Item | Value |
---|---|
geneid | 10198 |
ensemblid | ENSG00000051825.15 |
hgncid | 7215 |
symbol | MPHOSPH9 |
name | M-phase phosphoprotein 9 |
refseq_nuc | NM_022782.4 |
refseq_prot | NP_073619.3 |
ensembl_nuc | ENST00000606320.6 |
ensembl_prot | ENSP00000475489.1 |
mane_status | MANE Select |
chr | chr12 |
start | 123154215 |
end | 123233141 |
strand | - |
ver | v1.2 |
region | chr12:123154215-123233141 |
region5000 | chr12:123149215-123238141 |
regionname0 | MPHOSPH9_chr12_123154215_123233141 |
regionname5000 | MPHOSPH9_chr12_123149215_123238141 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1183 | 206 | 64 | 49 | 54 | 5 | 32 | 41 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | MEEFD others(1178): Show |
chr12 | 123149215 | 123238141 |
a0002 | 0/0 | 1183 | 50 | 2 | 5 | 39 | 0 | 4 | 29 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | MEEFD others(1178): Show |
chr12 | 123149215 | 123238141 |
a0003 | 0/0 | 1183 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | MEEFD others(1178): Show |
chr12 | 123149215 | 123238141 |
a0004 | 0/0 | 1183 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | MEEFD others(1178): Show |
chr12 | 123149215 | 123238141 |
a0005 | 0/0 | 1183 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | MEEFD others(1178): Show |
chr12 | 123149215 | 123238141 |
a0006 | 0/0 | 1183 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | MEEFD others(1178): Show |
chr12 | 123149215 | 123238141 |
a0007 | 0/0 | 1183 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | MEEFD others(1178): Show |
chr12 | 123149215 | 123238141 |
a0008 | 0/0 | 1183 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | MEEFD others(1178): Show |
chr12 | 123149215 | 123238141 |
a0009 | 0/0 | 1183 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | MEEFD others(1178): Show |
chr12 | 123149215 | 123238141 |
a0010 | 0/0 | 1183 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | MEEFD others(1178): Show |
chr12 | 123149215 | 123238141 |
a0011 | 0/0 | 1183 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | MEEFD others(1178): Show |
chr12 | 123149215 | 123238141 |
a0012 | 0/0 | 1183 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | MEEFD others(1178): Show |
chr12 | 123149215 | 123238141 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 3549 | 96 | 58 | 18 | 4 | 2 | 12 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | ATGGA others(3544): Show |
chr12 | 123149215 | 123238141 | ||
a0001c0002 | 0/0 | 3549 | 83 | 1 | 23 | 42 | 0 | 17 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | ATGGA others(3544): Show |
chr12 | 123149215 | 123238141 | ||
a0001c0004 | 0/0 | 3549 | 19 | 2 | 7 | 4 | 3 | 3 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | ATGGA others(3544): Show |
chr12 | 123149215 | 123238141 | ||
a0001c0005 | 0/0 | 3549 | 4 | 0 | 0 | 4 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | ATGGA others(3544): Show |
chr12 | 123149215 | 123238141 | ||
a0001c0007 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | ATGGA others(3544): Show |
chr12 | 123149215 | 123238141 | ||
a0001c0008 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | ATGGA others(3544): Show |
chr12 | 123149215 | 123238141 | ||
a0001c0009 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | ATGGA others(3544): Show |
chr12 | 123149215 | 123238141 | ||
a0001c0016 | 0/0 | 3549 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | ATGGA others(3544): Show |
chr12 | 123149215 | 123238141 | ||
a0002c0003 | 0/0 | 3549 | 46 | 2 | 5 | 35 | 0 | 4 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | ATGGA others(3544): Show |
chr12 | 123149215 | 123238141 | ||
a0002c0006 | 0/0 | 3549 | 3 | 0 | 0 | 3 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | ATGGA others(3544): Show |
chr12 | 123149215 | 123238141 | ||
a0002c0012 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | ATGGA others(3544): Show |
chr12 | 123149215 | 123238141 | ||
a0003c0019 | 0/0 | 3549 | 1 | 0 | 0 | 0 | 1 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | ATGGA others(3544): Show |
chr12 | 123149215 | 123238141 | ||
a0004c0013 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | ATGGA others(3544): Show |
chr12 | 123149215 | 123238141 | ||
a0005c0021 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | ATGGA others(3544): Show |
chr12 | 123149215 | 123238141 | ||
a0006c0011 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | ATGGA others(3544): Show |
chr12 | 123149215 | 123238141 | ||
a0007c0017 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | ATGGA others(3544): Show |
chr12 | 123149215 | 123238141 | ||
a0008c0015 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | ATGGA others(3544): Show |
chr12 | 123149215 | 123238141 | ||
a0009c0020 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | ATGGA others(3544): Show |
chr12 | 123149215 | 123238141 | ||
a0010c0010 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | ATGGA others(3544): Show |
chr12 | 123149215 | 123238141 | ||
a0011c0014 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | ATGGA others(3544): Show |
chr12 | 123149215 | 123238141 | ||
a0012c0018 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | ATGGA others(3544): Show |
chr12 | 123149215 | 123238141 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0003 | 0/0 | 6368 | 32 | 29 | 3 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6363): Show |
chr12 | 123149215 | 123238141 |
a0001c0001t0004 | 1/1 | 6369 | 26 | 3 | 13 | 0 | 1 | 7 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6364): Show |
chr12 | 123149215 | 123238141 |
a0001c0001t0005 | 0/0 | 6367 | 15 | 15 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6362): Show |
chr12 | 123149215 | 123238141 |
a0001c0001t0006 | 0/0 | 6368 | 9 | 0 | 0 | 4 | 0 | 5 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6363): Show |
chr12 | 123149215 | 123238141 |
a0001c0001t0009 | 0/0 | 6369 | 3 | 3 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6364): Show |
chr12 | 123149215 | 123238141 |
a0001c0001t0010 | 0/0 | 6364 | 3 | 0 | 2 | 0 | 1 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6359): Show |
chr12 | 123149215 | 123238141 |
a0001c0001t0012 | 0/0 | 6368 | 2 | 2 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6363): Show |
chr12 | 123149215 | 123238141 |
a0001c0001t0015 | 0/0 | 6369 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6364): Show |
chr12 | 123149215 | 123238141 |
a0001c0001t0020 | 0/0 | 6369 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6364): Show |
chr12 | 123149215 | 123238141 |
a0001c0001t0021 | 0/0 | 6369 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6364): Show |
chr12 | 123149215 | 123238141 |
a0001c0001t0023 | 0/0 | 6367 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6362): Show |
chr12 | 123149215 | 123238141 |
a0001c0001t0028 | 0/0 | 6368 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6363): Show |
chr12 | 123149215 | 123238141 |
a0001c0001t0030 | 0/0 | 6369 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6364): Show |
chr12 | 123149215 | 123238141 |
a0001c0002t0001 | 0/0 | 6365 | 71 | 1 | 22 | 37 | 0 | 11 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6360): Show |
chr12 | 123149215 | 123238141 |
a0001c0002t0007 | 0/0 | 6364 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6359): Show |
chr12 | 123149215 | 123238141 |
a0001c0002t0008 | 0/0 | 6364 | 4 | 0 | 0 | 2 | 0 | 2 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6359): Show |
chr12 | 123149215 | 123238141 |
a0001c0002t0013 | 0/0 | 6365 | 2 | 0 | 0 | 0 | 0 | 2 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6360): Show |
chr12 | 123149215 | 123238141 |
a0001c0002t0014 | 0/0 | 6365 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6360): Show |
chr12 | 123149215 | 123238141 |
a0001c0002t0016 | 0/0 | 6365 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6360): Show |
chr12 | 123149215 | 123238141 |
a0001c0002t0017 | 0/0 | 6363 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6358): Show |
chr12 | 123149215 | 123238141 |
a0001c0002t0018 | 0/0 | 6365 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6360): Show |
chr12 | 123149215 | 123238141 |
a0001c0002t0019 | 0/0 | 6365 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6360): Show |
chr12 | 123149215 | 123238141 |
a0001c0004t0001 | 0/0 | 6365 | 9 | 1 | 5 | 0 | 3 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6360): Show |
chr12 | 123149215 | 123238141 |
a0001c0004t0007 | 0/0 | 6364 | 7 | 0 | 1 | 4 | 0 | 2 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6359): Show |
chr12 | 123149215 | 123238141 |
a0001c0004t0011 | 0/0 | 6364 | 2 | 1 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6359): Show |
chr12 | 123149215 | 123238141 |
a0001c0004t0024 | 0/0 | 6364 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6359): Show |
chr12 | 123149215 | 123238141 |
a0001c0005t0001 | 0/0 | 6365 | 4 | 0 | 0 | 4 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6360): Show |
chr12 | 123149215 | 123238141 |
a0001c0007t0029 | 0/0 | 6368 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6363): Show |
chr12 | 123149215 | 123238141 |
a0001c0008t0003 | 0/0 | 6368 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6363): Show |
chr12 | 123149215 | 123238141 |
a0001c0009t0022 | 0/0 | 6368 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6363): Show |
chr12 | 123149215 | 123238141 |
a0001c0016t0001 | 0/0 | 6365 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6360): Show |
chr12 | 123149215 | 123238141 |
a0002c0003t0001 | 0/0 | 6365 | 2 | 0 | 0 | 1 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6360): Show |
chr12 | 123149215 | 123238141 |
a0002c0003t0002 | 0/0 | 6364 | 41 | 1 | 5 | 32 | 0 | 3 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6359): Show |
chr12 | 123149215 | 123238141 |
a0002c0003t0025 | 0/0 | 6364 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6359): Show |
chr12 | 123149215 | 123238141 |
a0002c0003t0026 | 0/0 | 6363 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6358): Show |
chr12 | 123149215 | 123238141 |
a0002c0003t0027 | 0/0 | 6365 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6360): Show |
chr12 | 123149215 | 123238141 |
a0002c0006t0002 | 0/0 | 6364 | 3 | 0 | 0 | 3 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6359): Show |
chr12 | 123149215 | 123238141 |
a0002c0012t0002 | 0/0 | 6364 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6359): Show |
chr12 | 123149215 | 123238141 |
a0003c0019t0004 | 0/0 | 6369 | 1 | 0 | 0 | 0 | 1 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6364): Show |
chr12 | 123149215 | 123238141 |
a0004c0013t0002 | 0/0 | 6364 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6359): Show |
chr12 | 123149215 | 123238141 |
a0005c0021t0001 | 0/0 | 6365 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6360): Show |
chr12 | 123149215 | 123238141 |
a0006c0011t0002 | 0/0 | 6364 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6359): Show |
chr12 | 123149215 | 123238141 |
a0007c0017t0005 | 0/0 | 6367 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6362): Show |
chr12 | 123149215 | 123238141 |
a0008c0015t0003 | 0/0 | 6368 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6363): Show |
chr12 | 123149215 | 123238141 |
a0009c0020t0005 | 0/0 | 6367 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6362): Show |
chr12 | 123149215 | 123238141 |
a0010c0010t0001 | 0/0 | 6365 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6360): Show |
chr12 | 123149215 | 123238141 |
a0011c0014t0002 | 0/0 | 6364 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6359): Show |
chr12 | 123149215 | 123238141 |
a0012c0018t0003 | 0/0 | 6368 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | CCCTC others(6363): Show |
chr12 | 123149215 | 123238141 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0004g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0004g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0004g0173 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0004g0176 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0004g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0004g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0004g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0006g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0006g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0006g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0006g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0006g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0006g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0006g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0006g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0006g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0009g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0009g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0009g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0010g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0010g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0010g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0012g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0012g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0015g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0020g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0021g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0023g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0028g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0001t0030g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0007g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0008g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0008g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0008g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0008g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0013g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0013g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0014g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0016g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0017g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0018g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0002t0019g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0004t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0004t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0004t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0004t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0004t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0004t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0004t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0004t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0004t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0004t0007g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0004t0007g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0004t0007g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0004t0007g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0004t0007g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0004t0007g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0004t0007g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0004t0011g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0004t0011g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0004t0024g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0005t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0005t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0005t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0005t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0007t0029g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0008t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0009t0022g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0001c0016t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0025g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0026g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0003t0027g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0006t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0006t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0006t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0002c0012t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0003c0019t0004g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0004c0013t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0005c0021t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0006c0011t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0007c0017t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0008c0015t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0009c0020t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0010c0010t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0011c0014t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
a0012c0018t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0010 | g0183 | EUR | GBR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG00140 | hp2 | a0001 | c0004 | t0001 | g0032 | EUR | GBR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG00558 | hp1 | a0002 | c0003 | t0002 | g0263 | EAS | CHS | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG00558 | hp2 | a0001 | c0002 | t0007 | g0037 | EAS | CHS | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG00597 | hp1 | a0001 | c0005 | t0001 | g0094 | EAS | CHS | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | CHS | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG00609 | hp1 | a0001 | c0005 | t0001 | g0095 | EAS | CHS | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG00609 | hp2 | a0002 | c0003 | t0002 | g0259 | EAS | CHS | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | CHS | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG00621 | hp2 | a0002 | c0003 | t0002 | g0242 | EAS | CHS | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0046 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0083 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG00642 | hp1 | a0001 | c0004 | t0001 | g0075 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG00642 | hp2 | a0002 | c0003 | t0002 | g0222 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | CHS | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG00673 | hp2 | a0002 | c0003 | t0002 | g0220 | EAS | CHS | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0030 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG00735 | hp2 | a0001 | c0004 | t0001 | g0004 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0026 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0186 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0172 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0064 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0028 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01069 | hp2 | a0002 | c0003 | t0002 | g0225 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01070 | hp1 | a0001 | c0001 | t0004 | g0191 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01070 | hp2 | a0002 | c0003 | t0002 | g0223 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0190 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01074 | hp1 | a0001 | c0001 | t0004 | g0182 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0170 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01081 | hp2 | a0001 | c0004 | t0001 | g0076 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0142 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0082 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01106 | hp1 | a0001 | c0004 | t0001 | g0073 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0179 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0146 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01109 | hp2 | a0001 | c0001 | t0010 | g0184 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01167 | hp1 | a0001 | c0001 | t0004 | g0181 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0063 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01175 | hp1 | a0001 | c0004 | t0011 | g0105 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0159 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01243 | hp2 | a0002 | c0003 | t0002 | g0213 | AMR | PUR | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0061 | AMR | CLM | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01256 | hp2 | a0001 | c0001 | t0010 | g0174 | AMR | CLM | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0068 | AMR | CLM | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0056 | AMR | CLM | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01261 | hp1 | a0001 | c0001 | t0004 | g0188 | AMR | CLM | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01261 | hp2 | a0001 | c0004 | t0001 | g0074 | AMR | CLM | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01361 | hp1 | a0001 | c0002 | t0016 | g0067 | AMR | CLM | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0066 | AMR | CLM | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01516 | hp1 | a0003 | c0019 | t0004 | g0196 | EUR | IBS | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01516 | hp2 | a0001 | c0004 | t0001 | g0005 | EUR | IBS | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0132 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0137 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01891 | hp1 | a0001 | c0001 | t0009 | g0164 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01952 | hp1 | a0001 | c0016 | t0001 | g0097 | AMR | PEL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01952 | hp2 | a0001 | c0004 | t0007 | g0109 | AMR | PEL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0096 | AMR | PEL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01975 | hp2 | a0001 | c0001 | t0004 | g0171 | AMR | PEL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0099 | AMR | PEL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01978 | hp2 | a0001 | c0001 | t0004 | g0195 | AMR | PEL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01993 | hp1 | a0001 | c0001 | t0004 | g0166 | AMR | PEL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0098 | AMR | PEL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02040 | hp1 | a0004 | c0013 | t0002 | g0248 | EAS | KHV | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | KHV | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02071 | hp1 | a0005 | c0021 | t0001 | g0088 | EAS | KHV | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02071 | hp2 | a0006 | c0011 | t0002 | g0219 | EAS | KHV | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | KHV | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02080 | hp2 | a0002 | c0003 | t0002 | g0233 | EAS | KHV | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02132 | hp1 | a0002 | c0006 | t0002 | g0251 | EAS | KHV | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02132 | hp2 | a0001 | c0004 | t0007 | g0111 | EAS | KHV | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02145 | hp1 | a0007 | c0017 | t0005 | g0203 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0136 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02155 | hp1 | a0002 | c0003 | t0002 | g0232 | EAS | CDX | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | CDX | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0121 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02258 | hp2 | a0001 | c0004 | t0001 | g0007 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02293 | hp1 | a0002 | c0003 | t0002 | g0235 | AMR | PEL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | PEL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02300 | hp1 | a0001 | c0001 | t0004 | g0194 | AMR | PEL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0038 | AMR | PEL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0180 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02451 | hp2 | a0001 | c0001 | t0009 | g0158 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | KHV | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02523 | hp2 | a0002 | c0003 | t0002 | g0228 | EAS | KHV | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0201 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0141 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02602 | hp1 | a0001 | c0002 | t0014 | g0008 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02602 | hp2 | a0001 | c0001 | t0006 | g0265 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0157 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02615 | hp2 | a0001 | c0001 | t0005 | g0208 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02622 | hp1 | a0001 | c0008 | t0003 | g0199 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0119 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0120 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02630 | hp2 | a0001 | c0001 | t0021 | g0205 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0123 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02647 | hp2 | a0001 | c0001 | t0005 | g0134 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02683 | hp1 | a0001 | c0004 | t0024 | g0102 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02683 | hp2 | a0001 | c0002 | t0019 | g0039 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0017 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0079 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02735 | hp1 | a0002 | c0003 | t0002 | g0258 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02735 | hp2 | a0001 | c0001 | t0004 | g0175 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02738 | hp1 | a0001 | c0004 | t0007 | g0103 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02738 | hp2 | a0001 | c0002 | t0008 | g0040 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0139 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02809 | hp2 | a0001 | c0009 | t0022 | g0162 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0128 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02886 | hp2 | a0008 | c0015 | t0003 | g0163 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02895 | hp1 | a0001 | c0001 | t0005 | g0126 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0161 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02896 | hp1 | a0001 | c0001 | t0030 | g0211 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0155 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0129 | AFR | GWD | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02922 | hp1 | a0001 | c0001 | t0012 | g0151 | AFR | ESN | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0169 | AFR | ESN | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0207 | AFR | ESN | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02965 | hp2 | a0001 | c0001 | t0009 | g0144 | AFR | ESN | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0154 | AFR | ESN | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02970 | hp2 | a0009 | c0020 | t0005 | g0104 | AFR | ESN | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02976 | hp1 | a0001 | c0001 | t0015 | g0107 | AFR | ESN | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | ESN | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0044 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0177 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03139 | hp1 | a0001 | c0007 | t0029 | g0210 | AFR | ESN | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0156 | AFR | ESN | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0204 | AFR | MSL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0135 | AFR | MSL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0081 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03239 | hp2 | a0001 | c0004 | t0007 | g0113 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | MSL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0167 | AFR | MSL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0200 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0015 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03491 | hp1 | a0001 | c0001 | t0006 | g0002 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0021 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03492 | hp2 | a0001 | c0001 | t0006 | g0003 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03516 | hp1 | a0002 | c0003 | t0002 | g0212 | AFR | ESN | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03516 | hp2 | a0001 | c0001 | t0020 | g0145 | AFR | ESN | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03654 | hp1 | a0001 | c0001 | t0004 | g0187 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0043 | SAS | PJL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03688 | hp1 | a0001 | c0001 | t0006 | g0264 | SAS | STU | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03688 | hp2 | a0001 | c0002 | t0013 | g0090 | SAS | STU | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03831 | hp1 | a0002 | c0003 | t0002 | g0214 | SAS | BEB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03831 | hp2 | a0001 | c0002 | t0008 | g0031 | SAS | BEB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03834 | hp1 | a0002 | c0003 | t0001 | g0229 | SAS | BEB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03834 | hp2 | a0001 | c0002 | t0013 | g0089 | SAS | BEB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0192 | SAS | BEB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0019 | SAS | BEB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG04199 | hp1 | a0001 | c0001 | t0006 | g0118 | SAS | STU | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0193 | SAS | STU | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0178 | SAS | STU | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0058 | SAS | STU | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG04228 | hp1 | a0002 | c0003 | t0002 | g0236 | SAS | STU | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0020 | SAS | STU | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0131 | AFR | YRI | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0153 | AFR | YRI | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18612 | hp1 | a0001 | c0002 | t0008 | g0060 | EAS | CHB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18612 | hp2 | a0002 | c0003 | t0002 | g0256 | EAS | CHB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18747 | hp2 | a0002 | c0003 | t0001 | g0231 | EAS | CHB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0138 | AFR | YRI | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18906 | hp2 | a0001 | c0001 | t0012 | g0150 | AFR | YRI | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18941 | hp2 | a0002 | c0003 | t0002 | g0243 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18942 | hp2 | a0002 | c0003 | t0002 | g0255 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18948 | hp1 | a0010 | c0010 | t0001 | g0033 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18948 | hp2 | a0002 | c0003 | t0002 | g0261 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18949 | hp1 | a0002 | c0006 | t0002 | g0240 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18951 | hp2 | a0001 | c0001 | t0006 | g0115 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18952 | hp2 | a0002 | c0006 | t0002 | g0260 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18953 | hp1 | a0001 | c0002 | t0008 | g0009 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18953 | hp2 | a0002 | c0003 | t0002 | g0234 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18957 | hp1 | a0002 | c0003 | t0002 | g0262 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18963 | hp1 | a0002 | c0003 | t0002 | g0217 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18972 | hp1 | a0001 | c0004 | t0007 | g0110 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18972 | hp2 | a0002 | c0003 | t0002 | g0241 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18974 | hp2 | a0002 | c0003 | t0002 | g0238 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18977 | hp2 | a0001 | c0001 | t0006 | g0117 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18979 | hp1 | a0001 | c0005 | t0001 | g0093 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18979 | hp2 | a0001 | c0002 | t0018 | g0084 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18982 | hp1 | a0002 | c0003 | t0025 | g0080 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18987 | hp1 | a0002 | c0003 | t0002 | g0254 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18987 | hp2 | a0001 | c0005 | t0001 | g0092 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18989 | hp1 | a0002 | c0003 | t0027 | g0227 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18989 | hp2 | a0001 | c0004 | t0007 | g0112 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18990 | hp2 | a0002 | c0003 | t0002 | g0239 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18991 | hp2 | a0002 | c0003 | t0002 | g0249 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18992 | hp1 | a0002 | c0003 | t0002 | g0246 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18993 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18993 | hp2 | a0002 | c0003 | t0002 | g0250 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18995 | hp1 | a0002 | c0003 | t0002 | g0237 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18999 | hp1 | a0002 | c0003 | t0002 | g0244 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19003 | hp2 | a0002 | c0003 | t0002 | g0230 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19005 | hp2 | a0001 | c0001 | t0006 | g0114 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19012 | hp1 | a0002 | c0003 | t0002 | g0245 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | LWK | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19030 | hp2 | a0001 | c0001 | t0005 | g0133 | AFR | LWK | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0125 | AFR | LWK | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0130 | AFR | LWK | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19054 | hp2 | a0002 | c0003 | t0002 | g0252 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19055 | hp1 | a0002 | c0003 | t0002 | g0247 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19055 | hp2 | a0001 | c0002 | t0017 | g0071 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19056 | hp1 | a0001 | c0004 | t0007 | g0108 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19057 | hp2 | a0001 | c0001 | t0006 | g0116 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19063 | hp1 | a0002 | c0012 | t0002 | g0224 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19063 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19064 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19064 | hp2 | a0002 | c0003 | t0002 | g0257 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19067 | hp1 | a0002 | c0003 | t0002 | g0215 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19082 | hp2 | a0002 | c0003 | t0002 | g0226 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19083 | hp1 | a0011 | c0014 | t0002 | g0221 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19084 | hp2 | a0002 | c0003 | t0002 | g0218 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19090 | hp1 | a0002 | c0003 | t0002 | g0216 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0197 | AFR | YRI | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA19240 | hp2 | a0001 | c0001 | t0023 | g0209 | AFR | YRI | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA20129 | hp1 | a0001 | c0004 | t0011 | g0106 | AFR | ASW | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0152 | AFR | ASW | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA20805 | hp1 | a0001 | c0004 | t0001 | g0072 | EUR | TSI | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0185 | EUR | TSI | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0160 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0189 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02486 | hp1 | a0001 | c0001 | t0005 | g0206 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02486 | hp2 | a0001 | c0001 | t0028 | g0165 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0198 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0202 | AFR | ACB | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | MSL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
HG03471 | hp2 | a0002 | c0003 | t0026 | g0253 | AFR | MSL | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0168 | AFR | USA | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA20300 | hp2 | a0012 | c0018 | t0003 | g0140 | AFR | USA | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA21309 | hp1 | a0001 | c0001 | t0005 | g0127 | AFR | LWK | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | LWK | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0173 | REF | REF | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0176 | REF | REF | MPHOSPH9_chr12_123149215_123238141 | MPHOSPH9 | chr12 | 123149215 | 123238141 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:123156874 | C | T | 1 | a0007 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.3485G>A | p.Arg1162Gln | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 3710/6369 | 3485/3552 | 1162/1183 | chr12 | 123156874 | |||
chr12:123163031 | A | C | 1 | a0008 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.3012T>G | p.Asn1004Lys | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 20/24 | 3237/6369 | 3012/3552 | 1004/1183 | chr12 | 123163031 | |||
chr12:123163083 | C | T | 1 | a0006 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.2960G>A | p.Arg987Gln | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 20/24 | 3185/6369 | 2960/3552 | 987/1183 | chr12 | 123163083 | |||
chr12:123202775 | T | C | 1 | a0004 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.1630A>G | p.Ser544Gly | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 10/24 | 1855/6369 | 1630/3552 | 544/1183 | chr12 | 123202775 | |||
chr12:123218389 | G | A | 1 | a0011 | 1 | NA19083.hp1 | missense_variant | MODERATE | c.983C>T | p.Thr328Ile | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/24 | 1208/6369 | 983/3552 | 328/1183 | chr12 | 123218389 | |||
chr12:123221415 | C | T | 4 | a0002 a0004 a0006 others(1): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
missense_variant | MODERATE | c.829G>A | p.Gly277Ser | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/24 | 1054/6369 | 829/3552 | 277/1183 | chr12 | 123221415 | |||
chr12:123221417 | A | G | 1 | a0010 | 1 | NA18948.hp1 | missense_variant | MODERATE | c.827T>C | p.Leu276Pro | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/24 | 1052/6369 | 827/3552 | 276/1183 | chr12 | 123221417 | |||
chr12:123221759 | C | A | 1 | a0012 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.485G>T | p.Arg162Ile | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/24 | 710/6369 | 485/3552 | 162/1183 | chr12 | 123221759 | |||
chr12:123221766 | T | G | 1 | a0003 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.478A>C | p.Ser160Arg | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/24 | 703/6369 | 478/3552 | 160/1183 | chr12 | 123221766 | |||
chr12:123221812 | G | C | 1 | a0009 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.432C>G | p.Asn144Lys | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/24 | 657/6369 | 432/3552 | 144/1183 | chr12 | 123221812 | |||
chr12:123230286 | G | C | 1 | a0005 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.79C>G | p.Leu27Val | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/24 | 304/6369 | 79/3552 | 27/1183 | chr12 | 123230286 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:123161256 | G | A | 12 | a0001c0002 a0001c0004 a0001c0005 others(9): Show |
162 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(159): Show |
synonymous_variant | LOW | c.3261C>T | p.Tyr1087Tyr | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 22/24 | 3486/6369 | 3261/3552 | 1087/1183 | chr12 | 123161256 | |||
chr12:123166771 | G | A | 1 | a0002c0012 | 1 | NA19063.hp1 | synonymous_variant | LOW | c.2475C>T | p.Asp825Asp | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 17/24 | 2700/6369 | 2475/3552 | 825/1183 | chr12 | 123166771 | |||
chr12:123179967 | G | A | 5 | a0001c0002 a0001c0005 a0001c0016 others(2): Show |
90 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(87): Show |
synonymous_variant | LOW | c.2313C>T | p.Asn771Asn | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/24 | 2538/6369 | 2313/3552 | 771/1183 | chr12 | 123179967 | |||
chr12:123198313 | A | G | 1 | a0001c0016 | 1 | HG01952.hp1 | synonymous_variant | LOW | c.1959T>C | p.Ala653Ala | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/24 | 2184/6369 | 1959/3552 | 653/1183 | chr12 | 123198313 | |||
chr12:123202854 | C | T | 1 | a0008c0015 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.1551G>A | p.Pro517Pro | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 10/24 | 1776/6369 | 1551/3552 | 517/1183 | chr12 | 123202854 | |||
chr12:123210125 | G | A | 3 | a0002c0006 a0002c0012 a0004c0013 |
5 | HG02040.hp1 HG02132.hp1 NA18949.hp1 others(2): Show |
synonymous_variant | LOW | c.1125C>T | p.His375His | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/24 | 1350/6369 | 1125/3552 | 375/1183 | chr12 | 123210125 | |||
chr12:123221473 | A | G | 1 | a0001c0009 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.771T>C | p.His257His | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/24 | 996/6369 | 771/3552 | 257/1183 | chr12 | 123221473 | |||
chr12:123221539 | C | T | 1 | a0001c0008 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.705G>A | p.Pro235Pro | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/24 | 930/6369 | 705/3552 | 235/1183 | chr12 | 123221539 | |||
chr12:123221560 | C | T | 1 | a0001c0007 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.684G>A | p.Gln228Gln | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/24 | 909/6369 | 684/3552 | 228/1183 | chr12 | 123221560 | |||
chr12:123221641 | G | T | 1 | a0001c0005 | 4 | HG00597.hp1 HG00609.hp1 NA18979.hp1 others(1): Show |
synonymous_variant | LOW | c.603C>A | p.Thr201Thr | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/24 | 828/6369 | 603/3552 | 201/1183 | chr12 | 123221641 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:123154322 | A | G | 1 | a0001c0009t0022 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2485T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 2485 | chr12 | 123154322 | ||||||
chr12:123154383 | G | A | 27 | a0001c0002t0001 a0001c0002t0007 a0001c0002t0008 others(24): Show |
162 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*2424C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 2424 | chr12 | 123154383 | ||||||
chr12:123154527 | C | T | 1 | a0002c0003t0025 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2280G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 2280 | chr12 | 123154527 | ||||||
chr12:123154636 | C | T | 2 | a0001c0004t0011 a0001c0004t0024 |
3 | HG01175.hp1 HG02683.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2171G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 2171 | chr12 | 123154636 | ||||||
chr12:123154877 | G | A | 1 | a0001c0002t0013 | 2 | HG03688.hp2 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1930C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 1930 | chr12 | 123154877 | ||||||
chr12:123154992 | T | TA | 27 | a0001c0001t0009 a0001c0001t0020 a0001c0002t0001 others(24): Show |
161 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*1814dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 1814 | chr12 | 123154992 | ||||||
chr12:123155214 | TAAATA | T | 28 | a0001c0001t0010 a0001c0002t0001 a0001c0002t0007 others(25): Show |
165 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*1588_*1592delTATT others(1): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 1588 | chr12 | 123155214 | ||||||
chr12:123155322 | G | C | 9 | a0002c0003t0002 a0002c0003t0025 a0002c0003t0026 others(6): Show |
51 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1485C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 1485 | chr12 | 123155322 | ||||||
chr12:123155415 | C | T | 1 | a0001c0004t0024 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1392G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 1392 | chr12 | 123155415 | ||||||
chr12:123155461 | G | C | 1 | a0001c0009t0022 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1346C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 1346 | chr12 | 123155461 | ||||||
chr12:123155500 | G | A | 1 | a0001c0001t0023 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1307C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 1307 | chr12 | 123155500 | ||||||
chr12:123155627 | T | C | 1 | a0001c0002t0018 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1180A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 1180 | chr12 | 123155627 | ||||||
chr12:123155694 | A | G | 1 | a0001c0002t0016 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1113T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 1113 | chr12 | 123155694 | ||||||
chr12:123155715 | G | C | 1 | a0001c0001t0006 | 9 | HG02602.hp2 HG03491.hp1 HG03492.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1092C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 1092 | chr12 | 123155715 | ||||||
chr12:123155814 | C | T | 1 | a0001c0001t0020 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*993G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 993 | chr12 | 123155814 | ||||||
chr12:123156117 | C | A | 27 | a0001c0002t0001 a0001c0002t0007 a0001c0002t0008 others(24): Show |
162 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*690G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 690 | chr12 | 123156117 | ||||||
chr12:123156306 | C | G | 41 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 others(38): Show |
223 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(220): Show |
3_prime_UTR_variant | MODIFIER | c.*501G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 501 | chr12 | 123156306 | ||||||
chr12:123156323 | T | G | 1 | a0001c0002t0019 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*484A>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 484 | chr12 | 123156323 | ||||||
chr12:123156653 | C | T | 14 | a0001c0002t0001 a0001c0002t0008 a0001c0002t0013 others(11): Show |
100 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*154G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 154 | chr12 | 123156653 | ||||||
chr12:123156771 | A | T | 1 | a0001c0001t0015 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*36T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 24/24 | 36 | chr12 | 123156771 | ||||||
chr12:123230393 | T | C | 1 | a0001c0002t0013 | 2 | HG03688.hp2 HG03834.hp2 |
5_prime_UTR_variant | MODIFIER | c.-29A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/24 | 29 | chr12 | 123230393 | ||||||
chr12:123230460 | T | C | 1 | a0001c0001t0028 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-96A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/24 | 96 | chr12 | 123230460 | ||||||
chr12:123230466 | G | C | 2 | a0001c0001t0030 a0001c0007t0029 |
2 | HG02896.hp1 HG03139.hp1 |
5_prime_UTR_variant | MODIFIER | c.-102C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/24 | 102 | chr12 | 123230466 | ||||||
chr12:123230516 | A | G | 1 | a0001c0002t0014 | 1 | HG02602.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-152T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/24 | chr12 | 123230516 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:123157207 | G | A | 1 | a0007c0017t0005g0203 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3451-299C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123157207 | |||||||
chr12:123157304 | C | T | 1 | a0001c0002t0001g0011 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3451-396G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123157304 | |||||||
chr12:123157352 | A | G | 3 | a0001c0002t0001g0006 a0001c0002t0001g0024 a0001c0002t0001g0064 |
3 | HG00733.hp1 HG00741.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.3451-444T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123157352 | |||||||
chr12:123157383 | TA | T | 191 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(188): Show |
192 | HG00140.hp2 HG00558.hp1 HG00597.hp1 others(189): Show |
intron_variant | MODIFIER | c.3451-476delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123157383 | |||||||
chr12:123157512 | C | G | 1 | a0012c0018t0003g0140 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3451-604G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123157512 | |||||||
chr12:123157673 | G | T | 99 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(96): Show |
100 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.3451-765C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123157673 | |||||||
chr12:123157835 | A | T | 1 | a0001c0001t0003g0146 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3451-927T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123157835 | |||||||
chr12:123157986 | A | AT | 11 | a0001c0001t0005g0126 a0001c0001t0005g0127 a0001c0001t0005g0128 others(8): Show |
11 | HG01884.hp1 HG02615.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.3451-1079dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123157986 | |||||||
chr12:123157991 | T | A | 162 | a0001c0001t0005g0204 a0001c0002t0001g0001 a0001c0002t0001g0006 others(159): Show |
163 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(160): Show |
intron_variant | MODIFIER | c.3451-1083A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123157991 | |||||||
chr12:123157992 | T | A | 1 | a0003c0019t0004g0196 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3451-1084A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123157992 | |||||||
chr12:123158193 | T | C | 9 | a0001c0001t0003g0157 a0001c0002t0007g0037 a0001c0004t0007g0103 others(6): Show |
9 | HG00558.hp2 HG01952.hp2 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.3451-1285A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123158193 | |||||||
chr12:123158387 | G | C | 1 | a0009c0020t0005g0104 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3451-1479C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123158387 | |||||||
chr12:123158408 | C | G | 161 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(158): Show |
162 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.3451-1500G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123158408 | |||||||
chr12:123158810 | T | C | 15 | a0001c0001t0005g0126 a0001c0001t0005g0127 a0001c0001t0005g0128 others(12): Show |
15 | HG01884.hp1 HG02486.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.3451-1902A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123158810 | |||||||
chr12:123158873 | T | C | 161 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(158): Show |
162 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.3450+1908A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123158873 | |||||||
chr12:123158906 | C | A | 8 | a0001c0002t0007g0037 a0001c0004t0007g0103 a0001c0004t0007g0108 others(5): Show |
8 | HG00558.hp2 HG01952.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.3450+1875G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123158906 | |||||||
chr12:123158963 | T | C | 1 | a0002c0003t0002g0259 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3450+1818A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123158963 | |||||||
chr12:123159142 | T | C | 161 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(158): Show |
162 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.3450+1639A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123159142 | |||||||
chr12:123159182 | A | G | 199 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(196): Show |
200 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(197): Show |
intron_variant | MODIFIER | c.3450+1599T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123159182 | |||||||
chr12:123159448 | C | T | 5 | a0001c0001t0003g0167 a0001c0001t0003g0197 a0001c0001t0003g0198 others(2): Show |
5 | HG02559.hp1 HG02572.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.3450+1333G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123159448 | |||||||
chr12:123159454 | C | T | 3 | a0001c0004t0011g0105 a0001c0004t0011g0106 a0001c0004t0024g0102 |
3 | HG01175.hp1 HG02683.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3450+1327G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123159454 | |||||||
chr12:123159496 | T | C | 51 | a0002c0003t0002g0212 a0002c0003t0002g0213 a0002c0003t0002g0214 others(48): Show |
51 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.3450+1285A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123159496 | |||||||
chr12:123159509 | C | A | 161 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(158): Show |
162 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.3450+1272G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123159509 | |||||||
chr12:123159543 | C | T | 1 | a0001c0009t0022g0162 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3450+1238G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123159543 | |||||||
chr12:123159806 | C | T | 1 | a0001c0001t0006g0265 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3450+975G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123159806 | |||||||
chr12:123159872 | T | TA | 3 | a0001c0004t0011g0105 a0001c0004t0011g0106 a0001c0004t0024g0102 |
3 | HG01175.hp1 HG02683.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3450+908_3450+909i others(3): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123159872 | |||||||
chr12:123159873 | T | A | 219 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(216): Show |
220 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(217): Show |
intron_variant | MODIFIER | c.3450+908A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123159873 | |||||||
chr12:123159955 | C | T | 2 | a0002c0003t0002g0212 a0002c0003t0002g0213 |
2 | HG01243.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3450+826G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123159955 | |||||||
chr12:123160086 | G | A | 1 | a0001c0002t0001g0079 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3450+695C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123160086 | |||||||
chr12:123160167 | A | G | 199 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(196): Show |
200 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(197): Show |
intron_variant | MODIFIER | c.3450+614T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123160167 | |||||||
chr12:123160261 | C | T | 8 | a0001c0002t0007g0037 a0001c0004t0007g0103 a0001c0004t0007g0108 others(5): Show |
8 | HG00558.hp2 HG01952.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.3450+520G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123160261 | |||||||
chr12:123160446 | C | G | 4 | a0002c0003t0002g0215 a0002c0003t0002g0226 a0002c0003t0002g0249 others(1): Show |
4 | NA18989.hp1 NA18991.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.3450+335G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123160446 | |||||||
chr12:123160684 | A | G | 1 | a0001c0004t0007g0113 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3450+97T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123160684 | |||||||
chr12:123160776 | T | C | 38 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(35): Show |
38 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(35): Show |
splice_region_variant&intron_variant | LOW | c.3450+5A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 23/23 | chr12 | 123160776 | |||||||
chr12:123161025 | T | C | 1 | a0002c0003t0002g0223 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.3381+111A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 22/23 | chr12 | 123161025 | |||||||
chr12:123161441 | T | C | 16 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(13): Show |
16 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.3134-58A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 21/23 | chr12 | 123161441 | |||||||
chr12:123161549 | T | C | 1 | a0001c0001t0006g0118 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3134-166A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 21/23 | chr12 | 123161549 | |||||||
chr12:123161642 | G | A | 1 | a0001c0004t0007g0103 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3134-259C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 21/23 | chr12 | 123161642 | |||||||
chr12:123161663 | C | CA | 28 | a0001c0001t0003g0136 a0001c0001t0003g0159 a0001c0001t0004g0188 others(25): Show |
29 | HG00642.hp2 HG01175.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.3134-281dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 21/23 | chr12 | 123161663 | |||||||
chr12:123162492 | C | T | 1 | a0001c0002t0001g0049 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3030-274G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 20/23 | chr12 | 123162492 | |||||||
chr12:123162866 | G | A | 1 | a0001c0002t0001g0049 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3029+148C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 20/23 | chr12 | 123162866 | |||||||
chr12:123163178 | G | C | 161 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(158): Show |
162 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.2909-44C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 19/23 | chr12 | 123163178 | |||||||
chr12:123163393 | G | A | 2 | a0001c0001t0006g0002 a0001c0001t0006g0003 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2909-259C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 19/23 | chr12 | 123163393 | |||||||
chr12:123163430 | A | G | 1 | a0001c0002t0001g0006 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2909-296T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 19/23 | chr12 | 123163430 | |||||||
chr12:123163485 | C | T | 99 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(96): Show |
100 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.2909-351G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 19/23 | chr12 | 123163485 | |||||||
chr12:123163592 | G | GC | 233 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(230): Show |
234 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(231): Show |
intron_variant | MODIFIER | c.2908+357_2908+358i others(3): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 19/23 | chr12 | 123163592 | |||||||
chr12:123164134 | C | G | 1 | a0002c0003t0002g0232 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2768-44G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 18/23 | chr12 | 123164134 | |||||||
chr12:123164334 | C | T | 161 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(158): Show |
162 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.2768-244G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 18/23 | chr12 | 123164334 | |||||||
chr12:123164612 | T | A | 1 | a0002c0003t0002g0232 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2768-522A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 18/23 | chr12 | 123164612 | |||||||
chr12:123164723 | G | A | 6 | a0001c0002t0001g0012 a0001c0002t0001g0038 a0001c0002t0001g0054 others(3): Show |
6 | HG01256.hp1 HG01258.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.2767+579C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 18/23 | chr12 | 123164723 | |||||||
chr12:123164939 | A | G | 199 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(196): Show |
200 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(197): Show |
intron_variant | MODIFIER | c.2767+363T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 18/23 | chr12 | 123164939 | |||||||
chr12:123165015 | C | CA | 140 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(137): Show |
141 | HG00140.hp2 HG00597.hp2 HG00621.hp1 others(138): Show |
intron_variant | MODIFIER | c.2767+286dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 18/23 | chr12 | 123165015 | |||||||
chr12:123165015 | C | CAA | 11 | a0001c0001t0020g0145 a0001c0002t0001g0006 a0001c0002t0001g0014 others(8): Show |
11 | HG00597.hp1 HG00609.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.2767+285_2767+286d others(4): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 18/23 | chr12 | 123165015 | |||||||
chr12:123165015 | CA | C | 51 | a0001c0001t0010g0183 a0001c0002t0007g0037 a0001c0004t0007g0103 others(48): Show |
51 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.2767+286delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 18/23 | chr12 | 123165015 | |||||||
chr12:123165757 | C | T | 1 | a0001c0001t0003g0161 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2592-280G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 17/23 | chr12 | 123165757 | |||||||
chr12:123165788 | C | T | 110 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(107): Show |
111 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.2592-311G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 17/23 | chr12 | 123165788 | |||||||
chr12:123166062 | C | T | 1 | a0001c0004t0007g0103 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2592-585G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 17/23 | chr12 | 123166062 | |||||||
chr12:123166089 | G | T | 1 | a0002c0003t0002g0238 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2591+566C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 17/23 | chr12 | 123166089 | |||||||
chr12:123166098 | G | A | 2 | a0001c0002t0007g0037 a0001c0004t0007g0109 |
2 | HG00558.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.2591+557C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 17/23 | chr12 | 123166098 | |||||||
chr12:123166163 | T | C | 1 | a0001c0001t0010g0174 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2591+492A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 17/23 | chr12 | 123166163 | |||||||
chr12:123166167 | A | G | 161 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(158): Show |
162 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.2591+488T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 17/23 | chr12 | 123166167 | |||||||
chr12:123166471 | T | C | 161 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(158): Show |
162 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.2591+184A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 17/23 | chr12 | 123166471 | |||||||
chr12:123166558 | A | C | 1 | a0001c0001t0021g0205 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2591+97T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 17/23 | chr12 | 123166558 | |||||||
chr12:123166615 | A | G | 161 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(158): Show |
162 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.2591+40T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 17/23 | chr12 | 123166615 | |||||||
chr12:123166908 | T | C | 1 | a0001c0004t0024g0102 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2457-119A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123166908 | |||||||
chr12:123167191 | G | A | 3 | a0001c0001t0010g0174 a0001c0001t0010g0183 a0001c0001t0010g0184 |
3 | HG00140.hp1 HG01109.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.2457-402C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123167191 | |||||||
chr12:123167419 | G | C | 161 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(158): Show |
162 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.2457-630C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123167419 | |||||||
chr12:123167514 | C | G | 14 | a0001c0001t0003g0143 a0001c0001t0003g0147 a0001c0001t0003g0148 others(11): Show |
14 | HG01243.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.2457-725G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123167514 | |||||||
chr12:123168182 | C | A | 8 | a0001c0002t0007g0037 a0001c0004t0007g0103 a0001c0004t0007g0108 others(5): Show |
8 | HG00558.hp2 HG01952.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.2457-1393G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123168182 | |||||||
chr12:123168223 | G | A | 2 | a0001c0002t0001g0086 a0001c0002t0016g0067 |
2 | HG01361.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.2457-1434C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123168223 | |||||||
chr12:123168236 | A | G | 21 | a0002c0003t0002g0216 a0002c0003t0002g0217 a0002c0003t0002g0220 others(18): Show |
21 | HG00673.hp2 HG01070.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.2457-1447T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123168236 | |||||||
chr12:123168341 | C | CT | 21 | a0001c0001t0004g0172 a0001c0001t0004g0189 a0001c0001t0005g0127 others(18): Show |
21 | HG00741.hp1 HG01175.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.2457-1553dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123168341 | |||||||
chr12:123168341 | C | CTT | 8 | a0001c0002t0007g0037 a0001c0004t0007g0103 a0001c0004t0007g0108 others(5): Show |
8 | HG00558.hp2 HG01952.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.2457-1554_2457-155 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123168341 | |||||||
chr12:123168341 | CT | C | 45 | a0001c0001t0004g0188 a0002c0003t0002g0214 a0002c0003t0002g0215 others(42): Show |
45 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.2457-1553delA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123168341 | |||||||
chr12:123168381 | A | G | 11 | a0001c0002t0007g0037 a0001c0004t0007g0103 a0001c0004t0007g0108 others(8): Show |
11 | HG00558.hp2 HG01175.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.2457-1592T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123168381 | |||||||
chr12:123168490 | T | C | 3 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 |
3 | HG00738.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2457-1701A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123168490 | |||||||
chr12:123168499 | G | C | 1 | a0001c0001t0028g0165 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2457-1710C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123168499 | |||||||
chr12:123168499 | G | T | 219 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(216): Show |
220 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(217): Show |
intron_variant | MODIFIER | c.2457-1710C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123168499 | |||||||
chr12:123168631 | C | T | 1 | a0001c0002t0016g0067 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2457-1842G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123168631 | |||||||
chr12:123168709 | CCCT | C | 91 | a0001c0001t0004g0187 a0001c0002t0001g0001 a0001c0002t0001g0006 others(88): Show |
92 | HG00140.hp2 HG00609.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.2457-1923_2457-192 others(7): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123168709 | |||||||
chr12:123168923 | C | T | 1 | a0001c0002t0008g0060 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2457-2134G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123168923 | |||||||
chr12:123169009 | C | T | 170 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(167): Show |
171 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(168): Show |
intron_variant | MODIFIER | c.2457-2220G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169009 | |||||||
chr12:123169034 | A | G | 2 | a0001c0001t0009g0158 a0001c0002t0016g0067 |
2 | HG01361.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2457-2245T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169034 | |||||||
chr12:123169045 | C | A | 162 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(159): Show |
163 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(160): Show |
intron_variant | MODIFIER | c.2457-2256G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169045 | |||||||
chr12:123169295 | A | G | 1 | a0001c0001t0005g0169 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2457-2506T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169295 | |||||||
chr12:123169358 | G | T | 1 | a0001c0001t0003g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2457-2569C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169358 | |||||||
chr12:123169494 | G | A | 1 | a0002c0003t0002g0237 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2457-2705C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169494 | |||||||
chr12:123169498 | TA | T | 9 | a0001c0001t0003g0155 a0001c0001t0005g0132 a0001c0001t0005g0204 others(6): Show |
9 | HG01069.hp2 HG01884.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.2457-2710delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169498 | |||||||
chr12:123169612 | T | C | 1 | a0012c0018t0003g0140 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2457-2823A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169612 | |||||||
chr12:123169818 | A | G | 1 | a0001c0002t0001g0019 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2457-3029T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169818 | |||||||
chr12:123169823 | T | C | 1 | a0001c0002t0001g0019 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2457-3034A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169823 | |||||||
chr12:123169832 | T | C | 1 | a0001c0002t0001g0019 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2457-3043A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169832 | |||||||
chr12:123169833 | G | A | 16 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(13): Show |
16 | HG01952.hp2 HG02132.hp2 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.2457-3044C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169833 | |||||||
chr12:123169834 | C | A | 16 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(13): Show |
16 | HG01952.hp2 HG02132.hp2 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.2457-3045G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169834 | |||||||
chr12:123169837 | A | G | 1 | a0001c0002t0001g0019 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2457-3048T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169837 | |||||||
chr12:123169841 | T | C | 1 | a0001c0002t0001g0019 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2457-3052A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169841 | |||||||
chr12:123169842 | G | A | 1 | a0001c0002t0001g0019 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2457-3053C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169842 | |||||||
chr12:123169845 | C | T | 1 | a0001c0002t0001g0019 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2457-3056G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169845 | |||||||
chr12:123169951 | G | A | 39 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(36): Show |
39 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.2457-3162C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169951 | |||||||
chr12:123169982 | CT | C | 7 | a0001c0001t0006g0116 a0001c0001t0009g0144 a0001c0001t0009g0158 others(4): Show |
7 | HG01891.hp1 HG02451.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2457-3194delA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123169982 | |||||||
chr12:123170124 | C | T | 19 | a0001c0001t0005g0126 a0001c0001t0005g0127 a0001c0001t0005g0128 others(16): Show |
19 | HG01884.hp1 HG02145.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.2457-3335G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123170124 | |||||||
chr12:123170231 | C | T | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2457-3442G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123170231 | |||||||
chr12:123170265 | T | C | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2457-3476A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123170265 | |||||||
chr12:123170347 | G | A | 1 | a0002c0003t0002g0216 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2457-3558C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123170347 | |||||||
chr12:123170502 | A | G | 234 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(231): Show |
235 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(232): Show |
intron_variant | MODIFIER | c.2457-3713T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123170502 | |||||||
chr12:123170910 | C | T | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2457-4121G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123170910 | |||||||
chr12:123170920 | T | G | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2457-4131A>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123170920 | |||||||
chr12:123170934 | A | C | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2457-4145T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123170934 | |||||||
chr12:123170987 | T | C | 1 | a0001c0016t0001g0097 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2457-4198A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123170987 | |||||||
chr12:123171180 | A | G | 1 | a0007c0017t0005g0203 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2457-4391T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123171180 | |||||||
chr12:123171523 | C | T | 1 | a0001c0002t0007g0037 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2457-4734G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123171523 | |||||||
chr12:123171749 | AAAACAAA others(1): Show |
A | 15 | a0001c0001t0005g0126 a0001c0001t0005g0127 a0001c0001t0005g0128 others(12): Show |
15 | HG01884.hp1 HG02486.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.2456+4931_2456+493 others(12): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123171749 | |||||||
chr12:123171986 | C | T | 163 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(160): Show |
164 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(161): Show |
intron_variant | MODIFIER | c.2456+4702G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123171986 | |||||||
chr12:123171997 | G | A | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2456+4691C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123171997 | |||||||
chr12:123172017 | C | A | 7 | a0001c0004t0007g0103 a0001c0004t0007g0108 a0001c0004t0007g0109 others(4): Show |
7 | HG01952.hp2 HG02132.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.2456+4671G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172017 | |||||||
chr12:123172021 | T | C | 1 | a0001c0008t0003g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2456+4667A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172021 | |||||||
chr12:123172136 | G | A | 1 | a0001c0002t0007g0037 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2456+4552C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172136 | |||||||
chr12:123172178 | G | T | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2456+4510C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172178 | |||||||
chr12:123172262 | G | A | 89 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(86): Show |
90 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.2456+4426C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172262 | |||||||
chr12:123172337 | C | CT | 5 | a0001c0001t0004g0168 a0001c0002t0001g0099 a0001c0002t0008g0009 others(2): Show |
5 | HG01978.hp1 HG02071.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.2456+4350dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172337 | |||||||
chr12:123172337 | CT | C | 11 | a0001c0001t0004g0181 a0001c0001t0005g0132 a0001c0001t0021g0205 others(8): Show |
11 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.2456+4350delA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172337 | |||||||
chr12:123172467 | G | C | 1 | a0001c0002t0001g0058 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2456+4221C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172467 | |||||||
chr12:123172535 | G | A | 1 | a0009c0020t0005g0104 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2456+4153C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172535 | |||||||
chr12:123172553 | G | A | 9 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(6): Show |
9 | HG02602.hp2 HG03491.hp1 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.2456+4135C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172553 | |||||||
chr12:123172558 | C | G | 1 | a0001c0004t0001g0076 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2456+4130G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172558 | |||||||
chr12:123172680 | T | C | 3 | a0001c0001t0004g0177 a0001c0001t0004g0193 a0001c0001t0004g0200 |
3 | HG03017.hp2 HG03490.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2456+4008A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172680 | |||||||
chr12:123172791 | T | C | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2456+3897A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172791 | |||||||
chr12:123172861 | T | C | 2 | a0002c0003t0002g0223 a0002c0003t0002g0235 |
2 | HG01070.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.2456+3827A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172861 | |||||||
chr12:123172871 | C | CT | 20 | a0001c0001t0003g0121 a0001c0001t0003g0125 a0001c0001t0003g0136 others(17): Show |
20 | HG01106.hp2 HG01109.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.2456+3816dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172871 | |||||||
chr12:123172871 | C | CTT | 7 | a0001c0001t0003g0201 a0001c0002t0001g0026 a0001c0002t0001g0027 others(4): Show |
7 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2456+3815_2456+381 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172871 | |||||||
chr12:123172871 | C | CTTT | 63 | a0001c0002t0001g0012 a0001c0002t0001g0015 a0001c0002t0001g0016 others(60): Show |
63 | HG00140.hp2 HG00558.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2456+3814_2456+381 others(7): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172871 | |||||||
chr12:123172871 | C | CTTTT | 63 | a0001c0001t0004g0181 a0001c0001t0004g0182 a0001c0002t0001g0001 others(60): Show |
64 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.2456+3813_2456+381 others(8): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172871 | |||||||
chr12:123172871 | C | CTTTTT | 23 | a0001c0001t0004g0172 a0001c0002t0001g0013 a0001c0002t0001g0042 others(20): Show |
23 | HG00621.hp1 HG00673.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.2456+3812_2456+381 others(9): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172871 | |||||||
chr12:123172871 | CTTTTTTT others(4): Show |
C | 1 | a0002c0003t0002g0228 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2456+3806_2456+381 others(15): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172871 | |||||||
chr12:123172871 | CTTTTTTT others(7): Show |
C | 3 | a0001c0004t0011g0105 a0001c0004t0011g0106 a0001c0004t0024g0102 |
3 | HG01175.hp1 HG02683.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2456+3803_2456+381 others(18): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123172871 | |||||||
chr12:123173169 | C | A | 1 | a0001c0002t0001g0079 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2456+3519G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123173169 | |||||||
chr12:123173194 | C | G | 1 | a0001c0001t0005g0169 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2456+3494G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123173194 | |||||||
chr12:123173206 | T | A | 1 | a0001c0002t0001g0010 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2456+3482A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123173206 | |||||||
chr12:123173467 | G | A | 3 | a0001c0004t0011g0105 a0001c0004t0011g0106 a0001c0004t0024g0102 |
3 | HG01175.hp1 HG02683.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2456+3221C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123173467 | |||||||
chr12:123173600 | T | TC | 39 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(36): Show |
39 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.2456+3087dupG | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123173600 | |||||||
chr12:123173711 | A | G | 229 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(226): Show |
230 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(227): Show |
intron_variant | MODIFIER | c.2456+2977T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123173711 | |||||||
chr12:123173841 | A | T | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2456+2847T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123173841 | |||||||
chr12:123174375 | A | ATT | 162 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(159): Show |
163 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(160): Show |
intron_variant | MODIFIER | c.2456+2311_2456+231 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123174375 | |||||||
chr12:123174375 | A | ATTT | 5 | a0001c0002t0001g0099 a0001c0002t0008g0040 a0001c0004t0007g0110 others(2): Show |
5 | HG01978.hp1 HG02738.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.2456+2310_2456+231 others(7): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123174375 | |||||||
chr12:123174635 | GTGCTGGG others(774): Show |
G | 1 | a0001c0001t0005g0169 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2456+1272_2456+205 others(4): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123174635 | |||||||
chr12:123174833 | G | C | 18 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(15): Show |
18 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2456+1855C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123174833 | |||||||
chr12:123174995 | C | T | 210 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(207): Show |
211 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(208): Show |
intron_variant | MODIFIER | c.2456+1693G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123174995 | |||||||
chr12:123175458 | C | A | 39 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(36): Show |
39 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.2456+1230G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123175458 | |||||||
chr12:123175472 | C | T | 1 | a0001c0001t0003g0138 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2456+1216G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123175472 | |||||||
chr12:123175489 | A | G | 1 | a0002c0003t0002g0233 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2456+1199T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123175489 | |||||||
chr12:123175553 | T | C | 54 | a0001c0001t0021g0205 a0002c0003t0001g0229 a0002c0003t0001g0231 others(51): Show |
54 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.2456+1135A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123175553 | |||||||
chr12:123175629 | A | G | 13 | a0001c0001t0003g0143 a0001c0001t0003g0147 a0001c0001t0003g0148 others(10): Show |
13 | HG01243.hp1 HG02109.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.2456+1059T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123175629 | |||||||
chr12:123175637 | C | T | 3 | a0001c0001t0003g0147 a0001c0001t0003g0149 a0001c0001t0003g0157 |
3 | HG02615.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2456+1051G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123175637 | |||||||
chr12:123175821 | T | TA | 6 | a0001c0001t0003g0148 a0001c0001t0003g0159 a0001c0001t0003g0161 others(3): Show |
6 | HG01243.hp1 HG02486.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2456+866dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123175821 | |||||||
chr12:123175821 | TA | T | 112 | a0001c0001t0005g0129 a0001c0001t0005g0132 a0001c0001t0006g0003 others(109): Show |
113 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.2456+866delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123175821 | |||||||
chr12:123175821 | TAA | T | 10 | a0001c0001t0006g0002 a0001c0002t0001g0046 a0001c0002t0001g0083 others(7): Show |
10 | HG00639.hp1 HG00639.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.2456+865_2456+866d others(4): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123175821 | |||||||
chr12:123175963 | A | G | 234 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(231): Show |
235 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(232): Show |
intron_variant | MODIFIER | c.2456+725T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123175963 | |||||||
chr12:123176011 | A | G | 1 | a0009c0020t0005g0104 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2456+677T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123176011 | |||||||
chr12:123176169 | T | G | 229 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(226): Show |
230 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(227): Show |
intron_variant | MODIFIER | c.2456+519A>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123176169 | |||||||
chr12:123176170 | T | C | 229 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(226): Show |
230 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(227): Show |
intron_variant | MODIFIER | c.2456+518A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123176170 | |||||||
chr12:123176174 | A | T | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2456+514T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123176174 | |||||||
chr12:123176228 | T | A | 1 | a0001c0002t0018g0084 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2456+460A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123176228 | |||||||
chr12:123176295 | T | C | 1 | a0001c0001t0003g0161 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2456+393A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123176295 | |||||||
chr12:123176586 | A | G | 1 | a0001c0004t0001g0007 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2456+102T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 16/23 | chr12 | 123176586 | |||||||
chr12:123177098 | G | C | 1 | a0012c0018t0003g0140 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2355-309C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123177098 | |||||||
chr12:123177217 | T | C | 9 | a0001c0004t0007g0103 a0001c0004t0007g0108 a0001c0004t0007g0109 others(6): Show |
9 | HG01952.hp2 HG02132.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.2355-428A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123177217 | |||||||
chr12:123177485 | G | A | 1 | a0001c0001t0003g0146 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2355-696C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123177485 | |||||||
chr12:123177508 | C | G | 4 | a0001c0005t0001g0092 a0001c0005t0001g0093 a0001c0005t0001g0094 others(1): Show |
4 | HG00597.hp1 HG00609.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.2355-719G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123177508 | |||||||
chr12:123177557 | CA | C | 11 | a0001c0001t0005g0126 a0001c0001t0005g0127 a0001c0001t0005g0128 others(8): Show |
11 | HG01884.hp1 HG02615.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.2355-769delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123177557 | |||||||
chr12:123177771 | T | A | 1 | a0002c0003t0002g0254 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2355-982A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123177771 | |||||||
chr12:123177773 | A | C | 1 | a0002c0003t0002g0254 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2355-984T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123177773 | |||||||
chr12:123177859 | A | AAC | 14 | a0001c0001t0006g0116 a0001c0001t0006g0264 a0001c0002t0001g0010 others(11): Show |
14 | HG00597.hp2 HG01175.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.2355-1071_2355-107 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123177859 | |||||||
chr12:123177860 | A | AC | 105 | a0001c0001t0005g0169 a0001c0001t0006g0002 a0001c0001t0006g0003 others(102): Show |
106 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.2355-1072_2355-107 others(5): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123177860 | |||||||
chr12:123178076 | C | T | 2 | a0001c0001t0012g0150 a0001c0001t0012g0151 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2355-1287G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123178076 | |||||||
chr12:123178127 | A | G | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2355-1338T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123178127 | |||||||
chr12:123178804 | G | A | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2354+1122C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123178804 | |||||||
chr12:123178975 | T | C | 2 | a0001c0001t0003g0143 a0001c0001t0003g0155 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2354+951A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123178975 | |||||||
chr12:123179113 | G | A | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2354+813C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123179113 | |||||||
chr12:123179161 | C | T | 14 | a0001c0001t0003g0143 a0001c0001t0003g0147 a0001c0001t0003g0148 others(11): Show |
14 | HG01243.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.2354+765G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123179161 | |||||||
chr12:123179294 | G | T | 1 | a0001c0004t0001g0007 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2354+632C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123179294 | |||||||
chr12:123179297 | G | A | 3 | a0001c0004t0011g0105 a0001c0004t0011g0106 a0001c0004t0024g0102 |
3 | HG01175.hp1 HG02683.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2354+629C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123179297 | |||||||
chr12:123179541 | C | T | 1 | a0001c0001t0004g0180 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2354+385G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123179541 | |||||||
chr12:123179658 | C | T | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2354+268G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123179658 | |||||||
chr12:123179716 | T | TA | 91 | a0001c0001t0004g0177 a0001c0001t0004g0178 a0001c0001t0004g0200 others(88): Show |
92 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.2354+209dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123179716 | |||||||
chr12:123179716 | TA | T | 12 | a0001c0001t0003g0124 a0001c0001t0003g0137 a0001c0001t0003g0157 others(9): Show |
12 | HG00558.hp1 HG01070.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.2354+209delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123179716 | |||||||
chr12:123179734 | A | G | 2 | a0002c0003t0002g0239 a0002c0003t0002g0262 |
2 | NA18957.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2354+192T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123179734 | |||||||
chr12:123179891 | A | C | 50 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0214 others(47): Show |
50 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.2354+35T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 15/23 | chr12 | 123179891 | |||||||
chr12:123180566 | G | C | 120 | a0001c0001t0003g0201 a0001c0001t0006g0002 a0001c0001t0006g0003 others(117): Show |
121 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.2290-576C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 14/23 | chr12 | 123180566 | |||||||
chr12:123180709 | C | T | 172 | a0001c0001t0003g0201 a0001c0001t0006g0002 a0001c0001t0006g0003 others(169): Show |
173 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(170): Show |
intron_variant | MODIFIER | c.2289+454G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 14/23 | chr12 | 123180709 | |||||||
chr12:123180742 | G | A | 1 | a0001c0002t0001g0034 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2289+421C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 14/23 | chr12 | 123180742 | |||||||
chr12:123180813 | T | C | 1 | a0002c0003t0002g0228 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2289+350A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 14/23 | chr12 | 123180813 | |||||||
chr12:123181148 | A | G | 172 | a0001c0001t0003g0201 a0001c0001t0006g0002 a0001c0001t0006g0003 others(169): Show |
173 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(170): Show |
intron_variant | MODIFIER | c.2289+15T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 14/23 | chr12 | 123181148 | |||||||
chr12:123181528 | G | A | 21 | a0001c0001t0003g0201 a0001c0001t0006g0002 a0001c0001t0006g0003 others(18): Show |
21 | HG01175.hp1 HG01952.hp2 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.2242-318C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123181528 | |||||||
chr12:123181667 | G | A | 1 | a0001c0001t0005g0169 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2242-457C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123181667 | |||||||
chr12:123181750 | T | G | 19 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(16): Show |
19 | HG01175.hp1 HG01952.hp2 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.2242-540A>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123181750 | |||||||
chr12:123181808 | A | C | 1 | a0001c0001t0005g0169 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2242-598T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123181808 | |||||||
chr12:123181991 | C | T | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2242-781G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123181991 | |||||||
chr12:123182011 | G | A | 1 | a0001c0004t0007g0109 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2242-801C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182011 | |||||||
chr12:123182102 | G | A | 98 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(95): Show |
99 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.2242-892C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182102 | |||||||
chr12:123182120 | T | C | 1 | a0002c0003t0002g0254 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2242-910A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182120 | |||||||
chr12:123182186 | G | A | 6 | a0001c0001t0003g0143 a0001c0001t0003g0153 a0001c0001t0003g0154 others(3): Show |
6 | HG02109.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2242-976C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182186 | |||||||
chr12:123182249 | G | GTT | 10 | a0001c0002t0001g0044 a0001c0004t0001g0004 a0001c0004t0001g0005 others(7): Show |
10 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.2242-1041_2242-104 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182249 | |||||||
chr12:123182260 | T | TTG | 47 | a0002c0003t0001g0229 a0002c0003t0002g0212 a0002c0003t0002g0215 others(44): Show |
47 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.2242-1051_2242-105 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182260 | |||||||
chr12:123182260 | T | TTTG | 18 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(15): Show |
18 | HG01175.hp1 HG01243.hp2 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.2242-1051_2242-105 others(7): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182260 | |||||||
chr12:123182261 | G | C | 1 | a0001c0002t0001g0085 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2242-1051C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182261 | |||||||
chr12:123182261 | G | T | 158 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(155): Show |
159 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.2242-1051C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182261 | |||||||
chr12:123182261 | GT | G | 14 | a0001c0001t0003g0143 a0001c0001t0003g0147 a0001c0001t0003g0148 others(11): Show |
14 | HG01243.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.2242-1052delA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182261 | |||||||
chr12:123182262 | T | TGTTC | 85 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(82): Show |
86 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.2242-1053_2242-105 others(8): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182262 | |||||||
chr12:123182263 | T | TC | 10 | a0001c0002t0001g0044 a0001c0004t0001g0004 a0001c0004t0001g0005 others(7): Show |
10 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.2242-1054_2242-105 others(5): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182263 | |||||||
chr12:123182375 | T | A | 1 | a0001c0002t0001g0011 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2242-1165A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182375 | |||||||
chr12:123182401 | A | G | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2242-1191T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182401 | |||||||
chr12:123182426 | G | A | 1 | a0001c0004t0001g0076 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2242-1216C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182426 | |||||||
chr12:123182431 | A | C | 1 | a0001c0004t0001g0076 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2242-1221T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182431 | |||||||
chr12:123182710 | G | A | 1 | a0001c0002t0001g0082 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2242-1500C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182710 | |||||||
chr12:123182732 | C | T | 1 | a0001c0002t0001g0021 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2242-1522G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182732 | |||||||
chr12:123182807 | G | T | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2242-1597C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182807 | |||||||
chr12:123182940 | G | A | 1 | a0001c0002t0008g0060 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2242-1730C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182940 | |||||||
chr12:123182951 | C | T | 1 | a0001c0001t0030g0211 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2242-1741G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182951 | |||||||
chr12:123182982 | G | A | 2 | a0001c0001t0015g0107 a0007c0017t0005g0203 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2242-1772C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123182982 | |||||||
chr12:123183051 | C | G | 1 | a0001c0002t0001g0079 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2242-1841G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183051 | |||||||
chr12:123183063 | A | T | 1 | a0009c0020t0005g0104 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2242-1853T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183063 | |||||||
chr12:123183237 | C | T | 1 | a0001c0002t0001g0036 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2242-2027G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183237 | |||||||
chr12:123183332 | G | C | 15 | a0001c0001t0005g0126 a0001c0001t0005g0127 a0001c0001t0005g0128 others(12): Show |
15 | HG01884.hp1 HG02486.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.2242-2122C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183332 | |||||||
chr12:123183403 | T | C | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2242-2193A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183403 | |||||||
chr12:123183405 | A | G | 97 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(94): Show |
98 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.2242-2195T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183405 | |||||||
chr12:123183475 | A | G | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2242-2265T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183475 | |||||||
chr12:123183496 | C | T | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2242-2286G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183496 | |||||||
chr12:123183515 | C | T | 1 | a0001c0002t0001g0055 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2242-2305G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183515 | |||||||
chr12:123183547 | C | CA | 29 | a0001c0001t0003g0156 a0001c0001t0003g0198 a0001c0001t0004g0168 others(26): Show |
29 | HG00738.hp2 HG01106.hp1 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.2242-2338dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183547 | |||||||
chr12:123183547 | C | CAA | 83 | a0001c0001t0006g0117 a0001c0001t0006g0118 a0001c0002t0001g0001 others(80): Show |
84 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.2242-2339_2242-233 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183547 | |||||||
chr12:123183547 | C | CAAA | 8 | a0001c0002t0001g0019 a0001c0002t0001g0038 a0001c0002t0001g0049 others(5): Show |
8 | HG00597.hp2 HG01081.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.2242-2340_2242-233 others(7): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183547 | |||||||
chr12:123183547 | CA | C | 6 | a0001c0001t0003g0161 a0001c0001t0010g0183 a0002c0003t0002g0217 others(3): Show |
6 | HG00140.hp1 HG02895.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.2242-2338delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183547 | |||||||
chr12:123183565 | A | G | 1 | a0002c0003t0002g0213 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2242-2355T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183565 | |||||||
chr12:123183571 | G | A | 8 | a0001c0002t0001g0010 a0001c0002t0001g0053 a0001c0002t0001g0055 others(5): Show |
8 | HG02040.hp2 NA18953.hp1 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.2242-2361C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183571 | |||||||
chr12:123183937 | G | A | 1 | a0001c0001t0009g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2242-2727C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183937 | |||||||
chr12:123183940 | C | A | 1 | a0012c0018t0003g0140 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2242-2730G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183940 | |||||||
chr12:123183954 | A | C | 7 | a0001c0001t0003g0125 a0001c0001t0003g0146 a0001c0001t0009g0144 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2242-2744T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123183954 | |||||||
chr12:123184113 | G | C | 7 | a0001c0002t0001g0012 a0001c0002t0001g0038 a0001c0002t0001g0049 others(4): Show |
7 | HG00597.hp2 HG01256.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2242-2903C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123184113 | |||||||
chr12:123184371 | G | A | 1 | a0001c0004t0001g0072 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2242-3161C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123184371 | |||||||
chr12:123184374 | C | T | 3 | a0001c0001t0003g0147 a0001c0001t0003g0149 a0001c0001t0003g0157 |
3 | HG02615.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2242-3164G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123184374 | |||||||
chr12:123184498 | AT | A | 209 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(206): Show |
210 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(207): Show |
intron_variant | MODIFIER | c.2242-3289delA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123184498 | |||||||
chr12:123184672 | G | C | 19 | a0001c0001t0005g0126 a0001c0001t0005g0127 a0001c0001t0005g0128 others(16): Show |
19 | HG01884.hp1 HG02145.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.2242-3462C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123184672 | |||||||
chr12:123184688 | C | T | 118 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(115): Show |
119 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.2242-3478G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123184688 | |||||||
chr12:123184750 | G | A | 4 | a0001c0002t0001g0098 a0001c0002t0001g0099 a0001c0002t0017g0071 others(1): Show |
4 | HG01952.hp1 HG01978.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.2242-3540C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123184750 | |||||||
chr12:123184793 | C | T | 7 | a0001c0004t0007g0103 a0001c0004t0007g0108 a0001c0004t0007g0109 others(4): Show |
7 | HG01952.hp2 HG02132.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.2242-3583G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123184793 | |||||||
chr12:123184855 | G | A | 1 | a0001c0002t0016g0067 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2242-3645C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123184855 | |||||||
chr12:123184921 | T | C | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2242-3711A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123184921 | |||||||
chr12:123184961 | A | G | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2242-3751T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123184961 | |||||||
chr12:123185057 | G | A | 1 | a0001c0001t0004g0172 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2242-3847C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123185057 | |||||||
chr12:123185328 | TA | T | 6 | a0001c0001t0003g0161 a0001c0001t0006g0115 a0001c0002t0001g0059 others(3): Show |
6 | HG00558.hp2 HG01099.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2242-4119delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123185328 | |||||||
chr12:123185926 | T | C | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2242-4716A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123185926 | |||||||
chr12:123185947 | C | T | 1 | a0001c0001t0003g0201 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2242-4737G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123185947 | |||||||
chr12:123185980 | A | G | 1 | a0002c0003t0002g0214 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2242-4770T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123185980 | |||||||
chr12:123186225 | C | A | 1 | a0001c0002t0017g0071 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2242-5015G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123186225 | |||||||
chr12:123186227 | CA | C | 38 | a0001c0001t0003g0119 a0001c0001t0003g0142 a0001c0001t0003g0146 others(35): Show |
38 | HG00738.hp2 HG01099.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2242-5018delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123186227 | |||||||
chr12:123186227 | CAA | C | 127 | a0001c0001t0003g0120 a0001c0001t0003g0122 a0001c0001t0003g0123 others(124): Show |
128 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.2242-5019_2242-501 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123186227 | |||||||
chr12:123186227 | CAAA | C | 63 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(60): Show |
63 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.2242-5020_2242-501 others(7): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123186227 | |||||||
chr12:123186227 | CAAAA | C | 8 | a0001c0001t0006g0115 a0001c0001t0006g0116 a0002c0003t0002g0217 others(5): Show |
8 | HG02293.hp1 HG02970.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.2242-5021_2242-501 others(8): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123186227 | |||||||
chr12:123186227 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0003g0121 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2242-5029_2242-501 others(16): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123186227 | |||||||
chr12:123186227 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0003g0139 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2242-5031_2242-501 others(18): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123186227 | |||||||
chr12:123186245 | A | C | 98 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(95): Show |
99 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.2242-5035T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123186245 | |||||||
chr12:123186763 | T | C | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2242-5553A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123186763 | |||||||
chr12:123186891 | G | A | 4 | a0001c0004t0001g0004 a0001c0004t0001g0005 a0001c0004t0001g0073 others(1): Show |
4 | HG00642.hp1 HG00735.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.2242-5681C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123186891 | |||||||
chr12:123186939 | C | T | 3 | a0001c0004t0011g0105 a0001c0004t0011g0106 a0001c0004t0024g0102 |
3 | HG01175.hp1 HG02683.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2242-5729G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123186939 | |||||||
chr12:123187118 | G | C | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2242-5908C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123187118 | |||||||
chr12:123187214 | T | C | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2242-6004A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123187214 | |||||||
chr12:123187425 | CAA | C | 3 | a0001c0004t0011g0105 a0001c0004t0011g0106 a0001c0004t0024g0102 |
3 | HG01175.hp1 HG02683.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2242-6217_2242-621 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123187425 | |||||||
chr12:123187534 | C | T | 1 | a0001c0002t0001g0079 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2242-6324G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123187534 | |||||||
chr12:123187535 | C | A | 1 | a0001c0002t0001g0079 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2242-6325G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123187535 | |||||||
chr12:123187539 | A | T | 1 | a0001c0002t0001g0079 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2242-6329T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123187539 | |||||||
chr12:123187542 | T | A | 1 | a0001c0002t0001g0079 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2242-6332A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123187542 | |||||||
chr12:123187546 | C | A | 1 | a0001c0002t0001g0079 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2242-6336G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123187546 | |||||||
chr12:123187628 | T | G | 1 | a0001c0002t0001g0063 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2242-6418A>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123187628 | |||||||
chr12:123187642 | C | G | 1 | a0001c0002t0001g0014 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2242-6432G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123187642 | |||||||
chr12:123187971 | A | C | 9 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(6): Show |
9 | HG02602.hp2 HG03491.hp1 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.2241+6415T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123187971 | |||||||
chr12:123187971 | A | G | 162 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(159): Show |
163 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(160): Show |
intron_variant | MODIFIER | c.2241+6415T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123187971 | |||||||
chr12:123188026 | T | C | 1 | a0001c0001t0003g0156 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2241+6360A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123188026 | |||||||
chr12:123188039 | T | C | 1 | a0009c0020t0005g0104 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2241+6347A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123188039 | |||||||
chr12:123188087 | T | C | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2241+6299A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123188087 | |||||||
chr12:123188110 | G | C | 3 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 |
3 | HG01884.hp2 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2241+6276C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123188110 | |||||||
chr12:123188153 | A | T | 1 | a0001c0002t0001g0058 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2241+6233T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123188153 | |||||||
chr12:123188155 | A | T | 1 | a0001c0002t0001g0058 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2241+6231T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123188155 | |||||||
chr12:123188156 | C | T | 1 | a0001c0002t0001g0058 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2241+6230G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123188156 | |||||||
chr12:123188327 | C | T | 1 | a0001c0001t0003g0161 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2241+6059G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123188327 | |||||||
chr12:123188412 | A | AT | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2241+5973dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123188412 | |||||||
chr12:123188414 | A | G | 1 | a0001c0001t0005g0169 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2241+5972T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123188414 | |||||||
chr12:123188711 | G | A | 97 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(94): Show |
98 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.2241+5675C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123188711 | |||||||
chr12:123188796 | C | T | 1 | a0002c0003t0002g0239 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2241+5590G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123188796 | |||||||
chr12:123188968 | CA | C | 3 | a0001c0004t0011g0105 a0001c0004t0011g0106 a0001c0004t0024g0102 |
3 | HG01175.hp1 HG02683.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2241+5417delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123188968 | |||||||
chr12:123189058 | G | A | 3 | a0001c0002t0001g0081 a0001c0002t0001g0082 a0001c0002t0001g0083 |
3 | HG00639.hp2 HG01099.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.2241+5328C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123189058 | |||||||
chr12:123189292 | C | T | 11 | a0001c0001t0005g0126 a0001c0001t0005g0127 a0001c0001t0005g0128 others(8): Show |
11 | HG01884.hp1 HG02615.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.2241+5094G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123189292 | |||||||
chr12:123189336 | C | T | 2 | a0001c0002t0008g0031 a0001c0002t0008g0040 |
2 | HG02738.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2241+5050G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123189336 | |||||||
chr12:123189608 | A | C | 1 | a0001c0002t0017g0071 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2241+4778T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123189608 | |||||||
chr12:123189701 | G | A | 2 | a0002c0003t0002g0212 a0002c0003t0002g0213 |
2 | HG01243.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2241+4685C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123189701 | |||||||
chr12:123189704 | G | A | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2241+4682C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123189704 | |||||||
chr12:123189710 | G | A | 1 | a0001c0001t0012g0151 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2241+4676C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123189710 | |||||||
chr12:123189921 | G | A | 1 | a0001c0001t0005g0169 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2241+4465C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123189921 | |||||||
chr12:123189975 | T | C | 1 | a0007c0017t0005g0203 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2241+4411A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123189975 | |||||||
chr12:123190191 | C | T | 1 | a0002c0003t0001g0229 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2241+4195G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123190191 | |||||||
chr12:123190235 | C | T | 1 | a0001c0001t0003g0146 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2241+4151G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123190235 | |||||||
chr12:123190634 | C | CAGGATAT others(2): Show |
3 | a0001c0001t0005g0202 a0001c0001t0005g0206 a0001c0001t0005g0207 |
3 | HG02486.hp1 HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2241+3743_2241+375 others(13): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123190634 | |||||||
chr12:123191010 | T | C | 2 | a0001c0001t0004g0175 a0001c0001t0004g0187 |
2 | HG02735.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.2241+3376A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123191010 | |||||||
chr12:123191112 | G | C | 1 | a0001c0004t0007g0113 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2241+3274C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123191112 | |||||||
chr12:123191509 | T | G | 1 | a0001c0001t0005g0130 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2241+2877A>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123191509 | |||||||
chr12:123191606 | T | C | 1 | a0001c0001t0006g0265 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2241+2780A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123191606 | |||||||
chr12:123191680 | A | C | 3 | a0001c0001t0005g0127 a0001c0001t0005g0130 a0001c0001t0005g0132 |
3 | HG01884.hp1 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2241+2706T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123191680 | |||||||
chr12:123192216 | G | A | 118 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(115): Show |
119 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.2241+2170C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192216 | |||||||
chr12:123192294 | T | C | 19 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(16): Show |
19 | HG01175.hp1 HG01952.hp2 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.2241+2092A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192294 | |||||||
chr12:123192426 | C | T | 1 | a0010c0010t0001g0033 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2241+1960G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192426 | |||||||
chr12:123192453 | CA | C | 5 | a0001c0001t0005g0131 a0001c0001t0015g0107 a0001c0001t0030g0211 others(2): Show |
5 | HG02896.hp1 HG02976.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.2241+1932delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192453 | |||||||
chr12:123192475 | A | G | 2 | a0002c0003t0002g0243 a0002c0003t0002g0246 |
2 | NA18941.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.2241+1911T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192475 | |||||||
chr12:123192490 | T | C | 2 | a0002c0003t0002g0212 a0002c0003t0002g0213 |
2 | HG01243.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2241+1896A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192490 | |||||||
chr12:123192560 | T | C | 1 | a0001c0002t0001g0083 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2241+1826A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192560 | |||||||
chr12:123192618 | G | A | 1 | a0001c0004t0007g0103 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2241+1768C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192618 | |||||||
chr12:123192624 | G | A | 20 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(17): Show |
20 | HG01175.hp1 HG01952.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.2241+1762C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192624 | |||||||
chr12:123192628 | C | CA | 9 | a0001c0001t0004g0170 a0001c0001t0004g0178 a0001c0001t0004g0181 others(6): Show |
9 | HG00738.hp2 HG01070.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.2241+1757dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192628 | |||||||
chr12:123192628 | CA | C | 13 | a0001c0002t0001g0022 a0001c0002t0001g0030 a0001c0002t0001g0038 others(10): Show |
13 | HG00621.hp1 HG00639.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.2241+1757delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192628 | |||||||
chr12:123192628 | CAA | C | 97 | a0001c0001t0003g0119 a0001c0001t0006g0265 a0001c0002t0001g0001 others(94): Show |
98 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.2241+1756_2241+175 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192628 | |||||||
chr12:123192628 | CAAA | C | 67 | a0001c0001t0003g0136 a0001c0001t0003g0138 a0001c0001t0003g0167 others(64): Show |
67 | HG00609.hp2 HG00621.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.2241+1755_2241+175 others(7): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192628 | |||||||
chr12:123192628 | CAAAA | C | 54 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(51): Show |
54 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.2241+1754_2241+175 others(8): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192628 | |||||||
chr12:123192630 | A | C | 1 | a0001c0002t0001g0070 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2241+1756T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192630 | |||||||
chr12:123192631 | A | C | 2 | a0001c0002t0001g0050 a0001c0002t0001g0059 |
2 | NA18974.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.2241+1755T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192631 | |||||||
chr12:123192744 | T | C | 1 | a0001c0002t0001g0063 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2241+1642A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192744 | |||||||
chr12:123192954 | C | T | 1 | a0001c0001t0004g0180 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2241+1432G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123192954 | |||||||
chr12:123193071 | CA | C | 17 | a0001c0001t0003g0119 a0001c0001t0003g0125 a0001c0001t0003g0135 others(14): Show |
17 | HG00738.hp2 HG01074.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.2241+1314delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193071 | |||||||
chr12:123193071 | CAAA | C | 14 | a0001c0001t0003g0159 a0001c0001t0004g0179 a0001c0001t0005g0207 others(11): Show |
14 | HG00558.hp1 HG00609.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.2241+1312_2241+131 others(7): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193071 | |||||||
chr12:123193071 | CAAAAA | C | 18 | a0001c0001t0003g0143 a0001c0001t0003g0152 a0001c0001t0003g0153 others(15): Show |
18 | HG00673.hp1 HG00735.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.2241+1310_2241+131 others(9): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193071 | |||||||
chr12:123193071 | CAAAAAAA | C | 16 | a0001c0001t0003g0147 a0001c0001t0003g0161 a0001c0002t0001g0017 others(13): Show |
16 | HG00733.hp2 HG00735.hp2 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.2241+1308_2241+131 others(11): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193071 | |||||||
chr12:123193071 | CAAAAAAA others(2): Show |
C | 12 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0013 others(9): Show |
12 | HG01258.hp1 HG01361.hp2 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.2241+1306_2241+131 others(13): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193071 | |||||||
chr12:123193071 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0006g0002 a0001c0001t0006g0003 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2241+1305_2241+131 others(14): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193071 | |||||||
chr12:123193087 | AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0006g0265 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2241+1288_2241+129 others(15): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193087 | |||||||
chr12:123193088 | AAAAAAAA others(3): Show |
A | 3 | a0001c0002t0001g0022 a0001c0002t0001g0028 a0001c0002t0001g0082 |
3 | HG01069.hp1 HG01099.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2241+1288_2241+129 others(14): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193088 | |||||||
chr12:123193089 | AAAAAAAA others(2): Show |
A | 58 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0012 others(55): Show |
59 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.2241+1288_2241+129 others(13): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193089 | |||||||
chr12:123193090 | A | ATAT | 3 | a0001c0001t0003g0148 a0001c0001t0005g0169 a0001c0001t0028g0165 |
3 | HG02486.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2241+1295_2241+129 others(7): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193090 | |||||||
chr12:123193090 | A | T | 9 | a0001c0001t0003g0125 a0001c0001t0006g0116 a0001c0001t0006g0117 others(6): Show |
9 | HG01175.hp1 HG02132.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.2241+1296T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193090 | |||||||
chr12:123193092 | A | T | 17 | a0001c0001t0003g0125 a0001c0001t0003g0148 a0001c0001t0003g0160 others(14): Show |
17 | HG01175.hp1 HG01952.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.2241+1294T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193092 | |||||||
chr12:123193094 | A | AT | 3 | a0001c0001t0012g0150 a0001c0007t0029g0210 a0003c0019t0004g0196 |
3 | HG01516.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2241+1291_2241+129 others(5): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193094 | |||||||
chr12:123193094 | A | T | 60 | a0001c0001t0003g0125 a0001c0001t0003g0138 a0001c0001t0003g0139 others(57): Show |
60 | HG00621.hp2 HG00642.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.2241+1292T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193094 | |||||||
chr12:123193096 | A | AT | 6 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(3): Show |
6 | HG02258.hp1 HG02630.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2241+1289_2241+129 others(5): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193096 | |||||||
chr12:123193096 | A | T | 131 | a0001c0001t0003g0125 a0001c0001t0003g0135 a0001c0001t0003g0136 others(128): Show |
131 | HG00140.hp1 HG00621.hp2 HG00642.hp2 others(128): Show |
intron_variant | MODIFIER | c.2241+1290T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193096 | |||||||
chr12:123193102 | T | C | 1 | a0001c0001t0003g0123 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2241+1284A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193102 | |||||||
chr12:123193104 | T | C | 3 | a0001c0001t0003g0123 a0001c0001t0003g0141 a0008c0015t0003g0163 |
3 | HG02572.hp2 HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2241+1282A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193104 | |||||||
chr12:123193106 | T | C | 16 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(13): Show |
16 | HG01884.hp2 HG02258.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.2241+1280A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193106 | |||||||
chr12:123193106 | TATACACA others(5): Show |
T | 1 | a0001c0004t0007g0109 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2241+1268_2241+127 others(16): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193106 | |||||||
chr12:123193108 | T | C | 24 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(21): Show |
24 | HG01081.hp1 HG01099.hp1 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.2241+1278A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193108 | |||||||
chr12:123193108 | T | TAC | 7 | a0001c0001t0004g0185 a0001c0001t0004g0190 a0001c0001t0004g0191 others(4): Show |
7 | HG00140.hp1 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.2241+1276_2241+127 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193108 | |||||||
chr12:123193108 | T | TACAC | 3 | a0001c0001t0003g0197 a0001c0001t0003g0198 a0001c0001t0003g0201 |
3 | HG02559.hp1 HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2241+1274_2241+127 others(8): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193108 | |||||||
chr12:123193108 | T | TACACACA others(3): Show |
1 | a0001c0001t0010g0184 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2241+1268_2241+127 others(14): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193108 | |||||||
chr12:123193108 | TACAC | T | 7 | a0001c0002t0001g0023 a0001c0002t0001g0025 a0001c0002t0001g0041 others(4): Show |
7 | HG00673.hp1 HG02040.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.2241+1274_2241+127 others(8): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193108 | |||||||
chr12:123193108 | TACACAC | T | 5 | a0001c0004t0007g0108 a0001c0004t0007g0110 a0001c0004t0007g0112 others(2): Show |
5 | HG03239.hp2 NA18972.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.2241+1272_2241+127 others(10): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193108 | |||||||
chr12:123193108 | TACACACA others(1): Show |
T | 16 | a0001c0001t0021g0205 a0001c0004t0007g0103 a0002c0003t0002g0228 others(13): Show |
16 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.2241+1270_2241+127 others(12): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193108 | |||||||
chr12:123193108 | TACACACA others(3): Show |
T | 47 | a0001c0001t0003g0161 a0001c0001t0006g0116 a0001c0001t0006g0117 others(44): Show |
47 | HG00642.hp2 HG00673.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.2241+1268_2241+127 others(14): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193108 | |||||||
chr12:123193108 | TACACACA others(15): Show |
T | 1 | a0001c0004t0007g0111 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2241+1256_2241+127 others(26): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193108 | |||||||
chr12:123193110 | C | T | 129 | a0001c0001t0003g0143 a0001c0001t0003g0147 a0001c0001t0003g0148 others(126): Show |
130 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(127): Show |
intron_variant | MODIFIER | c.2241+1276G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193110 | |||||||
chr12:123193112 | C | T | 95 | a0001c0001t0003g0147 a0001c0001t0003g0149 a0001c0001t0004g0178 others(92): Show |
96 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.2241+1274G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193112 | |||||||
chr12:123193114 | C | T | 81 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(78): Show |
81 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.2241+1272G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193114 | |||||||
chr12:123193116 | C | T | 14 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0265 others(11): Show |
14 | HG01256.hp1 HG01258.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.2241+1270G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193116 | |||||||
chr12:123193118 | C | T | 23 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0265 others(20): Show |
23 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.2241+1268G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193118 | |||||||
chr12:123193120 | C | T | 30 | a0001c0001t0003g0161 a0001c0001t0006g0118 a0001c0001t0021g0205 others(27): Show |
30 | HG00558.hp1 HG00609.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.2241+1266G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193120 | |||||||
chr12:123193122 | C | T | 1 | a0001c0001t0003g0161 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2241+1264G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193122 | |||||||
chr12:123193263 | A | G | 118 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(115): Show |
119 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.2241+1123T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193263 | |||||||
chr12:123193388 | G | T | 1 | a0001c0001t0004g0180 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2241+998C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193388 | |||||||
chr12:123193621 | A | T | 1 | a0001c0004t0001g0075 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2241+765T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193621 | |||||||
chr12:123193691 | T | A | 1 | a0001c0002t0001g0025 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2241+695A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193691 | |||||||
chr12:123193808 | C | A | 1 | a0001c0002t0001g0044 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2241+578G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193808 | |||||||
chr12:123193817 | GAC | G | 53 | a0001c0002t0001g0059 a0002c0003t0001g0229 a0002c0003t0001g0231 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2241+567_2241+568d others(4): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193817 | |||||||
chr12:123193820 | AC | A | 116 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(113): Show |
117 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.2241+565delG | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193820 | |||||||
chr12:123193821 | C | G | 1 | a0001c0004t0001g0074 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2241+565G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193821 | |||||||
chr12:123193822 | A | G | 116 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(113): Show |
117 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.2241+564T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193822 | |||||||
chr12:123193822 | A | T | 1 | a0001c0004t0001g0074 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2241+564T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193822 | |||||||
chr12:123193823 | G | GT | 6 | a0001c0001t0003g0167 a0001c0001t0003g0197 a0001c0001t0003g0198 others(3): Show |
6 | HG02559.hp1 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2241+562dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193823 | |||||||
chr12:123193823 | G | T | 117 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(114): Show |
118 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.2241+563C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193823 | |||||||
chr12:123193824 | T | G | 1 | a0002c0003t0002g0261 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2241+562A>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193824 | |||||||
chr12:123193922 | C | T | 7 | a0001c0002t0001g0011 a0001c0002t0001g0029 a0001c0002t0001g0066 others(4): Show |
7 | HG01258.hp1 HG01361.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.2241+464G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123193922 | |||||||
chr12:123194067 | G | A | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2241+319C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 13/23 | chr12 | 123194067 | |||||||
chr12:123194624 | A | AT | 94 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(91): Show |
94 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.2026-24dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123194624 | |||||||
chr12:123194624 | A | ATT | 112 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(109): Show |
113 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.2026-25_2026-24dup others(2): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123194624 | |||||||
chr12:123195075 | T | C | 1 | a0001c0004t0001g0007 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2026-474A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123195075 | |||||||
chr12:123195314 | CAGT | C | 38 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(35): Show |
38 | HG01099.hp1 HG01243.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.2026-716_2026-714d others(5): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123195314 | |||||||
chr12:123195391 | C | A | 1 | a0001c0004t0001g0004 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2026-790G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123195391 | |||||||
chr12:123195398 | A | G | 1 | a0001c0001t0003g0160 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2026-797T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123195398 | |||||||
chr12:123195737 | A | T | 1 | a0001c0001t0021g0205 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2026-1136T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123195737 | |||||||
chr12:123195845 | G | A | 5 | a0001c0001t0003g0148 a0001c0001t0003g0152 a0001c0001t0003g0159 others(2): Show |
5 | HG01243.hp1 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2026-1244C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123195845 | |||||||
chr12:123195852 | C | T | 3 | a0001c0002t0001g0098 a0001c0002t0001g0099 a0001c0016t0001g0097 |
3 | HG01952.hp1 HG01978.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.2026-1251G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123195852 | |||||||
chr12:123195910 | C | T | 1 | a0001c0002t0001g0020 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2026-1309G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123195910 | |||||||
chr12:123196016 | T | C | 98 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(95): Show |
99 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.2026-1415A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123196016 | |||||||
chr12:123196050 | A | T | 4 | a0001c0001t0004g0172 a0001c0001t0004g0181 a0001c0001t0004g0182 others(1): Show |
4 | HG00741.hp1 HG01074.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.2026-1449T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123196050 | |||||||
chr12:123196147 | C | T | 1 | a0001c0002t0001g0049 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2026-1546G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123196147 | |||||||
chr12:123196218 | T | C | 4 | a0001c0004t0001g0004 a0001c0004t0001g0005 a0001c0004t0001g0073 others(1): Show |
4 | HG00642.hp1 HG00735.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.2026-1617A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123196218 | |||||||
chr12:123196272 | C | T | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2026-1671G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123196272 | |||||||
chr12:123196388 | T | C | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2026-1787A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123196388 | |||||||
chr12:123196480 | C | T | 9 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(6): Show |
9 | HG02602.hp2 HG03491.hp1 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.2025+1767G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123196480 | |||||||
chr12:123196576 | G | A | 1 | a0009c0020t0005g0104 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2025+1671C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123196576 | |||||||
chr12:123196675 | G | A | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.2025+1572C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123196675 | |||||||
chr12:123196736 | T | C | 1 | a0012c0018t0003g0140 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2025+1511A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123196736 | |||||||
chr12:123196755 | T | C | 2 | a0001c0002t0001g0030 a0001c0002t0001g0046 |
2 | HG00639.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.2025+1492A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123196755 | |||||||
chr12:123197031 | G | GT | 39 | a0001c0001t0004g0168 a0001c0001t0004g0172 a0001c0001t0004g0186 others(36): Show |
39 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.2025+1215dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197031 | |||||||
chr12:123197031 | G | GTT | 23 | a0002c0003t0001g0231 a0002c0003t0002g0212 a0002c0003t0002g0213 others(20): Show |
23 | HG00642.hp2 HG00673.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.2025+1214_2025+121 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197031 | |||||||
chr12:123197031 | GT | G | 19 | a0001c0001t0003g0124 a0001c0001t0003g0125 a0001c0001t0003g0142 others(16): Show |
19 | HG01099.hp1 HG02451.hp2 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.2025+1215delA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197031 | |||||||
chr12:123197031 | GTT | G | 40 | a0001c0001t0003g0143 a0001c0001t0003g0157 a0001c0001t0003g0160 others(37): Show |
40 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.2025+1214_2025+121 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197031 | |||||||
chr12:123197031 | GTTT | G | 75 | a0001c0001t0003g0159 a0001c0001t0006g0002 a0001c0001t0006g0003 others(72): Show |
76 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.2025+1213_2025+121 others(7): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197031 | |||||||
chr12:123197031 | GTTTT | G | 5 | a0001c0002t0001g0022 a0001c0002t0001g0061 a0001c0004t0007g0108 others(2): Show |
5 | HG01256.hp1 HG02132.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.2025+1212_2025+121 others(8): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197031 | |||||||
chr12:123197069 | G | A | 3 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 |
3 | HG00738.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2025+1178C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197069 | |||||||
chr12:123197090 | G | C | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2025+1157C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197090 | |||||||
chr12:123197298 | C | A | 1 | a0001c0001t0003g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2025+949G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197298 | |||||||
chr12:123197365 | T | G | 2 | a0001c0004t0007g0110 a0001c0004t0007g0112 |
2 | NA18972.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.2025+882A>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197365 | |||||||
chr12:123197534 | G | A | 118 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(115): Show |
119 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.2025+713C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197534 | |||||||
chr12:123197714 | G | A | 1 | a0001c0001t0004g0185 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2025+533C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197714 | |||||||
chr12:123197769 | G | A | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2025+478C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197769 | |||||||
chr12:123197790 | G | GA | 13 | a0001c0001t0004g0180 a0001c0001t0006g0002 a0001c0001t0006g0003 others(10): Show |
13 | HG00642.hp1 HG01516.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.2025+456dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197790 | |||||||
chr12:123197790 | GA | G | 60 | a0001c0001t0003g0167 a0001c0001t0003g0197 a0001c0001t0003g0198 others(57): Show |
60 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.2025+456delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197790 | |||||||
chr12:123197849 | C | T | 151 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(148): Show |
152 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(149): Show |
intron_variant | MODIFIER | c.2025+398G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123197849 | |||||||
chr12:123198015 | C | G | 1 | a0002c0003t0002g0261 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2025+232G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123198015 | |||||||
chr12:123198047 | G | A | 98 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(95): Show |
99 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.2025+200C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123198047 | |||||||
chr12:123198083 | C | CA | 24 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(21): Show |
24 | HG00621.hp1 HG01175.hp1 HG01952.hp2 others(21): Show |
intron_variant | MODIFIER | c.2025+163dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123198083 | |||||||
chr12:123198196 | G | A | 1 | a0001c0001t0003g0121 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2025+51C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 12/23 | chr12 | 123198196 | |||||||
chr12:123198608 | A | G | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1938-274T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123198608 | |||||||
chr12:123198809 | C | CA | 44 | a0001c0001t0003g0123 a0001c0001t0003g0135 a0001c0001t0003g0136 others(41): Show |
44 | HG00558.hp1 HG00621.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1938-476dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123198809 | |||||||
chr12:123198809 | CA | C | 86 | a0001c0001t0003g0139 a0001c0001t0003g0152 a0001c0001t0003g0159 others(83): Show |
87 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.1938-476delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123198809 | |||||||
chr12:123198839 | A | AAAATAAT others(305): Show |
1 | a0002c0003t0002g0217 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1938-506_1938-505i others(314): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123198839 | |||||||
chr12:123198839 | A | AAAATAAT others(323): Show |
1 | a0002c0003t0002g0230 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1938-506_1938-505i others(332): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123198839 | |||||||
chr12:123198839 | A | AAAATAAT others(324): Show |
1 | a0002c0003t0002g0216 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1938-506_1938-505i others(333): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123198839 | |||||||
chr12:123198839 | A | AAAATAAT others(330): Show |
1 | a0002c0003t0002g0234 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1938-506_1938-505i others(339): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123198839 | |||||||
chr12:123198927 | A | G | 1 | a0001c0002t0008g0031 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1938-593T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123198927 | |||||||
chr12:123199016 | C | T | 170 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(167): Show |
171 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(168): Show |
intron_variant | MODIFIER | c.1938-682G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123199016 | |||||||
chr12:123199121 | T | C | 2 | a0001c0002t0001g0024 a0001c0002t0001g0064 |
2 | HG00733.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.1938-787A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123199121 | |||||||
chr12:123199228 | C | A | 5 | a0001c0001t0003g0167 a0001c0001t0003g0197 a0001c0001t0003g0198 others(2): Show |
5 | HG02559.hp1 HG02572.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1938-894G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123199228 | |||||||
chr12:123199429 | T | C | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1938-1095A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123199429 | |||||||
chr12:123199478 | A | G | 9 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(6): Show |
9 | HG02602.hp2 HG03491.hp1 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.1938-1144T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123199478 | |||||||
chr12:123199661 | C | T | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1938-1327G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123199661 | |||||||
chr12:123199788 | C | CA | 7 | a0001c0001t0021g0205 a0001c0002t0001g0012 a0001c0002t0001g0038 others(4): Show |
7 | HG01256.hp1 HG01258.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1938-1455dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123199788 | |||||||
chr12:123199991 | A | G | 1 | a0001c0002t0001g0036 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1938-1657T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123199991 | |||||||
chr12:123200147 | G | C | 10 | a0001c0002t0001g0022 a0001c0002t0001g0035 a0001c0002t0001g0057 others(7): Show |
10 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.1938-1813C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123200147 | |||||||
chr12:123200235 | GA | G | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1938-1902delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123200235 | |||||||
chr12:123200271 | T | C | 1 | a0001c0001t0003g0152 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1937+1893A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123200271 | |||||||
chr12:123200300 | CT | C | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1937+1863delA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123200300 | |||||||
chr12:123200567 | G | C | 1 | a0001c0001t0004g0188 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1937+1597C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123200567 | |||||||
chr12:123200651 | A | AT | 5 | a0001c0001t0004g0177 a0001c0001t0004g0178 a0001c0001t0004g0193 others(2): Show |
5 | HG02976.hp1 HG03017.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1937+1512dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123200651 | |||||||
chr12:123200651 | AT | A | 6 | a0001c0001t0004g0175 a0001c0001t0005g0204 a0001c0001t0030g0211 others(3): Show |
6 | HG01891.hp2 HG02735.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1937+1512delA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123200651 | |||||||
chr12:123200992 | A | G | 1 | a0002c0003t0002g0225 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1937+1172T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123200992 | |||||||
chr12:123201032 | C | T | 1 | a0001c0002t0001g0083 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1937+1132G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123201032 | |||||||
chr12:123201231 | C | CTGTTT | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1937+928_1937+932d others(7): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123201231 | |||||||
chr12:123201580 | A | C | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1937+584T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123201580 | |||||||
chr12:123201601 | A | T | 2 | a0001c0001t0015g0107 a0007c0017t0005g0203 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1937+563T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123201601 | |||||||
chr12:123201603 | C | T | 3 | a0001c0001t0004g0172 a0001c0001t0004g0181 a0001c0001t0004g0182 |
3 | HG00741.hp1 HG01074.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.1937+561G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123201603 | |||||||
chr12:123201677 | T | C | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1937+487A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123201677 | |||||||
chr12:123201809 | A | C | 1 | a0002c0003t0002g0230 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1937+355T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123201809 | |||||||
chr12:123201900 | T | A | 1 | a0001c0001t0003g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1937+264A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123201900 | |||||||
chr12:123202044 | A | C | 1 | a0001c0002t0001g0035 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1937+120T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 11/23 | chr12 | 123202044 | |||||||
chr12:123203125 | G | A | 9 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(6): Show |
9 | HG02602.hp2 HG03491.hp1 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.1321-41C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 9/23 | chr12 | 123203125 | |||||||
chr12:123203227 | C | T | 52 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(49): Show |
52 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1320+23G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 9/23 | chr12 | 123203227 | |||||||
chr12:123203681 | C | A | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1195-306G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123203681 | |||||||
chr12:123203736 | T | A | 1 | a0001c0001t0004g0179 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1195-361A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123203736 | |||||||
chr12:123203858 | A | T | 1 | a0001c0001t0004g0175 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1195-483T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123203858 | |||||||
chr12:123203937 | T | G | 119 | a0001c0001t0004g0180 a0001c0001t0006g0002 a0001c0001t0006g0003 others(116): Show |
120 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.1195-562A>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123203937 | |||||||
chr12:123204090 | G | A | 1 | a0001c0001t0004g0189 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1195-715C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123204090 | |||||||
chr12:123204233 | C | T | 3 | a0001c0004t0011g0105 a0001c0004t0011g0106 a0001c0004t0024g0102 |
3 | HG01175.hp1 HG02683.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1195-858G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123204233 | |||||||
chr12:123204236 | A | T | 2 | a0001c0002t0001g0100 a0001c0002t0001g0101 |
2 | NA18990.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1195-861T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123204236 | |||||||
chr12:123204258 | C | T | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1195-883G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123204258 | |||||||
chr12:123204302 | CA | C | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1195-928delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123204302 | |||||||
chr12:123204628 | G | C | 1 | a0001c0002t0001g0021 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1195-1253C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123204628 | |||||||
chr12:123204781 | G | A | 51 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0214 others(48): Show |
51 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.1195-1406C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123204781 | |||||||
chr12:123204839 | T | C | 229 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(226): Show |
230 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(227): Show |
intron_variant | MODIFIER | c.1195-1464A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123204839 | |||||||
chr12:123204974 | C | T | 234 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(231): Show |
235 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(232): Show |
intron_variant | MODIFIER | c.1195-1599G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123204974 | |||||||
chr12:123205127 | C | T | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1195-1752G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123205127 | |||||||
chr12:123205238 | T | C | 1 | a0001c0004t0001g0074 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1195-1863A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123205238 | |||||||
chr12:123205350 | G | A | 102 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(99): Show |
103 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.1195-1975C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123205350 | |||||||
chr12:123205383 | T | A | 1 | a0001c0001t0021g0205 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1195-2008A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123205383 | |||||||
chr12:123205383 | T | C | 1 | a0001c0002t0019g0039 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1195-2008A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123205383 | |||||||
chr12:123205477 | C | T | 1 | a0001c0004t0007g0103 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1195-2102G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123205477 | |||||||
chr12:123205561 | C | T | 1 | a0001c0009t0022g0162 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1195-2186G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123205561 | |||||||
chr12:123206122 | C | T | 1 | a0001c0001t0009g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1195-2747G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206122 | |||||||
chr12:123206192 | T | C | 2 | a0001c0001t0006g0002 a0001c0001t0006g0003 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1195-2817A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206192 | |||||||
chr12:123206302 | C | CA | 118 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(115): Show |
119 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.1195-2928dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206302 | |||||||
chr12:123206376 | C | T | 1 | a0001c0001t0003g0135 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1195-3001G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206376 | |||||||
chr12:123206496 | AGAGAG | A | 34 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0122 others(31): Show |
34 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.1195-3126_1195-312 others(9): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206496 | |||||||
chr12:123206511 | G | A | 5 | a0001c0001t0003g0121 a0001c0001t0003g0123 a0001c0001t0003g0138 others(2): Show |
5 | HG01099.hp1 HG02258.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1195-3136C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206511 | |||||||
chr12:123206511 | GGAGAAGA others(13): Show |
G | 5 | a0001c0001t0004g0166 a0001c0001t0004g0168 a0001c0001t0004g0190 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1195-3156_1195-313 others(24): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206511 | |||||||
chr12:123206531 | T | A | 12 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(9): Show |
12 | HG01099.hp1 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1195-3156A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206531 | |||||||
chr12:123206531 | TGAGAA | T | 117 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(114): Show |
118 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.1195-3161_1195-315 others(9): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206531 | |||||||
chr12:123206536 | A | T | 1 | a0001c0002t0001g0011 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1195-3161T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206536 | |||||||
chr12:123206609 | G | A | 1 | a0001c0001t0005g0132 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1195-3234C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206609 | |||||||
chr12:123206625 | T | C | 1 | a0001c0001t0023g0209 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1195-3250A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206625 | |||||||
chr12:123206709 | C | T | 2 | a0001c0002t0001g0065 a0010c0010t0001g0033 |
2 | NA18948.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1195-3334G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206709 | |||||||
chr12:123206824 | G | C | 3 | a0001c0002t0001g0081 a0001c0002t0001g0082 a0001c0002t0001g0083 |
3 | HG00639.hp2 HG01099.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1194+3232C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206824 | |||||||
chr12:123206940 | C | T | 1 | a0001c0001t0004g0178 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1194+3116G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206940 | |||||||
chr12:123206950 | C | T | 1 | a0008c0015t0003g0163 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1194+3106G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123206950 | |||||||
chr12:123207053 | TA | T | 6 | a0001c0001t0012g0150 a0001c0001t0012g0151 a0001c0002t0001g0059 others(3): Show |
6 | HG02922.hp1 NA18906.hp2 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.1194+3002delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207053 | |||||||
chr12:123207056 | A | T | 1 | a0001c0004t0007g0111 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1194+3000T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207056 | |||||||
chr12:123207099 | G | C | 1 | a0001c0001t0003g0146 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1194+2957C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207099 | |||||||
chr12:123207123 | T | A | 1 | a0002c0003t0002g0262 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1194+2933A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207123 | |||||||
chr12:123207146 | T | TA | 102 | a0001c0001t0003g0136 a0001c0002t0001g0001 a0001c0002t0001g0006 others(99): Show |
103 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.1194+2909dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207146 | |||||||
chr12:123207146 | T | TAA | 45 | a0001c0002t0001g0029 a0002c0003t0001g0229 a0002c0003t0001g0231 others(42): Show |
45 | HG00609.hp2 HG00621.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.1194+2908_1194+290 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207146 | |||||||
chr12:123207146 | TA | T | 20 | a0001c0001t0003g0124 a0001c0001t0003g0161 a0001c0001t0004g0181 others(17): Show |
20 | HG01167.hp1 HG01256.hp2 HG01516.hp1 others(17): Show |
intron_variant | MODIFIER | c.1194+2909delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207146 | |||||||
chr12:123207195 | T | G | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1194+2861A>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207195 | |||||||
chr12:123207758 | T | C | 170 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(167): Show |
171 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(168): Show |
intron_variant | MODIFIER | c.1194+2298A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207758 | |||||||
chr12:123207759 | G | C | 1 | a0001c0002t0001g0059 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1194+2297C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207759 | |||||||
chr12:123207800 | C | T | 1 | a0001c0002t0001g0014 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1194+2256G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207800 | |||||||
chr12:123207831 | C | T | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1194+2225G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207831 | |||||||
chr12:123207869 | G | A | 1 | a0002c0003t0001g0229 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1194+2187C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207869 | |||||||
chr12:123207869 | GA | G | 207 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(204): Show |
208 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(205): Show |
intron_variant | MODIFIER | c.1194+2186delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207869 | |||||||
chr12:123207870 | A | G | 1 | a0002c0003t0001g0229 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1194+2186T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207870 | |||||||
chr12:123207880 | A | T | 1 | a0001c0002t0001g0059 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1194+2176T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207880 | |||||||
chr12:123207881 | T | A | 1 | a0001c0002t0001g0059 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1194+2175A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207881 | |||||||
chr12:123207957 | G | A | 1 | a0001c0001t0005g0204 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1194+2099C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123207957 | |||||||
chr12:123208074 | C | T | 1 | a0001c0001t0003g0138 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1194+1982G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208074 | |||||||
chr12:123208119 | G | A | 1 | a0001c0002t0001g0058 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1194+1937C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208119 | |||||||
chr12:123208125 | G | A | 1 | a0001c0002t0001g0043 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1194+1931C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208125 | |||||||
chr12:123208184 | G | A | 7 | a0001c0004t0007g0103 a0001c0004t0007g0108 a0001c0004t0007g0109 others(4): Show |
7 | HG01952.hp2 HG02132.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1194+1872C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208184 | |||||||
chr12:123208188 | CA | C | 186 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(183): Show |
187 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(184): Show |
intron_variant | MODIFIER | c.1194+1867delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208188 | |||||||
chr12:123208188 | CAA | C | 6 | a0001c0001t0003g0161 a0001c0002t0001g0087 a0001c0002t0017g0071 others(3): Show |
6 | HG02895.hp2 NA18982.hp2 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.1194+1866_1194+186 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208188 | |||||||
chr12:123208209 | A | T | 1 | a0002c0003t0002g0262 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1194+1847T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208209 | |||||||
chr12:123208211 | T | A | 1 | a0002c0003t0002g0262 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1194+1845A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208211 | |||||||
chr12:123208261 | C | G | 1 | a0001c0002t0001g0059 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1194+1795G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208261 | |||||||
chr12:123208261 | C | T | 1 | a0001c0016t0001g0097 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1194+1795G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208261 | |||||||
chr12:123208262 | G | C | 1 | a0001c0002t0001g0059 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1194+1794C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208262 | |||||||
chr12:123208265 | C | A | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1194+1791G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208265 | |||||||
chr12:123208335 | G | A | 1 | a0001c0001t0015g0107 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1194+1721C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208335 | |||||||
chr12:123208408 | G | T | 1 | a0001c0004t0007g0103 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1194+1648C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208408 | |||||||
chr12:123208418 | A | T | 210 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(207): Show |
211 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(208): Show |
intron_variant | MODIFIER | c.1194+1638T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208418 | |||||||
chr12:123208438 | G | A | 7 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(4): Show |
7 | HG03491.hp1 HG03492.hp2 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.1194+1618C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208438 | |||||||
chr12:123208533 | C | CA | 54 | a0001c0001t0005g0202 a0001c0001t0005g0206 a0001c0002t0001g0065 others(51): Show |
54 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1194+1522dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208533 | |||||||
chr12:123208533 | C | CAA | 114 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(111): Show |
115 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.1194+1521_1194+152 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208533 | |||||||
chr12:123208705 | G | A | 1 | a0001c0004t0007g0111 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1194+1351C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208705 | |||||||
chr12:123208755 | T | C | 1 | a0001c0002t0001g0059 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1194+1301A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208755 | |||||||
chr12:123208768 | G | T | 1 | a0002c0003t0002g0218 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1194+1288C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208768 | |||||||
chr12:123208816 | C | A | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1194+1240G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208816 | |||||||
chr12:123208873 | T | C | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1194+1183A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123208873 | |||||||
chr12:123209055 | C | A | 1 | a0002c0003t0002g0225 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1194+1001G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209055 | |||||||
chr12:123209088 | A | C | 1 | a0002c0003t0002g0262 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1194+968T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209088 | |||||||
chr12:123209090 | G | A | 1 | a0001c0001t0005g0169 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1194+966C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209090 | |||||||
chr12:123209262 | A | T | 1 | a0001c0002t0001g0059 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1194+794T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209262 | |||||||
chr12:123209409 | GT | G | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1194+646delA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209409 | |||||||
chr12:123209411 | T | A | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1194+645A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209411 | |||||||
chr12:123209659 | T | C | 229 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(226): Show |
230 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(227): Show |
intron_variant | MODIFIER | c.1194+397A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209659 | |||||||
chr12:123209668 | C | T | 3 | a0001c0001t0003g0147 a0001c0001t0003g0149 a0001c0001t0003g0157 |
3 | HG02615.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1194+388G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209668 | |||||||
chr12:123209703 | C | T | 118 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(115): Show |
119 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.1194+353G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209703 | |||||||
chr12:123209737 | G | GT | 112 | a0001c0001t0003g0121 a0001c0001t0004g0178 a0001c0001t0004g0179 others(109): Show |
113 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.1194+318dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209737 | |||||||
chr12:123209737 | G | GTT | 13 | a0001c0001t0006g0115 a0001c0001t0006g0118 a0001c0001t0006g0264 others(10): Show |
13 | HG00621.hp1 HG01952.hp2 HG02738.hp1 others(10): Show |
intron_variant | MODIFIER | c.1194+317_1194+318d others(4): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209737 | |||||||
chr12:123209737 | G | T | 1 | a0001c0002t0001g0059 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1194+319C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209737 | |||||||
chr12:123209894 | G | A | 2 | a0001c0001t0015g0107 a0007c0017t0005g0203 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1194+162C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209894 | |||||||
chr12:123209898 | A | G | 2 | a0001c0001t0015g0107 a0007c0017t0005g0203 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1194+158T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209898 | |||||||
chr12:123209926 | C | T | 1 | a0001c0002t0001g0044 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1194+130G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123209926 | |||||||
chr12:123210025 | C | A | 1 | a0001c0001t0003g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1194+31G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123210025 | |||||||
chr12:123210044 | T | G | 1 | a0001c0002t0001g0059 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1194+12A>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 8/23 | chr12 | 123210044 | |||||||
chr12:123210177 | C | T | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1088-15G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123210177 | |||||||
chr12:123210529 | C | T | 1 | a0011c0014t0002g0221 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1088-367G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123210529 | |||||||
chr12:123210885 | C | T | 1 | a0001c0002t0001g0079 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1088-723G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123210885 | |||||||
chr12:123210977 | C | CT | 27 | a0001c0001t0003g0201 a0001c0001t0004g0168 a0001c0001t0004g0170 others(24): Show |
27 | HG00735.hp2 HG00741.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.1088-816dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123210977 | |||||||
chr12:123210977 | C | CTT | 8 | a0001c0001t0004g0193 a0001c0001t0023g0209 a0001c0004t0007g0103 others(5): Show |
8 | HG02132.hp2 HG02738.hp1 HG03239.hp2 others(5): Show |
intron_variant | MODIFIER | c.1088-817_1088-816d others(4): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123210977 | |||||||
chr12:123210977 | CT | C | 80 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(77): Show |
80 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.1088-816delA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123210977 | |||||||
chr12:123210982 | T | C | 1 | a0001c0009t0022g0162 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1088-820A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123210982 | |||||||
chr12:123210987 | T | C | 2 | a0002c0003t0002g0214 a0002c0003t0002g0218 |
2 | HG03831.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1088-825A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123210987 | |||||||
chr12:123210988 | T | C | 51 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(48): Show |
51 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.1088-826A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123210988 | |||||||
chr12:123211371 | C | T | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1088-1209G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123211371 | |||||||
chr12:123211410 | T | G | 1 | a0002c0003t0002g0262 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1088-1248A>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123211410 | |||||||
chr12:123211610 | C | G | 1 | a0002c0003t0002g0262 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1088-1448G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123211610 | |||||||
chr12:123211684 | C | CT | 5 | a0001c0001t0004g0192 a0001c0001t0004g0195 a0001c0001t0005g0128 others(2): Show |
5 | HG01978.hp2 HG02145.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1088-1523dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123211684 | |||||||
chr12:123211684 | CT | C | 145 | a0001c0001t0003g0125 a0001c0001t0003g0157 a0001c0001t0003g0161 others(142): Show |
146 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.1088-1523delA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123211684 | |||||||
chr12:123211684 | CTT | C | 14 | a0001c0002t0001g0010 a0001c0002t0001g0015 a0001c0002t0001g0022 others(11): Show |
14 | HG01070.hp2 HG01081.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.1088-1524_1088-152 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123211684 | |||||||
chr12:123211684 | CTTTTTTT others(1): Show |
C | 5 | a0001c0002t0001g0098 a0001c0002t0001g0099 a0001c0002t0014g0008 others(2): Show |
5 | HG01952.hp1 HG01978.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1088-1530_1088-152 others(12): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123211684 | |||||||
chr12:123211709 | T | C | 1 | a0002c0003t0002g0256 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1088-1547A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123211709 | |||||||
chr12:123212416 | G | A | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1088-2254C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212416 | |||||||
chr12:123212417 | C | T | 2 | a0002c0003t0002g0223 a0002c0003t0002g0235 |
2 | HG01070.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1088-2255G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212417 | |||||||
chr12:123212460 | C | T | 118 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(115): Show |
119 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.1087+2284G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212460 | |||||||
chr12:123212494 | G | A | 34 | a0001c0001t0003g0167 a0001c0001t0003g0197 a0001c0001t0003g0198 others(31): Show |
34 | HG00140.hp1 HG00738.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1087+2250C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212494 | |||||||
chr12:123212673 | C | T | 1 | a0001c0002t0001g0079 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1087+2071G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212673 | |||||||
chr12:123212711 | C | CA | 14 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0004g0192 others(11): Show |
14 | HG02132.hp2 HG02145.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1087+2032dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212711 | |||||||
chr12:123212711 | CA | C | 140 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(137): Show |
141 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.1087+2032delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212711 | |||||||
chr12:123212761 | G | A | 1 | a0001c0002t0001g0079 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1087+1983C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212761 | |||||||
chr12:123212766 | C | CT | 5 | a0001c0001t0004g0172 a0001c0001t0004g0175 a0002c0003t0002g0223 others(2): Show |
5 | HG00741.hp1 HG01070.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1087+1977dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212766 | |||||||
chr12:123212766 | C | CTT | 45 | a0001c0002t0001g0022 a0001c0002t0001g0028 a0002c0003t0001g0229 others(42): Show |
45 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.1087+1976_1087+197 others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212766 | |||||||
chr12:123212766 | C | CTTT | 109 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(106): Show |
110 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.1087+1975_1087+197 others(7): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212766 | |||||||
chr12:123212766 | C | CTTTT | 13 | a0001c0001t0006g0118 a0001c0001t0006g0264 a0001c0002t0001g0011 others(10): Show |
13 | HG00741.hp2 HG02071.hp1 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.1087+1974_1087+197 others(8): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212766 | |||||||
chr12:123212766 | C | T | 1 | a0002c0003t0002g0262 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1087+1978G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212766 | |||||||
chr12:123212766 | CT | C | 28 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(25): Show |
28 | HG01099.hp1 HG01109.hp1 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.1087+1977delA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212766 | |||||||
chr12:123212796 | T | C | 15 | a0001c0001t0005g0126 a0001c0001t0005g0127 a0001c0001t0005g0128 others(12): Show |
15 | HG01884.hp1 HG02486.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1087+1948A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212796 | |||||||
chr12:123212810 | T | C | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1087+1934A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212810 | |||||||
chr12:123212976 | C | T | 1 | a0001c0002t0001g0035 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1087+1768G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212976 | |||||||
chr12:123212984 | T | C | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1087+1760A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123212984 | |||||||
chr12:123213005 | G | A | 1 | a0001c0001t0005g0133 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1087+1739C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123213005 | |||||||
chr12:123213009 | G | A | 1 | a0001c0002t0001g0030 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1087+1735C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123213009 | |||||||
chr12:123213054 | T | C | 2 | a0001c0002t0001g0024 a0001c0002t0001g0064 |
2 | HG00733.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.1087+1690A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123213054 | |||||||
chr12:123213079 | T | A | 1 | a0002c0003t0002g0262 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1087+1665A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123213079 | |||||||
chr12:123213345 | A | AT | 9 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(6): Show |
9 | HG02602.hp2 HG03491.hp1 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.1087+1398dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123213345 | |||||||
chr12:123213351 | T | C | 98 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(95): Show |
99 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1087+1393A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123213351 | |||||||
chr12:123213425 | G | C | 3 | a0001c0004t0011g0105 a0001c0004t0011g0106 a0001c0004t0024g0102 |
3 | HG01175.hp1 HG02683.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1087+1319C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123213425 | |||||||
chr12:123213785 | G | C | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1087+959C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123213785 | |||||||
chr12:123213787 | GAAC | G | 2 | a0001c0001t0003g0152 a0001c0001t0003g0159 |
2 | HG01243.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1087+954_1087+956d others(5): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123213787 | |||||||
chr12:123213971 | T | G | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1087+773A>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123213971 | |||||||
chr12:123213972 | G | T | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1087+772C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123213972 | |||||||
chr12:123214056 | A | T | 233 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(230): Show |
234 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(231): Show |
intron_variant | MODIFIER | c.1087+688T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123214056 | |||||||
chr12:123214243 | T | C | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1087+501A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123214243 | |||||||
chr12:123214259 | C | T | 2 | a0002c0003t0002g0212 a0002c0003t0002g0213 |
2 | HG01243.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1087+485G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123214259 | |||||||
chr12:123214653 | GTTT | G | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1087+88_1087+90del others(3): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123214653 | |||||||
chr12:123214698 | G | A | 7 | a0001c0004t0007g0103 a0001c0004t0007g0108 a0001c0004t0007g0109 others(4): Show |
7 | HG01952.hp2 HG02132.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1087+46C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 7/23 | chr12 | 123214698 | |||||||
chr12:123214973 | A | G | 234 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(231): Show |
235 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(232): Show |
intron_variant | MODIFIER | c.997-139T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123214973 | |||||||
chr12:123215025 | C | T | 1 | a0001c0002t0007g0037 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.997-191G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123215025 | |||||||
chr12:123215058 | A | G | 1 | a0001c0002t0001g0077 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.997-224T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123215058 | |||||||
chr12:123215075 | C | T | 5 | a0001c0001t0003g0148 a0001c0001t0003g0152 a0001c0001t0003g0159 others(2): Show |
5 | HG01243.hp1 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.997-241G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123215075 | |||||||
chr12:123215146 | G | A | 4 | a0001c0001t0006g0114 a0001c0001t0006g0115 a0001c0001t0006g0116 others(1): Show |
4 | NA18951.hp2 NA18977.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.997-312C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123215146 | |||||||
chr12:123215202 | A | T | 2 | a0001c0005t0001g0092 a0001c0005t0001g0093 |
2 | NA18979.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.997-368T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123215202 | |||||||
chr12:123215678 | C | T | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.997-844G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123215678 | |||||||
chr12:123215687 | T | C | 2 | a0001c0001t0012g0150 a0001c0001t0012g0151 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.997-853A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123215687 | |||||||
chr12:123215916 | C | G | 1 | a0002c0003t0002g0252 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.997-1082G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123215916 | |||||||
chr12:123215929 | T | A | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.997-1095A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123215929 | |||||||
chr12:123215959 | C | T | 2 | a0002c0003t0002g0223 a0002c0003t0002g0235 |
2 | HG01070.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.997-1125G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123215959 | |||||||
chr12:123216216 | T | C | 1 | a0001c0002t0001g0066 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.997-1382A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123216216 | |||||||
chr12:123216320 | A | G | 39 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(36): Show |
39 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.997-1486T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123216320 | |||||||
chr12:123216423 | G | A | 1 | a0001c0001t0005g0134 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.997-1589C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123216423 | |||||||
chr12:123216463 | G | T | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.997-1629C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123216463 | |||||||
chr12:123216723 | A | C | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.996+1653T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123216723 | |||||||
chr12:123216806 | T | C | 118 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(115): Show |
119 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.996+1570A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123216806 | |||||||
chr12:123216859 | C | T | 1 | a0001c0002t0001g0036 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.996+1517G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123216859 | |||||||
chr12:123216992 | A | AAAAT | 3 | a0001c0001t0003g0121 a0001c0001t0021g0205 a0008c0015t0003g0163 |
3 | HG02258.hp1 HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.996+1380_996+1383d others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123216992 | |||||||
chr12:123216992 | AAAAT | A | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.996+1380_996+1383d others(6): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123216992 | |||||||
chr12:123217322 | C | T | 39 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(36): Show |
39 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.996+1054G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123217322 | |||||||
chr12:123217323 | G | A | 1 | a0002c0003t0002g0249 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.996+1053C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123217323 | |||||||
chr12:123217419 | G | A | 1 | a0001c0001t0003g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.996+957C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123217419 | |||||||
chr12:123217525 | T | A | 3 | a0001c0001t0003g0147 a0001c0001t0003g0149 a0001c0001t0003g0157 |
3 | HG02615.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.996+851A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123217525 | |||||||
chr12:123217828 | G | A | 1 | a0001c0001t0003g0141 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.996+548C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123217828 | |||||||
chr12:123217902 | G | A | 7 | a0001c0004t0007g0103 a0001c0004t0007g0108 a0001c0004t0007g0109 others(4): Show |
7 | HG01952.hp2 HG02132.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.996+474C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123217902 | |||||||
chr12:123217906 | G | A | 1 | a0001c0001t0003g0146 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.996+470C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123217906 | |||||||
chr12:123217952 | G | C | 1 | a0001c0002t0001g0025 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.996+424C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123217952 | |||||||
chr12:123218044 | C | CA | 17 | a0001c0001t0003g0159 a0001c0001t0004g0194 a0001c0002t0001g0070 others(14): Show |
17 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.996+331dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123218044 | |||||||
chr12:123218147 | G | A | 1 | a0004c0013t0002g0248 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.996+229C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123218147 | |||||||
chr12:123218220 | G | T | 3 | a0001c0004t0011g0105 a0001c0004t0011g0106 a0001c0004t0024g0102 |
3 | HG01175.hp1 HG02683.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.996+156C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123218220 | |||||||
chr12:123218246 | C | CA | 11 | a0001c0001t0003g0143 a0001c0001t0003g0148 a0001c0001t0003g0152 others(8): Show |
11 | HG01243.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.996+129dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 6/23 | chr12 | 123218246 | |||||||
chr12:123218525 | T | C | 1 | a0001c0001t0003g0198 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.873-26A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123218525 | |||||||
chr12:123218556 | T | C | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.873-57A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123218556 | |||||||
chr12:123218582 | G | A | 19 | a0001c0001t0005g0126 a0001c0001t0005g0127 a0001c0001t0005g0128 others(16): Show |
19 | HG01884.hp1 HG02145.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.873-83C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123218582 | |||||||
chr12:123218677 | C | T | 7 | a0001c0004t0007g0103 a0001c0004t0007g0108 a0001c0004t0007g0109 others(4): Show |
7 | HG01952.hp2 HG02132.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.873-178G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123218677 | |||||||
chr12:123218679 | T | A | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.873-180A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123218679 | |||||||
chr12:123218834 | A | T | 1 | a0009c0020t0005g0104 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.873-335T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123218834 | |||||||
chr12:123218875 | A | AGTT | 229 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(226): Show |
230 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(227): Show |
intron_variant | MODIFIER | c.873-379_873-377dup others(3): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123218875 | |||||||
chr12:123218893 | TTTTG | T | 118 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(115): Show |
119 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.873-398_873-395del others(4): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123218893 | |||||||
chr12:123218926 | CCTCT | C | 11 | a0001c0001t0005g0126 a0001c0001t0005g0127 a0001c0001t0005g0128 others(8): Show |
11 | HG01884.hp1 HG02615.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.873-431_873-428del others(4): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123218926 | |||||||
chr12:123218954 | C | T | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.873-455G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123218954 | |||||||
chr12:123219031 | T | C | 7 | a0001c0002t0001g0011 a0001c0002t0001g0029 a0001c0002t0001g0068 others(4): Show |
7 | HG01258.hp1 HG01361.hp1 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.873-532A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123219031 | |||||||
chr12:123219034 | A | C | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.873-535T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123219034 | |||||||
chr12:123219337 | G | A | 1 | a0001c0001t0003g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.873-838C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123219337 | |||||||
chr12:123219470 | G | A | 4 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(1): Show |
4 | HG00733.hp2 HG02698.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.873-971C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123219470 | |||||||
chr12:123219501 | C | T | 3 | a0001c0001t0003g0147 a0001c0001t0003g0149 a0001c0001t0003g0157 |
3 | HG02615.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.873-1002G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123219501 | |||||||
chr12:123219504 | G | T | 1 | a0001c0001t0003g0146 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.873-1005C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123219504 | |||||||
chr12:123219552 | C | CA | 18 | a0001c0001t0003g0157 a0001c0001t0003g0159 a0001c0001t0004g0195 others(15): Show |
18 | HG00673.hp2 HG01070.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.873-1054dupT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123219552 | |||||||
chr12:123219552 | CA | C | 9 | a0001c0001t0003g0125 a0001c0001t0005g0127 a0001c0001t0005g0204 others(6): Show |
9 | HG00733.hp2 HG02258.hp2 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.873-1054delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123219552 | |||||||
chr12:123219603 | T | C | 1 | a0001c0001t0003g0160 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.873-1104A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123219603 | |||||||
chr12:123219672 | G | A | 1 | a0001c0002t0017g0071 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.873-1173C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123219672 | |||||||
chr12:123219814 | A | C | 2 | a0002c0003t0002g0256 a0002c0003t0002g0259 |
2 | HG00609.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.873-1315T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123219814 | |||||||
chr12:123220022 | C | T | 228 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(225): Show |
229 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(226): Show |
intron_variant | MODIFIER | c.872+1350G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123220022 | |||||||
chr12:123220051 | G | A | 98 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(95): Show |
99 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.872+1321C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123220051 | |||||||
chr12:123220123 | G | A | 1 | a0009c0020t0005g0104 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.872+1249C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123220123 | |||||||
chr12:123220167 | C | G | 1 | a0001c0002t0001g0034 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.872+1205G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123220167 | |||||||
chr12:123220295 | G | A | 2 | a0002c0003t0002g0214 a0002c0003t0002g0236 |
2 | HG03831.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.872+1077C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123220295 | |||||||
chr12:123220297 | T | C | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.872+1075A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123220297 | |||||||
chr12:123220343 | G | A | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.872+1029C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123220343 | |||||||
chr12:123220695 | A | G | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.872+677T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123220695 | |||||||
chr12:123220714 | C | G | 19 | a0001c0001t0005g0126 a0001c0001t0005g0127 a0001c0001t0005g0128 others(16): Show |
19 | HG01884.hp1 HG02145.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.872+658G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123220714 | |||||||
chr12:123220777 | T | C | 1 | a0001c0001t0003g0142 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.872+595A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123220777 | |||||||
chr12:123220783 | A | C | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.872+589T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123220783 | |||||||
chr12:123221012 | G | A | 38 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(35): Show |
38 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.872+360C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123221012 | |||||||
chr12:123221055 | A | C | 1 | a0001c0002t0001g0100 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.872+317T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123221055 | |||||||
chr12:123221123 | T | A | 1 | a0001c0001t0003g0161 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.872+249A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 5/23 | chr12 | 123221123 | |||||||
chr12:123222106 | G | A | 1 | a0001c0004t0007g0111 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.349-211C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 4/23 | chr12 | 123222106 | |||||||
chr12:123222324 | CA | C | 165 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(162): Show |
166 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(163): Show |
intron_variant | MODIFIER | c.349-430delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 4/23 | chr12 | 123222324 | |||||||
chr12:123222324 | CAA | C | 18 | a0002c0003t0001g0229 a0002c0003t0002g0215 a0002c0003t0002g0218 others(15): Show |
18 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.349-431_349-430del others(2): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 4/23 | chr12 | 123222324 | |||||||
chr12:123222403 | C | T | 1 | a0001c0002t0001g0100 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.349-508G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 4/23 | chr12 | 123222403 | |||||||
chr12:123222608 | C | T | 1 | a0001c0001t0004g0172 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.348+430G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 4/23 | chr12 | 123222608 | |||||||
chr12:123222609 | G | A | 3 | a0001c0004t0011g0105 a0001c0004t0011g0106 a0001c0004t0024g0102 |
3 | HG01175.hp1 HG02683.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.348+429C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 4/23 | chr12 | 123222609 | |||||||
chr12:123222770 | T | C | 1 | a0001c0002t0001g0012 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.348+268A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 4/23 | chr12 | 123222770 | |||||||
chr12:123222962 | A | ATG | 32 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(29): Show |
32 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.348+74_348+75dupCA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 4/23 | chr12 | 123222962 | |||||||
chr12:123222962 | A | ATGTG | 4 | a0001c0001t0003g0148 a0001c0001t0009g0164 a0001c0001t0020g0145 others(1): Show |
4 | HG01891.hp1 HG02486.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+72_348+75dupCA others(2): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 4/23 | chr12 | 123222962 | |||||||
chr12:123222980 | GTA | G | 170 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(167): Show |
171 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(168): Show |
intron_variant | MODIFIER | c.348+56_348+57delTA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 4/23 | chr12 | 123222980 | |||||||
chr12:123222982 | A | G | 2 | a0001c0001t0004g0179 a0001c0004t0007g0103 |
2 | HG01106.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.348+56T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 4/23 | chr12 | 123222982 | |||||||
chr12:123223005 | TA | T | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.348+32delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 4/23 | chr12 | 123223005 | |||||||
chr12:123223279 | G | A | 1 | a0002c0003t0026g0253 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.259-152C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123223279 | |||||||
chr12:123223430 | C | T | 1 | a0001c0002t0001g0030 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.259-303G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123223430 | |||||||
chr12:123223516 | A | G | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.259-389T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123223516 | |||||||
chr12:123223939 | A | T | 1 | a0007c0017t0005g0203 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.259-812T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123223939 | |||||||
chr12:123223943 | T | A | 176 | a0001c0001t0003g0167 a0001c0001t0003g0197 a0001c0001t0003g0198 others(173): Show |
177 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(174): Show |
intron_variant | MODIFIER | c.259-816A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123223943 | |||||||
chr12:123224105 | C | T | 1 | a0002c0003t0002g0255 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.259-978G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224105 | |||||||
chr12:123224110 | T | TTA | 20 | a0001c0001t0004g0170 a0001c0001t0005g0126 a0001c0001t0005g0127 others(17): Show |
20 | HG01081.hp1 HG01175.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.259-985_259-984dup others(2): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | |||||||
chr12:123224110 | T | TTATATAT others(17): Show |
1 | a0002c0003t0002g0222 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.259-984_259-983ins others(24): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | |||||||
chr12:123224110 | T | TTATATAT others(21): Show |
2 | a0002c0003t0002g0225 a0002c0003t0025g0080 |
2 | HG01069.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.259-984_259-983ins others(28): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | |||||||
chr12:123224110 | T | TTTATATA others(24): Show |
1 | a0011c0014t0002g0221 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.259-984_259-983ins others(31): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | |||||||
chr12:123224110 | T | TTTTATAT others(11): Show |
1 | a0002c0003t0002g0223 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.259-984_259-983ins others(18): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | |||||||
chr12:123224110 | T | TTTTATAT others(17): Show |
6 | a0002c0003t0001g0231 a0002c0003t0002g0216 a0002c0003t0002g0217 others(3): Show |
6 | HG02080.hp2 HG02155.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-984_259-983ins others(24): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | |||||||
chr12:123224110 | T | TTTTATAT others(19): Show |
4 | a0002c0003t0002g0214 a0002c0003t0002g0234 a0002c0003t0002g0235 others(1): Show |
4 | HG02293.hp1 HG03831.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-984_259-983ins others(26): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | |||||||
chr12:123224110 | T | TTTTATAT others(21): Show |
7 | a0002c0003t0002g0218 a0002c0003t0002g0237 a0002c0003t0002g0238 others(4): Show |
7 | HG02071.hp2 NA18949.hp1 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-984_259-983ins others(28): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | |||||||
chr12:123224110 | T | TTTTATAT others(23): Show |
13 | a0002c0003t0002g0220 a0002c0003t0002g0226 a0002c0003t0002g0241 others(10): Show |
13 | HG00621.hp2 HG00673.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.259-984_259-983ins others(30): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | |||||||
chr12:123224110 | T | TTTTATAT others(25): Show |
7 | a0002c0003t0002g0228 a0002c0003t0002g0249 a0002c0003t0002g0250 others(4): Show |
7 | HG00558.hp1 HG02132.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-984_259-983ins others(32): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | |||||||
chr12:123224110 | T | TTTTATAT others(27): Show |
3 | a0002c0003t0002g0215 a0002c0003t0002g0254 a0002c0003t0002g0262 |
3 | NA18957.hp1 NA18987.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.259-984_259-983ins others(34): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | |||||||
chr12:123224110 | T | TTTTATAT others(29): Show |
4 | a0002c0003t0002g0255 a0002c0003t0002g0256 a0002c0003t0002g0257 others(1): Show |
4 | HG02735.hp1 NA18612.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-984_259-983ins others(36): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | |||||||
chr12:123224110 | T | TTTTATAT others(31): Show |
1 | a0002c0003t0002g0212 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.259-984_259-983ins others(38): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | |||||||
chr12:123224110 | T | TTTTATAT others(33): Show |
2 | a0002c0003t0002g0213 a0002c0003t0002g0259 |
2 | HG00609.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.259-984_259-983ins others(40): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | |||||||
chr12:123224110 | TTA | T | 28 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(25): Show |
28 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.259-985_259-984del others(2): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224110 | |||||||
chr12:123224125 | T | C | 6 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0146 others(3): Show |
6 | HG01109.hp1 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-998A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224125 | |||||||
chr12:123224127 | C | T | 99 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(96): Show |
100 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.259-1000G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224127 | |||||||
chr12:123224128 | AC | A | 6 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0146 others(3): Show |
6 | HG01109.hp1 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-1002delG | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224128 | |||||||
chr12:123224130 | A | AC | 9 | a0001c0002t0001g0017 a0001c0002t0001g0026 a0001c0002t0001g0030 others(6): Show |
9 | HG00140.hp2 HG00621.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.259-1004_259-1003i others(3): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224130 | |||||||
chr12:123224130 | A | AT | 10 | a0001c0001t0004g0172 a0001c0001t0005g0169 a0001c0001t0005g0202 others(7): Show |
10 | HG00741.hp1 HG01256.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.259-1004dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224130 | |||||||
chr12:123224130 | A | T | 6 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0146 others(3): Show |
6 | HG01109.hp1 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-1003T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224130 | |||||||
chr12:123224130 | AT | A | 15 | a0001c0001t0003g0201 a0001c0001t0004g0200 a0001c0001t0006g0002 others(12): Show |
15 | HG01975.hp1 HG02572.hp1 HG02602.hp2 others(12): Show |
intron_variant | MODIFIER | c.259-1004delA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224130 | |||||||
chr12:123224131 | T | A | 9 | a0001c0002t0001g0017 a0001c0002t0001g0026 a0001c0002t0001g0030 others(6): Show |
9 | HG00140.hp2 HG00621.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.259-1004A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224131 | |||||||
chr12:123224131 | T | C | 88 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(85): Show |
89 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.259-1004A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224131 | |||||||
chr12:123224132 | T | A | 87 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(84): Show |
88 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.259-1005A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224132 | |||||||
chr12:123224132 | T | C | 2 | a0001c0002t0001g0012 a0001c0002t0001g0096 |
2 | HG01975.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.259-1005A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224132 | |||||||
chr12:123224133 | T | A | 2 | a0001c0002t0001g0012 a0001c0002t0001g0096 |
2 | HG01975.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.259-1006A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224133 | |||||||
chr12:123224377 | G | A | 19 | a0001c0001t0005g0126 a0001c0001t0005g0127 a0001c0001t0005g0128 others(16): Show |
19 | HG01884.hp1 HG02145.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.259-1250C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224377 | |||||||
chr12:123224732 | T | C | 1 | a0001c0001t0009g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.259-1605A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224732 | |||||||
chr12:123224799 | C | T | 1 | a0001c0004t0007g0103 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.259-1672G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224799 | |||||||
chr12:123224859 | A | C | 3 | a0001c0004t0011g0105 a0001c0004t0011g0106 a0001c0004t0024g0102 |
3 | HG01175.hp1 HG02683.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.259-1732T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224859 | |||||||
chr12:123224862 | C | T | 98 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(95): Show |
99 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.259-1735G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123224862 | |||||||
chr12:123225065 | A | T | 3 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 |
3 | HG00738.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.259-1938T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225065 | |||||||
chr12:123225237 | AGT | A | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.259-2112_259-2111d others(4): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225237 | |||||||
chr12:123225242 | AAGACTAA others(12): Show |
A | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.259-2134_259-2116d others(21): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225242 | |||||||
chr12:123225262 | A | T | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.259-2135T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225262 | |||||||
chr12:123225269 | C | T | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.259-2142G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225269 | |||||||
chr12:123225270 | C | T | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.259-2143G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225270 | |||||||
chr12:123225274 | T | C | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.259-2147A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225274 | |||||||
chr12:123225275 | C | A | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.259-2148G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225275 | |||||||
chr12:123225277 | C | G | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.259-2150G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225277 | |||||||
chr12:123225279 | A | T | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.259-2152T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225279 | |||||||
chr12:123225281 | A | AT | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.259-2155_259-2154i others(3): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225281 | |||||||
chr12:123225284 | A | T | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.259-2157T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225284 | |||||||
chr12:123225285 | A | C | 53 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(50): Show |
53 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.259-2158T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225285 | |||||||
chr12:123225367 | C | A | 1 | a0002c0006t0002g0260 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.258+2096G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225367 | |||||||
chr12:123225380 | G | A | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.258+2083C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225380 | |||||||
chr12:123225443 | CA | C | 9 | a0001c0001t0003g0124 a0001c0001t0003g0143 a0001c0001t0004g0171 others(6): Show |
9 | HG01175.hp1 HG01975.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.258+2019delT | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225443 | |||||||
chr12:123225443 | CAA | C | 157 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(154): Show |
158 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.258+2018_258+2019d others(4): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225443 | |||||||
chr12:123225443 | CAAA | C | 11 | a0001c0002t0001g0015 a0001c0002t0001g0022 a0001c0002t0001g0023 others(8): Show |
11 | HG00733.hp1 HG01069.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.258+2017_258+2019d others(5): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225443 | |||||||
chr12:123225457 | A | G | 54 | a0001c0002t0001g0021 a0002c0003t0001g0229 a0002c0003t0001g0231 others(51): Show |
54 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.258+2006T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225457 | |||||||
chr12:123225739 | T | C | 1 | a0001c0002t0001g0013 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.258+1724A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225739 | |||||||
chr12:123225817 | C | T | 98 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(95): Show |
99 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.258+1646G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123225817 | |||||||
chr12:123226231 | TATA | T | 14 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(11): Show |
14 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.258+1229_258+1231d others(5): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123226231 | |||||||
chr12:123226288 | A | C | 101 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(98): Show |
102 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.258+1175T>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123226288 | |||||||
chr12:123226294 | C | A | 1 | a0001c0001t0005g0169 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.258+1169G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123226294 | |||||||
chr12:123226521 | C | CT | 20 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(17): Show |
20 | HG01175.hp1 HG01952.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.258+941dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123226521 | |||||||
chr12:123226521 | CT | C | 51 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(48): Show |
51 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.258+941delA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123226521 | |||||||
chr12:123226629 | T | C | 9 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(6): Show |
9 | HG02602.hp2 HG03491.hp1 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.258+834A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123226629 | |||||||
chr12:123226882 | C | T | 4 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(1): Show |
4 | HG00733.hp2 HG02698.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+581G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123226882 | |||||||
chr12:123227388 | A | G | 2 | a0001c0002t0001g0015 a0001c0002t0001g0016 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.258+75T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 3/23 | chr12 | 123227388 | |||||||
chr12:123227869 | G | A | 209 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(206): Show |
210 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(207): Show |
intron_variant | MODIFIER | c.105-253C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123227869 | |||||||
chr12:123228165 | G | T | 171 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(168): Show |
172 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.105-549C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123228165 | |||||||
chr12:123228300 | G | T | 1 | a0001c0001t0004g0170 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.105-684C>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123228300 | |||||||
chr12:123228465 | G | A | 1 | a0001c0001t0015g0107 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.105-849C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123228465 | |||||||
chr12:123228575 | C | A | 3 | a0001c0002t0001g0081 a0001c0002t0001g0082 a0001c0002t0001g0083 |
3 | HG00639.hp2 HG01099.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.105-959G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123228575 | |||||||
chr12:123229043 | C | T | 1 | a0001c0002t0001g0014 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.104+1218G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229043 | |||||||
chr12:123229210 | G | A | 9 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(6): Show |
9 | HG02602.hp2 HG03491.hp1 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.104+1051C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229210 | |||||||
chr12:123229314 | C | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+947G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229314 | |||||||
chr12:123229317 | G | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+944C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229317 | |||||||
chr12:123229318 | C | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+943G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229318 | |||||||
chr12:123229319 | T | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+942A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229319 | |||||||
chr12:123229320 | T | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+941A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229320 | |||||||
chr12:123229321 | G | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+940C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229321 | |||||||
chr12:123229322 | T | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+939A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229322 | |||||||
chr12:123229323 | C | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+938G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229323 | |||||||
chr12:123229325 | G | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+936C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229325 | |||||||
chr12:123229327 | C | T | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+934G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229327 | |||||||
chr12:123229330 | T | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+931A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229330 | |||||||
chr12:123229331 | G | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+930C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229331 | |||||||
chr12:123229332 | T | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+929A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229332 | |||||||
chr12:123229333 | G | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+928C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229333 | |||||||
chr12:123229334 | C | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+927G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229334 | |||||||
chr12:123229338 | T | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+923A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229338 | |||||||
chr12:123229339 | T | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+922A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229339 | |||||||
chr12:123229340 | G | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+921C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229340 | |||||||
chr12:123229344 | G | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+917C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229344 | |||||||
chr12:123229345 | T | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+916A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229345 | |||||||
chr12:123229349 | C | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+912G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229349 | |||||||
chr12:123229351 | G | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+910C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229351 | |||||||
chr12:123229352 | G | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+909C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229352 | |||||||
chr12:123229353 | C | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+908G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229353 | |||||||
chr12:123229354 | T | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+907A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229354 | |||||||
chr12:123229355 | C | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+906G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229355 | |||||||
chr12:123229356 | T | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+905A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229356 | |||||||
chr12:123229357 | G | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+904C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229357 | |||||||
chr12:123229360 | G | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+901C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229360 | |||||||
chr12:123229366 | C | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+895G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229366 | |||||||
chr12:123229370 | C | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+891G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229370 | |||||||
chr12:123229371 | C | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+890G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229371 | |||||||
chr12:123229376 | T | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+885A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229376 | |||||||
chr12:123229377 | C | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+884G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229377 | |||||||
chr12:123229378 | T | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+883A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229378 | |||||||
chr12:123229379 | G | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+882C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229379 | |||||||
chr12:123229380 | T | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+881A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229380 | |||||||
chr12:123229381 | G | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+880C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229381 | |||||||
chr12:123229382 | T | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+879A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229382 | |||||||
chr12:123229383 | T | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+878A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229383 | |||||||
chr12:123229386 | G | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+875C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229386 | |||||||
chr12:123229388 | C | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+873G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229388 | |||||||
chr12:123229389 | C | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+872G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229389 | |||||||
chr12:123229391 | T | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+870A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229391 | |||||||
chr12:123229392 | T | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+869A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229392 | |||||||
chr12:123229406 | C | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+855G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229406 | |||||||
chr12:123229407 | C | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+854G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229407 | |||||||
chr12:123229410 | T | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+851A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229410 | |||||||
chr12:123229411 | C | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+850G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229411 | |||||||
chr12:123229413 | C | T | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+848G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229413 | |||||||
chr12:123229415 | G | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+846C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229415 | |||||||
chr12:123229416 | G | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+845C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229416 | |||||||
chr12:123229418 | T | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+843A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229418 | |||||||
chr12:123229420 | G | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+841C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229420 | |||||||
chr12:123229421 | C | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+840G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229421 | |||||||
chr12:123229422 | T | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+839A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229422 | |||||||
chr12:123229423 | T | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+838A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229423 | |||||||
chr12:123229424 | A | T | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+837T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229424 | |||||||
chr12:123229429 | T | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+832A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229429 | |||||||
chr12:123229434 | T | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+827A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229434 | |||||||
chr12:123229435 | G | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+826C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229435 | |||||||
chr12:123229436 | C | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+825G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229436 | |||||||
chr12:123229439 | T | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+822A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229439 | |||||||
chr12:123229496 | A | G | 1 | a0001c0001t0005g0169 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.104+765T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229496 | |||||||
chr12:123229689 | A | G | 172 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(169): Show |
173 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(170): Show |
intron_variant | MODIFIER | c.104+572T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229689 | |||||||
chr12:123229821 | A | AT | 8 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0124 others(5): Show |
8 | HG02622.hp2 HG02630.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+439dupA | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229821 | |||||||
chr12:123229821 | A | ATT | 97 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0014 others(94): Show |
98 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.104+438_104+439dup others(2): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229821 | |||||||
chr12:123229821 | A | ATTT | 66 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(63): Show |
66 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.104+437_104+439dup others(3): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229821 | |||||||
chr12:123229821 | A | ATTTT | 8 | a0002c0003t0002g0214 a0002c0003t0002g0215 a0002c0003t0002g0216 others(5): Show |
8 | HG00673.hp2 HG02071.hp2 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+436_104+439dup others(4): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229821 | |||||||
chr12:123229866 | G | A | 1 | a0001c0001t0006g0117 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.104+395C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229866 | |||||||
chr12:123229911 | T | C | 2 | a0001c0002t0001g0085 a0001c0002t0001g0086 |
2 | NA18992.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.104+350A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123229911 | |||||||
chr12:123230069 | G | A | 1 | a0001c0002t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.104+192C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123230069 | |||||||
chr12:123230142 | T | C | 52 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(49): Show |
52 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.104+119A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123230142 | |||||||
chr12:123230189 | T | A | 52 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(49): Show |
52 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.104+72A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 2/23 | chr12 | 123230189 | |||||||
chr12:123230558 | A | G | 1 | a0001c0001t0003g0167 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-158-36T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123230558 | |||||||
chr12:123230566 | C | T | 172 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(169): Show |
173 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(170): Show |
intron_variant | MODIFIER | c.-158-44G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123230566 | |||||||
chr12:123230719 | T | C | 172 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(169): Show |
173 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(170): Show |
intron_variant | MODIFIER | c.-158-197A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123230719 | |||||||
chr12:123230921 | A | T | 1 | a0001c0001t0004g0166 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-158-399T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123230921 | |||||||
chr12:123230982 | C | A | 1 | a0001c0001t0006g0118 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-158-460G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123230982 | |||||||
chr12:123231145 | T | C | 1 | a0002c0003t0002g0262 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-158-623A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123231145 | |||||||
chr12:123231226 | C | A | 50 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0214 others(47): Show |
50 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.-158-704G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123231226 | |||||||
chr12:123231385 | G | C | 1 | a0002c0003t0002g0263 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-158-863C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123231385 | |||||||
chr12:123231576 | T | C | 9 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(6): Show |
9 | HG02602.hp2 HG03491.hp1 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.-158-1054A>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123231576 | |||||||
chr12:123231757 | GCTGGATA others(4): Show |
G | 5 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(2): Show |
5 | HG02258.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-158-1246_-158-123 others(15): Show |
MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123231757 | |||||||
chr12:123231769 | C | T | 5 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(2): Show |
5 | HG02258.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-158-1247G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123231769 | |||||||
chr12:123231829 | C | T | 172 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(169): Show |
173 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(170): Show |
intron_variant | MODIFIER | c.-159+1246G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123231829 | |||||||
chr12:123231919 | G | A | 52 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(49): Show |
52 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.-159+1156C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123231919 | |||||||
chr12:123231966 | C | T | 172 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0114 others(169): Show |
173 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(170): Show |
intron_variant | MODIFIER | c.-159+1109G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123231966 | |||||||
chr12:123232238 | G | C | 5 | a0001c0002t0001g0091 a0001c0005t0001g0092 a0001c0005t0001g0093 others(2): Show |
5 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.-159+837C>G | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123232238 | |||||||
chr12:123232383 | A | T | 219 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(216): Show |
220 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(217): Show |
intron_variant | MODIFIER | c.-159+692T>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123232383 | |||||||
chr12:123232593 | G | A | 1 | a0001c0002t0001g0096 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-159+482C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123232593 | |||||||
chr12:123232669 | G | A | 50 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0214 others(47): Show |
50 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.-159+406C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123232669 | |||||||
chr12:123232678 | T | A | 3 | a0001c0002t0001g0098 a0001c0002t0001g0099 a0001c0016t0001g0097 |
3 | HG01952.hp1 HG01978.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.-159+397A>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123232678 | |||||||
chr12:123232686 | G | A | 2 | a0001c0002t0001g0100 a0001c0002t0001g0101 |
2 | NA18990.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-159+389C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123232686 | |||||||
chr12:123232793 | A | G | 2 | a0001c0002t0001g0006 a0001c0004t0001g0007 |
2 | HG01175.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-159+282T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123232793 | |||||||
chr12:123232807 | C | A | 52 | a0002c0003t0001g0229 a0002c0003t0001g0231 a0002c0003t0002g0212 others(49): Show |
52 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.-159+268G>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123232807 | |||||||
chr12:123232815 | A | G | 99 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(96): Show |
100 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.-159+260T>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123232815 | |||||||
chr12:123232849 | G | A | 2 | a0001c0001t0006g0264 a0001c0001t0006g0265 |
2 | HG02602.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-159+226C>T | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123232849 | |||||||
chr12:123232897 | C | T | 2 | a0001c0004t0001g0004 a0001c0004t0001g0005 |
2 | HG00735.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-159+178G>A | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123232897 | |||||||
chr12:123232903 | C | G | 2 | a0001c0001t0006g0002 a0001c0001t0006g0003 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-159+172G>C | MPHOSPH9 | ENSG00000051825.15 | transcript | ENST00000606320.6 | protein_coding | 1/23 | chr12 | 123232903 |