Item | Value |
---|---|
geneid | 55247 |
ensemblid | ENSG00000109674.4 |
hgncid | 24573 |
symbol | NEIL3 |
name | nei like DNA glycosylase 3 |
refseq_nuc | NM_018248.3 |
refseq_prot | NP_060718.3 |
ensembl_nuc | ENST00000264596.4 |
ensembl_prot | ENSP00000264596.3 |
mane_status | MANE Select |
chr | chr4 |
start | 177309874 |
end | 177362936 |
strand | + |
ver | v1.2 |
region | chr4:177309874-177362936 |
region5000 | chr4:177304874-177367936 |
regionname0 | NEIL3_chr4_177309874_177362936 |
regionname5000 | NEIL3_chr4_177304874_177367936 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 605 | 142 | 16 | 18 | 90 | 3 | 15 | 75 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
a0002 | 0/0 | 605 | 117 | 22 | 36 | 41 | 6 | 12 | 33 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
a0003 | 0/0 | 605 | 32 | 0 | 6 | 17 | 3 | 6 | 15 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
a0004 | 0/0 | 605 | 20 | 20 | 0 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
a0005 | 0/0 | 605 | 16 | 2 | 0 | 10 | 0 | 4 | 7 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
a0006 | 0/0 | 605 | 13 | 2 | 3 | 6 | 1 | 1 | 6 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
a0007 | 0/0 | 605 | 9 | 1 | 0 | 7 | 0 | 1 | 4 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
a0008 | 1/0 | 605 | 8 | 1 | 3 | 2 | 1 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
a0009 | 0/0 | 605 | 8 | 4 | 0 | 0 | 0 | 4 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
a0010 | 0/0 | 605 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
a0011 | 0/0 | 605 | 6 | 1 | 2 | 2 | 0 | 1 | 2 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
a0012 | 0/0 | 605 | 5 | 0 | 1 | 2 | 0 | 2 | 2 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
a0013 | 0/0 | 605 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
a0014 | 0/1 | 605 | 3 | 0 | 2 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
a0015 | 0/0 | 605 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
a0016 | 0/0 | 605 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
a0017 | 0/0 | 605 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
a0018 | 0/0 | 605 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
a0019 | 0/0 | 605 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
a0020 | 0/0 | 605 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
a0021 | 0/0 | 605 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
a0022 | 0/0 | 605 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
a0023 | 0/0 | 605 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
a0024 | 0/0 | 605 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
a0025 | 0/0 | 605 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
a0026 | 0/0 | 605 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
a0027 | 0/0 | 605 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
a0028 | 0/0 | 605 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
a0029 | 0/0 | 605 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | MVEGP others(600): Show |
chr4 | 177304874 | 177367936 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1815 | 109 | 15 | 16 | 64 | 2 | 12 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0001c0003 | 0/0 | 1815 | 23 | 0 | 2 | 17 | 1 | 3 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0001c0015 | 0/0 | 1815 | 6 | 0 | 0 | 6 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0001c0027 | 0/0 | 1815 | 2 | 0 | 0 | 2 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0001c0030 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0001c0043 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0002c0002 | 0/0 | 1815 | 94 | 11 | 29 | 37 | 6 | 11 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0002c0008 | 0/0 | 1815 | 8 | 2 | 1 | 4 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0002c0010 | 0/0 | 1815 | 8 | 3 | 5 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0002c0020 | 0/0 | 1815 | 4 | 3 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0002c0028 | 0/0 | 1815 | 2 | 2 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0002c0032 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0003c0004 | 0/0 | 1815 | 22 | 0 | 4 | 10 | 3 | 5 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0003c0007 | 0/0 | 1815 | 10 | 0 | 2 | 7 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0004c0006 | 0/0 | 1815 | 12 | 12 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0004c0014 | 0/0 | 1815 | 7 | 7 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0004c0048 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0005c0009 | 0/0 | 1815 | 8 | 0 | 0 | 8 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0005c0016 | 0/0 | 1815 | 6 | 0 | 0 | 2 | 0 | 4 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0005c0025 | 0/0 | 1815 | 2 | 2 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0006c0005 | 0/0 | 1815 | 13 | 2 | 3 | 6 | 1 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0007c0011 | 0/0 | 1815 | 8 | 1 | 0 | 6 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0007c0031 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0008c0012 | 1/0 | 1815 | 7 | 1 | 3 | 2 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0008c0037 | 0/0 | 1815 | 1 | 0 | 0 | 0 | 1 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0009c0019 | 0/0 | 1815 | 5 | 2 | 0 | 0 | 0 | 3 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0009c0022 | 0/0 | 1815 | 3 | 2 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0010c0013 | 0/0 | 1815 | 7 | 6 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0011c0018 | 0/0 | 1815 | 5 | 0 | 2 | 2 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0011c0033 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0012c0017 | 0/0 | 1815 | 5 | 0 | 1 | 2 | 0 | 2 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0013c0023 | 0/0 | 1815 | 3 | 2 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0014c0021 | 0/1 | 1815 | 3 | 0 | 2 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0015c0024 | 0/0 | 1815 | 3 | 2 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0016c0040 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0016c0041 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0017c0026 | 0/0 | 1815 | 2 | 2 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0018c0042 | 0/0 | 1815 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0019c0044 | 0/0 | 1815 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0020c0036 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0021c0045 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0022c0038 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0023c0047 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0024c0046 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0025c0034 | 0/0 | 1815 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0026c0039 | 0/0 | 1815 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0027c0029 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0028c0035 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 | ||
a0029c0049 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | ATGGT others(1810): Show |
chr4 | 177304874 | 177367936 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2363 | 61 | 12 | 10 | 29 | 2 | 8 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0001c0001t0002 | 0/0 | 2363 | 33 | 0 | 5 | 28 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0001c0001t0003 | 0/0 | 2363 | 6 | 1 | 1 | 0 | 0 | 4 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0001c0001t0004 | 0/0 | 2363 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0001c0001t0005 | 0/0 | 2363 | 2 | 2 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0001c0001t0006 | 0/0 | 2363 | 6 | 0 | 0 | 6 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0001c0003t0001 | 0/0 | 2363 | 21 | 0 | 1 | 16 | 1 | 3 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0001c0003t0002 | 0/0 | 2363 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0001c0003t0003 | 0/0 | 2363 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0001c0015t0001 | 0/0 | 2363 | 6 | 0 | 0 | 6 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0001c0027t0001 | 0/0 | 2363 | 2 | 0 | 0 | 2 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0001c0030t0001 | 0/0 | 2363 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0001c0043t0001 | 0/0 | 2363 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0002c0002t0001 | 0/0 | 2363 | 72 | 5 | 24 | 26 | 6 | 11 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0002c0002t0002 | 0/0 | 2363 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0002c0002t0003 | 0/0 | 2363 | 4 | 3 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0002c0002t0004 | 0/0 | 2363 | 10 | 0 | 0 | 10 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0002c0002t0005 | 0/0 | 2363 | 3 | 3 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0002c0002t0007 | 0/0 | 2363 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0002c0002t0008 | 0/0 | 2359 | 3 | 0 | 3 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2354): Show |
chr4 | 177304874 | 177367936 |
a0002c0008t0001 | 0/0 | 2363 | 7 | 1 | 1 | 4 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0002c0008t0005 | 0/0 | 2363 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0002c0010t0001 | 0/0 | 2363 | 7 | 2 | 5 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0002c0010t0005 | 0/0 | 2363 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0002c0020t0001 | 0/0 | 2363 | 4 | 3 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0002c0028t0001 | 0/0 | 2363 | 2 | 2 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0002c0032t0001 | 0/0 | 2363 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0003c0004t0001 | 0/0 | 2363 | 22 | 0 | 4 | 10 | 3 | 5 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0003c0007t0001 | 0/0 | 2363 | 5 | 0 | 2 | 3 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0003c0007t0002 | 0/0 | 2363 | 3 | 0 | 0 | 3 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0003c0007t0003 | 0/0 | 2363 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0003c0007t0006 | 0/0 | 2363 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0004c0006t0001 | 0/0 | 2363 | 6 | 6 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0004c0006t0004 | 0/0 | 2363 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0004c0006t0005 | 0/0 | 2363 | 4 | 4 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0004c0006t0006 | 0/0 | 2363 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0004c0014t0001 | 0/0 | 2363 | 7 | 7 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0004c0048t0005 | 0/0 | 2363 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0005c0009t0001 | 0/0 | 2363 | 2 | 0 | 0 | 2 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0005c0009t0004 | 0/0 | 2363 | 6 | 0 | 0 | 6 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0005c0016t0001 | 0/0 | 2363 | 3 | 0 | 0 | 2 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0005c0016t0004 | 0/0 | 2363 | 3 | 0 | 0 | 0 | 0 | 3 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0005c0025t0005 | 0/0 | 2363 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0005c0025t0011 | 0/0 | 2363 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0006c0005t0001 | 0/0 | 2363 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0006c0005t0003 | 0/0 | 2363 | 11 | 1 | 3 | 5 | 1 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0006c0005t0010 | 0/0 | 2363 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0007c0011t0001 | 0/0 | 2363 | 2 | 1 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0007c0011t0002 | 0/0 | 2363 | 3 | 0 | 0 | 2 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0007c0011t0007 | 0/0 | 2363 | 3 | 0 | 0 | 3 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0007c0031t0001 | 0/0 | 2363 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0008c0012t0001 | 1/0 | 2363 | 1 | 0 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0008c0012t0002 | 0/0 | 2363 | 6 | 1 | 3 | 2 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0008c0037t0001 | 0/0 | 2363 | 1 | 0 | 0 | 0 | 1 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0009c0019t0001 | 0/0 | 2363 | 5 | 2 | 0 | 0 | 0 | 3 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0009c0022t0001 | 0/0 | 2363 | 3 | 2 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0010c0013t0001 | 0/0 | 2363 | 6 | 5 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0010c0013t0005 | 0/0 | 2363 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0011c0018t0001 | 0/0 | 2363 | 3 | 0 | 2 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0011c0018t0004 | 0/0 | 2363 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0011c0018t0009 | 0/0 | 2363 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0011c0033t0005 | 0/0 | 2363 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0012c0017t0001 | 0/0 | 2363 | 2 | 0 | 0 | 2 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0012c0017t0003 | 0/0 | 2363 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0012c0017t0004 | 0/0 | 2363 | 2 | 0 | 0 | 0 | 0 | 2 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0013c0023t0001 | 0/0 | 2363 | 2 | 1 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0013c0023t0005 | 0/0 | 2363 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0014c0021t0001 | 0/1 | 2363 | 3 | 0 | 2 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0015c0024t0001 | 0/0 | 2363 | 3 | 2 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0016c0040t0002 | 0/0 | 2363 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0016c0041t0002 | 0/0 | 2363 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0017c0026t0001 | 0/0 | 2363 | 2 | 2 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0018c0042t0003 | 0/0 | 2363 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0019c0044t0001 | 0/0 | 2363 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0020c0036t0001 | 0/0 | 2363 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0021c0045t0001 | 0/0 | 2363 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0022c0038t0005 | 0/0 | 2363 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0023c0047t0005 | 0/0 | 2363 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0024c0046t0001 | 0/0 | 2363 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0025c0034t0001 | 0/0 | 2363 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0026c0039t0001 | 0/0 | 2363 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0027c0029t0001 | 0/0 | 2363 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0028c0035t0001 | 0/0 | 2363 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
a0029c0049t0001 | 0/0 | 2363 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | AGTGC others(2358): Show |
chr4 | 177304874 | 177367936 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0001g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0006g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0006g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0006g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0006g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0006g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0001t0006g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0003t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0003t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0003t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0003t0003g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0015t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0015t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0015t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0015t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0015t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0015t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0027t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0027t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0030t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0001c0043t0001g0399 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0378 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0379 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0382 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0383 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0384 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0385 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0386 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0387 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0001g0396 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0003g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0004g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0005g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0005g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0005g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0007g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0008g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0008g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0002t0008g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0008t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0008t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0008t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0008t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0008t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0008t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0008t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0008t0005g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0010t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0010t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0010t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0010t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0010t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0010t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0010t0001g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0010t0005g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0020t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0020t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0020t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0020t0001g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0028t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0028t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0002c0032t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0004t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0004t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0004t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0004t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0004t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0004t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0004t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0004t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0004t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0004t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0004t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0004t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0004t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0004t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0004t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0004t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0004t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0004t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0004t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0004t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0007t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0007t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0007t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0007t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0007t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0007t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0007t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0007t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0007t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0003c0007t0006g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0004c0006t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0004c0006t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0004c0006t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0004c0006t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0004c0006t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0004c0006t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0004c0006t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0004c0006t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0004c0006t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0004c0006t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0004c0006t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0004c0006t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0004c0014t0001g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0004c0014t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0004c0014t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0004c0014t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0004c0048t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0005c0009t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0005c0009t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0005c0009t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0005c0009t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0005c0009t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0005c0009t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0005c0009t0004g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0005c0009t0004g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0005c0016t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0005c0016t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0005c0016t0001g0392 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0005c0016t0004g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0005c0016t0004g0377 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0005c0025t0005g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0005c0025t0011g0398 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0006c0005t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0006c0005t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0006c0005t0003g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0006c0005t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0006c0005t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0006c0005t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0006c0005t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0006c0005t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0006c0005t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0006c0005t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0006c0005t0003g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0006c0005t0003g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0006c0005t0010g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0007c0011t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0007c0011t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0007c0011t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0007c0011t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0007c0011t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0007c0011t0007g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0007c0011t0007g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0007c0011t0007g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0007c0031t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0008c0012t0001g0091 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0008c0012t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0008c0012t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0008c0012t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0008c0012t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0008c0012t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0008c0012t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0008c0037t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0009c0019t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0009c0019t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0009c0019t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0009c0019t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0009c0019t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0009c0022t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0009c0022t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0009c0022t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0010c0013t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0010c0013t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0010c0013t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0010c0013t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0010c0013t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0010c0013t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0010c0013t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0011c0018t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0011c0018t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0011c0018t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0011c0018t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0011c0018t0009g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0011c0033t0005g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0012c0017t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0012c0017t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0012c0017t0003g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0012c0017t0004g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0012c0017t0004g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0013c0023t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0013c0023t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0013c0023t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0014c0021t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0014c0021t0001g0287 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0014c0021t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0015c0024t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0015c0024t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0015c0024t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0016c0040t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0016c0041t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0017c0026t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0017c0026t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0018c0042t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0019c0044t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0020c0036t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0021c0045t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0022c0038t0005g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0023c0047t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0024c0046t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0025c0034t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0026c0039t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0027c0029t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0028c0035t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
a0029c0049t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0003 | c0004 | t0001 | g0005 | EUR | GBR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG00140 | hp2 | a0006 | c0005 | t0003 | g0277 | EUR | GBR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | FIN | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0359 | EUR | FIN | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG00408 | hp1 | a0016 | c0040 | t0002 | g0203 | EAS | CHS | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG00408 | hp2 | a0002 | c0008 | t0001 | g0325 | EAS | CHS | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG00423 | hp1 | a0002 | c0002 | t0004 | g0164 | EAS | CHS | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | CHS | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | CHS | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG00544 | hp2 | a0007 | c0031 | t0001 | g0336 | EAS | CHS | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG00597 | hp1 | a0003 | c0007 | t0001 | g0152 | EAS | CHS | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG00597 | hp2 | a0001 | c0001 | t0006 | g0188 | EAS | CHS | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG00609 | hp1 | a0005 | c0009 | t0004 | g0295 | EAS | CHS | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG00609 | hp2 | a0008 | c0012 | t0002 | g0225 | EAS | CHS | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | CHS | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG00621 | hp2 | a0001 | c0003 | t0001 | g0114 | EAS | CHS | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG00639 | hp2 | a0008 | c0012 | t0002 | g0246 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG00642 | hp1 | a0003 | c0004 | t0001 | g0303 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG00642 | hp2 | a0010 | c0013 | t0001 | g0233 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG00733 | hp1 | a0003 | c0007 | t0001 | g0360 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0147 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0358 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG00735 | hp2 | a0013 | c0023 | t0001 | g0259 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG00738 | hp1 | a0018 | c0042 | t0003 | g0066 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0059 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0026 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG00741 | hp2 | a0008 | c0012 | t0002 | g0262 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01069 | hp1 | a0002 | c0008 | t0001 | g0298 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01069 | hp2 | a0003 | c0004 | t0001 | g0023 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01070 | hp1 | a0002 | c0010 | t0001 | g0029 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01070 | hp2 | a0003 | c0007 | t0001 | g0357 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01071 | hp1 | a0003 | c0004 | t0001 | g0080 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01071 | hp2 | a0002 | c0010 | t0001 | g0055 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01074 | hp1 | a0002 | c0010 | t0001 | g0061 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0375 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0373 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01081 | hp2 | a0011 | c0018 | t0001 | g0302 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0132 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01099 | hp2 | a0014 | c0021 | t0001 | g0342 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01109 | hp1 | a0011 | c0018 | t0001 | g0300 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0086 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0370 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01168 | hp2 | a0012 | c0017 | t0003 | g0294 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0058 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0352 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01175 | hp1 | a0002 | c0010 | t0001 | g0111 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01175 | hp2 | a0001 | c0003 | t0003 | g0364 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0113 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01192 | hp2 | a0003 | c0004 | t0001 | g0005 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01243 | hp2 | a0002 | c0010 | t0001 | g0115 | AMR | PUR | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0097 | AMR | CLM | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0396 | AMR | CLM | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01257 | hp2 | a0019 | c0044 | t0001 | g0256 | AMR | CLM | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0350 | AMR | CLM | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0296 | AMR | CLM | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0110 | AMR | CLM | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | CLM | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | CLM | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | CLM | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01358 | hp2 | a0001 | c0003 | t0001 | g0064 | AMR | CLM | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0098 | AMR | CLM | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0088 | AMR | CLM | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01433 | hp1 | a0006 | c0005 | t0003 | g0275 | AMR | CLM | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01433 | hp2 | a0002 | c0020 | t0001 | g0346 | AMR | CLM | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0365 | AMR | CLM | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0355 | AMR | CLM | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0385 | EUR | IBS | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01515 | hp2 | a0008 | c0037 | t0001 | g0165 | EUR | IBS | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0366 | EUR | IBS | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01516 | hp2 | a0003 | c0004 | t0001 | g0309 | EUR | IBS | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0382 | EUR | IBS | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01517 | hp2 | a0003 | c0004 | t0001 | g0316 | EUR | IBS | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01884 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | ACB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01884 | hp2 | a0009 | c0022 | t0001 | g0354 | AFR | ACB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01891 | hp1 | a0002 | c0002 | t0005 | g0349 | AFR | ACB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01891 | hp2 | a0004 | c0006 | t0004 | g0253 | AFR | ACB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0356 | AMR | PEL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01943 | hp2 | a0002 | c0002 | t0002 | g0245 | AMR | PEL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0043 | AMR | PEL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PEL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01975 | hp2 | a0006 | c0005 | t0003 | g0341 | AMR | PEL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01978 | hp1 | a0002 | c0002 | t0008 | g0374 | AMR | PEL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01978 | hp2 | a0008 | c0012 | t0002 | g0252 | AMR | PEL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01981 | hp1 | a0015 | c0024 | t0001 | g0243 | AMR | PEL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01981 | hp2 | a0002 | c0002 | t0008 | g0081 | AMR | PEL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PEL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01993 | hp2 | a0002 | c0002 | t0008 | g0048 | AMR | PEL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02004 | hp1 | a0014 | c0021 | t0001 | g0278 | AMR | PEL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0035 | AMR | PEL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | KHV | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02027 | hp2 | a0001 | c0015 | t0001 | g0327 | EAS | KHV | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02040 | hp1 | a0007 | c0011 | t0002 | g0214 | EAS | KHV | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02040 | hp2 | a0001 | c0003 | t0001 | g0041 | EAS | KHV | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02055 | hp1 | a0002 | c0028 | t0001 | g0032 | AFR | ACB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02055 | hp2 | a0004 | c0006 | t0005 | g0240 | AFR | ACB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02056 | hp1 | a0005 | c0009 | t0001 | g0318 | EAS | KHV | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02056 | hp2 | a0007 | c0011 | t0002 | g0215 | EAS | KHV | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | KHV | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02074 | hp1 | a0016 | c0041 | t0002 | g0194 | EAS | KHV | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02074 | hp2 | a0002 | c0002 | t0004 | g0137 | EAS | KHV | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02080 | hp1 | a0005 | c0009 | t0004 | g0323 | EAS | KHV | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | KHV | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | KHV | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02132 | hp1 | a0001 | c0003 | t0001 | g0104 | EAS | KHV | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02132 | hp2 | a0020 | c0036 | t0001 | g0011 | EAS | KHV | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0371 | EAS | KHV | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | KHV | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | CDX | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CDX | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02257 | hp1 | a0002 | c0002 | t0003 | g0057 | AFR | ACB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0368 | AFR | ACB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0020 | AFR | ACB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02273 | hp1 | a0002 | c0002 | t0003 | g0351 | AMR | PEL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02273 | hp2 | a0006 | c0005 | t0003 | g0288 | AMR | PEL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0367 | AMR | PEL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0173 | AMR | PEL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02451 | hp1 | a0021 | c0045 | t0001 | g0255 | AFR | ACB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02451 | hp2 | a0004 | c0006 | t0001 | g0241 | AFR | ACB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02523 | hp2 | a0001 | c0027 | t0001 | g0100 | EAS | KHV | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02572 | hp1 | a0004 | c0014 | t0001 | g0184 | AFR | GWD | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02572 | hp2 | a0005 | c0025 | t0005 | g0320 | AFR | GWD | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0386 | SAS | PJL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0082 | SAS | PJL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02622 | hp1 | a0001 | c0043 | t0001 | g0399 | AFR | GWD | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02622 | hp2 | a0004 | c0014 | t0001 | g0234 | AFR | GWD | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02630 | hp1 | a0002 | c0010 | t0001 | g0343 | AFR | GWD | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02630 | hp2 | a0010 | c0013 | t0001 | g0265 | AFR | GWD | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02683 | hp1 | a0006 | c0005 | t0003 | g0273 | SAS | PJL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0169 | SAS | PJL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0379 | SAS | PJL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02717 | hp2 | a0010 | c0013 | t0005 | g0297 | AFR | GWD | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02723 | hp1 | a0004 | c0006 | t0005 | g0242 | AFR | GWD | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0389 | AFR | GWD | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0384 | SAS | PJL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0019 | SAS | PJL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02738 | hp2 | a0003 | c0007 | t0003 | g0156 | SAS | PJL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02809 | hp1 | a0004 | c0006 | t0001 | g0268 | AFR | GWD | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02809 | hp2 | a0004 | c0014 | t0001 | g0001 | AFR | GWD | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02895 | hp1 | a0022 | c0038 | t0005 | g0388 | AFR | GWD | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02895 | hp2 | a0004 | c0014 | t0001 | g0001 | AFR | GWD | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02896 | hp1 | a0010 | c0013 | t0001 | g0266 | AFR | GWD | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02896 | hp2 | a0004 | c0014 | t0001 | g0001 | AFR | GWD | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02897 | hp1 | a0004 | c0014 | t0001 | g0001 | AFR | GWD | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02897 | hp2 | a0010 | c0013 | t0001 | g0185 | AFR | GWD | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02922 | hp1 | a0015 | c0024 | t0001 | g0238 | AFR | ESN | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02922 | hp2 | a0004 | c0006 | t0005 | g0231 | AFR | ESN | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02965 | hp2 | a0015 | c0024 | t0001 | g0232 | AFR | ESN | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02970 | hp1 | a0002 | c0002 | t0005 | g0347 | AFR | ESN | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02976 | hp1 | a0007 | c0011 | t0001 | g0093 | AFR | ESN | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02976 | hp2 | a0002 | c0010 | t0005 | g0380 | AFR | ESN | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0153 | SAS | PJL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03017 | hp2 | a0009 | c0019 | t0001 | g0157 | SAS | PJL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03041 | hp1 | a0002 | c0002 | t0003 | g0030 | AFR | GWD | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03041 | hp2 | a0004 | c0048 | t0005 | g0236 | AFR | GWD | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03098 | hp2 | a0002 | c0032 | t0001 | g0306 | AFR | MSL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03130 | hp2 | a0002 | c0020 | t0001 | g0170 | AFR | ESN | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03139 | hp2 | a0017 | c0026 | t0001 | g0307 | AFR | ESN | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03195 | hp1 | a0013 | c0023 | t0001 | g0257 | AFR | ESN | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03195 | hp2 | a0004 | c0006 | t0006 | g0189 | AFR | ESN | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03209 | hp1 | a0002 | c0020 | t0001 | g0372 | AFR | MSL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03209 | hp2 | a0009 | c0019 | t0001 | g0056 | AFR | MSL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03225 | hp1 | a0006 | c0005 | t0003 | g0283 | AFR | MSL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03225 | hp2 | a0004 | c0006 | t0001 | g0263 | AFR | MSL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03239 | hp1 | a0003 | c0004 | t0001 | g0317 | SAS | PJL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0146 | SAS | PJL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03453 | hp1 | a0023 | c0047 | t0005 | g0258 | AFR | MSL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03453 | hp2 | a0002 | c0028 | t0001 | g0034 | AFR | MSL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03486 | hp1 | a0004 | c0006 | t0005 | g0239 | AFR | MSL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03486 | hp2 | a0024 | c0046 | t0001 | g0260 | AFR | MSL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03491 | hp1 | a0005 | c0016 | t0004 | g0007 | SAS | PJL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03491 | hp2 | a0002 | c0008 | t0001 | g0328 | SAS | PJL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03492 | hp1 | a0005 | c0016 | t0004 | g0007 | SAS | PJL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03516 | hp1 | a0002 | c0002 | t0005 | g0348 | AFR | ESN | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03516 | hp2 | a0017 | c0026 | t0001 | g0301 | AFR | ESN | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03540 | hp1 | a0002 | c0008 | t0001 | g0339 | AFR | GWD | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03540 | hp2 | a0001 | c0001 | t0005 | g0070 | AFR | GWD | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0344 | AFR | MSL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03654 | hp1 | a0012 | c0017 | t0004 | g0270 | SAS | PJL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0125 | SAS | PJL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0345 | SAS | PJL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03669 | hp2 | a0009 | c0022 | t0001 | g0168 | SAS | PJL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03688 | hp1 | a0005 | c0016 | t0004 | g0377 | SAS | STU | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | STU | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0009 | SAS | PJL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03704 | hp2 | a0005 | c0016 | t0001 | g0392 | SAS | PJL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0376 | SAS | PJL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03831 | hp1 | a0003 | c0004 | t0001 | g0310 | SAS | BEB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0387 | SAS | BEB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03834 | hp1 | a0003 | c0004 | t0001 | g0319 | SAS | BEB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03834 | hp2 | a0001 | c0003 | t0001 | g0073 | SAS | BEB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0045 | SAS | BEB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03927 | hp2 | a0009 | c0019 | t0001 | g0015 | SAS | BEB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03942 | hp1 | a0001 | c0003 | t0001 | g0112 | SAS | BEB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0053 | SAS | BEB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0018 | SAS | STU | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG04115 | hp2 | a0025 | c0034 | t0001 | g0154 | SAS | STU | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG04184 | hp1 | a0009 | c0019 | t0001 | g0085 | SAS | BEB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG04184 | hp2 | a0007 | c0011 | t0002 | g0216 | SAS | BEB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG04199 | hp1 | a0012 | c0017 | t0004 | g0274 | SAS | STU | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG04199 | hp2 | a0001 | c0003 | t0001 | g0069 | SAS | STU | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0378 | SAS | STU | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG04204 | hp2 | a0026 | c0039 | t0001 | g0117 | SAS | STU | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | STU | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG04228 | hp2 | a0003 | c0004 | t0001 | g0312 | SAS | STU | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18522 | hp1 | a0002 | c0008 | t0005 | g0338 | AFR | YRI | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18522 | hp2 | a0002 | c0010 | t0001 | g0381 | AFR | YRI | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18747 | hp1 | a0003 | c0004 | t0001 | g0329 | EAS | CHB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18747 | hp2 | a0027 | c0029 | t0001 | g0326 | EAS | CHB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18939 | hp1 | a0001 | c0015 | t0001 | g0292 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18939 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18940 | hp2 | a0003 | c0004 | t0001 | g0330 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18943 | hp1 | a0006 | c0005 | t0003 | g0280 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0362 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18946 | hp2 | a0001 | c0001 | t0006 | g0180 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18947 | hp1 | a0002 | c0002 | t0004 | g0077 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18948 | hp2 | a0007 | c0011 | t0007 | g0220 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18949 | hp1 | a0001 | c0003 | t0001 | g0159 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18949 | hp2 | a0005 | c0009 | t0001 | g0315 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18950 | hp1 | a0001 | c0001 | t0004 | g0200 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18950 | hp2 | a0001 | c0015 | t0001 | g0289 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18951 | hp1 | a0005 | c0009 | t0004 | g0324 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18952 | hp1 | a0002 | c0002 | t0004 | g0078 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18954 | hp1 | a0008 | c0012 | t0002 | g0204 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18956 | hp1 | a0005 | c0009 | t0004 | g0305 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18959 | hp1 | a0028 | c0035 | t0001 | g0187 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18960 | hp1 | a0003 | c0004 | t0001 | g0006 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18960 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0369 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18962 | hp1 | a0003 | c0007 | t0002 | g0226 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0395 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18965 | hp2 | a0011 | c0018 | t0009 | g0279 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18966 | hp1 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18968 | hp2 | a0007 | c0011 | t0007 | g0219 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18969 | hp1 | a0002 | c0002 | t0007 | g0186 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18971 | hp2 | a0002 | c0008 | t0001 | g0313 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18974 | hp2 | a0001 | c0003 | t0001 | g0042 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18975 | hp2 | a0003 | c0004 | t0001 | g0332 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18977 | hp1 | a0002 | c0008 | t0001 | g0304 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18977 | hp2 | a0001 | c0003 | t0001 | g0134 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18979 | hp1 | a0012 | c0017 | t0001 | g0271 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18979 | hp2 | a0001 | c0003 | t0001 | g0106 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0363 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18986 | hp2 | a0002 | c0008 | t0001 | g0340 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18987 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18987 | hp2 | a0003 | c0004 | t0001 | g0006 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18989 | hp1 | a0001 | c0015 | t0001 | g0293 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18993 | hp1 | a0001 | c0027 | t0001 | g0017 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18994 | hp2 | a0001 | c0003 | t0001 | g0024 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0394 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18999 | hp2 | a0007 | c0011 | t0007 | g0175 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19000 | hp2 | a0003 | c0004 | t0001 | g0334 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19002 | hp1 | a0003 | c0007 | t0002 | g0230 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19002 | hp2 | a0001 | c0003 | t0001 | g0158 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19003 | hp1 | a0001 | c0030 | t0001 | g0337 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19003 | hp2 | a0006 | c0005 | t0003 | g0281 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19005 | hp1 | a0006 | c0005 | t0003 | g0284 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19005 | hp2 | a0003 | c0004 | t0001 | g0321 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19006 | hp1 | a0006 | c0005 | t0003 | g0397 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19007 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19009 | hp1 | a0001 | c0001 | t0006 | g0223 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19009 | hp2 | a0003 | c0004 | t0001 | g0331 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19011 | hp1 | a0001 | c0003 | t0001 | g0040 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0361 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19012 | hp1 | a0003 | c0007 | t0001 | g0075 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19030 | hp1 | a0010 | c0013 | t0001 | g0267 | AFR | LWK | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19030 | hp2 | a0011 | c0033 | t0005 | g0299 | AFR | LWK | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19043 | hp1 | a0004 | c0006 | t0001 | g0183 | AFR | LWK | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19043 | hp2 | a0029 | c0049 | t0001 | g0237 | AFR | LWK | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19056 | hp1 | a0006 | c0005 | t0010 | g0285 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19056 | hp2 | a0003 | c0007 | t0001 | g0122 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19057 | hp2 | a0001 | c0015 | t0001 | g0290 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19058 | hp1 | a0003 | c0007 | t0006 | g0192 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19058 | hp2 | a0001 | c0001 | t0006 | g0177 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19060 | hp1 | a0005 | c0009 | t0004 | g0314 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19062 | hp1 | a0002 | c0002 | t0004 | g0163 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19063 | hp1 | a0003 | c0007 | t0002 | g0224 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0393 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19066 | hp1 | a0006 | c0005 | t0003 | g0276 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19066 | hp2 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19068 | hp1 | a0005 | c0016 | t0001 | g0120 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19068 | hp2 | a0001 | c0001 | t0006 | g0181 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19072 | hp2 | a0012 | c0017 | t0001 | g0286 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0390 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19077 | hp2 | a0003 | c0004 | t0001 | g0335 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19078 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19079 | hp2 | a0001 | c0003 | t0001 | g0102 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19080 | hp1 | a0001 | c0003 | t0002 | g0213 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19080 | hp2 | a0005 | c0016 | t0001 | g0012 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19081 | hp1 | a0011 | c0018 | t0004 | g0282 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19081 | hp2 | a0001 | c0003 | t0001 | g0028 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19082 | hp1 | a0003 | c0004 | t0001 | g0333 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19082 | hp2 | a0001 | c0003 | t0001 | g0105 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19085 | hp1 | a0005 | c0009 | t0004 | g0322 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19086 | hp2 | a0001 | c0001 | t0006 | g0197 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19087 | hp1 | a0001 | c0003 | t0001 | g0108 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19088 | hp1 | a0002 | c0002 | t0004 | g0162 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19088 | hp2 | a0002 | c0002 | t0004 | g0044 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0391 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19091 | hp2 | a0007 | c0011 | t0001 | g0167 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | YRI | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA20129 | hp1 | a0009 | c0019 | t0001 | g0072 | AFR | ASW | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA20129 | hp2 | a0010 | c0013 | t0001 | g0264 | AFR | ASW | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0063 | EUR | TSI | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA20752 | hp2 | a0001 | c0003 | t0001 | g0118 | EUR | TSI | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0383 | EUR | TSI | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0211 | EUR | TSI | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA20905 | hp1 | a0011 | c0018 | t0001 | g0308 | SAS | GIH | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA20905 | hp2 | a0003 | c0004 | t0001 | g0311 | SAS | GIH | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0060 | AMR | CLM | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | ACB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02109 | hp2 | a0006 | c0005 | t0001 | g0272 | AFR | ACB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02486 | hp1 | a0005 | c0025 | t0011 | g0398 | AFR | ACB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02486 | hp2 | a0002 | c0002 | t0003 | g0084 | AFR | ACB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02559 | hp1 | a0009 | c0022 | t0001 | g0353 | AFR | ACB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0144 | AFR | ACB | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | MSL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG03471 | hp2 | a0004 | c0014 | t0001 | g0235 | AFR | MSL | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG06807 | hp1 | a0004 | c0006 | t0001 | g0244 | AFR | USA | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
HG06807 | hp2 | a0004 | c0006 | t0001 | g0254 | AFR | USA | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18955 | hp1 | a0001 | c0015 | t0001 | g0291 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA18955 | hp2 | a0002 | c0002 | t0004 | g0151 | EAS | JPT | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA20300 | hp1 | a0008 | c0012 | t0002 | g0251 | AFR | USA | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA20300 | hp2 | a0002 | c0020 | t0001 | g0010 | AFR | USA | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA21309 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | LWK | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
NA21309 | hp2 | a0013 | c0023 | t0005 | g0261 | AFR | LWK | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
homoSapiens | chm13v2 | a0014 | c0021 | t0001 | g0287 | REF | REF | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
homoSapiens | grch38p0 | a0008 | c0012 | t0001 | g0091 | REF | REF | NEIL3_chr4_177304874_177367936 | NEIL3 | chr4 | 177304874 | 177367936 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:177310020 | G | A | 1 | a0025 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.67G>A | p.Ala23Thr | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/10 | 147/2363 | 67/1818 | 23/605 | chr4 | 177310020 | |||
chr4:177310065 | C | T | 9 | a0004 a0010 a0013 others(6): Show |
38 | HG00642.hp2 HG00735.hp2 HG01257.hp2 others(35): Show |
missense_variant | MODERATE | c.112C>T | p.Arg38Cys | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/10 | 192/2363 | 112/1818 | 38/605 | chr4 | 177310065 | |||
chr4:177322528 | G | A | 1 | a0027 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.226G>A | p.Val76Met | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/10 | 306/2363 | 226/1818 | 76/605 | chr4 | 177322528 | |||
chr4:177335759 | C | G | 4 | a0006 a0011 a0012 others(1): Show |
26 | HG00140.hp2 HG01081.hp2 HG01099.hp2 others(23): Show |
missense_variant | MODERATE | c.350C>G | p.Pro117Arg | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 3/10 | 430/2363 | 350/1818 | 117/605 | chr4 | 177335759 | |||
chr4:177336125 | A | C | 1 | a0018 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.431A>C | p.Gln144Pro | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/10 | 511/2363 | 431/1818 | 144/605 | chr4 | 177336125 | |||
chr4:177336134 | T | A | 1 | a0028 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.440T>A | p.Ile147Lys | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/10 | 520/2363 | 440/1818 | 147/605 | chr4 | 177336134 | |||
chr4:177336179 | T | C | 1 | a0020 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.485T>C | p.Phe162Ser | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/10 | 565/2363 | 485/1818 | 162/605 | chr4 | 177336179 | |||
chr4:177336210 | G | C | 5 | a0013 a0019 a0021 others(2): Show |
7 | HG00735.hp2 HG01257.hp2 HG02451.hp1 others(4): Show |
missense_variant | MODERATE | c.516G>C | p.Gln172His | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/10 | 596/2363 | 516/1818 | 172/605 | chr4 | 177336210 | |||
chr4:177336289 | C | G | 1 | a0016 | 2 | HG00408.hp1 HG02074.hp1 |
missense_variant | MODERATE | c.595C>G | p.Leu199Val | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/10 | 675/2363 | 595/1818 | 199/605 | chr4 | 177336289 | |||
chr4:177341630 | A | G | 4 | a0003 a0014 a0026 others(1): Show |
36 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(33): Show |
missense_variant | MODERATE | c.857A>G | p.His286Arg | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/10 | 937/2363 | 857/1818 | 286/605 | chr4 | 177341630 | |||
chr4:177351546 | A | G | 3 | a0005 a0017 a0023 |
19 | HG00609.hp1 HG02056.hp1 HG02080.hp1 others(16): Show |
missense_variant | MODERATE | c.1036A>G | p.Ile346Val | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 7/10 | 1116/2363 | 1036/1818 | 346/605 | chr4 | 177351546 | |||
chr4:177353596 | C | T | 17 | a0002 a0003 a0004 others(14): Show |
212 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(209): Show |
missense_variant | MODERATE | c.1328C>T | p.Pro443Leu | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/10 | 1408/2363 | 1328/1818 | 443/605 | chr4 | 177353596 | |||
chr4:177353681 | A | C | 19 | a0002 a0003 a0004 others(16): Show |
234 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(231): Show |
missense_variant | MODERATE | c.1413A>C | p.Gln471His | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/10 | 1493/2363 | 1413/1818 | 471/605 | chr4 | 177353681 | |||
chr4:177360600 | G | A | 23 | a0001 a0002 a0003 others(20): Show |
384 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(381): Show |
missense_variant | MODERATE | c.1558G>A | p.Gly520Arg | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 9/10 | 1638/2363 | 1558/1818 | 520/605 | chr4 | 177360600 | |||
chr4:177362320 | A | G | 2 | a0021 a0029 |
2 | HG02451.hp1 NA19043.hp2 |
missense_variant | MODERATE | c.1667A>G | p.His556Arg | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 10/10 | 1747/2363 | 1667/1818 | 556/605 | chr4 | 177362320 | |||
chr4:177362416 | A | G | 1 | a0022 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.1763A>G | p.Asn588Ser | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 10/10 | 1843/2363 | 1763/1818 | 588/605 | chr4 | 177362416 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:177309998 | C | A | 15 | a0001c0015 a0001c0030 a0002c0008 others(12): Show |
78 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(75): Show |
synonymous_variant | LOW | c.45C>A | p.Arg15Arg | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/10 | 125/2363 | 45/1818 | 15/605 | chr4 | 177309998 | |||
chr4:177322485 | C | T | 1 | a0001c0043 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.183C>T | p.Ser61Ser | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/10 | 263/2363 | 183/1818 | 61/605 | chr4 | 177322485 | |||
chr4:177341490 | A | T | 1 | a0002c0028 | 2 | HG02055.hp1 HG03453.hp2 |
synonymous_variant | LOW | c.717A>T | p.Gly239Gly | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/10 | 797/2363 | 717/1818 | 239/605 | chr4 | 177341490 | |||
chr4:177341529 | T | C | 10 | a0001c0003 a0001c0027 a0001c0030 others(7): Show |
42 | HG00408.hp1 HG00621.hp2 HG01070.hp1 others(39): Show |
synonymous_variant | LOW | c.756T>C | p.Pro252Pro | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/10 | 836/2363 | 756/1818 | 252/605 | chr4 | 177341529 | |||
chr4:177351389 | G | A | 1 | a0001c0027 | 2 | HG02523.hp2 NA18993.hp1 |
synonymous_variant | LOW | c.879G>A | p.Pro293Pro | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 7/10 | 959/2363 | 879/1818 | 293/605 | chr4 | 177351389 | |||
chr4:177353411 | A | G | 29 | a0002c0002 a0002c0008 a0002c0010 others(26): Show |
212 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(209): Show |
synonymous_variant | LOW | c.1143A>G | p.Arg381Arg | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/10 | 1223/2363 | 1143/1818 | 381/605 | chr4 | 177353411 | |||
chr4:177353540 | T | G | 22 | a0002c0002 a0002c0008 a0002c0010 others(19): Show |
194 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(191): Show |
synonymous_variant | LOW | c.1272T>G | p.Val424Val | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/10 | 1352/2363 | 1272/1818 | 424/605 | chr4 | 177353540 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:177309917 | G | A | 13 | a0001c0001t0002 a0001c0001t0006 a0001c0003t0002 others(10): Show |
61 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(58): Show |
5_prime_UTR_variant | MODIFIER | c.-37G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/10 | 37 | chr4 | 177309917 | ||||||
chr4:177362554 | ATATC | A | 1 | a0002c0002t0008 | 3 | HG01978.hp1 HG01981.hp2 HG01993.hp2 |
3_prime_UTR_variant | MODIFIER | c.*87_*90delCTAT | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 10/10 | 87 | INFO_REALIGN_3_PRIME | chr4 | 177362554 | |||||
chr4:177362603 | T | C | 9 | a0001c0001t0003 a0001c0003t0003 a0002c0002t0003 others(6): Show |
29 | HG00140.hp2 HG00733.hp2 HG00738.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*132T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 10/10 | 132 | chr4 | 177362603 | ||||||
chr4:177362644 | C | G | 32 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(29): Show |
80 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*173C>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 10/10 | 173 | chr4 | 177362644 | ||||||
chr4:177362733 | G | A | 1 | a0011c0018t0009 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*262G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 10/10 | 262 | chr4 | 177362733 | ||||||
chr4:177362790 | T | C | 4 | a0009c0019t0001 a0011c0018t0001 a0015c0024t0001 others(1): Show |
6 | HG01081.hp2 HG01109.hp1 HG01981.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*319T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 10/10 | 319 | chr4 | 177362790 | ||||||
chr4:177362813 | C | T | 21 | a0001c0001t0003 a0001c0001t0005 a0001c0003t0003 others(18): Show |
47 | HG00140.hp2 HG00733.hp2 HG00738.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*342C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 10/10 | 342 | chr4 | 177362813 | ||||||
chr4:177362842 | T | C | 1 | a0006c0005t0010 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*371T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 10/10 | 371 | chr4 | 177362842 | ||||||
chr4:177362843 | A | G | 1 | a0005c0025t0011 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*372A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 10/10 | 372 | chr4 | 177362843 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:177310222 | G | A | 1 | a0001c0001t0005g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.156+113G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177310222 | |||||||
chr4:177310229 | C | G | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.156+120C>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177310229 | |||||||
chr4:177310307 | G | A | 1 | a0002c0002t0001g0009 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.156+198G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177310307 | |||||||
chr4:177310308 | C | A | 1 | a0002c0002t0001g0009 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.156+199C>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177310308 | |||||||
chr4:177310358 | A | G | 1 | a0005c0025t0011g0398 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.156+249A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177310358 | |||||||
chr4:177310382 | C | G | 234 | a0001c0001t0001g0174 a0001c0001t0001g0193 a0001c0001t0001g0201 others(231): Show |
240 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.156+273C>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177310382 | |||||||
chr4:177310472 | T | C | 1 | a0002c0020t0001g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.156+363T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177310472 | |||||||
chr4:177310534 | G | A | 1 | a0002c0020t0001g0010 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.156+425G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177310534 | |||||||
chr4:177310802 | C | T | 1 | a0006c0005t0003g0397 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.156+693C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177310802 | |||||||
chr4:177310872 | G | A | 1 | a0002c0020t0001g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.156+763G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177310872 | |||||||
chr4:177310920 | T | C | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.156+811T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177310920 | |||||||
chr4:177311060 | G | A | 1 | a0001c0001t0002g0171 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.156+951G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177311060 | |||||||
chr4:177311190 | A | G | 2 | a0002c0002t0001g0169 a0009c0022t0001g0168 |
2 | HG02683.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.156+1081A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177311190 | |||||||
chr4:177311206 | G | C | 103 | a0001c0001t0001g0174 a0001c0001t0001g0193 a0001c0001t0001g0201 others(100): Show |
106 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.156+1097G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177311206 | |||||||
chr4:177311326 | C | T | 1 | a0001c0001t0002g0269 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.156+1217C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177311326 | |||||||
chr4:177311589 | G | A | 1 | a0002c0020t0001g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.156+1480G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177311589 | |||||||
chr4:177311604 | G | T | 1 | a0002c0020t0001g0010 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.156+1495G>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177311604 | |||||||
chr4:177311641 | C | T | 151 | a0001c0001t0001g0193 a0001c0001t0001g0201 a0001c0001t0001g0344 others(148): Show |
155 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.156+1532C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177311641 | |||||||
chr4:177311674 | C | CA | 12 | a0001c0001t0001g0344 a0001c0001t0001g0345 a0001c0027t0001g0017 others(9): Show |
13 | HG01346.hp2 HG01884.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.156+1586dupA | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177311674 | ||||||
chr4:177311674 | CA | C | 98 | a0001c0001t0001g0166 a0001c0001t0001g0193 a0001c0001t0001g0201 others(95): Show |
101 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.156+1586delA | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177311674 | ||||||
chr4:177311759 | A | T | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.156+1650A>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177311759 | |||||||
chr4:177311832 | A | G | 8 | a0001c0001t0001g0345 a0001c0001t0001g0394 a0002c0002t0001g0390 others(5): Show |
9 | HG03491.hp1 HG03492.hp1 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+1723A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177311832 | |||||||
chr4:177311978 | G | A | 1 | a0002c0002t0001g0009 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.156+1869G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177311978 | |||||||
chr4:177312200 | G | A | 1 | a0002c0002t0007g0186 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.156+2091G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177312200 | |||||||
chr4:177312341 | A | T | 3 | a0002c0002t0004g0162 a0002c0002t0004g0163 a0002c0002t0004g0164 |
3 | HG00423.hp1 NA19062.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.156+2232A>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177312341 | |||||||
chr4:177312439 | T | C | 1 | a0002c0002t0001g0020 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.156+2330T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177312439 | |||||||
chr4:177312551 | T | C | 2 | a0002c0002t0001g0009 a0002c0020t0001g0010 |
2 | HG03704.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.156+2442T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177312551 | |||||||
chr4:177312588 | T | G | 1 | a0002c0020t0001g0346 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.156+2479T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177312588 | |||||||
chr4:177312591 | G | A | 27 | a0001c0015t0001g0289 a0001c0015t0001g0290 a0001c0015t0001g0291 others(24): Show |
27 | HG00140.hp2 HG01099.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.156+2482G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177312591 | |||||||
chr4:177312591 | G | T | 96 | a0001c0001t0001g0193 a0001c0001t0001g0201 a0001c0001t0002g0171 others(93): Show |
99 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.156+2482G>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177312591 | |||||||
chr4:177312865 | G | GA | 10 | a0001c0001t0001g0345 a0001c0001t0001g0394 a0002c0002t0001g0390 others(7): Show |
11 | HG00609.hp1 HG03491.hp1 HG03492.hp1 others(8): Show |
intron_variant | MODIFIER | c.156+2766dupA | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177312865 | ||||||
chr4:177313010 | C | A | 1 | a0005c0025t0011g0398 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.156+2901C>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177313010 | |||||||
chr4:177313030 | G | T | 72 | a0001c0015t0001g0289 a0001c0015t0001g0290 a0001c0015t0001g0291 others(69): Show |
74 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.156+2921G>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177313030 | |||||||
chr4:177313075 | T | A | 1 | a0008c0037t0001g0165 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.156+2966T>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177313075 | |||||||
chr4:177313081 | C | T | 2 | a0012c0017t0003g0294 a0014c0021t0001g0342 |
2 | HG01099.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.156+2972C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177313081 | |||||||
chr4:177313138 | A | G | 6 | a0004c0006t0001g0268 a0010c0013t0001g0185 a0010c0013t0001g0264 others(3): Show |
6 | HG02630.hp2 HG02809.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.156+3029A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177313138 | |||||||
chr4:177313259 | T | G | 48 | a0001c0001t0001g0344 a0001c0001t0001g0356 a0001c0001t0001g0366 others(45): Show |
48 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.156+3150T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177313259 | |||||||
chr4:177313447 | A | G | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.156+3338A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177313447 | |||||||
chr4:177313514 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.156+3405G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177313514 | |||||||
chr4:177313673 | T | C | 8 | a0001c0001t0001g0345 a0001c0001t0001g0394 a0002c0002t0001g0390 others(5): Show |
9 | HG03491.hp1 HG03492.hp1 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+3564T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177313673 | |||||||
chr4:177313701 | T | C | 1 | a0002c0020t0001g0010 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.156+3592T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177313701 | |||||||
chr4:177313846 | G | A | 1 | a0002c0020t0001g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.156+3737G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177313846 | |||||||
chr4:177313974 | A | G | 1 | a0004c0006t0001g0263 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.156+3865A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177313974 | |||||||
chr4:177314155 | C | T | 1 | a0008c0012t0002g0262 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.156+4046C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177314155 | |||||||
chr4:177314180 | A | C | 238 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(235): Show |
244 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.156+4071A>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177314180 | |||||||
chr4:177314222 | C | T | 8 | a0004c0006t0001g0263 a0013c0023t0001g0257 a0013c0023t0001g0259 others(5): Show |
8 | HG00735.hp2 HG01257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.156+4113C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177314222 | |||||||
chr4:177314232 | A | T | 47 | a0001c0001t0001g0344 a0001c0001t0001g0356 a0001c0001t0001g0366 others(44): Show |
47 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.156+4123A>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177314232 | |||||||
chr4:177314364 | A | T | 2 | a0004c0006t0001g0254 a0004c0006t0004g0253 |
2 | HG01891.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.156+4255A>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177314364 | |||||||
chr4:177314584 | G | C | 1 | a0002c0002t0001g0009 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.156+4475G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177314584 | |||||||
chr4:177314612 | A | G | 2 | a0001c0003t0001g0158 a0001c0003t0001g0159 |
2 | NA18949.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.156+4503A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177314612 | |||||||
chr4:177314736 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.156+4627A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177314736 | |||||||
chr4:177314769 | G | C | 6 | a0013c0023t0001g0257 a0013c0023t0001g0259 a0019c0044t0001g0256 others(3): Show |
6 | HG00735.hp2 HG01257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.156+4660G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177314769 | |||||||
chr4:177314799 | C | T | 2 | a0002c0002t0001g0009 a0002c0020t0001g0010 |
2 | HG03704.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.156+4690C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177314799 | |||||||
chr4:177314805 | C | G | 2 | a0002c0008t0001g0339 a0002c0008t0005g0338 |
2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.156+4696C>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177314805 | |||||||
chr4:177314806 | G | A | 8 | a0001c0001t0001g0345 a0001c0001t0001g0394 a0002c0002t0001g0390 others(5): Show |
9 | HG03491.hp1 HG03492.hp1 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+4697G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177314806 | |||||||
chr4:177314933 | T | TGGGCGTG others(1): Show |
235 | a0001c0001t0001g0174 a0001c0001t0001g0193 a0001c0001t0001g0201 others(232): Show |
241 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.156+4824_156+4825i others(10): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177314933 | |||||||
chr4:177315000 | T | C | 1 | a0002c0002t0001g0009 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.156+4891T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177315000 | |||||||
chr4:177315015 | G | C | 1 | a0002c0020t0001g0010 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.156+4906G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177315015 | |||||||
chr4:177315030 | C | T | 1 | a0009c0019t0001g0157 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.156+4921C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177315030 | |||||||
chr4:177315048 | A | G | 8 | a0001c0001t0001g0345 a0001c0001t0001g0394 a0002c0002t0001g0390 others(5): Show |
9 | HG03491.hp1 HG03492.hp1 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+4939A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177315048 | |||||||
chr4:177315068 | C | CA | 30 | a0001c0001t0001g0027 a0001c0003t0001g0024 a0001c0003t0001g0158 others(27): Show |
30 | HG00140.hp2 HG00642.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.156+4980dupA | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177315068 | ||||||
chr4:177315068 | C | CAA | 6 | a0006c0005t0001g0272 a0006c0005t0003g0273 a0011c0033t0005g0299 others(3): Show |
6 | HG02109.hp2 HG02683.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.156+4979_156+4980d others(4): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177315068 | ||||||
chr4:177315068 | CA | C | 75 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0123 others(72): Show |
76 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.156+4980delA | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177315068 | ||||||
chr4:177315068 | CAA | C | 51 | a0001c0001t0001g0344 a0001c0001t0001g0345 a0001c0001t0001g0356 others(48): Show |
52 | HG00323.hp2 HG00597.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.156+4979_156+4980d others(4): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177315068 | ||||||
chr4:177315068 | CAAA | C | 74 | a0001c0001t0001g0174 a0001c0001t0001g0193 a0001c0001t0001g0201 others(71): Show |
74 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.156+4978_156+4980d others(5): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177315068 | ||||||
chr4:177315068 | CAAAA | C | 33 | a0001c0001t0002g0247 a0001c0001t0002g0248 a0001c0001t0002g0249 others(30): Show |
36 | HG00639.hp2 HG00642.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.156+4977_156+4980d others(6): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177315068 | ||||||
chr4:177315084 | A | C | 1 | a0002c0020t0001g0010 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.156+4975A>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177315084 | |||||||
chr4:177315102 | C | T | 104 | a0001c0001t0001g0174 a0001c0001t0001g0193 a0001c0001t0001g0201 others(101): Show |
107 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.156+4993C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177315102 | |||||||
chr4:177315109 | G | C | 26 | a0001c0001t0005g0008 a0004c0006t0001g0183 a0004c0006t0001g0241 others(23): Show |
29 | HG00642.hp2 HG01891.hp2 HG01981.hp1 others(26): Show |
intron_variant | MODIFIER | c.156+5000G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177315109 | |||||||
chr4:177315248 | T | C | 109 | a0001c0001t0001g0174 a0001c0001t0001g0193 a0001c0001t0001g0201 others(106): Show |
112 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.156+5139T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177315248 | |||||||
chr4:177315381 | A | T | 1 | a0002c0020t0001g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.156+5272A>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177315381 | |||||||
chr4:177315448 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.156+5339A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177315448 | |||||||
chr4:177315557 | T | C | 1 | a0021c0045t0001g0255 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.156+5448T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177315557 | |||||||
chr4:177315618 | G | A | 1 | a0002c0002t0001g0009 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.156+5509G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177315618 | |||||||
chr4:177315621 | A | T | 26 | a0001c0001t0005g0008 a0004c0006t0001g0183 a0004c0006t0001g0241 others(23): Show |
29 | HG00642.hp2 HG01891.hp2 HG01981.hp1 others(26): Show |
intron_variant | MODIFIER | c.156+5512A>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177315621 | |||||||
chr4:177315742 | T | G | 113 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(110): Show |
116 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.156+5633T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177315742 | |||||||
chr4:177315946 | T | A | 1 | a0005c0009t0004g0305 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.156+5837T>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177315946 | |||||||
chr4:177315963 | C | T | 1 | a0002c0002t0001g0020 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.156+5854C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177315963 | |||||||
chr4:177316499 | G | T | 1 | a0006c0005t0003g0288 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.157-5960G>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177316499 | |||||||
chr4:177316683 | A | G | 1 | a0002c0010t0001g0115 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.157-5776A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177316683 | |||||||
chr4:177316777 | G | A | 1 | a0026c0039t0001g0117 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.157-5682G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177316777 | |||||||
chr4:177316783 | C | G | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.157-5676C>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177316783 | |||||||
chr4:177316802 | A | C | 2 | a0004c0006t0001g0254 a0004c0006t0004g0253 |
2 | HG01891.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.157-5657A>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177316802 | |||||||
chr4:177316864 | C | G | 39 | a0001c0015t0001g0327 a0001c0030t0001g0337 a0002c0008t0001g0304 others(36): Show |
41 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.157-5595C>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177316864 | |||||||
chr4:177316983 | G | A | 1 | a0009c0019t0001g0157 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.157-5476G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177316983 | |||||||
chr4:177317099 | T | C | 8 | a0004c0006t0001g0183 a0013c0023t0001g0257 a0013c0023t0001g0259 others(5): Show |
8 | HG00735.hp2 HG01257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.157-5360T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177317099 | |||||||
chr4:177317108 | A | G | 3 | a0001c0001t0001g0344 a0001c0001t0001g0389 a0022c0038t0005g0388 |
3 | HG02723.hp2 HG02895.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.157-5351A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177317108 | |||||||
chr4:177317176 | G | A | 11 | a0004c0006t0005g0231 a0004c0006t0005g0239 a0004c0014t0001g0001 others(8): Show |
14 | HG00642.hp2 HG02572.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.157-5283G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177317176 | |||||||
chr4:177317363 | A | G | 1 | a0011c0018t0001g0302 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.157-5096A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177317363 | |||||||
chr4:177317420 | G | A | 2 | a0001c0001t0001g0356 a0002c0002t0001g0355 |
2 | HG01496.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.157-5039G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177317420 | |||||||
chr4:177317479 | G | A | 1 | a0009c0022t0001g0168 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.157-4980G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177317479 | |||||||
chr4:177317508 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.157-4951C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177317508 | |||||||
chr4:177317588 | CTTTCT | C | 31 | a0001c0015t0001g0327 a0001c0030t0001g0337 a0002c0008t0001g0304 others(28): Show |
33 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.157-4862_157-4858d others(7): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177317588 | ||||||
chr4:177317593 | TTTTC | T | 7 | a0002c0008t0001g0340 a0003c0004t0001g0310 a0003c0004t0001g0321 others(4): Show |
7 | HG02080.hp1 HG03831.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.157-4862_157-4859d others(6): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177317593 | ||||||
chr4:177317597 | C | CT | 82 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0002g0171 others(79): Show |
85 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.157-4838dupT | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177317597 | ||||||
chr4:177317597 | C | CTT | 68 | a0001c0001t0001g0027 a0001c0001t0001g0160 a0001c0001t0001g0161 others(65): Show |
68 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.157-4839_157-4838d others(4): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177317597 | ||||||
chr4:177317597 | C | CTTT | 17 | a0001c0001t0002g0222 a0001c0001t0002g0227 a0001c0001t0002g0228 others(14): Show |
17 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.157-4840_157-4838d others(5): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177317597 | ||||||
chr4:177317597 | C | CTTTT | 39 | a0001c0001t0001g0344 a0001c0001t0001g0356 a0001c0001t0001g0366 others(36): Show |
39 | HG01074.hp2 HG01081.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.157-4841_157-4838d others(6): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177317597 | ||||||
chr4:177317597 | C | CTTTTT | 6 | a0002c0002t0001g0382 a0002c0002t0001g0383 a0002c0002t0001g0384 others(3): Show |
6 | HG01515.hp1 HG01517.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.157-4842_157-4838d others(7): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177317597 | ||||||
chr4:177317597 | CT | C | 13 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0119 others(10): Show |
14 | HG01070.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.157-4838delT | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177317597 | ||||||
chr4:177317597 | CTTTTTTT | C | 8 | a0001c0001t0001g0345 a0001c0001t0001g0394 a0002c0002t0001g0390 others(5): Show |
9 | HG03491.hp1 HG03492.hp1 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.157-4844_157-4838d others(9): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177317597 | ||||||
chr4:177317597 | CTTTTTTT others(4): Show |
C | 2 | a0004c0006t0001g0241 a0004c0006t0005g0240 |
2 | HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.157-4848_157-4838d others(13): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177317597 | ||||||
chr4:177317704 | C | T | 3 | a0001c0001t0001g0394 a0002c0002t0001g0393 a0002c0002t0001g0395 |
3 | NA18965.hp1 NA18998.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.157-4755C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177317704 | |||||||
chr4:177317787 | A | C | 4 | a0001c0001t0001g0099 a0002c0002t0001g0097 a0002c0002t0001g0098 others(1): Show |
4 | HG01192.hp1 HG01255.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.157-4672A>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177317787 | |||||||
chr4:177317975 | C | G | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.157-4484C>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177317975 | |||||||
chr4:177318059 | G | A | 1 | a0011c0018t0001g0300 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.157-4400G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177318059 | |||||||
chr4:177318196 | A | G | 1 | a0008c0012t0002g0262 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.157-4263A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177318196 | |||||||
chr4:177318270 | G | T | 1 | a0002c0020t0001g0010 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.157-4189G>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177318270 | |||||||
chr4:177318323 | T | C | 67 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0193 others(64): Show |
67 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.157-4136T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177318323 | |||||||
chr4:177318373 | CA | C | 33 | a0001c0001t0005g0008 a0004c0006t0001g0183 a0004c0006t0001g0241 others(30): Show |
36 | HG00642.hp2 HG00735.hp2 HG01257.hp2 others(33): Show |
intron_variant | MODIFIER | c.157-4080delA | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177318373 | ||||||
chr4:177318463 | C | T | 5 | a0001c0015t0001g0289 a0001c0015t0001g0290 a0001c0015t0001g0291 others(2): Show |
5 | NA18939.hp1 NA18950.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.157-3996C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177318463 | |||||||
chr4:177318519 | G | A | 3 | a0002c0002t0001g0361 a0002c0002t0001g0362 a0002c0002t0001g0363 |
3 | NA18944.hp2 NA18983.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.157-3940G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177318519 | |||||||
chr4:177318546 | A | C | 1 | a0004c0006t0001g0244 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.157-3913A>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177318546 | |||||||
chr4:177318635 | A | G | 112 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(109): Show |
115 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.157-3824A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177318635 | |||||||
chr4:177318766 | A | G | 1 | a0004c0006t0006g0189 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.157-3693A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177318766 | |||||||
chr4:177318791 | G | A | 1 | a0001c0003t0001g0118 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.157-3668G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177318791 | |||||||
chr4:177318844 | C | T | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.157-3615C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177318844 | |||||||
chr4:177319003 | C | T | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.157-3456C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177319003 | |||||||
chr4:177319014 | T | G | 1 | a0001c0001t0002g0222 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.157-3445T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177319014 | |||||||
chr4:177319133 | A | G | 1 | a0008c0012t0002g0251 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.157-3326A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177319133 | |||||||
chr4:177319153 | G | A | 1 | a0002c0002t0001g0035 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.157-3306G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177319153 | |||||||
chr4:177319280 | G | A | 1 | a0004c0006t0001g0244 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.157-3179G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177319280 | |||||||
chr4:177319282 | A | G | 1 | a0004c0006t0001g0244 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.157-3177A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177319282 | |||||||
chr4:177319422 | A | T | 8 | a0001c0001t0001g0345 a0001c0001t0001g0394 a0002c0002t0001g0390 others(5): Show |
9 | HG03491.hp1 HG03492.hp1 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.157-3037A>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177319422 | |||||||
chr4:177319549 | C | A | 39 | a0001c0015t0001g0327 a0001c0030t0001g0337 a0002c0008t0001g0304 others(36): Show |
41 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.157-2910C>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177319549 | |||||||
chr4:177319552 | T | A | 39 | a0001c0015t0001g0327 a0001c0030t0001g0337 a0002c0008t0001g0304 others(36): Show |
41 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.157-2907T>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177319552 | |||||||
chr4:177319726 | C | A | 1 | a0001c0001t0001g0121 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.157-2733C>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177319726 | |||||||
chr4:177319734 | T | C | 25 | a0001c0001t0005g0008 a0004c0006t0001g0241 a0004c0006t0001g0244 others(22): Show |
28 | HG00642.hp2 HG01891.hp2 HG01981.hp1 others(25): Show |
intron_variant | MODIFIER | c.157-2725T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177319734 | |||||||
chr4:177319881 | G | C | 1 | a0026c0039t0001g0117 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.157-2578G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177319881 | |||||||
chr4:177319951 | C | G | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.157-2508C>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177319951 | |||||||
chr4:177320039 | C | G | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.157-2420C>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177320039 | |||||||
chr4:177320097 | G | A | 100 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0193 others(97): Show |
103 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.157-2362G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177320097 | |||||||
chr4:177320169 | C | G | 3 | a0011c0018t0001g0300 a0011c0018t0001g0302 a0011c0018t0001g0308 |
3 | HG01081.hp2 HG01109.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.157-2290C>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177320169 | |||||||
chr4:177320205 | A | G | 185 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0193 others(182): Show |
189 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.157-2254A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177320205 | |||||||
chr4:177320233 | T | C | 3 | a0001c0001t0001g0394 a0002c0002t0001g0393 a0002c0002t0001g0395 |
3 | NA18965.hp1 NA18998.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.157-2226T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177320233 | |||||||
chr4:177320263 | T | G | 6 | a0001c0001t0002g0247 a0001c0001t0002g0248 a0002c0002t0002g0245 others(3): Show |
6 | HG00639.hp2 HG01346.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.157-2196T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177320263 | |||||||
chr4:177320310 | C | T | 65 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0193 others(62): Show |
65 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.157-2149C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177320310 | |||||||
chr4:177320330 | T | C | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.157-2129T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177320330 | |||||||
chr4:177320423 | G | T | 1 | a0002c0002t0001g0009 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.157-2036G>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177320423 | |||||||
chr4:177320461 | GCTGT | G | 7 | a0001c0030t0001g0337 a0003c0004t0001g0310 a0003c0004t0001g0319 others(4): Show |
7 | HG00544.hp2 HG03831.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.157-1995_157-1992d others(6): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177320461 | ||||||
chr4:177320462 | CTGTCT | C | 27 | a0001c0015t0001g0327 a0002c0008t0001g0304 a0002c0008t0001g0313 others(24): Show |
29 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.157-1995_157-1991d others(7): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177320462 | ||||||
chr4:177320466 | CT | C | 128 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0037 others(125): Show |
131 | HG00597.hp1 HG00621.hp2 HG00639.hp1 others(128): Show |
intron_variant | MODIFIER | c.157-1964delT | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177320466 | ||||||
chr4:177320466 | CTT | C | 49 | a0001c0001t0002g0218 a0001c0001t0002g0221 a0001c0001t0002g0229 others(46): Show |
52 | HG00597.hp2 HG00642.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.157-1965_157-1964d others(4): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177320466 | ||||||
chr4:177320466 | CTTT | C | 54 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0193 others(51): Show |
54 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.157-1966_157-1964d others(5): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177320466 | ||||||
chr4:177320466 | CTTTTTTT others(10): Show |
C | 47 | a0001c0001t0001g0344 a0001c0001t0001g0356 a0001c0001t0001g0366 others(44): Show |
47 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.157-1980_157-1964d others(19): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177320466 | ||||||
chr4:177320466 | CTTTTTTT others(11): Show |
C | 1 | a0003c0007t0001g0357 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.157-1981_157-1964d others(20): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177320466 | ||||||
chr4:177320467 | T | C | 1 | a0001c0001t0006g0180 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.157-1992T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177320467 | |||||||
chr4:177320467 | T | TTGCTG | 22 | a0006c0005t0001g0272 a0006c0005t0003g0273 a0006c0005t0003g0275 others(19): Show |
22 | HG00140.hp2 HG01081.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.157-1991_157-1990i others(7): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177320467 | ||||||
chr4:177320468 | T | TGCTGTC | 6 | a0002c0002t0001g0009 a0002c0020t0001g0010 a0006c0005t0003g0284 others(3): Show |
6 | HG03654.hp1 HG03704.hp1 NA19005.hp1 others(3): Show |
intron_variant | MODIFIER | c.157-1991_157-1990i others(8): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177320468 | |||||||
chr4:177320469 | T | C | 24 | a0002c0008t0001g0339 a0002c0008t0005g0338 a0006c0005t0001g0272 others(21): Show |
24 | HG00140.hp2 HG01081.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.157-1990T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177320469 | |||||||
chr4:177320512 | G | C | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.157-1947G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177320512 | |||||||
chr4:177320546 | C | T | 127 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0193 others(124): Show |
130 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.157-1913C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177320546 | |||||||
chr4:177320547 | G | A | 1 | a0005c0016t0004g0007 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.157-1912G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177320547 | |||||||
chr4:177320570 | A | C | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.157-1889A>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177320570 | |||||||
chr4:177320579 | G | A | 1 | a0012c0017t0001g0271 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.157-1880G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177320579 | |||||||
chr4:177320597 | C | T | 1 | a0003c0004t0001g0333 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.157-1862C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177320597 | |||||||
chr4:177320602 | C | T | 1 | a0002c0020t0001g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.157-1857C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177320602 | |||||||
chr4:177320629 | C | T | 8 | a0001c0001t0001g0033 a0001c0001t0001g0121 a0001c0001t0001g0139 others(5): Show |
8 | HG00609.hp1 HG02129.hp1 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.157-1830C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177320629 | |||||||
chr4:177320634 | T | C | 1 | a0001c0001t0003g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.157-1825T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177320634 | |||||||
chr4:177320686 | C | T | 3 | a0001c0003t0001g0112 a0003c0004t0001g0023 a0003c0004t0001g0080 |
3 | HG01069.hp2 HG01071.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.157-1773C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177320686 | |||||||
chr4:177320709 | C | T | 1 | a0003c0004t0001g0332 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.157-1750C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177320709 | |||||||
chr4:177320756 | C | T | 1 | a0002c0010t0001g0115 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.157-1703C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177320756 | |||||||
chr4:177320871 | G | A | 18 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(15): Show |
18 | HG02040.hp2 HG02071.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.157-1588G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177320871 | |||||||
chr4:177320939 | T | C | 1 | a0005c0016t0004g0007 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.157-1520T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177320939 | |||||||
chr4:177320959 | CT | C | 10 | a0001c0003t0001g0028 a0002c0002t0001g0036 a0002c0002t0001g0043 others(7): Show |
10 | HG01257.hp2 HG01517.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.157-1486delT | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177320959 | ||||||
chr4:177320985 | T | G | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.157-1474T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177320985 | |||||||
chr4:177321063 | A | G | 1 | a0024c0046t0001g0260 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.157-1396A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177321063 | |||||||
chr4:177321201 | T | G | 1 | a0001c0001t0002g0190 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.157-1258T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177321201 | |||||||
chr4:177321244 | G | A | 128 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0193 others(125): Show |
131 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.157-1215G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177321244 | |||||||
chr4:177321273 | C | A | 1 | a0006c0005t0003g0275 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.157-1186C>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177321273 | |||||||
chr4:177321383 | C | T | 100 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0193 others(97): Show |
103 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.157-1076C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177321383 | |||||||
chr4:177321417 | T | G | 1 | a0005c0025t0005g0320 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.157-1042T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177321417 | |||||||
chr4:177321484 | C | T | 4 | a0002c0032t0001g0306 a0005c0025t0005g0320 a0017c0026t0001g0301 others(1): Show |
4 | HG02572.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.157-975C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177321484 | |||||||
chr4:177321543 | C | G | 11 | a0004c0006t0005g0231 a0004c0006t0005g0239 a0004c0014t0001g0001 others(8): Show |
14 | HG00642.hp2 HG02572.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.157-916C>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177321543 | |||||||
chr4:177321702 | A | G | 1 | a0008c0012t0002g0262 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.157-757A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177321702 | |||||||
chr4:177321705 | T | C | 1 | a0001c0003t0003g0364 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.157-754T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177321705 | |||||||
chr4:177321737 | G | A | 2 | a0004c0006t0005g0231 a0004c0006t0005g0239 |
2 | HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.157-722G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177321737 | |||||||
chr4:177321741 | G | A | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.157-718G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177321741 | |||||||
chr4:177321769 | C | A | 2 | a0004c0006t0001g0263 a0005c0025t0011g0398 |
2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.157-690C>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177321769 | |||||||
chr4:177321836 | G | A | 48 | a0001c0001t0001g0344 a0001c0001t0001g0356 a0001c0001t0001g0366 others(45): Show |
48 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.157-623G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177321836 | |||||||
chr4:177321853 | TC | T | 28 | a0002c0002t0001g0009 a0002c0020t0001g0010 a0006c0005t0001g0272 others(25): Show |
28 | HG00140.hp2 HG01081.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.157-605delC | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177321853 | |||||||
chr4:177321970 | C | T | 1 | a0004c0006t0006g0189 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.157-489C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177321970 | |||||||
chr4:177322080 | G | A | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.157-379G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177322080 | |||||||
chr4:177322146 | C | T | 1 | a0025c0034t0001g0154 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.157-313C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177322146 | |||||||
chr4:177322215 | C | A | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.157-244C>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177322215 | |||||||
chr4:177322277 | A | C | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.157-182A>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177322277 | |||||||
chr4:177322283 | A | G | 1 | a0006c0005t0003g0283 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.157-176A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177322283 | |||||||
chr4:177322289 | CAA | C | 7 | a0003c0004t0001g0006 a0003c0004t0001g0329 a0003c0004t0001g0330 others(4): Show |
8 | HG02056.hp1 NA18747.hp1 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.157-167_157-166del others(2): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 177322289 | ||||||
chr4:177322343 | C | T | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.157-116C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177322343 | |||||||
chr4:177322437 | G | A | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.157-22G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177322437 | |||||||
chr4:177322441 | A | G | 74 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(71): Show |
74 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.157-18A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | chr4 | 177322441 | |||||||
chr4:177322952 | T | C | 1 | a0003c0004t0001g0321 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.278+372T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177322952 | |||||||
chr4:177323328 | C | G | 1 | a0002c0002t0001g0018 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.278+748C>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177323328 | |||||||
chr4:177323345 | C | A | 5 | a0013c0023t0001g0257 a0013c0023t0001g0259 a0019c0044t0001g0256 others(2): Show |
5 | HG00735.hp2 HG01257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.278+765C>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177323345 | |||||||
chr4:177323370 | A | G | 1 | a0001c0015t0001g0327 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.278+790A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177323370 | |||||||
chr4:177323506 | T | C | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.278+926T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177323506 | |||||||
chr4:177323588 | A | G | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.278+1008A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177323588 | |||||||
chr4:177323611 | A | G | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.278+1031A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177323611 | |||||||
chr4:177323764 | G | C | 1 | a0001c0001t0002g0191 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.278+1184G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177323764 | |||||||
chr4:177323953 | G | A | 18 | a0001c0015t0001g0327 a0001c0030t0001g0337 a0002c0008t0001g0325 others(15): Show |
19 | HG00408.hp2 HG00544.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.278+1373G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177323953 | |||||||
chr4:177323954 | G | T | 1 | a0001c0001t0001g0138 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.278+1374G>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177323954 | |||||||
chr4:177323962 | A | G | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.278+1382A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177323962 | |||||||
chr4:177324015 | T | C | 236 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(233): Show |
242 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.278+1435T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177324015 | |||||||
chr4:177324075 | C | T | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.278+1495C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177324075 | |||||||
chr4:177324272 | G | T | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.278+1692G>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177324272 | |||||||
chr4:177324277 | A | G | 11 | a0001c0001t0001g0076 a0001c0003t0001g0003 a0001c0003t0001g0028 others(8): Show |
13 | NA18947.hp1 NA18952.hp1 NA18960.hp2 others(10): Show |
intron_variant | MODIFIER | c.278+1697A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177324277 | |||||||
chr4:177324292 | T | C | 1 | a0001c0001t0003g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.278+1712T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177324292 | |||||||
chr4:177324300 | A | G | 5 | a0002c0010t0001g0343 a0002c0010t0001g0381 a0002c0010t0005g0380 others(2): Show |
5 | HG01884.hp2 HG02559.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.278+1720A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177324300 | |||||||
chr4:177324364 | G | A | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.278+1784G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177324364 | |||||||
chr4:177324449 | G | A | 5 | a0002c0010t0001g0343 a0002c0010t0001g0381 a0002c0010t0005g0380 others(2): Show |
5 | HG01884.hp2 HG02559.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.278+1869G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177324449 | |||||||
chr4:177324575 | C | A | 5 | a0002c0010t0001g0343 a0002c0010t0001g0381 a0002c0010t0005g0380 others(2): Show |
5 | HG01884.hp2 HG02559.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.278+1995C>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177324575 | |||||||
chr4:177324590 | T | C | 1 | a0002c0002t0004g0044 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.278+2010T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177324590 | |||||||
chr4:177324672 | A | G | 3 | a0002c0010t0001g0343 a0002c0010t0001g0381 a0002c0010t0005g0380 |
3 | HG02630.hp1 HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.278+2092A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177324672 | |||||||
chr4:177324816 | G | A | 1 | a0002c0020t0001g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.278+2236G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177324816 | |||||||
chr4:177324823 | A | T | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.278+2243A>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177324823 | |||||||
chr4:177324910 | A | G | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.278+2330A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177324910 | |||||||
chr4:177324950 | C | CAGAT | 80 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(77): Show |
83 | HG00323.hp2 HG00423.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.278+2404_278+2407d others(6): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 177324950 | ||||||
chr4:177324950 | C | CAGATAGA others(1): Show |
89 | a0001c0001t0001g0096 a0001c0001t0001g0201 a0001c0001t0001g0345 others(86): Show |
89 | HG00140.hp2 HG00408.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.278+2400_278+2407d others(10): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 177324950 | ||||||
chr4:177324950 | C | CAGATAGA others(5): Show |
26 | a0001c0001t0001g0022 a0001c0001t0002g0182 a0001c0001t0002g0190 others(23): Show |
27 | HG00544.hp1 HG00597.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.278+2396_278+2407d others(14): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 177324950 | ||||||
chr4:177324950 | C | CAGATAGA others(9): Show |
1 | a0001c0001t0002g0250 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.278+2392_278+2407d others(18): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 177324950 | ||||||
chr4:177324950 | CAGAT | C | 117 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0033 others(114): Show |
119 | HG00323.hp1 HG00544.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.278+2404_278+2407d others(6): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 177324950 | ||||||
chr4:177324950 | CAGATAGA others(1): Show |
C | 36 | a0001c0015t0001g0327 a0001c0030t0001g0337 a0002c0008t0001g0304 others(33): Show |
38 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.278+2400_278+2407d others(10): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 177324950 | ||||||
chr4:177324950 | CAGATAGA others(5): Show |
C | 2 | a0002c0008t0005g0338 a0002c0020t0001g0170 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.278+2396_278+2407d others(14): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 177324950 | ||||||
chr4:177324965 | A | G | 1 | a0002c0020t0001g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.278+2385A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177324965 | |||||||
chr4:177324974 | T | C | 1 | a0003c0007t0001g0152 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.278+2394T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177324974 | |||||||
chr4:177325176 | C | T | 85 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(82): Show |
85 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.278+2596C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177325176 | |||||||
chr4:177325263 | T | C | 28 | a0002c0002t0001g0009 a0002c0020t0001g0010 a0006c0005t0001g0272 others(25): Show |
28 | HG00140.hp2 HG01081.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.278+2683T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177325263 | |||||||
chr4:177325275 | A | G | 48 | a0001c0001t0001g0344 a0001c0001t0001g0356 a0001c0001t0001g0366 others(45): Show |
48 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.278+2695A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177325275 | |||||||
chr4:177325332 | C | T | 48 | a0001c0001t0001g0344 a0001c0001t0001g0356 a0001c0001t0001g0366 others(45): Show |
48 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.278+2752C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177325332 | |||||||
chr4:177325460 | T | C | 1 | a0002c0008t0001g0339 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.278+2880T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177325460 | |||||||
chr4:177325488 | T | G | 9 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(6): Show |
9 | HG02040.hp2 HG02071.hp2 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.278+2908T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177325488 | |||||||
chr4:177325599 | T | C | 1 | a0025c0034t0001g0154 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.278+3019T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177325599 | |||||||
chr4:177325720 | G | T | 1 | a0002c0002t0001g0009 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.278+3140G>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177325720 | |||||||
chr4:177325781 | T | C | 26 | a0006c0005t0001g0272 a0006c0005t0003g0273 a0006c0005t0003g0275 others(23): Show |
26 | HG00140.hp2 HG01081.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.278+3201T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177325781 | |||||||
chr4:177325826 | G | A | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.278+3246G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177325826 | |||||||
chr4:177325828 | A | G | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.278+3248A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177325828 | |||||||
chr4:177325938 | G | A | 25 | a0006c0005t0001g0272 a0006c0005t0003g0273 a0006c0005t0003g0275 others(22): Show |
25 | HG00140.hp2 HG01081.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.278+3358G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177325938 | |||||||
chr4:177325995 | T | A | 75 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(72): Show |
75 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.278+3415T>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177325995 | |||||||
chr4:177326060 | T | TA | 83 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(80): Show |
83 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.278+3481dupA | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 177326060 | ||||||
chr4:177326091 | C | G | 8 | a0001c0001t0001g0345 a0001c0001t0001g0394 a0002c0002t0001g0390 others(5): Show |
9 | HG03491.hp1 HG03492.hp1 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.278+3511C>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177326091 | |||||||
chr4:177326092 | G | T | 113 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(110): Show |
113 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.278+3512G>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177326092 | |||||||
chr4:177326246 | G | A | 113 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(110): Show |
113 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.278+3666G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177326246 | |||||||
chr4:177326262 | G | T | 1 | a0002c0002t0001g0369 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.278+3682G>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177326262 | |||||||
chr4:177326308 | T | C | 28 | a0002c0002t0001g0009 a0002c0020t0001g0010 a0006c0005t0001g0272 others(25): Show |
28 | HG00140.hp2 HG01081.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.278+3728T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177326308 | |||||||
chr4:177326841 | A | G | 76 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(73): Show |
76 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.278+4261A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177326841 | |||||||
chr4:177326924 | T | C | 169 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(166): Show |
170 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.278+4344T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177326924 | |||||||
chr4:177327156 | T | C | 85 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(82): Show |
85 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.278+4576T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177327156 | |||||||
chr4:177327214 | C | T | 47 | a0001c0001t0001g0344 a0001c0001t0001g0356 a0001c0001t0001g0366 others(44): Show |
47 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.278+4634C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177327214 | |||||||
chr4:177327289 | T | C | 1 | a0002c0020t0001g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.278+4709T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177327289 | |||||||
chr4:177327423 | T | A | 3 | a0002c0002t0001g0074 a0002c0002t0001g0079 a0002c0002t0001g0109 |
3 | NA18972.hp1 NA19064.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.278+4843T>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177327423 | |||||||
chr4:177327486 | G | A | 237 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(234): Show |
243 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.278+4906G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177327486 | |||||||
chr4:177327516 | A | G | 1 | a0002c0028t0001g0032 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.278+4936A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177327516 | |||||||
chr4:177327546 | C | T | 1 | a0002c0002t0001g0211 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.278+4966C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177327546 | |||||||
chr4:177327587 | C | G | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.278+5007C>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177327587 | |||||||
chr4:177327660 | G | C | 8 | a0013c0023t0001g0257 a0013c0023t0001g0259 a0013c0023t0005g0261 others(5): Show |
8 | HG00735.hp2 HG01257.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.278+5080G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177327660 | |||||||
chr4:177327673 | G | A | 8 | a0013c0023t0001g0257 a0013c0023t0001g0259 a0013c0023t0005g0261 others(5): Show |
8 | HG00735.hp2 HG01257.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.278+5093G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177327673 | |||||||
chr4:177327791 | A | G | 1 | a0011c0018t0001g0302 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.278+5211A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177327791 | |||||||
chr4:177327909 | A | G | 1 | a0002c0020t0001g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.278+5329A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177327909 | |||||||
chr4:177327916 | G | A | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.278+5336G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177327916 | |||||||
chr4:177328071 | C | T | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.278+5491C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177328071 | |||||||
chr4:177328393 | G | A | 1 | a0011c0033t0005g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.278+5813G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177328393 | |||||||
chr4:177328461 | G | A | 143 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(140): Show |
144 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.278+5881G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177328461 | |||||||
chr4:177328463 | A | G | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.278+5883A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177328463 | |||||||
chr4:177328509 | A | G | 1 | a0001c0001t0002g0198 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.278+5929A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177328509 | |||||||
chr4:177328512 | T | C | 28 | a0002c0002t0001g0009 a0002c0020t0001g0010 a0006c0005t0001g0272 others(25): Show |
28 | HG00140.hp2 HG01081.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.278+5932T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177328512 | |||||||
chr4:177328535 | C | T | 28 | a0002c0002t0001g0009 a0002c0020t0001g0010 a0006c0005t0001g0272 others(25): Show |
28 | HG00140.hp2 HG01081.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.278+5955C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177328535 | |||||||
chr4:177328536 | G | A | 8 | a0001c0001t0001g0145 a0001c0001t0001g0149 a0001c0001t0001g0166 others(5): Show |
8 | HG00733.hp2 HG01167.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.278+5956G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177328536 | |||||||
chr4:177328600 | G | A | 1 | a0002c0002t0001g0009 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.278+6020G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177328600 | |||||||
chr4:177328757 | T | C | 1 | a0002c0002t0001g0009 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.278+6177T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177328757 | |||||||
chr4:177328785 | G | C | 1 | a0001c0001t0002g0212 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.278+6205G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177328785 | |||||||
chr4:177328856 | T | C | 1 | a0002c0002t0001g0046 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.278+6276T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177328856 | |||||||
chr4:177328904 | ATGT | A | 4 | a0001c0043t0001g0399 a0002c0002t0001g0009 a0002c0020t0001g0170 others(1): Show |
4 | HG02622.hp1 HG03130.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.278+6330_278+6332d others(5): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 177328904 | ||||||
chr4:177328994 | C | T | 2 | a0002c0002t0001g0088 a0002c0020t0001g0170 |
2 | HG01361.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.278+6414C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177328994 | |||||||
chr4:177329027 | T | C | 1 | a0002c0002t0001g0101 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.278+6447T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177329027 | |||||||
chr4:177329036 | A | G | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.278+6456A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177329036 | |||||||
chr4:177329097 | T | A | 110 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(107): Show |
110 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.278+6517T>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177329097 | |||||||
chr4:177329133 | C | T | 26 | a0006c0005t0001g0272 a0006c0005t0003g0273 a0006c0005t0003g0275 others(23): Show |
26 | HG00140.hp2 HG01081.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.278+6553C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177329133 | |||||||
chr4:177329139 | A | C | 1 | a0001c0001t0002g0212 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.279-6549A>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177329139 | |||||||
chr4:177329246 | T | G | 83 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(80): Show |
83 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.279-6442T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177329246 | |||||||
chr4:177329251 | G | A | 1 | a0013c0023t0005g0261 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.279-6437G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177329251 | |||||||
chr4:177329334 | C | T | 1 | a0024c0046t0001g0260 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.279-6354C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177329334 | |||||||
chr4:177329419 | A | G | 1 | a0004c0006t0001g0244 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.279-6269A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177329419 | |||||||
chr4:177329446 | C | T | 8 | a0013c0023t0001g0257 a0013c0023t0001g0259 a0013c0023t0005g0261 others(5): Show |
8 | HG00735.hp2 HG01257.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.279-6242C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177329446 | |||||||
chr4:177329544 | T | C | 1 | a0002c0002t0001g0383 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.279-6144T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177329544 | |||||||
chr4:177329772 | T | C | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.279-5916T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177329772 | |||||||
chr4:177330094 | T | A | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.279-5594T>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177330094 | |||||||
chr4:177330104 | G | A | 72 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(69): Show |
72 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.279-5584G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177330104 | |||||||
chr4:177330159 | G | A | 1 | a0004c0006t0005g0242 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.279-5529G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177330159 | |||||||
chr4:177330251 | C | T | 2 | a0002c0002t0001g0036 a0002c0002t0001g0043 |
2 | HG01952.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.279-5437C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177330251 | |||||||
chr4:177330473 | C | T | 1 | a0002c0002t0001g0009 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.279-5215C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177330473 | |||||||
chr4:177330553 | A | G | 1 | a0015c0024t0001g0243 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.279-5135A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177330553 | |||||||
chr4:177330592 | C | A | 8 | a0013c0023t0001g0257 a0013c0023t0001g0259 a0013c0023t0005g0261 others(5): Show |
8 | HG00735.hp2 HG01257.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.279-5096C>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177330592 | |||||||
chr4:177330660 | C | T | 1 | a0002c0020t0001g0010 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.279-5028C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177330660 | |||||||
chr4:177330670 | A | G | 1 | a0015c0024t0001g0243 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.279-5018A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177330670 | |||||||
chr4:177330784 | G | A | 168 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(165): Show |
169 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.279-4904G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177330784 | |||||||
chr4:177330847 | A | G | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.279-4841A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177330847 | |||||||
chr4:177330896 | T | G | 8 | a0001c0001t0001g0345 a0001c0001t0001g0394 a0002c0002t0001g0390 others(5): Show |
9 | HG03491.hp1 HG03492.hp1 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.279-4792T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177330896 | |||||||
chr4:177330970 | G | C | 1 | a0003c0007t0001g0122 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.279-4718G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177330970 | |||||||
chr4:177330977 | A | G | 4 | a0001c0001t0001g0366 a0002c0002t0001g0359 a0002c0002t0001g0367 others(1): Show |
4 | HG00323.hp2 HG01516.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.279-4711A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177330977 | |||||||
chr4:177331143 | A | G | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.279-4545A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177331143 | |||||||
chr4:177331176 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.279-4512C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177331176 | |||||||
chr4:177331193 | C | A | 2 | a0002c0002t0001g0352 a0002c0002t0001g0370 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.279-4495C>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177331193 | |||||||
chr4:177331279 | A | G | 1 | a0002c0002t0001g0378 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.279-4409A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177331279 | |||||||
chr4:177331316 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.279-4372G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177331316 | |||||||
chr4:177331527 | A | T | 8 | a0013c0023t0001g0257 a0013c0023t0001g0259 a0013c0023t0005g0261 others(5): Show |
8 | HG00735.hp2 HG01257.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.279-4161A>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177331527 | |||||||
chr4:177331600 | T | C | 8 | a0013c0023t0001g0257 a0013c0023t0001g0259 a0013c0023t0005g0261 others(5): Show |
8 | HG00735.hp2 HG01257.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.279-4088T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177331600 | |||||||
chr4:177331627 | G | A | 1 | a0006c0005t0001g0272 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.279-4061G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177331627 | |||||||
chr4:177331708 | G | A | 48 | a0001c0001t0001g0344 a0001c0001t0001g0356 a0001c0001t0001g0366 others(45): Show |
48 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.279-3980G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177331708 | |||||||
chr4:177331758 | C | T | 5 | a0002c0010t0001g0343 a0002c0010t0001g0381 a0002c0010t0005g0380 others(2): Show |
5 | HG01884.hp2 HG02559.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.279-3930C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177331758 | |||||||
chr4:177331766 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.279-3922T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177331766 | |||||||
chr4:177331972 | T | C | 1 | a0024c0046t0001g0260 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.279-3716T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177331972 | |||||||
chr4:177332135 | C | T | 28 | a0002c0002t0001g0009 a0002c0020t0001g0010 a0006c0005t0001g0272 others(25): Show |
28 | HG00140.hp2 HG01081.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.279-3553C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177332135 | |||||||
chr4:177332239 | G | T | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.279-3449G>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177332239 | |||||||
chr4:177332288 | G | A | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.279-3400G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177332288 | |||||||
chr4:177332376 | C | T | 1 | a0004c0006t0001g0241 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.279-3312C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177332376 | |||||||
chr4:177332384 | T | C | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.279-3304T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177332384 | |||||||
chr4:177332389 | C | T | 81 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(78): Show |
81 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.279-3299C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177332389 | |||||||
chr4:177332390 | T | C | 1 | a0002c0002t0001g0009 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.279-3298T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177332390 | |||||||
chr4:177332427 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.279-3261G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177332427 | |||||||
chr4:177332659 | C | T | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.279-3029C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177332659 | |||||||
chr4:177332778 | A | G | 1 | a0001c0001t0002g0212 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.279-2910A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177332778 | |||||||
chr4:177332823 | T | C | 1 | a0002c0002t0001g0009 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.279-2865T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177332823 | |||||||
chr4:177332946 | C | T | 1 | a0001c0001t0002g0210 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.279-2742C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177332946 | |||||||
chr4:177332947 | G | A | 1 | a0001c0003t0001g0102 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.279-2741G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177332947 | |||||||
chr4:177332994 | C | G | 28 | a0002c0002t0001g0009 a0002c0020t0001g0010 a0006c0005t0001g0272 others(25): Show |
28 | HG00140.hp2 HG01081.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.279-2694C>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177332994 | |||||||
chr4:177333032 | TA | T | 80 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(77): Show |
80 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.279-2655delA | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177333032 | |||||||
chr4:177333033 | A | T | 31 | a0001c0043t0001g0399 a0002c0002t0001g0009 a0002c0020t0001g0010 others(28): Show |
31 | HG00140.hp2 HG01081.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.279-2655A>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177333033 | |||||||
chr4:177333079 | T | A | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.279-2609T>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177333079 | |||||||
chr4:177333133 | T | C | 1 | a0003c0004t0001g0312 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.279-2555T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177333133 | |||||||
chr4:177333299 | C | T | 9 | a0001c0001t0001g0135 a0001c0001t0001g0345 a0001c0001t0001g0394 others(6): Show |
10 | HG03491.hp1 HG03492.hp1 HG03669.hp1 others(7): Show |
intron_variant | MODIFIER | c.279-2389C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177333299 | |||||||
chr4:177333336 | A | G | 1 | a0025c0034t0001g0154 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.279-2352A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177333336 | |||||||
chr4:177333455 | G | A | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.279-2233G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177333455 | |||||||
chr4:177333491 | G | C | 1 | a0002c0002t0001g0065 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.279-2197G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177333491 | |||||||
chr4:177333522 | T | C | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.279-2166T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177333522 | |||||||
chr4:177333547 | A | G | 1 | a0001c0027t0001g0100 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.279-2141A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177333547 | |||||||
chr4:177333624 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.279-2064C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177333624 | |||||||
chr4:177333633 | C | T | 37 | a0001c0015t0001g0327 a0001c0030t0001g0337 a0002c0008t0001g0304 others(34): Show |
39 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.279-2055C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177333633 | |||||||
chr4:177333639 | T | C | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.279-2049T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177333639 | |||||||
chr4:177333694 | G | C | 1 | a0018c0042t0003g0066 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.279-1994G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177333694 | |||||||
chr4:177333750 | G | A | 237 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(234): Show |
243 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.279-1938G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177333750 | |||||||
chr4:177333834 | A | G | 28 | a0002c0002t0001g0009 a0002c0020t0001g0010 a0006c0005t0001g0272 others(25): Show |
28 | HG00140.hp2 HG01081.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.279-1854A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177333834 | |||||||
chr4:177333870 | AC | A | 81 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(78): Show |
81 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.279-1817delC | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177333870 | |||||||
chr4:177333990 | T | C | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.279-1698T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177333990 | |||||||
chr4:177334007 | T | C | 57 | a0001c0001t0001g0344 a0001c0001t0001g0345 a0001c0001t0001g0356 others(54): Show |
58 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.279-1681T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177334007 | |||||||
chr4:177334057 | A | G | 27 | a0002c0020t0001g0010 a0006c0005t0001g0272 a0006c0005t0003g0273 others(24): Show |
27 | HG00140.hp2 HG01081.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.279-1631A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177334057 | |||||||
chr4:177334060 | A | G | 1 | a0015c0024t0001g0243 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.279-1628A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177334060 | |||||||
chr4:177334105 | G | A | 1 | a0001c0015t0001g0293 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.279-1583G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177334105 | |||||||
chr4:177334142 | TA | T | 36 | a0001c0003t0001g0064 a0001c0043t0001g0399 a0002c0002t0001g0009 others(33): Show |
36 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.279-1532delA | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 177334142 | ||||||
chr4:177334144 | A | T | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.279-1544A>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177334144 | |||||||
chr4:177334159 | A | G | 73 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(70): Show |
73 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.279-1529A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177334159 | |||||||
chr4:177334213 | A | G | 2 | a0004c0006t0001g0254 a0004c0006t0004g0253 |
2 | HG01891.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.279-1475A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177334213 | |||||||
chr4:177334246 | G | T | 1 | a0002c0002t0001g0063 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.279-1442G>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177334246 | |||||||
chr4:177334593 | A | G | 238 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(235): Show |
244 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.279-1095A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177334593 | |||||||
chr4:177334731 | G | A | 5 | a0002c0002t0001g0361 a0002c0002t0001g0362 a0002c0002t0001g0363 others(2): Show |
5 | HG02135.hp1 NA18944.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.279-957G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177334731 | |||||||
chr4:177334756 | G | A | 73 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(70): Show |
73 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.279-932G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177334756 | |||||||
chr4:177334936 | T | G | 27 | a0002c0008t0001g0298 a0006c0005t0001g0272 a0006c0005t0003g0273 others(24): Show |
27 | HG00140.hp2 HG01069.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.279-752T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177334936 | |||||||
chr4:177334944 | A | G | 1 | a0002c0002t0001g0009 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.279-744A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177334944 | |||||||
chr4:177334975 | G | A | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.279-713G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177334975 | |||||||
chr4:177334985 | G | A | 2 | a0012c0017t0003g0294 a0014c0021t0001g0342 |
2 | HG01099.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.279-703G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177334985 | |||||||
chr4:177334993 | A | G | 7 | a0013c0023t0001g0257 a0013c0023t0001g0259 a0013c0023t0005g0261 others(4): Show |
7 | HG00735.hp2 HG01257.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.279-695A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177334993 | |||||||
chr4:177335082 | C | T | 10 | a0006c0005t0003g0276 a0006c0005t0003g0280 a0006c0005t0003g0281 others(7): Show |
10 | HG01975.hp2 HG02273.hp2 NA18943.hp1 others(7): Show |
intron_variant | MODIFIER | c.279-606C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177335082 | |||||||
chr4:177335165 | A | G | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.279-523A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177335165 | |||||||
chr4:177335238 | G | A | 1 | a0002c0002t0004g0044 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.279-450G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177335238 | |||||||
chr4:177335415 | T | C | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.279-273T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | chr4 | 177335415 | |||||||
chr4:177335605 | CA | C | 168 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(165): Show |
169 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.279-73delA | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 177335605 | ||||||
chr4:177335824 | T | TA | 74 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(71): Show |
74 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.413+10dupA | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | 177335824 | ||||||
chr4:177335851 | G | A | 1 | a0002c0020t0001g0010 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.413+29G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 3/9 | chr4 | 177335851 | |||||||
chr4:177335888 | G | A | 2 | a0004c0006t0001g0263 a0005c0025t0011g0398 |
2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.413+66G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 3/9 | chr4 | 177335888 | |||||||
chr4:177335915 | G | C | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.413+93G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 3/9 | chr4 | 177335915 | |||||||
chr4:177336004 | A | T | 1 | a0014c0021t0001g0278 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.414-104A>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 3/9 | chr4 | 177336004 | |||||||
chr4:177336334 | T | A | 1 | a0002c0002t0001g0169 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.627+13T>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177336334 | |||||||
chr4:177336362 | G | A | 238 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(235): Show |
244 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.627+41G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177336362 | |||||||
chr4:177336469 | A | G | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.627+148A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177336469 | |||||||
chr4:177336518 | A | G | 1 | a0002c0020t0001g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.627+197A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177336518 | |||||||
chr4:177336522 | C | T | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.627+201C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177336522 | |||||||
chr4:177336683 | G | A | 4 | a0010c0013t0001g0233 a0015c0024t0001g0232 a0015c0024t0001g0238 others(1): Show |
4 | HG00642.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+362G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177336683 | |||||||
chr4:177336723 | C | A | 4 | a0002c0032t0001g0306 a0005c0025t0005g0320 a0017c0026t0001g0301 others(1): Show |
4 | HG02572.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+402C>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177336723 | |||||||
chr4:177336736 | T | G | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.627+415T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177336736 | |||||||
chr4:177336747 | T | C | 6 | a0001c0001t0001g0027 a0001c0001t0001g0047 a0002c0002t0001g0088 others(3): Show |
6 | HG01109.hp2 HG01255.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.627+426T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177336747 | |||||||
chr4:177336887 | A | T | 1 | a0002c0002t0001g0378 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.627+566A>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177336887 | |||||||
chr4:177337067 | A | G | 1 | a0001c0001t0006g0197 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.627+746A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177337067 | |||||||
chr4:177337093 | CA | C | 76 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(73): Show |
76 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.627+784delA | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 177337093 | ||||||
chr4:177337094 | A | C | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.627+773A>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177337094 | |||||||
chr4:177337162 | A | G | 1 | a0021c0045t0001g0255 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.627+841A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177337162 | |||||||
chr4:177337324 | C | G | 4 | a0002c0032t0001g0306 a0005c0025t0005g0320 a0017c0026t0001g0301 others(1): Show |
4 | HG02572.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+1003C>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177337324 | |||||||
chr4:177337458 | A | G | 74 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(71): Show |
74 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.627+1137A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177337458 | |||||||
chr4:177337597 | G | T | 4 | a0002c0032t0001g0306 a0005c0025t0005g0320 a0017c0026t0001g0301 others(1): Show |
4 | HG02572.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+1276G>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177337597 | |||||||
chr4:177337653 | A | G | 1 | a0002c0008t0005g0338 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.627+1332A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177337653 | |||||||
chr4:177337714 | A | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0087 |
2 | NA18994.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.627+1393A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177337714 | |||||||
chr4:177337812 | G | A | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.627+1491G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177337812 | |||||||
chr4:177337920 | G | A | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.627+1599G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177337920 | |||||||
chr4:177337995 | G | C | 1 | a0001c0001t0001g0139 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.627+1674G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177337995 | |||||||
chr4:177338003 | G | A | 1 | a0003c0004t0001g0333 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.627+1682G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177338003 | |||||||
chr4:177338022 | T | TCA | 79 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(76): Show |
79 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.627+1702_627+1703i others(4): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 177338022 | ||||||
chr4:177338022 | T | TCACA | 3 | a0001c0001t0002g0199 a0001c0001t0002g0218 a0001c0001t0002g0221 |
3 | NA18943.hp2 NA18971.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.627+1702_627+1703i others(6): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 177338022 | ||||||
chr4:177338024 | T | A | 108 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(105): Show |
108 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.627+1703T>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177338024 | |||||||
chr4:177338024 | T | TCA | 59 | a0001c0001t0001g0037 a0001c0001t0001g0123 a0001c0001t0001g0344 others(56): Show |
60 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.627+1728_627+1729d others(4): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 177338024 | ||||||
chr4:177338024 | T | TCACA | 5 | a0002c0002t0001g0382 a0002c0002t0001g0383 a0002c0002t0001g0384 others(2): Show |
5 | HG01515.hp1 HG01517.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.627+1726_627+1729d others(6): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 177338024 | ||||||
chr4:177338024 | T | TCACACA | 44 | a0001c0015t0001g0327 a0001c0030t0001g0337 a0002c0008t0001g0304 others(41): Show |
46 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.627+1724_627+1729d others(8): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 177338024 | ||||||
chr4:177338024 | T | TCTCA | 3 | a0004c0006t0005g0240 a0004c0014t0001g0235 a0004c0048t0005g0236 |
3 | HG02055.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.627+1704_627+1705i others(6): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 177338024 | ||||||
chr4:177338024 | T | TCTCACA | 22 | a0001c0001t0005g0008 a0004c0006t0001g0183 a0004c0006t0001g0241 others(19): Show |
25 | HG00642.hp2 HG01891.hp2 HG01981.hp1 others(22): Show |
intron_variant | MODIFIER | c.627+1704_627+1705i others(8): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 177338024 | ||||||
chr4:177338259 | A | G | 4 | a0002c0032t0001g0306 a0005c0025t0005g0320 a0017c0026t0001g0301 others(1): Show |
4 | HG02572.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-1524A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177338259 | |||||||
chr4:177338364 | G | A | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.628-1419G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177338364 | |||||||
chr4:177338376 | T | C | 3 | a0002c0002t0005g0347 a0002c0002t0005g0348 a0002c0002t0005g0349 |
3 | HG01891.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.628-1407T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177338376 | |||||||
chr4:177338529 | C | T | 1 | a0002c0020t0001g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.628-1254C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177338529 | |||||||
chr4:177338552 | T | TAG | 76 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0174 others(73): Show |
76 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.628-1229_628-1228d others(4): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 177338552 | ||||||
chr4:177338591 | G | C | 2 | a0001c0043t0001g0399 a0002c0020t0001g0170 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.628-1192G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177338591 | |||||||
chr4:177338699 | G | T | 1 | a0009c0019t0001g0157 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.628-1084G>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177338699 | |||||||
chr4:177338780 | C | T | 27 | a0002c0020t0001g0010 a0006c0005t0001g0272 a0006c0005t0003g0273 others(24): Show |
27 | HG00140.hp2 HG01081.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.628-1003C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177338780 | |||||||
chr4:177338857 | A | AT | 38 | a0001c0001t0002g0196 a0001c0015t0001g0327 a0001c0030t0001g0337 others(35): Show |
40 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.628-915dupT | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 177338857 | ||||||
chr4:177338881 | A | G | 1 | a0026c0039t0001g0117 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.628-902A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177338881 | |||||||
chr4:177339043 | A | C | 2 | a0002c0008t0001g0339 a0002c0008t0005g0338 |
2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.628-740A>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177339043 | |||||||
chr4:177339051 | C | T | 4 | a0002c0032t0001g0306 a0005c0025t0005g0320 a0017c0026t0001g0301 others(1): Show |
4 | HG02572.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-732C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177339051 | |||||||
chr4:177339085 | C | T | 20 | a0001c0001t0001g0366 a0001c0001t0001g0376 a0002c0002t0001g0352 others(17): Show |
20 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.628-698C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177339085 | |||||||
chr4:177339114 | G | A | 48 | a0001c0001t0001g0344 a0001c0001t0001g0356 a0001c0001t0001g0366 others(45): Show |
48 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.628-669G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177339114 | |||||||
chr4:177339331 | G | A | 12 | a0002c0020t0001g0346 a0004c0006t0001g0263 a0005c0025t0011g0398 others(9): Show |
12 | HG00735.hp2 HG01257.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.628-452G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177339331 | |||||||
chr4:177339501 | T | G | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.628-282T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177339501 | |||||||
chr4:177339531 | G | C | 99 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0038 others(96): Show |
101 | HG00323.hp1 HG00423.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.628-252G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177339531 | |||||||
chr4:177339654 | T | C | 2 | a0002c0020t0001g0010 a0010c0013t0005g0297 |
2 | HG02717.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.628-129T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177339654 | |||||||
chr4:177339718 | C | T | 84 | a0001c0001t0001g0107 a0001c0001t0001g0160 a0001c0001t0001g0161 others(81): Show |
86 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.628-65C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 4/9 | chr4 | 177339718 | |||||||
chr4:177339880 | GTGTAAAA | G | 29 | a0001c0003t0003g0364 a0002c0010t0001g0061 a0005c0009t0001g0318 others(26): Show |
29 | HG00140.hp2 HG00609.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.702+34_702+40delAA others(5): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 177339880 | ||||||
chr4:177340185 | A | G | 1 | a0008c0012t0002g0252 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.702+328A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 5/9 | chr4 | 177340185 | |||||||
chr4:177340205 | C | T | 1 | a0005c0016t0004g0377 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.702+348C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 5/9 | chr4 | 177340205 | |||||||
chr4:177340424 | C | T | 1 | a0015c0024t0001g0243 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.702+567C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 5/9 | chr4 | 177340424 | |||||||
chr4:177340497 | C | T | 1 | a0002c0002t0001g0079 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.702+640C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 5/9 | chr4 | 177340497 | |||||||
chr4:177340498 | A | C | 1 | a0002c0002t0001g0079 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.702+641A>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 5/9 | chr4 | 177340498 | |||||||
chr4:177340499 | T | A | 1 | a0002c0002t0001g0079 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.702+642T>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 5/9 | chr4 | 177340499 | |||||||
chr4:177340507 | A | G | 48 | a0001c0001t0001g0160 a0001c0003t0001g0003 a0001c0003t0001g0024 others(45): Show |
49 | HG00408.hp1 HG00621.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.702+650A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 5/9 | chr4 | 177340507 | |||||||
chr4:177340701 | T | G | 38 | a0002c0002t0003g0057 a0002c0002t0003g0084 a0003c0004t0001g0005 others(35): Show |
40 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.703-775T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 5/9 | chr4 | 177340701 | |||||||
chr4:177340741 | G | A | 40 | a0001c0003t0001g0003 a0001c0003t0001g0024 a0001c0003t0001g0028 others(37): Show |
41 | HG00408.hp1 HG00621.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.703-735G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 5/9 | chr4 | 177340741 | |||||||
chr4:177340813 | A | T | 1 | a0011c0033t0005g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.703-663A>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 5/9 | chr4 | 177340813 | |||||||
chr4:177340836 | A | C | 1 | a0001c0001t0001g0135 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.703-640A>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 5/9 | chr4 | 177340836 | |||||||
chr4:177341140 | G | T | 2 | a0001c0001t0006g0188 a0001c0001t0006g0197 |
2 | HG00597.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.703-336G>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 5/9 | chr4 | 177341140 | |||||||
chr4:177341157 | T | G | 40 | a0001c0003t0001g0003 a0001c0003t0001g0024 a0001c0003t0001g0028 others(37): Show |
41 | HG00408.hp1 HG00621.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.703-319T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 5/9 | chr4 | 177341157 | |||||||
chr4:177341164 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.703-312G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 5/9 | chr4 | 177341164 | |||||||
chr4:177341224 | T | A | 2 | a0005c0025t0011g0398 a0013c0023t0001g0257 |
2 | HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.703-252T>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 5/9 | chr4 | 177341224 | |||||||
chr4:177341231 | A | C | 4 | a0002c0020t0001g0170 a0004c0006t0001g0268 a0009c0019t0001g0072 others(1): Show |
4 | HG02809.hp1 HG03130.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.703-245A>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 5/9 | chr4 | 177341231 | |||||||
chr4:177341261 | A | G | 4 | a0001c0001t0001g0376 a0002c0002t0001g0009 a0012c0017t0004g0270 others(1): Show |
4 | HG03654.hp1 HG03704.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.703-215A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 5/9 | chr4 | 177341261 | |||||||
chr4:177341266 | T | C | 1 | a0001c0001t0001g0344 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.703-210T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 5/9 | chr4 | 177341266 | |||||||
chr4:177341300 | C | G | 52 | a0001c0001t0001g0031 a0001c0001t0001g0071 a0001c0001t0001g0356 others(49): Show |
52 | HG00323.hp2 HG00423.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.703-176C>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 5/9 | chr4 | 177341300 | |||||||
chr4:177341443 | A | G | 2 | a0001c0001t0002g0208 a0001c0001t0002g0209 |
2 | NA19062.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.703-33A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 5/9 | chr4 | 177341443 | |||||||
chr4:177341459 | G | GT | 8 | a0001c0001t0001g0135 a0002c0002t0001g0361 a0002c0002t0001g0362 others(5): Show |
8 | HG02135.hp1 HG03688.hp1 HG04228.hp1 others(5): Show |
splice_acceptor_variant&intron_variant | HIGH | c.703-3dupT | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 177341459 | ||||||
chr4:177341459 | GT | G | 40 | a0001c0003t0001g0003 a0001c0003t0001g0024 a0001c0003t0001g0028 others(37): Show |
41 | HG00408.hp1 HG00621.hp2 HG01070.hp1 others(38): Show |
splice_region_variant&intron_variant | LOW | c.703-3delT | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 177341459 | ||||||
chr4:177341651 | T | C | 38 | a0002c0002t0003g0057 a0002c0002t0003g0084 a0003c0004t0001g0005 others(35): Show |
40 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.869+9T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177341651 | |||||||
chr4:177341657 | T | C | 41 | a0001c0003t0001g0003 a0001c0003t0001g0024 a0001c0003t0001g0028 others(38): Show |
42 | HG00408.hp1 HG00621.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.869+15T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177341657 | |||||||
chr4:177341925 | T | C | 3 | a0004c0014t0001g0001 a0004c0014t0001g0184 a0004c0014t0001g0234 |
6 | HG02572.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.869+283T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177341925 | |||||||
chr4:177341937 | GA | G | 41 | a0001c0003t0001g0003 a0001c0003t0001g0024 a0001c0003t0001g0028 others(38): Show |
42 | HG00408.hp1 HG00621.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.869+302delA | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177341937 | ||||||
chr4:177342008 | T | G | 1 | a0002c0010t0005g0380 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.869+366T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177342008 | |||||||
chr4:177342028 | A | T | 41 | a0001c0003t0001g0003 a0001c0003t0001g0024 a0001c0003t0001g0028 others(38): Show |
42 | HG00408.hp1 HG00621.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.869+386A>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177342028 | |||||||
chr4:177342041 | A | C | 1 | a0002c0002t0001g0014 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.869+399A>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177342041 | |||||||
chr4:177342062 | C | T | 1 | a0001c0015t0001g0327 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.869+420C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177342062 | |||||||
chr4:177342086 | G | A | 1 | a0002c0002t0001g0097 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.869+444G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177342086 | |||||||
chr4:177342132 | G | A | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.869+490G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177342132 | |||||||
chr4:177342208 | G | A | 1 | a0001c0001t0006g0188 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.869+566G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177342208 | |||||||
chr4:177342236 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.869+594A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177342236 | |||||||
chr4:177342368 | G | A | 41 | a0001c0003t0001g0003 a0001c0003t0001g0024 a0001c0003t0001g0028 others(38): Show |
42 | HG00408.hp1 HG00621.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.869+726G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177342368 | |||||||
chr4:177342419 | A | G | 12 | a0002c0008t0001g0304 a0005c0009t0001g0315 a0005c0009t0004g0295 others(9): Show |
13 | HG00609.hp1 HG02080.hp1 HG03491.hp1 others(10): Show |
intron_variant | MODIFIER | c.869+777A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177342419 | |||||||
chr4:177342437 | A | G | 1 | a0004c0006t0001g0244 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.869+795A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177342437 | |||||||
chr4:177342478 | G | A | 1 | a0003c0004t0001g0311 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.869+836G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177342478 | |||||||
chr4:177342577 | G | T | 19 | a0005c0009t0001g0318 a0006c0005t0001g0272 a0006c0005t0003g0273 others(16): Show |
19 | HG00140.hp2 HG01433.hp1 HG01975.hp2 others(16): Show |
intron_variant | MODIFIER | c.869+935G>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177342577 | |||||||
chr4:177342665 | T | TA | 81 | a0001c0003t0001g0003 a0001c0003t0001g0024 a0001c0003t0001g0028 others(78): Show |
82 | HG00140.hp2 HG00408.hp1 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.869+1030dupA | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177342665 | ||||||
chr4:177343065 | C | T | 3 | a0002c0008t0001g0339 a0002c0008t0005g0338 a0004c0006t0005g0242 |
3 | HG02723.hp1 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.869+1423C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177343065 | |||||||
chr4:177343066 | G | A | 11 | a0001c0001t0005g0008 a0002c0002t0001g0018 a0004c0006t0001g0183 others(8): Show |
11 | HG01257.hp2 HG02451.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.869+1424G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177343066 | |||||||
chr4:177343209 | C | A | 1 | a0011c0033t0005g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.869+1567C>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177343209 | |||||||
chr4:177343359 | G | A | 2 | a0002c0008t0001g0339 a0002c0008t0005g0338 |
2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.869+1717G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177343359 | |||||||
chr4:177343469 | T | G | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.869+1827T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177343469 | |||||||
chr4:177343499 | T | G | 148 | a0001c0001t0001g0047 a0001c0001t0001g0071 a0001c0001t0001g0135 others(145): Show |
149 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.869+1857T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177343499 | |||||||
chr4:177343690 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.869+2048G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177343690 | |||||||
chr4:177343740 | TTA | T | 3 | a0001c0043t0001g0399 a0002c0020t0001g0170 a0004c0006t0001g0268 |
3 | HG02622.hp1 HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.869+2113_869+2114d others(4): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177343740 | ||||||
chr4:177343755 | T | A | 12 | a0002c0008t0001g0304 a0005c0009t0001g0315 a0005c0009t0004g0295 others(9): Show |
13 | HG00609.hp1 HG02080.hp1 HG03491.hp1 others(10): Show |
intron_variant | MODIFIER | c.869+2113T>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177343755 | |||||||
chr4:177343799 | AT | A | 103 | a0001c0001t0001g0071 a0001c0001t0001g0373 a0001c0001t0002g0269 others(100): Show |
106 | HG00140.hp1 HG00423.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.869+2166delT | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177343799 | ||||||
chr4:177343910 | G | A | 4 | a0002c0008t0001g0339 a0002c0008t0005g0338 a0004c0006t0005g0242 others(1): Show |
4 | HG02723.hp1 HG03540.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.869+2268G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177343910 | |||||||
chr4:177343932 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.869+2290A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177343932 | |||||||
chr4:177343936 | A | G | 1 | a0002c0020t0001g0346 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.869+2294A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177343936 | |||||||
chr4:177343992 | A | G | 167 | a0001c0001t0001g0031 a0001c0001t0001g0071 a0001c0001t0001g0366 others(164): Show |
174 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.869+2350A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177343992 | |||||||
chr4:177344115 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.869+2473G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177344115 | |||||||
chr4:177344319 | A | T | 1 | a0002c0002t0001g0019 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.869+2677A>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177344319 | |||||||
chr4:177344530 | T | C | 1 | a0006c0005t0003g0277 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.869+2888T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177344530 | |||||||
chr4:177344540 | A | G | 1 | a0009c0022t0001g0168 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.869+2898A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177344540 | |||||||
chr4:177344547 | G | A | 12 | a0005c0009t0001g0315 a0005c0009t0004g0295 a0005c0009t0004g0305 others(9): Show |
13 | HG00609.hp1 HG02080.hp1 HG03491.hp1 others(10): Show |
intron_variant | MODIFIER | c.869+2905G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177344547 | |||||||
chr4:177344561 | C | T | 81 | a0002c0002t0001g0016 a0002c0002t0001g0019 a0002c0002t0001g0036 others(78): Show |
86 | HG00408.hp2 HG00609.hp1 HG01069.hp1 others(83): Show |
intron_variant | MODIFIER | c.869+2919C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177344561 | |||||||
chr4:177344597 | G | C | 229 | a0001c0001t0001g0031 a0001c0001t0001g0071 a0001c0001t0001g0366 others(226): Show |
237 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.869+2955G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177344597 | |||||||
chr4:177344597 | G | GA | 75 | a0001c0001t0001g0027 a0001c0001t0001g0039 a0001c0001t0001g0047 others(72): Show |
75 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.869+2956dupA | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177344597 | ||||||
chr4:177344631 | G | C | 3 | a0010c0013t0001g0264 a0010c0013t0001g0265 a0010c0013t0001g0267 |
3 | HG02630.hp2 NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.869+2989G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177344631 | |||||||
chr4:177344647 | C | T | 2 | a0002c0020t0001g0170 a0004c0006t0001g0268 |
2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.869+3005C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177344647 | |||||||
chr4:177344648 | G | A | 1 | a0003c0007t0003g0156 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.869+3006G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177344648 | |||||||
chr4:177344857 | C | T | 1 | a0025c0034t0001g0154 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.869+3215C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177344857 | |||||||
chr4:177344979 | C | A | 83 | a0001c0001t0001g0135 a0002c0002t0001g0014 a0002c0002t0001g0016 others(80): Show |
88 | HG00408.hp2 HG00609.hp1 HG01069.hp1 others(85): Show |
intron_variant | MODIFIER | c.869+3337C>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177344979 | |||||||
chr4:177344980 | G | A | 83 | a0001c0001t0001g0135 a0002c0002t0001g0014 a0002c0002t0001g0016 others(80): Show |
88 | HG00408.hp2 HG00609.hp1 HG01069.hp1 others(85): Show |
intron_variant | MODIFIER | c.869+3338G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177344980 | |||||||
chr4:177345009 | G | A | 83 | a0001c0001t0001g0135 a0002c0002t0001g0014 a0002c0002t0001g0016 others(80): Show |
88 | HG00408.hp2 HG00609.hp1 HG01069.hp1 others(85): Show |
intron_variant | MODIFIER | c.869+3367G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177345009 | |||||||
chr4:177345011 | T | A | 52 | a0002c0002t0001g0014 a0002c0002t0001g0016 a0002c0002t0001g0019 others(49): Show |
53 | HG00408.hp2 HG01069.hp1 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.869+3369T>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177345011 | |||||||
chr4:177345115 | T | G | 1 | a0001c0003t0002g0213 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.869+3473T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177345115 | |||||||
chr4:177345337 | T | C | 83 | a0001c0001t0001g0135 a0002c0002t0001g0014 a0002c0002t0001g0016 others(80): Show |
88 | HG00408.hp2 HG00609.hp1 HG01069.hp1 others(85): Show |
intron_variant | MODIFIER | c.869+3695T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177345337 | |||||||
chr4:177345421 | G | C | 15 | a0001c0001t0001g0076 a0001c0001t0001g0139 a0001c0001t0001g0140 others(12): Show |
15 | HG00544.hp2 HG02040.hp1 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.869+3779G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177345421 | |||||||
chr4:177345464 | CT | C | 146 | a0001c0001t0001g0031 a0001c0001t0001g0071 a0001c0001t0001g0366 others(143): Show |
149 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.869+3834delT | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177345464 | ||||||
chr4:177345470 | T | TTA | 12 | a0005c0009t0001g0315 a0005c0009t0004g0295 a0005c0009t0004g0305 others(9): Show |
13 | HG00609.hp1 HG02080.hp1 HG03491.hp1 others(10): Show |
intron_variant | MODIFIER | c.869+3829_869+3830i others(4): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177345470 | ||||||
chr4:177345474 | T | A | 13 | a0005c0009t0001g0315 a0005c0009t0004g0295 a0005c0009t0004g0305 others(10): Show |
14 | HG00609.hp1 HG02080.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.869+3832T>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177345474 | |||||||
chr4:177345474 | T | TA | 3 | a0002c0002t0003g0057 a0002c0002t0003g0084 a0009c0019t0001g0056 |
3 | HG02257.hp1 HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.869+3832_869+3833i others(3): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177345474 | |||||||
chr4:177345474 | T | TTA | 68 | a0001c0001t0001g0135 a0002c0002t0001g0014 a0002c0002t0001g0016 others(65): Show |
72 | HG00408.hp2 HG01069.hp1 HG01081.hp2 others(69): Show |
intron_variant | MODIFIER | c.869+3833_869+3834i others(4): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177345474 | ||||||
chr4:177345616 | C | T | 1 | a0001c0001t0002g0229 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.869+3974C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177345616 | |||||||
chr4:177345617 | G | A | 1 | a0001c0003t0003g0364 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.869+3975G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177345617 | |||||||
chr4:177345661 | A | C | 1 | a0004c0006t0001g0183 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.869+4019A>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177345661 | |||||||
chr4:177345679 | C | CT | 65 | a0001c0001t0001g0027 a0001c0001t0001g0039 a0001c0001t0001g0062 others(62): Show |
66 | HG00423.hp2 HG00609.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.869+4062dupT | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177345679 | ||||||
chr4:177345679 | CT | C | 84 | a0001c0001t0001g0021 a0001c0001t0001g0089 a0001c0001t0005g0008 others(81): Show |
90 | HG00140.hp1 HG00423.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.869+4062delT | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177345679 | ||||||
chr4:177345679 | CTT | C | 45 | a0001c0001t0001g0031 a0001c0001t0001g0071 a0001c0001t0001g0366 others(42): Show |
46 | HG00323.hp2 HG00741.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.869+4061_869+4062d others(4): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177345679 | ||||||
chr4:177345679 | CTTT | C | 8 | a0002c0002t0001g0058 a0002c0002t0001g0352 a0002c0002t0001g0370 others(5): Show |
8 | HG01168.hp1 HG01169.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.869+4060_869+4062d others(5): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177345679 | ||||||
chr4:177345679 | CTTTTTTT others(3): Show |
C | 24 | a0002c0002t0003g0030 a0002c0002t0005g0347 a0002c0002t0005g0348 others(21): Show |
24 | HG00140.hp2 HG00738.hp1 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.869+4053_869+4062d others(12): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177345679 | ||||||
chr4:177345703 | T | C | 1 | a0001c0003t0001g0104 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.869+4061T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177345703 | |||||||
chr4:177345738 | G | A | 1 | a0003c0004t0001g0311 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.869+4096G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177345738 | |||||||
chr4:177345841 | T | C | 1 | a0001c0001t0001g0373 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.869+4199T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177345841 | |||||||
chr4:177345882 | G | C | 4 | a0006c0005t0003g0280 a0006c0005t0003g0281 a0006c0005t0003g0284 others(1): Show |
4 | NA18943.hp1 NA19003.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.869+4240G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177345882 | |||||||
chr4:177346081 | A | T | 6 | a0002c0010t0001g0343 a0002c0010t0001g0381 a0002c0010t0005g0380 others(3): Show |
6 | HG01884.hp2 HG02559.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.869+4439A>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177346081 | |||||||
chr4:177346153 | C | T | 64 | a0002c0002t0001g0014 a0002c0002t0001g0016 a0002c0002t0001g0019 others(61): Show |
66 | HG00408.hp2 HG00609.hp1 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.869+4511C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177346153 | |||||||
chr4:177346165 | T | C | 83 | a0001c0001t0001g0135 a0002c0002t0001g0014 a0002c0002t0001g0016 others(80): Show |
88 | HG00408.hp2 HG00609.hp1 HG01069.hp1 others(85): Show |
intron_variant | MODIFIER | c.869+4523T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177346165 | |||||||
chr4:177346232 | T | C | 1 | a0002c0028t0001g0034 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.869+4590T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177346232 | |||||||
chr4:177346251 | C | T | 1 | a0006c0005t0001g0272 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.869+4609C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177346251 | |||||||
chr4:177346334 | TTTTTTA | T | 83 | a0001c0001t0001g0135 a0002c0002t0001g0014 a0002c0002t0001g0016 others(80): Show |
88 | HG00408.hp2 HG00609.hp1 HG01069.hp1 others(85): Show |
intron_variant | MODIFIER | c.869+4705_869+4710d others(8): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177346334 | ||||||
chr4:177346497 | C | T | 83 | a0001c0001t0001g0135 a0002c0002t0001g0014 a0002c0002t0001g0016 others(80): Show |
88 | HG00408.hp2 HG00609.hp1 HG01069.hp1 others(85): Show |
intron_variant | MODIFIER | c.869+4855C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177346497 | |||||||
chr4:177346530 | C | T | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.870-4850C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177346530 | |||||||
chr4:177346744 | T | G | 83 | a0001c0001t0001g0135 a0002c0002t0001g0014 a0002c0002t0001g0016 others(80): Show |
88 | HG00408.hp2 HG00609.hp1 HG01069.hp1 others(85): Show |
intron_variant | MODIFIER | c.870-4636T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177346744 | |||||||
chr4:177346838 | A | G | 3 | a0002c0002t0003g0057 a0002c0002t0003g0084 a0009c0019t0001g0056 |
3 | HG02257.hp1 HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.870-4542A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177346838 | |||||||
chr4:177346960 | C | A | 52 | a0002c0002t0001g0014 a0002c0002t0001g0016 a0002c0002t0001g0019 others(49): Show |
53 | HG00408.hp2 HG01069.hp1 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.870-4420C>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177346960 | |||||||
chr4:177346977 | A | G | 85 | a0001c0001t0001g0135 a0001c0003t0003g0364 a0002c0002t0001g0014 others(82): Show |
90 | HG00408.hp2 HG00609.hp1 HG01069.hp1 others(87): Show |
intron_variant | MODIFIER | c.870-4403A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177346977 | |||||||
chr4:177346999 | C | T | 1 | a0001c0003t0003g0364 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.870-4381C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177346999 | |||||||
chr4:177347001 | C | CA | 7 | a0002c0010t0001g0343 a0002c0010t0001g0381 a0002c0010t0005g0380 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.870-4364dupA | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177347001 | ||||||
chr4:177347001 | CA | C | 156 | a0001c0001t0001g0031 a0001c0001t0001g0071 a0001c0001t0001g0148 others(153): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.870-4364delA | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177347001 | ||||||
chr4:177347010 | A | G | 1 | a0017c0026t0001g0301 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.870-4370A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177347010 | |||||||
chr4:177347097 | G | C | 95 | a0001c0001t0001g0135 a0001c0001t0005g0008 a0002c0002t0001g0014 others(92): Show |
100 | HG00408.hp2 HG00609.hp1 HG01069.hp1 others(97): Show |
intron_variant | MODIFIER | c.870-4283G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177347097 | |||||||
chr4:177347119 | C | G | 1 | a0001c0001t0001g0116 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.870-4261C>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177347119 | |||||||
chr4:177347125 | C | T | 1 | a0002c0002t0001g0386 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.870-4255C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177347125 | |||||||
chr4:177347131 | A | G | 5 | a0001c0001t0001g0068 a0001c0001t0001g0131 a0001c0001t0001g0148 others(2): Show |
5 | HG00323.hp1 NA18972.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.870-4249A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177347131 | |||||||
chr4:177347171 | T | C | 9 | a0002c0020t0001g0010 a0002c0032t0001g0306 a0004c0014t0001g0001 others(6): Show |
12 | HG01981.hp1 HG02572.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.870-4209T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177347171 | |||||||
chr4:177347223 | A | G | 1 | a0002c0002t0001g0365 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.870-4157A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177347223 | |||||||
chr4:177347296 | C | T | 40 | a0002c0002t0001g0025 a0002c0002t0001g0355 a0002c0008t0001g0304 others(37): Show |
42 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.870-4084C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177347296 | |||||||
chr4:177347393 | C | A | 22 | a0001c0001t0001g0135 a0002c0002t0003g0057 a0002c0002t0003g0084 others(19): Show |
22 | HG00609.hp1 HG01884.hp2 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.870-3987C>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177347393 | |||||||
chr4:177347509 | G | T | 165 | a0001c0001t0001g0031 a0001c0001t0001g0071 a0001c0001t0001g0135 others(162): Show |
168 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.870-3871G>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177347509 | |||||||
chr4:177347743 | A | G | 88 | a0001c0001t0001g0031 a0001c0001t0001g0071 a0001c0001t0001g0135 others(85): Show |
90 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.870-3637A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177347743 | |||||||
chr4:177347790 | A | G | 1 | a0001c0001t0006g0188 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.870-3590A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177347790 | |||||||
chr4:177347925 | T | A | 1 | a0005c0025t0011g0398 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.870-3455T>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177347925 | |||||||
chr4:177348035 | T | C | 2 | a0002c0002t0003g0057 a0002c0002t0003g0084 |
2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.870-3345T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348035 | |||||||
chr4:177348099 | A | G | 84 | a0001c0001t0001g0031 a0001c0001t0001g0071 a0001c0001t0001g0135 others(81): Show |
86 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(83): Show |
intron_variant | MODIFIER | c.870-3281A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348099 | |||||||
chr4:177348197 | G | A | 1 | a0002c0002t0007g0186 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.870-3183G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348197 | |||||||
chr4:177348250 | C | T | 7 | a0001c0001t0001g0068 a0001c0001t0001g0128 a0001c0001t0001g0129 others(4): Show |
7 | HG00323.hp1 NA18959.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.870-3130C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348250 | |||||||
chr4:177348329 | C | A | 1 | a0002c0020t0001g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.870-3051C>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348329 | |||||||
chr4:177348456 | T | C | 1 | a0002c0002t0001g0009 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.870-2924T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348456 | |||||||
chr4:177348512 | C | T | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2868C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348512 | |||||||
chr4:177348515 | A | C | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2865A>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348515 | |||||||
chr4:177348516 | A | C | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2864A>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348516 | |||||||
chr4:177348516 | A | G | 72 | a0002c0002t0001g0009 a0002c0002t0001g0014 a0002c0002t0001g0016 others(69): Show |
74 | HG00408.hp2 HG00609.hp1 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.870-2864A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348516 | |||||||
chr4:177348518 | A | T | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2862A>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348518 | |||||||
chr4:177348526 | G | C | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2854G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348526 | |||||||
chr4:177348527 | G | C | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2853G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348527 | |||||||
chr4:177348530 | A | G | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2850A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348530 | |||||||
chr4:177348531 | T | A | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2849T>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348531 | |||||||
chr4:177348534 | T | A | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2846T>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348534 | |||||||
chr4:177348540 | C | G | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2840C>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348540 | |||||||
chr4:177348543 | C | T | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2837C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348543 | |||||||
chr4:177348545 | A | T | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2835A>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348545 | |||||||
chr4:177348547 | G | C | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2833G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348547 | |||||||
chr4:177348549 | G | C | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2831G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348549 | |||||||
chr4:177348550 | C | T | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2830C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348550 | |||||||
chr4:177348551 | C | G | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2829C>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348551 | |||||||
chr4:177348559 | C | A | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2821C>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348559 | |||||||
chr4:177348560 | C | G | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2820C>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348560 | |||||||
chr4:177348571 | A | C | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2809A>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348571 | |||||||
chr4:177348572 | T | A | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2808T>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348572 | |||||||
chr4:177348574 | C | A | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2806C>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348574 | |||||||
chr4:177348575 | T | C | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2805T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348575 | |||||||
chr4:177348577 | T | A | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2803T>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348577 | |||||||
chr4:177348582 | C | A | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2798C>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348582 | |||||||
chr4:177348586 | A | T | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2794A>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348586 | |||||||
chr4:177348591 | G | C | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2789G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348591 | |||||||
chr4:177348592 | T | G | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2788T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348592 | |||||||
chr4:177348593 | G | T | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2787G>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348593 | |||||||
chr4:177348594 | G | T | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2786G>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348594 | |||||||
chr4:177348595 | T | C | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2785T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348595 | |||||||
chr4:177348601 | T | C | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2779T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348601 | |||||||
chr4:177348603 | T | A | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2777T>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348603 | |||||||
chr4:177348607 | T | C | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2773T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348607 | |||||||
chr4:177348608 | C | A | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2772C>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348608 | |||||||
chr4:177348613 | T | G | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2767T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348613 | |||||||
chr4:177348619 | T | G | 1 | a0002c0008t0001g0340 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.870-2761T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348619 | |||||||
chr4:177348642 | G | A | 1 | a0017c0026t0001g0301 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.870-2738G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348642 | |||||||
chr4:177348672 | C | T | 24 | a0006c0005t0001g0272 a0006c0005t0003g0273 a0006c0005t0003g0275 others(21): Show |
24 | HG00140.hp2 HG00544.hp2 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.870-2708C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348672 | |||||||
chr4:177348713 | G | A | 1 | a0002c0020t0001g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.870-2667G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348713 | |||||||
chr4:177348817 | C | CATGAGAT | 60 | a0002c0002t0001g0009 a0002c0002t0001g0014 a0002c0002t0001g0016 others(57): Show |
61 | HG00408.hp2 HG00738.hp1 HG01192.hp1 others(58): Show |
intron_variant | MODIFIER | c.870-2561_870-2555d others(9): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177348817 | ||||||
chr4:177348858 | A | AT | 51 | a0001c0001t0001g0033 a0001c0001t0001g0054 a0001c0001t0001g0068 others(48): Show |
52 | HG00597.hp1 HG00642.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.870-2495dupT | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177348858 | ||||||
chr4:177348858 | A | ATT | 19 | a0002c0002t0001g0025 a0002c0002t0001g0110 a0002c0020t0001g0372 others(16): Show |
20 | HG00609.hp1 HG01261.hp2 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.870-2496_870-2495d others(4): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177348858 | ||||||
chr4:177348858 | A | ATTT | 32 | a0001c0001t0001g0366 a0002c0002t0001g0026 a0002c0002t0001g0058 others(29): Show |
32 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.870-2497_870-2495d others(5): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177348858 | ||||||
chr4:177348858 | A | ATTTT | 27 | a0002c0002t0001g0002 a0002c0002t0001g0013 a0002c0002t0001g0020 others(24): Show |
28 | HG00423.hp1 HG00735.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.870-2498_870-2495d others(6): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177348858 | ||||||
chr4:177348858 | A | ATTTTT | 20 | a0001c0001t0001g0135 a0002c0002t0001g0035 a0002c0002t0001g0060 others(17): Show |
20 | HG01069.hp1 HG01123.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.870-2499_870-2495d others(7): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177348858 | ||||||
chr4:177348858 | A | ATTTTTT | 17 | a0002c0002t0001g0211 a0002c0002t0001g0383 a0002c0028t0001g0032 others(14): Show |
17 | HG00140.hp2 HG00544.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.870-2500_870-2495d others(8): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177348858 | ||||||
chr4:177348858 | A | ATTTTTTT | 7 | a0006c0005t0001g0272 a0006c0005t0003g0281 a0006c0005t0003g0284 others(4): Show |
7 | HG02040.hp1 HG02109.hp2 NA19003.hp2 others(4): Show |
intron_variant | MODIFIER | c.870-2501_870-2495d others(9): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177348858 | ||||||
chr4:177348858 | A | ATTTTTTT others(3): Show |
3 | a0002c0002t0008g0048 a0002c0002t0008g0081 a0004c0006t0001g0268 |
3 | HG01981.hp2 HG01993.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.870-2504_870-2495d others(12): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177348858 | ||||||
chr4:177348858 | A | ATTTTTTT others(7): Show |
9 | a0002c0002t0001g0050 a0002c0002t0001g0051 a0002c0002t0001g0065 others(6): Show |
9 | HG00408.hp2 HG03017.hp2 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.870-2508_870-2495d others(16): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177348858 | ||||||
chr4:177348858 | A | ATTTTTTT others(8): Show |
12 | a0002c0002t0001g0036 a0002c0002t0001g0049 a0002c0002t0001g0052 others(9): Show |
12 | HG01943.hp2 HG02135.hp2 HG03942.hp2 others(9): Show |
intron_variant | MODIFIER | c.870-2509_870-2495d others(17): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177348858 | ||||||
chr4:177348858 | A | ATTTTTTT others(9): Show |
7 | a0002c0002t0001g0043 a0002c0002t0001g0083 a0002c0002t0001g0390 others(4): Show |
8 | HG01952.hp1 HG02071.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.870-2510_870-2495d others(18): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177348858 | ||||||
chr4:177348858 | A | ATTTTTTT others(10): Show |
5 | a0002c0002t0001g0074 a0002c0002t0001g0391 a0003c0004t0001g0335 others(2): Show |
5 | HG02055.hp2 HG03486.hp1 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.870-2511_870-2495d others(19): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177348858 | ||||||
chr4:177348858 | A | ATTTTTTT others(11): Show |
6 | a0002c0002t0001g0046 a0002c0002t0003g0057 a0002c0002t0003g0084 others(3): Show |
6 | HG00738.hp1 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.870-2512_870-2495d others(20): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177348858 | ||||||
chr4:177348858 | A | ATTTTTTT others(12): Show |
1 | a0009c0019t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.870-2513_870-2495d others(21): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177348858 | ||||||
chr4:177348858 | A | ATTTTTTT others(13): Show |
2 | a0002c0002t0001g0016 a0002c0002t0001g0109 |
2 | NA19078.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.870-2514_870-2495d others(22): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177348858 | ||||||
chr4:177348858 | A | ATTTTTTT others(14): Show |
1 | a0002c0002t0001g0079 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.870-2515_870-2495d others(23): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177348858 | ||||||
chr4:177348858 | A | ATTTTTTT others(15): Show |
1 | a0002c0002t0001g0014 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.870-2516_870-2495d others(24): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177348858 | ||||||
chr4:177348858 | A | ATTTTTTT others(16): Show |
1 | a0002c0002t0005g0347 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.870-2517_870-2495d others(25): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177348858 | ||||||
chr4:177348858 | A | ATTTTTTT others(17): Show |
1 | a0002c0002t0005g0348 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.870-2518_870-2495d others(26): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177348858 | ||||||
chr4:177348858 | A | ATTTTTTT others(21): Show |
1 | a0002c0002t0005g0349 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.870-2495_870-2494i others(30): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177348858 | ||||||
chr4:177348858 | A | ATTTTTTT others(22): Show |
1 | a0002c0002t0001g0009 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.870-2495_870-2494i others(31): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177348858 | ||||||
chr4:177348858 | A | ATTTTTTT others(27): Show |
1 | a0002c0002t0001g0019 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.870-2495_870-2494i others(36): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177348858 | ||||||
chr4:177348858 | A | ATTTTTTT others(31): Show |
1 | a0009c0019t0001g0015 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.870-2495_870-2494i others(40): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177348858 | ||||||
chr4:177348858 | AT | A | 16 | a0001c0001t0001g0022 a0001c0001t0001g0031 a0001c0001t0001g0071 others(13): Show |
16 | HG01515.hp2 HG01884.hp2 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.870-2495delT | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177348858 | ||||||
chr4:177348858 | ATTTTTTT others(2): Show |
A | 6 | a0002c0020t0001g0010 a0002c0032t0001g0306 a0004c0014t0001g0001 others(3): Show |
9 | HG02572.hp1 HG02622.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.870-2503_870-2495d others(11): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177348858 | ||||||
chr4:177348961 | G | A | 1 | a0001c0043t0001g0399 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.870-2419G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177348961 | |||||||
chr4:177349034 | A | AT | 135 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0033 others(132): Show |
136 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.870-2325dupT | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177349034 | ||||||
chr4:177349034 | A | ATT | 65 | a0001c0001t0001g0031 a0001c0001t0001g0071 a0001c0001t0001g0142 others(62): Show |
70 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.870-2326_870-2325d others(4): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177349034 | ||||||
chr4:177349034 | A | ATTT | 9 | a0001c0001t0001g0054 a0001c0001t0001g0099 a0001c0001t0001g0127 others(6): Show |
9 | HG01123.hp1 HG01952.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.870-2327_870-2325d others(5): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177349034 | ||||||
chr4:177349034 | AT | A | 10 | a0002c0002t0001g0018 a0002c0002t0001g0035 a0002c0002t0001g0101 others(7): Show |
10 | HG01257.hp2 HG01496.hp1 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.870-2325delT | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177349034 | ||||||
chr4:177349034 | ATT | A | 122 | a0001c0001t0001g0135 a0001c0001t0001g0366 a0002c0002t0001g0002 others(119): Show |
124 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.870-2326_870-2325d others(4): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177349034 | ||||||
chr4:177349034 | ATTTT | A | 13 | a0005c0009t0001g0315 a0005c0009t0001g0318 a0005c0009t0004g0295 others(10): Show |
14 | HG00609.hp1 HG02056.hp1 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.870-2328_870-2325d others(6): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177349034 | ||||||
chr4:177349052 | T | G | 1 | a0005c0016t0001g0012 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.870-2328T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177349052 | |||||||
chr4:177349054 | T | G | 13 | a0005c0009t0001g0315 a0005c0009t0001g0318 a0005c0009t0004g0295 others(10): Show |
14 | HG00609.hp1 HG02056.hp1 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.870-2326T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177349054 | |||||||
chr4:177349113 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.870-2267A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177349113 | |||||||
chr4:177349177 | C | T | 1 | a0001c0001t0001g0394 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.870-2203C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177349177 | |||||||
chr4:177349189 | T | C | 1 | a0002c0002t0001g0088 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.870-2191T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177349189 | |||||||
chr4:177349200 | G | A | 73 | a0002c0002t0001g0009 a0002c0002t0001g0014 a0002c0002t0001g0016 others(70): Show |
75 | HG00408.hp2 HG00609.hp1 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.870-2180G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177349200 | |||||||
chr4:177349327 | A | G | 3 | a0001c0003t0003g0364 a0002c0020t0001g0170 a0013c0023t0005g0261 |
3 | HG01175.hp2 HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.870-2053A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177349327 | |||||||
chr4:177349339 | G | T | 1 | a0002c0002t0001g0009 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.870-2041G>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177349339 | |||||||
chr4:177349373 | C | T | 1 | a0002c0028t0001g0034 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.870-2007C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177349373 | |||||||
chr4:177349472 | T | G | 2 | a0012c0017t0004g0270 a0012c0017t0004g0274 |
2 | HG03654.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.870-1908T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177349472 | |||||||
chr4:177349563 | T | C | 2 | a0009c0019t0001g0072 a0024c0046t0001g0260 |
2 | HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.870-1817T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177349563 | |||||||
chr4:177349582 | A | C | 24 | a0006c0005t0001g0272 a0006c0005t0003g0273 a0006c0005t0003g0275 others(21): Show |
24 | HG00140.hp2 HG00544.hp2 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.870-1798A>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177349582 | |||||||
chr4:177349762 | A | G | 237 | a0001c0001t0001g0031 a0001c0001t0001g0071 a0001c0001t0001g0135 others(234): Show |
245 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.870-1618A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177349762 | |||||||
chr4:177349990 | G | A | 1 | a0002c0002t0001g0014 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.870-1390G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177349990 | |||||||
chr4:177350000 | T | C | 1 | a0003c0004t0001g0319 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.870-1380T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177350000 | |||||||
chr4:177350377 | A | G | 4 | a0002c0008t0001g0339 a0002c0008t0005g0338 a0004c0006t0005g0242 others(1): Show |
4 | HG02723.hp1 HG03540.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.870-1003A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177350377 | |||||||
chr4:177350448 | A | G | 78 | a0002c0002t0001g0009 a0002c0002t0001g0014 a0002c0002t0001g0016 others(75): Show |
80 | HG00408.hp2 HG00609.hp1 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.870-932A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177350448 | |||||||
chr4:177350508 | C | T | 1 | a0002c0002t0001g0371 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.870-872C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177350508 | |||||||
chr4:177350636 | T | C | 78 | a0002c0002t0001g0009 a0002c0002t0001g0014 a0002c0002t0001g0016 others(75): Show |
80 | HG00408.hp2 HG00609.hp1 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.870-744T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177350636 | |||||||
chr4:177350643 | G | T | 1 | a0007c0031t0001g0336 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.870-737G>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177350643 | |||||||
chr4:177350673 | A | G | 4 | a0002c0008t0001g0339 a0002c0008t0005g0338 a0004c0006t0005g0242 others(1): Show |
4 | HG02723.hp1 HG03540.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.870-707A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177350673 | |||||||
chr4:177350705 | A | G | 2 | a0009c0019t0001g0072 a0024c0046t0001g0260 |
2 | HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.870-675A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177350705 | |||||||
chr4:177350756 | A | T | 1 | a0007c0011t0002g0215 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.870-624A>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177350756 | |||||||
chr4:177350782 | A | G | 9 | a0002c0002t0003g0030 a0002c0002t0003g0057 a0002c0002t0003g0084 others(6): Show |
9 | HG00738.hp1 HG01891.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.870-598A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177350782 | |||||||
chr4:177350834 | G | A | 18 | a0005c0009t0001g0315 a0005c0009t0001g0318 a0005c0009t0004g0295 others(15): Show |
19 | HG00609.hp1 HG02056.hp1 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.870-546G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177350834 | |||||||
chr4:177350897 | AGGG | A | 18 | a0005c0009t0001g0315 a0005c0009t0001g0318 a0005c0009t0004g0295 others(15): Show |
19 | HG00609.hp1 HG02056.hp1 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.870-479_870-477del others(3): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177350897 | ||||||
chr4:177350996 | C | T | 1 | a0001c0003t0001g0159 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.870-384C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177350996 | |||||||
chr4:177351009 | A | AC | 18 | a0005c0009t0001g0315 a0005c0009t0001g0318 a0005c0009t0004g0295 others(15): Show |
19 | HG00609.hp1 HG02056.hp1 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.870-370dupC | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177351009 | ||||||
chr4:177351068 | C | T | 1 | a0006c0005t0003g0341 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.870-312C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177351068 | |||||||
chr4:177351164 | A | C | 13 | a0005c0009t0001g0315 a0005c0009t0001g0318 a0005c0009t0004g0295 others(10): Show |
14 | HG00609.hp1 HG02056.hp1 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.870-216A>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177351164 | |||||||
chr4:177351169 | G | A | 117 | a0001c0003t0003g0364 a0001c0015t0001g0290 a0002c0002t0001g0009 others(114): Show |
122 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.870-211G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | chr4 | 177351169 | |||||||
chr4:177351206 | C | CA | 56 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0037 others(53): Show |
56 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.870-142dupA | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177351206 | ||||||
chr4:177351206 | C | CAA | 9 | a0001c0001t0001g0095 a0001c0001t0001g0366 a0001c0001t0001g0373 others(6): Show |
9 | HG00544.hp1 HG01081.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.870-143_870-142dup others(2): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177351206 | ||||||
chr4:177351206 | C | CAAAAAAA others(8): Show |
1 | a0004c0014t0001g0184 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.870-156_870-142dup others(15): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177351206 | ||||||
chr4:177351206 | CA | C | 30 | a0001c0001t0001g0129 a0001c0015t0001g0290 a0002c0010t0001g0343 others(27): Show |
32 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.870-142delA | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177351206 | ||||||
chr4:177351206 | CAAAA | C | 7 | a0006c0005t0003g0273 a0006c0005t0003g0275 a0006c0005t0003g0276 others(4): Show |
7 | HG00140.hp2 HG01433.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.870-145_870-142del others(4): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177351206 | ||||||
chr4:177351206 | CAAAAA | C | 16 | a0006c0005t0001g0272 a0006c0005t0003g0281 a0006c0005t0003g0283 others(13): Show |
16 | HG00544.hp2 HG01975.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.870-146_870-142del others(5): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177351206 | ||||||
chr4:177351206 | CAAAAAA | C | 8 | a0002c0002t0005g0347 a0002c0002t0005g0348 a0002c0002t0005g0349 others(5): Show |
8 | HG01891.hp1 HG01891.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.870-147_870-142del others(6): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177351206 | ||||||
chr4:177351206 | CAAAAAAA | C | 28 | a0002c0002t0001g0018 a0002c0002t0001g0035 a0002c0002t0001g0088 others(25): Show |
28 | HG00408.hp2 HG00738.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.870-148_870-142del others(7): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177351206 | ||||||
chr4:177351206 | CAAAAAAA others(1): Show |
C | 103 | a0002c0002t0001g0002 a0002c0002t0001g0009 a0002c0002t0001g0013 others(100): Show |
105 | HG00323.hp2 HG00423.hp1 HG00735.hp1 others(102): Show |
intron_variant | MODIFIER | c.870-149_870-142del others(8): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177351206 | ||||||
chr4:177351206 | CAAAAAAA others(4): Show |
C | 2 | a0001c0003t0001g0158 a0001c0003t0001g0159 |
2 | NA18949.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.870-152_870-142del others(11): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177351206 | ||||||
chr4:177351206 | CAAAAAAA others(6): Show |
C | 1 | a0013c0023t0005g0261 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.870-154_870-142del others(13): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177351206 | ||||||
chr4:177351206 | CAAAAAAA others(7): Show |
C | 15 | a0001c0003t0001g0108 a0001c0003t0003g0364 a0005c0009t0001g0315 others(12): Show |
16 | HG00609.hp1 HG01175.hp2 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.870-155_870-142del others(14): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 177351206 | ||||||
chr4:177351594 | G | A | 71 | a0001c0003t0003g0364 a0002c0002t0001g0002 a0002c0002t0001g0013 others(68): Show |
72 | HG00323.hp2 HG00423.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.1039+45G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 7/9 | chr4 | 177351594 | |||||||
chr4:177351602 | T | C | 4 | a0005c0025t0005g0320 a0017c0026t0001g0301 a0017c0026t0001g0307 others(1): Show |
4 | HG02572.hp2 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039+53T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 7/9 | chr4 | 177351602 | |||||||
chr4:177351618 | TATCTTGC others(3): Show |
T | 3 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0038 |
3 | HG02071.hp2 HG02129.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1039+76_1039+85del others(10): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 177351618 | ||||||
chr4:177351692 | C | T | 151 | a0002c0002t0001g0002 a0002c0002t0001g0009 a0002c0002t0001g0013 others(148): Show |
154 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.1039+143C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 7/9 | chr4 | 177351692 | |||||||
chr4:177351762 | T | C | 60 | a0002c0002t0001g0009 a0002c0002t0001g0014 a0002c0002t0001g0016 others(57): Show |
61 | HG00408.hp2 HG00738.hp1 HG01192.hp1 others(58): Show |
intron_variant | MODIFIER | c.1039+213T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 7/9 | chr4 | 177351762 | |||||||
chr4:177351817 | A | C | 1 | a0002c0002t0001g0378 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1039+268A>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 7/9 | chr4 | 177351817 | |||||||
chr4:177351845 | C | T | 1 | a0006c0005t0003g0341 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1039+296C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 7/9 | chr4 | 177351845 | |||||||
chr4:177351851 | T | A | 1 | a0009c0019t0001g0015 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1039+302T>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 7/9 | chr4 | 177351851 | |||||||
chr4:177351876 | A | G | 93 | a0001c0001t0001g0135 a0001c0003t0003g0364 a0002c0002t0001g0009 others(90): Show |
94 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.1039+327A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 7/9 | chr4 | 177351876 | |||||||
chr4:177351879 | T | G | 5 | a0001c0043t0001g0399 a0002c0008t0001g0339 a0002c0008t0005g0338 others(2): Show |
5 | HG02622.hp1 HG02723.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1039+330T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 7/9 | chr4 | 177351879 | |||||||
chr4:177351956 | A | G | 178 | a0001c0003t0003g0364 a0002c0002t0001g0002 a0002c0002t0001g0009 others(175): Show |
181 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.1039+407A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 7/9 | chr4 | 177351956 | |||||||
chr4:177351993 | G | T | 27 | a0001c0003t0003g0364 a0005c0025t0011g0398 a0006c0005t0001g0272 others(24): Show |
27 | HG00140.hp2 HG00544.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.1039+444G>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 7/9 | chr4 | 177351993 | |||||||
chr4:177352232 | A | C | 18 | a0001c0043t0001g0399 a0002c0008t0001g0339 a0002c0008t0005g0338 others(15): Show |
21 | HG01433.hp2 HG02486.hp1 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.1039+683A>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 7/9 | chr4 | 177352232 | |||||||
chr4:177352483 | T | C | 66 | a0002c0002t0001g0009 a0002c0002t0001g0014 a0002c0002t0001g0016 others(63): Show |
67 | HG00408.hp2 HG00738.hp1 HG01192.hp1 others(64): Show |
intron_variant | MODIFIER | c.1040-825T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 7/9 | chr4 | 177352483 | |||||||
chr4:177352529 | A | G | 2 | a0004c0006t0005g0242 a0011c0033t0005g0299 |
2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1040-779A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 7/9 | chr4 | 177352529 | |||||||
chr4:177352626 | C | T | 1 | a0001c0015t0001g0293 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1040-682C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 7/9 | chr4 | 177352626 | |||||||
chr4:177352779 | G | A | 88 | a0002c0002t0001g0002 a0002c0002t0001g0013 a0002c0002t0001g0018 others(85): Show |
90 | HG00323.hp2 HG00423.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.1040-529G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 7/9 | chr4 | 177352779 | |||||||
chr4:177352787 | G | A | 5 | a0002c0008t0001g0339 a0002c0008t0005g0338 a0004c0006t0005g0242 others(2): Show |
5 | HG02723.hp1 HG03195.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1040-521G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 7/9 | chr4 | 177352787 | |||||||
chr4:177352839 | A | C | 10 | a0002c0002t0003g0030 a0002c0002t0003g0057 a0002c0002t0003g0084 others(7): Show |
10 | HG00738.hp1 HG01891.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1040-469A>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 7/9 | chr4 | 177352839 | |||||||
chr4:177352840 | A | G | 1 | a0005c0025t0011g0398 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1040-468A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 7/9 | chr4 | 177352840 | |||||||
chr4:177352841 | AAG | A | 58 | a0002c0002t0001g0002 a0002c0002t0001g0013 a0002c0002t0001g0020 others(55): Show |
59 | HG00323.hp2 HG00423.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.1040-465_1040-464d others(4): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 177352841 | ||||||
chr4:177353023 | G | A | 10 | a0002c0020t0001g0010 a0002c0020t0001g0170 a0002c0020t0001g0346 others(7): Show |
13 | HG01433.hp2 HG02486.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1040-285G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 7/9 | chr4 | 177353023 | |||||||
chr4:177353099 | C | T | 1 | a0001c0015t0001g0290 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1040-209C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 7/9 | chr4 | 177353099 | |||||||
chr4:177353201 | A | G | 1 | a0003c0007t0001g0357 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1040-107A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 7/9 | chr4 | 177353201 | |||||||
chr4:177353223 | T | C | 48 | a0002c0002t0001g0025 a0002c0002t0001g0060 a0002c0002t0001g0355 others(45): Show |
50 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.1040-85T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 7/9 | chr4 | 177353223 | |||||||
chr4:177353765 | C | CT | 22 | a0001c0001t0002g0228 a0001c0015t0001g0293 a0002c0002t0001g0079 others(19): Show |
25 | HG00140.hp2 HG00544.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.1460+55dupT | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | 177353765 | ||||||
chr4:177353765 | CT | C | 8 | a0001c0001t0001g0022 a0001c0001t0002g0171 a0001c0001t0002g0218 others(5): Show |
8 | HG01192.hp1 HG01255.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1460+55delT | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | 177353765 | ||||||
chr4:177353814 | A | G | 86 | a0001c0001t0001g0027 a0001c0001t0001g0039 a0001c0001t0001g0047 others(83): Show |
87 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1460+86A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177353814 | |||||||
chr4:177353903 | T | A | 4 | a0001c0001t0001g0062 a0001c0001t0001g0087 a0001c0001t0004g0200 others(1): Show |
4 | NA18946.hp2 NA18950.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.1460+175T>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177353903 | |||||||
chr4:177354066 | T | C | 233 | a0001c0001t0001g0344 a0001c0001t0001g0389 a0002c0002t0001g0002 others(230): Show |
241 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.1460+338T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177354066 | |||||||
chr4:177354067 | G | A | 1 | a0002c0008t0001g0298 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1460+339G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177354067 | |||||||
chr4:177354252 | G | GT | 105 | a0001c0001t0001g0121 a0001c0001t0001g0344 a0001c0001t0001g0389 others(102): Show |
110 | HG00323.hp2 HG00423.hp1 HG00735.hp1 others(107): Show |
intron_variant | MODIFIER | c.1460+536dupT | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | 177354252 | ||||||
chr4:177354374 | C | T | 43 | a0002c0002t0001g0025 a0002c0002t0001g0060 a0002c0002t0001g0355 others(40): Show |
45 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1460+646C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177354374 | |||||||
chr4:177354496 | C | T | 58 | a0002c0002t0001g0009 a0002c0002t0001g0014 a0002c0002t0001g0016 others(55): Show |
59 | HG00408.hp2 HG00738.hp1 HG01192.hp1 others(56): Show |
intron_variant | MODIFIER | c.1460+768C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177354496 | |||||||
chr4:177354515 | G | T | 58 | a0002c0002t0001g0009 a0002c0002t0001g0014 a0002c0002t0001g0016 others(55): Show |
59 | HG00408.hp2 HG00738.hp1 HG01192.hp1 others(56): Show |
intron_variant | MODIFIER | c.1460+787G>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177354515 | |||||||
chr4:177354541 | GTTTATT | G | 6 | a0007c0011t0002g0214 a0007c0011t0002g0215 a0007c0011t0002g0216 others(3): Show |
6 | HG00544.hp2 HG02040.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.1460+829_1460+834d others(8): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | 177354541 | ||||||
chr4:177354770 | C | T | 1 | a0002c0002t0001g0379 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1460+1042C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177354770 | |||||||
chr4:177354936 | GT | G | 10 | a0002c0002t0003g0030 a0002c0002t0003g0057 a0002c0002t0003g0084 others(7): Show |
10 | HG00738.hp1 HG01891.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1460+1209delT | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177354936 | |||||||
chr4:177355090 | A | G | 1 | a0013c0023t0001g0257 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1460+1362A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177355090 | |||||||
chr4:177355573 | G | A | 1 | a0002c0002t0001g0097 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1460+1845G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177355573 | |||||||
chr4:177355758 | C | T | 2 | a0009c0019t0001g0072 a0024c0046t0001g0260 |
2 | HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1460+2030C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177355758 | |||||||
chr4:177355894 | T | C | 6 | a0002c0008t0001g0339 a0002c0008t0005g0338 a0002c0020t0001g0170 others(3): Show |
6 | HG02723.hp1 HG03130.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1460+2166T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177355894 | |||||||
chr4:177355932 | T | C | 1 | a0001c0015t0001g0292 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1460+2204T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177355932 | |||||||
chr4:177356145 | T | C | 10 | a0002c0002t0001g0018 a0002c0002t0001g0211 a0004c0006t0001g0183 others(7): Show |
10 | HG01257.hp2 HG02451.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1460+2417T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177356145 | |||||||
chr4:177356480 | T | G | 1 | a0015c0024t0001g0243 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1460+2752T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177356480 | |||||||
chr4:177356699 | C | T | 1 | a0001c0001t0005g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1460+2971C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177356699 | |||||||
chr4:177356942 | G | C | 5 | a0002c0010t0001g0343 a0002c0010t0001g0381 a0002c0010t0005g0380 others(2): Show |
5 | HG01884.hp2 HG02559.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1460+3214G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177356942 | |||||||
chr4:177357335 | G | A | 336 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0033 others(333): Show |
345 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(342): Show |
intron_variant | MODIFIER | c.1461-3168G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177357335 | |||||||
chr4:177357341 | T | C | 125 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0038 others(122): Show |
129 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.1461-3162T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177357341 | |||||||
chr4:177357388 | C | T | 1 | a0002c0002t0001g0371 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1461-3115C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177357388 | |||||||
chr4:177357429 | ATTC | A | 60 | a0001c0001t0001g0039 a0001c0001t0001g0054 a0001c0001t0001g0107 others(57): Show |
60 | HG00140.hp2 HG00423.hp2 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.1461-3064_1461-306 others(7): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | 177357429 | ||||||
chr4:177357509 | A | T | 1 | a0002c0020t0001g0346 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1461-2994A>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177357509 | |||||||
chr4:177357631 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1461-2872G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177357631 | |||||||
chr4:177357741 | T | C | 1 | a0005c0025t0011g0398 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1461-2762T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177357741 | |||||||
chr4:177357767 | C | G | 181 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0033 others(178): Show |
186 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.1461-2736C>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177357767 | |||||||
chr4:177357818 | T | G | 7 | a0002c0002t0005g0347 a0002c0002t0005g0348 a0002c0002t0005g0349 others(4): Show |
7 | HG01891.hp1 HG02572.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1461-2685T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177357818 | |||||||
chr4:177357908 | C | A | 4 | a0004c0006t0004g0253 a0009c0019t0001g0056 a0013c0023t0005g0261 others(1): Show |
4 | HG01891.hp2 HG01981.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1461-2595C>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177357908 | |||||||
chr4:177357922 | T | C | 1 | a0001c0003t0001g0003 | 2 | NA18960.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1461-2581T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177357922 | |||||||
chr4:177358191 | G | C | 51 | a0001c0001t0001g0031 a0001c0001t0001g0071 a0001c0001t0001g0089 others(48): Show |
53 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.1461-2312G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177358191 | |||||||
chr4:177358210 | T | C | 11 | a0001c0001t0005g0008 a0001c0001t0005g0070 a0004c0006t0001g0183 others(8): Show |
11 | HG01981.hp1 HG02055.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.1461-2293T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177358210 | |||||||
chr4:177358257 | C | T | 29 | a0001c0001t0004g0200 a0001c0001t0006g0177 a0001c0001t0006g0180 others(26): Show |
31 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.1461-2246C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177358257 | |||||||
chr4:177358283 | C | T | 11 | a0008c0012t0002g0204 a0008c0012t0002g0225 a0008c0012t0002g0246 others(8): Show |
11 | HG00609.hp2 HG00639.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.1461-2220C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177358283 | |||||||
chr4:177358310 | T | G | 1 | a0001c0001t0001g0174 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1461-2193T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177358310 | |||||||
chr4:177358318 | G | GT | 9 | a0001c0001t0003g0045 a0001c0001t0003g0125 a0001c0001t0003g0144 others(6): Show |
9 | HG00733.hp2 HG01168.hp2 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.1461-2177dupT | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | 177358318 | ||||||
chr4:177358354 | C | A | 5 | a0002c0002t0001g0002 a0002c0002t0001g0013 a0002c0028t0001g0034 others(2): Show |
6 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1461-2149C>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177358354 | |||||||
chr4:177358413 | T | G | 40 | a0001c0001t0001g0138 a0001c0001t0001g0145 a0001c0001t0001g0174 others(37): Show |
42 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.1461-2090T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177358413 | |||||||
chr4:177358496 | G | A | 1 | a0001c0003t0001g0134 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1461-2007G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177358496 | |||||||
chr4:177358504 | A | G | 1 | a0001c0001t0002g0248 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1461-1999A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177358504 | |||||||
chr4:177358508 | T | C | 1 | a0005c0009t0001g0318 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1461-1995T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177358508 | |||||||
chr4:177358587 | G | A | 3 | a0002c0008t0005g0338 a0004c0006t0005g0242 a0011c0033t0005g0299 |
3 | HG02723.hp1 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1461-1916G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177358587 | |||||||
chr4:177358718 | A | T | 77 | a0001c0001t0002g0247 a0001c0001t0003g0045 a0001c0001t0003g0125 others(74): Show |
79 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.1461-1785A>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177358718 | |||||||
chr4:177358838 | A | G | 39 | a0001c0001t0002g0247 a0001c0001t0003g0045 a0001c0001t0003g0125 others(36): Show |
39 | HG00140.hp2 HG00733.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.1461-1665A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177358838 | |||||||
chr4:177358847 | G | A | 2 | a0012c0017t0004g0270 a0012c0017t0004g0274 |
2 | HG03654.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1461-1656G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177358847 | |||||||
chr4:177358877 | G | A | 348 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0027 others(345): Show |
355 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(352): Show |
intron_variant | MODIFIER | c.1461-1626G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177358877 | |||||||
chr4:177358988 | T | C | 3 | a0011c0018t0001g0300 a0011c0018t0001g0302 a0011c0018t0001g0308 |
3 | HG01081.hp2 HG01109.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1461-1515T>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177358988 | |||||||
chr4:177359114 | A | G | 3 | a0002c0002t0001g0065 a0002c0002t0001g0361 a0002c0002t0001g0362 |
3 | NA18944.hp2 NA19007.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1461-1389A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177359114 | |||||||
chr4:177359141 | A | G | 1 | a0002c0008t0005g0338 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1461-1362A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177359141 | |||||||
chr4:177359288 | G | C | 1 | a0004c0006t0001g0183 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1461-1215G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177359288 | |||||||
chr4:177359293 | T | A | 3 | a0001c0001t0001g0067 a0001c0001t0001g0124 a0001c0001t0001g0193 |
3 | NA18952.hp2 NA18970.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1461-1210T>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177359293 | |||||||
chr4:177359319 | A | G | 33 | a0001c0001t0003g0045 a0001c0001t0003g0125 a0001c0001t0003g0144 others(30): Show |
33 | HG00140.hp2 HG00733.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1461-1184A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177359319 | |||||||
chr4:177359617 | A | G | 1 | a0022c0038t0005g0388 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1461-886A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177359617 | |||||||
chr4:177359792 | A | G | 28 | a0001c0001t0004g0200 a0001c0001t0006g0177 a0001c0001t0006g0180 others(25): Show |
30 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.1461-711A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177359792 | |||||||
chr4:177359844 | G | A | 390 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0027 others(387): Show |
399 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(396): Show |
intron_variant | MODIFIER | c.1461-659G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177359844 | |||||||
chr4:177359892 | C | T | 2 | a0002c0002t0001g0136 a0002c0008t0001g0325 |
2 | HG00408.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1461-611C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177359892 | |||||||
chr4:177360027 | G | C | 7 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0038 others(4): Show |
7 | HG02056.hp2 HG02071.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.1461-476G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177360027 | |||||||
chr4:177360167 | A | T | 1 | a0002c0002t0001g0053 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1461-336A>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177360167 | |||||||
chr4:177360168 | G | C | 3 | a0001c0001t0001g0121 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG02523.hp1 NA18945.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.1461-335G>C | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177360168 | |||||||
chr4:177360498 | T | G | 1 | a0001c0001t0003g0144 | 1 | HG02559.hp2 | splice_region_variant&intron_variant | LOW | c.1461-5T>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 8/9 | chr4 | 177360498 | |||||||
chr4:177360819 | A | T | 4 | a0002c0002t0001g0018 a0002c0002t0001g0088 a0002c0002t0001g0211 others(1): Show |
4 | HG01257.hp2 HG01361.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1635+142A>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 9/9 | chr4 | 177360819 | |||||||
chr4:177360906 | A | G | 1 | a0004c0006t0004g0253 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1635+229A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 9/9 | chr4 | 177360906 | |||||||
chr4:177361037 | A | G | 3 | a0009c0019t0001g0072 a0015c0024t0001g0243 a0024c0046t0001g0260 |
3 | HG01981.hp1 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1635+360A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 9/9 | chr4 | 177361037 | |||||||
chr4:177361099 | G | A | 7 | a0002c0002t0005g0347 a0002c0002t0005g0348 a0002c0002t0005g0349 others(4): Show |
7 | HG01891.hp1 HG02572.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1635+422G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 9/9 | chr4 | 177361099 | |||||||
chr4:177361132 | A | ACC | 241 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0027 others(238): Show |
246 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.1635+456_1635+457d others(4): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 177361132 | ||||||
chr4:177361201 | A | G | 2 | a0002c0002t0001g0386 a0002c0002t0001g0387 |
2 | HG02602.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1635+524A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 9/9 | chr4 | 177361201 | |||||||
chr4:177361516 | A | G | 29 | a0001c0001t0003g0045 a0001c0001t0003g0125 a0001c0001t0003g0144 others(26): Show |
29 | HG00140.hp2 HG00733.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1636-773A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 9/9 | chr4 | 177361516 | |||||||
chr4:177361651 | T | A | 1 | a0004c0006t0004g0253 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1636-638T>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 9/9 | chr4 | 177361651 | |||||||
chr4:177361708 | C | G | 1 | a0004c0006t0004g0253 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1636-581C>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 9/9 | chr4 | 177361708 | |||||||
chr4:177361773 | C | T | 1 | a0002c0028t0001g0032 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1636-516C>T | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 9/9 | chr4 | 177361773 | |||||||
chr4:177361823 | C | A | 1 | a0004c0006t0004g0253 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1636-466C>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 9/9 | chr4 | 177361823 | |||||||
chr4:177362092 | A | G | 2 | a0006c0005t0003g0273 a0006c0005t0003g0275 |
2 | HG01433.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1636-197A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 9/9 | chr4 | 177362092 | |||||||
chr4:177362207 | ACTAATCA others(3): Show |
A | 1 | a0001c0001t0001g0376 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1636-81_1636-72del others(10): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 9/9 | chr4 | 177362207 | |||||||
chr4:177362216 | A | G | 6 | a0009c0019t0001g0072 a0011c0018t0001g0300 a0011c0018t0001g0302 others(3): Show |
6 | HG01081.hp2 HG01109.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1636-73A>G | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 9/9 | chr4 | 177362216 | |||||||
chr4:177362225 | G | A | 19 | a0001c0001t0005g0008 a0001c0001t0005g0070 a0002c0002t0005g0347 others(16): Show |
19 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.1636-64G>A | NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 9/9 | chr4 | 177362225 |