Item | Value |
---|---|
geneid | 8602 |
ensemblid | ENSG00000087269.16 |
hgncid | 16821 |
symbol | NOP14 |
name | NOP14 nucleolar protein |
refseq_nuc | NM_001291978.2 |
refseq_prot | NP_001278907.1 |
ensembl_nuc | ENST00000416614.7 |
ensembl_prot | ENSP00000405068.2 |
mane_status | MANE Select |
chr | chr4 |
start | 2937936 |
end | 2963406 |
strand | - |
ver | v1.2 |
region | chr4:2937936-2963406 |
region5000 | chr4:2932936-2968406 |
regionname0 | NOP14_chr4_2937936_2963406 |
regionname5000 | NOP14_chr4_2932936_2968406 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 857 | 253 | 32 | 45 | 136 | 8 | 31 | 97 | NOP14_chr4_2932936_2968406 | NOP14 | MAKAK others(852): Show |
chr4 | 2932936 | 2968406 |
a0002 | 0/0 | 857 | 123 | 49 | 27 | 26 | 10 | 11 | 21 | NOP14_chr4_2932936_2968406 | NOP14 | MAKAK others(852): Show |
chr4 | 2932936 | 2968406 |
a0003 | 0/0 | 857 | 10 | 8 | 2 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | MAKAK others(852): Show |
chr4 | 2932936 | 2968406 |
a0004 | 0/0 | 857 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | NOP14_chr4_2932936_2968406 | NOP14 | MAKAK others(852): Show |
chr4 | 2932936 | 2968406 |
a0005 | 0/0 | 857 | 3 | 0 | 1 | 0 | 0 | 2 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | MAKAK others(852): Show |
chr4 | 2932936 | 2968406 |
a0006 | 0/0 | 857 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | MAKAK others(852): Show |
chr4 | 2932936 | 2968406 |
a0007 | 0/0 | 857 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | NOP14_chr4_2932936_2968406 | NOP14 | MAKAK others(852): Show |
chr4 | 2932936 | 2968406 |
a0008 | 0/0 | 857 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | MAKAK others(852): Show |
chr4 | 2932936 | 2968406 |
a0009 | 0/0 | 857 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | MAKAK others(852): Show |
chr4 | 2932936 | 2968406 |
a0010 | 0/0 | 857 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | MAKAK others(852): Show |
chr4 | 2932936 | 2968406 |
a0011 | 0/0 | 857 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | MAKAK others(852): Show |
chr4 | 2932936 | 2968406 |
a0012 | 0/0 | 857 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | MAKAK others(852): Show |
chr4 | 2932936 | 2968406 |
a0013 | 0/1 | 857 | 2 | 0 | 0 | 0 | 0 | 1 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | MAKAK others(852): Show |
chr4 | 2932936 | 2968406 |
a0014 | 0/0 | 857 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | MAKAK others(852): Show |
chr4 | 2932936 | 2968406 |
a0015 | 0/0 | 857 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NOP14_chr4_2932936_2968406 | NOP14 | MAKAK others(852): Show |
chr4 | 2932936 | 2968406 |
a0016 | 0/0 | 804 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | MAKAK others(799): Show |
chr4 | 2932936 | 2968406 |
a0017 | 0/0 | 857 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | MAKAK others(852): Show |
chr4 | 2932936 | 2968406 |
a0018 | 0/0 | 857 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | MAKAK others(852): Show |
chr4 | 2932936 | 2968406 |
a0019 | 0/0 | 857 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | MAKAK others(852): Show |
chr4 | 2932936 | 2968406 |
a0020 | 0/0 | 857 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | MAKAK others(852): Show |
chr4 | 2932936 | 2968406 |
a0021 | 0/0 | 857 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | MAKAK others(852): Show |
chr4 | 2932936 | 2968406 |
a0022 | 0/0 | 381 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | MAKAK others(376): Show |
chr4 | 2932936 | 2968406 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2571 | 251 | 31 | 45 | 135 | 8 | 31 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0001c0024 | 0/0 | 2571 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0001c0025 | 0/0 | 2571 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0002c0002 | 0/0 | 2571 | 120 | 48 | 26 | 26 | 10 | 10 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0002c0014 | 0/0 | 2571 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0002c0018 | 0/0 | 2571 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0002c0020 | 0/0 | 2571 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0003c0003 | 0/0 | 2571 | 10 | 8 | 2 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0004c0004 | 0/0 | 2571 | 4 | 0 | 0 | 4 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0005c0006 | 0/0 | 2571 | 3 | 0 | 1 | 0 | 0 | 2 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0006c0015 | 0/0 | 2571 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0006c0016 | 0/0 | 2571 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0006c0017 | 0/0 | 2571 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0007c0005 | 0/0 | 2571 | 3 | 0 | 0 | 3 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0008c0026 | 0/0 | 2571 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0008c0028 | 0/0 | 2571 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0009c0008 | 0/0 | 2571 | 2 | 1 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0010c0010 | 0/0 | 2571 | 2 | 0 | 0 | 2 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0011c0012 | 0/0 | 2571 | 2 | 2 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0012c0007 | 0/0 | 2571 | 2 | 2 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0013c0009 | 0/1 | 2571 | 2 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0014c0011 | 0/0 | 2571 | 2 | 0 | 0 | 2 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0015c0013 | 0/0 | 2571 | 2 | 0 | 0 | 2 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0016c0027 | 0/0 | 2571 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0017c0023 | 0/0 | 2571 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0018c0022 | 0/0 | 2571 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0019c0029 | 0/0 | 2571 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0020c0030 | 0/0 | 2571 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0021c0021 | 0/0 | 2571 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2566): Show |
chr4 | 2932936 | 2968406 | ||
a0022c0019 | 0/0 | 2584 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | ATGGC others(2579): Show |
chr4 | 2932936 | 2968406 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3556 | 193 | 20 | 27 | 124 | 2 | 19 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0001c0001t0002 | 0/0 | 3556 | 37 | 0 | 14 | 6 | 5 | 12 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0001c0001t0003 | 0/0 | 3556 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0001c0001t0004 | 0/0 | 3556 | 4 | 4 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0001c0001t0005 | 0/0 | 3556 | 4 | 0 | 1 | 3 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0001c0001t0006 | 0/0 | 3556 | 4 | 4 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0001c0001t0007 | 0/0 | 3556 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0001c0001t0009 | 0/0 | 3556 | 2 | 2 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0001c0001t0016 | 0/0 | 3556 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0001c0001t0017 | 0/0 | 3556 | 1 | 0 | 0 | 0 | 1 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0001c0001t0021 | 0/0 | 3556 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0001c0001t0022 | 0/0 | 3556 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0001c0001t0024 | 0/0 | 3556 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0001c0024t0001 | 0/0 | 3556 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0001c0025t0001 | 0/0 | 3556 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0002c0002t0001 | 0/0 | 3556 | 98 | 34 | 23 | 23 | 10 | 8 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0002c0002t0002 | 0/0 | 3556 | 2 | 0 | 0 | 2 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0002c0002t0003 | 0/0 | 3556 | 8 | 6 | 0 | 0 | 0 | 2 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0002c0002t0004 | 0/0 | 3556 | 3 | 2 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0002c0002t0005 | 0/0 | 3556 | 2 | 0 | 1 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0002c0002t0008 | 0/0 | 3556 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0002c0002t0010 | 0/0 | 3556 | 2 | 2 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0002c0002t0011 | 0/0 | 3556 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0002c0002t0020 | 0/0 | 3556 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0002c0002t0023 | 0/0 | 3556 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0002c0002t0026 | 0/0 | 3556 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0002c0014t0012 | 0/0 | 3556 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0002c0018t0027 | 0/0 | 3556 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0002c0020t0001 | 0/0 | 3556 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0003c0003t0001 | 0/0 | 3556 | 6 | 4 | 2 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0003c0003t0003 | 0/0 | 3556 | 2 | 2 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0003c0003t0008 | 0/0 | 3556 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0003c0003t0025 | 0/0 | 3556 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0004c0004t0001 | 0/0 | 3556 | 4 | 0 | 0 | 4 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0005c0006t0001 | 0/0 | 3556 | 3 | 0 | 1 | 0 | 0 | 2 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0006c0015t0007 | 0/0 | 3556 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0006c0016t0012 | 0/0 | 3556 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0006c0017t0001 | 0/0 | 3556 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0007c0005t0001 | 0/0 | 3556 | 3 | 0 | 0 | 3 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0008c0026t0002 | 0/0 | 3556 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0008c0028t0002 | 0/0 | 3556 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0009c0008t0014 | 0/0 | 3556 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0009c0008t0015 | 0/0 | 3556 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0010c0010t0018 | 0/0 | 3556 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0010c0010t0019 | 0/0 | 3556 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0011c0012t0013 | 0/0 | 3556 | 2 | 2 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0012c0007t0007 | 0/0 | 3556 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0012c0007t0011 | 0/0 | 3556 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0013c0009t0001 | 0/1 | 3556 | 2 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0014c0011t0001 | 0/0 | 3556 | 2 | 0 | 0 | 2 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0015c0013t0001 | 0/0 | 3556 | 2 | 0 | 0 | 2 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0016c0027t0001 | 0/0 | 3556 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0017c0023t0002 | 0/0 | 3556 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0018c0022t0028 | 0/0 | 3556 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0019c0029t0001 | 0/0 | 3556 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0020c0030t0004 | 0/0 | 3556 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0021c0021t0001 | 0/0 | 3556 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3551): Show |
chr4 | 2932936 | 2968406 |
a0022c0019t0001 | 0/0 | 3569 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | GGTTC others(3564): Show |
chr4 | 2932936 | 2968406 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 18 | 0 | 7 | 8 | 1 | 2 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0003 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0016 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0061 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0002g0006 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0002g0018 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0002g0046 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0004g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0005g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0005g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0006g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0007g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0009g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0016g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0017g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0021g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0022g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0001t0024g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0024t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0001c0025t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0004 | 0/0 | 6 | 0 | 3 | 1 | 1 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0007 | 0/0 | 5 | 0 | 2 | 0 | 2 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0048 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0050 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0003g0051 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0004g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0005g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0005g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0008g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0010g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0010g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0011g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0020g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0023g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0002t0026g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0014t0012g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0018t0027g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0002c0020t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0003c0003t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0003c0003t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0003c0003t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0003c0003t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0003c0003t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0003c0003t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0003c0003t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0003c0003t0008g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0003c0003t0025g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0004c0004t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0004c0004t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0004c0004t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0004c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0005c0006t0001g0022 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0006c0015t0007g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0006c0016t0012g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0006c0017t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0007c0005t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0007c0005t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0007c0005t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0008c0026t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0008c0028t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0009c0008t0014g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0009c0008t0015g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0010c0010t0018g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0010c0010t0019g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0011c0012t0013g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0011c0012t0013g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0012c0007t0007g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0012c0007t0011g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0013c0009t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0013c0009t0001g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0014c0011t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0014c0011t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0015c0013t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0015c0013t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0016c0027t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0017c0023t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0018c0022t0028g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0019c0029t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0020c0030t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0021c0021t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
a0022c0019t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0143 | EUR | GBR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0048 | EUR | GBR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0156 | EUR | GBR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00140 | hp2 | a0001 | c0001 | t0017 | g0158 | EUR | GBR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0288 | EUR | FIN | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0300 | EUR | FIN | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0290 | EUR | FIN | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0082 | EUR | FIN | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00408 | hp1 | a0004 | c0004 | t0001 | g0201 | EAS | CHS | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | CHS | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00609 | hp1 | a0001 | c0001 | t0024 | g0139 | EAS | CHS | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0048 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00639 | hp2 | a0002 | c0002 | t0023 | g0081 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00642 | hp2 | a0002 | c0020 | t0001 | g0292 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0021 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00738 | hp2 | a0005 | c0006 | t0001 | g0022 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0276 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01069 | hp1 | a0003 | c0003 | t0001 | g0040 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01071 | hp2 | a0003 | c0003 | t0001 | g0040 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01081 | hp1 | a0008 | c0026 | t0002 | g0162 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0256 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01109 | hp2 | a0006 | c0016 | t0012 | g0299 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0075 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0021 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0021 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0273 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0291 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01243 | hp1 | a0002 | c0002 | t0004 | g0293 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01243 | hp2 | a0002 | c0002 | t0001 | g0093 | AMR | PUR | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01255 | hp1 | a0009 | c0008 | t0015 | g0053 | AMR | CLM | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0278 | AMR | CLM | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01261 | hp1 | a0016 | c0027 | t0001 | g0130 | AMR | CLM | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0295 | AMR | CLM | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | CLM | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0267 | AMR | CLM | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0024 | AMR | CLM | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0209 | AMR | CLM | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | IBS | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0050 | EUR | IBS | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0007 | EUR | IBS | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0046 | EUR | IBS | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0046 | EUR | IBS | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0050 | EUR | IBS | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01884 | hp1 | a0002 | c0018 | t0027 | g0151 | AFR | ACB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0308 | AFR | ACB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0088 | AFR | ACB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0259 | AMR | PEL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PEL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01975 | hp1 | a0001 | c0001 | t0016 | g0169 | AMR | PEL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01975 | hp2 | a0001 | c0001 | t0005 | g0194 | AMR | PEL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | PEL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0215 | AMR | PEL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01981 | hp2 | a0002 | c0002 | t0005 | g0264 | AMR | PEL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01993 | hp1 | a0017 | c0023 | t0002 | g0220 | AMR | PEL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0073 | AMR | PEL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PEL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0251 | AFR | ACB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0287 | AFR | ACB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0237 | EAS | KHV | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02135 | hp1 | a0010 | c0010 | t0018 | g0176 | EAS | KHV | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02135 | hp2 | a0007 | c0005 | t0001 | g0072 | EAS | KHV | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | ACB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02145 | hp2 | a0011 | c0012 | t0013 | g0059 | AFR | ACB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02148 | hp1 | a0001 | c0001 | t0021 | g0198 | AMR | PEL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0266 | AMR | PEL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02155 | hp1 | a0001 | c0001 | t0022 | g0226 | EAS | CDX | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CDX | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02165 | hp1 | a0002 | c0002 | t0002 | g0272 | EAS | CDX | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CDX | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0252 | AFR | ACB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02257 | hp2 | a0001 | c0001 | t0006 | g0233 | AFR | ACB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02258 | hp1 | a0003 | c0003 | t0003 | g0205 | AFR | ACB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02258 | hp2 | a0002 | c0002 | t0003 | g0282 | AFR | ACB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0024 | AMR | PEL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0227 | AFR | ACB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0263 | AFR | ACB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0298 | AFR | ACB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02572 | hp1 | a0018 | c0022 | t0028 | g0312 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02572 | hp2 | a0006 | c0017 | t0001 | g0301 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02615 | hp1 | a0001 | c0001 | t0009 | g0045 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0011 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02622 | hp1 | a0012 | c0007 | t0011 | g0297 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02630 | hp1 | a0002 | c0002 | t0004 | g0253 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02630 | hp2 | a0002 | c0002 | t0011 | g0087 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02647 | hp1 | a0002 | c0002 | t0003 | g0086 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02647 | hp2 | a0006 | c0015 | t0007 | g0255 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0235 | SAS | PJL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02698 | hp2 | a0019 | c0029 | t0001 | g0132 | SAS | PJL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02717 | hp1 | a0003 | c0003 | t0001 | g0241 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02717 | hp2 | a0002 | c0002 | t0026 | g0078 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02723 | hp1 | a0001 | c0024 | t0001 | g0126 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0258 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0238 | SAS | PJL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0084 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0083 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02818 | hp2 | a0002 | c0002 | t0001 | g0229 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0239 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0090 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0306 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02897 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0089 | AFR | ESN | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02922 | hp2 | a0002 | c0002 | t0003 | g0101 | AFR | ESN | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | ESN | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0307 | AFR | ESN | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02976 | hp2 | a0002 | c0002 | t0001 | g0257 | AFR | ESN | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0007 | SAS | PJL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03017 | hp2 | a0005 | c0006 | t0001 | g0022 | SAS | PJL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0284 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03041 | hp2 | a0002 | c0002 | t0003 | g0254 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | MSL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03098 | hp2 | a0002 | c0002 | t0001 | g0092 | AFR | MSL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03130 | hp1 | a0003 | c0003 | t0001 | g0106 | AFR | ESN | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03130 | hp2 | a0002 | c0002 | t0003 | g0261 | AFR | ESN | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0058 | AFR | ESN | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03139 | hp2 | a0009 | c0008 | t0014 | g0054 | AFR | ESN | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03195 | hp1 | a0001 | c0001 | t0006 | g0044 | AFR | ESN | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | ESN | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03209 | hp1 | a0001 | c0001 | t0006 | g0044 | AFR | MSL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03209 | hp2 | a0003 | c0003 | t0001 | g0165 | AFR | MSL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0091 | AFR | MSL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03225 | hp2 | a0002 | c0002 | t0020 | g0280 | AFR | MSL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0085 | SAS | PJL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03453 | hp2 | a0020 | c0030 | t0004 | g0311 | AFR | MSL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03486 | hp1 | a0001 | c0001 | t0006 | g0234 | AFR | MSL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03486 | hp2 | a0003 | c0003 | t0001 | g0208 | AFR | MSL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0232 | SAS | PJL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03490 | hp2 | a0002 | c0002 | t0003 | g0051 | SAS | PJL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0212 | SAS | PJL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0279 | SAS | PJL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03492 | hp1 | a0002 | c0002 | t0003 | g0051 | SAS | PJL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03516 | hp1 | a0002 | c0002 | t0010 | g0079 | AFR | ESN | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0305 | AFR | ESN | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0294 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0296 | AFR | MSL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03579 | hp2 | a0012 | c0007 | t0007 | g0285 | AFR | MSL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0236 | SAS | PJL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | STU | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03688 | hp2 | a0021 | c0021 | t0001 | g0274 | SAS | STU | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03704 | hp2 | a0002 | c0014 | t0012 | g0281 | SAS | PJL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | BEB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0246 | SAS | BEB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0166 | SAS | BEB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03927 | hp2 | a0013 | c0009 | t0001 | g0108 | SAS | BEB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0193 | SAS | BEB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | STU | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | STU | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | BEB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG04184 | hp2 | a0005 | c0006 | t0001 | g0022 | SAS | BEB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0170 | SAS | STU | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | STU | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | STU | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | STU | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | STU | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG04228 | hp2 | a0008 | c0028 | t0002 | g0174 | SAS | STU | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0052 | AFR | YRI | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18522 | hp2 | a0001 | c0001 | t0007 | g0152 | AFR | YRI | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18612 | hp2 | a0014 | c0011 | t0001 | g0131 | EAS | CHB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | CHB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | YRI | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18906 | hp2 | a0002 | c0002 | t0010 | g0080 | AFR | YRI | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18942 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18946 | hp1 | a0004 | c0004 | t0001 | g0133 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0289 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0283 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18959 | hp1 | a0001 | c0001 | t0005 | g0055 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18960 | hp1 | a0004 | c0004 | t0001 | g0116 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18964 | hp1 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18965 | hp1 | a0022 | c0019 | t0001 | g0071 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18965 | hp2 | a0004 | c0004 | t0001 | g0141 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18967 | hp2 | a0001 | c0025 | t0001 | g0124 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18968 | hp1 | a0007 | c0005 | t0001 | g0247 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18971 | hp2 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0275 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18986 | hp2 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18990 | hp1 | a0007 | c0005 | t0001 | g0066 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19000 | hp1 | a0002 | c0002 | t0002 | g0277 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19000 | hp2 | a0015 | c0013 | t0001 | g0309 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19003 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | LWK | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19043 | hp2 | a0002 | c0002 | t0003 | g0230 | AFR | LWK | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19055 | hp1 | a0010 | c0010 | t0019 | g0177 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19080 | hp2 | a0002 | c0002 | t0005 | g0268 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19081 | hp2 | a0014 | c0011 | t0001 | g0098 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19087 | hp1 | a0015 | c0013 | t0001 | g0310 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | YRI | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0094 | AFR | ASW | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ASW | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0303 | EUR | TSI | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0007 | EUR | TSI | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0004 | EUR | TSI | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | GIH | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0231 | SAS | GIH | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | CLM | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02109 | hp1 | a0001 | c0001 | t0009 | g0045 | AFR | ACB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02109 | hp2 | a0003 | c0003 | t0003 | g0206 | AFR | ACB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02559 | hp1 | a0002 | c0002 | t0008 | g0057 | AFR | ACB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0052 | AFR | ACB | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0302 | AFR | MSL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG03471 | hp2 | a0002 | c0002 | t0004 | g0240 | AFR | MSL | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | USA | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
HG06807 | hp2 | a0011 | c0012 | t0013 | g0060 | AFR | USA | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA20300 | hp1 | a0003 | c0003 | t0025 | g0207 | AFR | USA | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA20300 | hp2 | a0003 | c0003 | t0008 | g0111 | AFR | USA | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0286 | AFR | LWK | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0228 | AFR | LWK | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
homoSapiens | chm13v2 | a0013 | c0009 | t0001 | g0155 | REF | REF | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0061 | REF | REF | NOP14_chr4_2932936_2968406 | NOP14 | chr4 | 2932936 | 2968406 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:2939194 | A | G | 1 | a0004 | 4 | HG00408.hp1 NA18946.hp1 NA18960.hp1 others(1): Show |
missense_variant | MODERATE | c.2468T>C | p.Met823Thr | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 17/18 | 2555/3556 | 2468/2574 | 823/857 | chr4 | 2939194 | |||
chr4:2939248 | C | T | 1 | a0021 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.2414G>A | p.Arg805Gln | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 17/18 | 2501/3556 | 2414/2574 | 805/857 | chr4 | 2939248 | |||
chr4:2939249 | G | A | 1 | a0016 | 1 | HG01261.hp1 | stop_gained | HIGH | c.2413C>T | p.Arg805* | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 17/18 | 2500/3556 | 2413/2574 | 805/857 | chr4 | 2939249 | |||
chr4:2939539 | C | T | 1 | a0007 | 3 | HG02135.hp2 NA18968.hp1 NA18990.hp1 |
missense_variant | MODERATE | c.2306G>A | p.Arg769Gln | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 16/18 | 2393/3556 | 2306/2574 | 769/857 | chr4 | 2939539 | |||
chr4:2939590 | G | A | 1 | a0005 | 3 | HG00738.hp2 HG03017.hp2 HG04184.hp2 |
missense_variant | MODERATE | c.2255C>T | p.Pro752Leu | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 16/18 | 2342/3556 | 2255/2574 | 752/857 | chr4 | 2939590 | |||
chr4:2941634 | T | C | 12 | a0002 a0005 a0006 others(9): Show |
143 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
missense_variant | MODERATE | c.2147A>G | p.Gln716Arg | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/18 | 2234/3556 | 2147/2574 | 716/857 | chr4 | 2941634 | |||
chr4:2941691 | C | T | 1 | a0008 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.2090G>A | p.Arg697His | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/18 | 2177/3556 | 2090/2574 | 697/857 | chr4 | 2941691 | |||
chr4:2941692 | G | A | 1 | a0008 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.2089C>T | p.Arg697Cys | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/18 | 2176/3556 | 2089/2574 | 697/857 | chr4 | 2941692 | |||
chr4:2945193 | T | C | 1 | a0003 | 10 | HG01069.hp1 HG01071.hp2 HG02109.hp2 others(7): Show |
missense_variant | MODERATE | c.1672A>G | p.Thr558Ala | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 12/18 | 1759/3556 | 1672/2574 | 558/857 | chr4 | 2945193 | |||
chr4:2946476 | G | A | 1 | a0018 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.1571C>T | p.Ala524Val | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/18 | 1658/3556 | 1571/2574 | 524/857 | chr4 | 2946476 | |||
chr4:2949937 | C | T | 1 | a0017 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.1279G>A | p.Ala427Thr | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 8/18 | 1366/3556 | 1279/2574 | 427/857 | chr4 | 2949937 | |||
chr4:2949942 | G | C | 1 | a0010 | 2 | HG02135.hp1 NA19055.hp1 |
missense_variant | MODERATE | c.1274C>G | p.Thr425Arg | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 8/18 | 1361/3556 | 1274/2574 | 425/857 | chr4 | 2949942 | |||
chr4:2950077 | A | G | 11 | a0002 a0005 a0006 others(8): Show |
142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
missense_variant | MODERATE | c.1139T>C | p.Leu380Ser | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 8/18 | 1226/3556 | 1139/2574 | 380/857 | chr4 | 2950077 | |||
chr4:2950111 | C | CCTCTCTG others(6): Show |
1 | a0022 | 1 | NA18965.hp1 | frameshift_variant | HIGH | c.1104_1105insACGAGG others(7): Show |
p.Asp369fs | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 8/18 | 1191/3556 | 1104/2574 | 368/857 | chr4 | 2950111 | |||
chr4:2950113 | T | C | 1 | a0014 | 2 | NA18612.hp2 NA19081.hp2 |
missense_variant | MODERATE | c.1103A>G | p.Glu368Gly | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 8/18 | 1190/3556 | 1103/2574 | 368/857 | chr4 | 2950113 | |||
chr4:2950141 | C | T | 1 | a0012 | 2 | HG02622.hp1 HG03579.hp2 |
missense_variant | MODERATE | c.1075G>A | p.Glu359Lys | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 8/18 | 1162/3556 | 1075/2574 | 359/857 | chr4 | 2950141 | |||
chr4:2950182 | T | C | 1 | a0019 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.1034A>G | p.Gln345Arg | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 8/18 | 1121/3556 | 1034/2574 | 345/857 | chr4 | 2950182 | |||
chr4:2952330 | A | T | 1 | a0009 | 2 | HG01255.hp1 HG03139.hp2 |
missense_variant | MODERATE | c.815T>A | p.Met272Lys | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 6/18 | 902/3556 | 815/2574 | 272/857 | chr4 | 2952330 | |||
chr4:2952394 | C | T | 2 | a0006 a0012 |
5 | HG01109.hp2 HG02572.hp2 HG02622.hp1 others(2): Show |
missense_variant | MODERATE | c.751G>A | p.Asp251Asn | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 6/18 | 838/3556 | 751/2574 | 251/857 | chr4 | 2952394 | |||
chr4:2953634 | T | G | 1 | a0011 | 2 | HG02145.hp2 HG06807.hp2 |
missense_variant | MODERATE | c.624A>C | p.Gln208His | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 5/18 | 711/3556 | 624/2574 | 208/857 | chr4 | 2953634 | |||
chr4:2963156 | G | A | 1 | a0015 | 2 | NA19000.hp2 NA19087.hp1 |
missense_variant | MODERATE | c.164C>T | p.Pro55Leu | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/18 | 251/3556 | 164/2574 | 55/857 | chr4 | 2963156 | |||
chr4:2963261 | G | A | 1 | a0020 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.59C>T | p.Ala20Val | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/18 | 146/3556 | 59/2574 | 20/857 | chr4 | 2963261 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:2941591 | C | T | 1 | a0002c0020 | 1 | HG00642.hp2 | synonymous_variant | LOW | c.2190G>A | p.Gln730Gln | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/18 | 2277/3556 | 2190/2574 | 730/857 | chr4 | 2941591 | |||
chr4:2942287 | A | T | 1 | a0001c0025 | 1 | NA18967.hp2 | synonymous_variant | LOW | c.1956T>A | p.Ala652Ala | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 14/18 | 2043/3556 | 1956/2574 | 652/857 | chr4 | 2942287 | |||
chr4:2942323 | C | T | 1 | a0006c0016 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.1920G>A | p.Ala640Ala | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 14/18 | 2007/3556 | 1920/2574 | 640/857 | chr4 | 2942323 | |||
chr4:2946433 | C | T | 1 | a0018c0022 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.1614G>A | p.Ala538Ala | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/18 | 1701/3556 | 1614/2574 | 538/857 | chr4 | 2946433 | |||
chr4:2948362 | C | T | 1 | a0001c0024 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.1329G>A | p.Ser443Ser | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 9/18 | 1416/3556 | 1329/2574 | 443/857 | chr4 | 2948362 | |||
chr4:2952347 | C | T | 2 | a0002c0018 a0006c0015 |
2 | HG01884.hp1 HG02647.hp2 |
synonymous_variant | LOW | c.798G>A | p.Ala266Ala | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 6/18 | 885/3556 | 798/2574 | 266/857 | chr4 | 2952347 | |||
chr4:2954478 | C | T | 1 | a0002c0014 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.558G>A | p.Pro186Pro | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 4/18 | 645/3556 | 558/2574 | 186/857 | chr4 | 2954478 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:2938102 | G | A | 1 | a0002c0002t0023 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*729C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 18/18 | 729 | chr4 | 2938102 | ||||||
chr4:2938148 | G | A | 1 | a0009c0008t0015 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*683C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 18/18 | 683 | chr4 | 2938148 | ||||||
chr4:2938167 | C | T | 1 | a0001c0001t0022 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*664G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 18/18 | 664 | chr4 | 2938167 | ||||||
chr4:2938176 | C | T | 2 | a0002c0002t0020 a0018c0022t0028 |
2 | HG02572.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*655G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 18/18 | 655 | chr4 | 2938176 | ||||||
chr4:2938300 | T | C | 3 | a0002c0002t0010 a0002c0002t0026 a0011c0012t0013 |
5 | HG02145.hp2 HG02717.hp2 HG03516.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*531A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 18/18 | 531 | chr4 | 2938300 | ||||||
chr4:2938318 | C | T | 2 | a0002c0014t0012 a0006c0016t0012 |
2 | HG01109.hp2 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*513G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 18/18 | 513 | chr4 | 2938318 | ||||||
chr4:2938323 | C | T | 1 | a0001c0001t0021 | 1 | HG02148.hp1 | 3_prime_UTR_variant | MODIFIER | c.*508G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 18/18 | 508 | chr4 | 2938323 | ||||||
chr4:2938335 | A | T | 7 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0016 others(4): Show |
15 | HG01243.hp1 HG01884.hp2 HG01975.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*496T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 18/18 | 496 | chr4 | 2938335 | ||||||
chr4:2938350 | G | A | 1 | a0001c0001t0024 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*481C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 18/18 | 481 | chr4 | 2938350 | ||||||
chr4:2938389 | A | G | 3 | a0002c0002t0026 a0003c0003t0025 a0011c0012t0013 |
4 | HG02145.hp2 HG02717.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*442T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 18/18 | 442 | chr4 | 2938389 | ||||||
chr4:2938394 | T | C | 3 | a0002c0002t0026 a0003c0003t0025 a0011c0012t0013 |
4 | HG02145.hp2 HG02717.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*437A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 18/18 | 437 | chr4 | 2938394 | ||||||
chr4:2938510 | A | C | 2 | a0001c0001t0005 a0002c0002t0005 |
6 | HG01975.hp2 HG01981.hp2 NA18959.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*321T>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 18/18 | 321 | chr4 | 2938510 | ||||||
chr4:2938517 | T | G | 6 | a0001c0001t0007 a0002c0002t0011 a0006c0015t0007 others(3): Show |
7 | HG02145.hp2 HG02622.hp1 HG02630.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*314A>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 18/18 | 314 | chr4 | 2938517 | ||||||
chr4:2938573 | A | G | 1 | a0010c0010t0019 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*258T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 18/18 | 258 | chr4 | 2938573 | ||||||
chr4:2938617 | T | C | 1 | a0002c0018t0027 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*214A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 18/18 | 214 | chr4 | 2938617 | ||||||
chr4:2938631 | G | A | 6 | a0001c0001t0002 a0001c0001t0017 a0002c0002t0002 others(3): Show |
43 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*200C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 18/18 | 200 | chr4 | 2938631 | ||||||
chr4:2938657 | C | T | 1 | a0010c0010t0018 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*174G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 18/18 | 174 | chr4 | 2938657 | ||||||
chr4:2938659 | C | G | 9 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0017 others(6): Show |
18 | HG00140.hp2 HG01975.hp1 HG01981.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*172G>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 18/18 | 172 | chr4 | 2938659 | ||||||
chr4:2938702 | C | T | 3 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0016 |
7 | HG01975.hp1 HG02109.hp1 HG02257.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*129G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 18/18 | 129 | chr4 | 2938702 | ||||||
chr4:2938747 | A | G | 2 | a0002c0002t0008 a0003c0003t0008 |
2 | HG02559.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*84T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 18/18 | 84 | chr4 | 2938747 | ||||||
chr4:2963353 | C | G | 2 | a0009c0008t0014 a0009c0008t0015 |
2 | HG01255.hp1 HG03139.hp2 |
5_prime_UTR_variant | MODIFIER | c.-34G>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/18 | 34 | chr4 | 2963353 | ||||||
chr4:2963371 | C | A | 1 | a0018c0022t0028 | 1 | HG02572.hp1 | 5_prime_UTR_variant | MODIFIER | c.-52G>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/18 | 52 | chr4 | 2963371 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:2939045 | A | G | 6 | a0002c0002t0001g0229 a0002c0002t0004g0253 a0002c0002t0026g0078 others(3): Show |
6 | HG02145.hp2 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2475-115T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 17/17 | chr4 | 2939045 | |||||||
chr4:2939111 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0118 |
3 | NA18974.hp1 NA19058.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2474+77G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 17/17 | chr4 | 2939111 | |||||||
chr4:2939166 | C | T | 2 | a0011c0012t0013g0059 a0011c0012t0013g0060 |
2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2474+22G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 17/17 | chr4 | 2939166 | |||||||
chr4:2939167 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2474+21C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 17/17 | chr4 | 2939167 | |||||||
chr4:2939666 | G | A | 2 | a0002c0002t0010g0079 a0002c0002t0010g0080 |
2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2200-21C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2939666 | |||||||
chr4:2939691 | G | A | 12 | a0001c0001t0001g0076 a0001c0001t0001g0161 a0001c0001t0001g0164 others(9): Show |
17 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.2200-46C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2939691 | |||||||
chr4:2939698 | G | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0197 |
2 | HG00558.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.2200-53C>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2939698 | |||||||
chr4:2939789 | A | G | 1 | a0001c0001t0004g0306 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2200-144T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2939789 | |||||||
chr4:2939993 | CCAGA | C | 1 | a0005c0006t0001g0022 | 3 | HG00738.hp2 HG03017.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2200-352_2200-349d others(6): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2939993 | |||||||
chr4:2940000 | A | G | 1 | a0018c0022t0028g0312 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2200-355T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2940000 | |||||||
chr4:2940066 | C | T | 2 | a0001c0001t0004g0305 a0003c0003t0008g0111 |
2 | HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2200-421G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2940066 | |||||||
chr4:2940099 | T | G | 1 | a0001c0001t0001g0159 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2200-454A>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2940099 | |||||||
chr4:2940261 | T | C | 127 | a0001c0001t0001g0029 a0001c0001t0001g0135 a0001c0001t0001g0140 others(124): Show |
154 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.2200-616A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2940261 | |||||||
chr4:2940283 | C | T | 1 | a0002c0002t0001g0058 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2200-638G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2940283 | |||||||
chr4:2940332 | G | A | 1 | a0001c0001t0002g0178 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2200-687C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2940332 | |||||||
chr4:2940346 | T | C | 73 | a0001c0001t0001g0160 a0001c0001t0002g0032 a0002c0002t0001g0007 others(70): Show |
89 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.2200-701A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2940346 | |||||||
chr4:2940482 | T | G | 37 | a0001c0001t0006g0233 a0001c0001t0006g0234 a0002c0002t0001g0004 others(34): Show |
46 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.2200-837A>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2940482 | |||||||
chr4:2940569 | T | C | 4 | a0001c0001t0001g0015 a0001c0001t0001g0028 a0001c0001t0001g0148 others(1): Show |
7 | HG00408.hp2 HG00609.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.2200-924A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2940569 | |||||||
chr4:2940640 | C | T | 1 | a0002c0002t0001g0227 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2199+942G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2940640 | |||||||
chr4:2940812 | T | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(239): Show |
328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.2199+770A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2940812 | |||||||
chr4:2940814 | G | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(67): Show |
116 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.2199+768C>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2940814 | |||||||
chr4:2940838 | G | A | 1 | a0002c0002t0001g0279 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2199+744C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2940838 | |||||||
chr4:2940849 | T | C | 2 | a0002c0002t0010g0079 a0002c0002t0010g0080 |
2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2199+733A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2940849 | |||||||
chr4:2940955 | TGCCTTCG others(146): Show |
T | 5 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(2): Show |
5 | HG01884.hp2 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2199+474_2199+626d others(2): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2940955 | |||||||
chr4:2940958 | C | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(72): Show |
128 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.2199+624G>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2940958 | |||||||
chr4:2940976 | C | A | 1 | a0018c0022t0028g0312 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2199+606G>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2940976 | |||||||
chr4:2940988 | C | T | 1 | a0001c0024t0001g0126 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2199+594G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2940988 | |||||||
chr4:2941032 | C | T | 36 | a0002c0002t0001g0004 a0002c0002t0001g0011 a0002c0002t0001g0024 others(33): Show |
45 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.2199+550G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2941032 | |||||||
chr4:2941056 | G | C | 9 | a0003c0003t0001g0040 a0003c0003t0001g0106 a0003c0003t0001g0165 others(6): Show |
10 | HG01069.hp1 HG01071.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2199+526C>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2941056 | |||||||
chr4:2941096 | G | C | 2 | a0001c0001t0001g0164 a0008c0026t0002g0162 |
2 | HG01081.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.2199+486C>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2941096 | |||||||
chr4:2941174 | C | A | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG03669.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2199+408G>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2941174 | |||||||
chr4:2941176 | A | G | 5 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(2): Show |
5 | HG01884.hp2 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2199+406T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2941176 | |||||||
chr4:2941219 | T | C | 1 | a0002c0002t0001g0093 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2199+363A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2941219 | |||||||
chr4:2941259 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2199+323G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2941259 | |||||||
chr4:2941323 | G | A | 2 | a0001c0001t0001g0120 a0018c0022t0028g0312 |
2 | HG00673.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2199+259C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2941323 | |||||||
chr4:2941411 | T | A | 1 | a0001c0001t0001g0095 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2199+171A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2941411 | |||||||
chr4:2941478 | G | GACTT | 4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
4 | HG00673.hp1 HG02080.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.2199+100_2199+103d others(6): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2941478 | |||||||
chr4:2941518 | T | G | 1 | a0001c0001t0001g0110 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2199+64A>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2941518 | |||||||
chr4:2941538 | T | C | 1 | a0018c0022t0028g0312 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2199+44A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 15/17 | chr4 | 2941538 | |||||||
chr4:2941793 | C | G | 1 | a0002c0002t0001g0236 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2052-64G>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 14/17 | chr4 | 2941793 | |||||||
chr4:2941798 | C | A | 1 | a0002c0018t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2052-69G>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 14/17 | chr4 | 2941798 | |||||||
chr4:2941834 | C | A | 1 | a0002c0018t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2052-105G>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 14/17 | chr4 | 2941834 | |||||||
chr4:2941839 | G | A | 1 | a0002c0018t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2052-110C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 14/17 | chr4 | 2941839 | |||||||
chr4:2941846 | C | A | 1 | a0002c0018t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2052-117G>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 14/17 | chr4 | 2941846 | |||||||
chr4:2941890 | C | G | 1 | a0001c0001t0002g0214 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2052-161G>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 14/17 | chr4 | 2941890 | |||||||
chr4:2941945 | G | C | 115 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0011 others(112): Show |
140 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.2052-216C>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 14/17 | chr4 | 2941945 | |||||||
chr4:2941953 | G | A | 1 | a0002c0002t0011g0087 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2052-224C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 14/17 | chr4 | 2941953 | |||||||
chr4:2941991 | A | C | 2 | a0001c0001t0001g0161 a0001c0001t0001g0163 |
2 | HG00735.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2051+201T>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 14/17 | chr4 | 2941991 | |||||||
chr4:2942023 | A | G | 1 | a0002c0002t0020g0280 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2051+169T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 14/17 | chr4 | 2942023 | |||||||
chr4:2942366 | C | T | 1 | a0002c0002t0001g0228 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1892-15G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2942366 | |||||||
chr4:2942407 | A | C | 1 | a0001c0001t0007g0152 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1892-56T>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2942407 | |||||||
chr4:2942458 | C | T | 1 | a0002c0002t0001g0085 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1892-107G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2942458 | |||||||
chr4:2942502 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1892-151G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2942502 | |||||||
chr4:2942609 | G | A | 40 | a0002c0002t0001g0004 a0002c0002t0001g0011 a0002c0002t0001g0024 others(37): Show |
49 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.1892-258C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2942609 | |||||||
chr4:2942697 | G | C | 6 | a0001c0001t0002g0006 a0001c0001t0002g0172 a0001c0001t0002g0209 others(3): Show |
10 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.1892-346C>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2942697 | |||||||
chr4:2942750 | T | C | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(306): Show |
419 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(416): Show |
intron_variant | MODIFIER | c.1892-399A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2942750 | |||||||
chr4:2942782 | C | G | 1 | a0018c0022t0028g0312 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1892-431G>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2942782 | |||||||
chr4:2942791 | C | T | 1 | a0001c0001t0002g0175 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1892-440G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2942791 | |||||||
chr4:2942837 | T | C | 1 | a0018c0022t0028g0312 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1892-486A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2942837 | |||||||
chr4:2942844 | C | CGT | 117 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0011 others(114): Show |
142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1892-494_1892-493i others(4): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2942844 | |||||||
chr4:2942879 | A | G | 2 | a0009c0008t0014g0054 a0009c0008t0015g0053 |
2 | HG01255.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1892-528T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2942879 | |||||||
chr4:2942893 | T | C | 117 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0011 others(114): Show |
142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1892-542A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2942893 | |||||||
chr4:2942965 | C | T | 1 | a0002c0002t0001g0262 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1892-614G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2942965 | |||||||
chr4:2943019 | T | C | 122 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(119): Show |
147 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1892-668A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2943019 | |||||||
chr4:2943047 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1892-696C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2943047 | |||||||
chr4:2943063 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1892-712G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2943063 | |||||||
chr4:2943124 | G | A | 1 | a0018c0022t0028g0312 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1892-773C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2943124 | |||||||
chr4:2943144 | C | T | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0002c0002t0003g0086 |
3 | HG02486.hp1 HG02647.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1892-793G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2943144 | |||||||
chr4:2943164 | C | T | 1 | a0002c0002t0001g0058 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1892-813G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2943164 | |||||||
chr4:2943168 | G | T | 1 | a0002c0002t0001g0058 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1892-817C>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2943168 | |||||||
chr4:2943221 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1891+852G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2943221 | |||||||
chr4:2943382 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1891+691G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2943382 | |||||||
chr4:2943432 | C | G | 3 | a0002c0002t0001g0068 a0002c0002t0001g0069 a0022c0019t0001g0071 |
3 | NA18949.hp2 NA18965.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1891+641G>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2943432 | |||||||
chr4:2943611 | G | A | 1 | a0002c0002t0001g0058 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1891+462C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2943611 | |||||||
chr4:2943620 | G | T | 3 | a0002c0002t0001g0284 a0002c0002t0001g0287 a0002c0002t0003g0282 |
3 | HG02055.hp2 HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1891+453C>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2943620 | |||||||
chr4:2943658 | C | A | 1 | a0002c0002t0001g0227 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1891+415G>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2943658 | |||||||
chr4:2943664 | C | T | 5 | a0002c0002t0001g0075 a0002c0002t0001g0083 a0002c0002t0001g0084 others(2): Show |
5 | HG01167.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1891+409G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2943664 | |||||||
chr4:2943688 | T | G | 5 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(2): Show |
5 | HG01884.hp2 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1891+385A>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2943688 | |||||||
chr4:2943789 | A | G | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
323 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.1891+284T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2943789 | |||||||
chr4:2943866 | G | A | 1 | a0002c0002t0020g0280 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1891+207C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2943866 | |||||||
chr4:2943919 | C | T | 1 | a0002c0002t0004g0253 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1891+154G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2943919 | |||||||
chr4:2943946 | C | G | 1 | a0002c0002t0001g0064 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1891+127G>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 13/17 | chr4 | 2943946 | |||||||
chr4:2944301 | T | C | 1 | a0018c0022t0028g0312 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1738-75A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 12/17 | chr4 | 2944301 | |||||||
chr4:2944330 | C | T | 3 | a0002c0002t0001g0082 a0002c0002t0001g0085 a0002c0002t0023g0081 |
3 | HG00323.hp2 HG00639.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1738-104G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 12/17 | chr4 | 2944330 | |||||||
chr4:2944411 | A | AT | 78 | a0001c0001t0001g0180 a0001c0001t0002g0121 a0002c0002t0001g0007 others(75): Show |
94 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.1738-186dupA | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 12/17 | chr4 | 2944411 | |||||||
chr4:2944469 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1738-243G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 12/17 | chr4 | 2944469 | |||||||
chr4:2944499 | C | T | 1 | a0002c0002t0003g0086 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1738-273G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 12/17 | chr4 | 2944499 | |||||||
chr4:2944532 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1738-306C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 12/17 | chr4 | 2944532 | |||||||
chr4:2944575 | T | G | 1 | a0001c0001t0002g0121 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1738-349A>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 12/17 | chr4 | 2944575 | |||||||
chr4:2944597 | G | C | 3 | a0002c0002t0001g0082 a0002c0002t0001g0085 a0002c0002t0023g0081 |
3 | HG00323.hp2 HG00639.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1738-371C>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 12/17 | chr4 | 2944597 | |||||||
chr4:2944603 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1738-377G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 12/17 | chr4 | 2944603 | |||||||
chr4:2944649 | C | T | 75 | a0002c0002t0001g0007 a0002c0002t0001g0012 a0002c0002t0001g0021 others(72): Show |
91 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.1738-423G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 12/17 | chr4 | 2944649 | |||||||
chr4:2944687 | G | A | 5 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(2): Show |
5 | HG01884.hp2 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+441C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 12/17 | chr4 | 2944687 | |||||||
chr4:2944703 | G | T | 1 | a0001c0001t0001g0250 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1737+425C>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 12/17 | chr4 | 2944703 | |||||||
chr4:2944752 | C | T | 1 | a0002c0002t0001g0065 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1737+376G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 12/17 | chr4 | 2944752 | |||||||
chr4:2944754 | A | G | 64 | a0002c0002t0001g0007 a0002c0002t0001g0012 a0002c0002t0001g0021 others(61): Show |
77 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.1737+374T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 12/17 | chr4 | 2944754 | |||||||
chr4:2944770 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1737+358A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 12/17 | chr4 | 2944770 | |||||||
chr4:2944884 | T | G | 8 | a0002c0002t0001g0052 a0002c0002t0001g0286 a0002c0002t0001g0294 others(5): Show |
11 | HG00738.hp2 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1737+244A>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 12/17 | chr4 | 2944884 | |||||||
chr4:2945003 | C | T | 2 | a0002c0002t0001g0094 a0002c0002t0003g0101 |
2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1737+125G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 12/17 | chr4 | 2945003 | |||||||
chr4:2945072 | C | G | 2 | a0001c0001t0001g0102 a0001c0001t0001g0123 |
2 | HG00609.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.1737+56G>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 12/17 | chr4 | 2945072 | |||||||
chr4:2945075 | C | T | 8 | a0002c0002t0001g0052 a0002c0002t0001g0286 a0002c0002t0001g0294 others(5): Show |
11 | HG00738.hp2 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1737+53G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 12/17 | chr4 | 2945075 | |||||||
chr4:2945099 | G | A | 2 | a0002c0002t0010g0079 a0002c0002t0010g0080 |
2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1737+29C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 12/17 | chr4 | 2945099 | |||||||
chr4:2945274 | C | A | 1 | a0021c0021t0001g0274 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1636-45G>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2945274 | |||||||
chr4:2945457 | A | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0138 |
2 | NA18964.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1636-228T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2945457 | |||||||
chr4:2945545 | A | G | 1 | a0002c0002t0001g0227 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1636-316T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2945545 | |||||||
chr4:2945737 | A | C | 1 | a0002c0002t0011g0087 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1636-508T>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2945737 | |||||||
chr4:2945811 | G | T | 3 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0002g0036 |
6 | HG01167.hp2 HG01169.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.1636-582C>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2945811 | |||||||
chr4:2945903 | G | GCTGCCGT others(25): Show |
1 | a0001c0001t0001g0149 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1635+477_1635+508d others(34): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2945903 | |||||||
chr4:2945903 | GCTGCCGT others(25): Show |
G | 3 | a0001c0001t0001g0112 a0002c0002t0001g0256 a0002c0002t0003g0254 |
3 | HG01099.hp1 HG02071.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1635+477_1635+508d others(34): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2945903 | |||||||
chr4:2945903 | GCTGCCGT others(57): Show |
G | 71 | a0001c0001t0001g0250 a0002c0002t0001g0007 a0002c0002t0001g0012 others(68): Show |
87 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.1635+445_1635+508d others(66): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2945903 | |||||||
chr4:2945903 | GCTGCCGT others(89): Show |
G | 2 | a0001c0001t0005g0194 a0002c0002t0011g0087 |
2 | HG01975.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1635+413_1635+508d others(98): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2945903 | |||||||
chr4:2945903 | GCTGCCGT others(121): Show |
G | 3 | a0002c0002t0001g0259 a0002c0002t0001g0266 a0002c0002t0002g0277 |
3 | HG01928.hp1 HG02148.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1635+381_1635+508d others(2): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2945903 | |||||||
chr4:2945930 | C | G | 2 | a0009c0008t0014g0054 a0009c0008t0015g0053 |
2 | HG01255.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1635+482G>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2945930 | |||||||
chr4:2945951 | ACTCCAGA others(211): Show |
A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0100 a0001c0001t0001g0147 |
4 | HG02040.hp1 NA18747.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.1635+243_1635+460d others(2): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2945951 | |||||||
chr4:2945953 | T | TCCAGATC others(25): Show |
1 | a0003c0003t0003g0205 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1635+458_1635+459i others(34): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2945953 | |||||||
chr4:2945955 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1635+457G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2945955 | |||||||
chr4:2945985 | T | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(71): Show |
127 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.1635+427A>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2945985 | |||||||
chr4:2946063 | A | G | 38 | a0002c0002t0001g0004 a0002c0002t0001g0011 a0002c0002t0001g0024 others(35): Show |
47 | HG00738.hp1 HG01069.hp2 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.1635+349T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2946063 | |||||||
chr4:2946068 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0118 |
3 | NA18974.hp1 NA19058.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1635+344G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2946068 | |||||||
chr4:2946073 | ACTCTCAC others(27): Show |
A | 34 | a0002c0002t0001g0004 a0002c0002t0001g0011 a0002c0002t0001g0024 others(31): Show |
43 | HG00738.hp1 HG01069.hp2 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.1635+305_1635+338d others(36): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2946073 | |||||||
chr4:2946075 | TCTCACTC others(85): Show |
T | 1 | a0002c0002t0004g0253 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1635+245_1635+336d others(94): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2946075 | |||||||
chr4:2946081 | T | G | 1 | a0001c0001t0005g0194 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1635+331A>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2946081 | |||||||
chr4:2946095 | A | ACTGCCGT others(89): Show |
1 | a0003c0003t0008g0111 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1635+316_1635+317i others(98): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2946095 | |||||||
chr4:2946095 | A | ACTGCCGT others(25): Show |
8 | a0001c0001t0001g0167 a0001c0001t0001g0173 a0001c0001t0001g0190 others(5): Show |
9 | HG01070.hp2 HG01175.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1635+285_1635+316d others(34): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2946095 | |||||||
chr4:2946095 | A | G | 5 | a0002c0002t0001g0093 a0002c0002t0001g0094 a0002c0002t0003g0101 others(2): Show |
5 | HG01243.hp2 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1635+317T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2946095 | |||||||
chr4:2946105 | ACT | A | 4 | a0002c0002t0001g0093 a0002c0002t0001g0094 a0002c0002t0003g0101 others(1): Show |
4 | HG01243.hp2 HG02572.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1635+305_1635+306d others(4): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2946105 | |||||||
chr4:2946127 | G | A | 4 | a0003c0003t0008g0111 a0009c0008t0014g0054 a0009c0008t0015g0053 others(1): Show |
4 | HG01255.hp1 HG02572.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1635+285C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2946127 | |||||||
chr4:2946139 | TCA | T | 40 | a0002c0002t0001g0004 a0002c0002t0001g0011 a0002c0002t0001g0024 others(37): Show |
49 | HG00738.hp1 HG01069.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.1635+271_1635+272d others(4): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2946139 | |||||||
chr4:2946157 | A | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0097 a0001c0001t0001g0099 others(19): Show |
25 | HG00423.hp2 HG00438.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.1635+255T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2946157 | |||||||
chr4:2946169 | T | A | 1 | a0002c0002t0004g0253 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1635+243A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2946169 | |||||||
chr4:2946197 | T | TCTCA | 116 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0011 others(113): Show |
141 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1635+214_1635+215i others(6): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2946197 | |||||||
chr4:2946197 | T | TCTCCAGA others(89): Show |
4 | a0001c0001t0001g0017 a0001c0001t0001g0219 a0010c0010t0018g0176 others(1): Show |
6 | HG00621.hp2 HG02135.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.1635+214_1635+215i others(98): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2946197 | |||||||
chr4:2946213 | A | G | 2 | a0009c0008t0014g0054 a0009c0008t0015g0053 |
2 | HG01255.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1635+199T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2946213 | |||||||
chr4:2946219 | G | A | 1 | a0002c0002t0001g0262 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1635+193C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2946219 | |||||||
chr4:2946245 | A | G | 117 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0011 others(114): Show |
142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1635+167T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2946245 | |||||||
chr4:2946292 | A | T | 3 | a0002c0002t0001g0283 a0002c0002t0001g0289 a0002c0002t0002g0272 |
3 | HG02165.hp1 NA18950.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.1635+120T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2946292 | |||||||
chr4:2946347 | C | G | 1 | a0002c0002t0001g0227 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1635+65G>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2946347 | |||||||
chr4:2946372 | T | A | 1 | a0001c0001t0001g0039 | 2 | NA18939.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1635+40A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2946372 | |||||||
chr4:2946373 | T | A | 1 | a0001c0001t0001g0039 | 2 | NA18939.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1635+39A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 11/17 | chr4 | 2946373 | |||||||
chr4:2946593 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1500-46C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 10/17 | chr4 | 2946593 | |||||||
chr4:2946659 | T | C | 1 | a0018c0022t0028g0312 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1500-112A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 10/17 | chr4 | 2946659 | |||||||
chr4:2946698 | T | C | 1 | a0002c0002t0001g0093 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1500-151A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 10/17 | chr4 | 2946698 | |||||||
chr4:2946729 | G | A | 117 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0011 others(114): Show |
142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1500-182C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 10/17 | chr4 | 2946729 | |||||||
chr4:2946771 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1500-224C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 10/17 | chr4 | 2946771 | |||||||
chr4:2946787 | G | A | 1 | a0002c0002t0001g0075 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1500-240C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 10/17 | chr4 | 2946787 | |||||||
chr4:2947142 | A | G | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
418 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(415): Show |
intron_variant | MODIFIER | c.1499+384T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 10/17 | chr4 | 2947142 | |||||||
chr4:2947194 | C | G | 1 | a0001c0001t0001g0250 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1499+332G>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 10/17 | chr4 | 2947194 | |||||||
chr4:2947337 | C | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0189 a0001c0001t0002g0032 others(1): Show |
6 | HG00423.hp1 HG00642.hp1 HG00735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1499+189G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 10/17 | chr4 | 2947337 | |||||||
chr4:2947428 | T | G | 1 | a0001c0001t0001g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1499+98A>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 10/17 | chr4 | 2947428 | |||||||
chr4:2947787 | C | G | 1 | a0001c0001t0024g0139 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1414-176G>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 9/17 | chr4 | 2947787 | |||||||
chr4:2947930 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1414-319G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 9/17 | chr4 | 2947930 | |||||||
chr4:2947957 | ATCTGCCA others(14): Show |
A | 1 | a0002c0002t0001g0235 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1413+300_1413+320d others(23): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 9/17 | chr4 | 2947957 | |||||||
chr4:2948006 | T | C | 1 | a0002c0002t0001g0058 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1413+272A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 9/17 | chr4 | 2948006 | |||||||
chr4:2948070 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1413+208C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 9/17 | chr4 | 2948070 | |||||||
chr4:2948109 | C | T | 1 | a0002c0002t0001g0276 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1413+169G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 9/17 | chr4 | 2948109 | |||||||
chr4:2948151 | A | G | 35 | a0002c0002t0001g0004 a0002c0002t0001g0011 a0002c0002t0001g0024 others(32): Show |
44 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.1413+127T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 9/17 | chr4 | 2948151 | |||||||
chr4:2948409 | C | G | 1 | a0001c0001t0001g0150 | 1 | HG03688.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.1283-1G>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 8/17 | chr4 | 2948409 | |||||||
chr4:2948485 | C | T | 3 | a0002c0002t0001g0284 a0002c0002t0001g0287 a0002c0002t0003g0282 |
3 | HG02055.hp2 HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1283-77G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 8/17 | chr4 | 2948485 | |||||||
chr4:2948990 | G | A | 75 | a0002c0002t0001g0007 a0002c0002t0001g0012 a0002c0002t0001g0021 others(72): Show |
91 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.1283-582C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 8/17 | chr4 | 2948990 | |||||||
chr4:2949172 | T | C | 122 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(119): Show |
147 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1282+762A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 8/17 | chr4 | 2949172 | |||||||
chr4:2949255 | G | A | 1 | a0020c0030t0004g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1282+679C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 8/17 | chr4 | 2949255 | |||||||
chr4:2949298 | G | A | 18 | a0002c0002t0001g0012 a0002c0002t0001g0058 a0002c0002t0001g0082 others(15): Show |
20 | HG00323.hp2 HG00639.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1282+636C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 8/17 | chr4 | 2949298 | |||||||
chr4:2949402 | G | A | 1 | a0001c0001t0002g0246 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1282+532C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 8/17 | chr4 | 2949402 | |||||||
chr4:2949471 | T | C | 2 | a0002c0002t0001g0094 a0002c0002t0003g0101 |
2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1282+463A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 8/17 | chr4 | 2949471 | |||||||
chr4:2949582 | C | T | 17 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0095 others(14): Show |
21 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.1282+352G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 8/17 | chr4 | 2949582 | |||||||
chr4:2949792 | A | G | 117 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0011 others(114): Show |
142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1282+142T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 8/17 | chr4 | 2949792 | |||||||
chr4:2949921 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1282+13G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 8/17 | chr4 | 2949921 | |||||||
chr4:2950262 | G | C | 1 | a0022c0019t0001g0071 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1003-49C>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 7/17 | chr4 | 2950262 | |||||||
chr4:2950263 | C | G | 1 | a0022c0019t0001g0071 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1003-50G>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 7/17 | chr4 | 2950263 | |||||||
chr4:2950352 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1003-139G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 7/17 | chr4 | 2950352 | |||||||
chr4:2950374 | C | G | 1 | a0022c0019t0001g0071 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1003-161G>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 7/17 | chr4 | 2950374 | |||||||
chr4:2950480 | G | T | 1 | a0001c0001t0001g0157 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1003-267C>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 7/17 | chr4 | 2950480 | |||||||
chr4:2950539 | C | T | 2 | a0002c0002t0001g0094 a0002c0002t0003g0101 |
2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1003-326G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 7/17 | chr4 | 2950539 | |||||||
chr4:2950577 | G | A | 1 | a0019c0029t0001g0132 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1003-364C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 7/17 | chr4 | 2950577 | |||||||
chr4:2950590 | T | C | 1 | a0022c0019t0001g0071 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1003-377A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 7/17 | chr4 | 2950590 | |||||||
chr4:2950731 | A | T | 3 | a0002c0002t0010g0079 a0002c0002t0010g0080 a0002c0002t0026g0078 |
3 | HG02717.hp2 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1002+383T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 7/17 | chr4 | 2950731 | |||||||
chr4:2950779 | A | G | 117 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0011 others(114): Show |
142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1002+335T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 7/17 | chr4 | 2950779 | |||||||
chr4:2950790 | G | A | 1 | a0002c0018t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1002+324C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 7/17 | chr4 | 2950790 | |||||||
chr4:2950876 | CAGAG | C | 12 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(9): Show |
13 | HG01884.hp2 HG01928.hp1 HG02896.hp2 others(10): Show |
intron_variant | MODIFIER | c.1002+234_1002+237d others(6): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 7/17 | chr4 | 2950876 | |||||||
chr4:2950880 | G | C | 3 | a0002c0002t0001g0284 a0002c0002t0001g0287 a0002c0002t0003g0282 |
3 | HG02055.hp2 HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1002+234C>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 7/17 | chr4 | 2950880 | |||||||
chr4:2950885 | AGAGT | A | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(67): Show |
122 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.1002+225_1002+228d others(6): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 7/17 | chr4 | 2950885 | |||||||
chr4:2951299 | G | A | 1 | a0005c0006t0001g0022 | 3 | HG00738.hp2 HG03017.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.871-54C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 6/17 | chr4 | 2951299 | |||||||
chr4:2951303 | G | C | 1 | a0001c0001t0001g0199 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.871-58C>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 6/17 | chr4 | 2951303 | |||||||
chr4:2951375 | T | C | 1 | a0001c0001t0002g0156 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.871-130A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 6/17 | chr4 | 2951375 | |||||||
chr4:2951562 | A | G | 5 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(2): Show |
5 | HG01884.hp2 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.871-317T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 6/17 | chr4 | 2951562 | |||||||
chr4:2951936 | A | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0112 |
3 | HG02071.hp2 NA18999.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.870+339T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 6/17 | chr4 | 2951936 | |||||||
chr4:2951952 | C | G | 6 | a0002c0002t0001g0012 a0002c0002t0001g0090 a0002c0002t0001g0091 others(3): Show |
8 | HG02630.hp2 HG02647.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.870+323G>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 6/17 | chr4 | 2951952 | |||||||
chr4:2951976 | A | G | 123 | a0001c0001t0001g0146 a0001c0001t0006g0044 a0001c0001t0006g0233 others(120): Show |
150 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.870+299T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 6/17 | chr4 | 2951976 | |||||||
chr4:2952109 | G | GA | 58 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0161 others(55): Show |
72 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.870+165dupT | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 6/17 | chr4 | 2952109 | |||||||
chr4:2952109 | GA | G | 7 | a0001c0001t0001g0099 a0002c0002t0001g0068 a0002c0002t0001g0094 others(4): Show |
7 | HG02717.hp1 HG02922.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.870+165delT | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 6/17 | chr4 | 2952109 | |||||||
chr4:2952232 | C | T | 1 | a0002c0002t0026g0078 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.870+43G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 6/17 | chr4 | 2952232 | |||||||
chr4:2952768 | C | T | 1 | a0002c0002t0001g0093 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.748-371G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 5/17 | chr4 | 2952768 | |||||||
chr4:2952880 | T | A | 1 | a0001c0001t0001g0243 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.748-483A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 5/17 | chr4 | 2952880 | |||||||
chr4:2952957 | G | A | 1 | a0002c0002t0001g0073 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.747+554C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 5/17 | chr4 | 2952957 | |||||||
chr4:2952989 | G | C | 12 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0107 others(9): Show |
12 | HG00423.hp2 HG00673.hp1 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.747+522C>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 5/17 | chr4 | 2952989 | |||||||
chr4:2952990 | G | A | 34 | a0002c0002t0001g0004 a0002c0002t0001g0011 a0002c0002t0001g0024 others(31): Show |
43 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.747+521C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 5/17 | chr4 | 2952990 | |||||||
chr4:2953055 | A | T | 1 | a0001c0001t0001g0114 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.747+456T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 5/17 | chr4 | 2953055 | |||||||
chr4:2953163 | A | G | 1 | a0018c0022t0028g0312 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.747+348T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 5/17 | chr4 | 2953163 | |||||||
chr4:2953246 | A | G | 4 | a0001c0025t0001g0124 a0002c0002t0001g0284 a0002c0002t0001g0287 others(1): Show |
4 | HG02055.hp2 HG02258.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.747+265T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 5/17 | chr4 | 2953246 | |||||||
chr4:2953325 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.747+186G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 5/17 | chr4 | 2953325 | |||||||
chr4:2953390 | A | G | 1 | a0001c0001t0002g0303 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.747+121T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 5/17 | chr4 | 2953390 | |||||||
chr4:2953418 | T | C | 117 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0011 others(114): Show |
142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.747+93A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 5/17 | chr4 | 2953418 | |||||||
chr4:2953430 | C | A | 1 | a0002c0002t0001g0058 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.747+81G>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 5/17 | chr4 | 2953430 | |||||||
chr4:2953465 | C | G | 117 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0011 others(114): Show |
142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.747+46G>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 5/17 | chr4 | 2953465 | |||||||
chr4:2953485 | A | C | 1 | a0018c0022t0028g0312 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.747+26T>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 5/17 | chr4 | 2953485 | |||||||
chr4:2953738 | T | C | 117 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0011 others(114): Show |
142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.613-93A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 4/17 | chr4 | 2953738 | |||||||
chr4:2953798 | A | T | 1 | a0001c0001t0001g0123 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.613-153T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 4/17 | chr4 | 2953798 | |||||||
chr4:2953952 | G | A | 2 | a0001c0001t0001g0200 a0001c0001t0002g0143 |
2 | HG00099.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.613-307C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 4/17 | chr4 | 2953952 | |||||||
chr4:2953954 | G | A | 1 | a0002c0002t0001g0235 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.613-309C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 4/17 | chr4 | 2953954 | |||||||
chr4:2953959 | G | C | 1 | a0002c0002t0001g0227 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.613-314C>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 4/17 | chr4 | 2953959 | |||||||
chr4:2954031 | C | T | 1 | a0018c0022t0028g0312 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.613-386G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 4/17 | chr4 | 2954031 | |||||||
chr4:2954035 | C | A | 1 | a0001c0001t0001g0095 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.612+389G>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 4/17 | chr4 | 2954035 | |||||||
chr4:2954061 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.612+363A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 4/17 | chr4 | 2954061 | |||||||
chr4:2954190 | C | A | 3 | a0002c0002t0001g0093 a0002c0002t0001g0094 a0002c0002t0003g0101 |
3 | HG01243.hp2 HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.612+234G>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 4/17 | chr4 | 2954190 | |||||||
chr4:2954193 | C | T | 5 | a0002c0002t0001g0075 a0002c0002t0001g0083 a0002c0002t0001g0084 others(2): Show |
5 | HG01167.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.612+231G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 4/17 | chr4 | 2954193 | |||||||
chr4:2954652 | T | C | 3 | a0001c0001t0001g0037 a0001c0001t0001g0189 a0001c0001t0001g0190 |
4 | HG00423.hp1 HG02083.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.473-89A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2954652 | |||||||
chr4:2954819 | C | G | 2 | a0011c0012t0013g0059 a0011c0012t0013g0060 |
2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.473-256G>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2954819 | |||||||
chr4:2954976 | A | ACCACGGC others(22): Show |
1 | a0002c0002t0001g0275 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.473-414_473-413ins others(29): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2954976 | |||||||
chr4:2955004 | C | T | 57 | a0002c0002t0001g0007 a0002c0002t0001g0021 a0002c0002t0001g0047 others(54): Show |
71 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.473-441G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955004 | |||||||
chr4:2955073 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0200 |
8 | NA18945.hp2 NA18959.hp2 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.473-510A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955073 | |||||||
chr4:2955122 | A | G | 3 | a0001c0001t0001g0150 a0002c0002t0001g0082 a0002c0002t0001g0273 |
3 | HG00323.hp2 HG01175.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.473-559T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955122 | |||||||
chr4:2955150 | C | T | 1 | a0001c0001t0002g0178 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.473-587G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955150 | |||||||
chr4:2955175 | G | GCCACGGC others(20): Show |
1 | a0002c0002t0001g0227 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.473-639_473-613dup others(27): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955175 | |||||||
chr4:2955180 | G | A | 3 | a0002c0002t0001g0093 a0002c0002t0001g0094 a0002c0002t0003g0101 |
3 | HG01243.hp2 HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.473-617C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955180 | |||||||
chr4:2955182 | C | T | 1 | a0002c0002t0026g0078 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.473-619G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955182 | |||||||
chr4:2955183 | G | A | 34 | a0002c0002t0001g0004 a0002c0002t0001g0011 a0002c0002t0001g0024 others(31): Show |
43 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.473-620C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955183 | |||||||
chr4:2955236 | A | G | 117 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0011 others(114): Show |
142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.473-673T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955236 | |||||||
chr4:2955239 | G | A | 1 | a0002c0002t0001g0228 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.473-676C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955239 | |||||||
chr4:2955266 | G | A | 13 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0095 others(10): Show |
17 | HG00140.hp2 HG00642.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.473-703C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955266 | |||||||
chr4:2955299 | T | G | 117 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0011 others(114): Show |
142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.473-736A>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955299 | |||||||
chr4:2955319 | C | T | 1 | a0001c0001t0001g0192 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.473-756G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955319 | |||||||
chr4:2955340 | C | G | 34 | a0002c0002t0001g0004 a0002c0002t0001g0011 a0002c0002t0001g0024 others(31): Show |
43 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.473-777G>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955340 | |||||||
chr4:2955372 | C | T | 1 | a0002c0002t0001g0021 | 3 | HG00733.hp2 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.473-809G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955372 | |||||||
chr4:2955373 | G | GGCGCCCC others(74): Show |
1 | a0002c0002t0001g0291 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.473-891_473-811dup others(81): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955373 | |||||||
chr4:2955389 | A | C | 1 | a0001c0001t0024g0139 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.473-826T>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955389 | |||||||
chr4:2955432 | GCCCTCTA others(49): Show |
G | 2 | a0001c0001t0001g0107 a0002c0002t0026g0078 |
2 | HG02717.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.473-925_473-870del others(56): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955432 | |||||||
chr4:2955454 | A | AGCGCCCC others(163): Show |
3 | a0001c0001t0001g0001 a0001c0001t0005g0194 a0001c0001t0021g0198 |
6 | HG01257.hp2 HG01258.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.473-892_473-891ins others(170): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955454 | |||||||
chr4:2955477 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.473-914G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955477 | |||||||
chr4:2955485 | C | T | 1 | a0001c0001t0002g0018 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.473-922G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955485 | |||||||
chr4:2955510 | A | AGCGCCCC others(22): Show |
4 | a0001c0001t0001g0017 a0001c0001t0001g0219 a0010c0010t0018g0176 others(1): Show |
6 | HG00621.hp2 HG02135.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.473-976_473-948dup others(29): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955510 | |||||||
chr4:2955510 | AGCGCCCC others(22): Show |
A | 1 | a0001c0001t0001g0203 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.473-976_473-948del others(29): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955510 | |||||||
chr4:2955512 | C | T | 5 | a0006c0015t0007g0255 a0006c0016t0012g0299 a0006c0017t0001g0301 others(2): Show |
5 | HG01109.hp2 HG02572.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.473-949G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955512 | |||||||
chr4:2955516 | C | T | 1 | a0018c0022t0028g0312 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.473-953G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955516 | |||||||
chr4:2955568 | G | A | 1 | a0002c0002t0001g0058 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.473-1005C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955568 | |||||||
chr4:2955570 | C | T | 1 | a0002c0002t0026g0078 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.473-1007G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955570 | |||||||
chr4:2955571 | G | A | 1 | a0002c0002t0001g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.473-1008C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955571 | |||||||
chr4:2955598 | G | A | 1 | a0002c0018t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.473-1035C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955598 | |||||||
chr4:2955784 | G | A | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.472+886C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955784 | |||||||
chr4:2955940 | C | G | 1 | a0001c0001t0002g0026 | 2 | HG02602.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.472+730G>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955940 | |||||||
chr4:2955975 | T | C | 1 | a0001c0001t0001g0033 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.472+695A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2955975 | |||||||
chr4:2956127 | G | A | 8 | a0002c0002t0001g0052 a0002c0002t0001g0286 a0002c0002t0001g0294 others(5): Show |
11 | HG00738.hp2 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.472+543C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2956127 | |||||||
chr4:2956163 | T | C | 1 | a0002c0002t0001g0227 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.472+507A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2956163 | |||||||
chr4:2956170 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.472+500G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2956170 | |||||||
chr4:2956459 | A | G | 76 | a0002c0002t0001g0007 a0002c0002t0001g0012 a0002c0002t0001g0021 others(73): Show |
92 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.472+211T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2956459 | |||||||
chr4:2956635 | C | T | 3 | a0002c0002t0001g0265 a0002c0002t0005g0264 a0002c0002t0005g0268 |
3 | HG01981.hp2 NA18948.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.472+35G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 3/17 | chr4 | 2956635 | |||||||
chr4:2956919 | C | T | 2 | a0011c0012t0013g0059 a0011c0012t0013g0060 |
2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.331-108G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 2/17 | chr4 | 2956919 | |||||||
chr4:2957062 | A | C | 117 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0011 others(114): Show |
142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.331-251T>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 2/17 | chr4 | 2957062 | |||||||
chr4:2957135 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.331-324C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 2/17 | chr4 | 2957135 | |||||||
chr4:2957191 | G | A | 2 | a0001c0001t0001g0153 a0002c0002t0001g0227 |
2 | HG01515.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.331-380C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 2/17 | chr4 | 2957191 | |||||||
chr4:2957295 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.330+311G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 2/17 | chr4 | 2957295 | |||||||
chr4:2957352 | T | C | 2 | a0002c0002t0001g0227 a0002c0018t0027g0151 |
2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.330+254A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 2/17 | chr4 | 2957352 | |||||||
chr4:2957945 | A | G | 118 | a0001c0001t0001g0219 a0002c0002t0001g0004 a0002c0002t0001g0007 others(115): Show |
143 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.196-205T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2957945 | |||||||
chr4:2957985 | A | T | 2 | a0009c0008t0014g0054 a0009c0008t0015g0053 |
2 | HG01255.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.196-245T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2957985 | |||||||
chr4:2958019 | A | G | 1 | a0001c0001t0001g0034 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.196-279T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2958019 | |||||||
chr4:2958038 | C | T | 118 | a0001c0001t0001g0219 a0002c0002t0001g0004 a0002c0002t0001g0007 others(115): Show |
143 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.196-298G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2958038 | |||||||
chr4:2958086 | T | A | 1 | a0001c0001t0001g0250 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.196-346A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2958086 | |||||||
chr4:2958420 | G | C | 1 | a0001c0001t0001g0204 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.196-680C>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2958420 | |||||||
chr4:2958703 | C | T | 57 | a0002c0002t0001g0007 a0002c0002t0001g0021 a0002c0002t0001g0047 others(54): Show |
71 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.196-963G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2958703 | |||||||
chr4:2958734 | C | G | 1 | a0001c0001t0001g0304 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.196-994G>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2958734 | |||||||
chr4:2958977 | T | TAGAGCAC others(21): Show |
1 | a0001c0001t0004g0308 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.196-1265_196-1238d others(30): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2958977 | |||||||
chr4:2959312 | G | T | 1 | a0001c0001t0001g0164 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.196-1572C>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959312 | |||||||
chr4:2959317 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.196-1577C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959317 | |||||||
chr4:2959318 | C | T | 8 | a0001c0001t0001g0224 a0003c0003t0001g0040 a0003c0003t0001g0106 others(5): Show |
9 | HG01069.hp1 HG01071.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-1578G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959318 | |||||||
chr4:2959319 | G | A | 6 | a0003c0003t0001g0241 a0006c0015t0007g0255 a0006c0016t0012g0299 others(3): Show |
6 | HG01109.hp2 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-1579C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959319 | |||||||
chr4:2959320 | C | G | 5 | a0006c0015t0007g0255 a0006c0016t0012g0299 a0006c0017t0001g0301 others(2): Show |
5 | HG01109.hp2 HG02572.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-1580G>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959320 | |||||||
chr4:2959340 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.196-1600A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959340 | |||||||
chr4:2959349 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.196-1609G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959349 | |||||||
chr4:2959359 | A | G | 4 | a0002c0002t0001g0068 a0002c0002t0001g0069 a0002c0002t0001g0070 others(1): Show |
4 | NA18949.hp2 NA18965.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-1619T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959359 | |||||||
chr4:2959362 | G | GT | 4 | a0002c0002t0001g0068 a0002c0002t0001g0069 a0002c0002t0001g0070 others(1): Show |
4 | NA18949.hp2 NA18965.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-1623_196-1622i others(3): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959362 | |||||||
chr4:2959363 | C | G | 4 | a0002c0002t0001g0068 a0002c0002t0001g0069 a0002c0002t0001g0070 others(1): Show |
4 | NA18949.hp2 NA18965.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-1623G>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959363 | |||||||
chr4:2959364 | G | A | 3 | a0002c0002t0008g0057 a0009c0008t0014g0054 a0009c0008t0015g0053 |
3 | HG01255.hp1 HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.196-1624C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959364 | |||||||
chr4:2959370 | A | G | 4 | a0002c0002t0001g0068 a0002c0002t0001g0069 a0002c0002t0001g0070 others(1): Show |
4 | NA18949.hp2 NA18965.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-1630T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959370 | |||||||
chr4:2959374 | C | T | 5 | a0001c0001t0001g0168 a0002c0002t0001g0068 a0002c0002t0001g0069 others(2): Show |
5 | NA18949.hp2 NA18965.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-1634G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959374 | |||||||
chr4:2959375 | G | A | 1 | a0002c0002t0001g0064 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.196-1635C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959375 | |||||||
chr4:2959379 | T | C | 4 | a0002c0002t0001g0068 a0002c0002t0001g0069 a0002c0002t0001g0070 others(1): Show |
4 | NA18949.hp2 NA18965.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-1639A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959379 | |||||||
chr4:2959380 | T | C | 25 | a0001c0001t0001g0008 a0001c0001t0001g0103 a0001c0001t0001g0104 others(22): Show |
28 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.196-1640A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959380 | |||||||
chr4:2959383 | A | G | 19 | a0001c0001t0001g0008 a0001c0001t0001g0103 a0001c0001t0001g0104 others(16): Show |
22 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-1643T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959383 | |||||||
chr4:2959388 | C | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0103 a0001c0001t0002g0303 others(4): Show |
10 | NA18949.hp1 NA18949.hp2 NA18951.hp2 others(7): Show |
intron_variant | MODIFIER | c.196-1648G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959388 | |||||||
chr4:2959389 | A | G | 132 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(129): Show |
168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.196-1649T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959389 | |||||||
chr4:2959402 | G | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(132): Show |
191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.196-1662C>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959402 | |||||||
chr4:2959408 | T | C | 22 | a0001c0001t0001g0010 a0001c0001t0001g0217 a0001c0001t0001g0304 others(19): Show |
28 | HG01069.hp1 HG01071.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.196-1668A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959408 | |||||||
chr4:2959415 | A | G | 1 | a0002c0002t0001g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.196-1675T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959415 | |||||||
chr4:2959420 | G | A | 7 | a0001c0001t0001g0002 a0001c0001t0001g0202 a0001c0001t0001g0203 others(4): Show |
13 | HG00408.hp1 HG00597.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.196-1680C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959420 | |||||||
chr4:2959449 | C | T | 150 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0027 others(147): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.196-1709G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959449 | |||||||
chr4:2959453 | T | C | 147 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0076 others(144): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.196-1713A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959453 | |||||||
chr4:2959457 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.196-1717C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959457 | |||||||
chr4:2959461 | C | T | 134 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0033 others(131): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.196-1721G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959461 | |||||||
chr4:2959462 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.196-1722C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959462 | |||||||
chr4:2959466 | G | A | 10 | a0001c0001t0001g0144 a0001c0001t0001g0210 a0001c0001t0001g0244 others(7): Show |
15 | HG00099.hp1 HG00733.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.196-1726C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959466 | |||||||
chr4:2959509 | C | T | 1 | a0002c0002t0001g0227 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.196-1769G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959509 | |||||||
chr4:2959571 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.196-1831G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959571 | |||||||
chr4:2959583 | ACT | A | 114 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0011 others(111): Show |
139 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.196-1845_196-1844d others(4): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959583 | |||||||
chr4:2959598 | C | A | 1 | a0001c0001t0001g0211 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.196-1858G>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959598 | |||||||
chr4:2959598 | C | CA | 55 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0002c0002t0001g0004 others(52): Show |
66 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.196-1859dupT | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959598 | |||||||
chr4:2959607 | A | C | 1 | a0004c0004t0001g0116 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.196-1867T>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959607 | |||||||
chr4:2959617 | C | T | 36 | a0002c0002t0001g0007 a0002c0002t0001g0021 a0002c0002t0001g0047 others(33): Show |
47 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.196-1877G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959617 | |||||||
chr4:2959778 | A | G | 1 | a0003c0003t0008g0111 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.196-2038T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959778 | |||||||
chr4:2959836 | A | G | 36 | a0002c0002t0001g0007 a0002c0002t0001g0021 a0002c0002t0001g0047 others(33): Show |
47 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.196-2096T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959836 | |||||||
chr4:2959924 | C | T | 1 | a0001c0001t0001g0042 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.196-2184G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959924 | |||||||
chr4:2959927 | T | C | 1 | a0001c0001t0002g0172 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.196-2187A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959927 | |||||||
chr4:2959971 | CT | C | 16 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0100 others(13): Show |
26 | HG00438.hp2 HG00621.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.196-2232delA | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959971 | |||||||
chr4:2959986 | T | A | 90 | a0002c0002t0001g0007 a0002c0002t0001g0012 a0002c0002t0001g0021 others(87): Show |
106 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.196-2246A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2959986 | |||||||
chr4:2960056 | A | G | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(235): Show |
330 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.196-2316T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960056 | |||||||
chr4:2960100 | G | A | 5 | a0002c0002t0001g0011 a0002c0002t0001g0239 a0002c0002t0003g0254 others(2): Show |
8 | HG02145.hp1 HG02559.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.196-2360C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960100 | |||||||
chr4:2960115 | G | A | 1 | a0001c0001t0006g0234 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.196-2375C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960115 | |||||||
chr4:2960171 | C | T | 1 | a0002c0002t0001g0291 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.196-2431G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960171 | |||||||
chr4:2960306 | G | A | 1 | a0002c0002t0001g0093 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.196-2566C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960306 | |||||||
chr4:2960342 | G | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
7 | HG00438.hp2 HG00621.hp1 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.196-2602C>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960342 | |||||||
chr4:2960456 | G | A | 1 | a0001c0001t0001g0218 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.195+2669C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960456 | |||||||
chr4:2960523 | C | A | 1 | a0002c0002t0001g0258 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.195+2602G>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960523 | |||||||
chr4:2960523 | C | T | 2 | a0011c0012t0013g0059 a0011c0012t0013g0060 |
2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.195+2602G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960523 | |||||||
chr4:2960595 | C | T | 1 | a0002c0002t0001g0262 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.195+2530G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960595 | |||||||
chr4:2960662 | TTATTATA others(4): Show |
T | 9 | a0001c0001t0001g0001 a0002c0002t0001g0012 a0002c0002t0001g0088 others(6): Show |
12 | HG01891.hp2 HG02015.hp2 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.195+2452_195+2462d others(13): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960662 | |||||||
chr4:2960663 | T | C | 3 | a0002c0002t0001g0284 a0002c0002t0001g0287 a0002c0002t0003g0282 |
3 | HG02055.hp2 HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.195+2462A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960663 | |||||||
chr4:2960676 | T | A | 2 | a0009c0008t0014g0054 a0009c0008t0015g0053 |
2 | HG01255.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.195+2449A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960676 | |||||||
chr4:2960676 | T | TTAA | 3 | a0001c0001t0001g0103 a0002c0002t0010g0079 a0002c0002t0010g0080 |
3 | HG03516.hp1 NA18906.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.195+2448_195+2449i others(5): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960676 | |||||||
chr4:2960676 | T | TTATAATC others(13): Show |
1 | a0002c0002t0011g0087 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.195+2448_195+2449i others(22): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960676 | |||||||
chr4:2960676 | TTATATTA others(24): Show |
T | 24 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0020 others(21): Show |
32 | HG01070.hp2 HG01175.hp2 HG01358.hp1 others(29): Show |
intron_variant | MODIFIER | c.195+2418_195+2448d others(33): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960676 | |||||||
chr4:2960676 | TTATATTA others(55): Show |
T | 4 | a0001c0001t0001g0136 a0001c0001t0001g0199 a0001c0001t0005g0194 others(1): Show |
4 | HG00673.hp1 HG01975.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+2387_195+2448d others(64): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960676 | |||||||
chr4:2960694 | C | T | 103 | a0001c0001t0004g0308 a0002c0002t0001g0004 a0002c0002t0001g0007 others(100): Show |
126 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.195+2431G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960694 | |||||||
chr4:2960695 | A | G | 2 | a0009c0008t0014g0054 a0009c0008t0015g0053 |
2 | HG01255.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.195+2430T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960695 | |||||||
chr4:2960705 | T | C | 41 | a0002c0002t0001g0007 a0002c0002t0001g0021 a0002c0002t0001g0047 others(38): Show |
52 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.195+2420A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960705 | |||||||
chr4:2960725 | C | T | 67 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(64): Show |
81 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.195+2400G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960725 | |||||||
chr4:2960729 | TTAATATT others(27): Show |
T | 1 | a0001c0001t0001g0219 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.195+2362_195+2395d others(36): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960729 | |||||||
chr4:2960736 | T | C | 8 | a0001c0001t0001g0211 a0002c0002t0001g0049 a0002c0002t0001g0259 others(5): Show |
9 | HG01928.hp1 HG02027.hp1 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.195+2389A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960736 | |||||||
chr4:2960736 | TAATATAT others(83): Show |
T | 3 | a0009c0008t0014g0054 a0011c0012t0013g0059 a0011c0012t0013g0060 |
3 | HG02145.hp2 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.195+2299_195+2388d others(92): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960736 | |||||||
chr4:2960742 | A | G | 7 | a0002c0002t0001g0094 a0002c0002t0001g0228 a0002c0002t0001g0229 others(4): Show |
7 | HG02818.hp2 HG02922.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.195+2383T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960742 | |||||||
chr4:2960746 | ATAT | A | 45 | a0001c0001t0002g0193 a0002c0002t0001g0007 a0002c0002t0001g0021 others(42): Show |
58 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.195+2376_195+2378d others(5): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960746 | |||||||
chr4:2960750 | T | A | 1 | a0001c0001t0001g0129 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.195+2375A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960750 | |||||||
chr4:2960751 | A | T | 1 | a0001c0001t0001g0129 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.195+2374T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960751 | |||||||
chr4:2960753 | AATCACAT others(51): Show |
A | 1 | a0001c0001t0004g0308 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.195+2314_195+2371d others(60): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960753 | |||||||
chr4:2960754 | A | T | 1 | a0002c0002t0001g0267 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.195+2371T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960754 | |||||||
chr4:2960756 | C | A | 1 | a0002c0002t0001g0267 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.195+2369G>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960756 | |||||||
chr4:2960756 | C | T | 57 | a0002c0002t0001g0007 a0002c0002t0001g0021 a0002c0002t0001g0047 others(54): Show |
71 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.195+2369G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960756 | |||||||
chr4:2960758 | C | T | 1 | a0002c0002t0001g0267 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.195+2367G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960758 | |||||||
chr4:2960764 | T | C | 1 | a0002c0002t0001g0267 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.195+2361A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960764 | |||||||
chr4:2960764 | T | TATTAATA others(18): Show |
47 | a0002c0002t0001g0007 a0002c0002t0001g0021 a0002c0002t0001g0047 others(44): Show |
58 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.195+2336_195+2360d others(27): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960764 | |||||||
chr4:2960767 | T | C | 2 | a0001c0001t0001g0219 a0009c0008t0015g0053 |
2 | HG00621.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.195+2358A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960767 | |||||||
chr4:2960767 | TAATATAT others(52): Show |
T | 2 | a0002c0018t0027g0151 a0018c0022t0028g0312 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.195+2299_195+2357d others(61): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960767 | |||||||
chr4:2960773 | A | G | 8 | a0002c0002t0001g0093 a0002c0002t0001g0094 a0002c0002t0001g0228 others(5): Show |
8 | HG01243.hp2 HG02818.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.195+2352T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960773 | |||||||
chr4:2960777 | ATAT | A | 7 | a0002c0002t0001g0049 a0002c0002t0001g0259 a0002c0002t0001g0266 others(4): Show |
8 | HG01928.hp1 HG02148.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.195+2345_195+2347d others(5): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960777 | |||||||
chr4:2960787 | C | T | 10 | a0002c0002t0001g0049 a0002c0002t0001g0259 a0002c0002t0001g0266 others(7): Show |
11 | HG01255.hp1 HG01928.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.195+2338G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960787 | |||||||
chr4:2960789 | CATTAAT | C | 2 | a0005c0006t0001g0022 a0006c0015t0007g0255 |
4 | HG00738.hp2 HG02647.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+2330_195+2335d others(8): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960789 | |||||||
chr4:2960800 | A | T | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2325T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960800 | |||||||
chr4:2960804 | A | G | 3 | a0002c0002t0001g0094 a0002c0002t0001g0231 a0002c0002t0003g0101 |
3 | HG02922.hp2 NA20129.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.195+2321T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960804 | |||||||
chr4:2960805 | T | C | 1 | a0001c0001t0001g0009 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.195+2320A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960805 | |||||||
chr4:2960806 | T | C | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2319A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960806 | |||||||
chr4:2960814 | T | C | 1 | a0002c0002t0001g0084 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.195+2311A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960814 | |||||||
chr4:2960816 | A | T | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2309T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960816 | |||||||
chr4:2960818 | C | A | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2307G>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960818 | |||||||
chr4:2960818 | C | T | 2 | a0002c0002t0010g0079 a0002c0002t0010g0080 |
2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.195+2307G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960818 | |||||||
chr4:2960820 | C | T | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2305G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960820 | |||||||
chr4:2960822 | T | TTAA | 104 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0033 others(101): Show |
125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.195+2302_195+2303i others(5): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960822 | |||||||
chr4:2960822 | T | TTAATATT others(27): Show |
4 | a0002c0002t0001g0094 a0002c0002t0001g0229 a0002c0002t0003g0101 others(1): Show |
4 | HG00639.hp2 HG02818.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+2302_195+2303i others(36): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960822 | |||||||
chr4:2960823 | TATC | T | 7 | a0002c0002t0001g0049 a0002c0002t0001g0259 a0002c0002t0001g0266 others(4): Show |
8 | HG01928.hp1 HG02148.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.195+2299_195+2301d others(5): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960823 | |||||||
chr4:2960826 | C | T | 109 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0033 others(106): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.195+2299G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960826 | |||||||
chr4:2960828 | A | T | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2297T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960828 | |||||||
chr4:2960832 | A | T | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2293T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960832 | |||||||
chr4:2960842 | T | C | 5 | a0002c0002t0001g0082 a0002c0002t0001g0083 a0002c0002t0001g0084 others(2): Show |
5 | HG00323.hp2 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.195+2283A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960842 | |||||||
chr4:2960846 | C | T | 3 | a0002c0002t0001g0058 a0002c0002t0010g0079 a0002c0002t0010g0080 |
3 | HG03139.hp1 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.195+2279G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960846 | |||||||
chr4:2960847 | A | T | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2278T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960847 | |||||||
chr4:2960848 | CATTATCA others(24): Show |
C | 1 | a0002c0002t0001g0058 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.195+2246_195+2276d others(33): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960848 | |||||||
chr4:2960850 | T | A | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2275A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960850 | |||||||
chr4:2960850 | T | TTAA | 24 | a0001c0001t0001g0025 a0001c0001t0001g0095 a0001c0001t0001g0107 others(21): Show |
26 | HG00323.hp2 HG01167.hp1 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.195+2274_195+2275i others(5): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960850 | |||||||
chr4:2960854 | C | T | 24 | a0001c0001t0001g0025 a0001c0001t0001g0095 a0001c0001t0001g0107 others(21): Show |
26 | HG00323.hp2 HG01167.hp1 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.195+2271G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960854 | |||||||
chr4:2960855 | A | G | 1 | a0001c0001t0001g0010 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.195+2270T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960855 | |||||||
chr4:2960870 | T | C | 4 | a0002c0002t0001g0084 a0002c0002t0001g0085 a0002c0002t0001g0251 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+2255A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960870 | |||||||
chr4:2960873 | T | A | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2252A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960873 | |||||||
chr4:2960874 | T | C | 49 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0033 others(46): Show |
56 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.195+2251A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960874 | |||||||
chr4:2960876 | C | T | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2249G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960876 | |||||||
chr4:2960876 | CATT | C | 48 | a0002c0002t0001g0007 a0002c0002t0001g0021 a0002c0002t0001g0047 others(45): Show |
61 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.195+2246_195+2248d others(5): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960876 | |||||||
chr4:2960880 | ATTATT | A | 11 | a0002c0002t0001g0049 a0002c0002t0001g0082 a0002c0002t0001g0083 others(8): Show |
12 | HG00323.hp2 HG01928.hp1 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.195+2240_195+2244d others(7): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960880 | |||||||
chr4:2960881 | T | A | 7 | a0001c0001t0001g0107 a0002c0002t0001g0075 a0002c0002t0001g0085 others(4): Show |
7 | HG01167.hp1 HG01255.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+2244A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960881 | |||||||
chr4:2960882 | T | C | 32 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0033 others(29): Show |
38 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.195+2243A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960882 | |||||||
chr4:2960884 | T | A | 33 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0033 others(30): Show |
39 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.195+2241A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960884 | |||||||
chr4:2960884 | T | C | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2241A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960884 | |||||||
chr4:2960885 | T | TAATATAT others(2): Show |
4 | a0001c0001t0001g0107 a0002c0002t0001g0075 a0002c0002t0001g0085 others(1): Show |
4 | HG01167.hp1 HG03239.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+2239_195+2240i others(11): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960885 | |||||||
chr4:2960885 | T | TAATATAT others(33): Show |
2 | a0002c0002t0001g0251 a0002c0002t0001g0252 |
2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.195+2239_195+2240i others(42): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960885 | |||||||
chr4:2960887 | T | C | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2238A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960887 | |||||||
chr4:2960888 | ATTATTAT others(34): Show |
A | 1 | a0001c0001t0001g0168 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.195+2196_195+2236d others(43): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960888 | |||||||
chr4:2960889 | TTATTATA others(62): Show |
T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(149): Show |
231 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(228): Show |
intron_variant | MODIFIER | c.195+2167_195+2235d others(71): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960889 | |||||||
chr4:2960890 | TATTATAT others(1): Show |
T | 6 | a0001c0001t0001g0025 a0001c0001t0001g0095 a0001c0001t0001g0154 others(3): Show |
7 | HG01168.hp2 HG02523.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+2227_195+2234d others(10): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960890 | |||||||
chr4:2960891 | ATT | A | 25 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0109 others(22): Show |
30 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.195+2232_195+2233d others(4): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960891 | |||||||
chr4:2960892 | T | A | 12 | a0002c0002t0001g0049 a0002c0002t0001g0082 a0002c0002t0001g0083 others(9): Show |
13 | HG00323.hp2 HG01928.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.195+2233A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960892 | |||||||
chr4:2960893 | T | A | 6 | a0001c0001t0001g0107 a0002c0002t0001g0075 a0002c0002t0001g0085 others(3): Show |
6 | HG01167.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.195+2232A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960893 | |||||||
chr4:2960895 | T | TCAC | 5 | a0002c0002t0001g0075 a0002c0002t0001g0085 a0002c0002t0001g0251 others(2): Show |
5 | HG01167.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.195+2229_195+2230i others(5): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960895 | |||||||
chr4:2960896 | A | C | 1 | a0001c0001t0001g0107 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.195+2229T>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960896 | |||||||
chr4:2960897 | T | A | 1 | a0001c0001t0001g0107 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.195+2228A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960897 | |||||||
chr4:2960898 | C | T | 42 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0109 others(39): Show |
48 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.195+2227G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960898 | |||||||
chr4:2960900 | A | T | 26 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0107 others(23): Show |
31 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.195+2225T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960900 | |||||||
chr4:2960901 | T | A | 25 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0109 others(22): Show |
30 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.195+2224A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960901 | |||||||
chr4:2960903 | T | C | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2222A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960903 | |||||||
chr4:2960903 | T | TTAA | 6 | a0002c0002t0001g0075 a0002c0002t0001g0084 a0002c0002t0001g0085 others(3): Show |
6 | HG01167.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.195+2221_195+2222i others(5): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960903 | |||||||
chr4:2960906 | T | C | 25 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0109 others(22): Show |
30 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.195+2219A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960906 | |||||||
chr4:2960908 | T | A | 17 | a0001c0001t0001g0025 a0001c0001t0001g0095 a0001c0001t0001g0154 others(14): Show |
19 | HG00323.hp2 HG01168.hp2 HG01928.hp1 others(16): Show |
intron_variant | MODIFIER | c.195+2217A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960908 | |||||||
chr4:2960910 | A | C | 17 | a0001c0001t0001g0025 a0001c0001t0001g0095 a0001c0001t0001g0154 others(14): Show |
19 | HG00323.hp2 HG01168.hp2 HG01928.hp1 others(16): Show |
intron_variant | MODIFIER | c.195+2215T>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960910 | |||||||
chr4:2960911 | A | T | 25 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0109 others(22): Show |
30 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.195+2214T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960911 | |||||||
chr4:2960911 | ATAT | A | 52 | a0002c0002t0001g0007 a0002c0002t0001g0021 a0002c0002t0001g0047 others(49): Show |
65 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.195+2211_195+2213d others(5): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960911 | |||||||
chr4:2960911 | ATATTATA others(65): Show |
A | 1 | a0001c0001t0001g0148 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.195+2142_195+2213d others(74): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960911 | |||||||
chr4:2960912 | T | C | 17 | a0001c0001t0001g0025 a0001c0001t0001g0095 a0001c0001t0001g0154 others(14): Show |
19 | HG00323.hp2 HG01168.hp2 HG01928.hp1 others(16): Show |
intron_variant | MODIFIER | c.195+2213A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960912 | |||||||
chr4:2960917 | TATCGA | T | 16 | a0001c0001t0001g0025 a0001c0001t0001g0095 a0001c0001t0001g0154 others(13): Show |
18 | HG00323.hp2 HG01168.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+2203_195+2207d others(7): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960917 | |||||||
chr4:2960919 | T | A | 7 | a0001c0001t0001g0107 a0002c0002t0001g0075 a0002c0002t0001g0084 others(4): Show |
7 | HG01167.hp1 HG02055.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+2206A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960919 | |||||||
chr4:2960919 | TCGATATT others(32): Show |
T | 25 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0109 others(22): Show |
30 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.195+2167_195+2205d others(41): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960919 | |||||||
chr4:2960920 | C | T | 7 | a0001c0001t0001g0107 a0002c0002t0001g0075 a0002c0002t0001g0084 others(4): Show |
7 | HG01167.hp1 HG02055.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+2205G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960920 | |||||||
chr4:2960921 | G | A | 1 | a0002c0002t0010g0080 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.195+2204C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960921 | |||||||
chr4:2960921 | G | C | 7 | a0001c0001t0001g0107 a0002c0002t0001g0075 a0002c0002t0001g0084 others(4): Show |
7 | HG01167.hp1 HG02055.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+2204C>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960921 | |||||||
chr4:2960923 | T | C | 23 | a0001c0001t0001g0025 a0001c0001t0001g0095 a0001c0001t0001g0107 others(20): Show |
25 | HG00323.hp2 HG01167.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.195+2202A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960923 | |||||||
chr4:2960925 | T | A | 17 | a0001c0001t0001g0025 a0001c0001t0001g0095 a0001c0001t0001g0154 others(14): Show |
19 | HG00323.hp2 HG01168.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.195+2200A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960925 | |||||||
chr4:2960925 | T | TTATCAA | 6 | a0001c0001t0001g0107 a0002c0002t0001g0075 a0002c0002t0001g0084 others(3): Show |
6 | HG01167.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.195+2199_195+2200i others(8): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960925 | |||||||
chr4:2960929 | T | A | 23 | a0001c0001t0001g0025 a0001c0001t0001g0095 a0001c0001t0001g0107 others(20): Show |
25 | HG00323.hp2 HG01167.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.195+2196A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960929 | |||||||
chr4:2960929 | T | C | 1 | a0002c0002t0010g0079 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.195+2196A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960929 | |||||||
chr4:2960929 | TTTAATAT others(87): Show |
T | 1 | a0001c0001t0002g0166 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.195+2102_195+2195d others(96): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960929 | |||||||
chr4:2960930 | T | A | 2 | a0002c0002t0010g0079 a0002c0002t0010g0080 |
2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.195+2195A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960930 | |||||||
chr4:2960931 | T | A | 1 | a0002c0002t0010g0079 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.195+2194A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960931 | |||||||
chr4:2960932 | A | T | 1 | a0002c0002t0010g0079 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.195+2193T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960932 | |||||||
chr4:2960937 | T | A | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2188A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960937 | |||||||
chr4:2960938 | A | C | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2187T>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960938 | |||||||
chr4:2960941 | T | A | 25 | a0001c0001t0001g0025 a0001c0001t0001g0095 a0001c0001t0001g0107 others(22): Show |
27 | HG00323.hp2 HG01167.hp1 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.195+2184A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960941 | |||||||
chr4:2960942 | C | T | 25 | a0001c0001t0001g0025 a0001c0001t0001g0095 a0001c0001t0001g0107 others(22): Show |
27 | HG00323.hp2 HG01167.hp1 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.195+2183G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960942 | |||||||
chr4:2960943 | A | T | 24 | a0001c0001t0001g0025 a0001c0001t0001g0095 a0001c0001t0001g0107 others(21): Show |
26 | HG00323.hp2 HG01167.hp1 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.195+2182T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960943 | |||||||
chr4:2960944 | A | T | 1 | a0002c0002t0010g0080 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.195+2181T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960944 | |||||||
chr4:2960945 | T | C | 24 | a0001c0001t0001g0025 a0001c0001t0001g0095 a0001c0001t0001g0107 others(21): Show |
26 | HG00323.hp2 HG01167.hp1 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.195+2180A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960945 | |||||||
chr4:2960947 | T | A | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2178A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960947 | |||||||
chr4:2960950 | T | A | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2175A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960950 | |||||||
chr4:2960954 | A | T | 16 | a0001c0001t0001g0025 a0001c0001t0001g0095 a0001c0001t0001g0107 others(13): Show |
17 | HG00323.hp2 HG01167.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.195+2171T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960954 | |||||||
chr4:2960955 | T | A | 16 | a0001c0001t0001g0025 a0001c0001t0001g0095 a0001c0001t0001g0107 others(13): Show |
17 | HG00323.hp2 HG01167.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.195+2170A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960955 | |||||||
chr4:2960955 | TTAA | T | 9 | a0001c0001t0001g0168 a0002c0002t0001g0049 a0002c0002t0001g0259 others(6): Show |
10 | HG01928.hp1 HG02148.hp2 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.195+2167_195+2169d others(5): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960955 | |||||||
chr4:2960958 | A | T | 16 | a0001c0001t0001g0025 a0001c0001t0001g0095 a0001c0001t0001g0107 others(13): Show |
17 | HG00323.hp2 HG01167.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.195+2167T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960958 | |||||||
chr4:2960958 | ATAT | A | 5 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(2): Show |
5 | HG01884.hp2 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.195+2164_195+2166d others(5): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960958 | |||||||
chr4:2960958 | ATATTATA others(65): Show |
A | 1 | a0001c0001t0005g0055 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.195+2095_195+2166d others(74): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960958 | |||||||
chr4:2960965 | A | T | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2160T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960965 | |||||||
chr4:2960966 | T | A | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2159A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960966 | |||||||
chr4:2960967 | CAATATTA others(65): Show |
C | 1 | a0017c0023t0002g0220 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.195+2086_195+2157d others(74): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960967 | |||||||
chr4:2960969 | ATATTATA others(40): Show |
A | 2 | a0006c0015t0007g0255 a0006c0017t0001g0301 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.195+2109_195+2155d others(49): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960969 | |||||||
chr4:2960972 | T | A | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2153A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960972 | |||||||
chr4:2960975 | T | C | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+2150A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960975 | |||||||
chr4:2960978 | T | C | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+2147A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960978 | |||||||
chr4:2960978 | TA | T | 4 | a0002c0002t0001g0257 a0002c0002t0001g0258 a0002c0002t0001g0263 others(1): Show |
4 | HG02280.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+2146delT | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960978 | |||||||
chr4:2960980 | A | C | 6 | a0002c0002t0001g0228 a0002c0002t0001g0229 a0002c0002t0001g0231 others(3): Show |
6 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+2145T>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960980 | |||||||
chr4:2960980 | ATAT | A | 7 | a0002c0002t0001g0049 a0002c0002t0001g0259 a0002c0002t0001g0266 others(4): Show |
8 | HG01928.hp1 HG02148.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.195+2142_195+2144d others(5): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960980 | |||||||
chr4:2960983 | T | C | 100 | a0001c0001t0001g0063 a0001c0001t0001g0304 a0001c0001t0004g0305 others(97): Show |
124 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.195+2142A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960983 | |||||||
chr4:2960984 | T | G | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2141A>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960984 | |||||||
chr4:2960985 | A | C | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2140T>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960985 | |||||||
chr4:2960986 | T | C | 100 | a0001c0001t0001g0063 a0001c0001t0001g0304 a0001c0001t0004g0305 others(97): Show |
124 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.195+2139A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960986 | |||||||
chr4:2960990 | G | A | 101 | a0001c0001t0001g0063 a0001c0001t0001g0304 a0001c0001t0004g0305 others(98): Show |
125 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.195+2135C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960990 | |||||||
chr4:2960994 | T | C | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+2131A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960994 | |||||||
chr4:2960998 | T | A | 102 | a0001c0001t0001g0063 a0001c0001t0001g0304 a0001c0001t0004g0305 others(99): Show |
126 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.195+2127A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960998 | |||||||
chr4:2960999 | T | A | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2126A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2960999 | |||||||
chr4:2961005 | T | C | 100 | a0001c0001t0001g0063 a0001c0001t0001g0304 a0001c0001t0004g0305 others(97): Show |
124 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.195+2120A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961005 | |||||||
chr4:2961010 | T | A | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+2115A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961010 | |||||||
chr4:2961011 | C | A | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2114G>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961011 | |||||||
chr4:2961011 | C | T | 101 | a0001c0001t0001g0063 a0001c0001t0001g0304 a0001c0001t0004g0305 others(98): Show |
125 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.195+2114G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961011 | |||||||
chr4:2961012 | A | T | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2113T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961012 | |||||||
chr4:2961013 | ATAT | A | 3 | a0002c0002t0001g0085 a0002c0002t0010g0079 a0002c0002t0010g0080 |
3 | HG03239.hp2 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.195+2109_195+2111d others(5): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961013 | |||||||
chr4:2961019 | T | A | 2 | a0009c0008t0014g0054 a0009c0008t0015g0053 |
2 | HG01255.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.195+2106A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961019 | |||||||
chr4:2961019 | T | TAATAA | 97 | a0001c0001t0001g0063 a0001c0001t0001g0304 a0001c0001t0004g0305 others(94): Show |
121 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.195+2105_195+2106i others(7): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961019 | |||||||
chr4:2961020 | T | C | 5 | a0001c0001t0006g0044 a0001c0001t0006g0233 a0001c0001t0006g0234 others(2): Show |
7 | HG01975.hp1 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.195+2105A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961020 | |||||||
chr4:2961024 | T | C | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+2101A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961024 | |||||||
chr4:2961030 | T | A | 1 | a0002c0002t0026g0078 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.195+2095A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961030 | |||||||
chr4:2961030 | T | C | 2 | a0006c0015t0007g0255 a0006c0017t0001g0301 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.195+2095A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961030 | |||||||
chr4:2961031 | T | C | 1 | a0002c0002t0001g0256 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.195+2094A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961031 | |||||||
chr4:2961033 | T | C | 2 | a0006c0015t0007g0255 a0006c0017t0001g0301 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.195+2092A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961033 | |||||||
chr4:2961033 | TATC | T | 99 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(96): Show |
123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.195+2089_195+2091d others(5): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961033 | |||||||
chr4:2961036 | C | T | 3 | a0001c0001t0001g0063 a0002c0002t0026g0078 a0009c0008t0015g0053 |
3 | HG01255.hp1 HG02717.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.195+2089G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961036 | |||||||
chr4:2961041 | T | A | 100 | a0001c0001t0001g0063 a0001c0001t0001g0304 a0001c0001t0004g0305 others(97): Show |
124 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.195+2084A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961041 | |||||||
chr4:2961041 | T | TATAGTAA others(180): Show |
1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2083_195+2084i others(189): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961041 | |||||||
chr4:2961046 | T | A | 1 | a0002c0002t0026g0078 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.195+2079A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961046 | |||||||
chr4:2961048 | A | AAT | 29 | a0001c0001t0001g0063 a0001c0001t0001g0304 a0001c0001t0004g0305 others(26): Show |
38 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.195+2075_195+2076d others(4): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961048 | |||||||
chr4:2961051 | AC | A | 70 | a0002c0002t0001g0007 a0002c0002t0001g0012 a0002c0002t0001g0021 others(67): Show |
85 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.195+2073delG | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961051 | |||||||
chr4:2961052 | C | A | 1 | a0002c0002t0026g0078 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.195+2073G>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961052 | |||||||
chr4:2961055 | C | A | 29 | a0001c0001t0001g0063 a0001c0001t0001g0304 a0001c0001t0004g0305 others(26): Show |
38 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.195+2070G>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961055 | |||||||
chr4:2961055 | C | T | 5 | a0002c0002t0026g0078 a0006c0015t0007g0255 a0006c0017t0001g0301 others(2): Show |
5 | HG01255.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.195+2070G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961055 | |||||||
chr4:2961055 | CAT | C | 70 | a0002c0002t0001g0007 a0002c0002t0001g0012 a0002c0002t0001g0021 others(67): Show |
85 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.195+2068_195+2069d others(4): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961055 | |||||||
chr4:2961056 | A | T | 30 | a0001c0001t0001g0063 a0001c0001t0001g0304 a0001c0001t0004g0305 others(27): Show |
39 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.195+2069T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961056 | |||||||
chr4:2961057 | T | A | 30 | a0001c0001t0001g0063 a0001c0001t0001g0304 a0001c0001t0004g0305 others(27): Show |
39 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.195+2068A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961057 | |||||||
chr4:2961057 | T | C | 1 | a0002c0002t0026g0078 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.195+2068A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961057 | |||||||
chr4:2961058 | C | A | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2067G>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961058 | |||||||
chr4:2961058 | C | T | 102 | a0001c0001t0001g0063 a0001c0001t0001g0304 a0001c0001t0004g0305 others(99): Show |
126 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.195+2067G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961058 | |||||||
chr4:2961059 | A | G | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2066T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961059 | |||||||
chr4:2961060 | A | T | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2065T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961060 | |||||||
chr4:2961063 | T | A | 30 | a0001c0001t0001g0063 a0001c0001t0001g0304 a0001c0001t0004g0305 others(27): Show |
39 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.195+2062A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961063 | |||||||
chr4:2961063 | T | G | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2062A>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961063 | |||||||
chr4:2961065 | ATAT | A | 73 | a0002c0002t0001g0007 a0002c0002t0001g0012 a0002c0002t0001g0021 others(70): Show |
88 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.195+2057_195+2059d others(5): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961065 | |||||||
chr4:2961073 | A | ATG | 30 | a0001c0001t0001g0063 a0001c0001t0001g0304 a0001c0001t0004g0305 others(27): Show |
39 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.195+2051_195+2052i others(4): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961073 | |||||||
chr4:2961074 | C | A | 73 | a0002c0002t0001g0007 a0002c0002t0001g0012 a0002c0002t0001g0021 others(70): Show |
88 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.195+2051G>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961074 | |||||||
chr4:2961078 | A | T | 29 | a0001c0001t0001g0063 a0001c0001t0001g0304 a0001c0001t0004g0305 others(26): Show |
38 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.195+2047T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961078 | |||||||
chr4:2961079 | T | A | 29 | a0001c0001t0001g0063 a0001c0001t0001g0304 a0001c0001t0004g0305 others(26): Show |
38 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.195+2046A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961079 | |||||||
chr4:2961079 | T | G | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2046A>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961079 | |||||||
chr4:2961080 | T | C | 29 | a0001c0001t0001g0063 a0001c0001t0001g0304 a0001c0001t0004g0305 others(26): Show |
38 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.195+2045A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961080 | |||||||
chr4:2961082 | A | ATATGC | 71 | a0002c0002t0001g0007 a0002c0002t0001g0012 a0002c0002t0001g0021 others(68): Show |
86 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.195+2042_195+2043i others(7): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961082 | |||||||
chr4:2961082 | ATAT | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0104 others(5): Show |
15 | HG00438.hp2 HG00621.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.195+2040_195+2042d others(5): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961082 | |||||||
chr4:2961085 | T | A | 30 | a0001c0001t0001g0063 a0001c0001t0001g0304 a0001c0001t0004g0305 others(27): Show |
39 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.195+2040A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961085 | |||||||
chr4:2961086 | T | A | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2039A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961086 | |||||||
chr4:2961087 | A | T | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2038T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961087 | |||||||
chr4:2961087 | ATAATAAT others(12): Show |
A | 3 | a0002c0002t0001g0227 a0002c0002t0001g0248 a0007c0005t0001g0247 |
3 | HG02280.hp1 NA18966.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.195+2019_195+2037d others(21): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961087 | |||||||
chr4:2961088 | T | C | 71 | a0002c0002t0001g0007 a0002c0002t0001g0012 a0002c0002t0001g0021 others(68): Show |
86 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.195+2037A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961088 | |||||||
chr4:2961089 | A | T | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+2036T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961089 | |||||||
chr4:2961090 | A | T | 29 | a0001c0001t0001g0063 a0001c0001t0001g0304 a0001c0001t0004g0305 others(26): Show |
38 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.195+2035T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961090 | |||||||
chr4:2961097 | A | G | 29 | a0001c0001t0001g0063 a0001c0001t0001g0304 a0001c0001t0004g0305 others(26): Show |
38 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.195+2028T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961097 | |||||||
chr4:2961098 | T | C | 29 | a0001c0001t0001g0063 a0001c0001t0001g0304 a0001c0001t0004g0305 others(26): Show |
38 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.195+2027A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961098 | |||||||
chr4:2961101 | A | G | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2024T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961101 | |||||||
chr4:2961105 | T | A | 2 | a0009c0008t0014g0054 a0009c0008t0015g0053 |
2 | HG01255.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.195+2020A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961105 | |||||||
chr4:2961105 | T | G | 71 | a0002c0002t0001g0007 a0002c0002t0001g0012 a0002c0002t0001g0021 others(68): Show |
86 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.195+2020A>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961105 | |||||||
chr4:2961106 | T | A | 48 | a0001c0001t0001g0063 a0001c0001t0001g0304 a0001c0001t0004g0305 others(45): Show |
58 | HG00323.hp2 HG00438.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.195+2019A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961106 | |||||||
chr4:2961106 | T | C | 71 | a0002c0002t0001g0007 a0002c0002t0001g0012 a0002c0002t0001g0021 others(68): Show |
86 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.195+2019A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961106 | |||||||
chr4:2961112 | A | C | 3 | a0001c0001t0002g0303 a0003c0003t0001g0106 a0003c0003t0001g0165 |
3 | HG03130.hp1 HG03209.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.195+2013T>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961112 | |||||||
chr4:2961112 | A | G | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+2013T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961112 | |||||||
chr4:2961112 | A | T | 71 | a0002c0002t0001g0007 a0002c0002t0001g0012 a0002c0002t0001g0021 others(68): Show |
86 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.195+2013T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961112 | |||||||
chr4:2961117 | T | A | 71 | a0002c0002t0001g0007 a0002c0002t0001g0012 a0002c0002t0001g0021 others(68): Show |
86 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.195+2008A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961117 | |||||||
chr4:2961117 | T | C | 2 | a0002c0002t0010g0079 a0002c0002t0010g0080 |
2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.195+2008A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961117 | |||||||
chr4:2961117 | T | G | 1 | a0009c0008t0015g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+2008A>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961117 | |||||||
chr4:2961117 | T | TTAATATA others(1): Show |
15 | a0002c0002t0001g0049 a0002c0002t0001g0075 a0002c0002t0001g0082 others(12): Show |
16 | HG00323.hp2 HG01167.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.195+2007_195+2008i others(10): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961117 | |||||||
chr4:2961123 | T | TATAGTAA others(3): Show |
1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+2001_195+2002i others(12): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961123 | |||||||
chr4:2961123 | T | TATTAATA others(83): Show |
13 | a0002c0002t0001g0004 a0002c0002t0001g0024 a0002c0002t0001g0064 others(10): Show |
19 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.195+2001_195+2002i others(92): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961123 | |||||||
chr4:2961123 | T | TATTAATA others(205): Show |
1 | a0001c0001t0001g0063 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.195+2001_195+2002i others(214): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961123 | |||||||
chr4:2961124 | T | A | 17 | a0001c0001t0001g0149 a0001c0001t0001g0304 a0001c0001t0004g0305 others(14): Show |
20 | HG01081.hp2 HG01255.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.195+2001A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961124 | |||||||
chr4:2961124 | TATA | T | 68 | a0002c0002t0001g0007 a0002c0002t0001g0012 a0002c0002t0001g0021 others(65): Show |
83 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.195+1998_195+2000d others(5): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961124 | |||||||
chr4:2961125 | A | AT | 15 | a0001c0001t0001g0063 a0002c0002t0001g0004 a0002c0002t0001g0024 others(12): Show |
21 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.195+1999dupA | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961125 | |||||||
chr4:2961125 | A | T | 16 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(13): Show |
19 | HG01255.hp1 HG01884.hp2 HG02129.hp1 others(16): Show |
intron_variant | MODIFIER | c.195+2000T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961125 | |||||||
chr4:2961128 | A | ATATAT | 3 | a0002c0002t0001g0257 a0002c0002t0001g0302 a0002c0002t0003g0261 |
3 | HG02976.hp2 HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.195+1996_195+1997i others(7): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961128 | |||||||
chr4:2961128 | A | ATATTGT | 15 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(12): Show |
18 | HG01884.hp2 HG02129.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+1996_195+1997i others(8): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961128 | |||||||
chr4:2961131 | A | G | 15 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(12): Show |
18 | HG01884.hp2 HG02129.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+1994T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961131 | |||||||
chr4:2961133 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.195+1992T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961133 | |||||||
chr4:2961135 | A | AG | 16 | a0001c0001t0001g0063 a0002c0002t0001g0004 a0002c0002t0001g0024 others(13): Show |
22 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+1989_195+1990i others(3): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961135 | |||||||
chr4:2961138 | A | AGT | 13 | a0002c0002t0001g0004 a0002c0002t0001g0024 a0002c0002t0001g0064 others(10): Show |
19 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.195+1986_195+1987i others(4): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961138 | |||||||
chr4:2961139 | A | G | 3 | a0001c0001t0001g0063 a0009c0008t0014g0054 a0009c0008t0015g0053 |
3 | HG01255.hp1 HG03139.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.195+1986T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961139 | |||||||
chr4:2961142 | T | TATAGTA | 15 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(12): Show |
18 | HG01884.hp2 HG02129.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+1982_195+1983i others(8): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961142 | |||||||
chr4:2961143 | A | G | 18 | a0002c0002t0001g0049 a0002c0002t0001g0075 a0002c0002t0001g0082 others(15): Show |
19 | HG00323.hp2 HG01167.hp1 HG01928.hp1 others(16): Show |
intron_variant | MODIFIER | c.195+1982T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961143 | |||||||
chr4:2961144 | C | T | 87 | a0001c0001t0001g0063 a0002c0002t0001g0004 a0002c0002t0001g0007 others(84): Show |
108 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.195+1981G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961144 | |||||||
chr4:2961145 | T | C | 8 | a0002c0002t0001g0012 a0002c0002t0001g0088 a0002c0002t0001g0089 others(5): Show |
10 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.195+1980A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961145 | |||||||
chr4:2961146 | A | AAT | 18 | a0001c0001t0001g0063 a0002c0002t0001g0004 a0002c0002t0001g0024 others(15): Show |
24 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.195+1977_195+1978d others(4): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961146 | |||||||
chr4:2961147 | A | G | 1 | a0002c0002t0001g0257 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.195+1978T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961147 | |||||||
chr4:2961147 | A | T | 32 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(29): Show |
36 | HG00323.hp2 HG01167.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.195+1978T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961147 | |||||||
chr4:2961148 | T | A | 15 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(12): Show |
18 | HG01884.hp2 HG02129.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+1977A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961148 | |||||||
chr4:2961149 | A | AT | 67 | a0002c0002t0001g0007 a0002c0002t0001g0012 a0002c0002t0001g0021 others(64): Show |
82 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.195+1975dupA | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961149 | |||||||
chr4:2961149 | A | T | 15 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(12): Show |
18 | HG01884.hp2 HG02129.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+1976T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961149 | |||||||
chr4:2961150 | T | C | 17 | a0002c0002t0001g0049 a0002c0002t0001g0075 a0002c0002t0001g0082 others(14): Show |
18 | HG00323.hp2 HG01167.hp1 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+1975A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961150 | |||||||
chr4:2961151 | A | G | 67 | a0002c0002t0001g0007 a0002c0002t0001g0012 a0002c0002t0001g0021 others(64): Show |
82 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.195+1974T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961151 | |||||||
chr4:2961152 | A | G | 18 | a0001c0001t0001g0063 a0002c0002t0001g0004 a0002c0002t0001g0024 others(15): Show |
24 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.195+1973T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961152 | |||||||
chr4:2961152 | A | T | 69 | a0002c0002t0001g0007 a0002c0002t0001g0012 a0002c0002t0001g0021 others(66): Show |
84 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.195+1973T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961152 | |||||||
chr4:2961155 | A | AC | 18 | a0001c0001t0001g0063 a0002c0002t0001g0004 a0002c0002t0001g0024 others(15): Show |
24 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.195+1969_195+1970i others(3): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961155 | |||||||
chr4:2961155 | A | G | 68 | a0002c0002t0001g0007 a0002c0002t0001g0012 a0002c0002t0001g0021 others(65): Show |
83 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.195+1970T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961155 | |||||||
chr4:2961159 | A | AG | 15 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(12): Show |
18 | HG01884.hp2 HG02129.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+1965_195+1966i others(3): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961159 | |||||||
chr4:2961163 | A | G | 15 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(12): Show |
18 | HG01884.hp2 HG02129.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+1962T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961163 | |||||||
chr4:2961165 | A | AATAT | 15 | a0001c0001t0001g0063 a0002c0002t0001g0004 a0002c0002t0001g0024 others(12): Show |
21 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.195+1959_195+1960i others(6): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961165 | |||||||
chr4:2961166 | T | A | 17 | a0001c0001t0001g0063 a0002c0002t0001g0004 a0002c0002t0001g0024 others(14): Show |
23 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.195+1959A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961166 | |||||||
chr4:2961166 | T | TATA | 4 | a0002c0002t0001g0050 a0002c0002t0001g0228 a0002c0002t0001g0267 others(1): Show |
5 | HG01361.hp1 HG01515.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.195+1958_195+1959i others(5): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961166 | |||||||
chr4:2961166 | T | TATAGTA | 64 | a0002c0002t0001g0007 a0002c0002t0001g0012 a0002c0002t0001g0021 others(61): Show |
78 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.195+1958_195+1959i others(8): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961166 | |||||||
chr4:2961167 | G | A | 81 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(78): Show |
98 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.195+1958C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961167 | |||||||
chr4:2961167 | G | T | 2 | a0002c0002t0001g0302 a0002c0002t0003g0261 |
2 | HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.195+1958C>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961167 | |||||||
chr4:2961168 | C | A | 2 | a0002c0002t0001g0302 a0002c0002t0003g0261 |
2 | HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.195+1957G>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961168 | |||||||
chr4:2961168 | C | CTAA | 17 | a0002c0002t0001g0049 a0002c0002t0001g0075 a0002c0002t0001g0082 others(14): Show |
18 | HG00323.hp2 HG01167.hp1 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+1956_195+1957i others(5): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961168 | |||||||
chr4:2961168 | C | T | 36 | a0001c0001t0001g0063 a0001c0001t0001g0304 a0001c0001t0004g0305 others(33): Show |
46 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.195+1957G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961168 | |||||||
chr4:2961169 | T | A | 5 | a0002c0002t0001g0050 a0002c0002t0001g0228 a0002c0002t0001g0267 others(2): Show |
6 | HG01361.hp1 HG01515.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+1956A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961169 | |||||||
chr4:2961170 | A | AAT | 15 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(12): Show |
18 | HG01884.hp2 HG02129.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+1954_195+1955i others(4): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961170 | |||||||
chr4:2961170 | A | C | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1955T>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961170 | |||||||
chr4:2961171 | T | A | 16 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(13): Show |
19 | HG01884.hp2 HG02129.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.195+1954A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961171 | |||||||
chr4:2961171 | T | C | 4 | a0002c0002t0001g0050 a0002c0002t0001g0228 a0002c0002t0001g0267 others(1): Show |
5 | HG01361.hp1 HG01515.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.195+1954A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961171 | |||||||
chr4:2961171 | T | G | 17 | a0001c0001t0001g0063 a0002c0002t0001g0004 a0002c0002t0001g0024 others(14): Show |
23 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.195+1954A>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961171 | |||||||
chr4:2961172 | T | A | 65 | a0002c0002t0001g0007 a0002c0002t0001g0012 a0002c0002t0001g0021 others(62): Show |
79 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.195+1953A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961172 | |||||||
chr4:2961173 | A | T | 64 | a0002c0002t0001g0007 a0002c0002t0001g0012 a0002c0002t0001g0021 others(61): Show |
78 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.195+1952T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961173 | |||||||
chr4:2961174 | C | A | 1 | a0002c0002t0001g0257 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.195+1951G>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961174 | |||||||
chr4:2961174 | C | T | 117 | a0001c0001t0001g0063 a0001c0001t0001g0304 a0001c0001t0004g0305 others(114): Show |
142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.195+1951G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961174 | |||||||
chr4:2961175 | A | T | 2 | a0002c0002t0001g0257 a0009c0008t0014g0054 |
2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.195+1950T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961175 | |||||||
chr4:2961176 | A | G | 15 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(12): Show |
18 | HG01884.hp2 HG02129.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+1949T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961176 | |||||||
chr4:2961176 | A | T | 21 | a0001c0001t0001g0063 a0002c0002t0001g0004 a0002c0002t0001g0024 others(18): Show |
28 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.195+1949T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961176 | |||||||
chr4:2961179 | A | AC | 15 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(12): Show |
18 | HG01884.hp2 HG02129.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+1945_195+1946i others(3): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961179 | |||||||
chr4:2961179 | A | G | 1 | a0002c0002t0001g0257 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.195+1946T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961179 | |||||||
chr4:2961181 | A | T | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1944T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961181 | |||||||
chr4:2961183 | A | AG | 23 | a0002c0002t0001g0012 a0002c0002t0001g0058 a0002c0002t0001g0088 others(20): Show |
25 | HG00639.hp2 HG01243.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.195+1941_195+1942i others(3): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961183 | |||||||
chr4:2961183 | A | T | 17 | a0002c0002t0001g0049 a0002c0002t0001g0075 a0002c0002t0001g0082 others(14): Show |
18 | HG00323.hp2 HG01167.hp1 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+1942T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961183 | |||||||
chr4:2961184 | T | A | 17 | a0002c0002t0001g0049 a0002c0002t0001g0075 a0002c0002t0001g0082 others(14): Show |
18 | HG00323.hp2 HG01167.hp1 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+1941A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961184 | |||||||
chr4:2961184 | T | G | 45 | a0002c0002t0001g0007 a0002c0002t0001g0021 a0002c0002t0001g0047 others(42): Show |
58 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.195+1941A>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961184 | |||||||
chr4:2961184 | T | TAG | 17 | a0001c0001t0001g0063 a0002c0002t0001g0004 a0002c0002t0001g0024 others(14): Show |
23 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.195+1940_195+1941i others(4): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961184 | |||||||
chr4:2961185 | TA | T | 45 | a0002c0002t0001g0007 a0002c0002t0001g0021 a0002c0002t0001g0047 others(42): Show |
58 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.195+1939delT | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961185 | |||||||
chr4:2961186 | A | AAT | 15 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(12): Show |
18 | HG01884.hp2 HG02129.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+1937_195+1938d others(4): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961186 | |||||||
chr4:2961187 | A | AC | 17 | a0001c0001t0001g0063 a0002c0002t0001g0004 a0002c0002t0001g0024 others(14): Show |
23 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.195+1937_195+1938i others(3): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961187 | |||||||
chr4:2961187 | A | G | 23 | a0002c0002t0001g0012 a0002c0002t0001g0058 a0002c0002t0001g0088 others(20): Show |
25 | HG00639.hp2 HG01243.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.195+1938T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961187 | |||||||
chr4:2961190 | TGC | T | 45 | a0002c0002t0001g0007 a0002c0002t0001g0021 a0002c0002t0001g0047 others(42): Show |
58 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.195+1933_195+1934d others(4): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961190 | |||||||
chr4:2961191 | G | A | 72 | a0001c0001t0001g0063 a0001c0001t0001g0304 a0001c0001t0004g0305 others(69): Show |
84 | HG00323.hp2 HG00438.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.195+1934C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961191 | |||||||
chr4:2961192 | C | A | 1 | a0002c0002t0001g0257 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.195+1933G>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961192 | |||||||
chr4:2961192 | C | T | 58 | a0001c0001t0001g0063 a0002c0002t0001g0004 a0002c0002t0001g0012 others(55): Show |
67 | HG00323.hp2 HG00438.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.195+1933G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961192 | |||||||
chr4:2961195 | A | AC | 15 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(12): Show |
18 | HG01884.hp2 HG02129.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+1929_195+1930i others(3): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961195 | |||||||
chr4:2961195 | A | C | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1930T>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961195 | |||||||
chr4:2961195 | A | G | 1 | a0002c0002t0001g0257 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.195+1930T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961195 | |||||||
chr4:2961197 | AT | A | 70 | a0002c0002t0001g0007 a0002c0002t0001g0012 a0002c0002t0001g0021 others(67): Show |
85 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.195+1927delA | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961197 | |||||||
chr4:2961198 | T | A | 15 | a0001c0001t0001g0063 a0002c0002t0001g0004 a0002c0002t0001g0024 others(12): Show |
21 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.195+1927A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961198 | |||||||
chr4:2961198 | T | C | 1 | a0002c0002t0001g0257 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.195+1927A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961198 | |||||||
chr4:2961199 | T | A | 33 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(30): Show |
37 | HG00323.hp2 HG01167.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.195+1926A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961199 | |||||||
chr4:2961200 | A | G | 1 | a0002c0002t0003g0261 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.195+1925T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961200 | |||||||
chr4:2961200 | A | T | 32 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(29): Show |
36 | HG00323.hp2 HG01167.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.195+1925T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961200 | |||||||
chr4:2961202 | A | AG | 15 | a0001c0001t0001g0063 a0002c0002t0001g0004 a0002c0002t0001g0024 others(12): Show |
21 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.195+1922_195+1923i others(3): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961202 | |||||||
chr4:2961202 | A | T | 1 | a0002c0002t0003g0261 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.195+1923T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961202 | |||||||
chr4:2961203 | A | ATATTGT | 17 | a0002c0002t0001g0049 a0002c0002t0001g0075 a0002c0002t0001g0082 others(14): Show |
18 | HG00323.hp2 HG01167.hp1 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+1921_195+1922i others(8): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961203 | |||||||
chr4:2961203 | A | G | 69 | a0002c0002t0001g0007 a0002c0002t0001g0012 a0002c0002t0001g0021 others(66): Show |
84 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.195+1922T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961203 | |||||||
chr4:2961203 | A | T | 17 | a0001c0001t0001g0063 a0002c0002t0001g0004 a0002c0002t0001g0024 others(14): Show |
23 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.195+1922T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961203 | |||||||
chr4:2961204 | T | G | 1 | a0002c0002t0003g0261 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.195+1921A>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961204 | |||||||
chr4:2961205 | A | T | 1 | a0002c0002t0003g0261 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.195+1920T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961205 | |||||||
chr4:2961206 | A | AC | 69 | a0002c0002t0001g0007 a0002c0002t0001g0012 a0002c0002t0001g0021 others(66): Show |
84 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.195+1918_195+1919i others(3): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961206 | |||||||
chr4:2961206 | A | G | 32 | a0001c0001t0001g0063 a0002c0002t0001g0004 a0002c0002t0001g0024 others(29): Show |
39 | HG00323.hp2 HG00438.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.195+1919T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961206 | |||||||
chr4:2961210 | A | AG | 15 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(12): Show |
18 | HG01884.hp2 HG02129.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+1914_195+1915i others(3): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961210 | |||||||
chr4:2961210 | A | T | 2 | a0006c0015t0007g0255 a0006c0017t0001g0301 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.195+1915T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961210 | |||||||
chr4:2961211 | T | A | 2 | a0006c0015t0007g0255 a0006c0017t0001g0301 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.195+1914A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961211 | |||||||
chr4:2961211 | T | G | 1 | a0018c0022t0028g0312 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.195+1914A>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961211 | |||||||
chr4:2961214 | A | C | 5 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(2): Show |
5 | HG01884.hp2 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.195+1911T>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961214 | |||||||
chr4:2961214 | A | G | 10 | a0002c0002t0001g0011 a0002c0002t0001g0235 a0002c0002t0001g0236 others(7): Show |
13 | HG02129.hp1 HG02145.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.195+1911T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961214 | |||||||
chr4:2961216 | A | AATATAGT others(495): Show |
1 | a0011c0012t0013g0060 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.195+1908_195+1909i others(504): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961216 | |||||||
chr4:2961216 | A | AATATAGT others(573): Show |
1 | a0011c0012t0013g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.195+1908_195+1909i others(582): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961216 | |||||||
chr4:2961216 | A | ATTGTTAG others(240): Show |
1 | a0001c0001t0001g0225 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.195+1908_195+1909i others(249): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961216 | |||||||
chr4:2961219 | T | A | 3 | a0001c0001t0001g0225 a0011c0012t0013g0059 a0011c0012t0013g0060 |
3 | HG02071.hp1 HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.195+1906A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TACTAACT others(571): Show |
3 | a0002c0002t0001g0007 a0002c0002t0003g0051 a0002c0020t0001g0292 |
8 | HG00642.hp2 HG01123.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.195+1905_195+1906i others(580): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(7): Show |
15 | a0001c0001t0001g0063 a0002c0002t0001g0004 a0002c0002t0001g0024 others(12): Show |
21 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.195+1905_195+1906i others(16): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(645): Show |
2 | a0002c0002t0001g0049 a0002c0002t0002g0277 |
3 | NA18967.hp1 NA18986.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.195+1905_195+1906i others(654): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(684): Show |
1 | a0002c0002t0001g0275 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.195+1905_195+1906i others(693): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(723): Show |
1 | a0002c0002t0001g0271 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.195+1905_195+1906i others(732): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(762): Show |
1 | a0002c0002t0001g0269 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.195+1905_195+1906i others(771): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(801): Show |
1 | a0002c0002t0001g0266 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.195+1905_195+1906i others(810): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(642): Show |
1 | a0002c0002t0001g0259 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.195+1905_195+1906i others(651): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(360): Show |
1 | a0002c0002t0001g0296 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.195+1905_195+1906i others(369): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(1021): Show |
1 | a0002c0002t0003g0261 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.195+1905_195+1906i others(1030): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(472): Show |
1 | a0018c0022t0028g0312 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.195+1905_195+1906i others(481): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(1215): Show |
1 | a0002c0002t0004g0253 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.195+1905_195+1906i others(1224): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(880): Show |
3 | a0002c0002t0001g0083 a0002c0002t0001g0084 a0002c0002t0001g0251 |
3 | HG02055.hp1 HG02809.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.195+1905_195+1906i others(889): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(919): Show |
1 | a0002c0002t0001g0252 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.195+1905_195+1906i others(928): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(607): Show |
2 | a0002c0002t0010g0079 a0002c0002t0010g0080 |
2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.195+1905_195+1906i others(616): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(802): Show |
1 | a0002c0002t0001g0082 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.195+1905_195+1906i others(811): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(880): Show |
1 | a0002c0002t0001g0085 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.195+1905_195+1906i others(889): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(643): Show |
1 | a0002c0002t0001g0075 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.195+1905_195+1906i others(652): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(667): Show |
1 | a0002c0002t0002g0272 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.195+1905_195+1906i others(676): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(939): Show |
1 | a0002c0002t0001g0089 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.195+1905_195+1906i others(948): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(667): Show |
1 | a0002c0002t0020g0280 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.195+1905_195+1906i others(676): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(354): Show |
2 | a0002c0002t0001g0052 a0002c0002t0001g0302 |
3 | HG02559.hp2 HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.195+1905_195+1906i others(363): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(240): Show |
1 | a0002c0002t0001g0300 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.195+1905_195+1906i others(249): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(279): Show |
1 | a0006c0016t0012g0299 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.195+1905_195+1906i others(288): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(318): Show |
3 | a0002c0002t0001g0298 a0005c0006t0001g0022 a0012c0007t0011g0297 |
5 | HG00738.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.195+1905_195+1906i others(327): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(357): Show |
4 | a0002c0002t0001g0021 a0002c0002t0001g0294 a0002c0002t0001g0295 others(1): Show |
6 | HG00733.hp2 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+1905_195+1906i others(366): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(396): Show |
6 | a0002c0002t0001g0286 a0002c0002t0001g0287 a0002c0002t0001g0288 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+1905_195+1906i others(405): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(435): Show |
1 | a0002c0002t0001g0284 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.195+1905_195+1906i others(444): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(474): Show |
2 | a0002c0002t0001g0283 a0002c0002t0003g0282 |
2 | HG02258.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.195+1905_195+1906i others(483): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(513): Show |
1 | a0002c0014t0012g0281 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.195+1905_195+1906i others(522): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(552): Show |
4 | a0002c0002t0001g0050 a0002c0002t0001g0256 a0002c0002t0001g0278 others(1): Show |
5 | HG01099.hp1 HG01255.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.195+1905_195+1906i others(561): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(591): Show |
1 | a0002c0002t0001g0276 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.195+1905_195+1906i others(600): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(630): Show |
3 | a0002c0002t0001g0048 a0002c0002t0001g0273 a0021c0021t0001g0274 |
4 | HG00099.hp2 HG00639.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+1905_195+1906i others(639): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(669): Show |
1 | a0002c0002t0001g0270 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.195+1905_195+1906i others(678): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(708): Show |
3 | a0002c0002t0001g0047 a0002c0002t0001g0267 a0002c0002t0005g0268 |
4 | HG01361.hp1 NA18989.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+1905_195+1906i others(717): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(747): Show |
1 | a0002c0002t0001g0265 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.195+1905_195+1906i others(756): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(786): Show |
1 | a0002c0002t0005g0264 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.195+1905_195+1906i others(795): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(825): Show |
2 | a0002c0002t0001g0262 a0002c0002t0001g0263 |
2 | HG02280.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.195+1905_195+1906i others(834): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(571): Show |
1 | a0002c0002t0001g0291 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.195+1905_195+1906i others(580): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(546): Show |
1 | a0002c0002t0001g0258 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.195+1905_195+1906i others(555): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(393): Show |
1 | a0002c0002t0001g0058 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.195+1905_195+1906i others(402): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(432): Show |
1 | a0002c0002t0026g0078 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.195+1905_195+1906i others(441): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(588): Show |
1 | a0002c0002t0023g0081 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.195+1905_195+1906i others(597): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(861): Show |
1 | a0002c0002t0011g0087 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.195+1905_195+1906i others(870): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(939): Show |
1 | a0002c0002t0001g0088 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.195+1905_195+1906i others(948): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(1017): Show |
1 | a0002c0002t0001g0090 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.195+1905_195+1906i others(1026): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(1095): Show |
2 | a0002c0002t0001g0091 a0002c0002t0001g0092 |
2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.195+1905_195+1906i others(1104): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(1134): Show |
1 | a0002c0002t0001g0012 | 3 | HG02895.hp1 HG02897.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.195+1905_195+1906i others(1143): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(897): Show |
1 | a0002c0002t0003g0086 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.195+1905_195+1906i others(906): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(744): Show |
1 | a0002c0002t0001g0260 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.195+1905_195+1906i others(753): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(469): Show |
1 | a0002c0002t0001g0093 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.195+1905_195+1906i others(478): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(161): Show |
1 | a0020c0030t0004g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.195+1905_195+1906i others(170): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(313): Show |
1 | a0002c0018t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.195+1905_195+1906i others(322): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(200): Show |
4 | a0002c0002t0001g0228 a0002c0002t0001g0229 a0002c0002t0001g0231 others(1): Show |
4 | HG02818.hp2 NA19043.hp2 NA20905.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+1905_195+1906i others(209): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(278): Show |
1 | a0002c0002t0003g0101 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.195+1905_195+1906i others(287): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TAGTAACT others(317): Show |
1 | a0002c0002t0001g0094 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.195+1905_195+1906i others(326): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TATTAATA others(95): Show |
15 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(12): Show |
18 | HG01884.hp2 HG02129.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+1905_195+1906i others(104): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961219 | T | TTAATATA others(291): Show |
2 | a0006c0015t0007g0255 a0006c0017t0001g0301 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.195+1905_195+1906i others(300): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961219 | |||||||
chr4:2961226 | T | A | 122 | a0001c0001t0001g0063 a0001c0001t0001g0225 a0001c0001t0001g0304 others(119): Show |
147 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.195+1899A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961226 | |||||||
chr4:2961226 | T | TGTTACTA others(250): Show |
2 | a0001c0001t0001g0043 a0001c0001t0022g0226 |
3 | HG02155.hp1 NA18999.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.195+1898_195+1899i others(259): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961226 | |||||||
chr4:2961226 | T | TGTTAGTA others(206): Show |
2 | a0002c0002t0001g0248 a0007c0005t0001g0247 |
2 | NA18966.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.195+1898_195+1899i others(215): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961226 | |||||||
chr4:2961226 | T | TGTTAGTA others(32): Show |
1 | a0001c0001t0002g0062 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.195+1860_195+1898d others(41): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961226 | |||||||
chr4:2961226 | T | TGTTAGTA others(248): Show |
1 | a0002c0002t0001g0227 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.195+1898_195+1899i others(257): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961226 | |||||||
chr4:2961226 | T | TGTTAGTA others(287): Show |
1 | a0001c0001t0001g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.195+1898_195+1899i others(296): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961226 | |||||||
chr4:2961226 | T | TGTTAGTA others(209): Show |
6 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0244 others(3): Show |
7 | HG00733.hp1 HG00741.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.195+1898_195+1899i others(218): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961226 | |||||||
chr4:2961226 | T | TGTTAGTA others(248): Show |
82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
140 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.195+1898_195+1899i others(257): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961226 | |||||||
chr4:2961226 | T | TGTTAGTA others(287): Show |
56 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0015 others(53): Show |
70 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.195+1898_195+1899i others(296): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961226 | |||||||
chr4:2961226 | T | TGTTAGTA others(326): Show |
6 | a0001c0001t0001g0013 a0001c0001t0001g0097 a0001c0001t0001g0099 others(3): Show |
8 | HG00423.hp2 HG01256.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.195+1898_195+1899i others(335): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961226 | |||||||
chr4:2961226 | T | TGTTAGTA others(365): Show |
1 | a0015c0013t0001g0309 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.195+1898_195+1899i others(374): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961226 | |||||||
chr4:2961226 | T | TGTTAGTA others(248): Show |
1 | a0001c0001t0001g0076 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.195+1898_195+1899i others(257): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961226 | |||||||
chr4:2961226 | T | TGTTAGTA others(206): Show |
1 | a0001c0001t0002g0232 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.195+1898_195+1899i others(215): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961226 | |||||||
chr4:2961226 | T | TGTTAGTA others(287): Show |
5 | a0001c0001t0001g0008 a0001c0001t0001g0102 a0001c0001t0001g0103 others(2): Show |
8 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(5): Show |
intron_variant | MODIFIER | c.195+1898_195+1899i others(296): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961226 | |||||||
chr4:2961226 | T | TGTTAGTA others(209): Show |
4 | a0001c0001t0006g0044 a0001c0001t0006g0233 a0001c0001t0006g0234 others(1): Show |
6 | HG02109.hp1 HG02257.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.195+1898_195+1899i others(218): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961226 | |||||||
chr4:2961226 | T | TGTTAGTA others(184): Show |
1 | a0001c0001t0002g0077 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.195+1898_195+1899i others(193): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961226 | |||||||
chr4:2961226 | T | TGTTAGTA others(285): Show |
1 | a0001c0001t0001g0153 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.195+1898_195+1899i others(294): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961226 | |||||||
chr4:2961226 | T | TGTTAGTA others(244): Show |
13 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0154 others(10): Show |
17 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.195+1898_195+1899i others(253): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961226 | |||||||
chr4:2961226 | T | TGTTAGTA others(322): Show |
2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG01496.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.195+1898_195+1899i others(331): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961226 | |||||||
chr4:2961226 | T | TGTTAGTA others(209): Show |
1 | a0001c0001t0007g0152 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.195+1898_195+1899i others(218): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961226 | |||||||
chr4:2961266 | G | GTTAGTAT others(287): Show |
1 | a0001c0001t0001g0249 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.195+1858_195+1859i others(296): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961266 | |||||||
chr4:2961280 | A | ATATAGTA others(529): Show |
1 | a0002c0002t0001g0257 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.195+1844_195+1845i others(538): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961280 | |||||||
chr4:2961311 | T | A | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1814A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961311 | |||||||
chr4:2961314 | A | G | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1811T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961314 | |||||||
chr4:2961316 | A | T | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1809T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961316 | |||||||
chr4:2961321 | C | T | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1804G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961321 | |||||||
chr4:2961323 | T | C | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1802A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961323 | |||||||
chr4:2961326 | A | C | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1799T>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961326 | |||||||
chr4:2961329 | T | TGATCCAC others(302): Show |
1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1795_195+1796i others(311): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961329 | |||||||
chr4:2961331 | A | C | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1794T>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961331 | |||||||
chr4:2961332 | C | A | 1 | a0001c0001t0001g0250 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.195+1793G>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961332 | |||||||
chr4:2961333 | T | C | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1792A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961333 | |||||||
chr4:2961338 | T | C | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1787A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961338 | |||||||
chr4:2961345 | T | C | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1780A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961345 | |||||||
chr4:2961348 | T | G | 2 | a0002c0002t0001g0251 a0002c0002t0001g0252 |
2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.195+1777A>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961348 | |||||||
chr4:2961349 | T | C | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1776A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961349 | |||||||
chr4:2961350 | T | C | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1775A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961350 | |||||||
chr4:2961351 | C | A | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1774G>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961351 | |||||||
chr4:2961353 | G | C | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1772C>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961353 | |||||||
chr4:2961357 | T | C | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1768A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961357 | |||||||
chr4:2961358 | A | C | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1767T>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961358 | |||||||
chr4:2961359 | A | T | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1766T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961359 | |||||||
chr4:2961361 | G | C | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1764C>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961361 | |||||||
chr4:2961362 | A | C | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1763T>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961362 | |||||||
chr4:2961363 | A | C | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1762T>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961363 | |||||||
chr4:2961368 | A | T | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1757T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961368 | |||||||
chr4:2961372 | A | C | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1753T>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961372 | |||||||
chr4:2961378 | A | C | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1747T>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961378 | |||||||
chr4:2961379 | T | A | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1746A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961379 | |||||||
chr4:2961380 | A | C | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1745T>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961380 | |||||||
chr4:2961392 | T | A | 1 | a0009c0008t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+1733A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961392 | |||||||
chr4:2961513 | T | C | 1 | a0002c0002t0004g0253 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.195+1612A>G | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961513 | |||||||
chr4:2961551 | C | T | 2 | a0009c0008t0014g0054 a0009c0008t0015g0053 |
2 | HG01255.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.195+1574G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961551 | |||||||
chr4:2961558 | C | T | 1 | a0002c0002t0001g0256 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.195+1567G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961558 | |||||||
chr4:2961578 | A | G | 2 | a0011c0012t0013g0059 a0011c0012t0013g0060 |
2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.195+1547T>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961578 | |||||||
chr4:2961796 | C | T | 1 | a0002c0002t0001g0058 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.195+1329G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2961796 | |||||||
chr4:2962234 | A | T | 1 | a0002c0002t0008g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.195+891T>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2962234 | |||||||
chr4:2962370 | C | T | 1 | a0006c0015t0007g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.195+755G>A | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2962370 | |||||||
chr4:2962456 | G | A | 1 | a0002c0002t0003g0254 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.195+669C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2962456 | |||||||
chr4:2962661 | T | A | 57 | a0002c0002t0001g0007 a0002c0002t0001g0021 a0002c0002t0001g0047 others(54): Show |
71 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.195+464A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2962661 | |||||||
chr4:2962717 | C | G | 1 | a0001c0001t0001g0056 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.195+408G>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2962717 | |||||||
chr4:2962787 | T | A | 1 | a0001c0001t0002g0303 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.195+338A>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2962787 | |||||||
chr4:2962888 | C | G | 1 | a0018c0022t0028g0312 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.195+237G>C | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2962888 | |||||||
chr4:2962892 | TGGA | T | 2 | a0001c0001t0005g0023 a0001c0001t0005g0055 |
3 | NA18959.hp1 NA18964.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.195+230_195+232del others(3): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2962892 | |||||||
chr4:2962999 | G | A | 5 | a0001c0001t0001g0304 a0001c0001t0004g0305 a0001c0001t0004g0306 others(2): Show |
5 | HG01884.hp2 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.195+126C>T | NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | 2962999 |