Item | Value |
---|---|
geneid | 4131 |
ensemblid | ENSG00000131711.15 |
hgncid | 6836 |
symbol | MAP1B |
name | microtubule associated protein 1B |
refseq_nuc | NM_005909.5 |
refseq_prot | NP_005900.2 |
ensembl_nuc | ENST00000296755.12 |
ensembl_prot | ENSP00000296755.7 |
mane_status | MANE Select |
chr | chr5 |
start | 72107475 |
end | 72209565 |
strand | + |
ver | v1.2 |
region | chr5:72107475-72209565 |
region5000 | chr5:72102475-72214565 |
regionname0 | MAP1B_chr5_72107475_72209565 |
regionname5000 | MAP1B_chr5_72102475_72214565 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 2468 | 289 | 77 | 49 | 119 | 10 | 33 | 88 | MAP1B_chr5_72102475_72214565 | MAP1B | MATVV others(2463): Show |
chr5 | 72102475 | 72214565 |
a0002 | 1/0 | 2468 | 22 | 1 | 16 | 3 | 0 | 1 | 2 | MAP1B_chr5_72102475_72214565 | MAP1B | MATVV others(2463): Show |
chr5 | 72102475 | 72214565 |
a0003 | 0/0 | 2468 | 5 | 0 | 5 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | MATVV others(2463): Show |
chr5 | 72102475 | 72214565 |
a0004 | 0/0 | 2468 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | MATVV others(2463): Show |
chr5 | 72102475 | 72214565 |
a0005 | 0/0 | 2468 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | MATVV others(2463): Show |
chr5 | 72102475 | 72214565 |
a0006 | 0/0 | 2468 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | MAP1B_chr5_72102475_72214565 | MAP1B | MATVV others(2463): Show |
chr5 | 72102475 | 72214565 |
a0007 | 0/0 | 2468 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | MATVV others(2463): Show |
chr5 | 72102475 | 72214565 |
a0008 | 0/0 | 2468 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | MATVV others(2463): Show |
chr5 | 72102475 | 72214565 |
a0009 | 0/0 | 2468 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | MATVV others(2463): Show |
chr5 | 72102475 | 72214565 |
a0010 | 0/0 | 2472 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | MATVV others(2467): Show |
chr5 | 72102475 | 72214565 |
a0011 | 0/0 | 2468 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | MATVV others(2463): Show |
chr5 | 72102475 | 72214565 |
a0012 | 0/0 | 2468 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | MATVV others(2463): Show |
chr5 | 72102475 | 72214565 |
a0013 | 0/0 | 2468 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | MATVV others(2463): Show |
chr5 | 72102475 | 72214565 |
a0014 | 0/0 | 2468 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | MATVV others(2463): Show |
chr5 | 72102475 | 72214565 |
a0015 | 0/0 | 2468 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | MATVV others(2463): Show |
chr5 | 72102475 | 72214565 |
a0016 | 0/0 | 2468 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | MATVV others(2463): Show |
chr5 | 72102475 | 72214565 |
a0017 | 0/0 | 2468 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | MATVV others(2463): Show |
chr5 | 72102475 | 72214565 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 7404 | 122 | 30 | 22 | 48 | 3 | 18 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0001c0002 | 0/0 | 7404 | 100 | 10 | 17 | 58 | 5 | 10 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0001c0004 | 0/0 | 7404 | 18 | 6 | 3 | 4 | 2 | 3 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0001c0005 | 0/0 | 7404 | 17 | 16 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0001c0006 | 0/0 | 7404 | 7 | 6 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0001c0008 | 0/0 | 7404 | 4 | 0 | 0 | 4 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0001c0009 | 0/0 | 7404 | 4 | 1 | 3 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0001c0017 | 0/0 | 7404 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0001c0018 | 0/0 | 7404 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0001c0019 | 0/0 | 7404 | 2 | 1 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0001c0020 | 0/0 | 7404 | 2 | 1 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0001c0022 | 0/0 | 7404 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0001c0025 | 0/0 | 7404 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0001c0026 | 0/0 | 7404 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0001c0028 | 0/0 | 7404 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0001c0029 | 0/0 | 7404 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0001c0034 | 0/0 | 7404 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0001c0036 | 0/0 | 7404 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0001c0038 | 0/0 | 7404 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0001c0039 | 0/0 | 7404 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0002c0003 | 1/0 | 7404 | 18 | 1 | 14 | 1 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0002c0014 | 0/0 | 7404 | 2 | 0 | 2 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0002c0015 | 0/0 | 7404 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0003c0007 | 0/0 | 7404 | 5 | 0 | 5 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0004c0011 | 0/0 | 7404 | 4 | 3 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0005c0010 | 0/0 | 7404 | 4 | 4 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0006c0012 | 0/0 | 7404 | 3 | 0 | 0 | 3 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0006c0030 | 0/0 | 7404 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0007c0013 | 0/0 | 7404 | 3 | 3 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0008c0016 | 0/0 | 7404 | 2 | 1 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0009c0024 | 0/0 | 7404 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0010c0023 | 0/0 | 7416 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7411): Show |
chr5 | 72102475 | 72214565 | ||
a0011c0021 | 0/0 | 7404 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0012c0032 | 0/0 | 7404 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0013c0035 | 0/0 | 7404 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0014c0027 | 0/0 | 7404 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0015c0037 | 0/0 | 7404 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0016c0031 | 0/0 | 7404 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 | ||
a0017c0033 | 0/0 | 7404 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | ATGGC others(7399): Show |
chr5 | 72102475 | 72214565 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 11791 | 53 | 13 | 7 | 23 | 2 | 8 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0001c0001t0002 | 0/0 | 11791 | 12 | 0 | 1 | 9 | 0 | 2 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0001c0001t0003 | 0/1 | 11790 | 1 | 0 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11785): Show |
chr5 | 72102475 | 72214565 |
a0001c0001t0004 | 0/0 | 11780 | 15 | 2 | 7 | 0 | 1 | 5 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11775): Show |
chr5 | 72102475 | 72214565 |
a0001c0001t0005 | 0/0 | 11790 | 4 | 2 | 1 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11785): Show |
chr5 | 72102475 | 72214565 |
a0001c0001t0007 | 0/0 | 11792 | 4 | 3 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11787): Show |
chr5 | 72102475 | 72214565 |
a0001c0001t0009 | 0/0 | 11791 | 4 | 0 | 0 | 4 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGT others(11786): Show |
chr5 | 72102475 | 72214565 |
a0001c0001t0010 | 0/0 | 11791 | 6 | 0 | 3 | 3 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGT others(11786): Show |
chr5 | 72102475 | 72214565 |
a0001c0001t0011 | 0/0 | 11792 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11787): Show |
chr5 | 72102475 | 72214565 |
a0001c0001t0012 | 0/0 | 11790 | 7 | 7 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11785): Show |
chr5 | 72102475 | 72214565 |
a0001c0001t0014 | 0/0 | 11790 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11785): Show |
chr5 | 72102475 | 72214565 |
a0001c0001t0015 | 0/0 | 11787 | 2 | 1 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11782): Show |
chr5 | 72102475 | 72214565 |
a0001c0001t0019 | 0/0 | 11780 | 3 | 0 | 2 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGT others(11775): Show |
chr5 | 72102475 | 72214565 |
a0001c0001t0020 | 0/0 | 11791 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0001c0001t0021 | 0/0 | 11790 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11785): Show |
chr5 | 72102475 | 72214565 |
a0001c0001t0024 | 0/0 | 11789 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11784): Show |
chr5 | 72102475 | 72214565 |
a0001c0001t0026 | 0/0 | 11791 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0001c0001t0028 | 0/0 | 11791 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0001c0001t0035 | 0/0 | 11781 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11776): Show |
chr5 | 72102475 | 72214565 |
a0001c0001t0039 | 0/0 | 11792 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGT others(11787): Show |
chr5 | 72102475 | 72214565 |
a0001c0002t0001 | 0/0 | 11791 | 7 | 0 | 1 | 6 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0001c0002t0002 | 0/0 | 11791 | 32 | 4 | 2 | 18 | 0 | 8 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0001c0002t0003 | 0/0 | 11790 | 35 | 0 | 8 | 22 | 3 | 2 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11785): Show |
chr5 | 72102475 | 72214565 |
a0001c0002t0004 | 0/0 | 11780 | 4 | 0 | 2 | 0 | 2 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11775): Show |
chr5 | 72102475 | 72214565 |
a0001c0002t0009 | 0/0 | 11791 | 4 | 0 | 0 | 4 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGT others(11786): Show |
chr5 | 72102475 | 72214565 |
a0001c0002t0010 | 0/0 | 11791 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGT others(11786): Show |
chr5 | 72102475 | 72214565 |
a0001c0002t0011 | 0/0 | 11792 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11787): Show |
chr5 | 72102475 | 72214565 |
a0001c0002t0013 | 0/0 | 11790 | 6 | 1 | 3 | 2 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGT others(11785): Show |
chr5 | 72102475 | 72214565 |
a0001c0002t0014 | 0/0 | 11790 | 3 | 2 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11785): Show |
chr5 | 72102475 | 72214565 |
a0001c0002t0016 | 0/0 | 11789 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11784): Show |
chr5 | 72102475 | 72214565 |
a0001c0002t0023 | 0/0 | 11790 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGT others(11785): Show |
chr5 | 72102475 | 72214565 |
a0001c0002t0027 | 0/0 | 11789 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11784): Show |
chr5 | 72102475 | 72214565 |
a0001c0002t0030 | 0/0 | 11791 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0001c0002t0031 | 0/0 | 11780 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11775): Show |
chr5 | 72102475 | 72214565 |
a0001c0002t0032 | 0/0 | 11790 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11785): Show |
chr5 | 72102475 | 72214565 |
a0001c0004t0001 | 0/0 | 11791 | 3 | 3 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0001c0004t0002 | 0/0 | 11791 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0001c0004t0005 | 0/0 | 11790 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11785): Show |
chr5 | 72102475 | 72214565 |
a0001c0004t0007 | 0/0 | 11792 | 2 | 1 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11787): Show |
chr5 | 72102475 | 72214565 |
a0001c0004t0010 | 0/0 | 11791 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGT others(11786): Show |
chr5 | 72102475 | 72214565 |
a0001c0004t0011 | 0/0 | 11792 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11787): Show |
chr5 | 72102475 | 72214565 |
a0001c0004t0015 | 0/0 | 11787 | 3 | 0 | 0 | 2 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11782): Show |
chr5 | 72102475 | 72214565 |
a0001c0004t0017 | 0/0 | 11781 | 4 | 1 | 2 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11776): Show |
chr5 | 72102475 | 72214565 |
a0001c0004t0022 | 0/0 | 11792 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11787): Show |
chr5 | 72102475 | 72214565 |
a0001c0004t0034 | 0/0 | 11792 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11787): Show |
chr5 | 72102475 | 72214565 |
a0001c0005t0001 | 0/0 | 11791 | 3 | 3 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0001c0005t0005 | 0/0 | 11790 | 5 | 5 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11785): Show |
chr5 | 72102475 | 72214565 |
a0001c0005t0008 | 0/0 | 11790 | 7 | 6 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11785): Show |
chr5 | 72102475 | 72214565 |
a0001c0005t0020 | 0/0 | 11791 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0001c0005t0021 | 0/0 | 11790 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11785): Show |
chr5 | 72102475 | 72214565 |
a0001c0006t0005 | 0/0 | 11790 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11785): Show |
chr5 | 72102475 | 72214565 |
a0001c0006t0007 | 0/0 | 11792 | 2 | 1 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11787): Show |
chr5 | 72102475 | 72214565 |
a0001c0006t0018 | 0/0 | 11791 | 3 | 3 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0001c0006t0022 | 0/0 | 11792 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11787): Show |
chr5 | 72102475 | 72214565 |
a0001c0008t0002 | 0/0 | 11791 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0001c0008t0003 | 0/0 | 11790 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11785): Show |
chr5 | 72102475 | 72214565 |
a0001c0008t0037 | 0/0 | 11791 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0001c0009t0001 | 0/0 | 11791 | 3 | 0 | 3 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0001c0009t0007 | 0/0 | 11792 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11787): Show |
chr5 | 72102475 | 72214565 |
a0001c0017t0002 | 0/0 | 11791 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0001c0017t0003 | 0/0 | 11790 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11785): Show |
chr5 | 72102475 | 72214565 |
a0001c0018t0001 | 0/0 | 11791 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0001c0019t0007 | 0/0 | 11792 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11787): Show |
chr5 | 72102475 | 72214565 |
a0001c0019t0040 | 0/0 | 11792 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGT others(11787): Show |
chr5 | 72102475 | 72214565 |
a0001c0020t0007 | 0/0 | 11792 | 2 | 1 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11787): Show |
chr5 | 72102475 | 72214565 |
a0001c0022t0002 | 0/0 | 11791 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0001c0025t0001 | 0/0 | 11791 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0001c0026t0008 | 0/0 | 11790 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11785): Show |
chr5 | 72102475 | 72214565 |
a0001c0028t0025 | 0/0 | 11791 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0001c0029t0005 | 0/0 | 11790 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11785): Show |
chr5 | 72102475 | 72214565 |
a0001c0034t0005 | 0/0 | 11790 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11785): Show |
chr5 | 72102475 | 72214565 |
a0001c0036t0008 | 0/0 | 11790 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11785): Show |
chr5 | 72102475 | 72214565 |
a0001c0038t0013 | 0/0 | 11790 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGT others(11785): Show |
chr5 | 72102475 | 72214565 |
a0001c0039t0018 | 0/0 | 11791 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0002c0003t0006 | 0/0 | 11790 | 15 | 1 | 14 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11785): Show |
chr5 | 72102475 | 72214565 |
a0002c0003t0016 | 0/0 | 11789 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11784): Show |
chr5 | 72102475 | 72214565 |
a0002c0003t0023 | 0/0 | 11790 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGT others(11785): Show |
chr5 | 72102475 | 72214565 |
a0002c0003t0038 | 1/0 | 11790 | 1 | 0 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGT others(11785): Show |
chr5 | 72102475 | 72214565 |
a0002c0014t0004 | 0/0 | 11780 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11775): Show |
chr5 | 72102475 | 72214565 |
a0002c0014t0006 | 0/0 | 11790 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11785): Show |
chr5 | 72102475 | 72214565 |
a0002c0015t0016 | 0/0 | 11789 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11784): Show |
chr5 | 72102475 | 72214565 |
a0003c0007t0002 | 0/0 | 11791 | 5 | 0 | 5 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0004c0011t0001 | 0/0 | 11791 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0004c0011t0011 | 0/0 | 11792 | 3 | 2 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11787): Show |
chr5 | 72102475 | 72214565 |
a0005c0010t0005 | 0/0 | 11790 | 4 | 4 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11785): Show |
chr5 | 72102475 | 72214565 |
a0006c0012t0002 | 0/0 | 11791 | 3 | 0 | 0 | 3 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0006c0030t0002 | 0/0 | 11791 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0007c0013t0001 | 0/0 | 11791 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0007c0013t0029 | 0/0 | 11791 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0008c0016t0001 | 0/0 | 11791 | 2 | 1 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0009c0024t0003 | 0/0 | 11790 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11785): Show |
chr5 | 72102475 | 72214565 |
a0010c0023t0006 | 0/0 | 11802 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11797): Show |
chr5 | 72102475 | 72214565 |
a0011c0021t0036 | 0/0 | 11792 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11787): Show |
chr5 | 72102475 | 72214565 |
a0012c0032t0033 | 0/0 | 11792 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11787): Show |
chr5 | 72102475 | 72214565 |
a0013c0035t0005 | 0/0 | 11790 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11785): Show |
chr5 | 72102475 | 72214565 |
a0014c0027t0010 | 0/0 | 11791 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGT others(11786): Show |
chr5 | 72102475 | 72214565 |
a0015c0037t0002 | 0/0 | 11791 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11786): Show |
chr5 | 72102475 | 72214565 |
a0016c0031t0003 | 0/0 | 11790 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGA others(11785): Show |
chr5 | 72102475 | 72214565 |
a0017c0033t0009 | 0/0 | 11791 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | GCAGT others(11786): Show |
chr5 | 72102475 | 72214565 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0003g0322 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0004g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0005g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0005g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0007g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0007g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0007g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0007g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0009g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0009g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0009g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0009g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0010g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0010g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0010g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0010g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0010g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0010g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0011g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0011g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0012g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0012g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0012g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0012g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0012g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0012g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0012g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0014g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0014g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0015g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0015g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0019g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0019g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0019g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0020g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0021g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0024g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0026g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0028g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0035g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0001t0039g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0004g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0004g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0004g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0009g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0009g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0009g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0009g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0010g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0011g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0011g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0013g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0013g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0013g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0013g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0013g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0013g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0014g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0014g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0016g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0023g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0027g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0030g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0031g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0002t0032g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0005g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0007g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0007g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0010g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0011g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0015g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0015g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0015g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0017g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0017g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0017g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0017g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0022g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0004t0034g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0008g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0008g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0008g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0008g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0008g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0008g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0008g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0020g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0005t0021g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0006t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0006t0007g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0006t0007g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0006t0018g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0006t0018g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0006t0018g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0006t0022g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0008t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0008t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0008t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0008t0037g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0009t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0009t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0009t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0009t0007g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0017t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0017t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0018t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0018t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0019t0007g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0019t0040g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0020t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0020t0007g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0022t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0025t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0026t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0028t0025g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0029t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0034t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0036t0008g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0038t0013g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0001c0039t0018g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0006g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0016g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0023g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0003t0038g0223 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0014t0004g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0014t0006g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0015t0016g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0002c0015t0016g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0003c0007t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0003c0007t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0003c0007t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0003c0007t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0003c0007t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0004c0011t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0004c0011t0011g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0004c0011t0011g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0004c0011t0011g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0005c0010t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0005c0010t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0005c0010t0005g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0005c0010t0005g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0006c0012t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0006c0012t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0006c0012t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0006c0030t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0007c0013t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0007c0013t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0007c0013t0029g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0008c0016t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0008c0016t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0009c0024t0003g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0010c0023t0006g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0011c0021t0036g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0012c0032t0033g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0013c0035t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0014c0027t0010g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0015c0037t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0016c0031t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
a0017c0033t0009g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0004 | g0193 | EUR | GBR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00099 | hp2 | a0001 | c0002 | t0003 | g0176 | EUR | GBR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0309 | EUR | GBR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00140 | hp2 | a0001 | c0002 | t0003 | g0090 | EUR | GBR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | CHS | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | CHS | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00558 | hp1 | a0001 | c0004 | t0015 | g0301 | EAS | CHS | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00558 | hp2 | a0001 | c0002 | t0009 | g0230 | EAS | CHS | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00609 | hp1 | a0002 | c0015 | t0016 | g0205 | EAS | CHS | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0302 | EAS | CHS | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00621 | hp1 | a0001 | c0008 | t0002 | g0113 | EAS | CHS | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00621 | hp2 | a0001 | c0002 | t0013 | g0023 | EAS | CHS | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0148 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00639 | hp2 | a0001 | c0001 | t0010 | g0229 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00642 | hp2 | a0001 | c0001 | t0004 | g0296 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00673 | hp1 | a0001 | c0001 | t0026 | g0201 | EAS | CHS | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00673 | hp2 | a0001 | c0002 | t0003 | g0112 | EAS | CHS | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00733 | hp1 | a0002 | c0003 | t0006 | g0194 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00733 | hp2 | a0001 | c0004 | t0005 | g0107 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00735 | hp1 | a0002 | c0003 | t0006 | g0165 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0084 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00738 | hp1 | a0002 | c0003 | t0006 | g0002 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00738 | hp2 | a0001 | c0004 | t0017 | g0164 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00741 | hp1 | a0008 | c0016 | t0001 | g0330 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG00741 | hp2 | a0001 | c0005 | t0008 | g0041 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01069 | hp1 | a0001 | c0002 | t0004 | g0005 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01069 | hp2 | a0001 | c0001 | t0028 | g0175 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01070 | hp1 | a0001 | c0002 | t0023 | g0142 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01070 | hp2 | a0001 | c0001 | t0005 | g0155 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01071 | hp1 | a0001 | c0002 | t0004 | g0005 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01074 | hp1 | a0001 | c0002 | t0003 | g0173 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01074 | hp2 | a0004 | c0011 | t0011 | g0138 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01081 | hp1 | a0002 | c0003 | t0006 | g0002 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01081 | hp2 | a0001 | c0001 | t0019 | g0237 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01099 | hp2 | a0001 | c0002 | t0003 | g0306 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01106 | hp1 | a0002 | c0014 | t0006 | g0091 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0307 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01109 | hp1 | a0002 | c0014 | t0004 | g0085 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01109 | hp2 | a0001 | c0002 | t0002 | g0160 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01167 | hp1 | a0003 | c0007 | t0002 | g0098 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01167 | hp2 | a0001 | c0006 | t0007 | g0259 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01168 | hp1 | a0001 | c0002 | t0003 | g0147 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01168 | hp2 | a0001 | c0009 | t0001 | g0063 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01169 | hp1 | a0001 | c0009 | t0001 | g0062 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01169 | hp2 | a0003 | c0007 | t0002 | g0099 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0025 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01243 | hp2 | a0001 | c0020 | t0007 | g0260 | AMR | PUR | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0195 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01255 | hp2 | a0001 | c0002 | t0013 | g0225 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01257 | hp1 | a0002 | c0003 | t0006 | g0169 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0075 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01261 | hp1 | a0002 | c0003 | t0006 | g0014 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01261 | hp2 | a0001 | c0001 | t0010 | g0010 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01346 | hp1 | a0001 | c0002 | t0013 | g0226 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01346 | hp2 | a0001 | c0001 | t0004 | g0191 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01358 | hp1 | a0001 | c0002 | t0013 | g0021 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01358 | hp2 | a0001 | c0009 | t0001 | g0328 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01361 | hp1 | a0001 | c0001 | t0019 | g0241 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01361 | hp2 | a0009 | c0024 | t0003 | g0326 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01433 | hp1 | a0001 | c0019 | t0007 | g0029 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01433 | hp2 | a0003 | c0007 | t0002 | g0122 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0055 | EUR | IBS | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01515 | hp2 | a0001 | c0004 | t0010 | g0236 | EUR | IBS | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01884 | hp1 | a0001 | c0002 | t0014 | g0003 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01884 | hp2 | a0001 | c0005 | t0001 | g0008 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01891 | hp1 | a0001 | c0001 | t0007 | g0254 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01891 | hp2 | a0001 | c0002 | t0011 | g0265 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01928 | hp1 | a0001 | c0002 | t0003 | g0006 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01934 | hp1 | a0002 | c0003 | t0006 | g0293 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01934 | hp2 | a0001 | c0001 | t0004 | g0028 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01943 | hp1 | a0002 | c0003 | t0006 | g0167 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01943 | hp2 | a0001 | c0002 | t0003 | g0289 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01975 | hp1 | a0003 | c0007 | t0002 | g0083 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01975 | hp2 | a0002 | c0003 | t0006 | g0217 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01978 | hp1 | a0001 | c0002 | t0003 | g0015 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01978 | hp2 | a0001 | c0001 | t0010 | g0228 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01981 | hp1 | a0001 | c0002 | t0003 | g0088 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01981 | hp2 | a0002 | c0003 | t0006 | g0150 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01993 | hp1 | a0010 | c0023 | t0006 | g0166 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01993 | hp2 | a0002 | c0003 | t0006 | g0196 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02004 | hp1 | a0002 | c0003 | t0006 | g0170 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02004 | hp2 | a0003 | c0007 | t0002 | g0097 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02015 | hp1 | a0001 | c0002 | t0003 | g0203 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02055 | hp1 | a0001 | c0029 | t0005 | g0076 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0335 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02071 | hp1 | a0001 | c0001 | t0039 | g0022 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02071 | hp2 | a0001 | c0002 | t0002 | g0186 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02074 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02074 | hp2 | a0001 | c0002 | t0010 | g0224 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02080 | hp2 | a0001 | c0001 | t0015 | g0116 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0204 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02135 | hp1 | a0001 | c0001 | t0011 | g0108 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02135 | hp2 | a0001 | c0004 | t0011 | g0323 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02145 | hp1 | a0001 | c0005 | t0021 | g0136 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02145 | hp2 | a0001 | c0001 | t0015 | g0124 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02148 | hp1 | a0001 | c0002 | t0003 | g0218 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02148 | hp2 | a0001 | c0004 | t0017 | g0060 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02155 | hp1 | a0001 | c0038 | t0013 | g0024 | EAS | CDX | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02257 | hp1 | a0001 | c0005 | t0005 | g0128 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02257 | hp2 | a0001 | c0019 | t0040 | g0244 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0140 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02258 | hp2 | a0001 | c0001 | t0021 | g0268 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02280 | hp1 | a0001 | c0004 | t0017 | g0190 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02280 | hp2 | a0001 | c0005 | t0020 | g0258 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0291 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02300 | hp2 | a0002 | c0003 | t0006 | g0161 | AMR | PEL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02451 | hp1 | a0001 | c0006 | t0018 | g0071 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02451 | hp2 | a0001 | c0005 | t0005 | g0257 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | KHV | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02572 | hp1 | a0001 | c0001 | t0012 | g0311 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02572 | hp2 | a0001 | c0001 | t0007 | g0119 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0105 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02602 | hp2 | a0001 | c0001 | t0004 | g0068 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02622 | hp1 | a0001 | c0002 | t0002 | g0216 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02630 | hp1 | a0001 | c0005 | t0001 | g0270 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02630 | hp2 | a0001 | c0005 | t0008 | g0332 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02647 | hp1 | a0005 | c0010 | t0005 | g0329 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02647 | hp2 | a0001 | c0005 | t0008 | g0135 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02683 | hp1 | a0001 | c0001 | t0019 | g0246 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02683 | hp2 | a0001 | c0025 | t0001 | g0089 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02717 | hp2 | a0001 | c0004 | t0001 | g0189 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02723 | hp1 | a0001 | c0002 | t0002 | g0040 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02723 | hp2 | a0011 | c0021 | t0036 | g0045 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02738 | hp1 | a0001 | c0004 | t0034 | g0215 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02738 | hp2 | a0001 | c0002 | t0002 | g0013 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02818 | hp1 | a0001 | c0034 | t0005 | g0036 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02886 | hp1 | a0001 | c0026 | t0008 | g0030 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02886 | hp2 | a0001 | c0009 | t0007 | g0043 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02895 | hp1 | a0001 | c0001 | t0012 | g0056 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02895 | hp2 | a0001 | c0004 | t0007 | g0141 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02897 | hp1 | a0012 | c0032 | t0033 | g0221 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02897 | hp2 | a0001 | c0001 | t0012 | g0057 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02922 | hp1 | a0005 | c0010 | t0005 | g0255 | AFR | ESN | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02922 | hp2 | a0001 | c0002 | t0016 | g0152 | AFR | ESN | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02965 | hp1 | a0004 | c0011 | t0011 | g0137 | AFR | ESN | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02965 | hp2 | a0001 | c0005 | t0001 | g0304 | AFR | ESN | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02976 | hp1 | a0001 | c0005 | t0005 | g0154 | AFR | ESN | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03017 | hp2 | a0001 | c0002 | t0003 | g0121 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03041 | hp2 | a0001 | c0004 | t0001 | g0334 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03098 | hp1 | a0001 | c0005 | t0008 | g0033 | AFR | MSL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03098 | hp2 | a0001 | c0006 | t0022 | g0039 | AFR | MSL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03130 | hp1 | a0007 | c0013 | t0001 | g0126 | AFR | ESN | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03130 | hp2 | a0001 | c0005 | t0005 | g0046 | AFR | ESN | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03139 | hp1 | a0001 | c0005 | t0008 | g0110 | AFR | ESN | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03139 | hp2 | a0007 | c0013 | t0029 | g0127 | AFR | ESN | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03195 | hp1 | a0001 | c0005 | t0005 | g0220 | AFR | ESN | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03195 | hp2 | a0007 | c0013 | t0001 | g0264 | AFR | ESN | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03209 | hp1 | a0001 | c0005 | t0008 | g0252 | AFR | MSL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03225 | hp1 | a0004 | c0011 | t0001 | g0253 | AFR | MSL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03225 | hp2 | a0001 | c0001 | t0012 | g0012 | AFR | MSL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03239 | hp2 | a0001 | c0001 | t0007 | g0052 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03453 | hp1 | a0001 | c0002 | t0002 | g0267 | AFR | MSL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03453 | hp2 | a0008 | c0016 | t0001 | g0261 | AFR | MSL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03486 | hp1 | a0013 | c0035 | t0005 | g0047 | AFR | MSL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | MSL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03491 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03492 | hp2 | a0001 | c0002 | t0002 | g0095 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03516 | hp1 | a0001 | c0001 | t0007 | g0269 | AFR | ESN | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03540 | hp1 | a0001 | c0002 | t0002 | g0111 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03540 | hp2 | a0001 | c0036 | t0008 | g0125 | AFR | GWD | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03579 | hp1 | a0001 | c0005 | t0008 | g0035 | AFR | MSL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0321 | AFR | MSL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03654 | hp2 | a0001 | c0001 | t0035 | g0300 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03669 | hp1 | a0002 | c0003 | t0023 | g0242 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0151 | SAS | STU | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03688 | hp2 | a0001 | c0004 | t0017 | g0064 | SAS | STU | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03710 | hp1 | a0001 | c0001 | t0004 | g0100 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03831 | hp2 | a0001 | c0002 | t0002 | g0011 | SAS | BEB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0168 | SAS | BEB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG04115 | hp1 | a0001 | c0001 | t0004 | g0051 | SAS | STU | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG04115 | hp2 | a0001 | c0002 | t0003 | g0174 | SAS | STU | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG04199 | hp1 | a0001 | c0022 | t0002 | g0149 | SAS | STU | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0251 | SAS | STU | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0054 | SAS | STU | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG04204 | hp2 | a0001 | c0004 | t0015 | g0185 | SAS | STU | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18522 | hp1 | a0001 | c0002 | t0011 | g0153 | AFR | YRI | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0156 | AFR | YRI | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | CHB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18612 | hp2 | a0001 | c0002 | t0002 | g0200 | EAS | CHB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18747 | hp1 | a0001 | c0002 | t0002 | g0275 | EAS | CHB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | CHB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18906 | hp1 | a0004 | c0011 | t0011 | g0139 | AFR | YRI | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18906 | hp2 | a0001 | c0002 | t0014 | g0003 | AFR | YRI | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18941 | hp2 | a0001 | c0001 | t0010 | g0231 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18942 | hp2 | a0001 | c0002 | t0002 | g0101 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18943 | hp1 | a0001 | c0008 | t0003 | g0183 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18944 | hp2 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18945 | hp2 | a0001 | c0002 | t0003 | g0069 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18946 | hp2 | a0001 | c0002 | t0003 | g0171 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18947 | hp1 | a0001 | c0004 | t0002 | g0179 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18947 | hp2 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18953 | hp1 | a0001 | c0002 | t0003 | g0129 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18953 | hp2 | a0001 | c0001 | t0005 | g0285 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18957 | hp2 | a0001 | c0001 | t0014 | g0094 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18959 | hp1 | a0001 | c0002 | t0027 | g0103 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18959 | hp2 | a0001 | c0017 | t0002 | g0058 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18960 | hp1 | a0014 | c0027 | t0010 | g0234 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18960 | hp2 | a0001 | c0002 | t0003 | g0318 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18963 | hp1 | a0006 | c0012 | t0002 | g0319 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18963 | hp2 | a0001 | c0002 | t0003 | g0303 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18966 | hp1 | a0001 | c0018 | t0001 | g0080 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18966 | hp2 | a0002 | c0015 | t0016 | g0019 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18967 | hp2 | a0015 | c0037 | t0002 | g0315 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18968 | hp1 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18970 | hp1 | a0001 | c0002 | t0003 | g0102 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18970 | hp2 | a0001 | c0018 | t0001 | g0288 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18971 | hp1 | a0006 | c0030 | t0002 | g0294 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18971 | hp2 | a0001 | c0002 | t0013 | g0247 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18973 | hp1 | a0001 | c0001 | t0009 | g0240 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18973 | hp2 | a0006 | c0012 | t0002 | g0314 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18974 | hp1 | a0001 | c0002 | t0002 | g0282 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18974 | hp2 | a0001 | c0002 | t0003 | g0172 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18977 | hp1 | a0001 | c0002 | t0003 | g0287 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18978 | hp1 | a0001 | c0002 | t0003 | g0297 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18978 | hp2 | a0001 | c0002 | t0030 | g0070 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18979 | hp1 | a0001 | c0001 | t0009 | g0238 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18979 | hp2 | a0001 | c0002 | t0003 | g0211 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18982 | hp1 | a0001 | c0001 | t0024 | g0207 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18982 | hp2 | a0001 | c0004 | t0015 | g0271 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18983 | hp2 | a0001 | c0017 | t0003 | g0073 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18984 | hp2 | a0001 | c0002 | t0009 | g0248 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18985 | hp2 | a0016 | c0031 | t0003 | g0049 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18986 | hp1 | a0001 | c0002 | t0003 | g0278 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18986 | hp2 | a0001 | c0001 | t0010 | g0243 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18991 | hp2 | a0001 | c0002 | t0003 | g0106 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18995 | hp2 | a0001 | c0002 | t0003 | g0320 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18998 | hp2 | a0001 | c0001 | t0010 | g0245 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19002 | hp1 | a0001 | c0002 | t0009 | g0227 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0059 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19003 | hp1 | a0001 | c0002 | t0032 | g0273 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19007 | hp1 | a0001 | c0002 | t0014 | g0178 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19007 | hp2 | a0001 | c0001 | t0014 | g0093 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19009 | hp2 | a0001 | c0001 | t0009 | g0239 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19011 | hp1 | a0001 | c0008 | t0037 | g0078 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19011 | hp2 | a0001 | c0002 | t0003 | g0061 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | LWK | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19030 | hp2 | a0001 | c0006 | t0018 | g0038 | AFR | LWK | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19043 | hp1 | a0001 | c0028 | t0025 | g0042 | AFR | LWK | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19043 | hp2 | a0005 | c0010 | t0005 | g0134 | AFR | LWK | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19057 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19060 | hp2 | a0001 | c0002 | t0009 | g0235 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19062 | hp1 | a0002 | c0003 | t0016 | g0299 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19062 | hp2 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19063 | hp2 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19066 | hp1 | a0001 | c0002 | t0003 | g0305 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19066 | hp2 | a0001 | c0002 | t0002 | g0295 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19068 | hp2 | a0001 | c0008 | t0002 | g0280 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19077 | hp1 | a0001 | c0002 | t0002 | g0312 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19077 | hp2 | a0017 | c0033 | t0009 | g0233 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19081 | hp1 | a0006 | c0012 | t0002 | g0313 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19082 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19082 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19085 | hp2 | a0001 | c0001 | t0009 | g0232 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19086 | hp1 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19086 | hp2 | a0001 | c0002 | t0003 | g0087 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19087 | hp1 | a0001 | c0002 | t0003 | g0298 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19087 | hp2 | a0001 | c0002 | t0031 | g0206 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19088 | hp1 | a0001 | c0001 | t0011 | g0279 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19088 | hp2 | a0001 | c0002 | t0002 | g0109 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19240 | hp1 | a0001 | c0004 | t0022 | g0037 | AFR | YRI | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA19240 | hp2 | a0005 | c0010 | t0005 | g0331 | AFR | YRI | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA20129 | hp1 | a0001 | c0002 | t0013 | g0222 | AFR | ASW | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA20129 | hp2 | a0001 | c0006 | t0018 | g0214 | AFR | ASW | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA20752 | hp1 | a0001 | c0002 | t0003 | g0157 | EUR | TSI | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA20752 | hp2 | a0001 | c0002 | t0004 | g0192 | EUR | TSI | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA20805 | hp1 | a0001 | c0004 | t0007 | g0324 | EUR | TSI | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0212 | EUR | TSI | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG01123 | hp2 | a0002 | c0003 | t0006 | g0050 | AMR | CLM | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02109 | hp2 | a0001 | c0006 | t0005 | g0067 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02486 | hp1 | a0001 | c0001 | t0012 | g0048 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02486 | hp2 | a0001 | c0039 | t0018 | g0016 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02559 | hp1 | a0001 | c0001 | t0012 | g0144 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG02559 | hp2 | a0001 | c0001 | t0020 | g0131 | AFR | ACB | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03471 | hp1 | a0001 | c0006 | t0007 | g0262 | AFR | MSL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG03471 | hp2 | a0001 | c0001 | t0012 | g0034 | AFR | MSL | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0250 | AFR | USA | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | USA | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18955 | hp1 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | USA | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA20300 | hp2 | a0002 | c0003 | t0006 | g0292 | AFR | USA | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA21309 | hp1 | a0001 | c0020 | t0007 | g0133 | AFR | LWK | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
NA21309 | hp2 | a0001 | c0004 | t0001 | g0327 | AFR | LWK | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0322 | REF | REF | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
homoSapiens | grch38p0 | a0002 | c0003 | t0038 | g0223 | REF | REF | MAP1B_chr5_72102475_72214565 | MAP1B | chr5 | 72102475 | 72214565 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:72183772 | G | A | 1 | a0011 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.316G>A | p.Val106Ile | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/7 | 373/11790 | 316/7407 | 106/2468 | chr5 | 72183772 | |||
chr5:72194797 | C | T | 1 | a0015 | 1 | NA18967.hp2 | missense_variant | MODERATE | c.1442C>T | p.Ala481Val | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 1499/11790 | 1442/7407 | 481/2468 | chr5 | 72194797 | |||
chr5:72195135 | A | G | 15 | a0001 a0003 a0004 others(12): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
missense_variant | MODERATE | c.1780A>G | p.Ile594Val | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 1837/11790 | 1780/7407 | 594/2468 | chr5 | 72195135 | |||
chr5:72195415 | A | C | 1 | a0010 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.2060A>C | p.Glu687Ala | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 2117/11790 | 2060/7407 | 687/2468 | chr5 | 72195415 | |||
chr5:72195484 | A | G | 1 | a0004 | 4 | HG01074.hp2 HG02965.hp1 HG03225.hp1 others(1): Show |
missense_variant | MODERATE | c.2129A>G | p.Lys710Arg | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 2186/11790 | 2129/7407 | 710/2468 | chr5 | 72195484 | |||
chr5:72195741 | G | A | 1 | a0009 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.2386G>A | p.Ala796Thr | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 2443/11790 | 2386/7407 | 796/2468 | chr5 | 72195741 | |||
chr5:72195742 | C | T | 1 | a0013 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.2387C>T | p.Ala796Val | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 2444/11790 | 2387/7407 | 796/2468 | chr5 | 72195742 | |||
chr5:72195961 | A | G | 1 | a0007 | 3 | HG03130.hp1 HG03139.hp2 HG03195.hp2 |
missense_variant | MODERATE | c.2606A>G | p.Glu869Gly | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 2663/11790 | 2606/7407 | 869/2468 | chr5 | 72195961 | |||
chr5:72196294 | C | T | 1 | a0017 | 1 | NA19077.hp2 | missense_variant | MODERATE | c.2939C>T | p.Ala980Val | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 2996/11790 | 2939/7407 | 980/2468 | chr5 | 72196294 | |||
chr5:72196591 | G | A | 1 | a0008 | 2 | HG00741.hp1 HG03453.hp2 |
missense_variant | MODERATE | c.3236G>A | p.Arg1079Gln | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 3293/11790 | 3236/7407 | 1079/2468 | chr5 | 72196591 | |||
chr5:72197242 | C | T | 1 | a0005 | 4 | HG02647.hp1 HG02922.hp1 NA19043.hp2 others(1): Show |
missense_variant | MODERATE | c.3887C>T | p.Pro1296Leu | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 3944/11790 | 3887/7407 | 1296/2468 | chr5 | 72197242 | |||
chr5:72197388 | T | G | 1 | a0012 | 1 | HG02897.hp1 | missense_variant | MODERATE | c.4033T>G | p.Ser1345Ala | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4090/11790 | 4033/7407 | 1345/2468 | chr5 | 72197388 | |||
chr5:72197424 | C | T | 1 | a0016 | 1 | NA18985.hp2 | missense_variant | MODERATE | c.4069C>T | p.Pro1357Ser | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4126/11790 | 4069/7407 | 1357/2468 | chr5 | 72197424 | |||
chr5:72197866 | A | C | 1 | a0010 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.4511A>C | p.Gln1504Pro | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4568/11790 | 4511/7407 | 1504/2468 | chr5 | 72197866 | |||
chr5:72197867 | A | C | 1 | a0010 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.4512A>C | p.Gln1504His | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4569/11790 | 4512/7407 | 1504/2468 | chr5 | 72197867 | |||
chr5:72197869 | T | C | 1 | a0010 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.4514T>C | p.Ile1505Thr | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4571/11790 | 4514/7407 | 1505/2468 | chr5 | 72197869 | |||
chr5:72197871 | G | C | 1 | a0010 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.4516G>C | p.Asp1506His | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4573/11790 | 4516/7407 | 1506/2468 | chr5 | 72197871 | |||
chr5:72197877 | A | G | 1 | a0010 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.4522A>G | p.Ser1508Gly | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4579/11790 | 4522/7407 | 1508/2468 | chr5 | 72197877 | |||
chr5:72197878 | G | A | 1 | a0010 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.4523G>A | p.Ser1508Asn | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4580/11790 | 4523/7407 | 1508/2468 | chr5 | 72197878 | |||
chr5:72197879 | T | G | 1 | a0010 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.4524T>G | p.Ser1508Arg | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4581/11790 | 4524/7407 | 1508/2468 | chr5 | 72197879 | |||
chr5:72197881 | A | T | 1 | a0010 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.4526A>T | p.Gln1509Leu | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4583/11790 | 4526/7407 | 1509/2468 | chr5 | 72197881 | |||
chr5:72197917 | T | G | 1 | a0010 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.4562T>G | p.Ile1521Ser | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4619/11790 | 4562/7407 | 1521/2468 | chr5 | 72197917 | |||
chr5:72197982 | T | G | 1 | a0010 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.4627T>G | p.Tyr1543Asp | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4684/11790 | 4627/7407 | 1543/2468 | chr5 | 72197982 | |||
chr5:72197990 | T | G | 1 | a0010 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.4635T>G | p.His1545Gln | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4692/11790 | 4635/7407 | 1545/2468 | chr5 | 72197990 | |||
chr5:72197991 | A | T | 1 | a0010 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.4636A>T | p.Met1546Leu | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4693/11790 | 4636/7407 | 1546/2468 | chr5 | 72197991 | |||
chr5:72197998 | G | GGTGCAGC others(5): Show |
1 | a0010 | 1 | HG01993.hp1 | disruptive_inframe_insertion | MODERATE | c.4643_4644insGTGCAG others(6): Show |
p.Gly1548_Val1549ins others(12): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4701/11790 | 4644/7407 | 1548/2468 | chr5 | 72197998 | |||
chr5:72198853 | G | A | 1 | a0014 | 1 | NA18960.hp1 | missense_variant | MODERATE | c.5498G>A | p.Arg1833His | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 5555/11790 | 5498/7407 | 1833/2468 | chr5 | 72198853 | |||
chr5:72198867 | T | C | 1 | a0003 | 5 | HG01167.hp1 HG01169.hp2 HG01433.hp2 others(2): Show |
missense_variant | MODERATE | c.5512T>C | p.Phe1838Leu | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 5569/11790 | 5512/7407 | 1838/2468 | chr5 | 72198867 | |||
chr5:72199104 | A | C | 1 | a0009 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.5749A>C | p.Ser1917Arg | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 5806/11790 | 5749/7407 | 1917/2468 | chr5 | 72199104 | |||
chr5:72199362 | G | C | 1 | a0006 | 4 | NA18963.hp1 NA18971.hp1 NA18973.hp2 others(1): Show |
missense_variant | MODERATE | c.6007G>C | p.Asp2003His | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 6064/11790 | 6007/7407 | 2003/2468 | chr5 | 72199362 | |||
chr5:72199978 | G | A | 1 | a0006 | 4 | NA18963.hp1 NA18971.hp1 NA18973.hp2 others(1): Show |
missense_variant | MODERATE | c.6623G>A | p.Arg2208His | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 6680/11790 | 6623/7407 | 2208/2468 | chr5 | 72199978 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:72107627 | C | T | 1 | a0001c0039 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.96C>T | p.Phe32Phe | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/7 | 153/11790 | 96/7407 | 32/2468 | chr5 | 72107627 | |||
chr5:72115762 | A | G | 1 | a0001c0038 | 1 | HG02155.hp1 | synonymous_variant | LOW | c.249A>G | p.Val83Val | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/7 | 306/11790 | 249/7407 | 83/2468 | chr5 | 72115762 | |||
chr5:72193868 | C | T | 4 | a0001c0006 a0001c0020 a0001c0039 others(1): Show |
11 | HG01167.hp2 HG01243.hp2 HG02109.hp2 others(8): Show |
splice_region_variant&synonymous_variant | LOW | c.513C>T | p.Ile171Ile | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 570/11790 | 513/7407 | 171/2468 | chr5 | 72193868 | |||
chr5:72194798 | G | A | 1 | a0001c0022 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.1443G>A | p.Ala481Ala | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 1500/11790 | 1443/7407 | 481/2468 | chr5 | 72194798 | |||
chr5:72194850 | C | T | 1 | a0001c0036 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.1495C>T | p.Leu499Leu | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 1552/11790 | 1495/7407 | 499/2468 | chr5 | 72194850 | |||
chr5:72195134 | A | G | 1 | a0007c0013 | 3 | HG03130.hp1 HG03139.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.1779A>G | p.Pro593Pro | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 1836/11790 | 1779/7407 | 593/2468 | chr5 | 72195134 | |||
chr5:72195674 | C | T | 1 | a0002c0015 | 2 | HG00609.hp1 NA18966.hp2 |
synonymous_variant | LOW | c.2319C>T | p.Ala773Ala | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 2376/11790 | 2319/7407 | 773/2468 | chr5 | 72195674 | |||
chr5:72196037 | G | A | 3 | a0001c0006 a0001c0020 a0001c0039 |
10 | HG01167.hp2 HG01243.hp2 HG02109.hp2 others(7): Show |
synonymous_variant | LOW | c.2682G>A | p.Glu894Glu | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 2739/11790 | 2682/7407 | 894/2468 | chr5 | 72196037 | |||
chr5:72196082 | T | C | 1 | a0007c0013 | 3 | HG03130.hp1 HG03139.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.2727T>C | p.Pro909Pro | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 2784/11790 | 2727/7407 | 909/2468 | chr5 | 72196082 | |||
chr5:72196238 | C | T | 1 | a0001c0034 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.2883C>T | p.His961His | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 2940/11790 | 2883/7407 | 961/2468 | chr5 | 72196238 | |||
chr5:72196259 | G | A | 1 | a0001c0025 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.2904G>A | p.Lys968Lys | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 2961/11790 | 2904/7407 | 968/2468 | chr5 | 72196259 | |||
chr5:72196613 | T | C | 1 | a0001c0026 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.3258T>C | p.His1086His | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 3315/11790 | 3258/7407 | 1086/2468 | chr5 | 72196613 | |||
chr5:72196907 | C | T | 4 | a0001c0004 a0001c0019 a0001c0034 others(1): Show |
22 | HG00558.hp1 HG00733.hp2 HG00738.hp2 others(19): Show |
synonymous_variant | LOW | c.3552C>T | p.Asn1184Asn | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 3609/11790 | 3552/7407 | 1184/2468 | chr5 | 72196907 | |||
chr5:72197324 | A | G | 1 | a0001c0018 | 2 | NA18966.hp1 NA18970.hp2 |
synonymous_variant | LOW | c.3969A>G | p.Pro1323Pro | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4026/11790 | 3969/7407 | 1323/2468 | chr5 | 72197324 | |||
chr5:72197381 | C | T | 1 | a0001c0017 | 2 | NA18959.hp2 NA18983.hp2 |
synonymous_variant | LOW | c.4026C>T | p.Asp1342Asp | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4083/11790 | 4026/7407 | 1342/2468 | chr5 | 72197381 | |||
chr5:72197981 | G | T | 1 | a0010c0023 | 1 | HG01993.hp1 | synonymous_variant | LOW | c.4626G>T | p.Thr1542Thr | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4683/11790 | 4626/7407 | 1542/2468 | chr5 | 72197981 | |||
chr5:72198050 | A | T | 3 | a0001c0005 a0001c0026 a0001c0036 |
19 | HG00741.hp2 HG01884.hp2 HG02145.hp1 others(16): Show |
synonymous_variant | LOW | c.4695A>T | p.Pro1565Pro | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 4752/11790 | 4695/7407 | 1565/2468 | chr5 | 72198050 | |||
chr5:72198548 | C | A | 1 | a0001c0008 | 4 | HG00621.hp1 NA18943.hp1 NA19011.hp1 others(1): Show |
synonymous_variant | LOW | c.5193C>A | p.Ser1731Ser | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 5250/11790 | 5193/7407 | 1731/2468 | chr5 | 72198548 | |||
chr5:72199079 | G | A | 2 | a0001c0004 a0001c0009 |
22 | HG00558.hp1 HG00733.hp2 HG00738.hp2 others(19): Show |
synonymous_variant | LOW | c.5724G>A | p.Lys1908Lys | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 5781/11790 | 5724/7407 | 1908/2468 | chr5 | 72199079 | |||
chr5:72199145 | C | T | 1 | a0006c0030 | 1 | NA18971.hp1 | synonymous_variant | LOW | c.5790C>T | p.Thr1930Thr | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 5847/11790 | 5790/7407 | 1930/2468 | chr5 | 72199145 | |||
chr5:72199214 | T | C | 13 | a0001c0002 a0001c0008 a0001c0017 others(10): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(121): Show |
synonymous_variant | LOW | c.5859T>C | p.Gly1953Gly | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 5916/11790 | 5859/7407 | 1953/2468 | chr5 | 72199214 | |||
chr5:72199493 | G | A | 1 | a0001c0029 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.6138G>A | p.Glu2046Glu | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 6195/11790 | 6138/7407 | 2046/2468 | chr5 | 72199493 | |||
chr5:72199517 | A | C | 1 | a0001c0028 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.6162A>C | p.Ala2054Ala | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 6219/11790 | 6162/7407 | 2054/2468 | chr5 | 72199517 | |||
chr5:72199901 | C | T | 1 | a0004c0011 | 4 | HG01074.hp2 HG02965.hp1 HG03225.hp1 others(1): Show |
synonymous_variant | LOW | c.6546C>T | p.Asp2182Asp | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/7 | 6603/11790 | 6546/7407 | 2182/2468 | chr5 | 72199901 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:72107479 | T | A | 83 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(80): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
5_prime_UTR_variant | MODIFIER | c.-53T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/7 | 53 | chr5 | 72107479 | ||||||
chr5:72205473 | C | A | 1 | a0001c0001t0024 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*234C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 234 | chr5 | 72205473 | ||||||
chr5:72205571 | G | A | 4 | a0001c0005t0008 a0001c0026t0008 a0001c0028t0025 others(1): Show |
10 | HG00741.hp2 HG02630.hp2 HG02647.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*332G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 332 | chr5 | 72205571 | ||||||
chr5:72205795 | A | G | 1 | a0001c0008t0037 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*556A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 556 | chr5 | 72205795 | ||||||
chr5:72206699 | C | CT | 11 | a0001c0001t0007 a0001c0001t0035 a0001c0004t0007 others(8): Show |
17 | HG01167.hp2 HG01243.hp2 HG01433.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1469dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 1470 | INFO_REALIGN_3_PRIME | chr5 | 72206699 | |||||
chr5:72206717 | C | T | 10 | a0001c0001t0007 a0001c0001t0035 a0001c0004t0007 others(7): Show |
16 | HG01167.hp2 HG01243.hp2 HG01433.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1478C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 1478 | chr5 | 72206717 | ||||||
chr5:72206723 | A | G | 4 | a0001c0004t0022 a0001c0006t0018 a0001c0006t0022 others(1): Show |
6 | HG02451.hp1 HG02486.hp2 HG03098.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1484A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 1484 | chr5 | 72206723 | ||||||
chr5:72207295 | A | G | 1 | a0001c0002t0032 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2056A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 2056 | chr5 | 72207295 | ||||||
chr5:72207378 | C | G | 1 | a0001c0002t0031 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2139C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 2139 | chr5 | 72207378 | ||||||
chr5:72207588 | G | A | 2 | a0001c0001t0020 a0001c0005t0020 |
2 | HG02280.hp2 HG02559.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2349G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 2349 | chr5 | 72207588 | ||||||
chr5:72207680 | C | G | 72 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(69): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
3_prime_UTR_variant | MODIFIER | c.*2441C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 2441 | chr5 | 72207680 | ||||||
chr5:72207860 | C | A | 94 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(91): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
3_prime_UTR_variant | MODIFIER | c.*2621C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 2621 | chr5 | 72207860 | ||||||
chr5:72207946 | TTCTC | T | 3 | a0001c0001t0015 a0001c0004t0015 a0001c0004t0017 |
9 | HG00558.hp1 HG00738.hp2 HG02080.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2721_*2724delCTCT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 2721 | INFO_REALIGN_3_PRIME | chr5 | 72207946 | |||||
chr5:72207962 | C | CT | 22 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0011 others(19): Show |
81 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*2744dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 2745 | INFO_REALIGN_3_PRIME | chr5 | 72207962 | |||||
chr5:72207962 | CT | C | 16 | a0001c0001t0005 a0001c0001t0024 a0001c0002t0016 others(13): Show |
33 | HG00609.hp1 HG00733.hp2 HG00741.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2744delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 2744 | INFO_REALIGN_3_PRIME | chr5 | 72207962 | |||||
chr5:72207962 | CTTTTTTT others(4): Show |
C | 6 | a0001c0001t0004 a0001c0001t0019 a0001c0001t0035 others(3): Show |
25 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2734_*2744delTTTT others(7): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 2734 | INFO_REALIGN_3_PRIME | chr5 | 72207962 | |||||
chr5:72207964 | T | C | 11 | a0001c0001t0007 a0001c0001t0020 a0001c0001t0026 others(8): Show |
17 | HG00673.hp1 HG01167.hp2 HG01243.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2725T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 2725 | chr5 | 72207964 | ||||||
chr5:72207965 | T | C | 1 | a0001c0004t0034 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2726T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 2726 | chr5 | 72207965 | ||||||
chr5:72208086 | T | TA | 62 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(59): Show |
193 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*2848dupA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 2849 | INFO_REALIGN_3_PRIME | chr5 | 72208086 | |||||
chr5:72208450 | G | A | 1 | a0001c0001t0028 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3211G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3211 | chr5 | 72208450 | ||||||
chr5:72208466 | C | A | 2 | a0001c0001t0021 a0001c0005t0021 |
2 | HG02145.hp1 HG02258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3227C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3227 | chr5 | 72208466 | ||||||
chr5:72208794 | G | A | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3555G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3555 | chr5 | 72208794 | ||||||
chr5:72208795 | C | A | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3556C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3556 | chr5 | 72208795 | ||||||
chr5:72208797 | G | T | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3558G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3558 | chr5 | 72208797 | ||||||
chr5:72208798 | C | T | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3559C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3559 | chr5 | 72208798 | ||||||
chr5:72208799 | T | G | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3560T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3560 | chr5 | 72208799 | ||||||
chr5:72208800 | C | G | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3561C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3561 | chr5 | 72208800 | ||||||
chr5:72208806 | T | A | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3567T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3567 | chr5 | 72208806 | ||||||
chr5:72208807 | T | A | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3568T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3568 | chr5 | 72208807 | ||||||
chr5:72208808 | C | A | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3569C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3569 | chr5 | 72208808 | ||||||
chr5:72208813 | T | G | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3574T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3574 | chr5 | 72208813 | ||||||
chr5:72208814 | T | G | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3575T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3575 | chr5 | 72208814 | ||||||
chr5:72208817 | C | G | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3578C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3578 | chr5 | 72208817 | ||||||
chr5:72208819 | T | A | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3580T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3580 | chr5 | 72208819 | ||||||
chr5:72208820 | T | A | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3581T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3581 | chr5 | 72208820 | ||||||
chr5:72208821 | T | G | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3582T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3582 | chr5 | 72208821 | ||||||
chr5:72208822 | C | A | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3583C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3583 | chr5 | 72208822 | ||||||
chr5:72208825 | G | T | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3586G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3586 | chr5 | 72208825 | ||||||
chr5:72208832 | T | A | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3593T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3593 | chr5 | 72208832 | ||||||
chr5:72208840 | C | A | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3601C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3601 | chr5 | 72208840 | ||||||
chr5:72208841 | C | A | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3602C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3602 | chr5 | 72208841 | ||||||
chr5:72208852 | G | T | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3613G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3613 | chr5 | 72208852 | ||||||
chr5:72208853 | G | T | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3614G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3614 | chr5 | 72208853 | ||||||
chr5:72208855 | T | C | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3616T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3616 | chr5 | 72208855 | ||||||
chr5:72208856 | C | A | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3617C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3617 | chr5 | 72208856 | ||||||
chr5:72208859 | G | C | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3620G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3620 | chr5 | 72208859 | ||||||
chr5:72208860 | C | T | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3621C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3621 | chr5 | 72208860 | ||||||
chr5:72208864 | G | C | 1 | a0007c0013t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3625G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3625 | chr5 | 72208864 | ||||||
chr5:72208892 | CT | C | 3 | a0001c0001t0012 a0001c0001t0021 a0001c0005t0021 |
9 | HG02145.hp1 HG02258.hp2 HG02486.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3664delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3664 | INFO_REALIGN_3_PRIME | chr5 | 72208892 | |||||
chr5:72209045 | TTAAAAC | T | 1 | a0001c0004t0017 | 4 | HG00738.hp2 HG02148.hp2 HG02280.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3809_*3814delAAAC others(2): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3809 | INFO_REALIGN_3_PRIME | chr5 | 72209045 | |||||
chr5:72209135 | G | T | 1 | a0001c0002t0031 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3896G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 7/7 | 3896 | chr5 | 72209135 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:72107730 | G | GC | 6 | a0001c0001t0001g0333 a0001c0001t0001g0335 a0001c0004t0001g0334 others(3): Show |
6 | HG00741.hp1 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.184+20dupC | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 72107730 | ||||||
chr5:72107892 | G | C | 1 | a0001c0005t0001g0008 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.184+177G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72107892 | |||||||
chr5:72108044 | G | T | 1 | a0005c0010t0005g0329 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.184+329G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72108044 | |||||||
chr5:72108290 | G | GC | 23 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0027 others(20): Show |
23 | HG00621.hp2 HG00642.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.184+583dupC | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 72108290 | ||||||
chr5:72108349 | A | G | 1 | a0001c0009t0001g0328 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.184+634A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72108349 | |||||||
chr5:72108384 | T | C | 1 | a0001c0026t0008g0030 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.184+669T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72108384 | |||||||
chr5:72108487 | G | C | 1 | a0001c0001t0001g0009 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.184+772G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72108487 | |||||||
chr5:72108557 | T | C | 2 | a0001c0001t0002g0031 a0001c0002t0002g0032 |
2 | HG02523.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.184+842T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72108557 | |||||||
chr5:72108567 | C | G | 30 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 others(27): Show |
30 | HG00140.hp1 HG00741.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.184+852C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72108567 | |||||||
chr5:72108571 | G | A | 2 | a0001c0005t0008g0033 a0005c0010t0005g0329 |
2 | HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.184+856G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72108571 | |||||||
chr5:72108571 | G | C | 1 | a0001c0001t0012g0034 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.184+856G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72108571 | |||||||
chr5:72108572 | G | A | 2 | a0001c0005t0008g0035 a0001c0034t0005g0036 |
2 | HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.184+857G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72108572 | |||||||
chr5:72108580 | G | A | 1 | a0001c0001t0010g0010 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.184+865G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72108580 | |||||||
chr5:72108601 | G | A | 12 | a0001c0001t0001g0044 a0001c0001t0012g0048 a0001c0002t0002g0040 others(9): Show |
12 | HG00741.hp2 HG02486.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.184+886G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72108601 | |||||||
chr5:72108703 | C | A | 1 | a0001c0026t0008g0030 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.184+988C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72108703 | |||||||
chr5:72108750 | G | T | 2 | a0001c0001t0001g0335 a0008c0016t0001g0330 |
2 | HG00741.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.184+1035G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72108750 | |||||||
chr5:72108764 | C | T | 1 | a0001c0005t0001g0304 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.184+1049C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72108764 | |||||||
chr5:72109053 | C | A | 1 | a0016c0031t0003g0049 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.184+1338C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72109053 | |||||||
chr5:72109205 | C | T | 36 | a0001c0001t0001g0027 a0001c0001t0001g0272 a0001c0001t0001g0274 others(33): Show |
38 | HG00558.hp1 HG00609.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.184+1490C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72109205 | |||||||
chr5:72109235 | T | TA | 83 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0066 others(80): Show |
83 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.184+1532dupA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 72109235 | ||||||
chr5:72109248 | G | A | 1 | a0001c0001t0001g0335 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.184+1533G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72109248 | |||||||
chr5:72109248 | G | GA | 57 | a0001c0001t0001g0001 a0001c0001t0001g0044 a0001c0001t0001g0130 others(54): Show |
58 | HG00140.hp1 HG00741.hp1 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.184+1541dupA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 72109248 | ||||||
chr5:72109496 | A | G | 1 | a0001c0004t0015g0271 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.184+1781A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72109496 | |||||||
chr5:72109582 | G | T | 1 | a0001c0001t0001g0123 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.184+1867G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72109582 | |||||||
chr5:72109685 | C | T | 34 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0308 others(31): Show |
35 | HG00140.hp1 HG00741.hp1 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.184+1970C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72109685 | |||||||
chr5:72109759 | T | C | 1 | a0001c0005t0008g0033 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.184+2044T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72109759 | |||||||
chr5:72109902 | G | C | 1 | a0005c0010t0005g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.184+2187G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72109902 | |||||||
chr5:72109909 | C | T | 23 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 others(20): Show |
23 | HG00140.hp1 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.184+2194C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72109909 | |||||||
chr5:72109912 | T | C | 1 | a0001c0005t0008g0135 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.184+2197T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72109912 | |||||||
chr5:72110077 | A | T | 54 | a0001c0001t0001g0027 a0001c0001t0001g0256 a0001c0001t0001g0263 others(51): Show |
56 | HG00558.hp1 HG00609.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.184+2362A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72110077 | |||||||
chr5:72110234 | G | C | 6 | a0001c0001t0005g0140 a0001c0004t0007g0141 a0001c0005t0021g0136 others(3): Show |
6 | HG01074.hp2 HG02145.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.184+2519G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72110234 | |||||||
chr5:72110549 | A | G | 1 | a0003c0007t0002g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.184+2834A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72110549 | |||||||
chr5:72110661 | A | G | 1 | a0001c0002t0003g0121 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.184+2946A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72110661 | |||||||
chr5:72110730 | C | T | 2 | a0001c0001t0002g0031 a0001c0002t0002g0032 |
2 | HG02523.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.184+3015C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72110730 | |||||||
chr5:72110843 | T | C | 31 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0123 others(28): Show |
31 | HG00140.hp1 HG01070.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.184+3128T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72110843 | |||||||
chr5:72110866 | C | T | 1 | a0001c0001t0020g0131 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.184+3151C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72110866 | |||||||
chr5:72110950 | T | A | 4 | a0001c0002t0002g0040 a0001c0004t0022g0037 a0001c0006t0018g0038 others(1): Show |
4 | HG02723.hp1 HG03098.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.184+3235T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72110950 | |||||||
chr5:72111028 | T | A | 4 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0004g0307 others(1): Show |
4 | HG00140.hp1 HG01099.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.184+3313T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72111028 | |||||||
chr5:72111053 | T | G | 1 | a0001c0001t0001g0310 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.184+3338T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72111053 | |||||||
chr5:72111102 | C | CT | 17 | a0001c0001t0001g0044 a0001c0001t0001g0130 a0001c0001t0012g0048 others(14): Show |
17 | HG00741.hp2 HG02257.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.184+3392dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr5 | 72111102 | ||||||
chr5:72111250 | C | T | 1 | a0001c0039t0018g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.184+3535C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72111250 | |||||||
chr5:72111283 | A | T | 3 | a0001c0005t0008g0135 a0001c0005t0008g0252 a0004c0011t0001g0253 |
3 | HG02647.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.184+3568A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72111283 | |||||||
chr5:72111296 | T | A | 5 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0001t0015g0124 others(2): Show |
5 | HG02145.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.184+3581T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72111296 | |||||||
chr5:72111423 | A | T | 3 | a0001c0001t0004g0025 a0001c0001t0004g0250 a0001c0001t0004g0251 |
3 | HG01192.hp2 HG04199.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.184+3708A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72111423 | |||||||
chr5:72111604 | T | A | 2 | a0007c0013t0001g0126 a0007c0013t0029g0127 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.184+3889T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72111604 | |||||||
chr5:72111647 | A | T | 2 | a0001c0001t0001g0130 a0001c0002t0003g0129 |
2 | NA18945.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.184+3932A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72111647 | |||||||
chr5:72111717 | G | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(227): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.185-3981G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72111717 | |||||||
chr5:72111738 | A | G | 1 | a0001c0002t0004g0005 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.185-3960A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72111738 | |||||||
chr5:72111768 | C | T | 30 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0123 others(27): Show |
30 | HG00140.hp1 HG01070.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.185-3930C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72111768 | |||||||
chr5:72111831 | G | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(229): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.185-3867G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72111831 | |||||||
chr5:72111877 | T | G | 1 | a0001c0004t0017g0060 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.185-3821T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72111877 | |||||||
chr5:72112063 | T | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(227): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.185-3635T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72112063 | |||||||
chr5:72112173 | C | G | 1 | a0001c0005t0001g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.185-3525C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72112173 | |||||||
chr5:72112426 | C | T | 6 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0005t0008g0033 others(3): Show |
7 | HG02622.hp2 HG02886.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.185-3272C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72112426 | |||||||
chr5:72112488 | C | T | 1 | a0001c0038t0013g0024 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.185-3210C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72112488 | |||||||
chr5:72112641 | A | G | 1 | a0001c0001t0007g0269 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.185-3057A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72112641 | |||||||
chr5:72112923 | G | A | 1 | a0001c0001t0020g0131 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.185-2775G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72112923 | |||||||
chr5:72112984 | A | C | 18 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0333 others(15): Show |
19 | HG00741.hp1 HG02055.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.185-2714A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72112984 | |||||||
chr5:72113040 | A | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(227): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.185-2658A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72113040 | |||||||
chr5:72113092 | C | A | 54 | a0001c0001t0001g0027 a0001c0001t0001g0256 a0001c0001t0001g0263 others(51): Show |
56 | HG00558.hp1 HG00609.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.185-2606C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72113092 | |||||||
chr5:72113116 | A | G | 1 | a0001c0005t0005g0220 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.185-2582A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72113116 | |||||||
chr5:72113144 | C | A | 1 | a0001c0005t0008g0041 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.185-2554C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72113144 | |||||||
chr5:72113168 | T | G | 1 | a0001c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.185-2530T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72113168 | |||||||
chr5:72113184 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.185-2514A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72113184 | |||||||
chr5:72113297 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.185-2401A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72113297 | |||||||
chr5:72113388 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.185-2310C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72113388 | |||||||
chr5:72113482 | A | C | 30 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0123 others(27): Show |
30 | HG00140.hp1 HG01070.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.185-2216A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72113482 | |||||||
chr5:72113493 | A | C | 2 | a0001c0002t0003g0218 a0002c0003t0006g0217 |
2 | HG01975.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.185-2205A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72113493 | |||||||
chr5:72113556 | A | G | 49 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0055 others(46): Show |
49 | HG00140.hp1 HG00741.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.185-2142A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72113556 | |||||||
chr5:72113742 | A | C | 298 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(295): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.185-1956A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72113742 | |||||||
chr5:72113767 | T | C | 1 | a0002c0003t0006g0002 | 2 | HG00738.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.185-1931T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72113767 | |||||||
chr5:72113866 | G | C | 2 | a0001c0001t0001g0143 a0005c0010t0005g0134 |
2 | HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.185-1832G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72113866 | |||||||
chr5:72114028 | T | C | 1 | a0001c0039t0018g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.185-1670T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72114028 | |||||||
chr5:72114090 | T | C | 1 | a0001c0002t0002g0065 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.185-1608T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72114090 | |||||||
chr5:72114190 | T | C | 1 | a0001c0001t0001g0066 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.185-1508T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72114190 | |||||||
chr5:72114192 | T | C | 1 | a0001c0006t0005g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.185-1506T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72114192 | |||||||
chr5:72114220 | T | C | 1 | a0001c0001t0012g0144 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.185-1478T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72114220 | |||||||
chr5:72114227 | G | A | 107 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0143 others(104): Show |
111 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.185-1471G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72114227 | |||||||
chr5:72114243 | A | G | 107 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0143 others(104): Show |
111 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.185-1455A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72114243 | |||||||
chr5:72114285 | A | T | 30 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0123 others(27): Show |
30 | HG00140.hp1 HG01070.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.185-1413A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72114285 | |||||||
chr5:72114372 | A | G | 4 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0001t0015g0124 others(1): Show |
4 | HG02145.hp2 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.185-1326A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72114372 | |||||||
chr5:72114498 | T | G | 2 | a0001c0001t0002g0031 a0001c0002t0002g0032 |
2 | HG02523.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.185-1200T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72114498 | |||||||
chr5:72114507 | G | T | 1 | a0001c0039t0018g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.185-1191G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72114507 | |||||||
chr5:72114518 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.185-1180T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72114518 | |||||||
chr5:72114529 | G | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(227): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.185-1169G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72114529 | |||||||
chr5:72115095 | G | A | 2 | a0001c0001t0002g0031 a0001c0002t0002g0032 |
2 | HG02523.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.185-603G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72115095 | |||||||
chr5:72115172 | G | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0005t0008g0033 others(3): Show |
7 | HG02622.hp2 HG02886.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.185-526G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72115172 | |||||||
chr5:72115177 | T | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(227): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.185-521T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72115177 | |||||||
chr5:72115369 | C | T | 1 | a0005c0010t0005g0329 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.185-329C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72115369 | |||||||
chr5:72115465 | A | G | 4 | a0001c0001t0001g0266 a0001c0002t0002g0267 a0001c0002t0011g0265 others(1): Show |
4 | HG01891.hp2 HG02109.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.185-233A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72115465 | |||||||
chr5:72115479 | C | T | 62 | a0001c0001t0001g0066 a0001c0001t0001g0074 a0001c0001t0001g0086 others(59): Show |
62 | HG00140.hp2 HG00408.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.185-219C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72115479 | |||||||
chr5:72115593 | C | G | 2 | a0001c0001t0002g0031 a0001c0002t0002g0032 |
2 | HG02523.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.185-105C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 1/6 | chr5 | 72115593 | |||||||
chr5:72115845 | A | G | 1 | a0001c0001t0007g0119 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.286+46A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72115845 | |||||||
chr5:72115891 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(154): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.286+92T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72115891 | |||||||
chr5:72116040 | A | T | 52 | a0001c0001t0001g0027 a0001c0001t0001g0263 a0001c0001t0001g0266 others(49): Show |
54 | HG00558.hp1 HG00609.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.286+241A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72116040 | |||||||
chr5:72116049 | C | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(153): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.286+250C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72116049 | |||||||
chr5:72116118 | A | G | 8 | a0001c0001t0001g0333 a0001c0001t0001g0335 a0001c0001t0012g0311 others(5): Show |
8 | HG00741.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.286+319A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72116118 | |||||||
chr5:72116150 | T | C | 1 | a0001c0001t0012g0012 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.286+351T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72116150 | |||||||
chr5:72116309 | A | G | 6 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0005t0008g0033 others(3): Show |
7 | HG02622.hp2 HG02886.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+510A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72116309 | |||||||
chr5:72116386 | T | C | 13 | a0001c0001t0001g0333 a0001c0001t0001g0335 a0001c0001t0012g0056 others(10): Show |
13 | HG00741.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.286+587T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72116386 | |||||||
chr5:72116417 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.286+618T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72116417 | |||||||
chr5:72116465 | A | G | 51 | a0001c0001t0001g0027 a0001c0001t0001g0263 a0001c0001t0001g0266 others(48): Show |
53 | HG00558.hp1 HG00609.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.286+666A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72116465 | |||||||
chr5:72116544 | G | A | 7 | a0001c0001t0001g0333 a0001c0001t0001g0335 a0001c0004t0001g0334 others(4): Show |
7 | HG00741.hp1 HG02055.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.286+745G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72116544 | |||||||
chr5:72116546 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(154): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.286+747A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72116546 | |||||||
chr5:72116627 | T | G | 1 | a0016c0031t0003g0049 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.286+828T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72116627 | |||||||
chr5:72117121 | T | TGAAAAAT others(322): Show |
1 | a0001c0002t0032g0273 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.286+1337_286+1338i others(331): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | ||||||
chr5:72117121 | T | TGAAAAAT others(325): Show |
1 | a0001c0005t0001g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.286+1337_286+1338i others(334): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | ||||||
chr5:72117121 | T | TGAAAAAT others(330): Show |
1 | a0001c0001t0001g0274 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.286+1337_286+1338i others(339): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | ||||||
chr5:72117121 | T | TGAAAAAT others(331): Show |
8 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0002t0002g0216 others(5): Show |
8 | HG01167.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.286+1337_286+1338i others(340): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | ||||||
chr5:72117121 | T | TGAAAAAT others(332): Show |
12 | a0001c0001t0001g0263 a0001c0001t0001g0281 a0001c0001t0001g0283 others(9): Show |
12 | HG01099.hp1 HG01243.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.286+1337_286+1338i others(341): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | ||||||
chr5:72117121 | T | TGAAAAAT others(333): Show |
5 | a0001c0001t0001g0266 a0001c0001t0001g0286 a0001c0001t0005g0285 others(2): Show |
5 | HG02109.hp1 HG02258.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+1337_286+1338i others(342): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | ||||||
chr5:72117121 | T | TGAAAAAT others(337): Show |
1 | a0001c0002t0002g0267 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.286+1337_286+1338i others(346): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | ||||||
chr5:72117121 | T | TGAAAAAT others(338): Show |
4 | a0001c0002t0003g0287 a0001c0002t0003g0289 a0001c0017t0002g0058 others(1): Show |
4 | HG01943.hp2 NA18959.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+1337_286+1338i others(347): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | ||||||
chr5:72117121 | T | TGAAAAAT others(339): Show |
6 | a0001c0001t0001g0027 a0001c0001t0001g0290 a0001c0001t0002g0291 others(3): Show |
7 | HG01928.hp1 HG01934.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.286+1337_286+1338i others(348): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | ||||||
chr5:72117121 | T | TGAAAAAT others(340): Show |
2 | a0001c0002t0002g0295 a0006c0030t0002g0294 |
2 | NA18971.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.286+1337_286+1338i others(349): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | ||||||
chr5:72117121 | T | TGAAAAAT others(341): Show |
3 | a0001c0001t0004g0296 a0001c0002t0003g0007 a0001c0002t0003g0297 |
4 | HG00642.hp2 NA18978.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+1337_286+1338i others(350): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | ||||||
chr5:72117121 | T | TGAAAAAT others(342): Show |
3 | a0001c0002t0003g0298 a0001c0005t0001g0008 a0002c0003t0016g0299 |
3 | HG01884.hp2 NA19062.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.286+1337_286+1338i others(351): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | ||||||
chr5:72117121 | T | TGAAAAAT others(343): Show |
1 | a0001c0001t0035g0300 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.286+1337_286+1338i others(352): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | ||||||
chr5:72117121 | T | TGAAAAAT others(346): Show |
2 | a0001c0002t0001g0302 a0001c0004t0015g0301 |
2 | HG00558.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.286+1337_286+1338i others(355): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | ||||||
chr5:72117121 | T | TGAAAAAT others(348): Show |
1 | a0001c0002t0003g0303 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.286+1337_286+1338i others(357): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72117121 | ||||||
chr5:72117267 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.286+1468C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117267 | |||||||
chr5:72117268 | G | A | 209 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(206): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.286+1469G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117268 | |||||||
chr5:72117327 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(154): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.286+1528G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117327 | |||||||
chr5:72117376 | T | A | 1 | a0001c0001t0002g0146 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.286+1577T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117376 | |||||||
chr5:72117447 | T | C | 1 | a0001c0002t0003g0147 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.286+1648T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117447 | |||||||
chr5:72117492 | A | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(206): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.286+1693A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117492 | |||||||
chr5:72117516 | G | A | 4 | a0001c0005t0021g0136 a0004c0011t0011g0137 a0004c0011t0011g0138 others(1): Show |
4 | HG01074.hp2 HG02145.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+1717G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117516 | |||||||
chr5:72117530 | T | C | 1 | a0001c0002t0001g0148 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.286+1731T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117530 | |||||||
chr5:72117541 | T | C | 1 | a0001c0002t0001g0148 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.286+1742T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117541 | |||||||
chr5:72117624 | C | G | 1 | a0001c0001t0001g0325 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.286+1825C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117624 | |||||||
chr5:72117791 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.286+1992C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117791 | |||||||
chr5:72117801 | G | A | 70 | a0001c0001t0001g0066 a0001c0001t0001g0074 a0001c0001t0001g0086 others(67): Show |
70 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.286+2002G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117801 | |||||||
chr5:72117801 | G | T | 1 | a0001c0001t0012g0311 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286+2002G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117801 | |||||||
chr5:72117818 | T | G | 6 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0005t0008g0033 others(3): Show |
7 | HG02622.hp2 HG02886.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+2019T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117818 | |||||||
chr5:72117831 | T | A | 1 | a0001c0022t0002g0149 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.286+2032T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72117831 | |||||||
chr5:72118145 | A | G | 1 | a0001c0001t0020g0131 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.286+2346A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72118145 | |||||||
chr5:72118339 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(154): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.286+2540A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72118339 | |||||||
chr5:72118369 | T | C | 1 | a0001c0001t0020g0131 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.286+2570T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72118369 | |||||||
chr5:72118369 | TA | T | 51 | a0001c0001t0001g0027 a0001c0001t0001g0263 a0001c0001t0001g0266 others(48): Show |
53 | HG00558.hp1 HG00609.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.286+2579delA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72118369 | ||||||
chr5:72118380 | A | G | 6 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0005t0008g0033 others(3): Show |
7 | HG02622.hp2 HG02886.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+2581A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72118380 | |||||||
chr5:72118455 | T | C | 2 | a0001c0001t0012g0056 a0001c0001t0012g0057 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+2656T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72118455 | |||||||
chr5:72118637 | G | A | 1 | a0001c0039t0018g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.286+2838G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72118637 | |||||||
chr5:72118773 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0132 others(109): Show |
117 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.286+2974G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72118773 | |||||||
chr5:72118805 | A | G | 52 | a0001c0001t0001g0027 a0001c0001t0001g0263 a0001c0001t0001g0266 others(49): Show |
54 | HG00558.hp1 HG00609.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.286+3006A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72118805 | |||||||
chr5:72118832 | C | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0053 others(140): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.286+3033C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72118832 | |||||||
chr5:72118852 | G | A | 10 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0002t0002g0059 others(7): Show |
10 | NA18946.hp1 NA18960.hp2 NA18963.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+3053G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72118852 | |||||||
chr5:72118876 | T | G | 1 | a0001c0006t0005g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.286+3077T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72118876 | |||||||
chr5:72118973 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0053 others(153): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.286+3174A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72118973 | |||||||
chr5:72118985 | C | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0053 others(140): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.286+3186C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72118985 | |||||||
chr5:72119306 | C | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0053 others(153): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.286+3507C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72119306 | |||||||
chr5:72119329 | G | A | 1 | a0002c0003t0006g0150 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.286+3530G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72119329 | |||||||
chr5:72119569 | G | A | 2 | a0001c0009t0007g0043 a0001c0028t0025g0042 |
2 | HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.286+3770G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72119569 | |||||||
chr5:72119595 | C | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0132 others(111): Show |
119 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.286+3796C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72119595 | |||||||
chr5:72119755 | T | C | 1 | a0001c0001t0020g0131 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.286+3956T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72119755 | |||||||
chr5:72119802 | C | T | 29 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0123 others(26): Show |
29 | HG00140.hp1 HG01070.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.286+4003C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72119802 | |||||||
chr5:72119803 | G | A | 1 | a0001c0002t0002g0075 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.286+4004G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72119803 | |||||||
chr5:72119859 | A | C | 2 | a0001c0001t0002g0072 a0001c0001t0015g0116 |
2 | HG00408.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.286+4060A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72119859 | |||||||
chr5:72119990 | G | A | 1 | a0001c0020t0007g0260 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.286+4191G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72119990 | |||||||
chr5:72120095 | C | G | 52 | a0001c0001t0001g0027 a0001c0001t0001g0263 a0001c0001t0001g0266 others(49): Show |
54 | HG00558.hp1 HG00609.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.286+4296C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72120095 | |||||||
chr5:72120425 | CT | C | 53 | a0001c0001t0001g0027 a0001c0001t0001g0143 a0001c0001t0001g0263 others(50): Show |
55 | HG00558.hp1 HG00609.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.286+4643delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72120425 | ||||||
chr5:72120465 | C | G | 1 | a0001c0001t0001g0117 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.286+4666C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72120465 | |||||||
chr5:72120494 | G | T | 5 | a0001c0001t0001g0143 a0001c0005t0008g0135 a0001c0005t0008g0252 others(2): Show |
5 | HG02647.hp2 HG03041.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+4695G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72120494 | |||||||
chr5:72120518 | G | A | 1 | a0001c0001t0012g0311 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286+4719G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72120518 | |||||||
chr5:72120549 | C | T | 1 | a0001c0004t0034g0215 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.286+4750C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72120549 | |||||||
chr5:72120574 | A | G | 2 | a0001c0001t0002g0031 a0001c0002t0002g0032 |
2 | HG02523.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.286+4775A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72120574 | |||||||
chr5:72120590 | A | AT | 6 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0001t0015g0124 others(3): Show |
6 | HG02145.hp2 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+4800dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72120590 | ||||||
chr5:72120590 | AT | A | 5 | a0001c0001t0001g0017 a0001c0001t0012g0311 a0001c0005t0001g0008 others(2): Show |
5 | HG00642.hp1 HG01884.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+4800delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72120590 | ||||||
chr5:72120640 | A | C | 1 | a0001c0004t0001g0334 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.286+4841A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72120640 | |||||||
chr5:72120665 | A | C | 1 | a0001c0002t0002g0213 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.286+4866A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72120665 | |||||||
chr5:72120800 | A | G | 65 | a0001c0001t0001g0009 a0001c0001t0001g0066 a0001c0001t0001g0074 others(62): Show |
65 | HG00140.hp2 HG00408.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.286+5001A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72120800 | |||||||
chr5:72120857 | G | A | 2 | a0001c0001t0002g0031 a0001c0002t0002g0032 |
2 | HG02523.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.286+5058G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72120857 | |||||||
chr5:72121067 | C | T | 2 | a0001c0001t0002g0031 a0001c0002t0002g0032 |
2 | HG02523.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.286+5268C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72121067 | |||||||
chr5:72121111 | G | C | 1 | a0001c0002t0002g0082 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.286+5312G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72121111 | |||||||
chr5:72121213 | A | G | 2 | a0001c0005t0008g0135 a0004c0011t0001g0253 |
2 | HG02647.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.286+5414A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72121213 | |||||||
chr5:72121291 | T | C | 1 | a0001c0001t0020g0131 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.286+5492T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72121291 | |||||||
chr5:72121295 | C | T | 4 | a0001c0001t0004g0025 a0001c0001t0004g0212 a0001c0001t0004g0250 others(1): Show |
4 | HG01192.hp2 HG04199.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+5496C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72121295 | |||||||
chr5:72121337 | T | G | 6 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0005t0008g0033 others(3): Show |
7 | HG02622.hp2 HG02886.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+5538T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72121337 | |||||||
chr5:72121844 | A | G | 19 | a0001c0001t0001g0114 a0001c0001t0001g0210 a0001c0001t0001g0310 others(16): Show |
19 | HG00609.hp1 HG00621.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.286+6045A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72121844 | |||||||
chr5:72121938 | G | A | 11 | a0001c0001t0007g0269 a0001c0001t0012g0056 a0001c0001t0012g0057 others(8): Show |
11 | HG01167.hp2 HG01243.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.286+6139G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72121938 | |||||||
chr5:72121960 | T | C | 1 | a0001c0002t0002g0202 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.286+6161T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72121960 | |||||||
chr5:72121983 | G | T | 1 | a0001c0001t0026g0201 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.286+6184G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72121983 | |||||||
chr5:72122065 | G | A | 3 | a0001c0001t0001g0219 a0001c0004t0001g0327 a0001c0005t0008g0033 |
3 | HG03098.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.286+6266G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72122065 | |||||||
chr5:72122238 | G | A | 3 | a0001c0002t0011g0153 a0001c0002t0014g0003 a0001c0002t0016g0152 |
4 | HG01884.hp1 HG02922.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+6439G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72122238 | |||||||
chr5:72122281 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.286+6482C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72122281 | |||||||
chr5:72122301 | T | C | 1 | a0001c0001t0002g0031 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.286+6502T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72122301 | |||||||
chr5:72122376 | G | A | 1 | a0001c0005t0008g0033 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.286+6577G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72122376 | |||||||
chr5:72122556 | C | T | 2 | a0001c0017t0003g0073 a0002c0003t0016g0299 |
2 | NA18983.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.286+6757C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72122556 | |||||||
chr5:72122641 | C | CTTT | 7 | a0001c0001t0012g0034 a0001c0001t0012g0144 a0001c0001t0020g0131 others(4): Show |
7 | HG02559.hp1 HG02559.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+6857_286+6859d others(5): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72122641 | ||||||
chr5:72122641 | CT | C | 10 | a0001c0001t0001g0055 a0001c0001t0005g0155 a0001c0001t0005g0156 others(7): Show |
10 | HG01070.hp1 HG01070.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+6859delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72122641 | ||||||
chr5:72122737 | G | T | 3 | a0001c0001t0002g0072 a0001c0001t0015g0116 a0003c0007t0002g0083 |
3 | HG00408.hp1 HG01975.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.286+6938G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72122737 | |||||||
chr5:72122750 | T | C | 1 | a0001c0002t0002g0312 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.286+6951T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72122750 | |||||||
chr5:72122785 | C | CCCAGGAG | 7 | a0001c0001t0012g0034 a0001c0001t0012g0144 a0001c0001t0020g0131 others(4): Show |
7 | HG02559.hp1 HG02559.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+6990_286+6996d others(9): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72122785 | ||||||
chr5:72122811 | A | G | 3 | a0001c0001t0001g0009 a0001c0002t0001g0199 a0001c0002t0002g0200 |
3 | HG02155.hp2 NA18612.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.286+7012A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72122811 | |||||||
chr5:72122881 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.286+7082G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72122881 | |||||||
chr5:72123062 | C | G | 1 | a0008c0016t0001g0330 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.286+7263C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72123062 | |||||||
chr5:72123183 | A | G | 9 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0143 others(6): Show |
10 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+7384A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72123183 | |||||||
chr5:72123325 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.286+7526C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72123325 | |||||||
chr5:72123472 | G | GT | 165 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0044 others(162): Show |
170 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.286+7681dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72123472 | ||||||
chr5:72123481 | G | T | 1 | a0001c0002t0003g0211 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.286+7682G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72123481 | |||||||
chr5:72123505 | GA | G | 9 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0143 others(6): Show |
10 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+7707delA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72123505 | |||||||
chr5:72123523 | C | T | 10 | a0001c0001t0001g0074 a0001c0001t0007g0119 a0001c0002t0002g0111 others(7): Show |
10 | HG01074.hp2 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+7724C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72123523 | |||||||
chr5:72123585 | C | T | 2 | a0001c0001t0012g0311 a0001c0005t0001g0008 |
2 | HG01884.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.286+7786C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72123585 | |||||||
chr5:72123586 | G | A | 2 | a0001c0001t0002g0031 a0001c0039t0018g0016 |
2 | HG02486.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.286+7787G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72123586 | |||||||
chr5:72123607 | C | T | 1 | a0001c0005t0008g0332 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.286+7808C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72123607 | |||||||
chr5:72123728 | C | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0143 others(6): Show |
10 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+7929C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72123728 | |||||||
chr5:72123884 | A | G | 332 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(329): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.286+8085A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72123884 | |||||||
chr5:72123929 | C | T | 4 | a0001c0001t0012g0034 a0001c0001t0012g0144 a0001c0005t0005g0220 others(1): Show |
4 | HG02559.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+8130C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72123929 | |||||||
chr5:72124358 | T | G | 3 | a0001c0002t0011g0153 a0001c0002t0014g0003 a0001c0002t0016g0152 |
4 | HG01884.hp1 HG02922.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+8559T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72124358 | |||||||
chr5:72124385 | A | G | 1 | a0001c0001t0004g0100 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.286+8586A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72124385 | |||||||
chr5:72124450 | C | T | 8 | a0001c0001t0001g0286 a0001c0002t0001g0302 a0001c0002t0003g0278 others(5): Show |
8 | HG00609.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.286+8651C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72124450 | |||||||
chr5:72124460 | A | C | 1 | a0001c0005t0005g0128 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.286+8661A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72124460 | |||||||
chr5:72124466 | A | T | 1 | a0001c0005t0005g0128 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.286+8667A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72124466 | |||||||
chr5:72124534 | G | T | 1 | a0001c0039t0018g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.286+8735G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72124534 | |||||||
chr5:72124545 | G | A | 1 | a0001c0001t0007g0119 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.286+8746G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72124545 | |||||||
chr5:72124617 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.286+8818C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72124617 | |||||||
chr5:72124624 | T | C | 5 | a0001c0001t0004g0084 a0001c0002t0003g0157 a0002c0003t0006g0014 others(2): Show |
5 | HG00735.hp2 HG01109.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+8825T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72124624 | |||||||
chr5:72124862 | C | A | 3 | a0001c0002t0011g0153 a0001c0002t0014g0003 a0001c0002t0016g0152 |
4 | HG01884.hp1 HG02922.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+9063C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72124862 | |||||||
chr5:72124924 | G | T | 9 | a0001c0002t0002g0109 a0001c0002t0003g0006 a0001c0002t0003g0007 others(6): Show |
11 | HG01928.hp1 HG01943.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.286+9125G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72124924 | |||||||
chr5:72124956 | C | T | 1 | a0001c0001t0007g0119 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.286+9157C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72124956 | |||||||
chr5:72125160 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.286+9361C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72125160 | |||||||
chr5:72125204 | TAGG | T | 34 | a0001c0001t0001g0096 a0001c0001t0001g0123 a0001c0001t0001g0249 others(31): Show |
35 | HG00099.hp2 HG00408.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.286+9408_286+9410d others(5): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72125204 | ||||||
chr5:72125285 | T | C | 3 | a0001c0002t0002g0202 a0001c0002t0002g0204 a0001c0008t0002g0113 |
3 | HG00621.hp1 HG02132.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.286+9486T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72125285 | |||||||
chr5:72125658 | A | G | 2 | a0001c0001t0012g0311 a0001c0005t0001g0008 |
2 | HG01884.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.286+9859A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72125658 | |||||||
chr5:72125721 | A | AT | 133 | a0001c0001t0001g0027 a0001c0001t0001g0044 a0001c0001t0001g0066 others(130): Show |
137 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(134): Show |
intron_variant | MODIFIER | c.286+9923dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72125721 | ||||||
chr5:72125841 | G | A | 1 | a0001c0039t0018g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.286+10042G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72125841 | |||||||
chr5:72125880 | T | TAAGAATT others(308): Show |
1 | a0001c0001t0001g0198 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.286+10098_286+1009 others(319): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72125880 | ||||||
chr5:72125880 | T | TAAGAATT others(309): Show |
8 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0143 others(5): Show |
9 | HG02622.hp2 HG02897.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.286+10098_286+1009 others(320): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72125880 | ||||||
chr5:72125903 | A | G | 9 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0143 others(6): Show |
10 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+10104A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72125903 | |||||||
chr5:72126076 | C | G | 6 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0198 others(3): Show |
7 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+10277C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72126076 | |||||||
chr5:72126133 | G | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0143 others(6): Show |
10 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+10334G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72126133 | |||||||
chr5:72126181 | G | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0044 others(168): Show |
176 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(173): Show |
intron_variant | MODIFIER | c.286+10382G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72126181 | |||||||
chr5:72126275 | C | G | 9 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0143 others(6): Show |
10 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+10476C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72126275 | |||||||
chr5:72126338 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.286+10539G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72126338 | |||||||
chr5:72126359 | T | C | 152 | a0001c0001t0001g0027 a0001c0001t0001g0044 a0001c0001t0001g0066 others(149): Show |
156 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.286+10560T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72126359 | |||||||
chr5:72126361 | A | G | 1 | a0001c0001t0001g0333 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.286+10562A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72126361 | |||||||
chr5:72126525 | C | G | 2 | a0001c0001t0001g0143 a0005c0010t0005g0134 |
2 | HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.286+10726C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72126525 | |||||||
chr5:72126549 | A | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0143 others(8): Show |
12 | HG02486.hp2 HG02523.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.286+10750A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72126549 | |||||||
chr5:72126816 | C | A | 1 | a0001c0002t0003g0129 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.286+11017C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72126816 | |||||||
chr5:72126922 | T | C | 1 | a0003c0007t0002g0083 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.286+11123T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72126922 | |||||||
chr5:72127160 | T | C | 1 | a0001c0001t0002g0031 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.286+11361T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72127160 | |||||||
chr5:72127164 | G | A | 2 | a0001c0001t0002g0031 a0001c0005t0008g0033 |
2 | HG02523.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.286+11365G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72127164 | |||||||
chr5:72127172 | C | T | 4 | a0001c0001t0001g0096 a0001c0001t0001g0123 a0001c0001t0002g0146 others(1): Show |
4 | HG02738.hp2 HG03017.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+11373C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72127172 | |||||||
chr5:72127336 | T | C | 1 | a0001c0001t0020g0131 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.286+11537T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72127336 | |||||||
chr5:72127342 | T | G | 1 | a0001c0001t0001g0130 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.286+11543T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72127342 | |||||||
chr5:72127398 | A | G | 133 | a0001c0001t0001g0027 a0001c0001t0001g0044 a0001c0001t0001g0066 others(130): Show |
137 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(134): Show |
intron_variant | MODIFIER | c.286+11599A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72127398 | |||||||
chr5:72127414 | G | T | 9 | a0001c0001t0001g0333 a0001c0001t0001g0335 a0001c0004t0001g0334 others(6): Show |
9 | HG00741.hp1 HG00741.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.286+11615G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72127414 | |||||||
chr5:72127525 | A | G | 5 | a0001c0001t0004g0084 a0001c0002t0003g0157 a0002c0003t0006g0014 others(2): Show |
5 | HG00735.hp2 HG01109.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+11726A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72127525 | |||||||
chr5:72127599 | A | C | 9 | a0001c0001t0001g0074 a0001c0002t0002g0111 a0001c0005t0005g0046 others(6): Show |
9 | HG01074.hp2 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.286+11800A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72127599 | |||||||
chr5:72127741 | C | T | 2 | a0003c0007t0002g0098 a0003c0007t0002g0099 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.286+11942C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72127741 | |||||||
chr5:72127983 | G | A | 1 | a0001c0001t0002g0031 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.286+12184G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72127983 | |||||||
chr5:72128061 | A | C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0143 others(6): Show |
10 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+12262A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72128061 | |||||||
chr5:72128105 | C | T | 9 | a0001c0001t0001g0333 a0001c0001t0001g0335 a0001c0004t0001g0334 others(6): Show |
9 | HG00741.hp1 HG00741.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.286+12306C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72128105 | |||||||
chr5:72128178 | A | G | 1 | a0005c0010t0005g0329 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.286+12379A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72128178 | |||||||
chr5:72128408 | T | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0143 others(6): Show |
10 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+12609T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72128408 | |||||||
chr5:72128408 | TA | T | 153 | a0001c0001t0001g0027 a0001c0001t0001g0044 a0001c0001t0001g0066 others(150): Show |
157 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.286+12624delA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72128408 | ||||||
chr5:72128410 | A | T | 4 | a0001c0001t0001g0074 a0001c0001t0001g0219 a0001c0004t0001g0327 others(1): Show |
4 | HG03098.hp1 HG03209.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+12611A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72128410 | |||||||
chr5:72128420 | A | C | 1 | a0001c0001t0011g0108 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.286+12621A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72128420 | |||||||
chr5:72128664 | A | C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0143 others(6): Show |
10 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+12865A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72128664 | |||||||
chr5:72128834 | G | A | 15 | a0001c0001t0001g0066 a0001c0001t0001g0104 a0001c0001t0009g0238 others(12): Show |
15 | HG02135.hp1 NA18942.hp2 NA18943.hp1 others(12): Show |
intron_variant | MODIFIER | c.286+13035G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72128834 | |||||||
chr5:72128971 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.286+13172T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72128971 | |||||||
chr5:72129120 | TC | T | 3 | a0001c0002t0011g0153 a0001c0002t0014g0003 a0001c0002t0016g0152 |
4 | HG01884.hp1 HG02922.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+13323delC | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72129120 | ||||||
chr5:72129326 | T | C | 1 | a0001c0001t0012g0311 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286+13527T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72129326 | |||||||
chr5:72129384 | T | C | 3 | a0001c0001t0001g0182 a0001c0001t0004g0105 a0001c0022t0002g0149 |
3 | HG02602.hp1 HG03942.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.286+13585T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72129384 | |||||||
chr5:72129505 | C | T | 4 | a0001c0002t0003g0112 a0001c0002t0003g0203 a0001c0002t0013g0023 others(1): Show |
4 | HG00621.hp2 HG00673.hp2 HG02015.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+13706C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72129505 | |||||||
chr5:72129515 | C | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0143 others(6): Show |
10 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+13716C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72129515 | |||||||
chr5:72129530 | C | G | 2 | a0001c0001t0012g0311 a0001c0005t0001g0008 |
2 | HG01884.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.286+13731C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72129530 | |||||||
chr5:72129532 | A | G | 15 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0143 others(12): Show |
16 | HG02559.hp1 HG02559.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.286+13733A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72129532 | |||||||
chr5:72129547 | A | G | 40 | a0001c0001t0001g0117 a0001c0001t0001g0163 a0001c0001t0001g0274 others(37): Show |
41 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.286+13748A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72129547 | |||||||
chr5:72129555 | C | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0143 others(7): Show |
11 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.286+13756C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72129555 | |||||||
chr5:72129556 | T | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0143 others(7): Show |
11 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.286+13757T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72129556 | |||||||
chr5:72129657 | G | A | 1 | a0001c0001t0014g0094 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.286+13858G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72129657 | |||||||
chr5:72130098 | C | T | 9 | a0001c0001t0001g0333 a0001c0001t0001g0335 a0001c0004t0001g0334 others(6): Show |
9 | HG00741.hp1 HG00741.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.286+14299C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72130098 | |||||||
chr5:72130125 | A | T | 5 | a0001c0001t0012g0034 a0001c0001t0012g0144 a0001c0005t0005g0220 others(2): Show |
5 | HG02559.hp1 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+14326A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72130125 | |||||||
chr5:72130146 | T | A | 2 | a0001c0001t0001g0249 a0001c0002t0003g0171 |
2 | NA18946.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.286+14347T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72130146 | |||||||
chr5:72130194 | A | AAC | 8 | a0001c0001t0001g0286 a0001c0002t0001g0302 a0001c0002t0003g0278 others(5): Show |
8 | HG00609.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.286+14396_286+1439 others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72130194 | ||||||
chr5:72130194 | A | AC | 277 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0027 others(274): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.286+14395_286+1439 others(5): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72130194 | |||||||
chr5:72130213 | C | T | 9 | a0001c0001t0001g0333 a0001c0001t0001g0335 a0001c0004t0001g0334 others(6): Show |
9 | HG00741.hp1 HG00741.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.286+14414C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72130213 | |||||||
chr5:72130219 | G | A | 1 | a0001c0004t0011g0323 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.286+14420G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72130219 | |||||||
chr5:72130268 | C | T | 3 | a0001c0002t0011g0153 a0001c0002t0014g0003 a0001c0002t0016g0152 |
4 | HG01884.hp1 HG02922.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+14469C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72130268 | |||||||
chr5:72130302 | A | G | 1 | a0001c0001t0001g0017 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.286+14503A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72130302 | |||||||
chr5:72130392 | T | A | 2 | a0001c0001t0012g0311 a0001c0005t0001g0008 |
2 | HG01884.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.286+14593T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72130392 | |||||||
chr5:72130507 | A | G | 1 | a0001c0001t0004g0251 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.286+14708A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72130507 | |||||||
chr5:72130637 | A | G | 148 | a0001c0001t0001g0027 a0001c0001t0001g0044 a0001c0001t0001g0074 others(145): Show |
152 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.286+14838A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72130637 | |||||||
chr5:72130704 | G | A | 11 | a0001c0001t0001g0074 a0001c0001t0007g0119 a0001c0002t0002g0040 others(8): Show |
11 | HG01074.hp2 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.286+14905G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72130704 | |||||||
chr5:72130818 | G | A | 332 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(329): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.286+15019G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72130818 | |||||||
chr5:72131042 | A | G | 3 | a0001c0001t0001g0130 a0001c0002t0003g0129 a0001c0004t0005g0107 |
3 | HG00733.hp2 NA18945.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.286+15243A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72131042 | |||||||
chr5:72131083 | G | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0143 others(6): Show |
10 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+15284G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72131083 | |||||||
chr5:72131125 | T | C | 1 | a0001c0001t0026g0201 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.286+15326T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72131125 | |||||||
chr5:72131187 | G | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0143 others(6): Show |
10 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+15388G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72131187 | |||||||
chr5:72131309 | T | G | 3 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0039t0018g0016 |
3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+15510T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72131309 | |||||||
chr5:72131674 | G | A | 3 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0039t0018g0016 |
3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+15875G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72131674 | |||||||
chr5:72131818 | C | T | 11 | a0001c0001t0001g0074 a0001c0001t0007g0119 a0001c0002t0002g0040 others(8): Show |
11 | HG01074.hp2 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.286+16019C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72131818 | |||||||
chr5:72131896 | G | A | 1 | a0001c0005t0021g0136 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.286+16097G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72131896 | |||||||
chr5:72131957 | T | C | 9 | a0001c0001t0001g0333 a0001c0001t0001g0335 a0001c0004t0001g0334 others(6): Show |
9 | HG00741.hp1 HG00741.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.286+16158T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72131957 | |||||||
chr5:72132082 | A | G | 131 | a0001c0001t0001g0027 a0001c0001t0001g0044 a0001c0001t0001g0074 others(128): Show |
134 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.286+16283A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72132082 | |||||||
chr5:72132345 | C | T | 3 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0039t0018g0016 |
3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+16546C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72132345 | |||||||
chr5:72132467 | T | C | 2 | a0001c0006t0018g0071 a0011c0021t0036g0045 |
2 | HG02451.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.286+16668T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72132467 | |||||||
chr5:72132498 | G | A | 2 | a0001c0005t0005g0154 a0001c0005t0005g0257 |
2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.286+16699G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72132498 | |||||||
chr5:72132537 | A | G | 2 | a0001c0001t0012g0311 a0001c0005t0001g0008 |
2 | HG01884.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.286+16738A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72132537 | |||||||
chr5:72132699 | G | A | 8 | a0001c0001t0001g0145 a0001c0001t0005g0140 a0001c0001t0012g0048 others(5): Show |
8 | HG01243.hp1 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.286+16900G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72132699 | |||||||
chr5:72132858 | T | C | 1 | a0001c0005t0020g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.286+17059T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72132858 | |||||||
chr5:72132873 | T | C | 2 | a0001c0034t0005g0036 a0013c0035t0005g0047 |
2 | HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.286+17074T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72132873 | |||||||
chr5:72132964 | G | T | 7 | a0001c0001t0005g0140 a0001c0001t0012g0048 a0001c0001t0021g0268 others(4): Show |
7 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.286+17165G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72132964 | |||||||
chr5:72133319 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.286+17520C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72133319 | |||||||
chr5:72133358 | C | T | 3 | a0001c0001t0012g0311 a0001c0005t0001g0008 a0002c0003t0006g0170 |
3 | HG01884.hp2 HG02004.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.286+17559C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72133358 | |||||||
chr5:72133396 | C | A | 1 | a0001c0001t0005g0140 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.286+17597C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72133396 | |||||||
chr5:72133696 | T | A | 3 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0039t0018g0016 |
3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+17897T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72133696 | |||||||
chr5:72133733 | T | C | 1 | a0001c0004t0007g0141 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.286+17934T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72133733 | |||||||
chr5:72133764 | G | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0143 others(6): Show |
10 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+17965G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72133764 | |||||||
chr5:72133874 | G | A | 3 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0039t0018g0016 |
3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+18075G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72133874 | |||||||
chr5:72133935 | A | C | 3 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0039t0018g0016 |
3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+18136A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72133935 | |||||||
chr5:72134016 | C | T | 3 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0039t0018g0016 |
3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+18217C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72134016 | |||||||
chr5:72134102 | G | A | 3 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0039t0018g0016 |
3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+18303G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72134102 | |||||||
chr5:72134330 | T | C | 3 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0039t0018g0016 |
3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+18531T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72134330 | |||||||
chr5:72134345 | G | T | 1 | a0001c0001t0012g0048 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.286+18546G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72134345 | |||||||
chr5:72134410 | T | C | 329 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(326): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.286+18611T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72134410 | |||||||
chr5:72134410 | T | G | 2 | a0001c0001t0001g0219 a0001c0004t0001g0327 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.286+18611T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72134410 | |||||||
chr5:72134515 | TAAG | T | 117 | a0001c0001t0001g0027 a0001c0001t0001g0044 a0001c0001t0001g0074 others(114): Show |
120 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.286+18722_286+1872 others(7): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72134515 | ||||||
chr5:72134548 | C | T | 3 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0039t0018g0016 |
3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+18749C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72134548 | |||||||
chr5:72134590 | A | T | 1 | a0001c0006t0007g0262 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.286+18791A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72134590 | |||||||
chr5:72134795 | A | G | 3 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0039t0018g0016 |
3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+18996A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72134795 | |||||||
chr5:72134806 | G | T | 3 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0039t0018g0016 |
3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+19007G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72134806 | |||||||
chr5:72135068 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0027 others(162): Show |
170 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.286+19269G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72135068 | |||||||
chr5:72135106 | A | G | 38 | a0001c0001t0001g0096 a0001c0001t0001g0123 a0001c0001t0001g0249 others(35): Show |
39 | HG00099.hp2 HG00408.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.286+19307A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72135106 | |||||||
chr5:72135140 | C | A | 3 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0039t0018g0016 |
3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+19341C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72135140 | |||||||
chr5:72135397 | G | C | 3 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0039t0018g0016 |
3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+19598G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72135397 | |||||||
chr5:72135401 | T | G | 1 | a0001c0001t0001g0184 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.286+19602T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72135401 | |||||||
chr5:72135614 | A | T | 3 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0039t0018g0016 |
3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+19815A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72135614 | |||||||
chr5:72135708 | T | TGAAAAAG others(312): Show |
1 | a0001c0001t0012g0057 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.286+19921_286+1992 others(323): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72135708 | ||||||
chr5:72135708 | T | TGAAAAAG others(313): Show |
2 | a0001c0001t0012g0056 a0001c0039t0018g0016 |
2 | HG02486.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.286+19921_286+1992 others(324): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72135708 | ||||||
chr5:72135844 | T | C | 1 | a0001c0002t0002g0059 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.286+20045T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72135844 | |||||||
chr5:72135889 | G | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0027 others(155): Show |
163 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(160): Show |
intron_variant | MODIFIER | c.286+20090G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72135889 | |||||||
chr5:72135952 | T | A | 1 | a0001c0002t0003g0306 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.286+20153T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72135952 | |||||||
chr5:72136069 | C | T | 1 | a0001c0001t0004g0250 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.286+20270C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72136069 | |||||||
chr5:72136106 | T | C | 1 | a0001c0004t0015g0185 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.286+20307T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72136106 | |||||||
chr5:72136344 | T | C | 3 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0039t0018g0016 |
3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+20545T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72136344 | |||||||
chr5:72136393 | A | G | 15 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0143 others(12): Show |
16 | HG01884.hp2 HG02486.hp2 HG02523.hp2 others(13): Show |
intron_variant | MODIFIER | c.286+20594A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72136393 | |||||||
chr5:72136396 | C | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0143 others(8): Show |
12 | HG01884.hp2 HG02572.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.286+20597C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72136396 | |||||||
chr5:72136870 | C | T | 2 | a0001c0001t0001g0219 a0001c0004t0001g0327 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.286+21071C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72136870 | |||||||
chr5:72137163 | A | G | 3 | a0001c0002t0011g0153 a0001c0002t0014g0003 a0001c0002t0016g0152 |
4 | HG01884.hp1 HG02922.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+21364A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72137163 | |||||||
chr5:72137456 | G | C | 1 | a0001c0002t0032g0273 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.286+21657G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72137456 | |||||||
chr5:72137511 | A | G | 2 | a0001c0001t0001g0219 a0001c0004t0001g0327 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.286+21712A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72137511 | |||||||
chr5:72137615 | C | T | 3 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0039t0018g0016 |
3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+21816C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72137615 | |||||||
chr5:72137777 | C | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0143 others(6): Show |
10 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.286+21978C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72137777 | |||||||
chr5:72138483 | C | A | 2 | a0001c0034t0005g0036 a0013c0035t0005g0047 |
2 | HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.286+22684C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72138483 | |||||||
chr5:72138487 | C | T | 2 | a0001c0001t0012g0311 a0001c0005t0001g0008 |
2 | HG01884.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.286+22688C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72138487 | |||||||
chr5:72138674 | G | A | 3 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0039t0018g0016 |
3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+22875G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72138674 | |||||||
chr5:72138724 | T | C | 1 | a0001c0001t0002g0031 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.286+22925T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72138724 | |||||||
chr5:72139494 | A | G | 2 | a0001c0034t0005g0036 a0013c0035t0005g0047 |
2 | HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.286+23695A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72139494 | |||||||
chr5:72139508 | C | T | 1 | a0001c0002t0003g0121 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.286+23709C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72139508 | |||||||
chr5:72139509 | G | A | 1 | a0005c0010t0005g0329 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.286+23710G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72139509 | |||||||
chr5:72139526 | C | T | 2 | a0001c0001t0004g0028 a0001c0001t0004g0321 |
2 | HG01934.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.286+23727C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72139526 | |||||||
chr5:72139678 | G | T | 3 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0039t0018g0016 |
3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+23879G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72139678 | |||||||
chr5:72139747 | T | C | 130 | a0001c0001t0001g0027 a0001c0001t0001g0044 a0001c0001t0001g0074 others(127): Show |
133 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.286+23948T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72139747 | |||||||
chr5:72139868 | C | T | 3 | a0001c0001t0001g0283 a0001c0002t0002g0026 a0014c0027t0010g0234 |
3 | NA18960.hp1 NA19060.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.286+24069C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72139868 | |||||||
chr5:72139966 | C | CT | 9 | a0001c0001t0001g0017 a0001c0001t0001g0249 a0001c0001t0007g0269 others(6): Show |
9 | HG00642.hp1 HG01167.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.286+24180dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72139966 | ||||||
chr5:72139988 | G | T | 3 | a0001c0001t0004g0025 a0001c0001t0004g0250 a0001c0001t0004g0251 |
3 | HG01192.hp2 HG04199.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.286+24189G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72139988 | |||||||
chr5:72140024 | C | A | 1 | a0001c0001t0001g0017 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.286+24225C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72140024 | |||||||
chr5:72140024 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.286+24225C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72140024 | |||||||
chr5:72140333 | A | G | 1 | a0001c0001t0001g0333 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.286+24534A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72140333 | |||||||
chr5:72140432 | G | C | 1 | a0001c0002t0002g0186 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.286+24633G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72140432 | |||||||
chr5:72140527 | G | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0027 others(155): Show |
163 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(160): Show |
intron_variant | MODIFIER | c.286+24728G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72140527 | |||||||
chr5:72140564 | A | G | 1 | a0005c0010t0005g0329 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.286+24765A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72140564 | |||||||
chr5:72140897 | G | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0198 others(3): Show |
7 | HG02622.hp2 HG02818.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+25098G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72140897 | |||||||
chr5:72140923 | A | T | 1 | a0001c0001t0001g0284 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.286+25124A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72140923 | |||||||
chr5:72141028 | C | G | 1 | a0005c0010t0005g0329 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.286+25229C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72141028 | |||||||
chr5:72141035 | A | G | 9 | a0001c0001t0001g0333 a0001c0001t0001g0335 a0001c0004t0001g0334 others(6): Show |
9 | HG00741.hp1 HG00741.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.286+25236A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72141035 | |||||||
chr5:72141231 | C | G | 6 | a0001c0001t0001g0066 a0001c0001t0001g0104 a0001c0002t0002g0065 others(3): Show |
6 | NA18942.hp2 NA18943.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+25432C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72141231 | |||||||
chr5:72141266 | G | C | 1 | a0002c0003t0006g0161 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.286+25467G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72141266 | |||||||
chr5:72141435 | A | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0044 others(188): Show |
197 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(194): Show |
intron_variant | MODIFIER | c.286+25636A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72141435 | |||||||
chr5:72141641 | C | G | 8 | a0001c0001t0001g0286 a0001c0002t0001g0302 a0001c0002t0003g0278 others(5): Show |
8 | HG00609.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.286+25842C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72141641 | |||||||
chr5:72142054 | C | T | 1 | a0017c0033t0009g0233 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.286+26255C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72142054 | |||||||
chr5:72142222 | A | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0114 others(104): Show |
109 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.286+26423A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72142222 | |||||||
chr5:72142409 | C | T | 19 | a0001c0001t0001g0044 a0001c0001t0002g0188 a0001c0002t0002g0109 others(16): Show |
21 | HG00558.hp1 HG01928.hp1 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.286+26610C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72142409 | |||||||
chr5:72142610 | G | A | 1 | a0001c0022t0002g0149 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.286+26811G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72142610 | |||||||
chr5:72142641 | A | G | 2 | a0001c0001t0002g0072 a0001c0001t0015g0116 |
2 | HG00408.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.286+26842A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72142641 | |||||||
chr5:72142651 | A | G | 1 | a0001c0001t0002g0031 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.286+26852A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72142651 | |||||||
chr5:72142678 | A | T | 4 | a0001c0005t0008g0135 a0001c0005t0008g0252 a0004c0011t0001g0253 others(1): Show |
4 | HG02647.hp1 HG02647.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+26879A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72142678 | |||||||
chr5:72142731 | T | TA | 11 | a0001c0001t0002g0072 a0001c0001t0004g0212 a0001c0001t0015g0116 others(8): Show |
11 | HG00408.hp1 HG00733.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.286+26945dupA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72142731 | ||||||
chr5:72142829 | G | C | 5 | a0001c0001t0012g0311 a0001c0005t0008g0135 a0001c0005t0008g0252 others(2): Show |
5 | HG02572.hp1 HG02647.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+27030G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72142829 | |||||||
chr5:72142985 | T | C | 2 | a0001c0034t0005g0036 a0013c0035t0005g0047 |
2 | HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.286+27186T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72142985 | |||||||
chr5:72143109 | T | C | 4 | a0001c0005t0008g0135 a0001c0005t0008g0252 a0004c0011t0001g0253 others(1): Show |
4 | HG02647.hp1 HG02647.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+27310T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72143109 | |||||||
chr5:72143141 | A | G | 2 | a0001c0001t0004g0100 a0001c0001t0004g0250 |
2 | HG03710.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.286+27342A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72143141 | |||||||
chr5:72143349 | C | A | 7 | a0001c0001t0005g0140 a0001c0001t0007g0269 a0001c0001t0015g0124 others(4): Show |
7 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+27550C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72143349 | |||||||
chr5:72143436 | C | G | 3 | a0001c0005t0008g0041 a0007c0013t0001g0126 a0007c0013t0029g0127 |
3 | HG00741.hp2 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.286+27637C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72143436 | |||||||
chr5:72143447 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.286+27648C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72143447 | |||||||
chr5:72143560 | G | A | 4 | a0001c0005t0008g0135 a0001c0005t0008g0252 a0004c0011t0001g0253 others(1): Show |
4 | HG02647.hp1 HG02647.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+27761G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72143560 | |||||||
chr5:72143658 | A | G | 2 | a0001c0034t0005g0036 a0013c0035t0005g0047 |
2 | HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.286+27859A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72143658 | |||||||
chr5:72143673 | G | T | 1 | a0001c0001t0012g0311 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286+27874G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72143673 | |||||||
chr5:72143860 | TA | T | 10 | a0001c0001t0001g0219 a0001c0001t0001g0335 a0001c0004t0001g0327 others(7): Show |
10 | HG00741.hp1 HG00741.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.286+28062delA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72143860 | |||||||
chr5:72143933 | G | A | 1 | a0001c0002t0003g0106 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.286+28134G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72143933 | |||||||
chr5:72144067 | A | G | 12 | a0001c0001t0001g0145 a0001c0001t0001g0266 a0001c0001t0012g0048 others(9): Show |
12 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.286+28268A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144067 | |||||||
chr5:72144103 | A | C | 71 | a0001c0001t0001g0017 a0001c0001t0001g0074 a0001c0001t0001g0114 others(68): Show |
71 | HG00099.hp1 HG00621.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.286+28304A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144103 | |||||||
chr5:72144304 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.286+28505G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144304 | |||||||
chr5:72144328 | G | A | 14 | a0001c0001t0001g0086 a0001c0001t0001g0181 a0001c0001t0010g0010 others(11): Show |
14 | HG00558.hp2 HG00639.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.286+28529G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144328 | |||||||
chr5:72144329 | C | T | 4 | a0001c0005t0008g0135 a0001c0005t0008g0252 a0004c0011t0001g0253 others(1): Show |
4 | HG02647.hp1 HG02647.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+28530C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144329 | |||||||
chr5:72144374 | C | T | 4 | a0001c0001t0004g0212 a0001c0002t0002g0312 a0001c0009t0001g0328 others(1): Show |
4 | HG01358.hp2 HG01433.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+28575C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144374 | |||||||
chr5:72144429 | T | G | 1 | a0001c0002t0003g0173 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.286+28630T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144429 | |||||||
chr5:72144480 | A | C | 1 | a0001c0001t0020g0131 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.286+28681A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144480 | |||||||
chr5:72144550 | C | T | 2 | a0001c0002t0002g0040 a0001c0002t0002g0160 |
2 | HG01109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.286+28751C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144550 | |||||||
chr5:72144607 | C | A | 1 | a0001c0002t0002g0095 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.286+28808C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144607 | |||||||
chr5:72144699 | G | A | 4 | a0001c0001t0012g0034 a0001c0001t0012g0144 a0001c0005t0005g0220 others(1): Show |
4 | HG02559.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+28900G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144699 | |||||||
chr5:72144758 | G | A | 3 | a0001c0002t0011g0153 a0001c0002t0014g0003 a0001c0002t0016g0152 |
4 | HG01884.hp1 HG02922.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+28959G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144758 | |||||||
chr5:72144789 | T | C | 12 | a0001c0001t0005g0140 a0001c0001t0007g0269 a0001c0001t0012g0311 others(9): Show |
12 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.286+28990T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144789 | |||||||
chr5:72144848 | G | T | 12 | a0001c0001t0005g0140 a0001c0001t0007g0269 a0001c0001t0012g0311 others(9): Show |
12 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.286+29049G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144848 | |||||||
chr5:72144887 | A | G | 2 | a0001c0034t0005g0036 a0013c0035t0005g0047 |
2 | HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.286+29088A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72144887 | |||||||
chr5:72145307 | G | A | 1 | a0001c0002t0031g0206 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.286+29508G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72145307 | |||||||
chr5:72145374 | TA | T | 15 | a0001c0001t0004g0212 a0001c0001t0005g0140 a0001c0001t0007g0269 others(12): Show |
15 | HG01358.hp2 HG01433.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.286+29587delA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72145374 | ||||||
chr5:72145411 | T | C | 1 | a0001c0001t0012g0012 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.286+29612T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72145411 | |||||||
chr5:72145641 | A | T | 14 | a0001c0001t0001g0086 a0001c0001t0001g0181 a0001c0001t0010g0010 others(11): Show |
14 | HG00558.hp2 HG00639.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.286+29842A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72145641 | |||||||
chr5:72145736 | T | C | 1 | a0001c0002t0023g0142 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.286+29937T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72145736 | |||||||
chr5:72145762 | T | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0074 others(134): Show |
139 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(136): Show |
intron_variant | MODIFIER | c.286+29963T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72145762 | |||||||
chr5:72145847 | G | T | 14 | a0001c0001t0001g0086 a0001c0001t0001g0181 a0001c0001t0010g0010 others(11): Show |
14 | HG00558.hp2 HG00639.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.286+30048G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72145847 | |||||||
chr5:72145873 | G | A | 16 | a0001c0001t0004g0212 a0001c0001t0005g0140 a0001c0001t0007g0269 others(13): Show |
16 | HG01358.hp2 HG01433.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.286+30074G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72145873 | |||||||
chr5:72145886 | C | T | 15 | a0001c0001t0004g0212 a0001c0001t0005g0140 a0001c0001t0007g0269 others(12): Show |
15 | HG01358.hp2 HG01433.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.286+30087C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72145886 | |||||||
chr5:72146418 | T | C | 12 | a0001c0001t0001g0272 a0001c0002t0003g0015 a0001c0002t0003g0061 others(9): Show |
12 | HG00621.hp2 HG00673.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.286+30619T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72146418 | |||||||
chr5:72146680 | A | G | 1 | a0001c0001t0039g0022 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.286+30881A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72146680 | |||||||
chr5:72146861 | G | C | 1 | a0001c0001t0002g0031 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.286+31062G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72146861 | |||||||
chr5:72146961 | C | CT | 15 | a0001c0001t0001g0086 a0001c0001t0001g0181 a0001c0001t0010g0010 others(12): Show |
15 | HG00558.hp2 HG00639.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.286+31180dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72146961 | ||||||
chr5:72146961 | CT | C | 7 | a0001c0001t0001g0017 a0001c0001t0002g0031 a0001c0001t0005g0155 others(4): Show |
7 | HG00642.hp1 HG01070.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.286+31180delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72146961 | ||||||
chr5:72147182 | T | C | 3 | a0001c0001t0001g0009 a0001c0002t0001g0199 a0001c0002t0002g0200 |
3 | HG02155.hp2 NA18612.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.286+31383T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72147182 | |||||||
chr5:72147248 | C | T | 2 | a0001c0001t0001g0309 a0001c0002t0003g0172 |
2 | HG00140.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.286+31449C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72147248 | |||||||
chr5:72147389 | C | T | 4 | a0001c0001t0001g0143 a0001c0009t0007g0043 a0001c0028t0025g0042 others(1): Show |
4 | HG02886.hp2 HG03041.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+31590C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72147389 | |||||||
chr5:72147446 | A | G | 5 | a0001c0001t0001g0272 a0001c0002t0003g0015 a0001c0002t0003g0087 others(2): Show |
5 | HG01978.hp1 HG01981.hp1 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+31647A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72147446 | |||||||
chr5:72147484 | G | T | 1 | a0001c0005t0008g0033 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.286+31685G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72147484 | |||||||
chr5:72147501 | G | A | 1 | a0003c0007t0002g0083 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.286+31702G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72147501 | |||||||
chr5:72147588 | G | A | 1 | a0001c0001t0012g0311 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286+31789G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72147588 | |||||||
chr5:72147606 | C | T | 1 | a0001c0002t0002g0216 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.286+31807C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72147606 | |||||||
chr5:72147783 | G | A | 1 | a0001c0038t0013g0024 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.286+31984G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72147783 | |||||||
chr5:72147795 | T | C | 2 | a0001c0034t0005g0036 a0013c0035t0005g0047 |
2 | HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.286+31996T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72147795 | |||||||
chr5:72148064 | A | G | 2 | a0001c0006t0007g0259 a0001c0020t0007g0260 |
2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.286+32265A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72148064 | |||||||
chr5:72148447 | CT | C | 3 | a0001c0001t0011g0279 a0001c0002t0002g0275 a0001c0008t0002g0280 |
3 | NA18747.hp1 NA19068.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.286+32652delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72148447 | ||||||
chr5:72148517 | T | G | 15 | a0001c0001t0004g0212 a0001c0001t0005g0140 a0001c0001t0007g0269 others(12): Show |
15 | HG01358.hp2 HG01433.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.286+32718T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72148517 | |||||||
chr5:72148559 | AG | A | 15 | a0001c0001t0004g0212 a0001c0001t0005g0140 a0001c0001t0007g0269 others(12): Show |
15 | HG01358.hp2 HG01433.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.286+32762delG | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72148559 | ||||||
chr5:72148698 | G | A | 1 | a0001c0005t0005g0128 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.286+32899G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72148698 | |||||||
chr5:72148722 | T | C | 2 | a0001c0006t0007g0259 a0001c0020t0007g0260 |
2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.286+32923T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72148722 | |||||||
chr5:72148769 | A | G | 15 | a0001c0001t0004g0212 a0001c0001t0005g0140 a0001c0001t0007g0269 others(12): Show |
15 | HG01358.hp2 HG01433.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.286+32970A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72148769 | |||||||
chr5:72148805 | C | T | 2 | a0001c0006t0007g0259 a0001c0020t0007g0260 |
2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.286+33006C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72148805 | |||||||
chr5:72148871 | C | T | 7 | a0001c0001t0005g0140 a0001c0001t0007g0269 a0001c0001t0015g0124 others(4): Show |
7 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+33072C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72148871 | |||||||
chr5:72149209 | A | G | 1 | a0001c0001t0005g0285 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.286+33410A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72149209 | |||||||
chr5:72149238 | G | A | 1 | a0001c0001t0012g0311 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286+33439G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72149238 | |||||||
chr5:72149419 | C | T | 16 | a0001c0001t0004g0212 a0001c0001t0005g0140 a0001c0001t0007g0269 others(13): Show |
16 | HG01358.hp2 HG01433.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.286+33620C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72149419 | |||||||
chr5:72149522 | A | G | 15 | a0001c0001t0004g0212 a0001c0001t0005g0140 a0001c0001t0007g0269 others(12): Show |
15 | HG01358.hp2 HG01433.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.286+33723A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72149522 | |||||||
chr5:72149633 | T | C | 1 | a0001c0002t0002g0204 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.286+33834T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72149633 | |||||||
chr5:72149874 | C | T | 7 | a0001c0001t0005g0140 a0001c0001t0007g0269 a0001c0001t0015g0124 others(4): Show |
7 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.287-33869C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72149874 | |||||||
chr5:72150112 | A | G | 1 | a0001c0001t0002g0031 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.287-33631A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72150112 | |||||||
chr5:72150164 | A | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0074 others(149): Show |
154 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(151): Show |
intron_variant | MODIFIER | c.287-33579A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72150164 | |||||||
chr5:72150254 | T | C | 15 | a0001c0001t0004g0212 a0001c0001t0005g0140 a0001c0001t0007g0269 others(12): Show |
15 | HG01358.hp2 HG01433.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.287-33489T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72150254 | |||||||
chr5:72150380 | C | T | 69 | a0001c0001t0001g0017 a0001c0001t0001g0074 a0001c0001t0001g0114 others(66): Show |
69 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.287-33363C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72150380 | |||||||
chr5:72150596 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.287-33147C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72150596 | |||||||
chr5:72150701 | G | A | 1 | a0001c0005t0008g0332 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.287-33042G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72150701 | |||||||
chr5:72150935 | G | A | 2 | a0001c0001t0007g0119 a0001c0005t0008g0110 |
2 | HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.287-32808G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72150935 | |||||||
chr5:72150979 | G | A | 7 | a0001c0001t0005g0140 a0001c0001t0007g0269 a0001c0001t0015g0124 others(4): Show |
7 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.287-32764G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72150979 | |||||||
chr5:72151049 | G | GT | 136 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0074 others(133): Show |
138 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.287-32694_287-3269 others(5): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72151049 | |||||||
chr5:72151080 | A | G | 2 | a0001c0002t0002g0075 a0001c0004t0007g0324 |
2 | HG01257.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.287-32663A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72151080 | |||||||
chr5:72151092 | G | A | 1 | a0001c0026t0008g0030 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.287-32651G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72151092 | |||||||
chr5:72151190 | A | G | 1 | a0001c0001t0002g0031 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.287-32553A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72151190 | |||||||
chr5:72151316 | A | G | 12 | a0001c0001t0005g0140 a0001c0001t0007g0269 a0001c0001t0012g0056 others(9): Show |
12 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.287-32427A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72151316 | |||||||
chr5:72151380 | G | A | 70 | a0001c0001t0001g0017 a0001c0001t0001g0074 a0001c0001t0001g0114 others(67): Show |
70 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.287-32363G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72151380 | |||||||
chr5:72151406 | T | G | 2 | a0001c0001t0002g0072 a0001c0001t0015g0116 |
2 | HG00408.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.287-32337T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72151406 | |||||||
chr5:72151441 | T | C | 1 | a0001c0002t0016g0152 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.287-32302T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72151441 | |||||||
chr5:72151584 | A | G | 3 | a0001c0002t0011g0153 a0001c0002t0014g0003 a0001c0002t0016g0152 |
4 | HG01884.hp1 HG02922.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-32159A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72151584 | |||||||
chr5:72151737 | T | A | 14 | a0001c0001t0001g0086 a0001c0001t0001g0181 a0001c0001t0010g0010 others(11): Show |
14 | HG00558.hp2 HG00639.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.287-32006T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72151737 | |||||||
chr5:72151798 | A | G | 11 | a0001c0001t0009g0238 a0001c0001t0009g0239 a0001c0001t0009g0240 others(8): Show |
11 | HG02486.hp2 HG02895.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.287-31945A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72151798 | |||||||
chr5:72151862 | T | A | 1 | a0001c0001t0002g0208 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.287-31881T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72151862 | |||||||
chr5:72151906 | A | G | 1 | a0001c0001t0012g0311 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.287-31837A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72151906 | |||||||
chr5:72151973 | G | A | 1 | a0001c0019t0040g0244 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.287-31770G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72151973 | |||||||
chr5:72152113 | G | C | 1 | a0001c0004t0010g0236 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.287-31630G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152113 | |||||||
chr5:72152136 | T | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0074 others(149): Show |
154 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(151): Show |
intron_variant | MODIFIER | c.287-31607T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152136 | |||||||
chr5:72152176 | G | C | 11 | a0001c0001t0009g0238 a0001c0001t0009g0239 a0001c0001t0009g0240 others(8): Show |
11 | HG02486.hp2 HG02895.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.287-31567G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152176 | |||||||
chr5:72152178 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.287-31565A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152178 | |||||||
chr5:72152225 | G | A | 52 | a0001c0001t0001g0017 a0001c0001t0001g0114 a0001c0001t0001g0120 others(49): Show |
52 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.287-31518G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152225 | |||||||
chr5:72152237 | T | C | 1 | a0001c0005t0008g0033 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.287-31506T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152237 | |||||||
chr5:72152343 | C | T | 1 | a0001c0002t0002g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.287-31400C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152343 | |||||||
chr5:72152485 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.287-31258C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152485 | |||||||
chr5:72152508 | G | T | 2 | a0001c0001t0001g0143 a0005c0010t0005g0134 |
2 | HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.287-31235G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152508 | |||||||
chr5:72152539 | T | C | 2 | a0001c0001t0001g0286 a0001c0002t0003g0278 |
2 | NA18984.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.287-31204T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152539 | |||||||
chr5:72152541 | G | A | 1 | a0001c0005t0008g0035 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.287-31202G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152541 | |||||||
chr5:72152617 | C | A | 1 | a0001c0001t0001g0333 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.287-31126C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152617 | |||||||
chr5:72152760 | T | C | 23 | a0001c0001t0001g0086 a0001c0001t0001g0181 a0001c0001t0004g0028 others(20): Show |
23 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.287-30983T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152760 | |||||||
chr5:72152810 | T | A | 2 | a0001c0009t0001g0062 a0001c0009t0001g0063 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.287-30933T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152810 | |||||||
chr5:72152890 | C | T | 11 | a0001c0001t0009g0238 a0001c0001t0009g0239 a0001c0001t0009g0240 others(8): Show |
11 | HG02486.hp2 HG02895.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.287-30853C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152890 | |||||||
chr5:72152921 | G | A | 4 | a0001c0001t0004g0025 a0001c0001t0004g0100 a0001c0001t0004g0250 others(1): Show |
4 | HG01192.hp2 HG03710.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-30822G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72152921 | |||||||
chr5:72153255 | A | G | 3 | a0001c0001t0001g0333 a0001c0034t0005g0036 a0013c0035t0005g0047 |
3 | HG02818.hp1 HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.287-30488A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72153255 | |||||||
chr5:72153278 | G | C | 22 | a0001c0001t0001g0086 a0001c0001t0001g0181 a0001c0001t0004g0028 others(19): Show |
22 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.287-30465G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72153278 | |||||||
chr5:72153431 | G | T | 4 | a0001c0002t0002g0059 a0001c0018t0001g0080 a0006c0012t0002g0313 others(1): Show |
4 | NA18966.hp1 NA18971.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-30312G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72153431 | |||||||
chr5:72153520 | G | T | 4 | a0003c0007t0002g0097 a0003c0007t0002g0098 a0003c0007t0002g0099 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-30223G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72153520 | |||||||
chr5:72153537 | G | A | 1 | a0001c0002t0002g0312 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.287-30206G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72153537 | |||||||
chr5:72153903 | TAA | T | 8 | a0001c0001t0009g0238 a0001c0001t0009g0239 a0001c0001t0009g0240 others(5): Show |
8 | NA18943.hp1 NA18955.hp1 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-29831_287-2983 others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72153903 | ||||||
chr5:72154097 | A | G | 8 | a0001c0001t0009g0238 a0001c0001t0009g0239 a0001c0001t0009g0240 others(5): Show |
8 | NA18943.hp1 NA18955.hp1 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-29646A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72154097 | |||||||
chr5:72154118 | G | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0074 others(129): Show |
134 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.287-29625G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72154118 | |||||||
chr5:72154163 | C | T | 2 | a0001c0001t0012g0056 a0001c0001t0012g0057 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.287-29580C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72154163 | |||||||
chr5:72154188 | T | C | 22 | a0001c0001t0001g0074 a0001c0001t0001g0143 a0001c0001t0004g0212 others(19): Show |
22 | HG01074.hp2 HG01358.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.287-29555T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72154188 | |||||||
chr5:72154331 | C | T | 1 | a0001c0001t0002g0031 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.287-29412C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72154331 | |||||||
chr5:72154352 | C | A | 22 | a0001c0001t0001g0086 a0001c0001t0001g0181 a0001c0001t0004g0028 others(19): Show |
22 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.287-29391C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72154352 | |||||||
chr5:72154605 | AC | A | 3 | a0001c0005t0008g0135 a0001c0005t0008g0252 a0004c0011t0001g0253 |
3 | HG02647.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.287-29137delC | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72154605 | |||||||
chr5:72154766 | T | C | 4 | a0001c0001t0012g0311 a0001c0001t0015g0124 a0001c0001t0020g0131 others(1): Show |
4 | HG02145.hp2 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-28977T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72154766 | |||||||
chr5:72154931 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.287-28812A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72154931 | |||||||
chr5:72154948 | G | A | 28 | a0001c0001t0001g0086 a0001c0001t0001g0181 a0001c0001t0004g0028 others(25): Show |
28 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.287-28795G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72154948 | |||||||
chr5:72155085 | C | T | 35 | a0001c0001t0001g0086 a0001c0001t0001g0181 a0001c0001t0001g0219 others(32): Show |
35 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.287-28658C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72155085 | |||||||
chr5:72155128 | A | G | 27 | a0001c0001t0001g0086 a0001c0001t0001g0181 a0001c0001t0004g0028 others(24): Show |
27 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.287-28615A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72155128 | |||||||
chr5:72155333 | C | T | 209 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0053 others(206): Show |
212 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.287-28410C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72155333 | |||||||
chr5:72155348 | A | G | 46 | a0001c0001t0001g0086 a0001c0001t0001g0143 a0001c0001t0001g0181 others(43): Show |
46 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.287-28395A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72155348 | |||||||
chr5:72155383 | C | T | 33 | a0001c0001t0001g0086 a0001c0001t0001g0181 a0001c0001t0001g0219 others(30): Show |
33 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.287-28360C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72155383 | |||||||
chr5:72155599 | C | T | 2 | a0001c0006t0007g0259 a0001c0020t0007g0260 |
2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.287-28144C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72155599 | |||||||
chr5:72155654 | A | G | 1 | a0001c0004t0015g0271 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.287-28089A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72155654 | |||||||
chr5:72155693 | T | C | 287 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0053 others(284): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.287-28050T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72155693 | |||||||
chr5:72155766 | C | CT | 23 | a0001c0001t0001g0017 a0001c0001t0001g0316 a0001c0001t0001g0317 others(20): Show |
25 | HG00642.hp1 HG01099.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.287-27959dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72155766 | ||||||
chr5:72155766 | C | CTT | 40 | a0001c0001t0001g0114 a0001c0001t0001g0120 a0001c0001t0001g0159 others(37): Show |
40 | HG00099.hp1 HG00621.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.287-27960_287-2795 others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72155766 | ||||||
chr5:72155766 | C | CTTT | 7 | a0001c0001t0001g0197 a0001c0002t0001g0081 a0001c0004t0034g0215 others(4): Show |
7 | HG01928.hp2 HG01934.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.287-27961_287-2795 others(7): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72155766 | ||||||
chr5:72155766 | CT | C | 36 | a0001c0001t0001g0086 a0001c0001t0001g0143 a0001c0001t0001g0181 others(33): Show |
36 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.287-27959delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72155766 | ||||||
chr5:72155770 | T | TC | 13 | a0001c0001t0001g0074 a0001c0001t0007g0119 a0001c0002t0002g0111 others(10): Show |
13 | HG01074.hp2 HG02109.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.287-27973_287-2797 others(5): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72155770 | |||||||
chr5:72155799 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0114 others(85): Show |
90 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.287-27944C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72155799 | |||||||
chr5:72155881 | C | T | 7 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0001t0012g0311 others(4): Show |
7 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.287-27862C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72155881 | |||||||
chr5:72155995 | G | T | 3 | a0001c0001t0011g0279 a0001c0002t0002g0275 a0001c0008t0002g0280 |
3 | NA18747.hp1 NA19068.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.287-27748G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72155995 | |||||||
chr5:72156052 | C | G | 1 | a0001c0002t0002g0004 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.287-27691C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72156052 | |||||||
chr5:72156267 | G | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0053 others(229): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.287-27476G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72156267 | |||||||
chr5:72156275 | A | G | 8 | a0001c0001t0009g0238 a0001c0001t0009g0239 a0001c0001t0009g0240 others(5): Show |
8 | NA18943.hp1 NA18955.hp1 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-27468A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72156275 | |||||||
chr5:72156318 | G | A | 2 | a0001c0001t0012g0311 a0001c0001t0020g0131 |
2 | HG02559.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.287-27425G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72156318 | |||||||
chr5:72156423 | G | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0053 others(282): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.287-27320G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72156423 | |||||||
chr5:72156735 | G | T | 8 | a0001c0001t0009g0238 a0001c0001t0009g0239 a0001c0001t0009g0240 others(5): Show |
8 | NA18943.hp1 NA18955.hp1 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-27008G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72156735 | |||||||
chr5:72156753 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.287-26990C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72156753 | |||||||
chr5:72156998 | C | G | 1 | a0001c0001t0001g0333 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.287-26745C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72156998 | |||||||
chr5:72157021 | T | A | 2 | a0001c0001t0004g0028 a0001c0001t0004g0321 |
2 | HG01934.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.287-26722T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72157021 | |||||||
chr5:72157519 | C | G | 1 | a0001c0002t0003g0318 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.287-26224C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72157519 | |||||||
chr5:72157520 | G | A | 4 | a0001c0001t0001g0009 a0001c0002t0001g0199 a0001c0002t0002g0200 others(1): Show |
4 | HG02155.hp2 NA18612.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-26223G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72157520 | |||||||
chr5:72157574 | C | G | 2 | a0001c0006t0018g0038 a0001c0006t0022g0039 |
2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.287-26169C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72157574 | |||||||
chr5:72157959 | C | T | 1 | a0001c0002t0002g0202 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.287-25784C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72157959 | |||||||
chr5:72157987 | C | T | 1 | a0001c0001t0019g0246 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.287-25756C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72157987 | |||||||
chr5:72158006 | A | AT | 12 | a0001c0001t0001g0017 a0001c0001t0001g0044 a0001c0001t0001g0187 others(9): Show |
13 | HG00642.hp1 HG01109.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.287-25716dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72158006 | ||||||
chr5:72158006 | A | ATTT | 7 | a0001c0001t0009g0239 a0001c0001t0009g0240 a0001c0001t0014g0093 others(4): Show |
7 | NA18943.hp1 NA18955.hp1 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.287-25718_287-2571 others(7): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72158006 | ||||||
chr5:72158006 | AT | A | 51 | a0001c0001t0001g0086 a0001c0001t0001g0114 a0001c0001t0001g0181 others(48): Show |
51 | HG00558.hp2 HG00639.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.287-25716delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72158006 | ||||||
chr5:72158006 | ATT | A | 198 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0066 others(195): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.287-25717_287-2571 others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72158006 | ||||||
chr5:72158122 | C | T | 10 | a0001c0001t0001g0143 a0001c0001t0012g0056 a0001c0001t0012g0057 others(7): Show |
10 | HG02145.hp2 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.287-25621C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158122 | |||||||
chr5:72158233 | A | G | 2 | a0001c0006t0007g0259 a0001c0020t0007g0260 |
2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.287-25510A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158233 | |||||||
chr5:72158324 | T | C | 2 | a0001c0001t0001g0219 a0001c0004t0001g0327 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.287-25419T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158324 | |||||||
chr5:72158348 | T | C | 244 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0066 others(241): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.287-25395T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158348 | |||||||
chr5:72158360 | A | T | 1 | a0001c0001t0001g0017 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.287-25383A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158360 | |||||||
chr5:72158373 | A | G | 19 | a0001c0001t0001g0074 a0001c0001t0007g0119 a0001c0001t0009g0238 others(16): Show |
19 | HG01074.hp2 HG02109.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.287-25370A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158373 | |||||||
chr5:72158442 | G | A | 244 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0066 others(241): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.287-25301G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158442 | |||||||
chr5:72158445 | G | A | 1 | a0001c0002t0001g0148 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.287-25298G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158445 | |||||||
chr5:72158456 | A | G | 8 | a0001c0001t0009g0238 a0001c0001t0009g0239 a0001c0001t0009g0240 others(5): Show |
8 | NA18943.hp1 NA18955.hp1 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-25287A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158456 | |||||||
chr5:72158476 | A | G | 10 | a0001c0001t0001g0219 a0001c0001t0002g0031 a0001c0004t0001g0327 others(7): Show |
10 | HG00741.hp2 HG02523.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.287-25267A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158476 | |||||||
chr5:72158484 | T | C | 1 | a0001c0001t0015g0124 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.287-25259T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158484 | |||||||
chr5:72158510 | G | T | 1 | a0001c0001t0026g0201 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.287-25233G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158510 | |||||||
chr5:72158684 | T | C | 2 | a0001c0001t0012g0056 a0001c0001t0012g0057 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.287-25059T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158684 | |||||||
chr5:72158719 | C | T | 14 | a0001c0001t0001g0086 a0001c0001t0001g0181 a0001c0001t0010g0010 others(11): Show |
14 | HG00558.hp2 HG00639.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.287-25024C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158719 | |||||||
chr5:72158881 | T | C | 1 | a0001c0002t0002g0202 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.287-24862T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158881 | |||||||
chr5:72158955 | A | G | 2 | a0001c0001t0001g0143 a0005c0010t0005g0134 |
2 | HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.287-24788A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158955 | |||||||
chr5:72158956 | C | T | 231 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0066 others(228): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.287-24787C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72158956 | |||||||
chr5:72159087 | T | C | 5 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0034t0005g0036 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.287-24656T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72159087 | |||||||
chr5:72159433 | CAGAT | C | 241 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0066 others(238): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.287-24303_287-2430 others(8): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72159433 | ||||||
chr5:72159447 | A | G | 193 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0066 others(190): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.287-24296A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72159447 | |||||||
chr5:72159706 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0123 |
2 | HG03491.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.287-24037A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72159706 | |||||||
chr5:72159761 | C | T | 8 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0001t0012g0311 others(5): Show |
8 | HG02145.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.287-23982C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72159761 | |||||||
chr5:72159781 | C | A | 1 | a0001c0004t0034g0215 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.287-23962C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72159781 | |||||||
chr5:72159791 | A | G | 209 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0066 others(206): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.287-23952A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72159791 | |||||||
chr5:72159927 | G | A | 234 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0066 others(231): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.287-23816G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72159927 | |||||||
chr5:72159927 | G | T | 7 | a0001c0001t0001g0219 a0001c0001t0002g0031 a0001c0004t0001g0327 others(4): Show |
7 | HG00741.hp2 HG02523.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.287-23816G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72159927 | |||||||
chr5:72159985 | G | A | 2 | a0001c0001t0001g0143 a0005c0010t0005g0134 |
2 | HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.287-23758G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72159985 | |||||||
chr5:72160120 | C | T | 2 | a0001c0006t0005g0067 a0011c0021t0036g0045 |
2 | HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.287-23623C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72160120 | |||||||
chr5:72160218 | T | TA | 61 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0074 others(58): Show |
63 | HG00140.hp1 HG00642.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.287-23510dupA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72160218 | ||||||
chr5:72160218 | T | TAA | 216 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0066 others(213): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.287-23511_287-2351 others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72160218 | ||||||
chr5:72160266 | G | A | 4 | a0001c0001t0004g0212 a0001c0002t0002g0312 a0001c0009t0001g0328 others(1): Show |
4 | HG01358.hp2 HG01433.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-23477G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72160266 | |||||||
chr5:72160382 | A | G | 8 | a0001c0001t0009g0238 a0001c0001t0009g0239 a0001c0001t0009g0240 others(5): Show |
8 | NA18943.hp1 NA18955.hp1 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-23361A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72160382 | |||||||
chr5:72160660 | ATAGGCAA others(13): Show |
A | 1 | a0001c0002t0002g0213 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.287-23080_287-2306 others(24): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72160660 | ||||||
chr5:72160795 | A | G | 209 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0066 others(206): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.287-22948A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72160795 | |||||||
chr5:72161004 | C | T | 1 | a0002c0003t0006g0293 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.287-22739C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72161004 | |||||||
chr5:72161181 | C | T | 260 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0066 others(257): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.287-22562C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72161181 | |||||||
chr5:72161201 | G | A | 42 | a0001c0001t0001g0066 a0001c0001t0001g0104 a0001c0001t0001g0130 others(39): Show |
42 | HG00140.hp2 HG00621.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.287-22542G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72161201 | |||||||
chr5:72161358 | A | G | 19 | a0001c0001t0001g0074 a0001c0001t0007g0119 a0001c0001t0009g0238 others(16): Show |
19 | HG01074.hp2 HG02109.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.287-22385A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72161358 | |||||||
chr5:72161441 | T | C | 1 | a0001c0004t0017g0064 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.287-22302T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72161441 | |||||||
chr5:72161567 | C | T | 6 | a0001c0001t0001g0219 a0001c0004t0001g0327 a0001c0005t0008g0033 others(3): Show |
6 | HG00741.hp2 HG03098.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-22176C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72161567 | |||||||
chr5:72161618 | C | T | 1 | a0001c0001t0001g0333 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.287-22125C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72161618 | |||||||
chr5:72161685 | A | C | 5 | a0001c0001t0001g0143 a0001c0004t0001g0334 a0001c0005t0008g0332 others(2): Show |
5 | HG02630.hp2 HG03041.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-22058A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72161685 | |||||||
chr5:72161771 | A | G | 2 | a0001c0034t0005g0036 a0013c0035t0005g0047 |
2 | HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.287-21972A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72161771 | |||||||
chr5:72161906 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0010g0245 |
2 | NA18941.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.287-21837G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72161906 | |||||||
chr5:72161926 | C | G | 1 | a0001c0005t0008g0041 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.287-21817C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72161926 | |||||||
chr5:72161943 | C | T | 1 | a0001c0005t0008g0033 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.287-21800C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72161943 | |||||||
chr5:72161956 | C | CA | 29 | a0001c0001t0001g0086 a0001c0001t0001g0181 a0001c0001t0002g0209 others(26): Show |
29 | HG00558.hp2 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.287-21767dupA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72161956 | ||||||
chr5:72161956 | CA | C | 180 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0066 others(177): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.287-21767delA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72161956 | ||||||
chr5:72161956 | CAA | C | 29 | a0001c0001t0001g0074 a0001c0001t0001g0145 a0001c0001t0001g0256 others(26): Show |
29 | HG01074.hp2 HG01168.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.287-21768_287-2176 others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72161956 | ||||||
chr5:72161973 | A | AAAG | 6 | a0001c0001t0001g0219 a0001c0004t0001g0327 a0001c0005t0008g0033 others(3): Show |
6 | HG00741.hp2 HG03098.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-21768_287-2176 others(7): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72161973 | ||||||
chr5:72161974 | AAAG | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0187 others(19): Show |
24 | HG00140.hp1 HG00741.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.287-21766_287-2176 others(7): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72161974 | ||||||
chr5:72161974 | AAAGAAAG | A | 6 | a0001c0001t0010g0010 a0001c0001t0010g0228 a0001c0001t0010g0229 others(3): Show |
6 | HG00639.hp2 HG01106.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-21766_287-2176 others(11): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72161974 | ||||||
chr5:72161986 | A | G | 192 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0066 others(189): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.287-21757A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72161986 | |||||||
chr5:72162014 | ACAGC | A | 7 | a0001c0001t0001g0219 a0001c0001t0002g0031 a0001c0004t0001g0327 others(4): Show |
7 | HG00741.hp2 HG02523.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.287-21725_287-2172 others(8): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72162014 | ||||||
chr5:72162251 | A | G | 1 | a0005c0010t0005g0329 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.287-21492A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72162251 | |||||||
chr5:72162295 | C | T | 141 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0066 others(138): Show |
144 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.287-21448C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72162295 | |||||||
chr5:72162393 | G | A | 29 | a0001c0001t0001g0086 a0001c0001t0001g0181 a0001c0001t0002g0209 others(26): Show |
29 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.287-21350G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72162393 | |||||||
chr5:72162394 | G | A | 8 | a0001c0001t0009g0238 a0001c0001t0009g0239 a0001c0001t0009g0240 others(5): Show |
8 | NA18943.hp1 NA18955.hp1 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-21349G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72162394 | |||||||
chr5:72162403 | CT | C | 6 | a0001c0001t0001g0219 a0001c0004t0001g0327 a0001c0005t0008g0033 others(3): Show |
6 | HG00741.hp2 HG03098.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-21330delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72162403 | ||||||
chr5:72162602 | A | C | 1 | a0001c0004t0010g0236 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.287-21141A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72162602 | |||||||
chr5:72162644 | G | A | 241 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0066 others(238): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.287-21099G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72162644 | |||||||
chr5:72162691 | G | A | 2 | a0001c0006t0007g0259 a0001c0020t0007g0260 |
2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.287-21052G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72162691 | |||||||
chr5:72162704 | G | C | 1 | a0001c0001t0002g0031 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.287-21039G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72162704 | |||||||
chr5:72162784 | T | A | 1 | a0001c0004t0015g0301 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.287-20959T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72162784 | |||||||
chr5:72162992 | G | A | 1 | a0001c0005t0008g0033 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.287-20751G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72162992 | |||||||
chr5:72163012 | G | A | 1 | a0001c0001t0020g0131 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.287-20731G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163012 | |||||||
chr5:72163172 | G | A | 6 | a0001c0001t0001g0055 a0001c0001t0004g0051 a0001c0001t0007g0052 others(3): Show |
6 | HG01070.hp1 HG01515.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-20571G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163172 | |||||||
chr5:72163185 | G | A | 1 | a0001c0002t0002g0020 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.287-20558G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163185 | |||||||
chr5:72163227 | C | CA | 14 | a0001c0001t0001g0074 a0001c0001t0001g0333 a0001c0001t0001g0335 others(11): Show |
14 | HG01074.hp2 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.287-20495dupA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72163227 | ||||||
chr5:72163227 | CA | C | 195 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0096 others(192): Show |
198 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.287-20495delA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72163227 | ||||||
chr5:72163227 | CAA | C | 34 | a0001c0001t0001g0086 a0001c0001t0001g0181 a0001c0001t0002g0209 others(31): Show |
34 | HG00099.hp1 HG00558.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.287-20496_287-2049 others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72163227 | ||||||
chr5:72163245 | A | G | 2 | a0001c0004t0015g0271 a0001c0022t0002g0149 |
2 | HG04199.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.287-20498A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163245 | |||||||
chr5:72163307 | A | G | 1 | a0001c0008t0002g0113 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.287-20436A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163307 | |||||||
chr5:72163322 | G | A | 260 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0066 others(257): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.287-20421G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163322 | |||||||
chr5:72163448 | A | G | 1 | a0001c0001t0002g0031 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.287-20295A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163448 | |||||||
chr5:72163461 | G | A | 11 | a0001c0001t0001g0074 a0001c0001t0007g0119 a0001c0002t0002g0111 others(8): Show |
11 | HG01074.hp2 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.287-20282G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163461 | |||||||
chr5:72163497 | C | G | 1 | a0001c0005t0020g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.287-20246C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163497 | |||||||
chr5:72163639 | C | T | 20 | a0001c0001t0001g0114 a0001c0001t0001g0182 a0001c0001t0001g0210 others(17): Show |
20 | HG00621.hp1 HG00673.hp1 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.287-20104C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163639 | |||||||
chr5:72163643 | A | C | 27 | a0001c0001t0001g0086 a0001c0001t0001g0181 a0001c0001t0002g0209 others(24): Show |
27 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.287-20100A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163643 | |||||||
chr5:72163706 | G | T | 8 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0001t0012g0311 others(5): Show |
8 | HG02145.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.287-20037G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163706 | |||||||
chr5:72163904 | T | C | 6 | a0001c0002t0003g0112 a0001c0002t0003g0203 a0001c0002t0013g0023 others(3): Show |
6 | HG00621.hp2 HG00673.hp2 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-19839T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163904 | |||||||
chr5:72163916 | CT | C | 7 | a0001c0001t0001g0263 a0001c0001t0001g0266 a0001c0002t0002g0216 others(4): Show |
7 | HG01099.hp1 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.287-19814delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72163916 | ||||||
chr5:72163917 | TTTTTTTT others(6): Show |
T | 1 | a0001c0002t0003g0129 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.287-19813_287-1980 others(17): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72163917 | ||||||
chr5:72163925 | T | C | 1 | a0001c0004t0011g0323 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.287-19818T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163925 | |||||||
chr5:72163925 | T | TC | 33 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0132 others(30): Show |
35 | HG00140.hp1 HG00642.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.287-19818_287-1981 others(5): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163925 | |||||||
chr5:72163926 | T | C | 246 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0066 others(243): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.287-19817T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163926 | |||||||
chr5:72163927 | T | C | 1 | a0001c0002t0003g0088 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.287-19816T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163927 | |||||||
chr5:72163928 | TTC | T | 30 | a0001c0001t0001g0086 a0001c0001t0001g0181 a0001c0001t0002g0115 others(27): Show |
30 | HG00558.hp2 HG00639.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.287-19813_287-1981 others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72163928 | ||||||
chr5:72163929 | T | C | 1 | a0001c0002t0009g0235 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.287-19814T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163929 | |||||||
chr5:72163929 | TC | T | 178 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0066 others(175): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.287-19813delC | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163929 | |||||||
chr5:72163930 | C | CT | 21 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0187 others(18): Show |
21 | HG00140.hp1 HG00642.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.287-19792dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72163930 | ||||||
chr5:72163930 | C | CTT | 6 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0335 others(3): Show |
7 | HG01884.hp1 HG02055.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.287-19793_287-1979 others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72163930 | ||||||
chr5:72163930 | C | T | 48 | a0001c0001t0001g0104 a0001c0001t0001g0182 a0001c0001t0002g0291 others(45): Show |
48 | HG00609.hp2 HG00621.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.287-19813C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163930 | |||||||
chr5:72163931 | T | C | 11 | a0001c0001t0009g0238 a0001c0001t0009g0239 a0001c0001t0009g0240 others(8): Show |
11 | HG02630.hp2 HG03041.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.287-19812T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163931 | |||||||
chr5:72163932 | T | C | 17 | a0001c0001t0001g0074 a0001c0001t0001g0219 a0001c0001t0007g0119 others(14): Show |
17 | HG00741.hp2 HG01074.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.287-19811T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163932 | |||||||
chr5:72163933 | T | C | 1 | a0001c0005t0008g0033 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.287-19810T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163933 | |||||||
chr5:72163934 | T | C | 6 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0001t0020g0131 others(3): Show |
6 | HG02486.hp2 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-19809T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163934 | |||||||
chr5:72163935 | T | C | 5 | a0001c0001t0001g0143 a0001c0001t0015g0124 a0001c0009t0007g0043 others(2): Show |
5 | HG02145.hp2 HG02886.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.287-19808T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163935 | |||||||
chr5:72163939 | T | C | 1 | a0001c0002t0003g0129 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.287-19804T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163939 | |||||||
chr5:72163987 | A | G | 287 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0053 others(284): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.287-19756A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163987 | |||||||
chr5:72163994 | C | T | 241 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0066 others(238): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.287-19749C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72163994 | |||||||
chr5:72164168 | T | G | 232 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0066 others(229): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.287-19575T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72164168 | |||||||
chr5:72164169 | G | T | 1 | a0001c0004t0011g0323 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.287-19574G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72164169 | |||||||
chr5:72164248 | T | C | 2 | a0001c0006t0018g0038 a0001c0006t0022g0039 |
2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.287-19495T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72164248 | |||||||
chr5:72164414 | G | A | 2 | a0001c0006t0007g0259 a0001c0020t0007g0260 |
2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.287-19329G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72164414 | |||||||
chr5:72164665 | C | A | 3 | a0001c0002t0002g0202 a0001c0002t0002g0204 a0001c0008t0002g0113 |
3 | HG00621.hp1 HG02132.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.287-19078C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72164665 | |||||||
chr5:72164717 | C | T | 1 | a0001c0001t0010g0010 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.287-19026C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72164717 | |||||||
chr5:72164868 | T | G | 1 | a0001c0002t0013g0222 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.287-18875T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72164868 | |||||||
chr5:72164900 | T | C | 2 | a0001c0006t0018g0038 a0001c0006t0022g0039 |
2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.287-18843T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72164900 | |||||||
chr5:72164993 | T | C | 1 | a0001c0006t0018g0071 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.287-18750T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72164993 | |||||||
chr5:72165093 | T | C | 1 | a0001c0002t0002g0109 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.287-18650T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72165093 | |||||||
chr5:72165151 | T | C | 10 | a0001c0001t0001g0219 a0001c0001t0009g0238 a0001c0001t0009g0239 others(7): Show |
10 | NA18943.hp1 NA18955.hp1 NA18973.hp1 others(7): Show |
intron_variant | MODIFIER | c.287-18592T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72165151 | |||||||
chr5:72165264 | G | C | 1 | a0001c0002t0003g0305 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.287-18479G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72165264 | |||||||
chr5:72165267 | C | T | 147 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0066 others(144): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.287-18476C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72165267 | |||||||
chr5:72165347 | G | A | 1 | a0001c0002t0002g0011 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.287-18396G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72165347 | |||||||
chr5:72165428 | G | A | 2 | a0001c0009t0001g0062 a0001c0009t0001g0063 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.287-18315G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72165428 | |||||||
chr5:72165642 | T | C | 42 | a0001c0001t0001g0066 a0001c0001t0001g0104 a0001c0001t0001g0130 others(39): Show |
42 | HG00140.hp2 HG00621.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.287-18101T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72165642 | |||||||
chr5:72165662 | T | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0187 others(21): Show |
26 | HG00140.hp1 HG00741.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.287-18081T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72165662 | |||||||
chr5:72165753 | C | T | 1 | a0003c0007t0002g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.287-17990C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72165753 | |||||||
chr5:72165780 | A | T | 2 | a0001c0001t0004g0195 a0001c0004t0017g0064 |
2 | HG01255.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.287-17963A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72165780 | |||||||
chr5:72165900 | C | T | 3 | a0001c0001t0015g0124 a0001c0034t0005g0036 a0013c0035t0005g0047 |
3 | HG02145.hp2 HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.287-17843C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72165900 | |||||||
chr5:72165984 | A | G | 1 | a0001c0001t0019g0237 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.287-17759A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72165984 | |||||||
chr5:72166238 | C | T | 50 | a0001c0001t0001g0114 a0001c0001t0001g0120 a0001c0001t0001g0159 others(47): Show |
50 | HG00099.hp1 HG00621.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.287-17505C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72166238 | |||||||
chr5:72166283 | C | G | 11 | a0001c0001t0001g0074 a0001c0001t0007g0119 a0001c0002t0002g0111 others(8): Show |
11 | HG01074.hp2 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.287-17460C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72166283 | |||||||
chr5:72166329 | C | T | 1 | a0001c0002t0003g0306 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.287-17414C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72166329 | |||||||
chr5:72166518 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.287-17225C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72166518 | |||||||
chr5:72166646 | C | T | 1 | a0001c0034t0005g0036 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.287-17097C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72166646 | |||||||
chr5:72166682 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0010g0245 |
2 | NA18941.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.287-17061C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72166682 | |||||||
chr5:72166800 | T | G | 8 | a0001c0001t0009g0238 a0001c0001t0009g0239 a0001c0001t0009g0240 others(5): Show |
8 | NA18943.hp1 NA18955.hp1 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-16943T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72166800 | |||||||
chr5:72166805 | T | C | 287 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0053 others(284): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.287-16938T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72166805 | |||||||
chr5:72166899 | G | A | 1 | a0001c0002t0003g0174 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.287-16844G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72166899 | |||||||
chr5:72166915 | G | A | 4 | a0001c0001t0001g0143 a0001c0009t0007g0043 a0001c0028t0025g0042 others(1): Show |
4 | HG02886.hp2 HG03041.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-16828G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72166915 | |||||||
chr5:72166992 | T | G | 4 | a0001c0001t0001g0187 a0001c0001t0001g0308 a0001c0001t0001g0309 others(1): Show |
4 | HG00140.hp1 HG01106.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-16751T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72166992 | |||||||
chr5:72166996 | T | G | 1 | a0003c0007t0002g0083 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.287-16747T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72166996 | |||||||
chr5:72167010 | T | G | 4 | a0001c0002t0003g0090 a0001c0002t0013g0021 a0001c0002t0013g0225 others(1): Show |
4 | HG00140.hp2 HG01255.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-16733T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72167010 | |||||||
chr5:72167016 | C | CT | 19 | a0001c0001t0001g0219 a0001c0001t0001g0316 a0001c0001t0004g0212 others(16): Show |
19 | HG01358.hp2 HG01433.hp1 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.287-16711dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72167016 | ||||||
chr5:72167016 | C | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0143 a0001c0009t0007g0043 others(2): Show |
5 | HG00642.hp1 HG02886.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.287-16727C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72167016 | |||||||
chr5:72167016 | CT | C | 6 | a0001c0001t0007g0269 a0001c0002t0002g0275 a0001c0005t0008g0041 others(3): Show |
6 | HG00741.hp2 HG03130.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-16711delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72167016 | ||||||
chr5:72167016 | CTT | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0074 a0001c0001t0001g0086 others(107): Show |
113 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.287-16712_287-1671 others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72167016 | ||||||
chr5:72167029 | T | C | 3 | a0001c0004t0007g0141 a0001c0006t0007g0259 a0001c0020t0007g0260 |
3 | HG01167.hp2 HG01243.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.287-16714T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72167029 | |||||||
chr5:72167322 | A | G | 1 | a0001c0002t0002g0312 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.287-16421A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72167322 | |||||||
chr5:72167440 | T | C | 11 | a0001c0001t0001g0074 a0001c0001t0007g0119 a0001c0002t0002g0111 others(8): Show |
11 | HG01074.hp2 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.287-16303T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72167440 | |||||||
chr5:72167668 | C | T | 8 | a0001c0001t0009g0238 a0001c0001t0009g0239 a0001c0001t0009g0240 others(5): Show |
8 | NA18943.hp1 NA18955.hp1 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-16075C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72167668 | |||||||
chr5:72167711 | A | G | 1 | a0016c0031t0003g0049 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.287-16032A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72167711 | |||||||
chr5:72167774 | AC | A | 7 | a0001c0001t0001g0017 a0001c0001t0001g0143 a0001c0005t0005g0154 others(4): Show |
7 | HG00642.hp1 HG02451.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.287-15966delC | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72167774 | ||||||
chr5:72167909 | C | G | 2 | a0001c0006t0007g0259 a0001c0020t0007g0260 |
2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.287-15834C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72167909 | |||||||
chr5:72167910 | A | G | 1 | a0001c0002t0003g0172 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.287-15833A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72167910 | |||||||
chr5:72168006 | C | T | 1 | a0001c0001t0019g0246 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.287-15737C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72168006 | |||||||
chr5:72168010 | C | T | 8 | a0001c0002t0002g0095 a0002c0003t0006g0002 a0002c0003t0006g0161 others(5): Show |
9 | HG00735.hp1 HG00738.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.287-15733C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72168010 | |||||||
chr5:72168060 | G | C | 2 | a0001c0001t0001g0163 a0001c0001t0005g0155 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.287-15683G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72168060 | |||||||
chr5:72168353 | C | T | 11 | a0001c0001t0001g0074 a0001c0001t0007g0119 a0001c0002t0002g0111 others(8): Show |
11 | HG01074.hp2 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.287-15390C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72168353 | |||||||
chr5:72168417 | G | A | 11 | a0001c0001t0001g0074 a0001c0001t0007g0119 a0001c0002t0002g0111 others(8): Show |
11 | HG01074.hp2 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.287-15326G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72168417 | |||||||
chr5:72168441 | T | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0074 a0001c0001t0001g0086 others(115): Show |
121 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-15302T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72168441 | |||||||
chr5:72168483 | C | T | 1 | a0001c0001t0015g0116 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.287-15260C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72168483 | |||||||
chr5:72168587 | C | T | 1 | a0001c0002t0002g0168 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.287-15156C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72168587 | |||||||
chr5:72168640 | G | A | 72 | a0001c0001t0001g0086 a0001c0001t0001g0163 a0001c0001t0001g0181 others(69): Show |
73 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.287-15103G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72168640 | |||||||
chr5:72169027 | G | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0074 others(137): Show |
143 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.287-14716G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72169027 | |||||||
chr5:72169150 | C | T | 4 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0001t0020g0131 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-14593C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72169150 | |||||||
chr5:72169344 | C | G | 72 | a0001c0001t0001g0086 a0001c0001t0001g0163 a0001c0001t0001g0181 others(69): Show |
73 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.287-14399C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72169344 | |||||||
chr5:72169513 | A | C | 1 | a0001c0001t0020g0131 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.287-14230A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72169513 | |||||||
chr5:72169534 | T | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0074 a0001c0001t0001g0086 others(113): Show |
119 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.287-14209T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72169534 | |||||||
chr5:72169834 | T | C | 1 | a0001c0001t0012g0311 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.287-13909T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72169834 | |||||||
chr5:72169907 | A | G | 23 | a0001c0001t0001g0017 a0001c0001t0001g0143 a0001c0001t0001g0219 others(20): Show |
23 | HG00642.hp1 HG00741.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.287-13836A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72169907 | |||||||
chr5:72170028 | T | G | 1 | a0001c0002t0003g0087 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.287-13715T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72170028 | |||||||
chr5:72170094 | G | T | 27 | a0001c0001t0001g0017 a0001c0001t0001g0044 a0001c0001t0001g0143 others(24): Show |
27 | HG00642.hp1 HG00741.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.287-13649G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72170094 | |||||||
chr5:72170231 | CAAGGGCC others(1): Show |
C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0187 others(18): Show |
23 | HG00140.hp1 HG01106.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.287-13511_287-1350 others(12): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72170231 | |||||||
chr5:72170366 | G | T | 1 | a0001c0001t0012g0311 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.287-13377G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72170366 | |||||||
chr5:72170449 | C | A | 3 | a0001c0001t0012g0056 a0001c0001t0012g0057 a0001c0039t0018g0016 |
3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.287-13294C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72170449 | |||||||
chr5:72170802 | C | G | 3 | a0001c0005t0008g0041 a0007c0013t0001g0126 a0007c0013t0029g0127 |
3 | HG00741.hp2 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.287-12941C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72170802 | |||||||
chr5:72170806 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0074 others(137): Show |
143 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.287-12937A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72170806 | |||||||
chr5:72170875 | A | AG | 72 | a0001c0001t0001g0086 a0001c0001t0001g0163 a0001c0001t0001g0181 others(69): Show |
73 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.287-12866dupG | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72170875 | ||||||
chr5:72170942 | C | T | 3 | a0001c0001t0015g0124 a0001c0034t0005g0036 a0013c0035t0005g0047 |
3 | HG02145.hp2 HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.287-12801C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72170942 | |||||||
chr5:72171176 | T | C | 24 | a0001c0001t0001g0017 a0001c0001t0001g0143 a0001c0001t0001g0219 others(21): Show |
24 | HG00642.hp1 HG00741.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.287-12567T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72171176 | |||||||
chr5:72171243 | G | A | 18 | a0001c0001t0001g0114 a0001c0001t0001g0182 a0001c0001t0001g0310 others(15): Show |
18 | HG00621.hp1 HG00673.hp1 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.287-12500G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72171243 | |||||||
chr5:72171292 | T | A | 1 | a0005c0010t0005g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.287-12451T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72171292 | |||||||
chr5:72171352 | C | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0074 a0001c0001t0001g0086 others(113): Show |
119 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.287-12391C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72171352 | |||||||
chr5:72171372 | G | A | 18 | a0001c0001t0001g0017 a0001c0001t0001g0143 a0001c0001t0001g0219 others(15): Show |
18 | HG00642.hp1 HG00741.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.287-12371G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72171372 | |||||||
chr5:72171505 | A | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0074 others(138): Show |
144 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.287-12238A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72171505 | |||||||
chr5:72171597 | A | T | 2 | a0001c0001t0004g0028 a0001c0001t0004g0321 |
2 | HG01934.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.287-12146A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72171597 | |||||||
chr5:72171635 | A | G | 1 | a0001c0004t0015g0185 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.287-12108A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72171635 | |||||||
chr5:72171689 | T | G | 2 | a0001c0005t0001g0008 a0001c0005t0001g0270 |
2 | HG01884.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.287-12054T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72171689 | |||||||
chr5:72171820 | G | A | 1 | a0001c0002t0003g0174 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.287-11923G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72171820 | |||||||
chr5:72171843 | T | C | 72 | a0001c0001t0001g0086 a0001c0001t0001g0163 a0001c0001t0001g0181 others(69): Show |
73 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.287-11900T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72171843 | |||||||
chr5:72171871 | C | T | 1 | a0001c0004t0017g0190 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.287-11872C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72171871 | |||||||
chr5:72172109 | C | T | 8 | a0001c0001t0001g0333 a0001c0001t0012g0056 a0001c0001t0012g0057 others(5): Show |
8 | HG02145.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.287-11634C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72172109 | |||||||
chr5:72172135 | G | T | 1 | a0002c0003t0006g0050 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.287-11608G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72172135 | |||||||
chr5:72172233 | C | A | 1 | a0001c0002t0002g0004 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.287-11510C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72172233 | |||||||
chr5:72172279 | C | T | 2 | a0007c0013t0001g0126 a0007c0013t0029g0127 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.287-11464C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72172279 | |||||||
chr5:72172522 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.287-11221T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72172522 | |||||||
chr5:72172769 | T | C | 1 | a0001c0004t0015g0271 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.287-10974T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72172769 | |||||||
chr5:72172841 | C | T | 17 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0187 others(14): Show |
19 | HG00140.hp1 HG01106.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.287-10902C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72172841 | |||||||
chr5:72172974 | T | C | 23 | a0001c0001t0001g0219 a0001c0001t0001g0335 a0001c0001t0009g0238 others(20): Show |
23 | HG00741.hp1 HG02055.hp2 HG02559.hp1 others(20): Show |
intron_variant | MODIFIER | c.287-10769T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72172974 | |||||||
chr5:72173067 | C | T | 1 | a0001c0001t0014g0094 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.287-10676C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72173067 | |||||||
chr5:72173183 | T | C | 1 | a0001c0004t0017g0164 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.287-10560T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72173183 | |||||||
chr5:72173209 | C | T | 1 | a0001c0002t0003g0121 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.287-10534C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72173209 | |||||||
chr5:72173312 | G | A | 3 | a0001c0002t0011g0153 a0001c0002t0014g0003 a0001c0002t0016g0152 |
4 | HG01884.hp1 HG02922.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-10431G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72173312 | |||||||
chr5:72173629 | C | A | 4 | a0001c0001t0015g0124 a0001c0002t0003g0203 a0001c0034t0005g0036 others(1): Show |
4 | HG02015.hp1 HG02145.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-10114C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72173629 | |||||||
chr5:72173818 | C | T | 2 | a0001c0006t0007g0259 a0001c0020t0007g0260 |
2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.287-9925C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72173818 | |||||||
chr5:72173819 | C | G | 2 | a0001c0006t0007g0259 a0001c0020t0007g0260 |
2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.287-9924C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72173819 | |||||||
chr5:72173954 | C | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0027 others(211): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.287-9789C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72173954 | |||||||
chr5:72173964 | C | T | 22 | a0001c0001t0001g0096 a0001c0001t0001g0118 a0001c0001t0001g0123 others(19): Show |
23 | HG00609.hp2 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.287-9779C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72173964 | |||||||
chr5:72174054 | C | T | 22 | a0001c0001t0001g0096 a0001c0001t0001g0118 a0001c0001t0001g0123 others(19): Show |
23 | HG00609.hp2 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.287-9689C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72174054 | |||||||
chr5:72174072 | G | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0027 others(203): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.287-9671G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72174072 | |||||||
chr5:72174306 | A | G | 2 | a0001c0001t0007g0119 a0001c0005t0008g0110 |
2 | HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.287-9437A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72174306 | |||||||
chr5:72174335 | T | C | 1 | a0001c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.287-9408T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72174335 | |||||||
chr5:72174366 | C | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0027 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.287-9377C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72174366 | |||||||
chr5:72174438 | C | T | 1 | a0001c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.287-9305C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72174438 | |||||||
chr5:72174595 | C | G | 221 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0027 others(218): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.287-9148C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72174595 | |||||||
chr5:72174621 | C | T | 5 | a0001c0001t0012g0034 a0001c0001t0012g0056 a0001c0001t0012g0057 others(2): Show |
5 | HG02559.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-9122C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72174621 | |||||||
chr5:72174663 | C | T | 1 | a0013c0035t0005g0047 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.287-9080C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72174663 | |||||||
chr5:72174783 | C | T | 2 | a0001c0006t0007g0259 a0001c0020t0007g0260 |
2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.287-8960C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72174783 | |||||||
chr5:72174875 | T | TCTTC | 217 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0027 others(214): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.287-8850_287-8847d others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72174875 | ||||||
chr5:72174875 | TCTTCCTT others(1): Show |
T | 3 | a0001c0001t0015g0124 a0001c0034t0005g0036 a0013c0035t0005g0047 |
3 | HG02145.hp2 HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.287-8854_287-8847d others(10): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72174875 | ||||||
chr5:72174897 | C | T | 1 | a0001c0002t0003g0289 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.287-8846C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72174897 | |||||||
chr5:72174996 | TCCTTCCT others(10): Show |
T | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.287-8726_287-8710d others(19): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72174996 | ||||||
chr5:72175013 | CCCTT | C | 9 | a0001c0001t0001g0219 a0001c0001t0009g0238 a0001c0001t0009g0239 others(6): Show |
9 | NA18943.hp1 NA18955.hp1 NA18973.hp1 others(6): Show |
intron_variant | MODIFIER | c.287-8723_287-8720d others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72175013 | ||||||
chr5:72175017 | TCCTTCCC others(10): Show |
T | 1 | a0001c0001t0012g0311 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.287-8707_287-8691d others(19): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72175017 | ||||||
chr5:72175038 | T | C | 3 | a0001c0001t0015g0124 a0001c0034t0005g0036 a0013c0035t0005g0047 |
3 | HG02145.hp2 HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.287-8705T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72175038 | |||||||
chr5:72175086 | A | G | 9 | a0001c0001t0001g0335 a0001c0001t0012g0034 a0001c0001t0012g0056 others(6): Show |
9 | HG00741.hp1 HG02055.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.287-8657A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72175086 | |||||||
chr5:72175134 | G | A | 9 | a0001c0001t0001g0335 a0001c0001t0012g0034 a0001c0001t0012g0056 others(6): Show |
9 | HG00741.hp1 HG02055.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.287-8609G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72175134 | |||||||
chr5:72175135 | G | A | 1 | a0001c0009t0007g0043 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.287-8608G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72175135 | |||||||
chr5:72175196 | C | G | 1 | a0001c0028t0025g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.287-8547C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72175196 | |||||||
chr5:72175258 | T | A | 1 | a0001c0002t0002g0186 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.287-8485T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72175258 | |||||||
chr5:72175436 | C | A | 2 | a0001c0001t0004g0028 a0001c0001t0004g0321 |
2 | HG01934.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.287-8307C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72175436 | |||||||
chr5:72175487 | T | C | 50 | a0001c0001t0001g0009 a0001c0001t0001g0114 a0001c0001t0001g0120 others(47): Show |
50 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.287-8256T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72175487 | |||||||
chr5:72175502 | C | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0027 others(193): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.287-8241C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72175502 | |||||||
chr5:72175601 | T | C | 3 | a0001c0005t0008g0041 a0007c0013t0001g0126 a0007c0013t0029g0127 |
3 | HG00741.hp2 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.287-8142T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72175601 | |||||||
chr5:72175736 | G | GCACATGG others(3): Show |
1 | a0001c0001t0002g0209 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.287-8006_287-7997d others(12): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72175736 | ||||||
chr5:72175742 | G | A | 1 | a0001c0001t0012g0144 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.287-8001G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72175742 | |||||||
chr5:72175797 | C | A | 7 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0004g0051 others(4): Show |
7 | HG01070.hp1 HG01123.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.287-7946C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72175797 | |||||||
chr5:72175886 | T | C | 66 | a0001c0001t0001g0009 a0001c0001t0001g0114 a0001c0001t0001g0120 others(63): Show |
66 | HG00621.hp1 HG00639.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.287-7857T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72175886 | |||||||
chr5:72176191 | CCACACAC others(11): Show |
C | 1 | a0002c0003t0006g0194 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.287-7550_287-7533d others(20): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72176191 | ||||||
chr5:72176193 | A | G | 65 | a0001c0001t0001g0009 a0001c0001t0001g0114 a0001c0001t0001g0120 others(62): Show |
65 | HG00621.hp1 HG00639.hp1 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.287-7550A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176193 | |||||||
chr5:72176328 | A | C | 3 | a0001c0004t0007g0141 a0001c0006t0007g0259 a0001c0020t0007g0260 |
3 | HG01167.hp2 HG01243.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.287-7415A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176328 | |||||||
chr5:72176331 | T | G | 1 | a0001c0005t0008g0033 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.287-7412T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176331 | |||||||
chr5:72176393 | G | A | 6 | a0001c0001t0001g0290 a0001c0002t0002g0180 a0001c0002t0003g0305 others(3): Show |
6 | HG02056.hp2 HG02074.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-7350G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176393 | |||||||
chr5:72176422 | C | G | 1 | a0001c0001t0012g0311 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.287-7321C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176422 | |||||||
chr5:72176466 | C | G | 1 | a0001c0001t0019g0237 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.287-7277C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176466 | |||||||
chr5:72176471 | G | A | 1 | a0001c0001t0002g0072 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.287-7272G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176471 | |||||||
chr5:72176561 | G | A | 3 | a0001c0002t0011g0153 a0001c0002t0014g0003 a0001c0002t0016g0152 |
4 | HG01884.hp1 HG02922.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-7182G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176561 | |||||||
chr5:72176588 | A | G | 2 | a0001c0001t0004g0028 a0001c0001t0004g0321 |
2 | HG01934.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.287-7155A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176588 | |||||||
chr5:72176622 | T | C | 1 | a0001c0001t0001g0333 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.287-7121T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176622 | |||||||
chr5:72176638 | A | G | 3 | a0001c0004t0001g0334 a0001c0005t0008g0332 a0005c0010t0005g0331 |
3 | HG02630.hp2 HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.287-7105A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176638 | |||||||
chr5:72176697 | G | A | 1 | a0002c0003t0006g0050 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.287-7046G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176697 | |||||||
chr5:72176705 | G | T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0187 others(10): Show |
14 | HG00140.hp1 HG01106.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.287-7038G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176705 | |||||||
chr5:72176756 | C | T | 3 | a0001c0001t0002g0188 a0002c0015t0016g0019 a0002c0015t0016g0205 |
3 | HG00609.hp1 HG02523.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.287-6987C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176756 | |||||||
chr5:72176758 | C | T | 1 | a0017c0033t0009g0233 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.287-6985C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176758 | |||||||
chr5:72176869 | C | T | 3 | a0001c0004t0001g0334 a0001c0005t0008g0332 a0005c0010t0005g0331 |
3 | HG02630.hp2 HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.287-6874C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72176869 | |||||||
chr5:72177009 | G | A | 6 | a0001c0001t0012g0034 a0001c0001t0012g0056 a0001c0001t0012g0057 others(3): Show |
6 | HG02559.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-6734G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72177009 | |||||||
chr5:72177077 | C | A | 10 | a0001c0001t0001g0074 a0001c0001t0007g0119 a0001c0002t0002g0111 others(7): Show |
10 | HG01074.hp2 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.287-6666C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72177077 | |||||||
chr5:72177294 | C | T | 1 | a0001c0005t0008g0041 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.287-6449C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72177294 | |||||||
chr5:72177350 | T | C | 1 | a0002c0003t0023g0242 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.287-6393T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72177350 | |||||||
chr5:72177358 | T | TAGAAATG others(324): Show |
1 | a0001c0001t0012g0144 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.287-6368_287-6367i others(333): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72177358 | ||||||
chr5:72177358 | T | TAGAAATG others(323): Show |
5 | a0001c0001t0012g0034 a0001c0001t0012g0056 a0001c0001t0012g0057 others(2): Show |
5 | HG02895.hp1 HG02897.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.287-6368_287-6367i others(332): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72177358 | ||||||
chr5:72177580 | G | A | 3 | a0001c0001t0001g0263 a0001c0002t0002g0216 a0001c0002t0002g0267 |
3 | HG01099.hp1 HG02622.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.287-6163G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72177580 | |||||||
chr5:72177898 | A | T | 2 | a0001c0001t0002g0146 a0001c0002t0002g0013 |
2 | HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.287-5845A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72177898 | |||||||
chr5:72178025 | C | T | 1 | a0001c0002t0001g0018 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.287-5718C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178025 | |||||||
chr5:72178054 | G | C | 1 | a0001c0001t0001g0117 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.287-5689G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178054 | |||||||
chr5:72178078 | C | T | 6 | a0001c0001t0012g0034 a0001c0001t0012g0056 a0001c0001t0012g0057 others(3): Show |
6 | HG02559.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-5665C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178078 | |||||||
chr5:72178121 | G | T | 3 | a0001c0001t0001g0143 a0005c0010t0005g0134 a0005c0010t0005g0329 |
3 | HG02647.hp1 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.287-5622G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178121 | |||||||
chr5:72178232 | A | G | 1 | a0001c0001t0020g0131 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.287-5511A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178232 | |||||||
chr5:72178245 | C | T | 2 | a0001c0002t0002g0295 a0001c0002t0003g0287 |
2 | NA18977.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.287-5498C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178245 | |||||||
chr5:72178246 | A | G | 3 | a0001c0002t0002g0032 a0001c0002t0002g0295 a0001c0002t0003g0287 |
3 | NA18955.hp1 NA18977.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.287-5497A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178246 | |||||||
chr5:72178268 | C | G | 1 | a0001c0004t0017g0190 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.287-5475C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178268 | |||||||
chr5:72178314 | C | T | 3 | a0001c0002t0011g0153 a0001c0002t0014g0003 a0001c0002t0016g0152 |
4 | HG01884.hp1 HG02922.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-5429C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178314 | |||||||
chr5:72178371 | T | G | 7 | a0001c0002t0002g0111 a0001c0004t0001g0334 a0001c0009t0007g0043 others(4): Show |
7 | HG01074.hp2 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.287-5372T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178371 | |||||||
chr5:72178388 | G | A | 1 | a0013c0035t0005g0047 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.287-5355G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178388 | |||||||
chr5:72178447 | C | T | 62 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(59): Show |
64 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.287-5296C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178447 | |||||||
chr5:72178460 | C | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(193): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.287-5283C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178460 | |||||||
chr5:72178725 | G | GGT | 69 | a0001c0001t0001g0055 a0001c0001t0001g0086 a0001c0001t0001g0143 others(66): Show |
70 | HG00558.hp1 HG00609.hp2 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.287-4973_287-4972d others(4): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72178725 | ||||||
chr5:72178725 | G | GGTGT | 25 | a0001c0001t0001g0044 a0001c0001t0001g0145 a0001c0001t0001g0266 others(22): Show |
25 | HG00621.hp1 HG00621.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.287-4975_287-4972d others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72178725 | ||||||
chr5:72178725 | G | GGTGTGT | 7 | a0001c0001t0001g0017 a0001c0001t0002g0115 a0001c0001t0010g0231 others(4): Show |
7 | HG00642.hp1 HG02080.hp2 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.287-4977_287-4972d others(8): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72178725 | ||||||
chr5:72178725 | G | GT | 3 | a0001c0002t0002g0180 a0001c0002t0002g0213 a0001c0017t0003g0073 |
3 | NA18944.hp1 NA18983.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.287-5018_287-5017i others(3): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178725 | |||||||
chr5:72178725 | G | T | 1 | a0001c0002t0003g0174 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.287-5018G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178725 | |||||||
chr5:72178725 | GGT | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0053 others(94): Show |
101 | HG00408.hp1 HG00609.hp1 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.287-4973_287-4972d others(4): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72178725 | ||||||
chr5:72178725 | GGTGT | G | 14 | a0001c0001t0001g0187 a0001c0001t0004g0084 a0001c0001t0012g0034 others(11): Show |
15 | HG00099.hp2 HG00735.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.287-4975_287-4972d others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72178725 | ||||||
chr5:72178725 | GGTGTGTG others(3): Show |
G | 1 | a0001c0001t0012g0144 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.287-4981_287-4972d others(12): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72178725 | ||||||
chr5:72178725 | GGTGTGTG others(19): Show |
G | 1 | a0001c0004t0001g0334 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.287-4997_287-4972d others(28): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72178725 | ||||||
chr5:72178727 | T | G | 17 | a0001c0001t0001g0114 a0001c0001t0001g0182 a0001c0001t0001g0316 others(14): Show |
17 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.287-5016T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178727 | |||||||
chr5:72178729 | T | G | 2 | a0001c0004t0007g0141 a0001c0005t0008g0332 |
2 | HG02630.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.287-5014T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72178729 | |||||||
chr5:72179038 | C | T | 3 | a0007c0013t0001g0126 a0007c0013t0001g0264 a0007c0013t0029g0127 |
3 | HG03130.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.287-4705C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72179038 | |||||||
chr5:72179105 | C | T | 1 | a0001c0028t0025g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.287-4638C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72179105 | |||||||
chr5:72179106 | G | A | 1 | a0001c0004t0017g0190 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.287-4637G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72179106 | |||||||
chr5:72179129 | A | G | 37 | a0001c0001t0001g0009 a0001c0001t0001g0044 a0001c0001t0001g0055 others(34): Show |
37 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.287-4614A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72179129 | |||||||
chr5:72179318 | G | A | 1 | a0002c0015t0016g0205 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.287-4425G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72179318 | |||||||
chr5:72179599 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.287-4144G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72179599 | |||||||
chr5:72179601 | G | A | 9 | a0001c0001t0005g0140 a0001c0001t0007g0269 a0001c0005t0008g0033 others(6): Show |
9 | HG02055.hp1 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.287-4142G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72179601 | |||||||
chr5:72179785 | C | A | 1 | a0001c0002t0002g0111 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.287-3958C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72179785 | |||||||
chr5:72179859 | T | C | 1 | a0001c0002t0003g0121 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.287-3884T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72179859 | |||||||
chr5:72179948 | C | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0044 others(159): Show |
166 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(163): Show |
intron_variant | MODIFIER | c.287-3795C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72179948 | |||||||
chr5:72180015 | G | A | 2 | a0008c0016t0001g0261 a0008c0016t0001g0330 |
2 | HG00741.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.287-3728G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72180015 | |||||||
chr5:72180024 | C | A | 26 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0004g0028 others(23): Show |
28 | HG00642.hp2 HG00733.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.287-3719C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72180024 | |||||||
chr5:72180268 | C | T | 1 | a0001c0005t0008g0110 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.287-3475C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72180268 | |||||||
chr5:72180459 | T | C | 1 | a0001c0005t0008g0332 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.287-3284T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72180459 | |||||||
chr5:72180904 | T | C | 1 | a0001c0001t0001g0159 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.287-2839T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72180904 | |||||||
chr5:72180965 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.287-2778G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72180965 | |||||||
chr5:72181078 | C | T | 44 | a0001c0001t0001g0009 a0001c0001t0001g0086 a0001c0001t0001g0096 others(41): Show |
45 | HG00099.hp2 HG00621.hp1 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.287-2665C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72181078 | |||||||
chr5:72181124 | T | C | 10 | a0001c0001t0021g0268 a0001c0002t0013g0225 a0001c0004t0001g0334 others(7): Show |
10 | HG01167.hp2 HG01255.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.287-2619T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72181124 | |||||||
chr5:72181130 | G | A | 219 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0066 others(216): Show |
224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.287-2613G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72181130 | |||||||
chr5:72181288 | G | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0053 a0001c0001t0001g0132 others(161): Show |
166 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(163): Show |
intron_variant | MODIFIER | c.287-2455G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72181288 | |||||||
chr5:72181482 | G | C | 1 | a0001c0002t0002g0004 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.287-2261G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72181482 | |||||||
chr5:72181723 | A | AT | 171 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0027 others(168): Show |
174 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(171): Show |
intron_variant | MODIFIER | c.287-2004dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72181723 | ||||||
chr5:72181723 | A | ATT | 83 | a0001c0001t0001g0009 a0001c0001t0002g0072 a0001c0001t0002g0079 others(80): Show |
83 | HG00408.hp1 HG00642.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.287-2005_287-2004d others(4): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72181723 | ||||||
chr5:72181755 | A | G | 1 | a0001c0004t0005g0107 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.287-1988A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72181755 | |||||||
chr5:72181823 | G | A | 12 | a0001c0002t0014g0003 a0001c0002t0016g0152 a0001c0005t0001g0304 others(9): Show |
13 | HG01167.hp2 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.287-1920G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72181823 | |||||||
chr5:72181824 | C | T | 12 | a0001c0002t0002g0111 a0001c0005t0008g0033 a0001c0005t0008g0035 others(9): Show |
12 | HG02145.hp1 HG02280.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.287-1919C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72181824 | |||||||
chr5:72181842 | A | G | 3 | a0001c0005t0005g0128 a0001c0005t0005g0154 a0001c0005t0005g0257 |
3 | HG02257.hp1 HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.287-1901A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72181842 | |||||||
chr5:72182023 | C | CT | 35 | a0001c0001t0001g0145 a0001c0001t0035g0300 a0001c0002t0002g0111 others(32): Show |
36 | HG00558.hp1 HG00738.hp2 HG01168.hp2 others(33): Show |
intron_variant | MODIFIER | c.287-1699dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72182023 | ||||||
chr5:72182023 | C | CTT | 13 | a0001c0001t0001g0086 a0001c0001t0001g0130 a0001c0001t0001g0210 others(10): Show |
13 | HG02015.hp2 HG02135.hp2 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.287-1700_287-1699d others(4): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72182023 | ||||||
chr5:72182023 | C | CTTT | 72 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(69): Show |
73 | HG00140.hp1 HG00609.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.287-1701_287-1699d others(5): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72182023 | ||||||
chr5:72182023 | C | CTTTT | 17 | a0001c0001t0001g0027 a0001c0001t0001g0249 a0001c0001t0001g0277 others(14): Show |
17 | HG00673.hp1 HG01192.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.287-1702_287-1699d others(6): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72182023 | ||||||
chr5:72182023 | CT | C | 8 | a0001c0001t0001g0219 a0001c0001t0004g0051 a0001c0001t0004g0084 others(5): Show |
8 | HG00735.hp2 HG01168.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-1699delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72182023 | ||||||
chr5:72182023 | CTT | C | 44 | a0001c0001t0002g0072 a0001c0001t0002g0079 a0001c0001t0002g0115 others(41): Show |
44 | HG00408.hp1 HG00642.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.287-1700_287-1699d others(4): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72182023 | ||||||
chr5:72182023 | CTTT | C | 10 | a0001c0005t0001g0304 a0001c0006t0005g0067 a0001c0006t0007g0259 others(7): Show |
10 | HG01167.hp2 HG01243.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.287-1701_287-1699d others(5): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72182023 | ||||||
chr5:72182023 | CTTTTTT | C | 55 | a0001c0001t0001g0066 a0001c0001t0001g0096 a0001c0001t0001g0114 others(52): Show |
56 | HG00558.hp2 HG00621.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.287-1704_287-1699d others(8): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | 72182023 | ||||||
chr5:72182050 | C | A | 18 | a0001c0001t0001g0272 a0001c0001t0001g0274 a0001c0001t0001g0276 others(15): Show |
18 | HG00609.hp2 HG02056.hp2 NA18942.hp1 others(15): Show |
intron_variant | MODIFIER | c.287-1693C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72182050 | |||||||
chr5:72182185 | A | G | 2 | a0001c0004t0022g0037 a0001c0028t0025g0042 |
2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.287-1558A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72182185 | |||||||
chr5:72182195 | C | T | 3 | a0001c0002t0013g0021 a0001c0002t0013g0225 a0001c0002t0013g0226 |
3 | HG01255.hp2 HG01346.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.287-1548C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72182195 | |||||||
chr5:72182438 | C | T | 6 | a0001c0001t0001g0066 a0001c0001t0001g0114 a0001c0002t0002g0032 others(3): Show |
6 | NA18941.hp1 NA18943.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-1305C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72182438 | |||||||
chr5:72182726 | A | G | 1 | a0001c0002t0003g0015 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.287-1017A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72182726 | |||||||
chr5:72182768 | A | G | 15 | a0001c0001t0001g0256 a0001c0004t0005g0107 a0001c0005t0001g0304 others(12): Show |
15 | HG00733.hp2 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.287-975A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72182768 | |||||||
chr5:72182912 | A | C | 1 | a0001c0001t0012g0012 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.287-831A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72182912 | |||||||
chr5:72182996 | A | G | 9 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0143 others(6): Show |
10 | HG01891.hp2 HG02055.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.287-747A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72182996 | |||||||
chr5:72183108 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.287-635A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72183108 | |||||||
chr5:72183694 | C | T | 1 | a0001c0002t0009g0227 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.287-49C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | chr5 | 72183694 | |||||||
chr5:72184010 | T | C | 1 | a0001c0001t0001g0335 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.369+185T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72184010 | |||||||
chr5:72184217 | A | C | 3 | a0001c0004t0001g0189 a0001c0004t0001g0327 a0001c0004t0001g0334 |
3 | HG02717.hp2 HG03041.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.369+392A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72184217 | |||||||
chr5:72184588 | G | A | 1 | a0001c0002t0003g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.369+763G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72184588 | |||||||
chr5:72184969 | G | A | 4 | a0001c0002t0003g0173 a0001c0002t0003g0176 a0001c0002t0004g0005 others(1): Show |
5 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.369+1144G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72184969 | |||||||
chr5:72185027 | T | A | 1 | a0013c0035t0005g0047 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.369+1202T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72185027 | |||||||
chr5:72185072 | G | A | 3 | a0007c0013t0001g0126 a0007c0013t0001g0264 a0007c0013t0029g0127 |
3 | HG03130.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.369+1247G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72185072 | |||||||
chr5:72185118 | G | A | 2 | a0001c0002t0001g0077 a0001c0002t0010g0224 |
2 | HG00408.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.369+1293G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72185118 | |||||||
chr5:72185210 | C | G | 3 | a0007c0013t0001g0126 a0007c0013t0001g0264 a0007c0013t0029g0127 |
3 | HG03130.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.369+1385C>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72185210 | |||||||
chr5:72185227 | C | T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0143 |
4 | HG02622.hp2 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-1387C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72185227 | |||||||
chr5:72185235 | C | A | 4 | a0004c0011t0001g0253 a0004c0011t0011g0137 a0004c0011t0011g0138 others(1): Show |
4 | HG01074.hp2 HG02965.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-1379C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72185235 | |||||||
chr5:72185423 | G | T | 1 | a0001c0008t0003g0183 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.370-1191G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72185423 | |||||||
chr5:72185438 | A | C | 2 | a0001c0004t0007g0141 a0012c0032t0033g0221 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.370-1176A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72185438 | |||||||
chr5:72185545 | G | A | 4 | a0005c0010t0005g0134 a0005c0010t0005g0255 a0005c0010t0005g0329 others(1): Show |
4 | HG02647.hp1 HG02922.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.370-1069G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72185545 | |||||||
chr5:72185576 | G | T | 2 | a0003c0007t0002g0098 a0003c0007t0002g0099 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.370-1038G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72185576 | |||||||
chr5:72185608 | GA | G | 290 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(287): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.370-990delA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr5 | 72185608 | ||||||
chr5:72185608 | GAA | G | 12 | a0001c0001t0001g0184 a0001c0004t0002g0179 a0001c0004t0007g0324 others(9): Show |
12 | HG00558.hp1 HG00738.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.370-991_370-990del others(2): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr5 | 72185608 | ||||||
chr5:72185974 | C | T | 1 | a0001c0001t0001g0281 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.370-640C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72185974 | |||||||
chr5:72185980 | C | T | 1 | a0001c0002t0002g0111 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.370-634C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72185980 | |||||||
chr5:72186060 | C | T | 308 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(305): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.370-554C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72186060 | |||||||
chr5:72186131 | G | A | 1 | a0001c0006t0007g0262 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.370-483G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72186131 | |||||||
chr5:72186218 | C | T | 2 | a0003c0007t0002g0098 a0003c0007t0002g0099 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.370-396C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72186218 | |||||||
chr5:72186340 | AC | A | 3 | a0001c0005t0005g0128 a0001c0005t0005g0154 a0001c0005t0005g0257 |
3 | HG02257.hp1 HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.370-273delC | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72186340 | |||||||
chr5:72186354 | C | T | 1 | a0001c0006t0018g0214 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.370-260C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 3/6 | chr5 | 72186354 | |||||||
chr5:72186768 | T | C | 1 | a0002c0003t0023g0242 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.510+14T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72186768 | |||||||
chr5:72186853 | C | T | 5 | a0001c0001t0012g0034 a0001c0001t0012g0056 a0001c0001t0012g0057 others(2): Show |
5 | HG02258.hp2 HG02559.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+99C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72186853 | |||||||
chr5:72187070 | G | A | 1 | a0001c0002t0002g0040 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.510+316G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72187070 | |||||||
chr5:72187329 | T | G | 1 | a0001c0004t0017g0064 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.510+575T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72187329 | |||||||
chr5:72187379 | G | T | 1 | a0001c0002t0002g0075 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.510+625G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72187379 | |||||||
chr5:72187386 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.510+632G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72187386 | |||||||
chr5:72187624 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(94): Show |
98 | HG00140.hp1 HG00609.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.510+870G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72187624 | |||||||
chr5:72187660 | A | G | 3 | a0001c0004t0001g0189 a0001c0004t0001g0334 a0012c0032t0033g0221 |
3 | HG02717.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.510+906A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72187660 | |||||||
chr5:72187914 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(94): Show |
98 | HG00140.hp1 HG00609.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.510+1160G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72187914 | |||||||
chr5:72188217 | G | A | 9 | a0001c0006t0005g0067 a0001c0006t0007g0259 a0001c0006t0007g0262 others(6): Show |
9 | HG01167.hp2 HG01243.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.510+1463G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72188217 | |||||||
chr5:72188285 | A | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(101): Show |
105 | HG00140.hp1 HG00609.hp2 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.510+1531A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72188285 | |||||||
chr5:72188336 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.510+1582A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72188336 | |||||||
chr5:72188570 | G | A | 1 | a0001c0001t0019g0246 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.510+1816G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72188570 | |||||||
chr5:72188605 | C | T | 1 | a0001c0004t0005g0107 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.510+1851C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72188605 | |||||||
chr5:72188986 | A | G | 3 | a0007c0013t0001g0126 a0007c0013t0001g0264 a0007c0013t0029g0127 |
3 | HG03130.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.510+2232A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72188986 | |||||||
chr5:72188991 | T | G | 309 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(306): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.510+2237T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72188991 | |||||||
chr5:72189038 | C | A | 2 | a0001c0006t0005g0067 a0001c0006t0018g0071 |
2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.510+2284C>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72189038 | |||||||
chr5:72189508 | G | C | 2 | a0001c0002t0002g0040 a0001c0002t0002g0160 |
2 | HG01109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.510+2754G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72189508 | |||||||
chr5:72189556 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0114 |
2 | NA18941.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.510+2802G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72189556 | |||||||
chr5:72189694 | T | TA | 16 | a0001c0001t0007g0119 a0001c0001t0007g0254 a0001c0001t0007g0269 others(13): Show |
16 | HG00621.hp2 HG01891.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.510+2953dupA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr5 | 72189694 | ||||||
chr5:72189694 | TA | T | 7 | a0001c0001t0001g0001 a0001c0006t0005g0067 a0001c0006t0018g0071 others(4): Show |
8 | HG01074.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.510+2953delA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr5 | 72189694 | ||||||
chr5:72189884 | A | G | 1 | a0001c0005t0008g0135 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.510+3130A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72189884 | |||||||
chr5:72189950 | A | T | 1 | a0001c0001t0001g0181 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.510+3196A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72189950 | |||||||
chr5:72190100 | T | C | 1 | a0012c0032t0033g0221 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.510+3346T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72190100 | |||||||
chr5:72190401 | C | T | 36 | a0001c0001t0002g0072 a0001c0001t0002g0079 a0001c0001t0002g0115 others(33): Show |
36 | HG00408.hp1 HG00642.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.511-3465C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72190401 | |||||||
chr5:72190472 | T | C | 1 | a0001c0002t0002g0151 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.511-3394T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72190472 | |||||||
chr5:72190474 | G | A | 1 | a0001c0004t0002g0179 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.511-3392G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72190474 | |||||||
chr5:72190807 | A | T | 1 | a0002c0003t0006g0150 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.511-3059A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72190807 | |||||||
chr5:72190819 | T | C | 5 | a0001c0001t0001g0074 a0001c0001t0001g0266 a0001c0001t0007g0119 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.511-3047T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72190819 | |||||||
chr5:72190885 | G | A | 19 | a0001c0001t0001g0145 a0001c0005t0005g0046 a0001c0005t0005g0128 others(16): Show |
19 | HG00741.hp2 HG01243.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.511-2981G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72190885 | |||||||
chr5:72190958 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(151): Show |
155 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(152): Show |
intron_variant | MODIFIER | c.511-2908C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72190958 | |||||||
chr5:72191036 | G | C | 1 | a0001c0002t0001g0092 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.511-2830G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72191036 | |||||||
chr5:72191059 | TAAGAACC others(14): Show |
T | 1 | a0010c0023t0006g0166 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.511-2806_511-2786d others(23): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72191059 | |||||||
chr5:72191517 | G | A | 4 | a0004c0011t0001g0253 a0004c0011t0011g0137 a0004c0011t0011g0138 others(1): Show |
4 | HG01074.hp2 HG02965.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-2349G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72191517 | |||||||
chr5:72191519 | A | G | 1 | a0010c0023t0006g0166 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.511-2347A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72191519 | |||||||
chr5:72191526 | G | A | 3 | a0001c0002t0002g0011 a0001c0002t0002g0054 a0001c0002t0023g0142 |
3 | HG01070.hp1 HG03831.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.511-2340G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72191526 | |||||||
chr5:72191974 | C | T | 309 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(306): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.511-1892C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72191974 | |||||||
chr5:72192236 | T | C | 1 | a0001c0006t0007g0259 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.511-1630T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72192236 | |||||||
chr5:72193074 | G | A | 4 | a0005c0010t0005g0134 a0005c0010t0005g0255 a0005c0010t0005g0329 others(1): Show |
4 | HG02647.hp1 HG02922.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-792G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72193074 | |||||||
chr5:72193077 | C | T | 43 | a0001c0001t0002g0072 a0001c0001t0002g0079 a0001c0001t0002g0115 others(40): Show |
43 | HG00408.hp1 HG00642.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.511-789C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72193077 | |||||||
chr5:72193094 | A | G | 2 | a0001c0005t0008g0332 a0001c0036t0008g0125 |
2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.511-772A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72193094 | |||||||
chr5:72193164 | A | G | 1 | a0001c0001t0004g0068 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.511-702A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72193164 | |||||||
chr5:72193172 | G | A | 1 | a0002c0003t0023g0242 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.511-694G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72193172 | |||||||
chr5:72193238 | G | A | 1 | a0001c0001t0015g0124 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.511-628G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72193238 | |||||||
chr5:72193255 | G | GT | 268 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(265): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.511-605dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr5 | 72193255 | ||||||
chr5:72193342 | C | CT | 35 | a0001c0001t0002g0072 a0001c0001t0002g0079 a0001c0001t0002g0146 others(32): Show |
35 | HG00408.hp1 HG00642.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-506dupT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr5 | 72193342 | ||||||
chr5:72193342 | CT | C | 247 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(244): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.511-506delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr5 | 72193342 | ||||||
chr5:72193348 | T | A | 3 | a0007c0013t0001g0126 a0007c0013t0001g0264 a0007c0013t0029g0127 |
3 | HG03130.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.511-518T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72193348 | |||||||
chr5:72193459 | ATC | A | 2 | a0001c0002t0014g0003 a0001c0002t0016g0152 |
3 | HG01884.hp1 HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.511-405_511-404del others(2): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr5 | 72193459 | ||||||
chr5:72193478 | G | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(93): Show |
97 | HG00140.hp1 HG00609.hp2 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.511-388G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72193478 | |||||||
chr5:72193677 | G | A | 1 | a0001c0002t0011g0265 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.511-189G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | chr5 | 72193677 | |||||||
chr5:72193833 | TTTTCTTT others(5): Show |
T | 1 | a0001c0002t0003g0287 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.511-21_511-10delCT others(10): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr5 | 72193833 | ||||||
chr5:72200441 | T | C | 1 | a0001c0001t0004g0195 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.7012+74T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72200441 | |||||||
chr5:72200466 | A | C | 1 | a0001c0001t0001g0027 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.7012+99A>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72200466 | |||||||
chr5:72200513 | C | T | 1 | a0001c0005t0001g0304 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.7012+146C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72200513 | |||||||
chr5:72200592 | A | G | 49 | a0001c0001t0001g0187 a0001c0001t0002g0031 a0001c0001t0002g0072 others(46): Show |
50 | HG00099.hp1 HG00408.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.7012+225A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72200592 | |||||||
chr5:72200702 | C | T | 1 | a0013c0035t0005g0047 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.7012+335C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72200702 | |||||||
chr5:72200831 | A | T | 4 | a0004c0011t0001g0253 a0004c0011t0011g0137 a0004c0011t0011g0138 others(1): Show |
4 | HG01074.hp2 HG02965.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.7012+464A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72200831 | |||||||
chr5:72200838 | A | T | 3 | a0001c0004t0007g0141 a0001c0004t0034g0215 a0012c0032t0033g0221 |
3 | HG02738.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.7012+471A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72200838 | |||||||
chr5:72200839 | T | A | 1 | a0001c0001t0001g0120 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.7012+472T>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72200839 | |||||||
chr5:72200988 | A | G | 1 | a0011c0021t0036g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.7012+621A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72200988 | |||||||
chr5:72201077 | G | T | 41 | a0001c0001t0007g0052 a0001c0001t0020g0131 a0001c0004t0001g0189 others(38): Show |
41 | HG00733.hp2 HG00741.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.7012+710G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72201077 | |||||||
chr5:72201199 | C | CA | 6 | a0001c0004t0001g0189 a0001c0004t0001g0327 a0001c0004t0001g0334 others(3): Show |
6 | HG02717.hp2 HG02738.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.7012+845dupA | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr5 | 72201199 | ||||||
chr5:72201218 | TTTAATTA others(21): Show |
T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(105): Show |
109 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.7012+855_7012+882d others(30): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr5 | 72201218 | ||||||
chr5:72201247 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.7012+880T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72201247 | |||||||
chr5:72201432 | G | A | 1 | a0001c0002t0003g0172 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.7012+1065G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72201432 | |||||||
chr5:72201449 | GT | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(193): Show |
198 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.7012+1087delT | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr5 | 72201449 | ||||||
chr5:72201492 | A | T | 1 | a0002c0003t0006g0217 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.7012+1125A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72201492 | |||||||
chr5:72202110 | A | T | 1 | a0001c0004t0017g0190 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.7013-1453A>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72202110 | |||||||
chr5:72202112 | G | A | 8 | a0001c0001t0002g0188 a0001c0002t0002g0026 a0001c0002t0002g0059 others(5): Show |
8 | HG00621.hp1 HG02523.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.7013-1451G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72202112 | |||||||
chr5:72202245 | G | A | 1 | a0001c0002t0001g0148 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.7013-1318G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72202245 | |||||||
chr5:72202284 | C | T | 1 | a0001c0002t0030g0070 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.7013-1279C>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72202284 | |||||||
chr5:72202556 | G | A | 16 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0118 others(13): Show |
16 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.7013-1007G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72202556 | |||||||
chr5:72202574 | G | T | 1 | a0001c0001t0001g0219 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.7013-989G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72202574 | |||||||
chr5:72202593 | A | G | 3 | a0004c0011t0011g0137 a0004c0011t0011g0138 a0004c0011t0011g0139 |
3 | HG01074.hp2 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.7013-970A>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72202593 | |||||||
chr5:72202840 | G | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(106): Show |
110 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.7013-723G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72202840 | |||||||
chr5:72203020 | T | G | 1 | a0002c0003t0006g0293 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.7013-543T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72203020 | |||||||
chr5:72203254 | G | T | 1 | a0008c0016t0001g0330 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.7013-309G>T | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72203254 | |||||||
chr5:72203488 | G | A | 4 | a0001c0001t0001g0066 a0001c0001t0001g0114 a0001c0001t0001g0117 others(1): Show |
4 | NA18941.hp1 NA18943.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.7013-75G>A | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | chr5 | 72203488 | |||||||
chr5:72203548 | G | GTC | 4 | a0005c0010t0005g0134 a0005c0010t0005g0255 a0005c0010t0005g0329 others(1): Show |
4 | HG02647.hp1 HG02922.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.7013-14_7013-13ins others(2): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr5 | 72203548 | ||||||
chr5:72204347 | T | G | 2 | a0001c0001t0020g0131 a0001c0005t0020g0258 |
2 | HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.7251+546T>G | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 6/6 | chr5 | 72204347 | |||||||
chr5:72204801 | T | C | 2 | a0001c0001t0007g0119 a0001c0001t0007g0254 |
2 | HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.7252-283T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 6/6 | chr5 | 72204801 | |||||||
chr5:72204932 | T | C | 2 | a0001c0002t0014g0003 a0001c0002t0016g0152 |
3 | HG01884.hp1 HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.7252-152T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 6/6 | chr5 | 72204932 | |||||||
chr5:72204981 | T | C | 1 | a0001c0002t0002g0004 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.7252-103T>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 6/6 | chr5 | 72204981 | |||||||
chr5:72204985 | CCTT | C | 4 | a0001c0001t0001g0074 a0001c0001t0001g0266 a0001c0005t0001g0008 others(1): Show |
4 | HG01884.hp2 HG02109.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.7252-91_7252-89del others(3): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr5 | 72204985 | ||||||
chr5:72204998 | G | C | 17 | a0001c0001t0007g0052 a0001c0001t0007g0119 a0001c0001t0007g0254 others(14): Show |
17 | HG01167.hp2 HG01243.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.7252-86G>C | MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 6/6 | chr5 | 72204998 |