||
| chr8:98256706 | G | A | 3 | a0001c0001t0001g0180 a0001c0001t0003g0043 a0001c0002t0001g0181 |
3 | HG00735.hp1 HG01433.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.136-2619C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98256706 | |||||||
| chr8:98257056 | G | T | 1 | a0001c0002t0006g0264 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.136-2969C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98257056 | |||||||
| chr8:98257328 | T | C | 4 | a0001c0002t0001g0046 a0001c0002t0001g0062 a0001c0002t0001g0063 others(1): Show |
4 | HG01109.hp2 HG01192.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-3241A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98257328 | |||||||
| chr8:98257336 | T | A | 7 | a0001c0005t0001g0026 a0001c0005t0001g0030 a0001c0005t0001g0035 others(4): Show |
7 | HG02145.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-3249A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98257336 | |||||||
| chr8:98257349 | TTTTTTTT others(24): Show |
T | 203 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(200): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.136-3293_136-3263d others(33): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98257349 | |||||||
| chr8:98257724 | T | C | 2 | a0001c0002t0004g0294 a0001c0002t0004g0295 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.136-3637A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98257724 | |||||||
| chr8:98257728 | C | T | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-3641G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98257728 | |||||||
| chr8:98257866 | C | T | 7 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(4): Show |
7 | HG01109.hp1 HG01496.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-3779G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98257866 | |||||||
| chr8:98257899 | GA | G | 11 | a0001c0001t0003g0134 a0001c0001t0003g0135 a0001c0001t0005g0136 others(8): Show |
11 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.136-3813delT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98257899 | |||||||
| chr8:98258399 | T | C | 5 | a0001c0001t0001g0120 a0001c0001t0003g0115 a0001c0001t0003g0116 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-4312A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98258399 | |||||||
| chr8:98258477 | A | C | 248 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(245): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.136-4390T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98258477 | |||||||
| chr8:98258539 | C | T | 2 | a0001c0002t0001g0199 a0001c0002t0001g0245 |
2 | HG00597.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.136-4452G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98258539 | |||||||
| chr8:98258612 | G | A | 1 | a0001c0002t0004g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.136-4525C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98258612 | |||||||
| chr8:98258630 | A | G | 1 | a0001c0002t0004g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.136-4543T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98258630 | |||||||
| chr8:98258650 | A | G | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-4563T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98258650 | |||||||
| chr8:98258748 | A | G | 2 | a0001c0002t0004g0306 a0002c0004t0001g0222 |
2 | HG00609.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.136-4661T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98258748 | |||||||
| chr8:98258779 | CT | C | 292 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(289): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.136-4693delA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98258779 | |||||||
| chr8:98258851 | T | A | 1 | a0001c0001t0003g0050 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.136-4764A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98258851 | |||||||
| chr8:98258862 | C | T | 1 | a0001c0001t0009g0013 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.136-4775G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98258862 | |||||||
| chr8:98258942 | T | C | 5 | a0001c0001t0001g0120 a0001c0001t0003g0115 a0001c0001t0003g0116 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-4855A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98258942 | |||||||
| chr8:98258951 | A | T | 5 | a0001c0001t0001g0120 a0001c0001t0003g0115 a0001c0001t0003g0116 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-4864T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98258951 | |||||||
| chr8:98259019 | T | C | 2 | a0001c0002t0001g0319 a0001c0002t0019g0320 |
2 | HG00738.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.136-4932A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259019 | |||||||
| chr8:98259069 | C | CTTT | 4 | a0001c0001t0002g0091 a0001c0001t0003g0244 a0001c0001t0010g0140 others(1): Show |
4 | HG01069.hp2 HG01070.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-4983_136-4982i others(5): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | |||||||
| chr8:98259069 | C | CTTTT | 55 | a0001c0001t0001g0290 a0001c0001t0002g0036 a0001c0001t0002g0048 others(52): Show |
56 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.136-4983_136-4982i others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | |||||||
| chr8:98259069 | C | CTTTTT | 13 | a0001c0001t0002g0047 a0001c0001t0002g0054 a0001c0001t0002g0100 others(10): Show |
13 | HG01346.hp2 HG02080.hp1 HG02738.hp1 others(10): Show |
intron_variant | MODIFIER | c.136-4983_136-4982i others(7): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | |||||||
| chr8:98259069 | C | CTTTTTTT others(4): Show |
1 | a0001c0002t0004g0305 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.136-4983_136-4982i others(13): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | |||||||
| chr8:98259069 | C | CTTTTTTT others(5): Show |
2 | a0001c0002t0004g0114 a0001c0002t0004g0304 |
2 | HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.136-4983_136-4982i others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | |||||||
| chr8:98259069 | C | CTTTTTTT others(6): Show |
1 | a0001c0002t0004g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.136-4983_136-4982i others(15): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | |||||||
| chr8:98259069 | C | CTTTTTTT others(8): Show |
2 | a0001c0001t0002g0322 a0001c0001t0002g0324 |
2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.136-4983_136-4982i others(17): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | |||||||
| chr8:98259069 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0002g0323 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.136-4983_136-4982i others(18): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | |||||||
| chr8:98259069 | C | CTTTTTTT others(10): Show |
2 | a0001c0002t0004g0084 a0001c0002t0004g0325 |
2 | HG01243.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.136-4983_136-4982i others(19): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | |||||||
| chr8:98259069 | C | CTTTTTTT others(12): Show |
3 | a0001c0002t0004g0082 a0001c0002t0004g0083 a0001c0002t0020g0086 |
3 | HG02723.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.136-4983_136-4982i others(21): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | |||||||
| chr8:98259069 | C | CTTTTTTT others(13): Show |
1 | a0001c0001t0002g0085 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.136-4983_136-4982i others(22): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | |||||||
| chr8:98259069 | C | CTTTTTTT others(17): Show |
1 | a0001c0002t0004g0087 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.136-4983_136-4982i others(26): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | |||||||
| chr8:98259069 | CCT | C | 4 | a0001c0001t0001g0120 a0001c0001t0003g0115 a0001c0002t0004g0294 others(1): Show |
4 | HG02055.hp1 HG02109.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-4984_136-4983d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | |||||||
| chr8:98259069 | CCTT | C | 12 | a0001c0001t0001g0152 a0001c0001t0001g0197 a0001c0001t0001g0237 others(9): Show |
12 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(9): Show |
intron_variant | MODIFIER | c.136-4985_136-4983d others(5): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | |||||||
| chr8:98259069 | CCTTT | C | 115 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(112): Show |
116 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.136-4986_136-4983d others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | |||||||
| chr8:98259069 | CCTTTT | C | 9 | a0001c0001t0001g0146 a0001c0002t0001g0202 a0001c0005t0001g0026 others(6): Show |
9 | HG02145.hp1 HG02486.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.136-4987_136-4983d others(7): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | |||||||
| chr8:98259069 | CCTTTTT | C | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(1): Show |
4 | HG01109.hp1 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-4988_136-4983d others(8): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | |||||||
| chr8:98259069 | CCTTTTTT others(1): Show |
C | 3 | a0001c0001t0001g0118 a0001c0001t0003g0018 a0001c0002t0004g0081 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136-4990_136-4983d others(10): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | |||||||
| chr8:98259069 | CCTTTTTT others(3): Show |
C | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-4992_136-4983d others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | |||||||
| chr8:98259070 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0009g0012 a0001c0002t0004g0011 |
2 | HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.136-4993_136-4984d others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259070 | |||||||
| chr8:98259070 | C | CTTTTTTT others(4): Show |
4 | a0001c0001t0001g0014 a0001c0001t0002g0311 a0001c0001t0009g0013 others(1): Show |
4 | HG01884.hp1 HG02809.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-4994_136-4984d others(13): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259070 | |||||||
| chr8:98259070 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0001g0016 a0001c0001t0002g0309 |
2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.136-4995_136-4984d others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259070 | |||||||
| chr8:98259070 | C | CTTTTTTT others(6): Show |
1 | a0001c0002t0004g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.136-4996_136-4984d others(15): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259070 | |||||||
| chr8:98259070 | C | T | 88 | a0001c0001t0001g0290 a0001c0001t0002g0036 a0001c0001t0002g0047 others(85): Show |
89 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.136-4983G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259070 | |||||||
| chr8:98259107 | C | T | 75 | a0001c0001t0001g0016 a0001c0001t0001g0290 a0001c0001t0002g0036 others(72): Show |
76 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.136-5020G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259107 | |||||||
| chr8:98259108 | G | A | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-5021C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259108 | |||||||
| chr8:98259138 | G | A | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-5051C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259138 | |||||||
| chr8:98259163 | G | A | 2 | a0001c0001t0001g0239 a0001c0001t0001g0241 |
2 | HG02683.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.136-5076C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259163 | |||||||
| chr8:98259222 | G | A | 10 | a0001c0001t0001g0118 a0001c0002t0004g0081 a0001c0002t0004g0306 others(7): Show |
10 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.136-5135C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259222 | |||||||
| chr8:98259223 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.136-5136G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259223 | |||||||
| chr8:98259326 | C | T | 13 | a0001c0001t0001g0118 a0001c0001t0003g0018 a0001c0002t0004g0081 others(10): Show |
13 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.136-5239G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259326 | |||||||
| chr8:98259355 | G | A | 74 | a0001c0001t0001g0290 a0001c0001t0002g0036 a0001c0001t0002g0047 others(71): Show |
75 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.136-5268C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259355 | |||||||
| chr8:98259436 | T | C | 3 | a0001c0002t0001g0127 a0001c0002t0001g0128 a0001c0002t0001g0266 |
3 | HG01099.hp1 HG02683.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.136-5349A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259436 | |||||||
| chr8:98259523 | T | A | 2 | a0001c0001t0003g0134 a0001c0002t0001g0260 |
2 | HG02602.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.136-5436A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259523 | |||||||
| chr8:98259545 | G | A | 7 | a0001c0005t0001g0026 a0001c0005t0001g0030 a0001c0005t0001g0035 others(4): Show |
7 | HG02145.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-5458C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259545 | |||||||
| chr8:98259552 | T | C | 1 | a0001c0001t0002g0261 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.136-5465A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259552 | |||||||
| chr8:98259567 | G | T | 4 | a0001c0002t0001g0046 a0001c0002t0001g0062 a0001c0002t0001g0063 others(1): Show |
4 | HG01109.hp2 HG01192.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-5480C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259567 | |||||||
| chr8:98259575 | A | T | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-5488T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259575 | |||||||
| chr8:98259633 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.136-5546C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259633 | |||||||
| chr8:98259810 | G | A | 2 | a0001c0001t0001g0239 a0001c0001t0001g0241 |
2 | HG02683.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.136-5723C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259810 | |||||||
| chr8:98259923 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0001g0151 |
2 | NA18970.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.136-5836G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259923 | |||||||
| chr8:98260045 | G | A | 1 | a0001c0002t0004g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.136-5958C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260045 | |||||||
| chr8:98260090 | A | T | 5 | a0001c0001t0002g0085 a0001c0002t0004g0082 a0001c0002t0004g0083 others(2): Show |
5 | HG02723.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-6003T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260090 | |||||||
| chr8:98260157 | A | T | 7 | a0001c0005t0001g0026 a0001c0005t0001g0030 a0001c0005t0001g0035 others(4): Show |
7 | HG02145.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-6070T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260157 | |||||||
| chr8:98260286 | C | T | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-6199G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260286 | |||||||
| chr8:98260303 | G | A | 1 | a0001c0001t0002g0248 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.136-6216C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260303 | |||||||
| chr8:98260326 | G | T | 4 | a0001c0001t0003g0252 a0002c0004t0001g0222 a0002c0004t0001g0225 others(1): Show |
4 | HG00438.hp1 HG00609.hp2 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-6239C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260326 | |||||||
| chr8:98260419 | G | A | 3 | a0001c0001t0003g0252 a0002c0004t0001g0222 a0002c0004t0001g0225 |
3 | HG00438.hp1 HG00609.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.136-6332C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260419 | |||||||
| chr8:98260436 | C | T | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-6349G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260436 | |||||||
| chr8:98260534 | T | G | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-6447A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260534 | |||||||
| chr8:98260550 | C | T | 1 | a0002c0003t0001g0273 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.136-6463G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260550 | |||||||
| chr8:98260594 | G | A | 1 | a0001c0002t0004g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.136-6507C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260594 | |||||||
| chr8:98260639 | G | A | 1 | a0001c0001t0002g0094 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.136-6552C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260639 | |||||||
| chr8:98260644 | G | A | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-6557C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260644 | |||||||
| chr8:98260650 | T | C | 1 | a0001c0001t0003g0134 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.136-6563A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260650 | |||||||
| chr8:98260679 | C | G | 1 | a0001c0001t0002g0112 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.136-6592G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260679 | |||||||
| chr8:98260766 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0308 |
2 | HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.136-6679G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260766 | |||||||
| chr8:98260782 | A | T | 7 | a0001c0001t0002g0085 a0001c0002t0004g0082 a0001c0002t0004g0083 others(4): Show |
7 | HG01243.hp1 HG01243.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-6695T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260782 | |||||||
| chr8:98260800 | C | T | 1 | a0001c0001t0002g0258 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.136-6713G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260800 | |||||||
| chr8:98260817 | C | A | 129 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(126): Show |
130 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.136-6730G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260817 | |||||||
| chr8:98260850 | C | G | 1 | a0001c0002t0001g0189 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.136-6763G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260850 | |||||||
| chr8:98261154 | T | G | 1 | a0001c0001t0003g0149 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.136-7067A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98261154 | |||||||
| chr8:98261336 | C | T | 3 | a0001c0001t0001g0152 a0001c0001t0001g0237 a0003c0007t0002g0236 |
3 | HG00099.hp1 HG00280.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.136-7249G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98261336 | |||||||
| chr8:98261454 | A | C | 1 | a0001c0002t0001g0199 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.136-7367T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98261454 | |||||||
| chr8:98261462 | C | T | 3 | a0001c0001t0001g0118 a0001c0001t0003g0018 a0001c0002t0004g0081 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136-7375G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98261462 | |||||||
| chr8:98261619 | G | A | 25 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0274 others(22): Show |
27 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.136-7532C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98261619 | |||||||
| chr8:98261666 | A | G | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-7579T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98261666 | |||||||
| chr8:98261732 | A | G | 1 | a0001c0002t0001g0249 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.136-7645T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98261732 | |||||||
| chr8:98261734 | C | T | 1 | a0001c0002t0001g0249 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.136-7647G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98261734 | |||||||
| chr8:98261744 | C | A | 2 | a0001c0002t0001g0313 a0001c0002t0001g0317 |
2 | HG03710.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.136-7657G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98261744 | |||||||
| chr8:98261816 | A | C | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-7729T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98261816 | |||||||
| chr8:98261886 | G | A | 57 | a0001c0001t0002g0036 a0001c0001t0002g0047 a0001c0001t0002g0048 others(54): Show |
58 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.136-7799C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98261886 | |||||||
| chr8:98261959 | G | C | 11 | a0001c0001t0002g0067 a0001c0001t0003g0052 a0001c0001t0003g0055 others(8): Show |
11 | HG01257.hp2 HG01258.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.136-7872C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98261959 | |||||||
| chr8:98262041 | G | A | 1 | a0001c0001t0014g0069 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.136-7954C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262041 | |||||||
| chr8:98262047 | G | T | 1 | a0001c0001t0001g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.136-7960C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262047 | |||||||
| chr8:98262101 | C | A | 1 | a0001c0006t0002g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.136-8014G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262101 | |||||||
| chr8:98262272 | A | G | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-8185T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262272 | |||||||
| chr8:98262374 | C | G | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-8287G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262374 | |||||||
| chr8:98262391 | G | A | 2 | a0001c0001t0003g0134 a0001c0002t0001g0260 |
2 | HG02602.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.136-8304C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262391 | |||||||
| chr8:98262551 | A | C | 2 | a0001c0002t0004g0294 a0001c0002t0004g0295 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.136-8464T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262551 | |||||||
| chr8:98262553 | G | T | 3 | a0001c0001t0001g0118 a0001c0001t0003g0018 a0001c0002t0004g0081 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136-8466C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262553 | |||||||
| chr8:98262677 | A | C | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-8590T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262677 | |||||||
| chr8:98262729 | A | C | 7 | a0001c0005t0001g0026 a0001c0005t0001g0030 a0001c0005t0001g0035 others(4): Show |
7 | HG02145.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-8642T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262729 | |||||||
| chr8:98262761 | C | T | 1 | a0001c0002t0001g0190 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.136-8674G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262761 | |||||||
| chr8:98262840 | G | A | 1 | a0001c0001t0002g0274 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.136-8753C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262840 | |||||||
| chr8:98262871 | C | T | 5 | a0001c0001t0001g0160 a0001c0001t0001g0302 a0001c0001t0002g0166 others(2): Show |
5 | HG00323.hp2 HG00741.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-8784G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262871 | |||||||
| chr8:98262897 | A | C | 2 | a0001c0002t0004g0294 a0001c0002t0004g0295 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.136-8810T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262897 | |||||||
| chr8:98262934 | G | C | 1 | a0001c0005t0001g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.136-8847C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262934 | |||||||
| chr8:98262985 | C | T | 70 | a0001c0001t0001g0290 a0001c0001t0002g0036 a0001c0001t0002g0047 others(67): Show |
71 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.136-8898G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262985 | |||||||
| chr8:98262986 | G | A | 15 | a0001c0001t0001g0120 a0001c0001t0002g0085 a0001c0001t0002g0322 others(12): Show |
15 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.136-8899C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262986 | |||||||
| chr8:98263041 | C | T | 1 | a0001c0002t0001g0105 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.136-8954G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263041 | |||||||
| chr8:98263259 | G | C | 2 | a0001c0001t0003g0135 a0001c0001t0003g0296 |
2 | HG02738.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.136-9172C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263259 | |||||||
| chr8:98263376 | C | T | 2 | a0001c0001t0001g0016 a0002c0004t0001g0253 |
2 | HG02451.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.136-9289G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263376 | |||||||
| chr8:98263536 | T | G | 5 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(2): Show |
5 | HG01109.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-9449A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263536 | |||||||
| chr8:98263549 | G | A | 1 | a0001c0001t0016g0293 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.136-9462C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263549 | |||||||
| chr8:98263574 | A | C | 1 | a0001c0002t0022g0303 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.136-9487T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263574 | |||||||
| chr8:98263601 | G | C | 15 | a0001c0001t0001g0120 a0001c0001t0002g0085 a0001c0001t0002g0322 others(12): Show |
15 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.136-9514C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263601 | |||||||
| chr8:98263615 | T | G | 15 | a0001c0001t0001g0120 a0001c0001t0002g0085 a0001c0001t0002g0322 others(12): Show |
15 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.136-9528A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263615 | |||||||
| chr8:98263635 | C | T | 3 | a0001c0001t0002g0322 a0001c0001t0002g0323 a0001c0001t0002g0324 |
3 | HG03098.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.136-9548G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263635 | |||||||
| chr8:98263641 | T | C | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-9554A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263641 | |||||||
| chr8:98263650 | C | A | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-9563G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263650 | |||||||
| chr8:98263727 | T | C | 1 | a0001c0001t0014g0187 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.136-9640A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263727 | |||||||
| chr8:98263794 | T | A | 1 | a0001c0002t0004g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.136-9707A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263794 | |||||||
| chr8:98263862 | A | G | 1 | a0001c0001t0002g0108 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.136-9775T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263862 | |||||||
| chr8:98263979 | C | T | 8 | a0001c0001t0001g0153 a0001c0001t0001g0156 a0001c0001t0001g0157 others(5): Show |
8 | HG00544.hp1 HG00621.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.136-9892G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263979 | |||||||
| chr8:98264128 | G | T | 2 | a0001c0001t0002g0022 a0001c0001t0002g0023 |
2 | HG01069.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.136-10041C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98264128 | |||||||
| chr8:98264158 | C | A | 1 | a0001c0002t0004g0084 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.136-10071G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98264158 | |||||||
| chr8:98264169 | T | C | 2 | a0001c0001t0002g0022 a0001c0001t0002g0023 |
2 | HG01069.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.136-10082A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98264169 | |||||||
| chr8:98264277 | C | G | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-10190G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98264277 | |||||||
| chr8:98264304 | A | C | 1 | a0001c0001t0002g0010 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.136-10217T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98264304 | |||||||
| chr8:98264355 | C | T | 1 | a0001c0001t0002g0277 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.136-10268G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98264355 | |||||||
| chr8:98264384 | T | A | 1 | a0001c0001t0001g0232 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.136-10297A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98264384 | |||||||
| chr8:98264483 | G | A | 1 | a0003c0007t0002g0236 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.136-10396C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98264483 | |||||||
| chr8:98264487 | T | C | 1 | a0003c0007t0002g0236 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.136-10400A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98264487 | |||||||
| chr8:98264518 | C | T | 57 | a0001c0001t0002g0036 a0001c0001t0002g0047 a0001c0001t0002g0048 others(54): Show |
58 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.136-10431G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98264518 | |||||||
| chr8:98264548 | A | C | 3 | a0001c0001t0003g0130 a0001c0001t0003g0131 a0001c0001t0003g0132 |
3 | HG02258.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.136-10461T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98264548 | |||||||
| chr8:98264667 | G | A | 11 | a0001c0001t0001g0098 a0001c0001t0001g0146 a0001c0001t0001g0147 others(8): Show |
11 | HG00544.hp1 HG00621.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.136-10580C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98264667 | |||||||
| chr8:98265144 | A | C | 6 | a0001c0001t0002g0085 a0001c0002t0004g0082 a0001c0002t0004g0083 others(3): Show |
6 | HG01243.hp2 HG02723.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-11057T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265144 | |||||||
| chr8:98265154 | G | C | 1 | a0001c0002t0006g0264 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.136-11067C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265154 | |||||||
| chr8:98265156 | T | C | 1 | a0001c0002t0006g0264 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.136-11069A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265156 | |||||||
| chr8:98265158 | G | C | 1 | a0001c0002t0006g0264 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.136-11071C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265158 | |||||||
| chr8:98265352 | G | A | 3 | a0001c0001t0001g0118 a0001c0001t0003g0018 a0001c0002t0004g0081 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136-11265C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265352 | |||||||
| chr8:98265353 | A | C | 3 | a0001c0001t0001g0118 a0001c0001t0003g0018 a0001c0002t0004g0081 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136-11266T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265353 | |||||||
| chr8:98265405 | A | C | 1 | a0001c0002t0001g0256 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.136-11318T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265405 | |||||||
| chr8:98265431 | A | G | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-11344T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265431 | |||||||
| chr8:98265455 | T | A | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-11368A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265455 | |||||||
| chr8:98265468 | G | A | 1 | a0001c0002t0022g0303 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.136-11381C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265468 | |||||||
| chr8:98265504 | T | A | 2 | a0001c0001t0001g0184 a0001c0001t0003g0243 |
2 | HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.136-11417A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265504 | |||||||
| chr8:98265509 | T | C | 278 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(275): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.136-11422A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265509 | |||||||
| chr8:98265547 | G | A | 15 | a0001c0001t0001g0120 a0001c0001t0002g0085 a0001c0001t0002g0322 others(12): Show |
15 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.136-11460C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265547 | |||||||
| chr8:98265646 | G | A | 2 | a0001c0002t0004g0294 a0001c0002t0004g0295 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.136-11559C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265646 | |||||||
| chr8:98265747 | G | A | 4 | a0001c0001t0002g0033 a0001c0001t0008g0031 a0001c0001t0008g0032 others(1): Show |
4 | NA18960.hp1 NA19062.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-11660C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265747 | |||||||
| chr8:98265858 | G | A | 4 | a0001c0001t0001g0118 a0001c0001t0003g0018 a0001c0002t0004g0081 others(1): Show |
4 | HG02922.hp2 HG02970.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-11771C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265858 | |||||||
| chr8:98265858 | G | C | 5 | a0001c0001t0001g0120 a0001c0001t0003g0115 a0001c0001t0003g0116 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-11771C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265858 | |||||||
| chr8:98265864 | A | G | 3 | a0001c0005t0001g0030 a0001c0005t0001g0035 a0001c0005t0004g0029 |
3 | HG02145.hp1 HG02486.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.136-11777T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265864 | |||||||
| chr8:98265881 | C | T | 3 | a0001c0001t0002g0322 a0001c0001t0002g0323 a0001c0001t0002g0324 |
3 | HG03098.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.136-11794G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265881 | |||||||
| chr8:98265998 | T | A | 1 | a0001c0002t0001g0220 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.136-11911A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265998 | |||||||
| chr8:98266026 | G | A | 1 | a0001c0001t0002g0210 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.136-11939C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266026 | |||||||
| chr8:98266048 | C | T | 4 | a0001c0001t0002g0210 a0001c0001t0002g0234 a0001c0001t0003g0164 others(1): Show |
4 | HG00735.hp2 NA18961.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-11961G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266048 | |||||||
| chr8:98266137 | TG | T | 7 | a0001c0005t0001g0026 a0001c0005t0001g0030 a0001c0005t0001g0035 others(4): Show |
7 | HG02145.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-12051delC | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266137 | |||||||
| chr8:98266143 | G | A | 8 | a0001c0005t0001g0026 a0001c0005t0001g0030 a0001c0005t0001g0035 others(5): Show |
8 | HG02145.hp1 HG02486.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.136-12056C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266143 | |||||||
| chr8:98266172 | G | A | 248 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(245): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.136-12085C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266172 | |||||||
| chr8:98266202 | C | T | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-12115G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266202 | |||||||
| chr8:98266213 | C | T | 1 | a0001c0001t0002g0095 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.136-12126G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266213 | |||||||
| chr8:98266282 | T | TA | 245 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(242): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.136-12196dupT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266282 | |||||||
| chr8:98266282 | T | TAA | 8 | a0001c0001t0001g0118 a0001c0001t0002g0322 a0001c0001t0002g0323 others(5): Show |
8 | HG01069.hp2 HG02922.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.136-12197_136-1219 others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266282 | |||||||
| chr8:98266300 | GA | G | 16 | a0001c0001t0001g0120 a0001c0001t0002g0085 a0001c0001t0002g0322 others(13): Show |
16 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.136-12214delT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266300 | |||||||
| chr8:98266327 | C | T | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-12240G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266327 | |||||||
| chr8:98266553 | C | CA | 29 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0156 others(26): Show |
29 | HG00544.hp1 HG01175.hp2 HG01517.hp1 others(26): Show |
intron_variant | MODIFIER | c.136-12467dupT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266553 | |||||||
| chr8:98266553 | CA | C | 10 | a0001c0002t0001g0220 a0001c0002t0004g0306 a0001c0005t0001g0026 others(7): Show |
10 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.136-12467delT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266553 | |||||||
| chr8:98266595 | T | G | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-12508A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266595 | |||||||
| chr8:98266641 | G | C | 4 | a0001c0002t0001g0226 a0001c0002t0001g0227 a0001c0002t0001g0229 others(1): Show |
4 | NA18998.hp1 NA19060.hp1 NA19083.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-12554C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266641 | |||||||
| chr8:98266651 | C | T | 1 | a0002c0003t0002g0065 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.136-12564G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266651 | |||||||
| chr8:98266898 | C | T | 3 | a0001c0001t0001g0118 a0001c0001t0003g0018 a0001c0002t0004g0081 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136-12811G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266898 | |||||||
| chr8:98266973 | T | A | 4 | a0001c0001t0002g0033 a0001c0001t0008g0031 a0001c0001t0008g0032 others(1): Show |
4 | NA18960.hp1 NA19062.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-12886A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266973 | |||||||
| chr8:98266973 | TA | T | 12 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(9): Show |
12 | HG01109.hp1 HG02145.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.136-12887delT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266973 | |||||||
| chr8:98267086 | T | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(2): Show |
5 | HG01109.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-12999A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98267086 | |||||||
| chr8:98267327 | CT | C | 6 | a0001c0001t0001g0237 a0001c0001t0002g0102 a0001c0001t0002g0261 others(3): Show |
6 | HG01074.hp1 HG01167.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-13241delA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98267327 | |||||||
| chr8:98267380 | G | A | 1 | a0001c0001t0005g0136 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.136-13293C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98267380 | |||||||
| chr8:98267415 | C | T | 3 | a0001c0001t0001g0118 a0001c0001t0003g0018 a0001c0002t0004g0081 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136-13328G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98267415 | |||||||
| chr8:98267744 | A | T | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-13657T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98267744 | |||||||
| chr8:98267832 | T | G | 1 | a0001c0001t0002g0010 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.136-13745A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98267832 | |||||||
| chr8:98267893 | T | G | 1 | a0001c0001t0001g0239 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.136-13806A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98267893 | |||||||
| chr8:98267901 | T | C | 1 | a0001c0001t0002g0124 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.136-13814A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98267901 | |||||||
| chr8:98268011 | T | G | 1 | a0001c0001t0003g0129 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.136-13924A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98268011 | |||||||
| chr8:98268044 | G | A | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-13957C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98268044 | |||||||
| chr8:98268080 | T | C | 10 | a0001c0001t0002g0091 a0001c0001t0002g0094 a0001c0001t0002g0095 others(7): Show |
10 | HG00408.hp1 NA18747.hp2 NA18942.hp1 others(7): Show |
intron_variant | MODIFIER | c.136-13993A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98268080 | |||||||
| chr8:98268296 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.136-14209C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98268296 | |||||||
| chr8:98268545 | C | G | 3 | a0001c0001t0003g0001 a0001c0001t0003g0281 a0001c0001t0003g0282 |
5 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-14458G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98268545 | |||||||
| chr8:98268549 | A | G | 1 | a0001c0002t0001g0045 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.136-14462T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98268549 | |||||||
| chr8:98268621 | AG | A | 3 | a0001c0001t0002g0322 a0001c0001t0002g0323 a0001c0001t0002g0324 |
3 | HG03098.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.136-14535delC | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98268621 | |||||||
| chr8:98268622 | GA | G | 134 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(131): Show |
135 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.136-14536delT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98268622 | |||||||
| chr8:98268637 | C | G | 3 | a0001c0001t0001g0118 a0001c0001t0003g0018 a0001c0002t0004g0081 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136-14550G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98268637 | |||||||
| chr8:98268647 | GA | G | 5 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(2): Show |
5 | HG01109.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-14561delT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98268647 | |||||||
| chr8:98268666 | A | T | 3 | a0001c0001t0001g0118 a0001c0001t0003g0018 a0001c0002t0004g0081 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136-14579T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98268666 | |||||||
| chr8:98268933 | C | G | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-14846G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98268933 | |||||||
| chr8:98268996 | C | T | 1 | a0001c0001t0008g0161 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.136-14909G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98268996 | |||||||
| chr8:98269010 | C | G | 130 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(127): Show |
131 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.136-14923G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98269010 | |||||||
| chr8:98269305 | CTATT | C | 3 | a0001c0001t0001g0118 a0001c0001t0003g0018 a0001c0002t0004g0081 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136-15222_136-1521 others(8): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98269305 | |||||||
| chr8:98269435 | C | T | 1 | a0001c0001t0015g0195 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.136-15348G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98269435 | |||||||
| chr8:98269615 | C | G | 7 | a0001c0005t0001g0026 a0001c0005t0001g0030 a0001c0005t0001g0035 others(4): Show |
7 | HG02145.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-15528G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98269615 | |||||||
| chr8:98269697 | T | C | 204 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(201): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.136-15610A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98269697 | |||||||
| chr8:98269750 | C | T | 1 | a0001c0005t0001g0030 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.136-15663G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98269750 | |||||||
| chr8:98269809 | C | A | 1 | a0001c0001t0002g0112 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.136-15722G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98269809 | |||||||
| chr8:98269846 | C | T | 7 | a0001c0005t0001g0026 a0001c0005t0001g0030 a0001c0005t0001g0035 others(4): Show |
7 | HG02145.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-15759G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98269846 | |||||||
| chr8:98269946 | C | T | 204 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(201): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.136-15859G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98269946 | |||||||
| chr8:98269980 | T | G | 211 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(208): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.136-15893A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98269980 | |||||||
| chr8:98270020 | TC | T | 4 | a0001c0001t0002g0033 a0001c0001t0008g0031 a0001c0001t0008g0032 others(1): Show |
4 | NA18960.hp1 NA19062.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-15934delG | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98270020 | |||||||
| chr8:98270085 | T | C | 15 | a0001c0001t0001g0120 a0001c0001t0002g0085 a0001c0001t0002g0322 others(12): Show |
15 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.136-15998A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98270085 | |||||||
| chr8:98270165 | T | C | 5 | a0001c0001t0001g0160 a0001c0001t0001g0302 a0001c0001t0002g0166 others(2): Show |
5 | HG00323.hp2 HG00741.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-16078A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98270165 | |||||||
| chr8:98270555 | C | T | 1 | a0001c0002t0001g0089 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.136-16468G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98270555 | |||||||
| chr8:98270743 | G | T | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-16656C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98270743 | |||||||
| chr8:98270766 | T | TTGC | 6 | a0001c0001t0001g0118 a0001c0001t0003g0018 a0001c0002t0004g0081 others(3): Show |
6 | HG02559.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-16682_136-1668 others(7): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98270766 | |||||||
| chr8:98270769 | C | T | 12 | a0001c0001t0003g0134 a0001c0001t0003g0135 a0001c0001t0003g0296 others(9): Show |
12 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.136-16682G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98270769 | |||||||
| chr8:98271051 | C | T | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-16964G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98271051 | |||||||
| chr8:98271449 | G | C | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-17362C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98271449 | |||||||
| chr8:98271522 | G | A | 4 | a0001c0002t0006g0061 a0001c0002t0006g0079 a0002c0003t0002g0075 others(1): Show |
4 | NA18947.hp2 NA18993.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-17435C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98271522 | |||||||
| chr8:98271600 | T | C | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-17513A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98271600 | |||||||
| chr8:98271660 | C | T | 5 | a0001c0001t0001g0160 a0001c0001t0001g0302 a0001c0001t0002g0166 others(2): Show |
5 | HG00323.hp2 HG00741.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-17573G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98271660 | |||||||
| chr8:98271711 | A | C | 7 | a0001c0005t0001g0026 a0001c0005t0001g0030 a0001c0005t0001g0035 others(4): Show |
7 | HG02145.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-17624T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98271711 | |||||||
| chr8:98271866 | G | A | 1 | a0001c0001t0002g0010 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.136-17779C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98271866 | |||||||
| chr8:98271896 | T | G | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-17809A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98271896 | |||||||
| chr8:98271938 | G | A | 1 | a0001c0001t0003g0129 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.136-17851C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98271938 | |||||||
| chr8:98272240 | T | C | 1 | a0001c0002t0004g0325 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.136-18153A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98272240 | |||||||
| chr8:98272300 | G | A | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-18213C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98272300 | |||||||
| chr8:98272346 | A | G | 2 | a0001c0001t0011g0004 a0001c0001t0011g0005 |
2 | NA18942.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.136-18259T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98272346 | |||||||
| chr8:98272389 | G | A | 1 | a0001c0002t0004g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.136-18302C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98272389 | |||||||
| chr8:98272519 | A | T | 1 | a0001c0002t0004g0325 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.136-18432T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98272519 | |||||||
| chr8:98272616 | CT | C | 7 | a0001c0001t0002g0311 a0001c0001t0003g0244 a0001c0001t0005g0143 others(4): Show |
8 | HG00280.hp1 HG01074.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.136-18530delA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98272616 | |||||||
| chr8:98272676 | A | G | 1 | a0001c0002t0004g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.136-18589T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98272676 | |||||||
| chr8:98272810 | A | G | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-18723T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98272810 | |||||||
| chr8:98272869 | C | T | 1 | a0001c0002t0001g0145 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.136-18782G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98272869 | |||||||
| chr8:98272909 | G | A | 7 | a0001c0002t0001g0211 a0001c0002t0001g0214 a0001c0002t0001g0215 others(4): Show |
7 | NA18953.hp2 NA18962.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-18822C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98272909 | |||||||
| chr8:98273017 | A | T | 2 | a0001c0001t0003g0283 a0001c0001t0021g0285 |
2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.136-18930T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98273017 | |||||||
| chr8:98273038 | A | G | 1 | a0001c0001t0005g0002 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.136-18951T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98273038 | |||||||
| chr8:98273080 | G | A | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-18993C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98273080 | |||||||
| chr8:98273449 | T | G | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-19362A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98273449 | |||||||
| chr8:98273459 | T | C | 2 | a0001c0002t0004g0017 a0001c0002t0022g0303 |
2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.136-19372A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98273459 | |||||||
| chr8:98273646 | C | T | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-19559G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98273646 | |||||||
| chr8:98273659 | C | A | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-19572G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98273659 | |||||||
| chr8:98273736 | A | G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(1): Show |
4 | HG01109.hp1 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-19649T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98273736 | |||||||
| chr8:98273744 | G | A | 3 | a0001c0001t0003g0130 a0001c0001t0003g0131 a0001c0001t0003g0132 |
3 | HG02258.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.136-19657C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98273744 | |||||||
| chr8:98273830 | T | C | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-19743A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98273830 | |||||||
| chr8:98274023 | G | A | 230 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(227): Show |
232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.136-19936C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98274023 | |||||||
| chr8:98274250 | CATCT | C | 3 | a0001c0001t0001g0314 a0001c0001t0005g0002 a0001c0001t0008g0161 |
4 | HG01256.hp2 HG01258.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+19749_135+1975 others(8): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98274250 | |||||||
| chr8:98274419 | C | A | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+19584G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98274419 | |||||||
| chr8:98274506 | A | G | 3 | a0001c0001t0002g0322 a0001c0001t0002g0323 a0001c0001t0002g0324 |
3 | HG03098.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.135+19497T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98274506 | |||||||
| chr8:98274619 | G | T | 2 | a0001c0001t0003g0018 a0001c0002t0004g0081 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.135+19384C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98274619 | |||||||
| chr8:98274742 | C | T | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+19261G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98274742 | |||||||
| chr8:98274891 | T | C | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+19112A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98274891 | |||||||
| chr8:98274902 | C | T | 5 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(2): Show |
5 | HG01109.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+19101G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98274902 | |||||||
| chr8:98275077 | A | T | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+18926T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275077 | |||||||
| chr8:98275081 | T | C | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+18922A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275081 | |||||||
| chr8:98275087 | A | G | 1 | a0001c0002t0004g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.135+18916T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275087 | |||||||
| chr8:98275091 | C | G | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+18912G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275091 | |||||||
| chr8:98275120 | G | A | 15 | a0001c0001t0001g0120 a0001c0001t0002g0085 a0001c0001t0002g0322 others(12): Show |
15 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.135+18883C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275120 | |||||||
| chr8:98275248 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.135+18755G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275248 | |||||||
| chr8:98275249 | G | T | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+18754C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275249 | |||||||
| chr8:98275261 | T | A | 4 | a0001c0001t0003g0252 a0002c0004t0001g0222 a0002c0004t0001g0225 others(1): Show |
4 | HG00438.hp1 HG00609.hp2 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+18742A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275261 | |||||||
| chr8:98275331 | C | A | 1 | a0001c0001t0001g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.135+18672G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275331 | |||||||
| chr8:98275435 | A | G | 2 | a0001c0001t0002g0258 a0001c0001t0002g0259 |
2 | HG00408.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.135+18568T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275435 | |||||||
| chr8:98275547 | A | G | 1 | a0001c0002t0001g0266 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.135+18456T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275547 | |||||||
| chr8:98275566 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0009g0012 a0001c0001t0009g0013 |
3 | HG02451.hp1 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.135+18437C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275566 | |||||||
| chr8:98275642 | G | T | 4 | a0001c0005t0001g0026 a0001c0005t0001g0030 a0001c0005t0001g0035 others(1): Show |
4 | HG02145.hp1 HG02486.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+18361C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275642 | |||||||
| chr8:98275647 | T | C | 1 | a0001c0002t0001g0097 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.135+18356A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275647 | |||||||
| chr8:98275926 | T | A | 2 | a0001c0001t0001g0193 a0001c0001t0009g0185 |
2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.135+18077A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275926 | |||||||
| chr8:98276268 | C | G | 1 | a0001c0001t0002g0178 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.135+17735G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98276268 | |||||||
| chr8:98276301 | A | C | 5 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0002t0001g0265 others(2): Show |
5 | HG00438.hp2 HG02015.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+17702T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98276301 | |||||||
| chr8:98276630 | G | A | 1 | a0001c0001t0002g0091 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.135+17373C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98276630 | |||||||
| chr8:98277016 | C | T | 15 | a0001c0001t0001g0120 a0001c0001t0002g0085 a0001c0001t0002g0322 others(12): Show |
15 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.135+16987G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98277016 | |||||||
| chr8:98277051 | TGA | T | 70 | a0001c0001t0001g0290 a0001c0001t0002g0036 a0001c0001t0002g0047 others(67): Show |
71 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.135+16950_135+1695 others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98277051 | |||||||
| chr8:98277064 | C | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | NA18612.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.135+16939G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98277064 | |||||||
| chr8:98277115 | C | T | 1 | a0001c0005t0001g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.135+16888G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98277115 | |||||||
| chr8:98277315 | G | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0009g0012 others(2): Show |
5 | HG02451.hp1 HG02809.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+16688C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98277315 | |||||||
| chr8:98277427 | G | C | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+16576C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98277427 | |||||||
| chr8:98277451 | C | A | 57 | a0001c0001t0002g0036 a0001c0001t0002g0047 a0001c0001t0002g0048 others(54): Show |
58 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.135+16552G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98277451 | |||||||
| chr8:98277478 | A | T | 1 | a0001c0001t0002g0178 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.135+16525T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98277478 | |||||||
| chr8:98277498 | T | C | 15 | a0001c0001t0001g0120 a0001c0001t0002g0085 a0001c0001t0002g0322 others(12): Show |
15 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.135+16505A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98277498 | |||||||
| chr8:98277635 | G | A | 57 | a0001c0001t0002g0036 a0001c0001t0002g0047 a0001c0001t0002g0048 others(54): Show |
58 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.135+16368C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98277635 | |||||||
| chr8:98277661 | G | A | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+16342C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98277661 | |||||||
| chr8:98277765 | T | C | 11 | a0001c0001t0001g0197 a0001c0001t0003g0126 a0001c0001t0005g0196 others(8): Show |
11 | HG00558.hp1 HG00597.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.135+16238A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98277765 | |||||||
| chr8:98277841 | A | T | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+16162T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98277841 | |||||||
| chr8:98277991 | A | C | 1 | a0001c0002t0001g0278 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.135+16012T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98277991 | |||||||
| chr8:98278064 | G | T | 3 | a0001c0001t0001g0118 a0001c0001t0003g0018 a0001c0002t0004g0081 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.135+15939C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98278064 | |||||||
| chr8:98278224 | TTTTG | T | 7 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0005g0138 others(4): Show |
7 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+15775_135+1577 others(8): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98278224 | |||||||
| chr8:98278240 | G | C | 1 | a0001c0001t0003g0235 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.135+15763C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98278240 | |||||||
| chr8:98278652 | G | A | 1 | a0001c0002t0001g0317 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.135+15351C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98278652 | |||||||
| chr8:98278653 | C | T | 129 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(126): Show |
130 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.135+15350G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98278653 | |||||||
| chr8:98278837 | T | G | 1 | a0001c0001t0003g0018 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.135+15166A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98278837 | |||||||
| chr8:98279222 | A | G | 12 | a0001c0001t0003g0134 a0001c0001t0003g0135 a0001c0001t0003g0296 others(9): Show |
12 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.135+14781T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98279222 | |||||||
| chr8:98279361 | T | C | 3 | a0001c0001t0003g0001 a0001c0001t0003g0281 a0001c0001t0003g0282 |
5 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+14642A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98279361 | |||||||
| chr8:98279578 | T | C | 3 | a0001c0001t0001g0118 a0001c0001t0003g0018 a0001c0002t0004g0081 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.135+14425A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98279578 | |||||||
| chr8:98279701 | C | T | 2 | a0002c0004t0001g0078 a0002c0004t0001g0297 |
2 | NA18612.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.135+14302G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98279701 | |||||||
| chr8:98279866 | G | A | 8 | a0001c0001t0001g0109 a0001c0001t0002g0108 a0001c0001t0002g0110 others(5): Show |
8 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.135+14137C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98279866 | |||||||
| chr8:98279945 | T | G | 1 | a0001c0002t0001g0107 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.135+14058A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98279945 | |||||||
| chr8:98280028 | C | T | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+13975G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280028 | |||||||
| chr8:98280077 | C | G | 1 | a0001c0002t0004g0114 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.135+13926G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280077 | |||||||
| chr8:98280217 | G | A | 1 | a0001c0002t0001g0267 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.135+13786C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280217 | |||||||
| chr8:98280331 | T | G | 203 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(200): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.135+13672A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280331 | |||||||
| chr8:98280339 | C | T | 17 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(14): Show |
17 | HG01109.hp1 HG02145.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.135+13664G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280339 | |||||||
| chr8:98280343 | T | G | 1 | a0001c0001t0003g0052 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.135+13660A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280343 | |||||||
| chr8:98280486 | T | C | 222 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(219): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.135+13517A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280486 | |||||||
| chr8:98280699 | T | G | 214 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(211): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.135+13304A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280699 | |||||||
| chr8:98280736 | C | CTA | 3 | a0001c0001t0002g0279 a0001c0002t0001g0211 a0001c0002t0001g0278 |
3 | NA18942.hp2 NA18986.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.135+13265_135+1326 others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280736 | |||||||
| chr8:98280736 | C | CTATA | 4 | a0001c0001t0002g0033 a0001c0001t0002g0047 a0001c0001t0008g0032 others(1): Show |
4 | NA18960.hp1 NA19054.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+13263_135+1326 others(8): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280736 | |||||||
| chr8:98280736 | C | CTATATAT others(1): Show |
6 | a0001c0001t0002g0048 a0001c0001t0002g0049 a0001c0001t0002g0073 others(3): Show |
6 | HG01099.hp1 HG02132.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.135+13259_135+1326 others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280736 | |||||||
| chr8:98280736 | C | CTATATAT others(3): Show |
2 | a0001c0002t0001g0045 a0001c0002t0001g0046 |
2 | HG01070.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.135+13257_135+1326 others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280736 | |||||||
| chr8:98280736 | C | CTATATAT others(17): Show |
1 | a0001c0001t0001g0146 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.135+13243_135+1326 others(28): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280736 | |||||||
| chr8:98280736 | C | CTATATAT others(19): Show |
1 | a0001c0001t0001g0147 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.135+13241_135+1326 others(30): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280736 | |||||||
| chr8:98280736 | C | CTATATAT others(23): Show |
1 | a0001c0001t0002g0148 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.135+13266_135+1326 others(34): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280736 | |||||||
| chr8:98280736 | CTA | C | 4 | a0001c0001t0001g0016 a0001c0001t0009g0013 a0001c0002t0004g0015 others(1): Show |
4 | HG02055.hp2 HG02451.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+13265_135+1326 others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280736 | |||||||
| chr8:98280755 | T | G | 3 | a0001c0001t0002g0113 a0001c0001t0002g0182 a0002c0004t0001g0253 |
3 | HG01255.hp2 HG02723.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.135+13248A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280755 | |||||||
| chr8:98280757 | T | G | 13 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0182 others(10): Show |
13 | HG00438.hp1 HG01175.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.135+13246A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280757 | |||||||
| chr8:98280757 | T | TAGAGAGA others(3): Show |
1 | a0001c0001t0002g0095 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.135+13245_135+1324 others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280757 | |||||||
| chr8:98280759 | T | G | 26 | a0001c0001t0002g0091 a0001c0001t0002g0094 a0001c0001t0002g0095 others(23): Show |
27 | HG00438.hp1 HG00609.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.135+13244A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280759 | |||||||
| chr8:98280759 | T | TAG | 5 | a0001c0001t0003g0001 a0001c0001t0003g0281 a0001c0001t0003g0282 others(2): Show |
7 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+13243_135+1324 others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280759 | |||||||
| chr8:98280759 | T | TAGAGAGA others(3): Show |
2 | a0001c0001t0011g0005 a0001c0002t0004g0257 |
2 | HG02886.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.135+13243_135+1324 others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280759 | |||||||
| chr8:98280759 | T | TAGAGAGA others(5): Show |
3 | a0001c0001t0011g0004 a0001c0002t0001g0249 a0002c0003t0002g0068 |
3 | HG02523.hp1 NA18992.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.135+13243_135+1324 others(16): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280759 | |||||||
| chr8:98280761 | T | G | 58 | a0001c0001t0001g0016 a0001c0001t0001g0109 a0001c0001t0001g0289 others(55): Show |
61 | HG00438.hp1 HG00609.hp2 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.135+13242A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TAG | 4 | a0001c0001t0002g0277 a0001c0001t0002g0280 a0001c0002t0001g0090 others(1): Show |
4 | HG00408.hp1 HG00741.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+13240_135+1324 others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TAGAG | 5 | a0001c0001t0002g0054 a0001c0001t0002g0103 a0001c0001t0002g0284 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+13238_135+1324 others(8): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TAGAGAG | 4 | a0001c0001t0002g0022 a0001c0002t0001g0272 a0001c0002t0006g0264 others(1): Show |
4 | HG00438.hp2 HG04204.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+13236_135+1324 others(10): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TAGAGAGA others(1): Show |
8 | a0001c0001t0002g0036 a0001c0001t0002g0067 a0001c0001t0002g0274 others(5): Show |
8 | HG00280.hp1 HG00544.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+13234_135+1324 others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TAGAGAGA others(3): Show |
2 | a0001c0002t0001g0247 a0001c0006t0002g0117 |
2 | HG02976.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.135+13232_135+1324 others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TAGAGAGA others(5): Show |
1 | a0001c0001t0003g0018 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.135+13230_135+1324 others(16): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATAGAG | 3 | a0001c0001t0003g0269 a0001c0002t0001g0127 a0001c0002t0001g0270 |
3 | HG02015.hp1 HG02683.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(10): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATAGAGA others(1): Show |
8 | a0001c0001t0014g0069 a0001c0002t0001g0062 a0001c0002t0001g0063 others(5): Show |
8 | HG00621.hp1 HG01109.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATAGAGA others(3): Show |
4 | a0001c0001t0001g0308 a0001c0002t0001g0093 a0001c0002t0001g0204 others(1): Show |
4 | HG00558.hp1 HG03471.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATAGAGA others(5): Show |
1 | a0001c0001t0005g0136 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(16): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATAGAGA others(13): Show |
1 | a0001c0001t0002g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(24): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATAG | 4 | a0001c0001t0003g0126 a0001c0001t0005g0196 a0001c0002t0001g0221 others(1): Show |
4 | HG02056.hp1 NA18979.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(10): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATAGA others(1): Show |
6 | a0001c0001t0003g0055 a0001c0002t0001g0056 a0001c0002t0001g0059 others(3): Show |
6 | HG01257.hp2 HG01258.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATAGA others(3): Show |
5 | a0001c0001t0003g0134 a0001c0001t0010g0137 a0001c0002t0001g0199 others(2): Show |
5 | HG00642.hp1 HG02602.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATAGA others(5): Show |
1 | a0001c0002t0001g0205 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(16): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATAGA others(9): Show |
1 | a0001c0002t0001g0254 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(20): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATAGA others(11): Show |
1 | a0001c0001t0001g0241 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(22): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATAGA others(13): Show |
1 | a0001c0001t0002g0172 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(24): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATAGA others(19): Show |
2 | a0001c0001t0003g0276 a0001c0002t0001g0328 |
2 | HG01169.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(30): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(1): Show |
3 | a0001c0001t0003g0052 a0001c0001t0003g0101 a0001c0001t0003g0268 |
3 | HG01256.hp1 HG02004.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(3): Show |
3 | a0001c0001t0003g0060 a0001c0002t0001g0198 a0001c0002t0006g0061 |
3 | HG00099.hp2 NA18966.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(5): Show |
1 | a0001c0002t0001g0092 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(16): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(7): Show |
2 | a0001c0001t0010g0139 a0001c0001t0010g0140 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(18): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(9): Show |
1 | a0001c0002t0001g0227 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(20): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(11): Show |
1 | a0001c0001t0002g0106 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(22): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(13): Show |
1 | a0001c0002t0001g0229 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(24): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(15): Show |
1 | a0001c0001t0018g0163 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(26): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(17): Show |
1 | a0001c0001t0003g0209 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(28): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(19): Show |
1 | a0001c0001t0003g0174 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(30): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(3): Show |
2 | a0001c0001t0001g0197 a0001c0002t0001g0245 |
2 | HG00597.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(5): Show |
2 | a0001c0001t0002g0259 a0001c0002t0006g0079 |
2 | NA18997.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(16): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(7): Show |
3 | a0001c0001t0003g0135 a0001c0001t0005g0138 a0001c0002t0001g0260 |
3 | HG03239.hp2 HG03710.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(18): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(9): Show |
1 | a0001c0002t0001g0226 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(20): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(11): Show |
2 | a0001c0001t0001g0186 a0002c0004t0001g0206 |
2 | HG01169.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(22): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(13): Show |
5 | a0001c0001t0002g0039 a0001c0001t0002g0169 a0001c0001t0002g0258 others(2): Show |
5 | HG00408.hp2 HG02300.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(24): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(15): Show |
3 | a0001c0001t0001g0044 a0001c0001t0001g0099 a0001c0001t0002g0171 |
3 | HG02896.hp2 HG02897.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(26): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(17): Show |
1 | a0001c0002t0001g0256 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(28): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(23): Show |
1 | a0001c0005t0001g0030 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(34): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(5): Show |
2 | a0001c0001t0003g0296 a0002c0004t0001g0053 |
2 | HG01975.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(16): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(9): Show |
1 | a0001c0001t0001g0177 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(20): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(11): Show |
8 | a0001c0001t0001g0118 a0001c0001t0001g0184 a0001c0001t0003g0130 others(5): Show |
8 | HG01167.hp1 HG01517.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(22): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(13): Show |
4 | a0001c0001t0001g0157 a0001c0001t0002g0144 a0001c0001t0002g0173 others(1): Show |
4 | HG00323.hp1 HG00597.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(24): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(15): Show |
3 | a0001c0001t0001g0121 a0001c0001t0001g0160 a0001c0002t0023g0231 |
3 | HG00323.hp2 HG03017.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(26): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(17): Show |
3 | a0001c0001t0003g0122 a0001c0002t0001g0145 a0001c0002t0001g0191 |
3 | HG01123.hp1 HG02523.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(28): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(19): Show |
4 | a0001c0002t0001g0326 a0001c0002t0001g0327 a0001c0002t0020g0086 others(1): Show |
4 | HG01943.hp2 HG01993.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(30): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(23): Show |
2 | a0001c0001t0002g0166 a0002c0003t0002g0194 |
2 | HG01257.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(34): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(25): Show |
1 | a0001c0002t0004g0305 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(36): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(7): Show |
2 | a0001c0001t0002g0102 a0001c0001t0005g0143 |
2 | HG01074.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(18): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(9): Show |
1 | a0001c0001t0003g0129 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(20): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(11): Show |
2 | a0001c0001t0003g0243 a0001c0001t0005g0002 |
3 | HG01256.hp2 HG01258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(22): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(13): Show |
3 | a0001c0001t0001g0239 a0001c0002t0001g0142 a0001c0002t0004g0037 |
3 | HG01515.hp1 HG03209.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(24): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(15): Show |
2 | a0001c0001t0002g0168 a0001c0001t0003g0207 |
2 | HG00558.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(26): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(17): Show |
2 | a0001c0001t0001g0042 a0001c0001t0003g0170 |
2 | HG02258.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(28): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(19): Show |
3 | a0001c0001t0001g0242 a0001c0001t0005g0233 a0001c0002t0001g0071 |
3 | HG03669.hp1 HG03942.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(30): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(21): Show |
3 | a0001c0001t0003g0164 a0001c0002t0001g0321 a0001c0002t0004g0087 |
3 | HG00735.hp2 HG02698.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(32): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(23): Show |
1 | a0001c0005t0001g0035 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(34): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(25): Show |
1 | a0001c0001t0001g0028 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(36): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(9): Show |
1 | a0002c0003t0002g0167 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(20): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(11): Show |
1 | a0001c0001t0003g0230 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(22): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(15): Show |
2 | a0001c0001t0002g0133 a0001c0001t0003g0115 |
2 | HG02109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(26): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(17): Show |
4 | a0001c0001t0002g0124 a0001c0001t0002g0248 a0001c0001t0014g0187 others(1): Show |
4 | HG01358.hp2 HG03491.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(28): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(19): Show |
4 | a0001c0002t0001g0255 a0001c0002t0004g0082 a0001c0002t0004g0083 others(1): Show |
4 | HG01243.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(30): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(21): Show |
4 | a0001c0001t0001g0024 a0001c0001t0002g0085 a0001c0002t0001g0072 others(1): Show |
4 | HG02280.hp1 HG03225.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(32): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(23): Show |
2 | a0001c0001t0001g0025 a0001c0001t0001g0193 |
2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(34): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(25): Show |
1 | a0001c0002t0004g0304 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(36): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(15): Show |
2 | a0001c0002t0001g0202 a0002c0003t0002g0201 |
2 | HG02080.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(26): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(17): Show |
4 | a0001c0001t0001g0290 a0001c0001t0002g0125 a0001c0001t0003g0116 others(1): Show |
4 | HG00738.hp1 HG02257.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(28): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(19): Show |
5 | a0001c0001t0001g0232 a0001c0001t0001g0240 a0001c0001t0001g0302 others(2): Show |
5 | HG01106.hp1 HG01433.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(30): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(25): Show |
1 | a0001c0001t0002g0238 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(36): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(27): Show |
1 | a0001c0001t0001g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(38): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(15): Show |
1 | a0001c0001t0001g0176 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(26): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(17): Show |
2 | a0001c0001t0003g0203 a0001c0001t0024g0150 |
2 | HG00733.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(28): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(21): Show |
4 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0002t0001g0189 others(1): Show |
4 | HG01884.hp2 HG02165.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(32): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(23): Show |
1 | a0001c0002t0001g0190 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(34): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(25): Show |
1 | a0001c0002t0004g0294 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(36): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(31): Show |
1 | a0001c0005t0004g0029 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(42): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(19): Show |
4 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0002g0178 others(1): Show |
4 | HG00735.hp1 NA18906.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(30): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(21): Show |
3 | a0001c0001t0001g0070 a0001c0001t0001g0237 a0003c0007t0002g0236 |
3 | HG00099.hp1 HG02280.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(32): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(23): Show |
2 | a0001c0001t0001g0123 a0001c0001t0002g0301 |
2 | HG00609.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(34): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(27): Show |
1 | a0001c0001t0001g0162 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(38): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(19): Show |
2 | a0001c0001t0001g0120 a0001c0001t0003g0043 |
2 | HG01975.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(30): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(21): Show |
5 | a0001c0001t0001g0151 a0001c0001t0002g0323 a0001c0001t0005g0006 others(2): Show |
5 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(32): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(23): Show |
1 | a0001c0002t0004g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(34): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(25): Show |
1 | a0001c0001t0005g0008 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(36): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(21): Show |
1 | a0001c0001t0001g0098 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(32): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(23): Show |
2 | a0001c0001t0001g0152 a0001c0002t0001g0181 |
2 | HG00280.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(34): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(25): Show |
1 | a0001c0001t0007g0291 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(36): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(27): Show |
1 | a0001c0001t0002g0324 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(38): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(29): Show |
1 | a0001c0001t0008g0161 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(40): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(25): Show |
3 | a0001c0001t0001g0153 a0001c0001t0003g0235 a0001c0002t0001g0154 |
3 | HG02135.hp1 NA18947.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(36): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(27): Show |
5 | a0001c0001t0001g0156 a0001c0001t0002g0286 a0001c0001t0007g0292 others(2): Show |
5 | HG00544.hp1 HG00738.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(38): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(23): Show |
1 | a0001c0001t0003g0149 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(34): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(27): Show |
1 | a0001c0002t0001g0155 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(38): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(29): Show |
1 | a0001c0002t0006g0246 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(40): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(31): Show |
1 | a0001c0002t0001g0228 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(42): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(37): Show |
1 | a0001c0002t0004g0295 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(48): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280761 | T | TATATATA others(35): Show |
2 | a0001c0001t0001g0159 a0001c0002t0001g0158 |
2 | HG02165.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(46): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | |||||||
| chr8:98280763 | G | T | 11 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0002g0210 others(8): Show |
11 | HG01070.hp1 HG02273.hp1 HG03453.hp1 others(8): Show |
intron_variant | MODIFIER | c.135+13240C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280763 | |||||||
| chr8:98280765 | G | T | 5 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0002g0210 others(2): Show |
5 | NA18612.hp2 NA18992.hp2 NA19062.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+13238C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280765 | |||||||
| chr8:98280792 | A | AG | 9 | a0001c0001t0001g0025 a0001c0001t0001g0070 a0001c0001t0002g0144 others(6): Show |
9 | HG00323.hp1 HG00597.hp1 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.135+13210_135+1321 others(5): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280792 | |||||||
| chr8:98280921 | T | C | 6 | a0001c0001t0005g0138 a0001c0001t0010g0137 a0001c0001t0010g0139 others(3): Show |
6 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.135+13082A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280921 | |||||||
| chr8:98280930 | C | T | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+13073G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280930 | |||||||
| chr8:98281269 | A | G | 1 | a0001c0001t0005g0233 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.135+12734T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98281269 | |||||||
| chr8:98281406 | G | C | 1 | a0001c0001t0008g0034 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.135+12597C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98281406 | |||||||
| chr8:98281903 | T | G | 1 | a0001c0001t0014g0069 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.135+12100A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98281903 | |||||||
| chr8:98282336 | G | T | 1 | a0001c0002t0004g0114 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.135+11667C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98282336 | |||||||
| chr8:98282382 | T | A | 6 | a0001c0001t0002g0085 a0001c0002t0004g0082 a0001c0002t0004g0083 others(3): Show |
6 | HG01243.hp2 HG02723.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.135+11621A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98282382 | |||||||
| chr8:98282723 | T | G | 1 | a0001c0001t0003g0243 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.135+11280A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98282723 | |||||||
| chr8:98283192 | T | C | 3 | a0001c0002t0004g0304 a0001c0002t0004g0305 a0001c0002t0004g0306 |
3 | HG02559.hp2 HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.135+10811A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98283192 | |||||||
| chr8:98283436 | C | A | 57 | a0001c0001t0002g0036 a0001c0001t0002g0047 a0001c0001t0002g0048 others(54): Show |
58 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.135+10567G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98283436 | |||||||
| chr8:98284058 | T | A | 1 | a0001c0001t0021g0285 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.135+9945A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98284058 | |||||||
| chr8:98284399 | TTC | T | 25 | a0001c0001t0001g0121 a0001c0001t0001g0197 a0001c0001t0002g0248 others(22): Show |
25 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.135+9602_135+9603d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98284399 | |||||||
| chr8:98284418 | T | A | 1 | a0001c0001t0003g0230 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.135+9585A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98284418 | |||||||
| chr8:98284418 | T | TCA | 8 | a0001c0001t0001g0109 a0001c0001t0002g0023 a0001c0001t0002g0108 others(5): Show |
8 | HG01069.hp1 HG02109.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+9583_135+9584d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98284418 | |||||||
| chr8:98284418 | TCA | T | 201 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.135+9583_135+9584d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98284418 | |||||||
| chr8:98284418 | TCACACA | T | 16 | a0001c0001t0001g0118 a0001c0001t0002g0085 a0001c0001t0002g0322 others(13): Show |
16 | HG01243.hp1 HG01243.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.135+9579_135+9584d others(8): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98284418 | |||||||
| chr8:98284420 | A | T | 5 | a0001c0001t0001g0314 a0001c0001t0002g0277 a0001c0001t0007g0307 others(2): Show |
5 | HG00741.hp2 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+9583T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98284420 | |||||||
| chr8:98284422 | A | T | 13 | a0001c0001t0001g0024 a0001c0001t0001g0040 a0001c0001t0001g0041 others(10): Show |
13 | HG01884.hp2 HG02015.hp2 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.135+9581T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98284422 | |||||||
| chr8:98284593 | T | C | 3 | a0001c0002t0001g0326 a0001c0002t0001g0327 a0001c0002t0001g0328 |
3 | HG01943.hp2 HG01993.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.135+9410A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98284593 | |||||||
| chr8:98284967 | G | A | 1 | a0001c0001t0002g0301 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.135+9036C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98284967 | |||||||
| chr8:98284992 | G | A | 22 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(19): Show |
22 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.135+9011C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98284992 | |||||||
| chr8:98285259 | G | C | 1 | a0001c0002t0023g0231 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.135+8744C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285259 | |||||||
| chr8:98285396 | G | A | 1 | a0001c0001t0003g0018 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.135+8607C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285396 | |||||||
| chr8:98285434 | A | G | 35 | a0001c0001t0001g0098 a0001c0001t0001g0123 a0001c0001t0001g0146 others(32): Show |
36 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.135+8569T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285434 | |||||||
| chr8:98285474 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.135+8529C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285474 | |||||||
| chr8:98285523 | C | T | 10 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0003g0115 others(7): Show |
10 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.135+8480G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285523 | |||||||
| chr8:98285535 | G | A | 11 | a0001c0001t0002g0085 a0001c0001t0003g0018 a0001c0002t0004g0081 others(8): Show |
11 | HG01243.hp1 HG01243.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.135+8468C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285535 | |||||||
| chr8:98285541 | G | A | 1 | a0001c0001t0016g0293 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.135+8462C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285541 | |||||||
| chr8:98285542 | C | A | 1 | a0001c0002t0004g0325 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.135+8461G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285542 | |||||||
| chr8:98285647 | A | C | 30 | a0001c0001t0002g0085 a0001c0001t0002g0322 a0001c0001t0002g0323 others(27): Show |
30 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.135+8356T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285647 | |||||||
| chr8:98285676 | T | C | 3 | a0001c0001t0002g0094 a0001c0001t0002g0095 a0001c0006t0002g0117 |
3 | HG02976.hp1 NA19070.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.135+8327A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285676 | |||||||
| chr8:98285715 | A | C | 1 | a0001c0002t0001g0265 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.135+8288T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285715 | |||||||
| chr8:98285744 | G | A | 1 | a0001c0001t0005g0233 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.135+8259C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285744 | |||||||
| chr8:98285752 | C | A | 17 | a0001c0001t0002g0085 a0001c0001t0002g0133 a0001c0001t0003g0018 others(14): Show |
17 | HG01243.hp1 HG01243.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.135+8251G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285752 | |||||||
| chr8:98285756 | C | T | 1 | a0001c0001t0002g0234 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.135+8247G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285756 | |||||||
| chr8:98285913 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.135+8090C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285913 | |||||||
| chr8:98286214 | C | A | 5 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0290 others(2): Show |
5 | HG02055.hp1 HG02818.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+7789G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286214 | |||||||
| chr8:98286325 | G | A | 23 | a0001c0001t0001g0109 a0001c0001t0002g0085 a0001c0001t0002g0108 others(20): Show |
23 | HG01243.hp1 HG01243.hp2 HG02004.hp1 others(20): Show |
intron_variant | MODIFIER | c.135+7678C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286325 | |||||||
| chr8:98286435 | G | A | 1 | a0001c0002t0001g0080 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.135+7568C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286435 | |||||||
| chr8:98286478 | C | G | 50 | a0001c0001t0001g0308 a0001c0001t0001g0314 a0001c0001t0002g0022 others(47): Show |
52 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.135+7525G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286478 | |||||||
| chr8:98286611 | C | T | 1 | a0001c0001t0016g0293 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.135+7392G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286611 | |||||||
| chr8:98286722 | T | A | 9 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0009g0012 others(6): Show |
9 | HG02451.hp1 HG02559.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.135+7281A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286722 | |||||||
| chr8:98286812 | C | CA | 43 | a0001c0001t0001g0070 a0001c0001t0001g0237 a0001c0001t0001g0239 others(40): Show |
43 | HG00099.hp1 HG00438.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.135+7190dupT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286812 | |||||||
| chr8:98286823 | A | C | 5 | a0001c0001t0001g0308 a0001c0001t0002g0309 a0001c0001t0002g0311 others(2): Show |
5 | HG01884.hp1 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+7180T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286823 | |||||||
| chr8:98286824 | A | AC | 3 | a0001c0001t0002g0322 a0001c0001t0002g0323 a0001c0001t0002g0324 |
3 | HG03098.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.135+7178_135+7179i others(3): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286824 | |||||||
| chr8:98286824 | A | C | 10 | a0001c0001t0003g0134 a0001c0001t0003g0135 a0001c0001t0005g0136 others(7): Show |
10 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.135+7179T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286824 | |||||||
| chr8:98286828 | A | C | 1 | a0001c0001t0002g0023 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.135+7175T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286828 | |||||||
| chr8:98286829 | A | C | 41 | a0001c0001t0001g0308 a0001c0001t0001g0314 a0001c0001t0002g0022 others(38): Show |
43 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.135+7174T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286829 | |||||||
| chr8:98286830 | A | C | 33 | a0001c0001t0001g0109 a0001c0001t0002g0085 a0001c0001t0002g0108 others(30): Show |
33 | HG01243.hp1 HG01243.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.135+7173T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286830 | |||||||
| chr8:98286831 | AAAAC | A | 9 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0009g0012 others(6): Show |
9 | HG02451.hp1 HG02559.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.135+7168_135+7171d others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286831 | |||||||
| chr8:98286832 | AAAC | A | 9 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(6): Show |
9 | HG02280.hp1 HG02486.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.135+7168_135+7170d others(5): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286832 | |||||||
| chr8:98286834 | AC | A | 41 | a0001c0001t0001g0308 a0001c0001t0001g0314 a0001c0001t0002g0022 others(38): Show |
43 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.135+7168delG | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286834 | |||||||
| chr8:98286835 | C | A | 37 | a0001c0001t0001g0109 a0001c0001t0002g0085 a0001c0001t0002g0108 others(34): Show |
37 | HG01243.hp1 HG01243.hp2 HG02004.hp1 others(34): Show |
intron_variant | MODIFIER | c.135+7168G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286835 | |||||||
| chr8:98287051 | G | T | 1 | a0001c0002t0004g0017 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.135+6952C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98287051 | |||||||
| chr8:98287052 | A | G | 4 | a0001c0001t0001g0120 a0001c0001t0001g0290 a0001c0002t0004g0294 others(1): Show |
4 | HG02055.hp1 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+6951T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98287052 | |||||||
| chr8:98287434 | G | A | 17 | a0001c0001t0001g0109 a0001c0001t0002g0085 a0001c0001t0002g0108 others(14): Show |
17 | HG01243.hp1 HG01243.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.135+6569C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98287434 | |||||||
| chr8:98287507 | A | C | 1 | a0001c0001t0003g0001 | 3 | HG01070.hp2 HG01071.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.135+6496T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98287507 | |||||||
| chr8:98287741 | T | C | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+6262A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98287741 | |||||||
| chr8:98287753 | C | G | 25 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0274 others(22): Show |
27 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.135+6250G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98287753 | |||||||
| chr8:98287754 | G | A | 1 | a0001c0002t0001g0256 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.135+6249C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98287754 | |||||||
| chr8:98287853 | T | G | 29 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0109 others(26): Show |
29 | HG01243.hp1 HG01243.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.135+6150A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98287853 | |||||||
| chr8:98287952 | T | C | 4 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0008 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+6051A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98287952 | |||||||
| chr8:98288094 | G | T | 1 | a0001c0001t0003g0126 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.135+5909C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98288094 | |||||||
| chr8:98288146 | C | T | 17 | a0001c0001t0001g0109 a0001c0001t0002g0085 a0001c0001t0002g0108 others(14): Show |
17 | HG01243.hp1 HG01243.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.135+5857G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98288146 | |||||||
| chr8:98288147 | G | A | 1 | a0001c0002t0004g0257 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.135+5856C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98288147 | |||||||
| chr8:98288230 | C | T | 2 | a0001c0001t0003g0115 a0001c0001t0003g0116 |
2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.135+5773G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98288230 | |||||||
| chr8:98288231 | T | C | 2 | a0001c0001t0002g0258 a0001c0001t0002g0259 |
2 | HG00408.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.135+5772A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98288231 | |||||||
| chr8:98288309 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0009g0012 a0001c0001t0009g0013 |
3 | HG02451.hp1 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.135+5694G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98288309 | |||||||
| chr8:98288330 | G | T | 1 | a0001c0001t0002g0036 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.135+5673C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98288330 | |||||||
| chr8:98288411 | A | G | 1 | a0001c0002t0001g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.135+5592T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98288411 | |||||||
| chr8:98288502 | C | T | 1 | a0004c0008t0003g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+5501G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98288502 | |||||||
| chr8:98288503 | G | A | 15 | a0001c0001t0001g0109 a0001c0001t0002g0085 a0001c0001t0002g0108 others(12): Show |
15 | HG01243.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.135+5500C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98288503 | |||||||
| chr8:98288610 | C | T | 3 | a0001c0002t0004g0304 a0001c0002t0004g0305 a0001c0002t0004g0306 |
3 | HG02559.hp2 HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.135+5393G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98288610 | |||||||
| chr8:98288828 | C | T | 2 | a0001c0001t0002g0124 a0001c0001t0002g0125 |
2 | NA18953.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.135+5175G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98288828 | |||||||
| chr8:98288831 | G | A | 25 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0109 others(22): Show |
25 | HG01243.hp1 HG01243.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.135+5172C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98288831 | |||||||
| chr8:98288893 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.135+5110T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98288893 | |||||||
| chr8:98289009 | T | C | 1 | a0001c0002t0001g0260 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.135+4994A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98289009 | |||||||
| chr8:98289051 | A | T | 15 | a0001c0001t0001g0109 a0001c0001t0002g0085 a0001c0001t0002g0108 others(12): Show |
15 | HG01243.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.135+4952T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98289051 | |||||||
| chr8:98289256 | T | G | 29 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0109 others(26): Show |
29 | HG01243.hp1 HG01243.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.135+4747A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98289256 | |||||||
| chr8:98289514 | CT | C | 65 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(62): Show |
67 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.135+4488delA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98289514 | |||||||
| chr8:98289569 | T | G | 3 | a0001c0001t0001g0300 a0001c0001t0003g0298 a0001c0002t0001g0299 |
3 | NA18945.hp2 NA18990.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.135+4434A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98289569 | |||||||
| chr8:98289640 | C | G | 1 | a0001c0001t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.135+4363G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98289640 | |||||||
| chr8:98290081 | G | T | 2 | a0001c0001t0001g0121 a0001c0001t0003g0122 |
2 | HG03017.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.135+3922C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98290081 | |||||||
| chr8:98290102 | A | T | 55 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(52): Show |
57 | HG00738.hp1 HG00741.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.135+3901T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98290102 | |||||||
| chr8:98290103 | T | A | 10 | a0001c0001t0002g0091 a0001c0001t0002g0094 a0001c0001t0002g0095 others(7): Show |
10 | HG00408.hp1 NA18747.hp2 NA18942.hp1 others(7): Show |
intron_variant | MODIFIER | c.135+3900A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98290103 | |||||||
| chr8:98290498 | G | A | 4 | a0001c0001t0002g0033 a0001c0001t0008g0031 a0001c0001t0008g0032 others(1): Show |
4 | NA18960.hp1 NA19062.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+3505C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98290498 | |||||||
| chr8:98290556 | G | A | 1 | a0001c0002t0001g0096 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.135+3447C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98290556 | |||||||
| chr8:98290557 | T | G | 55 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(52): Show |
57 | HG00738.hp1 HG00741.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.135+3446A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98290557 | |||||||
| chr8:98290642 | G | C | 1 | a0001c0001t0003g0276 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.135+3361C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98290642 | |||||||
| chr8:98290670 | A | G | 1 | a0001c0001t0007g0307 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.135+3333T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98290670 | |||||||
| chr8:98290756 | G | A | 55 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(52): Show |
57 | HG00738.hp1 HG00741.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.135+3247C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98290756 | |||||||
| chr8:98291071 | T | A | 1 | a0001c0002t0001g0097 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.135+2932A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98291071 | |||||||
| chr8:98291299 | C | A | 1 | a0002c0004t0001g0287 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.135+2704G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98291299 | |||||||
| chr8:98291442 | T | C | 2 | a0001c0001t0001g0289 a0001c0001t0002g0288 |
2 | NA18973.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.135+2561A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98291442 | |||||||
| chr8:98291921 | C | A | 6 | a0001c0001t0001g0120 a0001c0001t0001g0290 a0001c0001t0007g0291 others(3): Show |
6 | HG00733.hp1 HG00738.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.135+2082G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98291921 | |||||||
| chr8:98292484 | A | G | 3 | a0001c0002t0004g0304 a0001c0002t0004g0305 a0001c0002t0004g0306 |
3 | HG02559.hp2 HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.135+1519T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98292484 | |||||||
| chr8:98292575 | A | G | 47 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(44): Show |
47 | HG00733.hp1 HG00738.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.135+1428T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98292575 | |||||||
| chr8:98292726 | A | AT | 23 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0109 others(20): Show |
23 | HG00280.hp1 HG01167.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.135+1276dupA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98292726 | |||||||
| chr8:98292726 | A | ATT | 66 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0041 others(63): Show |
66 | HG00099.hp2 HG00408.hp1 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.135+1275_135+1276d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98292726 | |||||||
| chr8:98292726 | A | ATTT | 9 | a0001c0001t0001g0014 a0001c0001t0002g0322 a0001c0001t0002g0323 others(6): Show |
9 | HG02630.hp2 HG02698.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.135+1274_135+1276d others(5): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98292726 | |||||||
| chr8:98292726 | AT | A | 6 | a0001c0001t0001g0290 a0001c0001t0007g0291 a0001c0001t0007g0292 others(3): Show |
6 | HG00733.hp1 HG00738.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.135+1276delA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98292726 | |||||||
| chr8:98292768 | T | C | 1 | a0001c0001t0003g0296 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.135+1235A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98292768 | |||||||
| chr8:98292794 | T | C | 4 | a0001c0001t0001g0300 a0001c0001t0003g0298 a0001c0002t0001g0299 others(1): Show |
4 | NA18945.hp2 NA18990.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+1209A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98292794 | |||||||
| chr8:98293135 | G | A | 35 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(32): Show |
35 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.135+868C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98293135 | |||||||
| chr8:98293272 | T | C | 2 | a0001c0001t0001g0302 a0001c0001t0002g0301 |
2 | HG01123.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.135+731A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98293272 | |||||||
| chr8:98293311 | A | T | 49 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(46): Show |
49 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.135+692T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98293311 | |||||||
| chr8:98293406 | T | G | 23 | a0001c0001t0001g0308 a0001c0001t0001g0314 a0001c0001t0002g0309 others(20): Show |
23 | HG00738.hp1 HG01175.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.135+597A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98293406 | |||||||
| chr8:98293667 | G | C | 3 | a0001c0002t0001g0326 a0001c0002t0001g0327 a0001c0002t0001g0328 |
3 | HG01943.hp2 HG01993.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.135+336C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98293667 | |||||||
| chr8:98293699 | C | T | 5 | a0001c0001t0002g0010 a0001c0001t0005g0006 a0001c0001t0005g0007 others(2): Show |
5 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+304G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98293699 |