Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54888 |
| ensemblid | ENSG00000037474.15 |
| hgncid | 25994 |
| symbol | NSUN2 |
| name | NOP2/Sun RNA methyltransferase 2 |
| refseq_nuc | NM_017755.6 |
| refseq_prot | NP_060225.4 |
| ensembl_nuc | ENST00000264670.11 |
| ensembl_prot | ENSP00000264670.6 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 6599239 |
| end | 6633044 |
| strand | - |
| ver | v1.2 |
| region | chr5:6599239-6633044 |
| region5000 | chr5:6594239-6638044 |
| regionname0 | NSUN2_chr5_6599239_6633044 |
| regionname5000 | NSUN2_chr5_6594239_6638044 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 767 | 389 | 83 | 72 | 176 | 15 | 41 | 133 | NSUN2_chr5_6594239_6638044 | NSUN2 | MGRRS others(762): Show |
chr5 | 6594239 | 6638044 |
| a0002 | 0/0 | 767 | 20 | 8 | 7 | 0 | 1 | 4 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | MGRRS others(762): Show |
chr5 | 6594239 | 6638044 |
| a0003 | 0/0 | 767 | 17 | 0 | 0 | 17 | 0 | 0 | 12 | NSUN2_chr5_6594239_6638044 | NSUN2 | MGRRS others(762): Show |
chr5 | 6594239 | 6638044 |
| a0004 | 0/0 | 767 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | MGRRS others(762): Show |
chr5 | 6594239 | 6638044 |
| a0005 | 0/0 | 767 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | MGRRS others(762): Show |
chr5 | 6594239 | 6638044 |
| a0006 | 0/0 | 767 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | MGRRS others(762): Show |
chr5 | 6594239 | 6638044 |
| a0007 | 0/0 | 767 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | MGRRS others(762): Show |
chr5 | 6594239 | 6638044 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2301 | 111 | 43 | 20 | 33 | 8 | 6 | NSUN2_chr5_6594239_6638044 | NSUN2 | ATGGG others(2296): Show |
chr5 | 6594239 | 6638044 | ||
| a0001c0002 | 0/0 | 2301 | 101 | 4 | 9 | 74 | 1 | 13 | NSUN2_chr5_6594239_6638044 | NSUN2 | ATGGG others(2296): Show |
chr5 | 6594239 | 6638044 | ||
| a0001c0003 | 0/1 | 2301 | 75 | 14 | 20 | 29 | 3 | 8 | NSUN2_chr5_6594239_6638044 | NSUN2 | ATGGG others(2296): Show |
chr5 | 6594239 | 6638044 | ||
| a0001c0004 | 0/0 | 2301 | 73 | 9 | 12 | 39 | 2 | 11 | NSUN2_chr5_6594239_6638044 | NSUN2 | ATGGG others(2296): Show |
chr5 | 6594239 | 6638044 | ||
| a0001c0009 | 0/0 | 2301 | 7 | 7 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | ATGGG others(2296): Show |
chr5 | 6594239 | 6638044 | ||
| a0001c0010 | 0/0 | 2301 | 6 | 0 | 5 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | ATGGG others(2296): Show |
chr5 | 6594239 | 6638044 | ||
| a0001c0011 | 0/0 | 2301 | 4 | 0 | 1 | 0 | 1 | 2 | NSUN2_chr5_6594239_6638044 | NSUN2 | ATGGG others(2296): Show |
chr5 | 6594239 | 6638044 | ||
| a0001c0012 | 0/0 | 2301 | 4 | 0 | 4 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | ATGGG others(2296): Show |
chr5 | 6594239 | 6638044 | ||
| a0001c0013 | 0/0 | 2301 | 4 | 4 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | ATGGG others(2296): Show |
chr5 | 6594239 | 6638044 | ||
| a0001c0015 | 0/0 | 2301 | 2 | 1 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | ATGGG others(2296): Show |
chr5 | 6594239 | 6638044 | ||
| a0001c0018 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | ATGGG others(2296): Show |
chr5 | 6594239 | 6638044 | ||
| a0001c0019 | 0/0 | 2301 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | ATGGG others(2296): Show |
chr5 | 6594239 | 6638044 | ||
| a0002c0006 | 0/0 | 2301 | 8 | 5 | 3 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | ATGGG others(2296): Show |
chr5 | 6594239 | 6638044 | ||
| a0002c0007 | 0/0 | 2301 | 8 | 2 | 4 | 0 | 1 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | ATGGG others(2296): Show |
chr5 | 6594239 | 6638044 | ||
| a0002c0014 | 0/0 | 2301 | 3 | 0 | 0 | 0 | 0 | 3 | NSUN2_chr5_6594239_6638044 | NSUN2 | ATGGG others(2296): Show |
chr5 | 6594239 | 6638044 | ||
| a0002c0017 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | ATGGG others(2296): Show |
chr5 | 6594239 | 6638044 | ||
| a0003c0005 | 0/0 | 2301 | 17 | 0 | 0 | 17 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | ATGGG others(2296): Show |
chr5 | 6594239 | 6638044 | ||
| a0004c0008 | 0/0 | 2301 | 8 | 7 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | ATGGG others(2296): Show |
chr5 | 6594239 | 6638044 | ||
| a0005c0016 | 0/0 | 2301 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | ATGGG others(2296): Show |
chr5 | 6594239 | 6638044 | ||
| a0006c0020 | 0/0 | 2301 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | ATGGG others(2296): Show |
chr5 | 6594239 | 6638044 | ||
| a0007c0021 | 0/0 | 2301 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | ATGGG others(2296): Show |
chr5 | 6594239 | 6638044 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3056 | 99 | 39 | 17 | 29 | 7 | 6 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0001c0001t0002 | 0/0 | 3056 | 9 | 1 | 3 | 4 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0001c0001t0004 | 0/0 | 3056 | 3 | 3 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0001c0002t0001 | 0/0 | 3056 | 100 | 4 | 9 | 74 | 1 | 12 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0001c0002t0007 | 0/0 | 3056 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0001c0003t0001 | 0/1 | 3056 | 73 | 14 | 19 | 28 | 3 | 8 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0001c0003t0002 | 0/0 | 3056 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0001c0003t0006 | 0/0 | 3056 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0001c0004t0001 | 0/0 | 3056 | 9 | 7 | 1 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0001c0004t0002 | 0/0 | 3056 | 62 | 2 | 11 | 37 | 2 | 10 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0001c0004t0005 | 0/0 | 3056 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0001c0004t0008 | 0/0 | 3056 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0001c0009t0001 | 0/0 | 3056 | 7 | 7 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0001c0010t0001 | 0/0 | 3056 | 4 | 0 | 3 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0001c0010t0002 | 0/0 | 3056 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0001c0011t0001 | 0/0 | 3056 | 4 | 0 | 1 | 0 | 1 | 2 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0001c0012t0002 | 0/0 | 3056 | 4 | 0 | 4 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0001c0013t0001 | 0/0 | 3056 | 4 | 4 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0001c0015t0001 | 0/0 | 3056 | 2 | 1 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0001c0018t0001 | 0/0 | 3056 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0001c0019t0002 | 0/0 | 3056 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0002c0006t0001 | 0/0 | 3056 | 4 | 4 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0002c0006t0003 | 0/0 | 3055 | 3 | 0 | 3 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3050): Show |
chr5 | 6594239 | 6638044 |
| a0002c0006t0009 | 0/0 | 3056 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTGGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0002c0007t0001 | 0/0 | 3056 | 4 | 2 | 1 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0002c0007t0003 | 0/0 | 3055 | 4 | 0 | 3 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3050): Show |
chr5 | 6594239 | 6638044 |
| a0002c0014t0001 | 0/0 | 3056 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0002c0014t0003 | 0/0 | 3055 | 2 | 0 | 0 | 0 | 0 | 2 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3050): Show |
chr5 | 6594239 | 6638044 |
| a0002c0017t0001 | 0/0 | 3056 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0003c0005t0001 | 0/0 | 3056 | 17 | 0 | 0 | 17 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0004c0008t0001 | 0/0 | 3056 | 8 | 7 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0005c0016t0002 | 0/0 | 3056 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0006c0020t0001 | 0/0 | 3056 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| a0007c0021t0001 | 0/0 | 3056 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | GTAGG others(3051): Show |
chr5 | 6594239 | 6638044 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 6 | 0 | 0 | 3 | 2 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0001t0004g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0002t0007g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0107 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0003t0006g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0002 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0003 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0005g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0004t0008g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0009t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0009t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0009t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0009t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0009t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0009t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0009t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0010t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0010t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0010t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0010t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0010t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0010t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0011t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0011t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0011t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0012t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0012t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0012t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0012t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0013t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0013t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0013t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0013t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0015t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0015t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0018t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0001c0019t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0002c0006t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0002c0006t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0002c0006t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0002c0006t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0002c0006t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0002c0006t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0002c0006t0009g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0002c0007t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0002c0007t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0002c0007t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0002c0007t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0002c0007t0003g0006 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0002c0014t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0002c0014t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0002c0014t0003g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0002c0017t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0003c0005t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0003c0005t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0003c0005t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0003c0005t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0003c0005t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0003c0005t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0003c0005t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0003c0005t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0003c0005t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0003c0005t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0003c0005t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0003c0005t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0003c0005t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0003c0005t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0003c0005t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0003c0005t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0004c0008t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0004c0008t0001g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0004c0008t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0004c0008t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0004c0008t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0004c0008t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0005c0016t0002g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0006c0020t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| a0007c0021t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0344 | EUR | GBR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0026 | EUR | GBR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0297 | EUR | GBR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00140 | hp2 | a0001 | c0004 | t0002 | g0166 | EUR | GBR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00280 | hp1 | a0001 | c0004 | t0002 | g0176 | EUR | FIN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0295 | EUR | FIN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00408 | hp1 | a0001 | c0003 | t0001 | g0017 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00408 | hp2 | a0001 | c0004 | t0002 | g0028 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00423 | hp1 | a0001 | c0003 | t0001 | g0082 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00423 | hp2 | a0003 | c0005 | t0001 | g0246 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0273 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00558 | hp1 | a0001 | c0003 | t0001 | g0081 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00558 | hp2 | a0003 | c0005 | t0001 | g0256 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00597 | hp1 | a0001 | c0004 | t0002 | g0177 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0315 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00609 | hp2 | a0003 | c0005 | t0001 | g0238 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00621 | hp1 | a0001 | c0004 | t0002 | g0174 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00621 | hp2 | a0001 | c0004 | t0002 | g0358 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00639 | hp1 | a0001 | c0003 | t0001 | g0057 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0106 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00642 | hp2 | a0002 | c0007 | t0003 | g0006 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0363 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00673 | hp2 | a0001 | c0003 | t0001 | g0019 | EAS | CHS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00735 | hp1 | a0001 | c0003 | t0001 | g0120 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00735 | hp2 | a0001 | c0003 | t0001 | g0022 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0119 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00741 | hp1 | a0001 | c0004 | t0002 | g0201 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG00741 | hp2 | a0001 | c0003 | t0001 | g0101 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01069 | hp1 | a0001 | c0012 | t0002 | g0152 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01069 | hp2 | a0001 | c0003 | t0001 | g0100 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01070 | hp2 | a0001 | c0004 | t0002 | g0002 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01071 | hp1 | a0001 | c0004 | t0002 | g0002 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01071 | hp2 | a0001 | c0012 | t0002 | g0151 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01074 | hp1 | a0001 | c0010 | t0002 | g0104 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01074 | hp2 | a0002 | c0007 | t0001 | g0130 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0333 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0022 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01099 | hp1 | a0002 | c0007 | t0003 | g0006 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0345 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01106 | hp1 | a0002 | c0006 | t0003 | g0093 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01106 | hp2 | a0001 | c0004 | t0002 | g0200 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01109 | hp2 | a0001 | c0003 | t0001 | g0110 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01167 | hp1 | a0002 | c0006 | t0003 | g0095 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0237 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01168 | hp1 | a0002 | c0007 | t0003 | g0006 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0037 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01192 | hp2 | a0001 | c0011 | t0001 | g0046 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01243 | hp1 | a0002 | c0006 | t0003 | g0094 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01243 | hp2 | a0004 | c0008 | t0001 | g0045 | AMR | PUR | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01256 | hp1 | a0001 | c0010 | t0001 | g0059 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01257 | hp1 | a0005 | c0016 | t0002 | g0027 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01257 | hp2 | a0001 | c0010 | t0001 | g0060 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01258 | hp1 | a0005 | c0016 | t0002 | g0027 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0193 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0109 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01346 | hp1 | a0001 | c0004 | t0002 | g0025 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01358 | hp1 | a0001 | c0003 | t0001 | g0108 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01358 | hp2 | a0001 | c0003 | t0001 | g0016 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01361 | hp2 | a0001 | c0003 | t0001 | g0072 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0102 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01496 | hp1 | a0001 | c0015 | t0001 | g0086 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0248 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01515 | hp1 | a0001 | c0011 | t0001 | g0047 | EUR | IBS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0021 | EUR | IBS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01517 | hp2 | a0001 | c0003 | t0001 | g0021 | EUR | IBS | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01891 | hp2 | a0001 | c0009 | t0001 | g0048 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01928 | hp1 | a0001 | c0004 | t0002 | g0002 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0348 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0343 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01934 | hp2 | a0001 | c0004 | t0002 | g0025 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0360 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01943 | hp2 | a0001 | c0003 | t0006 | g0114 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01952 | hp1 | a0001 | c0004 | t0001 | g0185 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01975 | hp1 | a0001 | c0010 | t0001 | g0061 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01975 | hp2 | a0001 | c0012 | t0002 | g0149 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0285 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01978 | hp2 | a0001 | c0012 | t0002 | g0150 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01981 | hp1 | a0001 | c0004 | t0002 | g0002 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0037 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01993 | hp1 | a0001 | c0003 | t0001 | g0117 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01993 | hp2 | a0001 | c0004 | t0002 | g0167 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02004 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02004 | hp2 | a0001 | c0004 | t0002 | g0003 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02015 | hp2 | a0003 | c0005 | t0001 | g0236 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02040 | hp1 | a0001 | c0004 | t0001 | g0159 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02040 | hp2 | a0001 | c0004 | t0002 | g0024 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02055 | hp1 | a0001 | c0004 | t0001 | g0202 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02055 | hp2 | a0001 | c0009 | t0001 | g0054 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02056 | hp1 | a0001 | c0003 | t0001 | g0096 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02071 | hp1 | a0001 | c0003 | t0001 | g0105 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02071 | hp2 | a0001 | c0003 | t0001 | g0078 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0307 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0364 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02080 | hp1 | a0001 | c0004 | t0002 | g0003 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02080 | hp2 | a0001 | c0003 | t0001 | g0076 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02083 | hp1 | a0001 | c0003 | t0001 | g0075 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02083 | hp2 | a0003 | c0005 | t0001 | g0269 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02129 | hp1 | a0001 | c0004 | t0002 | g0148 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02132 | hp1 | a0001 | c0004 | t0002 | g0147 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02135 | hp2 | a0001 | c0004 | t0002 | g0195 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | CDX | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0223 | EAS | CDX | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02165 | hp1 | a0001 | c0003 | t0001 | g0092 | EAS | CDX | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02165 | hp2 | a0001 | c0004 | t0002 | g0188 | EAS | CDX | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02257 | hp2 | a0001 | c0004 | t0002 | g0155 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02258 | hp1 | a0002 | c0006 | t0009 | g0371 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02273 | hp1 | a0001 | c0003 | t0001 | g0115 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0056 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02293 | hp1 | a0001 | c0010 | t0002 | g0118 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0320 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02300 | hp1 | a0001 | c0004 | t0002 | g0002 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02300 | hp2 | a0001 | c0003 | t0001 | g0007 | AMR | PEL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02451 | hp1 | a0004 | c0008 | t0001 | g0045 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0211 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0365 | EAS | KHV | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02572 | hp2 | a0002 | c0006 | t0001 | g0065 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02602 | hp1 | a0001 | c0010 | t0001 | g0058 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02602 | hp2 | a0001 | c0004 | t0002 | g0208 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0023 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02615 | hp2 | a0001 | c0009 | t0001 | g0050 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02622 | hp1 | a0004 | c0008 | t0001 | g0044 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02622 | hp2 | a0002 | c0007 | t0001 | g0132 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02630 | hp1 | a0001 | c0013 | t0001 | g0215 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0235 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0137 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0282 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02683 | hp2 | a0002 | c0014 | t0003 | g0245 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02698 | hp2 | a0001 | c0004 | t0002 | g0138 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02717 | hp2 | a0002 | c0007 | t0001 | g0128 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02723 | hp1 | a0002 | c0006 | t0001 | g0067 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02723 | hp2 | a0001 | c0004 | t0001 | g0153 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02735 | hp1 | a0001 | c0004 | t0002 | g0178 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02735 | hp2 | a0001 | c0011 | t0001 | g0013 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02738 | hp1 | a0001 | c0004 | t0002 | g0197 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02738 | hp2 | a0002 | c0014 | t0003 | g0261 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02809 | hp1 | a0004 | c0008 | t0001 | g0368 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02809 | hp2 | a0001 | c0018 | t0001 | g0136 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0023 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02886 | hp1 | a0001 | c0004 | t0001 | g0008 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02895 | hp1 | a0001 | c0009 | t0001 | g0053 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02897 | hp1 | a0001 | c0009 | t0001 | g0051 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02922 | hp2 | a0001 | c0004 | t0001 | g0154 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0207 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0091 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0083 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0103 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03017 | hp2 | a0001 | c0004 | t0002 | g0205 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03041 | hp1 | a0004 | c0008 | t0001 | g0369 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0121 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | MSL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0068 | AFR | MSL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0077 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03130 | hp2 | a0001 | c0003 | t0001 | g0066 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0064 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03195 | hp1 | a0004 | c0008 | t0001 | g0044 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03195 | hp2 | a0001 | c0009 | t0001 | g0052 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03209 | hp1 | a0002 | c0006 | t0001 | g0014 | AFR | MSL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03209 | hp2 | a0001 | c0013 | t0001 | g0214 | AFR | MSL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0063 | AFR | MSL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0251 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03239 | hp2 | a0002 | c0007 | t0001 | g0131 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03453 | hp1 | a0001 | c0015 | t0001 | g0069 | AFR | MSL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03486 | hp2 | a0001 | c0009 | t0001 | g0049 | AFR | MSL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03490 | hp1 | a0006 | c0020 | t0001 | g0281 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0290 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03491 | hp1 | a0001 | c0003 | t0001 | g0018 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03491 | hp2 | a0001 | c0002 | t0007 | g0228 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03492 | hp1 | a0001 | c0003 | t0001 | g0018 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0291 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0097 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | GWD | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03579 | hp2 | a0001 | c0004 | t0001 | g0156 | AFR | MSL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0227 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0234 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03688 | hp1 | a0001 | c0011 | t0001 | g0013 | SAS | STU | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | STU | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0244 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0308 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03710 | hp2 | a0001 | c0003 | t0001 | g0098 | SAS | PJL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0249 | SAS | BEB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03831 | hp2 | a0001 | c0004 | t0002 | g0024 | SAS | BEB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | BEB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0346 | SAS | BEB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0296 | SAS | BEB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03942 | hp1 | a0001 | c0004 | t0002 | g0209 | SAS | BEB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0263 | SAS | BEB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG04115 | hp1 | a0001 | c0004 | t0002 | g0210 | SAS | STU | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG04115 | hp2 | a0001 | c0004 | t0002 | g0194 | SAS | STU | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0113 | SAS | BEB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG04184 | hp2 | a0001 | c0004 | t0005 | g0175 | SAS | BEB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | STU | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0260 | SAS | STU | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG04228 | hp1 | a0001 | c0004 | t0002 | g0199 | SAS | STU | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG04228 | hp2 | a0001 | c0003 | t0001 | g0116 | SAS | STU | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18522 | hp1 | a0004 | c0008 | t0001 | g0367 | AFR | YRI | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18522 | hp2 | a0001 | c0013 | t0001 | g0213 | AFR | YRI | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18612 | hp1 | a0001 | c0004 | t0002 | g0357 | EAS | CHB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | CHB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18747 | hp1 | a0001 | c0004 | t0002 | g0192 | EAS | CHB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | CHB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | YRI | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18906 | hp2 | a0001 | c0004 | t0002 | g0143 | AFR | YRI | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18940 | hp1 | a0001 | c0003 | t0001 | g0088 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18941 | hp1 | a0001 | c0004 | t0002 | g0133 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18942 | hp1 | a0001 | c0003 | t0001 | g0020 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18943 | hp1 | a0001 | c0003 | t0001 | g0085 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18943 | hp2 | a0003 | c0005 | t0001 | g0034 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18944 | hp2 | a0001 | c0004 | t0002 | g0003 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18945 | hp1 | a0001 | c0004 | t0002 | g0172 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18945 | hp2 | a0003 | c0005 | t0001 | g0229 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18947 | hp1 | a0001 | c0004 | t0002 | g0003 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18950 | hp1 | a0001 | c0003 | t0001 | g0062 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18950 | hp2 | a0003 | c0005 | t0001 | g0271 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18952 | hp1 | a0001 | c0003 | t0001 | g0084 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18952 | hp2 | a0003 | c0005 | t0001 | g0034 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18953 | hp2 | a0001 | c0004 | t0002 | g0196 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18954 | hp2 | a0001 | c0004 | t0002 | g0173 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18956 | hp1 | a0001 | c0003 | t0001 | g0074 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0300 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18957 | hp1 | a0001 | c0004 | t0002 | g0184 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18962 | hp2 | a0001 | c0004 | t0002 | g0029 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0264 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18963 | hp2 | a0001 | c0004 | t0002 | g0169 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0289 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18967 | hp1 | a0003 | c0005 | t0001 | g0254 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18968 | hp1 | a0001 | c0004 | t0002 | g0319 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18969 | hp1 | a0003 | c0005 | t0001 | g0233 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18969 | hp2 | a0007 | c0021 | t0001 | g0361 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18970 | hp2 | a0003 | c0005 | t0001 | g0224 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18971 | hp1 | a0001 | c0004 | t0002 | g0134 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18975 | hp1 | a0001 | c0004 | t0002 | g0182 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18980 | hp1 | a0001 | c0019 | t0002 | g0198 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18981 | hp1 | a0003 | c0005 | t0001 | g0286 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18982 | hp1 | a0001 | c0003 | t0002 | g0099 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0301 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18983 | hp1 | a0001 | c0003 | t0001 | g0073 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18983 | hp2 | a0001 | c0004 | t0002 | g0171 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0294 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18988 | hp2 | a0001 | c0004 | t0002 | g0146 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18991 | hp2 | a0001 | c0004 | t0002 | g0139 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18994 | hp1 | a0001 | c0003 | t0001 | g0020 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0316 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18998 | hp1 | a0003 | c0005 | t0001 | g0270 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19000 | hp2 | a0001 | c0003 | t0001 | g0089 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19001 | hp2 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0312 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19003 | hp2 | a0001 | c0003 | t0001 | g0079 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19004 | hp1 | a0001 | c0003 | t0001 | g0017 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19004 | hp2 | a0001 | c0004 | t0002 | g0003 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19005 | hp1 | a0001 | c0003 | t0001 | g0090 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0299 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0313 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19030 | hp1 | a0002 | c0017 | t0001 | g0055 | AFR | LWK | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0122 | AFR | LWK | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | LWK | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | LWK | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19056 | hp1 | a0001 | c0004 | t0002 | g0191 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0292 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19060 | hp1 | a0001 | c0004 | t0002 | g0180 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19065 | hp1 | a0001 | c0004 | t0002 | g0189 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19065 | hp2 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19066 | hp1 | a0001 | c0003 | t0001 | g0071 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0362 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19068 | hp2 | a0001 | c0004 | t0002 | g0317 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19072 | hp2 | a0003 | c0005 | t0001 | g0226 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19075 | hp2 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19077 | hp1 | a0001 | c0003 | t0001 | g0087 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19079 | hp1 | a0001 | c0004 | t0008 | g0370 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0305 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19080 | hp1 | a0001 | c0004 | t0002 | g0158 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19081 | hp1 | a0001 | c0003 | t0001 | g0080 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19081 | hp2 | a0003 | c0005 | t0001 | g0247 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19083 | hp1 | a0001 | c0004 | t0002 | g0028 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19084 | hp2 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0293 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19089 | hp2 | a0001 | c0004 | t0002 | g0135 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19090 | hp1 | a0001 | c0004 | t0002 | g0029 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0310 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19091 | hp2 | a0003 | c0005 | t0001 | g0284 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | YRI | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | YRI | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0321 | AFR | ASW | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | ASW | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA20752 | hp1 | a0002 | c0007 | t0003 | g0006 | EUR | TSI | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0043 | EUR | TSI | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0338 | EUR | TSI | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA20805 | hp2 | a0001 | c0003 | t0001 | g0111 | EUR | TSI | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA20905 | hp1 | a0001 | c0003 | t0001 | g0070 | SAS | GIH | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA20905 | hp2 | a0002 | c0014 | t0001 | g0232 | SAS | GIH | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0112 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0356 | AMR | CLM | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02109 | hp1 | a0002 | c0006 | t0001 | g0014 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0259 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02486 | hp2 | a0001 | c0004 | t0001 | g0008 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02559 | hp1 | a0004 | c0008 | t0001 | g0366 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | ACB | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0008 | AFR | MSL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | MSL | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | USA | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | USA | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA18955 | hp2 | a0001 | c0004 | t0002 | g0318 | EAS | JPT | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | USA | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0243 | AFR | USA | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA21309 | hp1 | a0001 | c0013 | t0001 | g0212 | AFR | LWK | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0322 | AFR | LWK | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0107 | REF | REF | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | NSUN2_chr5_6594239_6638044 | NSUN2 | chr5 | 6594239 | 6638044 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:6599930 | C | T | 1 | a0005 | 2 | HG01257.hp1 HG01258.hp1 |
missense_variant | MODERATE | c.2300G>A | p.Arg767Gln | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 19/19 | 2365/3056 | 2300/2304 | 767/767 | chr5 | 6599930 | |||
| chr5:6599951 | G | T | 1 | a0002 | 20 | HG00642.hp2 HG01074.hp2 HG01099.hp1 others(17): Show |
missense_variant | MODERATE | c.2279C>A | p.Pro760Gln | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 19/19 | 2344/3056 | 2279/2304 | 760/767 | chr5 | 6599951 | |||
| chr5:6604216 | C | T | 1 | a0003 | 17 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(14): Show |
missense_variant | MODERATE | c.1879G>A | p.Val627Ile | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/19 | 1944/3056 | 1879/2304 | 627/767 | chr5 | 6604216 | |||
| chr5:6604654 | C | T | 1 | a0006 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.1769G>A | p.Arg590Lys | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 16/19 | 1834/3056 | 1769/2304 | 590/767 | chr5 | 6604654 | |||
| chr5:6631920 | G | C | 1 | a0007 | 1 | NA18969.hp2 | missense_variant | MODERATE | c.312C>G | p.Asp104Glu | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/19 | 377/3056 | 312/2304 | 104/767 | chr5 | 6631920 | |||
| chr5:6632958 | G | A | 1 | a0004 | 8 | HG01243.hp2 HG02451.hp1 HG02559.hp1 others(5): Show |
missense_variant | MODERATE | c.22C>T | p.Arg8Trp | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 1/19 | 87/3056 | 22/2304 | 8/767 | chr5 | 6632958 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:6600007 | G | A | 1 | a0001c0015 | 2 | HG01496.hp1 HG03453.hp1 |
synonymous_variant | LOW | c.2223C>T | p.Pro741Pro | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 19/19 | 2288/3056 | 2223/2304 | 741/767 | chr5 | 6600007 | |||
| chr5:6600037 | G | A | 5 | a0001c0004 a0001c0010 a0001c0011 others(2): Show |
88 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(85): Show |
synonymous_variant | LOW | c.2193C>T | p.Asp731Asp | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 19/19 | 2258/3056 | 2193/2304 | 731/767 | chr5 | 6600037 | |||
| chr5:6604674 | C | T | 4 | a0001c0002 a0002c0014 a0003c0005 others(1): Show |
122 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(119): Show |
synonymous_variant | LOW | c.1749G>A | p.Thr583Thr | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 16/19 | 1814/3056 | 1749/2304 | 583/767 | chr5 | 6604674 | |||
| chr5:6607250 | A | G | 1 | a0001c0019 | 1 | NA18980.hp1 | synonymous_variant | LOW | c.1458T>C | p.His486His | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 13/19 | 1523/3056 | 1458/2304 | 486/767 | chr5 | 6607250 | |||
| chr5:6622026 | G | T | 3 | a0001c0009 a0001c0018 a0002c0017 |
9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
synonymous_variant | LOW | c.612C>A | p.Val204Val | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/19 | 677/3056 | 612/2304 | 204/767 | chr5 | 6622026 | |||
| chr5:6623241 | C | T | 1 | a0001c0012 | 4 | HG01069.hp1 HG01071.hp2 HG01975.hp2 others(1): Show |
synonymous_variant | LOW | c.510G>A | p.Leu170Leu | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/19 | 575/3056 | 510/2304 | 170/767 | chr5 | 6623241 | |||
| chr5:6632730 | G | A | 1 | a0001c0013 | 4 | HG02630.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
synonymous_variant | LOW | c.123C>T | p.Ile41Ile | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 2/19 | 188/3056 | 123/2304 | 41/767 | chr5 | 6632730 | |||
| chr5:6632929 | C | T | 6 | a0001c0003 a0001c0009 a0001c0010 others(3): Show |
98 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(95): Show |
synonymous_variant | LOW | c.51G>A | p.Glu17Glu | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 1/19 | 116/3056 | 51/2304 | 17/767 | chr5 | 6632929 | |||
| chr5:6632959 | A | G | 1 | a0001c0011 | 4 | HG01192.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
synonymous_variant | LOW | c.21T>C | p.Gly7Gly | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 1/19 | 86/3056 | 21/2304 | 7/767 | chr5 | 6632959 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:6599302 | T | C | 1 | a0001c0003t0006 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*624A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 19/19 | 624 | chr5 | 6599302 | ||||||
| chr5:6599345 | A | G | 1 | a0001c0001t0004 | 3 | HG02647.hp1 HG02965.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*581T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 19/19 | 581 | chr5 | 6599345 | ||||||
| chr5:6599363 | G | A | 1 | a0001c0002t0007 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*563C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 19/19 | 563 | chr5 | 6599363 | ||||||
| chr5:6599379 | TG | T | 3 | a0002c0006t0003 a0002c0007t0003 a0002c0014t0003 |
9 | HG00642.hp2 HG01099.hp1 HG01106.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*546delC | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 19/19 | 546 | chr5 | 6599379 | ||||||
| chr5:6599704 | A | G | 1 | a0001c0004t0005 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*222T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 19/19 | 222 | chr5 | 6599704 | ||||||
| chr5:6599827 | C | T | 9 | a0001c0001t0002 a0001c0003t0002 a0001c0004t0002 others(6): Show |
83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*99G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 19/19 | 99 | chr5 | 6599827 | ||||||
| chr5:6633016 | G | A | 1 | a0001c0004t0008 | 1 | NA19079.hp1 | 5_prime_UTR_variant | MODIFIER | c.-37C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 1/19 | 37 | chr5 | 6633016 | ||||||
| chr5:6633042 | T | C | 1 | a0002c0006t0009 | 1 | HG02258.hp1 | 5_prime_UTR_variant | MODIFIER | c.-63A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 1/19 | 63 | chr5 | 6633042 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:6600276 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1998-44A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600276 | |||||||
| chr5:6600379 | G | GT | 241 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(238): Show |
278 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(275): Show |
intron_variant | MODIFIER | c.1998-148_1998-147i others(3): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600379 | |||||||
| chr5:6600384 | CG | C | 3 | a0001c0002t0001g0267 a0001c0002t0001g0268 a0001c0002t0001g0287 |
3 | NA18965.hp1 NA18975.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.1998-153delC | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600384 | |||||||
| chr5:6600385 | GA | G | 226 | a0001c0001t0001g0031 a0001c0001t0001g0042 a0001c0001t0001g0123 others(223): Show |
262 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(259): Show |
intron_variant | MODIFIER | c.1998-154delT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600385 | |||||||
| chr5:6600490 | A | C | 13 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0141 others(10): Show |
15 | HG00639.hp2 HG02257.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1998-258T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600490 | |||||||
| chr5:6600551 | C | T | 1 | a0001c0002t0001g0302 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1998-319G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600551 | |||||||
| chr5:6600552 | G | A | 5 | a0001c0003t0001g0097 a0001c0013t0001g0212 a0001c0013t0001g0213 others(2): Show |
5 | HG02630.hp1 HG03209.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1998-320C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600552 | |||||||
| chr5:6600559 | C | G | 5 | a0001c0003t0001g0097 a0001c0013t0001g0212 a0001c0013t0001g0213 others(2): Show |
5 | HG02630.hp1 HG03209.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1998-327G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600559 | |||||||
| chr5:6600589 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0164 |
5 | HG02280.hp2 HG02451.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1998-357C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600589 | |||||||
| chr5:6600654 | T | TGGGAGAC others(41): Show |
1 | a0001c0001t0002g0181 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1998-470_1998-423d others(50): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600654 | |||||||
| chr5:6600654 | TGGGAGAC others(41): Show |
T | 1 | a0001c0004t0002g0173 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1998-470_1998-423d others(50): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600654 | |||||||
| chr5:6600680 | T | C | 239 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(236): Show |
277 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.1998-448A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600680 | |||||||
| chr5:6600751 | T | C | 245 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(242): Show |
282 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.1998-519A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600751 | |||||||
| chr5:6600891 | T | C | 110 | a0001c0001t0001g0031 a0001c0001t0001g0129 a0001c0001t0001g0161 others(107): Show |
134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1998-659A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600891 | |||||||
| chr5:6600942 | A | T | 245 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(242): Show |
282 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.1998-710T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600942 | |||||||
| chr5:6600952 | G | GT | 5 | a0001c0003t0001g0097 a0001c0013t0001g0212 a0001c0013t0001g0213 others(2): Show |
5 | HG02630.hp1 HG03209.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1998-721_1998-720i others(3): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600952 | |||||||
| chr5:6600953 | C | T | 112 | a0001c0001t0001g0030 a0001c0001t0001g0141 a0001c0001t0001g0142 others(109): Show |
131 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.1998-721G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600953 | |||||||
| chr5:6600963 | G | A | 1 | a0001c0011t0001g0047 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1998-731C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600963 | |||||||
| chr5:6600966 | G | A | 1 | a0001c0003t0001g0121 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1998-734C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6600966 | |||||||
| chr5:6601009 | T | C | 1 | a0001c0002t0001g0314 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1998-777A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601009 | |||||||
| chr5:6601031 | T | TCTGACCT others(25): Show |
2 | a0001c0009t0001g0054 a0002c0017t0001g0055 |
2 | HG02055.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1998-831_1998-800d others(34): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601031 | |||||||
| chr5:6601057 | G | A | 2 | a0001c0002t0001g0364 a0001c0002t0001g0365 |
2 | HG02074.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1998-825C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601057 | |||||||
| chr5:6601124 | T | C | 1 | a0001c0001t0001g0043 | 2 | HG01168.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1998-892A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601124 | |||||||
| chr5:6601144 | T | C | 27 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0125 others(24): Show |
31 | HG00642.hp1 HG01074.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.1998-912A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601144 | |||||||
| chr5:6601163 | TA | T | 116 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0333 others(113): Show |
136 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1998-932delT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601163 | |||||||
| chr5:6601163 | TAA | T | 91 | a0001c0001t0001g0042 a0001c0001t0001g0123 a0001c0001t0001g0140 others(88): Show |
103 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.1998-933_1998-932d others(4): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601163 | |||||||
| chr5:6601163 | TAAA | T | 112 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0124 others(109): Show |
133 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1998-934_1998-932d others(5): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601163 | |||||||
| chr5:6601196 | C | T | 317 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(314): Show |
371 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(368): Show |
intron_variant | MODIFIER | c.1998-964G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601196 | |||||||
| chr5:6601333 | CA | C | 4 | a0001c0004t0001g0185 a0001c0012t0002g0150 a0001c0012t0002g0151 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1998-1102delT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601333 | |||||||
| chr5:6601336 | AC | A | 97 | a0001c0001t0001g0042 a0001c0001t0001g0124 a0001c0001t0001g0161 others(94): Show |
117 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.1998-1105delG | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601336 | |||||||
| chr5:6601385 | C | G | 82 | a0001c0001t0001g0126 a0001c0001t0001g0141 a0001c0001t0001g0161 others(79): Show |
98 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.1997+1076G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601385 | |||||||
| chr5:6601570 | C | G | 3 | a0001c0001t0001g0219 a0001c0003t0001g0097 a0002c0006t0009g0371 |
3 | HG02258.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1997+891G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601570 | |||||||
| chr5:6601586 | C | A | 26 | a0001c0001t0001g0274 a0001c0001t0001g0332 a0001c0003t0001g0016 others(23): Show |
31 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.1997+875G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601586 | |||||||
| chr5:6601600 | A | ATCCC | 159 | a0001c0001t0001g0031 a0001c0001t0001g0043 a0001c0001t0001g0129 others(156): Show |
186 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1997+857_1997+860d others(6): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601600 | |||||||
| chr5:6601606 | C | T | 1 | a0001c0003t0001g0105 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1997+855G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601606 | |||||||
| chr5:6601687 | G | A | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1997+774C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601687 | |||||||
| chr5:6601830 | C | T | 1 | a0001c0009t0001g0048 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1997+631G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601830 | |||||||
| chr5:6601831 | G | A | 2 | a0003c0005t0001g0270 a0003c0005t0001g0271 |
2 | NA18950.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1997+630C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601831 | |||||||
| chr5:6601910 | G | A | 6 | a0001c0001t0001g0266 a0001c0003t0001g0063 a0001c0003t0001g0066 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1997+551C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6601910 | |||||||
| chr5:6602040 | G | A | 1 | a0001c0001t0001g0351 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1997+421C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6602040 | |||||||
| chr5:6602162 | C | T | 5 | a0001c0003t0001g0007 a0001c0003t0001g0115 a0001c0003t0001g0116 others(2): Show |
7 | HG01943.hp2 HG01993.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.1997+299G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6602162 | |||||||
| chr5:6602259 | T | TGAGTGTT others(147): Show |
2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1997+201_1997+202i others(156): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6602259 | |||||||
| chr5:6602314 | G | T | 1 | a0001c0003t0001g0115 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1997+147C>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6602314 | |||||||
| chr5:6602431 | T | C | 249 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(246): Show |
287 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(284): Show |
intron_variant | MODIFIER | c.1997+30A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6602431 | |||||||
| chr5:6602432 | G | A | 2 | a0001c0002t0007g0228 a0001c0003t0001g0120 |
2 | HG00735.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1997+29C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 18/18 | chr5 | 6602432 | |||||||
| chr5:6602555 | G | C | 114 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(111): Show |
131 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1958-55C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6602555 | |||||||
| chr5:6602581 | T | C | 6 | a0001c0001t0001g0266 a0001c0003t0001g0063 a0001c0003t0001g0066 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1958-81A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6602581 | |||||||
| chr5:6602693 | A | G | 1 | a0001c0001t0001g0342 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1958-193T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6602693 | |||||||
| chr5:6602698 | G | A | 6 | a0001c0001t0001g0266 a0001c0003t0001g0063 a0001c0003t0001g0066 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1958-198C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6602698 | |||||||
| chr5:6602730 | A | G | 2 | a0001c0002t0001g0249 a0001c0002t0001g0260 |
2 | HG03831.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1958-230T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6602730 | |||||||
| chr5:6602806 | T | C | 1 | a0001c0002t0001g0259 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1958-306A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6602806 | |||||||
| chr5:6602865 | C | T | 3 | a0001c0011t0001g0013 a0001c0011t0001g0046 a0001c0011t0001g0047 |
4 | HG01192.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1958-365G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6602865 | |||||||
| chr5:6602887 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1958-387T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6602887 | |||||||
| chr5:6603104 | C | G | 1 | a0001c0001t0001g0127 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1958-604G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603104 | |||||||
| chr5:6603110 | G | C | 9 | a0001c0009t0001g0048 a0001c0009t0001g0049 a0001c0009t0001g0050 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1958-610C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603110 | |||||||
| chr5:6603159 | A | C | 1 | a0001c0004t0001g0185 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1958-659T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603159 | |||||||
| chr5:6603220 | G | A | 9 | a0001c0009t0001g0048 a0001c0009t0001g0049 a0001c0009t0001g0050 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1958-720C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603220 | |||||||
| chr5:6603400 | C | G | 1 | a0001c0013t0001g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1957+738G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603400 | |||||||
| chr5:6603430 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1957+708C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603430 | |||||||
| chr5:6603552 | G | A | 11 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0162 others(8): Show |
14 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1957+586C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603552 | |||||||
| chr5:6603566 | T | C | 6 | a0001c0001t0001g0266 a0001c0003t0001g0063 a0001c0003t0001g0066 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1957+572A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603566 | |||||||
| chr5:6603598 | G | A | 120 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(117): Show |
137 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1957+540C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603598 | |||||||
| chr5:6603599 | G | T | 1 | a0001c0002t0007g0228 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1957+539C>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603599 | |||||||
| chr5:6603625 | G | C | 3 | a0001c0011t0001g0013 a0001c0011t0001g0046 a0001c0011t0001g0047 |
4 | HG01192.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1957+513C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603625 | |||||||
| chr5:6603638 | C | T | 1 | a0001c0004t0002g0180 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1957+500G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603638 | |||||||
| chr5:6603751 | G | A | 1 | a0001c0003t0001g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1957+387C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603751 | |||||||
| chr5:6603829 | C | T | 114 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(111): Show |
131 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1957+309G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603829 | |||||||
| chr5:6603833 | G | A | 1 | a0001c0004t0002g0197 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1957+305C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603833 | |||||||
| chr5:6603925 | A | G | 1 | a0001c0013t0001g0213 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1957+213T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6603925 | |||||||
| chr5:6604026 | A | C | 5 | a0001c0001t0001g0031 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
6 | HG00639.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1957+112T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6604026 | |||||||
| chr5:6604092 | A | G | 120 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0266 others(117): Show |
141 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.1957+46T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 17/18 | chr5 | 6604092 | |||||||
| chr5:6604329 | G | A | 6 | a0001c0001t0001g0266 a0001c0003t0001g0063 a0001c0003t0001g0066 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1819-53C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 16/18 | chr5 | 6604329 | |||||||
| chr5:6604420 | AC | A | 243 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(240): Show |
281 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(278): Show |
intron_variant | MODIFIER | c.1819-145delG | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 16/18 | chr5 | 6604420 | |||||||
| chr5:6604427 | C | G | 9 | a0001c0009t0001g0048 a0001c0009t0001g0049 a0001c0009t0001g0050 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1819-151G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 16/18 | chr5 | 6604427 | |||||||
| chr5:6604451 | G | A | 9 | a0001c0009t0001g0048 a0001c0009t0001g0049 a0001c0009t0001g0050 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1818+154C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 16/18 | chr5 | 6604451 | |||||||
| chr5:6604752 | G | A | 1 | a0001c0001t0001g0331 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1738-67C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 15/18 | chr5 | 6604752 | |||||||
| chr5:6604818 | C | T | 206 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0126 others(203): Show |
239 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.1738-133G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 15/18 | chr5 | 6604818 | |||||||
| chr5:6604829 | C | T | 1 | a0001c0002t0001g0216 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1738-144G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 15/18 | chr5 | 6604829 | |||||||
| chr5:6604830 | G | A | 1 | a0001c0001t0001g0339 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1738-145C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 15/18 | chr5 | 6604830 | |||||||
| chr5:6604839 | C | T | 28 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0123 others(25): Show |
33 | HG00639.hp2 HG01074.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.1738-154G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 15/18 | chr5 | 6604839 | |||||||
| chr5:6604857 | G | A | 200 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0126 others(197): Show |
233 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.1738-172C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 15/18 | chr5 | 6604857 | |||||||
| chr5:6604858 | T | C | 1 | a0001c0002t0001g0285 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1738-173A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 15/18 | chr5 | 6604858 | |||||||
| chr5:6604899 | A | T | 5 | a0001c0003t0001g0097 a0001c0013t0001g0212 a0001c0013t0001g0213 others(2): Show |
5 | HG02630.hp1 HG03209.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-214T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 15/18 | chr5 | 6604899 | |||||||
| chr5:6604963 | G | A | 1 | a0001c0003t0001g0121 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1738-278C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 15/18 | chr5 | 6604963 | |||||||
| chr5:6605158 | G | A | 259 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0031 others(256): Show |
300 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(297): Show |
intron_variant | MODIFIER | c.1737+115C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 15/18 | chr5 | 6605158 | |||||||
| chr5:6605176 | G | C | 9 | a0001c0009t0001g0048 a0001c0009t0001g0049 a0001c0009t0001g0050 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1737+97C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 15/18 | chr5 | 6605176 | |||||||
| chr5:6605212 | C | T | 1 | a0001c0002t0001g0308 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1737+61G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 15/18 | chr5 | 6605212 | |||||||
| chr5:6605227 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0170 |
2 | HG00544.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1737+46G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 15/18 | chr5 | 6605227 | |||||||
| chr5:6605256 | G | A | 3 | a0001c0011t0001g0013 a0001c0011t0001g0046 a0001c0011t0001g0047 |
4 | HG01192.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+17C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 15/18 | chr5 | 6605256 | |||||||
| chr5:6605419 | C | A | 248 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(245): Show |
286 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(283): Show |
intron_variant | MODIFIER | c.1602-11G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6605419 | |||||||
| chr5:6605422 | CATT | C | 5 | a0001c0001t0001g0031 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
6 | HG00639.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1602-17_1602-15del others(3): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6605422 | |||||||
| chr5:6605427 | T | C | 4 | a0001c0003t0001g0103 a0001c0003t0001g0106 a0001c0003t0001g0112 others(1): Show |
4 | HG00642.hp1 HG01074.hp1 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.1602-19A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6605427 | |||||||
| chr5:6605566 | T | G | 1 | a0001c0004t0002g0155 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1602-158A>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6605566 | |||||||
| chr5:6605658 | C | T | 1 | a0001c0004t0002g0134 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1602-250G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6605658 | |||||||
| chr5:6605716 | G | T | 89 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0001g0145 others(86): Show |
103 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1602-308C>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6605716 | |||||||
| chr5:6605720 | T | C | 2 | a0003c0005t0001g0233 a0003c0005t0001g0246 |
2 | HG00423.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1602-312A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6605720 | |||||||
| chr5:6605823 | T | C | 1 | a0001c0001t0001g0356 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1602-415A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6605823 | |||||||
| chr5:6605857 | AT | A | 200 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0126 others(197): Show |
233 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.1602-450delA | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6605857 | |||||||
| chr5:6605906 | A | G | 206 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0126 others(203): Show |
239 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.1602-498T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6605906 | |||||||
| chr5:6605975 | T | A | 3 | a0001c0011t0001g0013 a0001c0011t0001g0046 a0001c0011t0001g0047 |
4 | HG01192.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1602-567A>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6605975 | |||||||
| chr5:6606180 | T | C | 1 | a0001c0002t0001g0223 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1601+640A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606180 | |||||||
| chr5:6606190 | C | T | 200 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0126 others(197): Show |
233 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.1601+630G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606190 | |||||||
| chr5:6606210 | T | C | 243 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(240): Show |
281 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(278): Show |
intron_variant | MODIFIER | c.1601+610A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606210 | |||||||
| chr5:6606332 | G | A | 88 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0001g0145 others(85): Show |
101 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.1601+488C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606332 | |||||||
| chr5:6606342 | G | A | 1 | a0001c0002t0001g0216 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1601+478C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606342 | |||||||
| chr5:6606362 | C | A | 34 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0123 others(31): Show |
39 | HG00639.hp2 HG01074.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.1601+458G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606362 | |||||||
| chr5:6606440 | C | T | 1 | a0001c0001t0001g0360 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1601+380G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606440 | |||||||
| chr5:6606441 | G | A | 3 | a0001c0011t0001g0013 a0001c0011t0001g0046 a0001c0011t0001g0047 |
4 | HG01192.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1601+379C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606441 | |||||||
| chr5:6606531 | C | T | 6 | a0001c0001t0001g0266 a0001c0003t0001g0063 a0001c0003t0001g0066 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1601+289G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606531 | |||||||
| chr5:6606574 | C | T | 28 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0123 others(25): Show |
33 | HG00639.hp2 HG01074.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.1601+246G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606574 | |||||||
| chr5:6606587 | G | GT | 9 | a0001c0009t0001g0048 a0001c0009t0001g0049 a0001c0009t0001g0050 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1601+232dupA | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606587 | |||||||
| chr5:6606618 | A | G | 3 | a0001c0004t0002g0169 a0001c0004t0002g0184 a0001c0004t0002g0195 |
3 | HG02135.hp2 NA18957.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.1601+202T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606618 | |||||||
| chr5:6606633 | CTTAAA | C | 6 | a0001c0001t0001g0266 a0001c0003t0001g0063 a0001c0003t0001g0066 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1601+182_1601+186d others(7): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606633 | |||||||
| chr5:6606694 | G | A | 90 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0001g0145 others(87): Show |
105 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1601+126C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606694 | |||||||
| chr5:6606697 | TA | T | 14 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(11): Show |
17 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1601+122delT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606697 | |||||||
| chr5:6606697 | TAA | T | 34 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0123 others(31): Show |
39 | HG00639.hp2 HG01074.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.1601+121_1601+122d others(4): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606697 | |||||||
| chr5:6606697 | TAAA | T | 198 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0126 others(195): Show |
231 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.1601+120_1601+122d others(5): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 14/18 | chr5 | 6606697 | |||||||
| chr5:6607009 | A | G | 1 | a0001c0010t0002g0118 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1509-97T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 13/18 | chr5 | 6607009 | |||||||
| chr5:6607012 | GAAC | G | 243 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(240): Show |
281 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(278): Show |
intron_variant | MODIFIER | c.1509-103_1509-101d others(5): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 13/18 | chr5 | 6607012 | |||||||
| chr5:6607022 | C | T | 35 | a0001c0001t0001g0231 a0001c0001t0001g0274 a0001c0001t0001g0275 others(32): Show |
40 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.1509-110G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 13/18 | chr5 | 6607022 | |||||||
| chr5:6607031 | T | C | 6 | a0001c0001t0001g0266 a0001c0003t0001g0063 a0001c0003t0001g0066 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1509-119A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 13/18 | chr5 | 6607031 | |||||||
| chr5:6607042 | C | T | 3 | a0001c0001t0004g0137 a0001c0001t0004g0207 a0001c0001t0004g0322 |
3 | HG02647.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1509-130G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 13/18 | chr5 | 6607042 | |||||||
| chr5:6607110 | C | T | 6 | a0001c0001t0001g0266 a0001c0003t0001g0063 a0001c0003t0001g0066 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1508+90G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 13/18 | chr5 | 6607110 | |||||||
| chr5:6607416 | A | C | 1 | a0001c0001t0001g0329 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1324-32T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6607416 | |||||||
| chr5:6607495 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1324-111G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6607495 | |||||||
| chr5:6607504 | T | G | 5 | a0001c0003t0001g0097 a0001c0013t0001g0212 a0001c0013t0001g0213 others(2): Show |
5 | HG02630.hp1 HG03209.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1324-120A>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6607504 | |||||||
| chr5:6607627 | T | C | 9 | a0001c0009t0001g0048 a0001c0009t0001g0049 a0001c0009t0001g0050 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1324-243A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6607627 | |||||||
| chr5:6607803 | T | C | 243 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(240): Show |
281 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(278): Show |
intron_variant | MODIFIER | c.1324-419A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6607803 | |||||||
| chr5:6607837 | AG | A | 5 | a0001c0001t0001g0266 a0001c0003t0001g0063 a0001c0003t0001g0066 others(2): Show |
5 | HG02257.hp1 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1324-454delC | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6607837 | |||||||
| chr5:6607935 | T | C | 4 | a0002c0006t0003g0093 a0002c0006t0003g0094 a0002c0006t0003g0095 others(1): Show |
7 | HG00642.hp2 HG01099.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.1324-551A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6607935 | |||||||
| chr5:6607943 | G | A | 27 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0123 others(24): Show |
32 | HG00639.hp2 HG01074.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.1324-559C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6607943 | |||||||
| chr5:6607986 | TTTTTAAC others(1): Show |
T | 6 | a0001c0001t0001g0266 a0001c0003t0001g0063 a0001c0003t0001g0066 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1324-610_1324-603d others(10): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6607986 | |||||||
| chr5:6608037 | T | C | 207 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0126 others(204): Show |
240 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.1324-653A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608037 | |||||||
| chr5:6608223 | G | C | 3 | a0001c0002t0001g0225 a0001c0002t0001g0253 a0001c0002t0001g0363 |
3 | HG00673.hp1 NA18941.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1324-839C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608223 | |||||||
| chr5:6608228 | C | A | 16 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0127 others(13): Show |
19 | HG01074.hp2 HG01243.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1324-844G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608228 | |||||||
| chr5:6608248 | C | A | 105 | a0001c0002t0001g0005 a0001c0002t0001g0009 a0001c0002t0001g0010 others(102): Show |
122 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.1324-864G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608248 | |||||||
| chr5:6608317 | T | C | 1 | a0001c0004t0002g0173 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1324-933A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608317 | |||||||
| chr5:6608326 | A | C | 9 | a0001c0009t0001g0048 a0001c0009t0001g0049 a0001c0009t0001g0050 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1324-942T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608326 | |||||||
| chr5:6608421 | A | T | 259 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0031 others(256): Show |
300 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(297): Show |
intron_variant | MODIFIER | c.1324-1037T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608421 | |||||||
| chr5:6608516 | A | G | 39 | a0001c0001t0001g0231 a0001c0001t0001g0274 a0001c0001t0001g0275 others(36): Show |
45 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.1324-1132T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608516 | |||||||
| chr5:6608609 | A | C | 6 | a0001c0001t0001g0266 a0001c0003t0001g0063 a0001c0003t0001g0066 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1323+1217T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608609 | |||||||
| chr5:6608670 | A | G | 1 | a0001c0003t0001g0072 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1323+1156T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608670 | |||||||
| chr5:6608676 | G | A | 1 | a0001c0002t0001g0314 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1323+1150C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608676 | |||||||
| chr5:6608764 | A | G | 339 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0031 others(336): Show |
396 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(393): Show |
intron_variant | MODIFIER | c.1323+1062T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608764 | |||||||
| chr5:6608844 | T | C | 205 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0126 others(202): Show |
238 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(235): Show |
intron_variant | MODIFIER | c.1323+982A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608844 | |||||||
| chr5:6608911 | C | T | 30 | a0001c0003t0001g0007 a0001c0003t0001g0021 a0001c0003t0001g0022 others(27): Show |
34 | HG00639.hp1 HG00642.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.1323+915G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608911 | |||||||
| chr5:6608912 | G | A | 2 | a0001c0004t0002g0139 a0001c0004t0002g0191 |
2 | NA18991.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1323+914C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608912 | |||||||
| chr5:6608953 | C | T | 6 | a0001c0001t0001g0266 a0001c0003t0001g0063 a0001c0003t0001g0066 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1323+873G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608953 | |||||||
| chr5:6608975 | C | A | 152 | a0001c0001t0001g0042 a0001c0001t0001g0126 a0001c0001t0001g0144 others(149): Show |
179 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.1323+851G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608975 | |||||||
| chr5:6608979 | G | A | 6 | a0001c0001t0001g0266 a0001c0003t0001g0063 a0001c0003t0001g0066 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1323+847C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608979 | |||||||
| chr5:6608999 | G | A | 156 | a0001c0001t0001g0042 a0001c0001t0001g0126 a0001c0001t0001g0144 others(153): Show |
183 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.1323+827C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6608999 | |||||||
| chr5:6609001 | C | A | 11 | a0001c0001t0001g0125 a0001c0001t0001g0142 a0001c0009t0001g0048 others(8): Show |
11 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1323+825G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6609001 | |||||||
| chr5:6609011 | C | T | 1 | a0001c0002t0001g0306 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1323+815G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6609011 | |||||||
| chr5:6609025 | C | T | 2 | a0001c0003t0001g0064 a0001c0003t0001g0091 |
2 | HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1323+801G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6609025 | |||||||
| chr5:6609026 | G | A | 196 | a0001c0001t0001g0042 a0001c0001t0001g0126 a0001c0001t0001g0144 others(193): Show |
229 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.1323+800C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6609026 | |||||||
| chr5:6609051 | G | A | 2 | a0001c0001t0004g0137 a0001c0001t0004g0207 |
2 | HG02647.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1323+775C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6609051 | |||||||
| chr5:6609157 | C | A | 1 | a0001c0001t0001g0129 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1323+669G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6609157 | |||||||
| chr5:6609246 | G | A | 1 | a0001c0004t0002g0192 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1323+580C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6609246 | |||||||
| chr5:6609283 | G | A | 1 | a0001c0002t0001g0248 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1323+543C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6609283 | |||||||
| chr5:6609315 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1323+511G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6609315 | |||||||
| chr5:6609401 | G | A | 1 | a0001c0004t0001g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1323+425C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6609401 | |||||||
| chr5:6609760 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1323+66G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 12/18 | chr5 | 6609760 | |||||||
| chr5:6610054 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1227-132A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610054 | |||||||
| chr5:6610065 | A | AT | 10 | a0001c0001t0001g0030 a0001c0001t0001g0140 a0001c0001t0001g0141 others(7): Show |
11 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1227-144dupA | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610065 | |||||||
| chr5:6610065 | A | ATT | 8 | a0001c0009t0001g0048 a0001c0009t0001g0049 a0001c0009t0001g0050 others(5): Show |
8 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1227-145_1227-144d others(4): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610065 | |||||||
| chr5:6610065 | AT | A | 32 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(29): Show |
35 | HG00140.hp1 HG01074.hp2 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1227-144delA | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610065 | |||||||
| chr5:6610082 | G | T | 1 | a0001c0001t0001g0341 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1227-160C>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610082 | |||||||
| chr5:6610124 | T | C | 206 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0126 others(203): Show |
239 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.1227-202A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610124 | |||||||
| chr5:6610124 | T | G | 1 | a0004c0008t0001g0045 | 2 | HG01243.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1227-202A>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610124 | |||||||
| chr5:6610127 | G | A | 5 | a0001c0003t0001g0097 a0001c0013t0001g0212 a0001c0013t0001g0213 others(2): Show |
5 | HG02630.hp1 HG03209.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1227-205C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610127 | |||||||
| chr5:6610136 | C | T | 215 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0126 others(212): Show |
248 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.1227-214G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610136 | |||||||
| chr5:6610149 | C | T | 3 | a0001c0001t0004g0137 a0001c0001t0004g0207 a0001c0001t0004g0322 |
3 | HG02647.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1227-227G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610149 | |||||||
| chr5:6610150 | G | A | 206 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0126 others(203): Show |
239 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.1227-228C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610150 | |||||||
| chr5:6610199 | G | A | 1 | a0001c0002t0001g0255 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1227-277C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610199 | |||||||
| chr5:6610224 | T | G | 2 | a0001c0003t0001g0100 a0001c0003t0001g0101 |
2 | HG00741.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.1227-302A>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610224 | |||||||
| chr5:6610238 | A | G | 1 | a0001c0003t0001g0015 | 2 | NA19001.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1227-316T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610238 | |||||||
| chr5:6610246 | T | TC | 4 | a0001c0001t0001g0004 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
7 | HG02280.hp2 HG02451.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1227-325_1227-324i others(3): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610246 | |||||||
| chr5:6610278 | T | C | 243 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(240): Show |
281 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(278): Show |
intron_variant | MODIFIER | c.1227-356A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610278 | |||||||
| chr5:6610332 | C | T | 1 | a0001c0003t0001g0018 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1227-410G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610332 | |||||||
| chr5:6610363 | C | T | 9 | a0001c0009t0001g0048 a0001c0009t0001g0049 a0001c0009t0001g0050 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1227-441G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610363 | |||||||
| chr5:6610613 | G | A | 1 | a0001c0001t0004g0322 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1226+342C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610613 | |||||||
| chr5:6610673 | G | T | 200 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0126 others(197): Show |
233 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.1226+282C>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610673 | |||||||
| chr5:6610683 | CA | C | 196 | a0001c0001t0001g0042 a0001c0001t0001g0126 a0001c0001t0001g0144 others(193): Show |
229 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.1226+271delT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610683 | |||||||
| chr5:6610755 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1226+200T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610755 | |||||||
| chr5:6610785 | G | A | 1 | a0001c0004t0002g0143 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1226+170C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610785 | |||||||
| chr5:6610798 | T | C | 90 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0001g0145 others(87): Show |
105 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1226+157A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610798 | |||||||
| chr5:6610951 | T | A | 1 | a0001c0002t0001g0235 | 1 | HG02630.hp2 | splice_region_variant&intron_variant | LOW | c.1226+4A>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 11/18 | chr5 | 6610951 | |||||||
| chr5:6611102 | T | C | 16 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0032 others(13): Show |
22 | HG00438.hp2 HG00673.hp1 HG02155.hp2 others(19): Show |
intron_variant | MODIFIER | c.1096-17A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611102 | |||||||
| chr5:6611155 | G | A | 1 | a0002c0007t0001g0132 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1096-70C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611155 | |||||||
| chr5:6611252 | A | G | 2 | a0001c0004t0002g0134 a0001c0004t0002g0135 |
2 | NA18971.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1096-167T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611252 | |||||||
| chr5:6611448 | T | TA | 9 | a0001c0003t0001g0023 a0001c0003t0001g0068 a0001c0003t0001g0121 others(6): Show |
12 | HG02257.hp2 HG02486.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1095+276dupT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | |||||||
| chr5:6611448 | T | TAAAAAA | 89 | a0001c0001t0001g0266 a0001c0002t0001g0005 a0001c0002t0001g0009 others(86): Show |
104 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.1095+271_1095+276d others(8): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | |||||||
| chr5:6611448 | T | TAAAAAAA | 17 | a0001c0002t0001g0038 a0001c0002t0001g0040 a0001c0002t0001g0211 others(14): Show |
19 | HG02056.hp2 HG02523.hp1 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.1095+270_1095+276d others(9): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | |||||||
| chr5:6611448 | T | TAAAAAAA others(3): Show |
1 | a0004c0008t0001g0368 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1095+267_1095+276d others(12): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | |||||||
| chr5:6611448 | T | TAAAAAAA others(4): Show |
16 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0127 others(13): Show |
19 | HG00423.hp1 HG01074.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1095+266_1095+276d others(13): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | |||||||
| chr5:6611448 | T | TAAAAAAA others(7): Show |
1 | a0001c0003t0001g0100 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1095+263_1095+276d others(16): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | |||||||
| chr5:6611448 | T | TAAAAAAA others(8): Show |
17 | a0001c0001t0001g0126 a0001c0001t0001g0144 a0001c0001t0001g0145 others(14): Show |
19 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.1095+262_1095+276d others(17): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | |||||||
| chr5:6611448 | T | TAAAAAAA others(9): Show |
15 | a0001c0001t0001g0275 a0001c0003t0001g0016 a0001c0003t0001g0071 others(12): Show |
16 | HG00642.hp1 HG00738.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1095+261_1095+276d others(18): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | |||||||
| chr5:6611448 | T | TAAAAAAA others(10): Show |
22 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 others(19): Show |
25 | HG01109.hp1 HG01261.hp2 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.1095+260_1095+276d others(19): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | |||||||
| chr5:6611448 | T | TAAAAAAA others(11): Show |
13 | a0001c0001t0001g0042 a0001c0001t0001g0231 a0001c0001t0001g0279 others(10): Show |
15 | HG00408.hp1 HG00597.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.1095+276_1095+277i others(20): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | |||||||
| chr5:6611448 | T | TAAAAAAA others(12): Show |
9 | a0001c0001t0001g0274 a0001c0001t0001g0324 a0001c0001t0001g0326 others(6): Show |
12 | HG00438.hp1 HG00558.hp1 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.1095+276_1095+277i others(21): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | |||||||
| chr5:6611448 | T | TAAAAAAA others(13): Show |
6 | a0001c0001t0001g0329 a0001c0001t0001g0331 a0001c0001t0004g0137 others(3): Show |
6 | HG00735.hp1 HG01952.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1095+276_1095+277i others(22): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | |||||||
| chr5:6611448 | T | TAAAAAAA others(14): Show |
1 | a0001c0001t0004g0322 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1095+276_1095+277i others(23): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | |||||||
| chr5:6611448 | T | TAAAAAAA others(15): Show |
1 | a0001c0003t0001g0122 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1095+276_1095+277i others(24): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | |||||||
| chr5:6611448 | TA | T | 6 | a0001c0001t0001g0340 a0001c0004t0002g0167 a0002c0006t0003g0093 others(3): Show |
9 | HG00642.hp2 HG01099.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1095+276delT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | |||||||
| chr5:6611448 | TAAA | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
6 | HG00639.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1095+274_1095+276d others(5): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | |||||||
| chr5:6611448 | TAAAAAAA others(2): Show |
T | 9 | a0001c0009t0001g0048 a0001c0009t0001g0049 a0001c0009t0001g0050 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1095+268_1095+276d others(11): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611448 | |||||||
| chr5:6611519 | G | GA | 10 | a0001c0002t0001g0264 a0001c0009t0001g0048 a0001c0009t0001g0049 others(7): Show |
10 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1095+205dupT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611519 | |||||||
| chr5:6611520 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1095+205T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611520 | |||||||
| chr5:6611528 | A | C | 1 | a0001c0004t0002g0166 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1095+197T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611528 | |||||||
| chr5:6611644 | A | T | 203 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0126 others(200): Show |
236 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.1095+81T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611644 | |||||||
| chr5:6611712 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1095+13C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 10/18 | chr5 | 6611712 | |||||||
| chr5:6611870 | C | A | 200 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0126 others(197): Show |
233 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.1022-72G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6611870 | |||||||
| chr5:6611914 | T | C | 86 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0001g0145 others(83): Show |
98 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1022-116A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6611914 | |||||||
| chr5:6611935 | G | A | 3 | a0001c0011t0001g0013 a0001c0011t0001g0046 a0001c0011t0001g0047 |
4 | HG01192.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1022-137C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6611935 | |||||||
| chr5:6611956 | C | T | 23 | a0001c0003t0001g0021 a0001c0003t0001g0022 a0001c0003t0001g0057 others(20): Show |
25 | HG00639.hp1 HG00642.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.1022-158G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6611956 | |||||||
| chr5:6611960 | G | A | 1 | a0004c0008t0001g0045 | 2 | HG01243.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1022-162C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6611960 | |||||||
| chr5:6612083 | G | A | 1 | a0001c0001t0001g0353 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1022-285C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612083 | |||||||
| chr5:6612130 | A | G | 218 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0126 others(215): Show |
251 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(248): Show |
intron_variant | MODIFIER | c.1022-332T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612130 | |||||||
| chr5:6612259 | G | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0162 a0001c0001t0001g0163 others(3): Show |
9 | HG02280.hp2 HG02451.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1022-461C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612259 | |||||||
| chr5:6612272 | A | G | 6 | a0001c0001t0001g0266 a0001c0003t0001g0063 a0001c0003t0001g0066 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1022-474T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612272 | |||||||
| chr5:6612293 | G | A | 4 | a0001c0003t0001g0020 a0001c0003t0001g0087 a0001c0003t0001g0088 others(1): Show |
5 | NA18940.hp1 NA18942.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.1022-495C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612293 | |||||||
| chr5:6612311 | A | G | 5 | a0001c0001t0001g0031 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
6 | HG00639.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1022-513T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612311 | |||||||
| chr5:6612319 | CA | C | 6 | a0001c0001t0001g0266 a0001c0003t0001g0063 a0001c0003t0001g0066 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1022-522delT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612319 | |||||||
| chr5:6612351 | A | G | 259 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0031 others(256): Show |
300 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(297): Show |
intron_variant | MODIFIER | c.1022-553T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612351 | |||||||
| chr5:6612409 | G | A | 1 | a0001c0001t0004g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1022-611C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612409 | |||||||
| chr5:6612540 | C | A | 5 | a0001c0003t0001g0097 a0001c0013t0001g0212 a0001c0013t0001g0213 others(2): Show |
5 | HG02630.hp1 HG03209.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1022-742G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612540 | |||||||
| chr5:6612557 | G | A | 9 | a0001c0009t0001g0048 a0001c0009t0001g0049 a0001c0009t0001g0050 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1022-759C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612557 | |||||||
| chr5:6612557 | G | C | 1 | a0001c0004t0001g0153 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1022-759C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612557 | |||||||
| chr5:6612662 | G | A | 5 | a0001c0001t0001g0031 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
6 | HG00639.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1022-864C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612662 | |||||||
| chr5:6612767 | C | T | 4 | a0001c0001t0002g0183 a0001c0001t0002g0193 a0001c0004t0002g0182 others(1): Show |
4 | HG01256.hp2 HG01258.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.1022-969G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612767 | |||||||
| chr5:6612782 | A | G | 1 | a0001c0001t0001g0336 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1022-984T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612782 | |||||||
| chr5:6612793 | G | C | 16 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0127 others(13): Show |
19 | HG01074.hp2 HG01243.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1022-995C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612793 | |||||||
| chr5:6612796 | G | A | 4 | a0002c0006t0003g0093 a0002c0006t0003g0094 a0002c0006t0003g0095 others(1): Show |
7 | HG00642.hp2 HG01099.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.1022-998C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612796 | |||||||
| chr5:6612866 | A | G | 1 | a0001c0001t0002g0181 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1022-1068T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612866 | |||||||
| chr5:6612873 | C | A | 1 | a0001c0002t0001g0302 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1022-1075G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6612873 | |||||||
| chr5:6613030 | G | C | 1 | a0001c0012t0002g0149 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1022-1232C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6613030 | |||||||
| chr5:6613033 | A | G | 209 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0126 others(206): Show |
242 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(239): Show |
intron_variant | MODIFIER | c.1022-1235T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6613033 | |||||||
| chr5:6613045 | G | C | 5 | a0001c0002t0001g0039 a0001c0002t0001g0303 a0001c0002t0001g0304 others(2): Show |
6 | NA18942.hp2 NA18948.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.1022-1247C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6613045 | |||||||
| chr5:6613305 | G | A | 203 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0126 others(200): Show |
236 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.1022-1507C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6613305 | |||||||
| chr5:6613404 | C | T | 105 | a0001c0002t0001g0005 a0001c0002t0001g0009 a0001c0002t0001g0010 others(102): Show |
122 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.1022-1606G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6613404 | |||||||
| chr5:6613456 | G | C | 9 | a0001c0009t0001g0048 a0001c0009t0001g0049 a0001c0009t0001g0050 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1022-1658C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6613456 | |||||||
| chr5:6613571 | G | A | 1 | a0001c0004t0002g0155 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1022-1773C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6613571 | |||||||
| chr5:6613641 | G | A | 4 | a0002c0006t0003g0093 a0002c0006t0003g0094 a0002c0006t0003g0095 others(1): Show |
7 | HG00642.hp2 HG01099.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.1022-1843C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6613641 | |||||||
| chr5:6613706 | G | A | 9 | a0001c0009t0001g0048 a0001c0009t0001g0049 a0001c0009t0001g0050 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1022-1908C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6613706 | |||||||
| chr5:6613709 | C | A | 1 | a0001c0002t0001g0265 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1022-1911G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6613709 | |||||||
| chr5:6613714 | T | C | 237 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(234): Show |
275 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(272): Show |
intron_variant | MODIFIER | c.1022-1916A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6613714 | |||||||
| chr5:6613821 | G | A | 5 | a0001c0001t0001g0160 a0001c0001t0001g0165 a0001c0001t0001g0203 others(2): Show |
5 | HG02258.hp2 HG06807.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.1022-2023C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6613821 | |||||||
| chr5:6613889 | G | C | 1 | a0001c0002t0001g0234 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1022-2091C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6613889 | |||||||
| chr5:6613922 | C | A | 9 | a0001c0009t0001g0048 a0001c0009t0001g0049 a0001c0009t0001g0050 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1022-2124G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6613922 | |||||||
| chr5:6614053 | G | A | 2 | a0001c0001t0004g0137 a0001c0001t0004g0207 |
2 | HG02647.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1022-2255C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614053 | |||||||
| chr5:6614093 | CG | C | 7 | a0001c0009t0001g0048 a0001c0009t0001g0049 a0001c0009t0001g0051 others(4): Show |
7 | HG01891.hp2 HG02809.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1022-2296delC | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614093 | |||||||
| chr5:6614095 | G | A | 234 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(231): Show |
272 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(269): Show |
intron_variant | MODIFIER | c.1022-2297C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614095 | |||||||
| chr5:6614095 | G | GA | 57 | a0001c0001t0001g0012 a0001c0001t0001g0161 a0001c0001t0001g0335 others(54): Show |
69 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1022-2298dupT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614095 | |||||||
| chr5:6614095 | GA | G | 6 | a0001c0001t0001g0004 a0001c0001t0001g0162 a0001c0001t0001g0163 others(3): Show |
9 | HG02280.hp2 HG02451.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1022-2298delT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614095 | |||||||
| chr5:6614110 | A | C | 12 | a0001c0003t0001g0056 a0002c0006t0001g0014 a0002c0007t0001g0128 others(9): Show |
15 | HG01074.hp2 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1022-2312T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614110 | |||||||
| chr5:6614111 | A | C | 4 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0127 others(1): Show |
4 | HG01891.hp1 HG02698.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.1022-2313T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614111 | |||||||
| chr5:6614119 | A | ACCCTCC | 123 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0144 others(120): Show |
147 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.1022-2322_1022-232 others(10): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614119 | |||||||
| chr5:6614119 | A | C | 15 | a0001c0001t0004g0137 a0001c0002t0001g0272 a0001c0003t0001g0096 others(12): Show |
18 | HG00642.hp2 HG01099.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1022-2321T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614119 | |||||||
| chr5:6614120 | A | ACCCTCCC | 61 | a0001c0001t0001g0030 a0001c0001t0001g0042 a0001c0001t0001g0140 others(58): Show |
66 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1022-2323_1022-232 others(11): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614120 | |||||||
| chr5:6614120 | A | C | 138 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0144 others(135): Show |
165 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.1022-2322T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614120 | |||||||
| chr5:6614121 | A | C | 15 | a0001c0001t0004g0137 a0001c0002t0001g0272 a0001c0003t0001g0096 others(12): Show |
18 | HG00642.hp2 HG01099.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1022-2323T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614121 | |||||||
| chr5:6614122 | A | C | 219 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(216): Show |
254 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(251): Show |
intron_variant | MODIFIER | c.1022-2324T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614122 | |||||||
| chr5:6614122 | A | T | 15 | a0001c0001t0004g0137 a0001c0002t0001g0272 a0001c0003t0001g0096 others(12): Show |
18 | HG00642.hp2 HG01099.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1022-2324T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614122 | |||||||
| chr5:6614124 | C | CCTCCCAC others(2): Show |
9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0127 others(6): Show |
9 | HG01109.hp2 HG01123.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1022-2327_1022-232 others(13): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614124 | |||||||
| chr5:6614124 | C | CTCCCACC others(1): Show |
35 | a0001c0001t0001g0031 a0001c0001t0001g0141 a0001c0001t0001g0142 others(32): Show |
41 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1022-2327_1022-232 others(12): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614124 | |||||||
| chr5:6614124 | C | T | 184 | a0001c0001t0001g0030 a0001c0001t0001g0042 a0001c0001t0001g0125 others(181): Show |
213 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(210): Show |
intron_variant | MODIFIER | c.1022-2326G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614124 | |||||||
| chr5:6614127 | C | CCTCA | 15 | a0001c0001t0004g0137 a0001c0002t0001g0272 a0001c0003t0001g0096 others(12): Show |
18 | HG00642.hp2 HG01099.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1022-2330_1022-232 others(8): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614127 | |||||||
| chr5:6614128 | A | C | 15 | a0001c0001t0004g0137 a0001c0002t0001g0272 a0001c0003t0001g0096 others(12): Show |
18 | HG00642.hp2 HG01099.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1022-2330T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614128 | |||||||
| chr5:6614129 | AC | A | 228 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(225): Show |
263 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(260): Show |
intron_variant | MODIFIER | c.1022-2332delG | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614129 | |||||||
| chr5:6614130 | C | A | 15 | a0001c0001t0004g0137 a0001c0002t0001g0272 a0001c0003t0001g0096 others(12): Show |
18 | HG00642.hp2 HG01099.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1022-2332G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614130 | |||||||
| chr5:6614200 | C | T | 1 | a0001c0002t0001g0240 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1022-2402G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614200 | |||||||
| chr5:6614311 | C | A | 1 | a0001c0004t0002g0148 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1021+2416G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614311 | |||||||
| chr5:6614462 | C | A | 1 | a0001c0003t0001g0122 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1021+2265G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614462 | |||||||
| chr5:6614467 | G | A | 5 | a0001c0001t0001g0031 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
6 | HG00639.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1021+2260C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614467 | |||||||
| chr5:6614540 | G | C | 209 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0126 others(206): Show |
242 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(239): Show |
intron_variant | MODIFIER | c.1021+2187C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614540 | |||||||
| chr5:6614542 | T | C | 203 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0126 others(200): Show |
236 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.1021+2185A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614542 | |||||||
| chr5:6614651 | C | T | 206 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0126 others(203): Show |
239 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.1021+2076G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614651 | |||||||
| chr5:6614767 | T | G | 1 | a0001c0004t0002g0178 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1021+1960A>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614767 | |||||||
| chr5:6614850 | G | A | 203 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0126 others(200): Show |
236 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.1021+1877C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614850 | |||||||
| chr5:6614850 | G | C | 9 | a0001c0009t0001g0048 a0001c0009t0001g0049 a0001c0009t0001g0050 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1021+1877C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614850 | |||||||
| chr5:6614856 | A | G | 203 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0126 others(200): Show |
236 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.1021+1871T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614856 | |||||||
| chr5:6614947 | A | C | 203 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0126 others(200): Show |
236 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.1021+1780T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614947 | |||||||
| chr5:6614979 | A | C | 203 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0126 others(200): Show |
236 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.1021+1748T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6614979 | |||||||
| chr5:6615042 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG01255.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1021+1685G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6615042 | |||||||
| chr5:6615275 | A | G | 6 | a0001c0001t0001g0004 a0001c0001t0001g0162 a0001c0001t0001g0163 others(3): Show |
9 | HG02280.hp2 HG02451.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1021+1452T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6615275 | |||||||
| chr5:6615388 | C | A | 3 | a0001c0002t0001g0267 a0001c0002t0001g0268 a0001c0002t0001g0287 |
3 | NA18965.hp1 NA18975.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.1021+1339G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6615388 | |||||||
| chr5:6615430 | T | C | 219 | a0001c0001t0001g0031 a0001c0001t0001g0042 a0001c0001t0001g0125 others(216): Show |
250 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.1021+1297A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6615430 | |||||||
| chr5:6615510 | T | C | 1 | a0002c0006t0003g0094 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1021+1217A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6615510 | |||||||
| chr5:6615516 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1021+1211A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6615516 | |||||||
| chr5:6615615 | GC | G | 251 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(248): Show |
289 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.1021+1111delG | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6615615 | |||||||
| chr5:6615627 | C | T | 10 | a0001c0001t0001g0042 a0001c0001t0001g0323 a0001c0001t0001g0324 others(7): Show |
11 | HG01261.hp2 HG01884.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.1021+1100G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6615627 | |||||||
| chr5:6615878 | G | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0140 a0001c0001t0001g0141 others(1): Show |
5 | HG02572.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1021+849C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6615878 | |||||||
| chr5:6615884 | C | A | 1 | a0002c0006t0001g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1021+843G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6615884 | |||||||
| chr5:6615991 | A | G | 12 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0127 others(9): Show |
14 | HG01891.hp1 HG02572.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1021+736T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6615991 | |||||||
| chr5:6616107 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1021+620G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616107 | |||||||
| chr5:6616121 | A | G | 57 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0144 others(54): Show |
64 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1021+606T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616121 | |||||||
| chr5:6616141 | T | C | 1 | a0001c0002t0001g0268 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1021+586A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616141 | |||||||
| chr5:6616164 | A | G | 184 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0031 others(181): Show |
221 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1021+563T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616164 | |||||||
| chr5:6616214 | C | G | 1 | a0001c0002t0001g0289 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1021+513G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616214 | |||||||
| chr5:6616253 | G | C | 1 | a0001c0004t0002g0155 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1021+474C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616253 | |||||||
| chr5:6616270 | G | A | 2 | a0001c0003t0001g0022 a0001c0003t0001g0110 |
3 | HG00735.hp2 HG01081.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.1021+457C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616270 | |||||||
| chr5:6616290 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1021+437C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616290 | |||||||
| chr5:6616295 | T | C | 184 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0160 others(181): Show |
212 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.1021+432A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616295 | |||||||
| chr5:6616419 | T | C | 228 | a0001c0001t0001g0030 a0001c0001t0001g0042 a0001c0001t0001g0123 others(225): Show |
265 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(262): Show |
intron_variant | MODIFIER | c.1021+308A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616419 | |||||||
| chr5:6616455 | G | T | 2 | a0001c0002t0001g0290 a0001c0002t0001g0291 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1021+272C>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616455 | |||||||
| chr5:6616623 | C | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
6 | HG00639.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1021+104G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616623 | |||||||
| chr5:6616669 | CAT | C | 245 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(242): Show |
283 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(280): Show |
intron_variant | MODIFIER | c.1021+56_1021+57del others(2): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616669 | |||||||
| chr5:6616675 | C | A | 245 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(242): Show |
283 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(280): Show |
intron_variant | MODIFIER | c.1021+52G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616675 | |||||||
| chr5:6616676 | A | T | 245 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(242): Show |
283 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(280): Show |
intron_variant | MODIFIER | c.1021+51T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616676 | |||||||
| chr5:6616678 | A | AAAAATTT others(237): Show |
1 | a0001c0002t0001g0299 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1021+48_1021+49ins others(244): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616678 | |||||||
| chr5:6616678 | A | AAAAATTT others(238): Show |
244 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(241): Show |
282 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.1021+48_1021+49ins others(245): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616678 | |||||||
| chr5:6616681 | A | G | 4 | a0001c0001t0001g0030 a0001c0001t0001g0140 a0001c0001t0001g0141 others(1): Show |
5 | HG02572.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1021+46T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 9/18 | chr5 | 6616681 | |||||||
| chr5:6616886 | G | C | 3 | a0001c0001t0001g0274 a0001c0002t0001g0272 a0001c0002t0001g0273 |
3 | HG00438.hp1 HG00544.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.891-29C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 8/18 | chr5 | 6616886 | |||||||
| chr5:6616898 | C | A | 245 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(242): Show |
283 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(280): Show |
intron_variant | MODIFIER | c.891-41G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 8/18 | chr5 | 6616898 | |||||||
| chr5:6617044 | AT | A | 5 | a0001c0003t0001g0063 a0001c0003t0001g0066 a0002c0006t0001g0065 others(2): Show |
5 | HG02258.hp1 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.891-188delA | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 8/18 | chr5 | 6617044 | |||||||
| chr5:6617108 | A | G | 1 | a0001c0001t0001g0324 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.891-251T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 8/18 | chr5 | 6617108 | |||||||
| chr5:6617368 | C | T | 116 | a0001c0001t0001g0231 a0001c0001t0001g0266 a0001c0001t0001g0274 others(113): Show |
133 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.891-511G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 8/18 | chr5 | 6617368 | |||||||
| chr5:6617429 | A | G | 1 | a0001c0002t0001g0235 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.890+521T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 8/18 | chr5 | 6617429 | |||||||
| chr5:6617498 | C | T | 3 | a0001c0004t0002g0002 a0001c0004t0002g0025 a0001c0004t0002g0167 |
8 | HG01070.hp2 HG01071.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.890+452G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 8/18 | chr5 | 6617498 | |||||||
| chr5:6617601 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.890+349G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 8/18 | chr5 | 6617601 | |||||||
| chr5:6618073 | T | C | 245 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(242): Show |
283 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(280): Show |
intron_variant | MODIFIER | c.816-49A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6618073 | |||||||
| chr5:6618210 | G | C | 245 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(242): Show |
283 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(280): Show |
intron_variant | MODIFIER | c.816-186C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6618210 | |||||||
| chr5:6618302 | G | A | 1 | a0001c0002t0001g0289 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.816-278C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6618302 | |||||||
| chr5:6618317 | A | C | 5 | a0001c0003t0001g0063 a0001c0003t0001g0066 a0002c0006t0001g0065 others(2): Show |
5 | HG02258.hp1 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.816-293T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6618317 | |||||||
| chr5:6618334 | T | C | 5 | a0001c0001t0001g0160 a0001c0001t0001g0165 a0001c0001t0001g0203 others(2): Show |
5 | HG02258.hp2 HG06807.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.816-310A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6618334 | |||||||
| chr5:6618546 | T | C | 1 | a0001c0001t0004g0207 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.816-522A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6618546 | |||||||
| chr5:6618590 | T | C | 245 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(242): Show |
283 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(280): Show |
intron_variant | MODIFIER | c.816-566A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6618590 | |||||||
| chr5:6618643 | T | C | 81 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0001g0145 others(78): Show |
93 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.816-619A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6618643 | |||||||
| chr5:6618761 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.816-737T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6618761 | |||||||
| chr5:6618839 | G | A | 6 | a0001c0003t0001g0019 a0001c0003t0001g0020 a0001c0003t0001g0062 others(3): Show |
8 | HG00673.hp2 NA18940.hp1 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.816-815C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6618839 | |||||||
| chr5:6618882 | A | G | 9 | a0001c0009t0001g0048 a0001c0009t0001g0049 a0001c0009t0001g0050 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.816-858T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6618882 | |||||||
| chr5:6618896 | T | G | 9 | a0001c0009t0001g0048 a0001c0009t0001g0049 a0001c0009t0001g0050 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.816-872A>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6618896 | |||||||
| chr5:6618903 | G | A | 3 | a0001c0011t0001g0013 a0001c0011t0001g0046 a0001c0011t0001g0047 |
4 | HG01192.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.816-879C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6618903 | |||||||
| chr5:6619105 | G | A | 1 | a0001c0002t0007g0228 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.815+1001C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6619105 | |||||||
| chr5:6619167 | A | T | 9 | a0001c0009t0001g0048 a0001c0009t0001g0049 a0001c0009t0001g0050 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.815+939T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6619167 | |||||||
| chr5:6619182 | T | C | 1 | a0001c0004t0002g0199 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.815+924A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6619182 | |||||||
| chr5:6619265 | G | A | 3 | a0001c0010t0001g0059 a0001c0010t0001g0060 a0001c0010t0001g0061 |
3 | HG01256.hp1 HG01257.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.815+841C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6619265 | |||||||
| chr5:6619351 | G | A | 3 | a0002c0006t0003g0093 a0002c0006t0003g0094 a0002c0006t0003g0095 |
3 | HG01106.hp1 HG01167.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.815+755C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6619351 | |||||||
| chr5:6619458 | C | T | 1 | a0001c0002t0001g0234 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.815+648G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6619458 | |||||||
| chr5:6619587 | T | C | 3 | a0001c0002t0001g0041 a0001c0002t0001g0315 a0001c0002t0001g0316 |
4 | HG00609.hp1 NA18991.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.815+519A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6619587 | |||||||
| chr5:6619620 | C | T | 250 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(247): Show |
288 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(285): Show |
intron_variant | MODIFIER | c.815+486G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6619620 | |||||||
| chr5:6619766 | G | A | 5 | a0001c0003t0001g0063 a0001c0003t0001g0066 a0002c0006t0001g0065 others(2): Show |
5 | HG02258.hp1 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.815+340C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6619766 | |||||||
| chr5:6619785 | A | G | 9 | a0001c0009t0001g0048 a0001c0009t0001g0049 a0001c0009t0001g0050 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.815+321T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6619785 | |||||||
| chr5:6619797 | AACAC | A | 5 | a0001c0003t0001g0063 a0001c0003t0001g0066 a0002c0006t0001g0065 others(2): Show |
5 | HG02258.hp1 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.815+305_815+308del others(4): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6619797 | |||||||
| chr5:6619810 | A | G | 84 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0001g0145 others(81): Show |
96 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.815+296T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6619810 | |||||||
| chr5:6619848 | CTGTTT | C | 26 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0123 others(23): Show |
34 | HG00639.hp2 HG00642.hp2 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.815+253_815+257del others(5): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6619848 | |||||||
| chr5:6619979 | C | T | 84 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0001g0145 others(81): Show |
96 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.815+127G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6619979 | |||||||
| chr5:6620034 | A | G | 5 | a0001c0003t0001g0063 a0001c0003t0001g0066 a0002c0006t0001g0065 others(2): Show |
5 | HG02258.hp1 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.815+72T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6620034 | |||||||
| chr5:6620080 | G | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
6 | HG00639.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.815+26C>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 7/18 | chr5 | 6620080 | |||||||
| chr5:6620346 | A | G | 248 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(245): Show |
286 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(283): Show |
intron_variant | MODIFIER | c.623-48T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6620346 | |||||||
| chr5:6620546 | G | T | 119 | a0001c0001t0001g0231 a0001c0001t0001g0266 a0001c0001t0001g0274 others(116): Show |
137 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.623-248C>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6620546 | |||||||
| chr5:6620597 | C | CA | 10 | a0001c0009t0001g0048 a0001c0009t0001g0049 a0001c0009t0001g0050 others(7): Show |
10 | HG01496.hp1 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.623-300dupT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6620597 | |||||||
| chr5:6620731 | C | A | 26 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0123 others(23): Show |
34 | HG00639.hp2 HG00642.hp2 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.623-433G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6620731 | |||||||
| chr5:6620816 | A | C | 9 | a0001c0009t0001g0048 a0001c0009t0001g0049 a0001c0009t0001g0050 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.623-518T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6620816 | |||||||
| chr5:6620874 | T | G | 7 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(4): Show |
7 | HG00597.hp2 HG02135.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.623-576A>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6620874 | |||||||
| chr5:6620918 | A | G | 245 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(242): Show |
283 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(280): Show |
intron_variant | MODIFIER | c.623-620T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6620918 | |||||||
| chr5:6621046 | C | G | 1 | a0001c0001t0001g0356 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.623-748G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621046 | |||||||
| chr5:6621097 | A | G | 250 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(247): Show |
288 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(285): Show |
intron_variant | MODIFIER | c.623-799T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621097 | |||||||
| chr5:6621105 | A | C | 116 | a0001c0001t0001g0231 a0001c0001t0001g0266 a0001c0001t0001g0274 others(113): Show |
133 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.623-807T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621105 | |||||||
| chr5:6621171 | G | A | 2 | a0001c0002t0001g0282 a0006c0020t0001g0281 |
2 | HG02683.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.622+845C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621171 | |||||||
| chr5:6621224 | G | A | 2 | a0001c0001t0001g0329 a0001c0001t0001g0332 |
2 | HG02886.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.622+792C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621224 | |||||||
| chr5:6621304 | T | C | 1 | a0001c0002t0001g0307 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.622+712A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621304 | |||||||
| chr5:6621335 | C | T | 17 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0127 others(14): Show |
23 | HG00642.hp2 HG01074.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.622+681G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621335 | |||||||
| chr5:6621368 | A | G | 3 | a0001c0004t0002g0166 a0001c0004t0002g0200 a0001c0004t0002g0201 |
3 | HG00140.hp2 HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.622+648T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621368 | |||||||
| chr5:6621476 | T | C | 14 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0162 others(11): Show |
17 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.622+540A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621476 | |||||||
| chr5:6621486 | C | T | 2 | a0004c0008t0001g0366 a0004c0008t0001g0367 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.622+530G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621486 | |||||||
| chr5:6621487 | A | G | 18 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0162 others(15): Show |
21 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.622+529T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621487 | |||||||
| chr5:6621488 | C | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0162 others(8): Show |
14 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.622+528G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621488 | |||||||
| chr5:6621515 | A | G | 3 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 |
3 | HG02818.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.622+501T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621515 | |||||||
| chr5:6621527 | T | G | 1 | a0001c0003t0001g0111 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.622+489A>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621527 | |||||||
| chr5:6621533 | G | A | 2 | a0002c0006t0003g0093 a0002c0006t0003g0095 |
2 | HG01106.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.622+483C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621533 | |||||||
| chr5:6621564 | T | C | 5 | a0001c0002t0001g0283 a0001c0003t0001g0020 a0001c0003t0001g0087 others(2): Show |
6 | NA18940.hp1 NA18942.hp1 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.622+452A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621564 | |||||||
| chr5:6621576 | G | A | 2 | a0001c0001t0004g0137 a0001c0001t0004g0207 |
2 | HG02647.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.622+440C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621576 | |||||||
| chr5:6621597 | A | T | 1 | a0001c0001t0001g0161 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.622+419T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621597 | |||||||
| chr5:6621606 | G | A | 1 | a0004c0008t0001g0367 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.622+410C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621606 | |||||||
| chr5:6621653 | C | G | 1 | a0001c0001t0001g0335 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.622+363G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621653 | |||||||
| chr5:6621747 | C | CA | 222 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(219): Show |
254 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(251): Show |
intron_variant | MODIFIER | c.622+268dupT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621747 | |||||||
| chr5:6621747 | C | CAA | 16 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0127 others(13): Show |
22 | HG00642.hp2 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.622+267_622+268dup others(2): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621747 | |||||||
| chr5:6621904 | T | G | 89 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0001g0145 others(86): Show |
101 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.622+112A>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6621904 | |||||||
| chr5:6622009 | T | A | 1 | a0002c0007t0003g0006 | 4 | HG00642.hp2 HG01099.hp1 HG01168.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.622+7A>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6622009 | |||||||
| chr5:6622012 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG06807.hp2 | splice_region_variant&intron_variant | LOW | c.622+4T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 6/18 | chr5 | 6622012 | |||||||
| chr5:6622103 | A | T | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | splice_region_variant&intron_variant | LOW | c.538-3T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622103 | |||||||
| chr5:6622106 | A | G | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | splice_region_variant&intron_variant | LOW | c.538-6T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622106 | |||||||
| chr5:6622107 | A | G | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | splice_region_variant&intron_variant | LOW | c.538-7T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622107 | |||||||
| chr5:6622109 | A | T | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-9T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622109 | |||||||
| chr5:6622114 | A | C | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-14T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622114 | |||||||
| chr5:6622116 | G | T | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-16C>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622116 | |||||||
| chr5:6622124 | T | G | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-24A>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622124 | |||||||
| chr5:6622127 | A | T | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-27T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622127 | |||||||
| chr5:6622129 | G | C | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-29C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622129 | |||||||
| chr5:6622134 | T | G | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-34A>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622134 | |||||||
| chr5:6622142 | C | G | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-42G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622142 | |||||||
| chr5:6622145 | A | G | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-45T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622145 | |||||||
| chr5:6622147 | A | G | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-47T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622147 | |||||||
| chr5:6622150 | C | G | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-50G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622150 | |||||||
| chr5:6622152 | A | T | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-52T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622152 | |||||||
| chr5:6622156 | T | A | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-56A>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622156 | |||||||
| chr5:6622158 | A | C | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-58T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622158 | |||||||
| chr5:6622159 | A | C | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-59T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622159 | |||||||
| chr5:6622163 | A | G | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-63T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622163 | |||||||
| chr5:6622164 | A | C | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-64T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622164 | |||||||
| chr5:6622165 | A | C | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-65T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622165 | |||||||
| chr5:6622166 | G | C | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-66C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622166 | |||||||
| chr5:6622169 | A | C | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-69T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622169 | |||||||
| chr5:6622172 | C | G | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-72G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622172 | |||||||
| chr5:6622174 | A | T | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-74T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622174 | |||||||
| chr5:6622175 | G | GATGGGGT others(8): Show |
1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-76_538-75insAA others(13): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622175 | |||||||
| chr5:6622187 | C | G | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-87G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622187 | |||||||
| chr5:6622192 | C | T | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-92G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622192 | |||||||
| chr5:6622201 | A | G | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-101T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622201 | |||||||
| chr5:6622202 | A | G | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-102T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622202 | |||||||
| chr5:6622208 | C | G | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-108G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622208 | |||||||
| chr5:6622209 | T | C | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-109A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622209 | |||||||
| chr5:6622210 | T | C | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-110A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622210 | |||||||
| chr5:6622215 | A | T | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-115T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622215 | |||||||
| chr5:6622222 | C | G | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-122G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622222 | |||||||
| chr5:6622223 | T | A | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-123A>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622223 | |||||||
| chr5:6622224 | A | G | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-124T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622224 | |||||||
| chr5:6622229 | A | G | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-129T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622229 | |||||||
| chr5:6622233 | C | G | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-133G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622233 | |||||||
| chr5:6622233 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.538-133G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622233 | |||||||
| chr5:6622235 | T | A | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-135A>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622235 | |||||||
| chr5:6622241 | A | T | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-141T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622241 | |||||||
| chr5:6622243 | TTTTAGGG others(12): Show |
T | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-162_538-144del others(19): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622243 | |||||||
| chr5:6622267 | A | T | 1 | a0001c0004t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.538-167T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622267 | |||||||
| chr5:6622469 | T | C | 2 | a0001c0004t0002g0134 a0001c0004t0002g0135 |
2 | NA18971.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.538-369A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622469 | |||||||
| chr5:6622555 | A | C | 1 | a0001c0001t0001g0231 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.538-455T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622555 | |||||||
| chr5:6622589 | T | C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0218 a0001c0001t0001g0219 others(3): Show |
7 | HG00639.hp2 HG02818.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.538-489A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622589 | |||||||
| chr5:6622622 | C | T | 4 | a0001c0001t0001g0030 a0001c0001t0001g0140 a0001c0001t0001g0141 others(1): Show |
5 | HG02572.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.538-522G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622622 | |||||||
| chr5:6622676 | C | T | 25 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0123 others(22): Show |
32 | HG00639.hp2 HG00642.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.537+538G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622676 | |||||||
| chr5:6622677 | G | A | 81 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0001g0145 others(78): Show |
93 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.537+537C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622677 | |||||||
| chr5:6622717 | C | T | 9 | a0001c0009t0001g0048 a0001c0009t0001g0049 a0001c0009t0001g0050 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.537+497G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622717 | |||||||
| chr5:6622747 | T | A | 1 | a0001c0003t0001g0112 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.537+467A>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622747 | |||||||
| chr5:6622790 | T | C | 1 | a0001c0001t0001g0042 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.537+424A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622790 | |||||||
| chr5:6622847 | C | CA | 6 | a0001c0002t0001g0230 a0001c0002t0001g0285 a0001c0003t0001g0056 others(3): Show |
6 | HG01074.hp2 HG01978.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.537+366dupT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622847 | |||||||
| chr5:6622847 | C | CAA | 206 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0126 others(203): Show |
236 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.537+365_537+366dup others(2): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622847 | |||||||
| chr5:6622911 | A | G | 1 | a0003c0005t0001g0229 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.537+303T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622911 | |||||||
| chr5:6622965 | C | T | 1 | a0004c0008t0001g0366 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.537+249G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622965 | |||||||
| chr5:6622972 | T | C | 211 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0126 others(208): Show |
241 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(238): Show |
intron_variant | MODIFIER | c.537+242A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622972 | |||||||
| chr5:6622975 | G | A | 1 | a0003c0005t0001g0284 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.537+239C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6622975 | |||||||
| chr5:6623044 | GA | G | 38 | a0001c0001t0001g0030 a0001c0001t0001g0123 a0001c0001t0001g0124 others(35): Show |
46 | HG00642.hp2 HG00738.hp1 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.537+169delT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6623044 | |||||||
| chr5:6623044 | GAA | G | 5 | a0001c0001t0001g0031 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
6 | HG00639.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.537+168_537+169del others(2): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6623044 | |||||||
| chr5:6623074 | G | A | 4 | a0001c0013t0001g0212 a0001c0013t0001g0213 a0001c0013t0001g0214 others(1): Show |
4 | HG02630.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.537+140C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6623074 | |||||||
| chr5:6623097 | G | C | 1 | a0001c0010t0002g0118 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.537+117C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6623097 | |||||||
| chr5:6623110 | A | T | 3 | a0001c0011t0001g0013 a0001c0011t0001g0046 a0001c0011t0001g0047 |
4 | HG01192.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.537+104T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6623110 | |||||||
| chr5:6623137 | A | G | 4 | a0001c0010t0001g0058 a0001c0010t0001g0059 a0001c0010t0001g0060 others(1): Show |
4 | HG01256.hp1 HG01257.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.537+77T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6623137 | |||||||
| chr5:6623205 | A | G | 6 | a0001c0004t0001g0008 a0001c0004t0001g0153 a0001c0004t0001g0154 others(3): Show |
8 | HG02257.hp2 HG02486.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.537+9T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6623205 | |||||||
| chr5:6623206 | T | C | 1 | a0002c0006t0003g0094 | 1 | HG01243.hp1 | splice_region_variant&intron_variant | LOW | c.537+8A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 5/18 | chr5 | 6623206 | |||||||
| chr5:6623319 | G | A | 5 | a0001c0001t0001g0031 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
6 | HG00639.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.466-34C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6623319 | |||||||
| chr5:6623319 | G | GA | 307 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0042 others(304): Show |
363 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(360): Show |
intron_variant | MODIFIER | c.466-35dupT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6623319 | |||||||
| chr5:6623319 | G | GAA | 25 | a0001c0001t0001g0288 a0001c0001t0001g0330 a0001c0001t0001g0331 others(22): Show |
25 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.466-36_466-35dupTT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6623319 | |||||||
| chr5:6623334 | C | T | 3 | a0001c0011t0001g0013 a0001c0011t0001g0046 a0001c0011t0001g0047 |
4 | HG01192.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-49G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6623334 | |||||||
| chr5:6623585 | G | C | 9 | a0001c0009t0001g0048 a0001c0009t0001g0049 a0001c0009t0001g0050 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.466-300C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6623585 | |||||||
| chr5:6623855 | CCT | C | 90 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0001g0145 others(87): Show |
102 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.466-572_466-571del others(2): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6623855 | |||||||
| chr5:6623955 | C | G | 3 | a0001c0004t0002g0024 a0001c0004t0002g0147 a0001c0004t0002g0148 |
4 | HG02040.hp2 HG02129.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.466-670G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6623955 | |||||||
| chr5:6624181 | C | A | 90 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0001g0145 others(87): Show |
102 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.466-896G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6624181 | |||||||
| chr5:6624258 | C | T | 81 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0001g0145 others(78): Show |
93 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.466-973G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6624258 | |||||||
| chr5:6624282 | G | A | 121 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0231 others(118): Show |
139 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.466-997C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6624282 | |||||||
| chr5:6624406 | A | G | 1 | a0001c0003t0001g0098 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.466-1121T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6624406 | |||||||
| chr5:6624482 | C | T | 5 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0066 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+1082G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6624482 | |||||||
| chr5:6624787 | G | C | 4 | a0001c0001t0001g0030 a0001c0001t0001g0140 a0001c0001t0001g0141 others(1): Show |
5 | HG02572.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.465+777C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6624787 | |||||||
| chr5:6624808 | TTAGAAAA | T | 90 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0001g0145 others(87): Show |
102 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.465+749_465+755del others(7): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6624808 | |||||||
| chr5:6624861 | C | A | 120 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0231 others(117): Show |
138 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.465+703G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6624861 | |||||||
| chr5:6625018 | T | C | 1 | a0001c0002t0001g0289 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.465+546A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6625018 | |||||||
| chr5:6625078 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.465+486C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6625078 | |||||||
| chr5:6625102 | G | GAA | 14 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0129 others(11): Show |
19 | HG00642.hp2 HG01074.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.465+460_465+461dup others(2): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6625102 | |||||||
| chr5:6625478 | G | A | 2 | a0001c0002t0001g0290 a0001c0002t0001g0291 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.465+86C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 4/18 | chr5 | 6625478 | |||||||
| chr5:6625844 | A | C | 1 | a0001c0001t0001g0333 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.360-175T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6625844 | |||||||
| chr5:6625935 | T | G | 5 | a0001c0002t0001g0036 a0001c0002t0001g0216 a0001c0002t0001g0292 others(2): Show |
6 | NA18988.hp1 NA18989.hp2 NA19010.hp1 others(3): Show |
intron_variant | MODIFIER | c.360-266A>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6625935 | |||||||
| chr5:6625978 | G | A | 61 | a0001c0003t0001g0007 a0001c0003t0001g0015 a0001c0003t0001g0016 others(58): Show |
71 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.360-309C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6625978 | |||||||
| chr5:6626060 | C | T | 1 | a0001c0004t0002g0146 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.360-391G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6626060 | |||||||
| chr5:6626117 | A | G | 3 | a0001c0011t0001g0013 a0001c0011t0001g0046 a0001c0011t0001g0047 |
4 | HG01192.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.360-448T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6626117 | |||||||
| chr5:6626125 | T | C | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.360-456A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6626125 | |||||||
| chr5:6626133 | T | C | 4 | a0001c0002t0001g0041 a0001c0002t0001g0314 a0001c0002t0001g0315 others(1): Show |
5 | HG00609.hp1 NA18991.hp1 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.360-464A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6626133 | |||||||
| chr5:6626325 | T | C | 1 | a0001c0001t0004g0207 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.360-656A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6626325 | |||||||
| chr5:6626380 | CT | C | 103 | a0001c0001t0001g0231 a0001c0001t0001g0266 a0001c0001t0001g0274 others(100): Show |
118 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.360-712delA | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6626380 | |||||||
| chr5:6626424 | T | C | 1 | a0002c0007t0001g0132 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.360-755A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6626424 | |||||||
| chr5:6626448 | T | C | 245 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(242): Show |
282 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.360-779A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6626448 | |||||||
| chr5:6626560 | C | G | 249 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0042 others(246): Show |
286 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(283): Show |
intron_variant | MODIFIER | c.360-891G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6626560 | |||||||
| chr5:6626595 | C | A | 3 | a0001c0011t0001g0013 a0001c0011t0001g0046 a0001c0011t0001g0047 |
4 | HG01192.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.360-926G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6626595 | |||||||
| chr5:6626697 | G | A | 1 | a0001c0004t0002g0205 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.360-1028C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6626697 | |||||||
| chr5:6626884 | T | C | 1 | a0001c0003t0001g0121 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.360-1215A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6626884 | |||||||
| chr5:6626945 | A | C | 3 | a0001c0011t0001g0013 a0001c0011t0001g0046 a0001c0011t0001g0047 |
4 | HG01192.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.360-1276T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6626945 | |||||||
| chr5:6627087 | C | T | 6 | a0001c0001t0001g0031 a0001c0001t0001g0218 a0001c0001t0001g0219 others(3): Show |
7 | HG00639.hp2 HG02818.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.360-1418G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6627087 | |||||||
| chr5:6627299 | T | C | 6 | a0001c0003t0001g0007 a0001c0003t0001g0115 a0001c0003t0001g0116 others(3): Show |
8 | HG01943.hp2 HG01993.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.360-1630A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6627299 | |||||||
| chr5:6627376 | A | T | 9 | a0001c0009t0001g0048 a0001c0009t0001g0049 a0001c0009t0001g0050 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.360-1707T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6627376 | |||||||
| chr5:6627542 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.360-1873C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6627542 | |||||||
| chr5:6627761 | T | A | 1 | a0001c0003t0001g0092 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.360-2092A>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6627761 | |||||||
| chr5:6627866 | A | G | 3 | a0001c0002t0001g0032 a0001c0002t0001g0217 a0001c0002t0001g0223 |
4 | HG02155.hp2 NA18971.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.360-2197T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6627866 | |||||||
| chr5:6627884 | C | G | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0004g0322 |
3 | HG01255.hp2 HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.360-2215G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6627884 | |||||||
| chr5:6627997 | G | A | 3 | a0002c0006t0003g0093 a0002c0006t0003g0094 a0002c0006t0003g0095 |
3 | HG01106.hp1 HG01167.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.360-2328C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6627997 | |||||||
| chr5:6628068 | C | T | 9 | a0001c0009t0001g0048 a0001c0009t0001g0049 a0001c0009t0001g0050 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.360-2399G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6628068 | |||||||
| chr5:6628085 | T | C | 15 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0127 others(12): Show |
20 | HG00642.hp2 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.360-2416A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6628085 | |||||||
| chr5:6628351 | A | T | 126 | a0001c0001t0001g0030 a0001c0001t0001g0125 a0001c0001t0001g0126 others(123): Show |
145 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.360-2682T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6628351 | |||||||
| chr5:6628414 | A | C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0218 a0001c0001t0001g0219 others(3): Show |
7 | HG00639.hp2 HG02818.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.360-2745T>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6628414 | |||||||
| chr5:6628419 | A | T | 1 | a0001c0003t0001g0063 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.360-2750T>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6628419 | |||||||
| chr5:6628522 | T | A | 1 | a0001c0002t0001g0296 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.360-2853A>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6628522 | |||||||
| chr5:6628928 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.359+2945G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6628928 | |||||||
| chr5:6628929 | G | A | 2 | a0001c0013t0001g0214 a0001c0013t0001g0215 |
2 | HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.359+2944C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6628929 | |||||||
| chr5:6629368 | C | G | 1 | a0001c0004t0002g0143 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.359+2505G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6629368 | |||||||
| chr5:6629500 | T | A | 1 | a0001c0003t0001g0096 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.359+2373A>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6629500 | |||||||
| chr5:6629721 | G | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0140 a0001c0001t0001g0141 others(1): Show |
5 | HG02572.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.359+2152C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6629721 | |||||||
| chr5:6629756 | C | A | 1 | a0001c0003t0001g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.359+2117G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6629756 | |||||||
| chr5:6629817 | G | A | 115 | a0001c0001t0001g0004 a0001c0001t0001g0144 a0001c0001t0001g0145 others(112): Show |
138 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.359+2056C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6629817 | |||||||
| chr5:6629925 | C | T | 4 | a0001c0013t0001g0212 a0001c0013t0001g0213 a0001c0013t0001g0214 others(1): Show |
4 | HG02630.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.359+1948G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6629925 | |||||||
| chr5:6629990 | A | G | 1 | a0001c0002t0001g0217 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.359+1883T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6629990 | |||||||
| chr5:6630005 | T | G | 1 | a0001c0001t0001g0206 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.359+1868A>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6630005 | |||||||
| chr5:6630161 | A | G | 1 | a0001c0002t0001g0222 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.359+1712T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6630161 | |||||||
| chr5:6630435 | G | C | 2 | a0001c0002t0001g0037 a0001c0002t0001g0297 |
3 | HG00140.hp1 HG01175.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.359+1438C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6630435 | |||||||
| chr5:6630496 | G | C | 2 | a0001c0002t0001g0364 a0001c0002t0001g0365 |
2 | HG02074.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.359+1377C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6630496 | |||||||
| chr5:6630826 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0004g0207 |
3 | HG02572.hp1 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.359+1047C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6630826 | |||||||
| chr5:6630870 | G | A | 3 | a0001c0004t0002g0208 a0001c0004t0002g0209 a0001c0004t0002g0210 |
3 | HG02602.hp2 HG03942.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.359+1003C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6630870 | |||||||
| chr5:6630880 | G | A | 115 | a0001c0001t0001g0231 a0001c0001t0001g0266 a0001c0001t0001g0274 others(112): Show |
132 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.359+993C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6630880 | |||||||
| chr5:6630913 | A | G | 90 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0140 others(87): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.359+960T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6630913 | |||||||
| chr5:6631222 | C | T | 1 | a0001c0002t0001g0216 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.359+651G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6631222 | |||||||
| chr5:6631229 | G | A | 1 | a0001c0001t0001g0359 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.359+644C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6631229 | |||||||
| chr5:6631282 | TACA | T | 4 | a0001c0010t0001g0058 a0001c0010t0001g0059 a0001c0010t0001g0060 others(1): Show |
4 | HG01256.hp1 HG01257.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.359+588_359+590del others(3): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6631282 | |||||||
| chr5:6631377 | C | A | 10 | a0001c0003t0001g0056 a0001c0009t0001g0048 a0001c0009t0001g0049 others(7): Show |
11 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.359+496G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6631377 | |||||||
| chr5:6631394 | T | C | 1 | a0001c0001t0001g0360 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.359+479A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6631394 | |||||||
| chr5:6631527 | G | A | 26 | a0001c0002t0001g0038 a0001c0002t0001g0039 a0001c0002t0001g0040 others(23): Show |
30 | HG00609.hp1 HG02074.hp1 HG02523.hp1 others(27): Show |
intron_variant | MODIFIER | c.359+346C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6631527 | |||||||
| chr5:6631653 | C | G | 1 | a0001c0013t0001g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.359+220G>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6631653 | |||||||
| chr5:6631692 | A | G | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.359+181T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6631692 | |||||||
| chr5:6631823 | G | C | 10 | a0001c0003t0001g0056 a0001c0009t0001g0048 a0001c0009t0001g0049 others(7): Show |
11 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.359+50C>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 3/18 | chr5 | 6631823 | |||||||
| chr5:6632011 | A | G | 1 | a0001c0003t0001g0057 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.255-34T>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 2/18 | chr5 | 6632011 | |||||||
| chr5:6632030 | T | C | 2 | a0001c0003t0001g0119 a0001c0003t0001g0120 |
2 | HG00735.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.255-53A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 2/18 | chr5 | 6632030 | |||||||
| chr5:6632052 | C | T | 4 | a0001c0013t0001g0212 a0001c0013t0001g0213 a0001c0013t0001g0214 others(1): Show |
4 | HG02630.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.255-75G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 2/18 | chr5 | 6632052 | |||||||
| chr5:6632182 | T | G | 90 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0140 others(87): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.255-205A>C | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 2/18 | chr5 | 6632182 | |||||||
| chr5:6632207 | C | A | 246 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0031 others(243): Show |
288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.255-230G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 2/18 | chr5 | 6632207 | |||||||
| chr5:6632211 | A | AT | 246 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0031 others(243): Show |
288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.255-235_255-234ins others(1): Show |
NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 2/18 | chr5 | 6632211 | |||||||
| chr5:6632228 | CA | C | 3 | a0001c0011t0001g0013 a0001c0011t0001g0046 a0001c0011t0001g0047 |
4 | HG01192.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.255-252delT | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 2/18 | chr5 | 6632228 | |||||||
| chr5:6632254 | T | C | 1 | a0001c0002t0001g0362 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.255-277A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 2/18 | chr5 | 6632254 | |||||||
| chr5:6632316 | T | C | 2 | a0001c0003t0001g0023 a0001c0003t0001g0121 |
3 | HG02615.hp1 HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.254+283A>G | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 2/18 | chr5 | 6632316 | |||||||
| chr5:6632500 | G | A | 3 | a0001c0002t0001g0363 a0001c0002t0001g0364 a0001c0002t0001g0365 |
3 | HG00673.hp1 HG02074.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.254+99C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 2/18 | chr5 | 6632500 | |||||||
| chr5:6632762 | G | A | 86 | a0001c0003t0001g0007 a0001c0003t0001g0015 a0001c0003t0001g0016 others(83): Show |
98 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(95): Show |
splice_region_variant&intron_variant | LOW | c.97-6C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 1/18 | chr5 | 6632762 | |||||||
| chr5:6632796 | G | A | 197 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0123 others(194): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.97-40C>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 1/18 | chr5 | 6632796 | |||||||
| chr5:6632829 | G | T | 197 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0123 others(194): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.96+55C>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 1/18 | chr5 | 6632829 | |||||||
| chr5:6632832 | C | A | 1 | a0001c0003t0001g0122 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.96+52G>T | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 1/18 | chr5 | 6632832 | |||||||
| chr5:6632867 | C | T | 2 | a0004c0008t0001g0366 a0004c0008t0001g0367 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.96+17G>A | NSUN2 | ENSG00000037474.15 | transcript | ENST00000264670.11 | protein_coding | 1/18 | chr5 | 6632867 |