Item | Value |
---|---|
geneid | 6672 |
ensemblid | ENSG00000067066.17 |
hgncid | 11206 |
symbol | SP100 |
name | SP100 nuclear antigen |
refseq_nuc | NM_001080391.2 |
refseq_prot | NP_001073860.1 |
ensembl_nuc | ENST00000340126.9 |
ensembl_prot | ENSP00000343023.4 |
mane_status | MANE Select |
chr | chr2 |
start | 230416201 |
end | 230545606 |
strand | + |
ver | v1.2 |
region | chr2:230416201-230545606 |
region5000 | chr2:230411201-230550606 |
regionname0 | SP100_chr2_230416201_230545606 |
regionname5000 | SP100_chr2_230411201_230550606 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 885 | 147 | 55 | 33 | 39 | 4 | 16 | 27 | SP100_chr2_230411201_230550606 | SP100 | MAGGG others(880): Show |
chr2 | 230411201 | 230550606 |
a0002 | 1/1 | 885 | 86 | 23 | 13 | 43 | 1 | 4 | 34 | SP100_chr2_230411201_230550606 | SP100 | MAGGG others(880): Show |
chr2 | 230411201 | 230550606 |
a0003 | 0/0 | 885 | 37 | 5 | 16 | 3 | 7 | 6 | 2 | SP100_chr2_230411201_230550606 | SP100 | MAGGG others(880): Show |
chr2 | 230411201 | 230550606 |
a0004 | 0/0 | 885 | 7 | 0 | 0 | 1 | 2 | 4 | 0 | SP100_chr2_230411201_230550606 | SP100 | MAGGG others(880): Show |
chr2 | 230411201 | 230550606 |
a0005 | 0/0 | 885 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | MAGGG others(880): Show |
chr2 | 230411201 | 230550606 |
a0006 | 0/0 | 885 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | MAGGG others(880): Show |
chr2 | 230411201 | 230550606 |
a0007 | 0/0 | 885 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | SP100_chr2_230411201_230550606 | SP100 | MAGGG others(880): Show |
chr2 | 230411201 | 230550606 |
a0008 | 0/0 | 885 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | MAGGG others(880): Show |
chr2 | 230411201 | 230550606 |
a0009 | 0/0 | 885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | MAGGG others(880): Show |
chr2 | 230411201 | 230550606 |
a0010 | 0/0 | 885 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | MAGGG others(880): Show |
chr2 | 230411201 | 230550606 |
a0011 | 0/0 | 885 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | MAGGG others(880): Show |
chr2 | 230411201 | 230550606 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2655 | 94 | 31 | 18 | 26 | 4 | 15 | SP100_chr2_230411201_230550606 | SP100 | ATGGC others(2650): Show |
chr2 | 230411201 | 230550606 | ||
a0001c0003 | 0/0 | 2655 | 44 | 19 | 11 | 13 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | ATGGC others(2650): Show |
chr2 | 230411201 | 230550606 | ||
a0001c0007 | 0/0 | 2655 | 4 | 4 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | ATGGC others(2650): Show |
chr2 | 230411201 | 230550606 | ||
a0001c0009 | 0/0 | 2655 | 3 | 0 | 3 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | ATGGC others(2650): Show |
chr2 | 230411201 | 230550606 | ||
a0001c0017 | 0/0 | 2655 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | ATGGC others(2650): Show |
chr2 | 230411201 | 230550606 | ||
a0001c0019 | 0/0 | 2655 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | ATGGC others(2650): Show |
chr2 | 230411201 | 230550606 | ||
a0002c0002 | 1/1 | 2655 | 55 | 13 | 10 | 25 | 1 | 4 | SP100_chr2_230411201_230550606 | SP100 | ATGGC others(2650): Show |
chr2 | 230411201 | 230550606 | ||
a0002c0005 | 0/0 | 2655 | 29 | 9 | 3 | 17 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | ATGGC others(2650): Show |
chr2 | 230411201 | 230550606 | ||
a0002c0020 | 0/0 | 2655 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | ATGGC others(2650): Show |
chr2 | 230411201 | 230550606 | ||
a0002c0021 | 0/0 | 2655 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | ATGGC others(2650): Show |
chr2 | 230411201 | 230550606 | ||
a0003c0004 | 0/0 | 2655 | 37 | 5 | 16 | 3 | 7 | 6 | SP100_chr2_230411201_230550606 | SP100 | ATGGC others(2650): Show |
chr2 | 230411201 | 230550606 | ||
a0004c0006 | 0/0 | 2655 | 6 | 0 | 0 | 0 | 2 | 4 | SP100_chr2_230411201_230550606 | SP100 | ATGGC others(2650): Show |
chr2 | 230411201 | 230550606 | ||
a0004c0015 | 0/0 | 2655 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | ATGGC others(2650): Show |
chr2 | 230411201 | 230550606 | ||
a0005c0008 | 0/0 | 2655 | 4 | 3 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | ATGGC others(2650): Show |
chr2 | 230411201 | 230550606 | ||
a0005c0013 | 0/0 | 2655 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | ATGGC others(2650): Show |
chr2 | 230411201 | 230550606 | ||
a0006c0014 | 0/0 | 2655 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | ATGGC others(2650): Show |
chr2 | 230411201 | 230550606 | ||
a0006c0016 | 0/0 | 2655 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | ATGGC others(2650): Show |
chr2 | 230411201 | 230550606 | ||
a0007c0010 | 0/0 | 2655 | 2 | 0 | 0 | 0 | 0 | 2 | SP100_chr2_230411201_230550606 | SP100 | ATGGC others(2650): Show |
chr2 | 230411201 | 230550606 | ||
a0008c0022 | 0/0 | 2655 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | ATGGC others(2650): Show |
chr2 | 230411201 | 230550606 | ||
a0009c0018 | 0/0 | 2655 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | ATGGC others(2650): Show |
chr2 | 230411201 | 230550606 | ||
a0010c0012 | 0/0 | 2655 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | ATGGC others(2650): Show |
chr2 | 230411201 | 230550606 | ||
a0011c0011 | 0/0 | 2655 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | ATGGC others(2650): Show |
chr2 | 230411201 | 230550606 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 5414 | 35 | 2 | 12 | 10 | 2 | 9 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0001c0001t0003 | 0/0 | 5416 | 10 | 0 | 4 | 5 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5411): Show |
chr2 | 230411201 | 230550606 |
a0001c0001t0004 | 0/0 | 5414 | 7 | 5 | 1 | 0 | 1 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0001c0001t0005 | 0/0 | 5415 | 8 | 8 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5410): Show |
chr2 | 230411201 | 230550606 |
a0001c0001t0006 | 0/0 | 5414 | 6 | 0 | 0 | 6 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0001c0001t0007 | 0/0 | 5414 | 3 | 2 | 0 | 0 | 1 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0001c0001t0008 | 0/0 | 5415 | 7 | 7 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5410): Show |
chr2 | 230411201 | 230550606 |
a0001c0001t0010 | 0/0 | 5414 | 6 | 0 | 1 | 1 | 0 | 4 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0001c0001t0014 | 0/0 | 5413 | 3 | 0 | 0 | 3 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5408): Show |
chr2 | 230411201 | 230550606 |
a0001c0001t0015 | 0/0 | 5414 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0001c0001t0017 | 0/0 | 5414 | 2 | 2 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0001c0001t0018 | 0/0 | 5414 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0001c0001t0019 | 0/0 | 5414 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0001c0001t0020 | 0/0 | 5415 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5410): Show |
chr2 | 230411201 | 230550606 |
a0001c0001t0021 | 0/0 | 5414 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0001c0001t0025 | 0/0 | 5414 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0001c0001t0026 | 0/0 | 5414 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0001c0003t0002 | 0/0 | 5414 | 7 | 1 | 6 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0001c0003t0003 | 0/0 | 5416 | 13 | 0 | 1 | 12 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5411): Show |
chr2 | 230411201 | 230550606 |
a0001c0003t0004 | 0/0 | 5414 | 3 | 3 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0001c0003t0005 | 0/0 | 5415 | 2 | 2 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5410): Show |
chr2 | 230411201 | 230550606 |
a0001c0003t0007 | 0/0 | 5414 | 6 | 2 | 4 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0001c0003t0008 | 0/0 | 5415 | 2 | 2 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5410): Show |
chr2 | 230411201 | 230550606 |
a0001c0003t0010 | 0/0 | 5414 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0001c0003t0012 | 0/0 | 5414 | 6 | 6 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0001c0003t0014 | 0/0 | 5413 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5408): Show |
chr2 | 230411201 | 230550606 |
a0001c0003t0015 | 0/0 | 5414 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0001c0003t0016 | 0/0 | 5414 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0001c0003t0018 | 0/0 | 5414 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0001c0007t0005 | 0/0 | 5415 | 3 | 3 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5410): Show |
chr2 | 230411201 | 230550606 |
a0001c0007t0016 | 0/0 | 5414 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0001c0009t0002 | 0/0 | 5414 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0001c0009t0007 | 0/0 | 5414 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0001c0009t0010 | 0/0 | 5414 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0001c0017t0002 | 0/0 | 5414 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0001c0019t0015 | 0/0 | 5414 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0002c0002t0001 | 1/1 | 5414 | 38 | 5 | 7 | 19 | 1 | 4 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0002c0002t0009 | 0/0 | 5414 | 8 | 0 | 2 | 6 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0002c0002t0011 | 0/0 | 5415 | 6 | 6 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5410): Show |
chr2 | 230411201 | 230550606 |
a0002c0002t0013 | 0/0 | 5414 | 2 | 2 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0002c0002t0023 | 0/0 | 5414 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0002c0005t0001 | 0/0 | 5414 | 21 | 6 | 2 | 13 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0002c0005t0006 | 0/0 | 5414 | 4 | 0 | 0 | 4 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0002c0005t0013 | 0/0 | 5414 | 4 | 3 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0002c0020t0022 | 0/0 | 5414 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0002c0021t0001 | 0/0 | 5414 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0003c0004t0002 | 0/0 | 5414 | 9 | 1 | 7 | 0 | 1 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0003c0004t0003 | 0/0 | 5416 | 25 | 3 | 8 | 3 | 5 | 6 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5411): Show |
chr2 | 230411201 | 230550606 |
a0003c0004t0004 | 0/0 | 5414 | 3 | 1 | 1 | 0 | 1 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0004c0006t0004 | 0/0 | 5414 | 6 | 0 | 0 | 0 | 2 | 4 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0004c0015t0004 | 0/0 | 5414 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0005c0008t0002 | 0/0 | 5414 | 2 | 2 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0005c0008t0003 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5411): Show |
chr2 | 230411201 | 230550606 |
a0005c0008t0005 | 0/0 | 5415 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5410): Show |
chr2 | 230411201 | 230550606 |
a0005c0013t0024 | 0/0 | 5414 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0006c0014t0004 | 0/0 | 5414 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0006c0016t0004 | 0/0 | 5414 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0007c0010t0001 | 0/0 | 5414 | 2 | 0 | 0 | 0 | 0 | 2 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0008c0022t0006 | 0/0 | 5414 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0009c0018t0004 | 0/0 | 5414 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0010c0012t0009 | 0/0 | 5414 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5409): Show |
chr2 | 230411201 | 230550606 |
a0011c0011t0003 | 0/0 | 5416 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | GCTTG others(5411): Show |
chr2 | 230411201 | 230550606 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0004g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0005g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0006g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0006g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0006g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0006g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0006g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0007g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0007g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0007g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0008g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0008g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0008g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0008g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0010g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0010g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0010g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0010g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0010g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0010g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0014g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0014g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0014g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0015g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0017g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0017g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0018g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0019g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0020g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0021g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0025g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0001t0026g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0007g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0007g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0007g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0007g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0007g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0007g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0008g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0010g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0012g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0012g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0012g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0012g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0012g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0012g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0014g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0015g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0016g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0003t0018g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0007t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0007t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0007t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0007t0016g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0009t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0009t0007g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0009t0010g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0017t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0001c0019t0015g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0192 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0211 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0009g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0009g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0009g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0009g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0009g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0009g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0009g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0011g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0011g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0011g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0011g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0011g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0011g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0013g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0013g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0002t0023g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0006g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0006g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0006g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0006g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0013g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0013g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0013g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0005t0013g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0020t0022g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0002c0021t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0003g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0004g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0003c0004t0004g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0004c0006t0004g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0004c0006t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0004c0006t0004g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0004c0006t0004g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0004c0006t0004g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0004c0006t0004g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0004c0015t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0005c0008t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0005c0008t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0005c0008t0003g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0005c0008t0005g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0005c0013t0024g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0006c0014t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0006c0016t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0007c0010t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0007c0010t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0008c0022t0006g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0009c0018t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0010c0012t0009g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
a0011c0011t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0004 | t0003 | g0241 | EUR | GBR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG00099 | hp2 | a0001 | c0001 | t0004 | g0098 | EUR | GBR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG00140 | hp1 | a0004 | c0006 | t0004 | g0238 | EUR | GBR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG00140 | hp2 | a0003 | c0004 | t0002 | g0152 | EUR | GBR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0284 | EUR | FIN | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG00280 | hp2 | a0003 | c0004 | t0003 | g0264 | EUR | FIN | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0107 | EUR | FIN | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG00323 | hp2 | a0003 | c0004 | t0003 | g0208 | EUR | FIN | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | CHS | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG00408 | hp2 | a0001 | c0003 | t0003 | g0110 | EAS | CHS | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG00544 | hp1 | a0002 | c0005 | t0001 | g0084 | EAS | CHS | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG00544 | hp2 | a0001 | c0003 | t0003 | g0227 | EAS | CHS | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG00558 | hp1 | a0002 | c0005 | t0001 | g0155 | EAS | CHS | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG00558 | hp2 | a0002 | c0002 | t0009 | g0215 | EAS | CHS | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG00673 | hp1 | a0001 | c0001 | t0006 | g0230 | EAS | CHS | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | CHS | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0209 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG00733 | hp2 | a0001 | c0003 | t0003 | g0273 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0193 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG00735 | hp2 | a0003 | c0004 | t0003 | g0137 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG00738 | hp2 | a0001 | c0009 | t0007 | g0272 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01070 | hp1 | a0003 | c0004 | t0003 | g0262 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01070 | hp2 | a0003 | c0004 | t0002 | g0134 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0267 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01071 | hp2 | a0003 | c0004 | t0003 | g0263 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01074 | hp2 | a0001 | c0003 | t0002 | g0275 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01081 | hp1 | a0001 | c0017 | t0002 | g0018 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01081 | hp2 | a0001 | c0003 | t0002 | g0109 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0017 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0210 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01106 | hp1 | a0002 | c0005 | t0013 | g0106 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01109 | hp1 | a0005 | c0008 | t0005 | g0004 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01109 | hp2 | a0001 | c0003 | t0002 | g0276 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01167 | hp1 | a0002 | c0002 | t0009 | g0001 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01167 | hp2 | a0001 | c0009 | t0002 | g0082 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01168 | hp1 | a0003 | c0004 | t0002 | g0117 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01168 | hp2 | a0003 | c0004 | t0003 | g0133 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01169 | hp1 | a0003 | c0004 | t0003 | g0116 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01169 | hp2 | a0002 | c0002 | t0009 | g0001 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0191 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01192 | hp2 | a0001 | c0003 | t0002 | g0281 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01243 | hp1 | a0003 | c0004 | t0004 | g0104 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01255 | hp1 | a0003 | c0004 | t0002 | g0151 | AMR | CLM | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01255 | hp2 | a0001 | c0009 | t0010 | g0064 | AMR | CLM | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01256 | hp1 | a0003 | c0004 | t0003 | g0222 | AMR | CLM | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01256 | hp2 | a0001 | c0003 | t0007 | g0250 | AMR | CLM | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0231 | AMR | CLM | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01258 | hp1 | a0001 | c0003 | t0007 | g0251 | AMR | CLM | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01261 | hp1 | a0001 | c0003 | t0002 | g0013 | AMR | CLM | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01261 | hp2 | a0006 | c0016 | t0004 | g0280 | AMR | CLM | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01346 | hp1 | a0001 | c0001 | t0010 | g0260 | AMR | CLM | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01346 | hp2 | a0003 | c0004 | t0002 | g0113 | AMR | CLM | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01358 | hp1 | a0003 | c0004 | t0003 | g0142 | AMR | CLM | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01358 | hp2 | a0003 | c0004 | t0002 | g0163 | AMR | CLM | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0274 | AMR | CLM | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01361 | hp2 | a0002 | c0002 | t0023 | g0219 | AMR | CLM | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0268 | AMR | CLM | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01433 | hp2 | a0001 | c0003 | t0002 | g0108 | AMR | CLM | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01496 | hp1 | a0003 | c0004 | t0002 | g0259 | AMR | CLM | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01496 | hp2 | a0003 | c0004 | t0003 | g0081 | AMR | CLM | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01516 | hp1 | a0003 | c0004 | t0003 | g0112 | EUR | IBS | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01516 | hp2 | a0004 | c0006 | t0004 | g0153 | EUR | IBS | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01884 | hp1 | a0001 | c0001 | t0008 | g0132 | AFR | ACB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0270 | AFR | ACB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01891 | hp1 | a0003 | c0004 | t0003 | g0162 | AFR | ACB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01891 | hp2 | a0002 | c0020 | t0022 | g0036 | AFR | ACB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01943 | hp1 | a0001 | c0003 | t0007 | g0055 | AMR | PEL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01943 | hp2 | a0002 | c0005 | t0001 | g0201 | AMR | PEL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01978 | hp1 | a0003 | c0004 | t0002 | g0265 | AMR | PEL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01978 | hp2 | a0001 | c0003 | t0007 | g0136 | AMR | PEL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0074 | AMR | PEL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01993 | hp1 | a0002 | c0005 | t0001 | g0076 | AMR | PEL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0232 | AMR | PEL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02040 | hp1 | a0008 | c0022 | t0006 | g0014 | EAS | KHV | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0225 | EAS | KHV | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02055 | hp1 | a0001 | c0003 | t0004 | g0249 | AFR | ACB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0118 | AFR | ACB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02071 | hp1 | a0001 | c0001 | t0006 | g0240 | EAS | KHV | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0218 | EAS | KHV | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0166 | EAS | KHV | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02074 | hp2 | a0003 | c0004 | t0003 | g0239 | EAS | KHV | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | KHV | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02129 | hp2 | a0004 | c0015 | t0004 | g0154 | EAS | KHV | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02132 | hp1 | a0001 | c0003 | t0003 | g0202 | EAS | KHV | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02132 | hp2 | a0002 | c0002 | t0009 | g0207 | EAS | KHV | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02145 | hp1 | a0002 | c0005 | t0013 | g0128 | AFR | ACB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02145 | hp2 | a0001 | c0001 | t0005 | g0124 | AFR | ACB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0285 | AMR | PEL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0077 | AMR | PEL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02155 | hp1 | a0002 | c0005 | t0001 | g0080 | EAS | CDX | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | CDX | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02257 | hp1 | a0001 | c0001 | t0017 | g0178 | AFR | ACB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02257 | hp2 | a0002 | c0005 | t0001 | g0256 | AFR | ACB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02258 | hp1 | a0001 | c0003 | t0012 | g0046 | AFR | ACB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02258 | hp2 | a0003 | c0004 | t0003 | g0016 | AFR | ACB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02280 | hp1 | a0001 | c0001 | t0025 | g0060 | AFR | ACB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02280 | hp2 | a0001 | c0003 | t0004 | g0125 | AFR | ACB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0085 | AMR | PEL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0244 | AMR | PEL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0190 | AFR | ACB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0176 | AFR | ACB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | KHV | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02523 | hp2 | a0001 | c0003 | t0003 | g0063 | EAS | KHV | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02572 | hp1 | a0001 | c0001 | t0008 | g0054 | AFR | GWD | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02572 | hp2 | a0001 | c0019 | t0015 | g0035 | AFR | GWD | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0105 | SAS | PJL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0283 | SAS | PJL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02615 | hp1 | a0001 | c0003 | t0015 | g0170 | AFR | GWD | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02615 | hp2 | a0001 | c0003 | t0012 | g0048 | AFR | GWD | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02622 | hp1 | a0001 | c0003 | t0007 | g0115 | AFR | GWD | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02622 | hp2 | a0002 | c0002 | t0011 | g0159 | AFR | GWD | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0097 | AFR | GWD | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02630 | hp2 | a0001 | c0007 | t0005 | g0030 | AFR | GWD | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02647 | hp1 | a0002 | c0002 | t0011 | g0119 | AFR | GWD | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02647 | hp2 | a0001 | c0001 | t0005 | g0091 | AFR | GWD | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0203 | SAS | PJL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02683 | hp2 | a0007 | c0010 | t0001 | g0168 | SAS | PJL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02698 | hp1 | a0001 | c0003 | t0010 | g0020 | SAS | PJL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0217 | SAS | PJL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02723 | hp1 | a0001 | c0007 | t0005 | g0033 | AFR | GWD | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | GWD | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02735 | hp1 | a0003 | c0004 | t0003 | g0255 | SAS | PJL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02735 | hp2 | a0001 | c0001 | t0010 | g0120 | SAS | PJL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0095 | AFR | GWD | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02809 | hp2 | a0001 | c0003 | t0008 | g0002 | AFR | GWD | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02818 | hp2 | a0002 | c0002 | t0011 | g0145 | AFR | GWD | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02886 | hp1 | a0002 | c0002 | t0011 | g0157 | AFR | GWD | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02886 | hp2 | a0003 | c0004 | t0004 | g0051 | AFR | GWD | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02896 | hp1 | a0001 | c0001 | t0008 | g0172 | AFR | GWD | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02896 | hp2 | a0005 | c0008 | t0002 | g0123 | AFR | GWD | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02897 | hp1 | a0005 | c0008 | t0002 | g0122 | AFR | GWD | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02897 | hp2 | a0001 | c0003 | t0005 | g0092 | AFR | GWD | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02922 | hp1 | a0009 | c0018 | t0004 | g0043 | AFR | ESN | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02922 | hp2 | a0002 | c0002 | t0013 | g0059 | AFR | ESN | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02965 | hp1 | a0001 | c0003 | t0012 | g0247 | AFR | ESN | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0044 | AFR | ESN | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0127 | AFR | ESN | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02970 | hp2 | a0001 | c0001 | t0017 | g0177 | AFR | ESN | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03017 | hp1 | a0001 | c0001 | t0010 | g0130 | SAS | PJL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03017 | hp2 | a0001 | c0001 | t0010 | g0245 | SAS | PJL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03041 | hp1 | a0002 | c0005 | t0001 | g0129 | AFR | GWD | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03041 | hp2 | a0001 | c0001 | t0008 | g0040 | AFR | GWD | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03098 | hp1 | a0001 | c0007 | t0005 | g0032 | AFR | MSL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03098 | hp2 | a0005 | c0013 | t0024 | g0161 | AFR | MSL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03130 | hp1 | a0001 | c0001 | t0020 | g0286 | AFR | ESN | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03130 | hp2 | a0001 | c0001 | t0007 | g0258 | AFR | ESN | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03139 | hp1 | a0001 | c0003 | t0004 | g0099 | AFR | ESN | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03139 | hp2 | a0001 | c0001 | t0019 | g0126 | AFR | ESN | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03195 | hp1 | a0002 | c0002 | t0011 | g0160 | AFR | ESN | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03195 | hp2 | a0001 | c0003 | t0012 | g0042 | AFR | ESN | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0093 | AFR | MSL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0034 | AFR | MSL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03225 | hp1 | a0002 | c0005 | t0001 | g0052 | AFR | MSL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03225 | hp2 | a0001 | c0003 | t0016 | g0138 | AFR | MSL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03239 | hp1 | a0003 | c0004 | t0003 | g0114 | SAS | PJL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0131 | SAS | PJL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0096 | AFR | MSL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03486 | hp2 | a0002 | c0005 | t0001 | g0179 | AFR | MSL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03491 | hp2 | a0004 | c0006 | t0004 | g0182 | SAS | PJL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03540 | hp1 | a0001 | c0001 | t0007 | g0173 | AFR | GWD | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03540 | hp2 | a0001 | c0003 | t0002 | g0100 | AFR | GWD | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03579 | hp1 | a0001 | c0001 | t0008 | g0039 | AFR | MSL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03579 | hp2 | a0001 | c0001 | t0015 | g0089 | AFR | MSL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03654 | hp1 | a0004 | c0006 | t0004 | g0277 | SAS | PJL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03654 | hp2 | a0001 | c0001 | t0026 | g0021 | SAS | PJL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03669 | hp1 | a0007 | c0010 | t0001 | g0121 | SAS | PJL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03669 | hp2 | a0003 | c0004 | t0003 | g0146 | SAS | PJL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0253 | SAS | BEB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0204 | SAS | BEB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0278 | SAS | BEB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03927 | hp2 | a0004 | c0006 | t0004 | g0180 | SAS | BEB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03942 | hp1 | a0004 | c0006 | t0004 | g0282 | SAS | BEB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0174 | SAS | BEB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0167 | SAS | STU | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG04115 | hp2 | a0003 | c0004 | t0003 | g0271 | SAS | STU | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0056 | SAS | BEB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0015 | SAS | BEB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0171 | SAS | STU | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG04199 | hp2 | a0003 | c0004 | t0003 | g0189 | SAS | STU | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG04228 | hp1 | a0001 | c0001 | t0010 | g0169 | SAS | STU | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG04228 | hp2 | a0003 | c0004 | t0003 | g0103 | SAS | STU | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18522 | hp1 | a0003 | c0004 | t0002 | g0269 | AFR | YRI | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0252 | AFR | YRI | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | CHB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18612 | hp2 | a0001 | c0003 | t0003 | g0197 | EAS | CHB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | YRI | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18906 | hp2 | a0001 | c0003 | t0005 | g0047 | AFR | YRI | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18939 | hp1 | a0001 | c0001 | t0014 | g0206 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18939 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18948 | hp1 | a0001 | c0001 | t0014 | g0149 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18948 | hp2 | a0002 | c0005 | t0001 | g0224 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18950 | hp2 | a0002 | c0021 | t0001 | g0101 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18954 | hp1 | a0002 | c0005 | t0001 | g0083 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18957 | hp1 | a0001 | c0003 | t0003 | g0022 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18957 | hp2 | a0001 | c0001 | t0010 | g0187 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18969 | hp2 | a0001 | c0001 | t0006 | g0237 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18970 | hp1 | a0002 | c0005 | t0001 | g0164 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18970 | hp2 | a0010 | c0012 | t0009 | g0087 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18973 | hp1 | a0002 | c0002 | t0009 | g0213 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18973 | hp2 | a0003 | c0004 | t0003 | g0061 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18974 | hp1 | a0001 | c0003 | t0003 | g0188 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18975 | hp1 | a0002 | c0005 | t0006 | g0198 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18975 | hp2 | a0001 | c0003 | t0003 | g0288 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18977 | hp1 | a0002 | c0002 | t0009 | g0246 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18977 | hp2 | a0006 | c0014 | t0004 | g0205 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18978 | hp1 | a0002 | c0005 | t0001 | g0010 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18978 | hp2 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0243 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18984 | hp1 | a0001 | c0001 | t0006 | g0135 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18989 | hp1 | a0002 | c0005 | t0006 | g0023 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18994 | hp1 | a0002 | c0005 | t0001 | g0011 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA18994 | hp2 | a0002 | c0002 | t0009 | g0214 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19002 | hp1 | a0001 | c0001 | t0018 | g0066 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19002 | hp2 | a0011 | c0011 | t0003 | g0086 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19003 | hp1 | a0002 | c0005 | t0006 | g0012 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19003 | hp2 | a0001 | c0003 | t0003 | g0183 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19005 | hp1 | a0002 | c0005 | t0001 | g0069 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19009 | hp1 | a0003 | c0004 | t0003 | g0165 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0242 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19010 | hp1 | a0001 | c0003 | t0003 | g0212 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19010 | hp2 | a0002 | c0005 | t0001 | g0068 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0102 | AFR | LWK | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19030 | hp2 | a0001 | c0007 | t0016 | g0031 | AFR | LWK | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19043 | hp1 | a0001 | c0003 | t0012 | g0045 | AFR | LWK | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19043 | hp2 | a0002 | c0005 | t0001 | g0058 | AFR | LWK | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19054 | hp1 | a0002 | c0005 | t0006 | g0024 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19055 | hp1 | a0001 | c0003 | t0014 | g0221 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19062 | hp2 | a0001 | c0001 | t0014 | g0229 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19067 | hp1 | a0002 | c0005 | t0001 | g0186 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19067 | hp2 | a0001 | c0003 | t0003 | g0185 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19080 | hp1 | a0001 | c0003 | t0003 | g0139 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19081 | hp1 | a0001 | c0001 | t0006 | g0223 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19082 | hp1 | a0002 | c0002 | t0009 | g0226 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19082 | hp2 | a0002 | c0005 | t0001 | g0075 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19087 | hp1 | a0001 | c0001 | t0006 | g0156 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19090 | hp2 | a0002 | c0005 | t0001 | g0141 | EAS | JPT | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19240 | hp1 | a0001 | c0001 | t0008 | g0053 | AFR | YRI | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA19240 | hp2 | a0002 | c0002 | t0011 | g0158 | AFR | YRI | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA20129 | hp1 | a0002 | c0005 | t0013 | g0287 | AFR | ASW | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA20129 | hp2 | a0005 | c0008 | t0003 | g0003 | AFR | ASW | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA20752 | hp1 | a0003 | c0004 | t0004 | g0248 | EUR | TSI | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA20752 | hp2 | a0003 | c0004 | t0003 | g0261 | EUR | TSI | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0279 | EUR | TSI | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA20805 | hp2 | a0001 | c0001 | t0007 | g0079 | EUR | TSI | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0070 | AMR | CLM | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0266 | AMR | CLM | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02109 | hp1 | a0001 | c0003 | t0018 | g0181 | AFR | ACB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02109 | hp2 | a0002 | c0005 | t0001 | g0057 | AFR | ACB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02486 | hp1 | a0002 | c0002 | t0013 | g0038 | AFR | ACB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02486 | hp2 | a0001 | c0001 | t0021 | g0090 | AFR | ACB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02559 | hp1 | a0001 | c0003 | t0007 | g0111 | AFR | ACB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG02559 | hp2 | a0001 | c0003 | t0008 | g0002 | AFR | ACB | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0050 | AFR | MSL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG03471 | hp2 | a0001 | c0001 | t0008 | g0041 | AFR | MSL | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG06807 | hp1 | a0002 | c0005 | t0013 | g0037 | AFR | USA | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
HG06807 | hp2 | a0003 | c0004 | t0003 | g0062 | AFR | USA | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA21309 | hp1 | a0001 | c0003 | t0012 | g0257 | AFR | LWK | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
NA21309 | hp2 | a0001 | c0001 | t0005 | g0088 | AFR | LWK | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0192 | REF | REF | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0211 | REF | REF | SP100_chr2_230411201_230550606 | SP100 | chr2 | 230411201 | 230550606 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:230416312 | G | A | 2 | a0010 a0011 |
2 | NA18970.hp2 NA19002.hp2 |
missense_variant | MODERATE | c.16G>A | p.Gly6Ser | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 1/29 | 112/5414 | 16/2658 | 6/885 | chr2 | 230416312 | |||
chr2:230443002 | A | G | 1 | a0008 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.173A>G | p.Lys58Arg | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 3/29 | 269/5414 | 173/2658 | 58/885 | chr2 | 230443002 | |||
chr2:230461284 | C | G | 1 | a0009 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.843C>G | p.Asn281Lys | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 9/29 | 939/5414 | 843/2658 | 281/885 | chr2 | 230461284 | |||
chr2:230461366 | T | C | 2 | a0005 a0007 |
7 | HG01109.hp1 HG02683.hp2 HG02896.hp2 others(4): Show |
missense_variant | MODERATE | c.925T>C | p.Cys309Arg | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 9/29 | 1021/5414 | 925/2658 | 309/885 | chr2 | 230461366 | |||
chr2:230469048 | A | G | 2 | a0003 a0004 |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
missense_variant | MODERATE | c.1297A>G | p.Met433Val | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 14/29 | 1393/5414 | 1297/2658 | 433/885 | chr2 | 230469048 | |||
chr2:230541355 | G | A | 2 | a0004 a0006 |
9 | HG00140.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
missense_variant | MODERATE | c.2386G>A | p.Ala796Thr | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 27/29 | 2482/5414 | 2386/2658 | 796/885 | chr2 | 230541355 | |||
chr2:230541965 | T | C | 8 | a0001 a0003 a0004 others(5): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
missense_variant | MODERATE | c.2477T>C | p.Met826Thr | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 28/29 | 2573/5414 | 2477/2658 | 826/885 | chr2 | 230541965 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:230443048 | A | G | 1 | a0002c0021 | 1 | NA18950.hp2 | synonymous_variant | LOW | c.219A>G | p.Pro73Pro | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 3/29 | 315/5414 | 219/2658 | 73/885 | chr2 | 230443048 | |||
chr2:230443054 | C | T | 2 | a0001c0019 a0002c0020 |
2 | HG01891.hp2 HG02572.hp2 |
synonymous_variant | LOW | c.225C>T | p.Leu75Leu | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 3/29 | 321/5414 | 225/2658 | 75/885 | chr2 | 230443054 | |||
chr2:230449658 | G | A | 1 | a0001c0007 | 4 | HG02630.hp2 HG02723.hp1 HG03098.hp1 others(1): Show |
synonymous_variant | LOW | c.684G>A | p.Ser228Ser | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 7/29 | 780/5414 | 684/2658 | 228/885 | chr2 | 230449658 | |||
chr2:230462469 | C | T | 1 | a0001c0017 | 1 | HG01081.hp1 | synonymous_variant | LOW | c.1008C>T | p.Asp336Asp | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/29 | 1104/5414 | 1008/2658 | 336/885 | chr2 | 230462469 | |||
chr2:230462505 | G | A | 1 | a0001c0009 | 3 | HG00738.hp2 HG01167.hp2 HG01255.hp2 |
synonymous_variant | LOW | c.1044G>A | p.Pro348Pro | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/29 | 1140/5414 | 1044/2658 | 348/885 | chr2 | 230462505 | |||
chr2:230467181 | G | A | 12 | a0001c0001 a0001c0007 a0001c0009 others(9): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
synonymous_variant | LOW | c.1257G>A | p.Ser419Ser | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/29 | 1353/5414 | 1257/2658 | 419/885 | chr2 | 230467181 | |||
chr2:230467184 | C | T | 1 | a0004c0015 | 1 | HG02129.hp2 | synonymous_variant | LOW | c.1260C>T | p.Ser420Ser | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/29 | 1356/5414 | 1260/2658 | 420/885 | chr2 | 230467184 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:230542948 | C | T | 21 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0010 others(18): Show |
86 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*2C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 2 | chr2 | 230542948 | ||||||
chr2:230542989 | C | T | 1 | a0001c0001t0025 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*43C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 43 | chr2 | 230542989 | ||||||
chr2:230543041 | C | T | 1 | a0005c0013t0024 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*95C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 95 | chr2 | 230543041 | ||||||
chr2:230543082 | G | A | 1 | a0001c0001t0019 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*136G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 136 | chr2 | 230543082 | ||||||
chr2:230543133 | A | G | 2 | a0002c0002t0013 a0002c0005t0013 |
6 | HG01106.hp1 HG02145.hp1 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*187A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 187 | chr2 | 230543133 | ||||||
chr2:230543148 | G | GA | 51 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(48): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*203dupA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 204 | INFO_REALIGN_3_PRIME | chr2 | 230543148 | |||||
chr2:230543332 | A | C | 2 | a0001c0003t0016 a0001c0007t0016 |
2 | HG03225.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*386A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 386 | chr2 | 230543332 | ||||||
chr2:230543380 | C | G | 50 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(47): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*434C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 434 | chr2 | 230543380 | ||||||
chr2:230543422 | C | G | 2 | a0001c0003t0016 a0001c0007t0016 |
2 | HG03225.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*476C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 476 | chr2 | 230543422 | ||||||
chr2:230543463 | C | T | 1 | a0002c0020t0022 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*517C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 517 | chr2 | 230543463 | ||||||
chr2:230543472 | A | C | 1 | a0002c0020t0022 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*526A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 526 | chr2 | 230543472 | ||||||
chr2:230543566 | T | A | 52 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(49): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*620T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 620 | chr2 | 230543566 | ||||||
chr2:230543632 | C | T | 37 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(34): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*686C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 686 | chr2 | 230543632 | ||||||
chr2:230543962 | C | G | 3 | a0001c0001t0015 a0001c0003t0015 a0001c0019t0015 |
3 | HG02572.hp2 HG02615.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1016C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 1016 | chr2 | 230543962 | ||||||
chr2:230543994 | C | T | 1 | a0001c0001t0026 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1048C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 1048 | chr2 | 230543994 | ||||||
chr2:230544026 | T | C | 1 | a0001c0001t0020 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1080T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 1080 | chr2 | 230544026 | ||||||
chr2:230544054 | A | G | 1 | a0002c0002t0011 | 6 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1108A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 1108 | chr2 | 230544054 | ||||||
chr2:230544205 | G | C | 3 | a0002c0002t0009 a0002c0002t0023 a0010c0012t0009 |
10 | HG00558.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1259G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 1259 | chr2 | 230544205 | ||||||
chr2:230544233 | C | A | 49 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(46): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
3_prime_UTR_variant | MODIFIER | c.*1287C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 1287 | chr2 | 230544233 | ||||||
chr2:230544399 | G | C | 49 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(46): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
3_prime_UTR_variant | MODIFIER | c.*1453G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 1453 | chr2 | 230544399 | ||||||
chr2:230544455 | T | C | 52 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(49): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*1509T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 1509 | chr2 | 230544455 | ||||||
chr2:230544493 | C | CT | 5 | a0001c0001t0003 a0001c0003t0003 a0003c0004t0003 others(2): Show |
50 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1558dupT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 1559 | INFO_REALIGN_3_PRIME | chr2 | 230544493 | |||||
chr2:230544493 | CT | C | 38 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(35): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*1558delT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 1558 | INFO_REALIGN_3_PRIME | chr2 | 230544493 | |||||
chr2:230544533 | G | A | 1 | a0001c0001t0017 | 2 | HG02257.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1587G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 1587 | chr2 | 230544533 | ||||||
chr2:230544549 | G | A | 5 | a0001c0001t0006 a0001c0001t0018 a0001c0003t0018 others(2): Show |
13 | HG00673.hp1 HG02040.hp1 HG02071.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1603G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 1603 | chr2 | 230544549 | ||||||
chr2:230544656 | A | G | 1 | a0001c0001t0021 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1710A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 1710 | chr2 | 230544656 | ||||||
chr2:230544686 | G | C | 1 | a0002c0002t0011 | 6 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1740G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 1740 | chr2 | 230544686 | ||||||
chr2:230544709 | G | A | 5 | a0001c0001t0007 a0001c0001t0018 a0001c0003t0007 others(2): Show |
12 | HG00738.hp2 HG01256.hp2 HG01258.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1763G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 1763 | chr2 | 230544709 | ||||||
chr2:230544894 | C | T | 1 | a0002c0020t0022 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1948C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 1948 | chr2 | 230544894 | ||||||
chr2:230545036 | G | A | 5 | a0001c0001t0003 a0001c0003t0003 a0003c0004t0003 others(2): Show |
50 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*2090G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 2090 | chr2 | 230545036 | ||||||
chr2:230545045 | G | A | 27 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(24): Show |
74 | HG00099.hp2 HG00140.hp1 HG00673.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*2099G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 2099 | chr2 | 230545045 | ||||||
chr2:230545135 | A | G | 1 | a0001c0001t0021 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2189A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 2189 | chr2 | 230545135 | ||||||
chr2:230545139 | C | T | 18 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0014 others(15): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*2193C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 2193 | chr2 | 230545139 | ||||||
chr2:230545347 | AG | A | 2 | a0001c0001t0014 a0001c0003t0014 |
4 | NA18939.hp1 NA18948.hp1 NA19055.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2403delG | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 2403 | INFO_REALIGN_3_PRIME | chr2 | 230545347 | |||||
chr2:230545348 | G | T | 3 | a0001c0001t0005 a0001c0003t0005 a0002c0002t0011 |
16 | HG02145.hp2 HG02622.hp2 HG02630.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2402G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 2402 | chr2 | 230545348 | ||||||
chr2:230545434 | G | A | 30 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(27): Show |
147 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*2488G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 2488 | chr2 | 230545434 | ||||||
chr2:230545470 | T | G | 1 | a0002c0002t0023 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2524T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 2524 | chr2 | 230545470 | ||||||
chr2:230545499 | C | T | 3 | a0001c0001t0015 a0001c0003t0015 a0001c0019t0015 |
3 | HG02572.hp2 HG02615.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2553C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 29/29 | 2553 | chr2 | 230545499 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:230416467 | T | A | 2 | a0005c0008t0003g0003 a0005c0008t0005g0004 |
2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.32+139T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 1/28 | chr2 | 230416467 | |||||||
chr2:230416495 | T | G | 2 | a0005c0008t0003g0003 a0005c0008t0005g0004 |
2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.32+167T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 1/28 | chr2 | 230416495 | |||||||
chr2:230416571 | T | C | 29 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(26): Show |
29 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.32+243T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 1/28 | chr2 | 230416571 | |||||||
chr2:230416651 | C | T | 1 | a0001c0003t0003g0288 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.32+323C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 1/28 | chr2 | 230416651 | |||||||
chr2:230416980 | C | G | 2 | a0001c0001t0020g0286 a0002c0005t0013g0287 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.33-611C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 1/28 | chr2 | 230416980 | |||||||
chr2:230416986 | G | C | 66 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0071 others(63): Show |
66 | HG00408.hp1 HG00544.hp1 HG01123.hp1 others(63): Show |
intron_variant | MODIFIER | c.33-605G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 1/28 | chr2 | 230416986 | |||||||
chr2:230417227 | A | G | 11 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0283 others(8): Show |
11 | HG00280.hp1 HG01074.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.33-364A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 1/28 | chr2 | 230417227 | |||||||
chr2:230417236 | A | T | 103 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0071 others(100): Show |
104 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.33-355A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 1/28 | chr2 | 230417236 | |||||||
chr2:230417519 | A | G | 6 | a0001c0001t0020g0286 a0001c0007t0005g0030 a0001c0007t0005g0032 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-72A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 1/28 | chr2 | 230417519 | |||||||
chr2:230417804 | G | A | 2 | a0001c0001t0002g0254 a0002c0002t0001g0005 |
2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.107+139G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230417804 | |||||||
chr2:230417819 | C | CT | 99 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0071 others(96): Show |
99 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.107+161dupT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230417819 | ||||||
chr2:230417990 | G | A | 2 | a0001c0019t0015g0035 a0002c0020t0022g0036 |
2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.107+325G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230417990 | |||||||
chr2:230418007 | CT | C | 87 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0071 others(84): Show |
87 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.107+343delT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230418007 | |||||||
chr2:230418076 | C | T | 40 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0071 others(37): Show |
40 | HG00408.hp1 HG00544.hp1 HG01123.hp1 others(37): Show |
intron_variant | MODIFIER | c.107+411C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230418076 | |||||||
chr2:230418109 | A | T | 1 | a0002c0002t0001g0253 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.107+444A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230418109 | |||||||
chr2:230418266 | G | A | 4 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(1): Show |
4 | HG00738.hp1 HG01074.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.107+601G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230418266 | |||||||
chr2:230418284 | T | C | 1 | a0002c0002t0001g0005 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.107+619T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230418284 | |||||||
chr2:230418410 | C | A | 4 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(1): Show |
4 | HG02630.hp2 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+745C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230418410 | |||||||
chr2:230418495 | G | A | 1 | a0001c0001t0004g0098 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.107+830G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230418495 | |||||||
chr2:230418586 | A | T | 2 | a0001c0003t0008g0002 a0002c0005t0001g0256 |
3 | HG02257.hp2 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.107+921A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230418586 | |||||||
chr2:230418590 | T | C | 3 | a0002c0005t0001g0010 a0002c0005t0001g0011 a0002c0005t0006g0012 |
3 | NA18978.hp1 NA18994.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.107+925T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230418590 | |||||||
chr2:230418595 | CT | C | 27 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(24): Show |
27 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.107+941delT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230418595 | ||||||
chr2:230418709 | G | C | 5 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(2): Show |
5 | HG02486.hp1 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+1044G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230418709 | |||||||
chr2:230418950 | A | T | 2 | a0001c0001t0020g0286 a0002c0005t0013g0287 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.107+1285A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230418950 | |||||||
chr2:230418991 | G | A | 6 | a0001c0003t0012g0042 a0001c0003t0012g0045 a0001c0003t0012g0046 others(3): Show |
6 | HG02258.hp1 HG02922.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.107+1326G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230418991 | |||||||
chr2:230418996 | T | C | 126 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0071 others(123): Show |
127 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.107+1331T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230418996 | |||||||
chr2:230419212 | C | A | 7 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(4): Show |
7 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.107+1547C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230419212 | |||||||
chr2:230419233 | C | T | 1 | a0001c0001t0002g0254 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.107+1568C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230419233 | |||||||
chr2:230419841 | T | C | 26 | a0001c0001t0002g0254 a0001c0001t0002g0266 a0001c0001t0002g0267 others(23): Show |
26 | HG00280.hp2 HG00733.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.107+2176T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230419841 | |||||||
chr2:230419868 | G | A | 2 | a0001c0019t0015g0035 a0002c0020t0022g0036 |
2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.107+2203G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230419868 | |||||||
chr2:230420735 | C | CAT | 15 | a0001c0001t0002g0027 a0001c0001t0002g0254 a0001c0001t0002g0266 others(12): Show |
15 | HG00280.hp2 HG00733.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.107+3084_107+3085d others(4): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230420735 | ||||||
chr2:230420855 | A | C | 35 | a0001c0001t0002g0254 a0001c0001t0002g0266 a0001c0001t0002g0267 others(32): Show |
35 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.107+3190A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230420855 | |||||||
chr2:230421064 | ATGT | A | 36 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0071 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.107+3404_107+3406d others(5): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230421064 | ||||||
chr2:230421091 | A | G | 123 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0071 others(120): Show |
124 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.107+3426A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230421091 | |||||||
chr2:230421229 | A | G | 2 | a0001c0003t0002g0100 a0002c0002t0001g0034 |
2 | HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.107+3564A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230421229 | |||||||
chr2:230421324 | C | T | 1 | a0002c0002t0001g0253 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.107+3659C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230421324 | |||||||
chr2:230421504 | C | CAT | 74 | a0001c0001t0002g0105 a0001c0001t0002g0254 a0001c0001t0002g0266 others(71): Show |
74 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.107+3856_107+3857d others(4): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230421504 | ||||||
chr2:230421504 | C | CATAT | 31 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(28): Show |
32 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.107+3854_107+3857d others(6): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230421504 | ||||||
chr2:230421504 | C | CATATAT | 4 | a0001c0001t0007g0258 a0001c0003t0002g0100 a0010c0012t0009g0087 others(1): Show |
4 | HG03130.hp2 HG03540.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.107+3852_107+3857d others(8): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230421504 | ||||||
chr2:230421504 | C | CATATATA others(1): Show |
34 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0071 others(31): Show |
34 | HG00408.hp1 HG00544.hp1 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.107+3850_107+3857d others(10): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230421504 | ||||||
chr2:230421504 | C | CATATATA others(3): Show |
1 | a0001c0001t0003g0056 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.107+3848_107+3857d others(12): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230421504 | ||||||
chr2:230421504 | C | CATATATA others(5): Show |
1 | a0001c0003t0007g0055 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.107+3846_107+3857d others(14): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230421504 | ||||||
chr2:230421504 | C | CATATATA others(13): Show |
1 | a0001c0003t0005g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.107+3857_107+3858i others(22): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230421504 | ||||||
chr2:230421516 | T | TAC | 8 | a0001c0001t0020g0286 a0001c0007t0005g0030 a0001c0007t0005g0032 others(5): Show |
8 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.107+3852_107+3853i others(4): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230421516 | ||||||
chr2:230421553 | CTA | C | 167 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(164): Show |
168 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.107+3905_107+3906d others(4): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230421553 | ||||||
chr2:230421788 | C | A | 70 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(67): Show |
70 | HG00408.hp1 HG00544.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.107+4123C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230421788 | |||||||
chr2:230421842 | T | G | 25 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(22): Show |
25 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.107+4177T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230421842 | |||||||
chr2:230421960 | C | A | 1 | a0001c0003t0003g0288 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.107+4295C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230421960 | |||||||
chr2:230422115 | C | A | 220 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(217): Show |
221 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.107+4450C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230422115 | |||||||
chr2:230422223 | T | G | 38 | a0001c0001t0002g0254 a0001c0001t0002g0266 a0001c0001t0002g0267 others(35): Show |
38 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.107+4558T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230422223 | |||||||
chr2:230422274 | G | C | 1 | a0001c0003t0005g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.107+4609G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230422274 | |||||||
chr2:230422570 | T | C | 25 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(22): Show |
25 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.107+4905T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230422570 | |||||||
chr2:230422621 | G | C | 54 | a0001c0001t0002g0254 a0001c0001t0002g0266 a0001c0001t0002g0267 others(51): Show |
54 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.107+4956G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230422621 | |||||||
chr2:230422681 | A | T | 2 | a0001c0019t0015g0035 a0002c0020t0022g0036 |
2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.107+5016A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230422681 | |||||||
chr2:230422896 | C | T | 25 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(22): Show |
25 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.107+5231C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230422896 | |||||||
chr2:230422897 | G | A | 2 | a0001c0003t0004g0125 a0003c0004t0002g0269 |
2 | HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.107+5232G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230422897 | |||||||
chr2:230422902 | T | C | 1 | a0001c0001t0008g0132 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.107+5237T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230422902 | |||||||
chr2:230422915 | G | A | 1 | a0001c0001t0002g0105 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.107+5250G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230422915 | |||||||
chr2:230423167 | C | T | 36 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0071 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.107+5502C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230423167 | |||||||
chr2:230423232 | G | T | 1 | a0002c0002t0009g0246 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.107+5567G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230423232 | |||||||
chr2:230423546 | C | T | 2 | a0002c0005t0001g0083 a0002c0005t0001g0084 |
2 | HG00544.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.107+5881C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230423546 | |||||||
chr2:230423823 | G | A | 8 | a0001c0001t0002g0102 a0001c0001t0004g0049 a0001c0001t0004g0050 others(5): Show |
8 | HG01106.hp1 HG02572.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.107+6158G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230423823 | |||||||
chr2:230423846 | C | T | 24 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0283 others(21): Show |
24 | HG00280.hp1 HG00738.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.107+6181C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230423846 | |||||||
chr2:230423905 | G | A | 2 | a0005c0008t0003g0003 a0005c0008t0005g0004 |
2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.107+6240G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230423905 | |||||||
chr2:230423964 | T | A | 24 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0283 others(21): Show |
24 | HG00280.hp1 HG00738.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.107+6299T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230423964 | |||||||
chr2:230424607 | T | G | 1 | a0002c0005t0001g0057 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.107+6942T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230424607 | |||||||
chr2:230424668 | C | CA | 72 | a0001c0001t0002g0009 a0001c0001t0002g0065 a0001c0001t0002g0067 others(69): Show |
73 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.107+7020dupA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230424668 | ||||||
chr2:230424668 | C | CAA | 36 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(33): Show |
36 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.107+7019_107+7020d others(4): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230424668 | ||||||
chr2:230424691 | G | A | 1 | a0001c0003t0003g0183 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.107+7026G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230424691 | |||||||
chr2:230424712 | T | C | 2 | a0003c0004t0002g0134 a0003c0004t0003g0133 |
2 | HG01070.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.107+7047T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230424712 | |||||||
chr2:230425131 | A | G | 1 | a0001c0003t0018g0181 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.107+7466A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230425131 | |||||||
chr2:230425193 | A | G | 1 | a0001c0001t0010g0245 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.107+7528A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230425193 | |||||||
chr2:230425261 | T | C | 36 | a0001c0001t0002g0254 a0001c0001t0002g0266 a0001c0001t0002g0267 others(33): Show |
36 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.107+7596T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230425261 | |||||||
chr2:230425532 | C | T | 1 | a0001c0003t0004g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.107+7867C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230425532 | |||||||
chr2:230425613 | C | T | 2 | a0001c0019t0015g0035 a0002c0020t0022g0036 |
2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.107+7948C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230425613 | |||||||
chr2:230425801 | A | AT | 39 | a0001c0001t0002g0254 a0001c0001t0002g0266 a0001c0001t0002g0267 others(36): Show |
39 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.107+8147dupT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230425801 | ||||||
chr2:230425888 | T | C | 1 | a0001c0001t0002g0184 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.107+8223T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230425888 | |||||||
chr2:230425898 | G | A | 6 | a0001c0001t0020g0286 a0001c0007t0005g0030 a0001c0007t0005g0032 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.107+8233G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230425898 | |||||||
chr2:230426195 | A | T | 1 | a0001c0003t0005g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.107+8530A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230426195 | |||||||
chr2:230426274 | C | G | 1 | a0001c0001t0002g0285 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.107+8609C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230426274 | |||||||
chr2:230426429 | G | A | 37 | a0001c0001t0002g0102 a0001c0001t0002g0105 a0001c0001t0002g0274 others(34): Show |
37 | HG00323.hp1 HG00408.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.107+8764G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230426429 | |||||||
chr2:230426526 | A | ATTAT | 161 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(158): Show |
162 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.107+8862_107+8865d others(6): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230426526 | ||||||
chr2:230426572 | G | A | 4 | a0001c0001t0025g0060 a0002c0002t0013g0059 a0002c0005t0001g0057 others(1): Show |
4 | HG02109.hp2 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.107+8907G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230426572 | |||||||
chr2:230426669 | T | C | 4 | a0001c0001t0006g0135 a0001c0001t0010g0187 a0001c0003t0003g0185 others(1): Show |
4 | NA18957.hp2 NA18984.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+9004T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230426669 | |||||||
chr2:230426935 | G | A | 1 | a0001c0003t0007g0136 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.107+9270G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230426935 | |||||||
chr2:230426953 | AGTT | A | 6 | a0001c0003t0012g0042 a0001c0003t0012g0045 a0001c0003t0012g0046 others(3): Show |
6 | HG02258.hp1 HG02922.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.107+9294_107+9296d others(5): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230426953 | ||||||
chr2:230427155 | G | GTC | 12 | a0001c0001t0002g0254 a0001c0001t0002g0266 a0001c0001t0002g0267 others(9): Show |
12 | HG00280.hp2 HG00733.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.107+9502_107+9503d others(4): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230427155 | ||||||
chr2:230427223 | G | T | 4 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(1): Show |
4 | HG02630.hp2 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+9558G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230427223 | |||||||
chr2:230427389 | C | T | 1 | a0001c0003t0005g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.107+9724C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230427389 | |||||||
chr2:230427408 | G | T | 4 | a0001c0001t0004g0176 a0001c0001t0017g0177 a0001c0001t0017g0178 others(1): Show |
4 | HG02257.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.107+9743G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230427408 | |||||||
chr2:230427505 | G | T | 1 | a0003c0004t0002g0269 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.107+9840G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230427505 | |||||||
chr2:230427506 | T | G | 1 | a0001c0007t0005g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.107+9841T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230427506 | |||||||
chr2:230427575 | G | A | 10 | a0001c0001t0005g0124 a0001c0001t0010g0120 a0002c0002t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.107+9910G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230427575 | |||||||
chr2:230427582 | C | T | 41 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0071 others(38): Show |
41 | HG00408.hp1 HG00544.hp1 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.107+9917C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230427582 | |||||||
chr2:230427645 | T | G | 1 | a0003c0004t0003g0137 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.107+9980T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230427645 | |||||||
chr2:230427696 | C | A | 1 | a0001c0003t0003g0273 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.107+10031C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230427696 | |||||||
chr2:230427969 | G | A | 1 | a0001c0003t0016g0138 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.107+10304G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230427969 | |||||||
chr2:230428124 | G | A | 36 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0071 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.107+10459G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230428124 | |||||||
chr2:230428307 | C | T | 2 | a0001c0019t0015g0035 a0002c0020t0022g0036 |
2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.107+10642C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230428307 | |||||||
chr2:230428391 | C | T | 2 | a0002c0002t0001g0243 a0002c0002t0001g0244 |
2 | HG02293.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.107+10726C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230428391 | |||||||
chr2:230428394 | G | A | 1 | a0001c0001t0004g0049 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.107+10729G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230428394 | |||||||
chr2:230428424 | C | T | 12 | a0001c0001t0002g0254 a0001c0001t0002g0266 a0001c0001t0002g0267 others(9): Show |
12 | HG00280.hp2 HG00733.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.107+10759C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230428424 | |||||||
chr2:230428438 | G | T | 1 | a0001c0001t0002g0175 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.107+10773G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230428438 | |||||||
chr2:230428439 | C | T | 1 | a0001c0001t0002g0175 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.107+10774C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230428439 | |||||||
chr2:230428446 | CT | C | 52 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0071 others(49): Show |
52 | HG00408.hp1 HG00544.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.107+10795delT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230428446 | ||||||
chr2:230428544 | G | A | 1 | a0002c0002t0001g0118 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.107+10879G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230428544 | |||||||
chr2:230428609 | T | A | 137 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(134): Show |
138 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.107+10944T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230428609 | |||||||
chr2:230428641 | A | T | 82 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0071 others(79): Show |
82 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.107+10976A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230428641 | |||||||
chr2:230428693 | C | T | 5 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(2): Show |
5 | HG02486.hp1 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+11028C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230428693 | |||||||
chr2:230428828 | G | A | 1 | a0001c0003t0005g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.107+11163G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230428828 | |||||||
chr2:230428909 | A | G | 112 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(109): Show |
113 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.107+11244A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230428909 | |||||||
chr2:230428965 | G | T | 26 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0283 others(23): Show |
26 | HG00280.hp1 HG00738.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.107+11300G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230428965 | |||||||
chr2:230429132 | G | A | 1 | a0003c0004t0003g0061 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.107+11467G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230429132 | |||||||
chr2:230429155 | T | C | 158 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(155): Show |
159 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.107+11490T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230429155 | |||||||
chr2:230429170 | T | G | 41 | a0001c0001t0002g0102 a0001c0001t0002g0105 a0001c0001t0002g0274 others(38): Show |
41 | HG00323.hp1 HG00408.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.107+11505T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230429170 | |||||||
chr2:230429235 | A | C | 10 | a0001c0001t0005g0124 a0001c0001t0010g0120 a0002c0002t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.107+11570A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230429235 | |||||||
chr2:230429268 | T | C | 41 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0071 others(38): Show |
41 | HG00408.hp1 HG00544.hp1 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.107+11603T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230429268 | |||||||
chr2:230429472 | G | A | 1 | a0001c0003t0002g0013 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.107+11807G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230429472 | |||||||
chr2:230429519 | C | T | 4 | a0001c0001t0025g0060 a0002c0002t0013g0059 a0002c0005t0001g0057 others(1): Show |
4 | HG02109.hp2 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.107+11854C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230429519 | |||||||
chr2:230429740 | T | C | 158 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(155): Show |
159 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.107+12075T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230429740 | |||||||
chr2:230429993 | C | T | 6 | a0001c0003t0012g0042 a0001c0003t0012g0045 a0001c0003t0012g0046 others(3): Show |
6 | HG02258.hp1 HG02922.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.107+12328C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230429993 | |||||||
chr2:230430059 | G | A | 2 | a0001c0003t0003g0273 a0003c0004t0002g0259 |
2 | HG00733.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.107+12394G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230430059 | |||||||
chr2:230430224 | C | A | 1 | a0003c0004t0003g0189 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.107+12559C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230430224 | |||||||
chr2:230430321 | C | G | 7 | a0001c0001t0007g0258 a0001c0003t0012g0042 a0001c0003t0012g0045 others(4): Show |
7 | HG02258.hp1 HG02922.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.108-12616C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230430321 | |||||||
chr2:230430361 | C | A | 1 | a0001c0001t0007g0258 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.108-12576C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230430361 | |||||||
chr2:230430449 | G | T | 3 | a0001c0001t0010g0130 a0001c0009t0007g0272 a0003c0004t0003g0271 |
3 | HG00738.hp2 HG03017.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.108-12488G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230430449 | |||||||
chr2:230430457 | C | T | 128 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(125): Show |
128 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.108-12480C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230430457 | |||||||
chr2:230430469 | C | G | 146 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(143): Show |
147 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.108-12468C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230430469 | |||||||
chr2:230430551 | G | T | 1 | a0001c0001t0007g0258 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.108-12386G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230430551 | |||||||
chr2:230430641 | G | A | 41 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0071 others(38): Show |
41 | HG00408.hp1 HG00544.hp1 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.108-12296G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230430641 | |||||||
chr2:230430826 | T | A | 6 | a0001c0003t0012g0042 a0001c0003t0012g0045 a0001c0003t0012g0046 others(3): Show |
6 | HG02258.hp1 HG02922.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.108-12111T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230430826 | |||||||
chr2:230431038 | C | G | 2 | a0001c0003t0002g0100 a0002c0002t0001g0034 |
2 | HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.108-11899C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230431038 | |||||||
chr2:230431257 | C | T | 2 | a0001c0001t0020g0286 a0002c0005t0013g0287 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.108-11680C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230431257 | |||||||
chr2:230431357 | T | C | 2 | a0001c0003t0008g0002 a0002c0005t0001g0256 |
3 | HG02257.hp2 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.108-11580T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230431357 | |||||||
chr2:230431382 | G | A | 1 | a0002c0002t0001g0028 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.108-11555G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230431382 | |||||||
chr2:230431669 | A | T | 4 | a0001c0001t0005g0124 a0002c0002t0001g0118 a0005c0008t0002g0122 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-11268A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230431669 | |||||||
chr2:230431982 | T | G | 141 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(138): Show |
142 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.108-10955T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230431982 | |||||||
chr2:230432131 | C | T | 1 | a0001c0003t0004g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.108-10806C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230432131 | |||||||
chr2:230432133 | A | G | 1 | a0002c0002t0001g0242 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.108-10804A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230432133 | |||||||
chr2:230432208 | G | A | 1 | a0001c0007t0016g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.108-10729G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230432208 | |||||||
chr2:230432471 | C | T | 5 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(2): Show |
5 | HG02486.hp1 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.108-10466C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230432471 | |||||||
chr2:230432556 | A | G | 158 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(155): Show |
159 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.108-10381A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230432556 | |||||||
chr2:230432598 | T | C | 1 | a0001c0001t0004g0270 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.108-10339T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230432598 | |||||||
chr2:230432618 | C | T | 99 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(96): Show |
99 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.108-10319C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230432618 | |||||||
chr2:230432801 | T | C | 3 | a0001c0003t0003g0139 a0002c0002t0001g0140 a0002c0005t0001g0141 |
3 | NA18974.hp2 NA19080.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.108-10136T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230432801 | |||||||
chr2:230433014 | T | TG | 27 | a0001c0001t0002g0102 a0001c0001t0002g0105 a0001c0001t0002g0274 others(24): Show |
27 | HG00323.hp1 HG00408.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.108-9917dupG | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230433014 | ||||||
chr2:230433217 | T | C | 1 | a0003c0004t0003g0062 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.108-9720T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230433217 | |||||||
chr2:230433515 | T | G | 1 | a0003c0004t0003g0142 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.108-9422T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230433515 | |||||||
chr2:230433760 | C | T | 6 | a0001c0001t0002g0274 a0001c0003t0004g0249 a0001c0003t0007g0250 others(3): Show |
6 | HG01256.hp2 HG01258.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-9177C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230433760 | |||||||
chr2:230433997 | A | T | 2 | a0010c0012t0009g0087 a0011c0011t0003g0086 |
2 | NA18970.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.108-8940A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230433997 | |||||||
chr2:230434403 | G | A | 24 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0283 others(21): Show |
24 | HG00280.hp1 HG00738.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.108-8534G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230434403 | |||||||
chr2:230434448 | T | C | 27 | a0001c0001t0002g0102 a0001c0001t0002g0105 a0001c0001t0002g0274 others(24): Show |
27 | HG00323.hp1 HG00408.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.108-8489T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230434448 | |||||||
chr2:230434462 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.108-8475C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230434462 | |||||||
chr2:230434511 | G | T | 1 | a0003c0004t0003g0241 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.108-8426G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230434511 | |||||||
chr2:230434523 | A | T | 4 | a0001c0001t0006g0135 a0001c0001t0010g0187 a0001c0003t0003g0185 others(1): Show |
4 | NA18957.hp2 NA18984.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.108-8414A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230434523 | |||||||
chr2:230434589 | T | A | 27 | a0001c0001t0002g0102 a0001c0001t0002g0105 a0001c0001t0002g0274 others(24): Show |
27 | HG00323.hp1 HG00408.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.108-8348T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230434589 | |||||||
chr2:230434631 | G | A | 2 | a0001c0003t0008g0002 a0002c0005t0001g0256 |
3 | HG02257.hp2 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.108-8306G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230434631 | |||||||
chr2:230434638 | G | A | 76 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(73): Show |
77 | HG00408.hp1 HG00544.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.108-8299G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230434638 | |||||||
chr2:230434667 | A | G | 1 | a0001c0001t0002g0175 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.108-8270A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230434667 | |||||||
chr2:230434850 | G | A | 129 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(126): Show |
130 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.108-8087G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230434850 | |||||||
chr2:230434947 | G | A | 2 | a0002c0002t0001g0190 a0002c0002t0001g0191 |
2 | HG01192.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.108-7990G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230434947 | |||||||
chr2:230435310 | T | C | 73 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(70): Show |
73 | HG00408.hp1 HG00544.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.108-7627T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230435310 | |||||||
chr2:230435355 | G | A | 41 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0071 others(38): Show |
41 | HG00408.hp1 HG00544.hp1 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.108-7582G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230435355 | |||||||
chr2:230435593 | G | C | 26 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0283 others(23): Show |
26 | HG00280.hp1 HG00738.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.108-7344G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230435593 | |||||||
chr2:230435649 | G | A | 19 | a0001c0001t0002g0105 a0001c0001t0002g0274 a0001c0003t0002g0108 others(16): Show |
19 | HG00323.hp1 HG00408.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.108-7288G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230435649 | |||||||
chr2:230435701 | T | A | 12 | a0001c0001t0002g0254 a0001c0001t0002g0266 a0001c0001t0002g0267 others(9): Show |
12 | HG00280.hp2 HG00733.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.108-7236T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230435701 | |||||||
chr2:230435933 | AATGAGAT others(37): Show |
A | 1 | a0001c0001t0006g0240 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.108-7001_108-6958d others(46): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230435933 | ||||||
chr2:230435940 | TCATGTCC others(29): Show |
T | 24 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0283 others(21): Show |
24 | HG00280.hp1 HG00738.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.108-6993_108-6958d others(38): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230435940 | ||||||
chr2:230436186 | A | G | 160 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(157): Show |
161 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.108-6751A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230436186 | |||||||
chr2:230436196 | C | T | 3 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0002c0005t0013g0106 |
3 | HG01106.hp1 HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.108-6741C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230436196 | |||||||
chr2:230436263 | G | C | 102 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(99): Show |
103 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.108-6674G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230436263 | |||||||
chr2:230436369 | C | T | 73 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(70): Show |
73 | HG00408.hp1 HG00544.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.108-6568C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230436369 | |||||||
chr2:230436419 | G | A | 12 | a0001c0001t0002g0254 a0001c0001t0002g0266 a0001c0001t0002g0267 others(9): Show |
12 | HG00280.hp2 HG00733.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.108-6518G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230436419 | |||||||
chr2:230436438 | TGTTCTCA others(13): Show |
T | 31 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0071 others(28): Show |
31 | HG00408.hp1 HG00544.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.108-6488_108-6469d others(22): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230436438 | ||||||
chr2:230436494 | C | T | 2 | a0001c0003t0008g0002 a0002c0005t0001g0256 |
3 | HG02257.hp2 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.108-6443C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230436494 | |||||||
chr2:230436495 | G | A | 1 | a0003c0004t0003g0133 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.108-6442G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230436495 | |||||||
chr2:230436556 | G | A | 1 | a0002c0002t0001g0005 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.108-6381G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230436556 | |||||||
chr2:230436755 | T | C | 1 | a0001c0003t0012g0048 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.108-6182T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230436755 | |||||||
chr2:230436866 | G | GTATATGT others(13): Show |
1 | a0003c0004t0002g0269 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.108-6051_108-6032d others(22): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230436866 | ||||||
chr2:230436866 | G | GTATATGT others(33): Show |
10 | a0001c0001t0002g0105 a0001c0001t0004g0050 a0001c0001t0010g0130 others(7): Show |
10 | HG00323.hp1 HG00738.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.108-6032_108-6031i others(42): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230436866 | ||||||
chr2:230436866 | G | GTATATGT others(53): Show |
3 | a0001c0001t0004g0270 a0001c0001t0005g0095 a0002c0005t0001g0129 |
3 | HG01884.hp2 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.108-6032_108-6031i others(62): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230436866 | ||||||
chr2:230436866 | G | GTATATGT others(73): Show |
3 | a0001c0001t0005g0127 a0001c0001t0019g0126 a0002c0005t0013g0128 |
3 | HG02145.hp1 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.108-6032_108-6031i others(82): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230436866 | ||||||
chr2:230436866 | G | GTATATGT others(33): Show |
49 | a0001c0001t0002g0065 a0001c0001t0002g0072 a0001c0001t0002g0274 others(46): Show |
49 | HG00408.hp2 HG01106.hp1 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.108-6033_108-6032i others(42): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230436866 | ||||||
chr2:230436884 | A | ACG | 2 | a0001c0003t0008g0002 a0002c0005t0001g0256 |
3 | HG02257.hp2 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.108-6052_108-6051i others(4): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230436884 | ||||||
chr2:230436891 | T | TGTGTATA others(7): Show |
2 | a0001c0003t0008g0002 a0002c0005t0001g0256 |
3 | HG02257.hp2 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.108-6033_108-6032i others(16): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230436891 | ||||||
chr2:230436899 | C | CACACACG others(13): Show |
62 | a0001c0001t0002g0065 a0001c0001t0002g0072 a0001c0001t0002g0105 others(59): Show |
62 | HG00323.hp1 HG00408.hp2 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.108-6031_108-6012d others(22): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230436899 | ||||||
chr2:230436899 | C | CACACATA others(53): Show |
13 | a0001c0001t0002g0067 a0001c0001t0002g0071 a0001c0001t0003g0070 others(10): Show |
13 | HG00408.hp1 HG00544.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.108-6033_108-6032i others(62): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230436899 | ||||||
chr2:230436899 | C | CACACATA others(51): Show |
1 | a0001c0001t0002g0102 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.108-6033_108-6032i others(60): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230436899 | ||||||
chr2:230436899 | C | CACACATA others(11): Show |
25 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(22): Show |
25 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.108-6033_108-6032i others(20): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230436899 | ||||||
chr2:230436904 | ACG | A | 14 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0283 others(11): Show |
14 | HG00280.hp1 HG01074.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.108-6031_108-6030d others(4): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230436904 | ||||||
chr2:230436906 | G | A | 26 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(23): Show |
26 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.108-6031G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230436906 | |||||||
chr2:230436925 | C | CACATAT | 3 | a0001c0001t0002g0283 a0001c0001t0002g0284 a0001c0001t0002g0285 |
3 | HG00280.hp1 HG02148.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.108-6011_108-6010i others(8): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230436925 | ||||||
chr2:230436925 | C | CACATATA others(1): Show |
2 | a0001c0003t0008g0002 a0002c0005t0001g0256 |
3 | HG02257.hp2 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.108-6011_108-6010i others(10): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230436925 | ||||||
chr2:230436925 | C | CACATATA others(19): Show |
10 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0003t0002g0275 others(7): Show |
10 | HG01074.hp2 HG01109.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.108-6011_108-6010i others(28): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230436925 | ||||||
chr2:230436927 | A | AGTGTATA others(15): Show |
2 | a0001c0001t0007g0173 a0001c0001t0008g0172 |
2 | HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.108-5995_108-5974d others(24): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230436927 | ||||||
chr2:230436927 | A | C | 25 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(22): Show |
25 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.108-6010A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230436927 | |||||||
chr2:230436927 | A | T | 17 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0283 others(14): Show |
18 | HG00280.hp1 HG01074.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.108-6010A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230436927 | |||||||
chr2:230436928 | G | GCATATA | 26 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(23): Show |
26 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.108-6009_108-6008i others(8): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230436928 | |||||||
chr2:230436932 | A | G | 26 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(23): Show |
26 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.108-6005A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230436932 | |||||||
chr2:230436935 | C | T | 26 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(23): Show |
26 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.108-6002C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230436935 | |||||||
chr2:230436941 | C | T | 5 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(2): Show |
5 | HG02486.hp1 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.108-5996C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230436941 | |||||||
chr2:230436943 | C | CATATATG others(15): Show |
7 | a0001c0003t0005g0047 a0001c0003t0012g0042 a0001c0003t0012g0045 others(4): Show |
7 | HG02258.hp1 HG02922.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.108-5950_108-5929d others(24): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230436943 | ||||||
chr2:230436943 | CATATATG others(15): Show |
C | 4 | a0003c0004t0002g0134 a0003c0004t0003g0133 a0005c0008t0003g0003 others(1): Show |
4 | HG01070.hp2 HG01109.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-5950_108-5929d others(24): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230436943 | ||||||
chr2:230436943 | CATATATG others(37): Show |
C | 1 | a0002c0002t0001g0218 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.108-5972_108-5929d others(46): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230436943 | ||||||
chr2:230436949 | T | A | 1 | a0001c0003t0004g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.108-5988T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230436949 | |||||||
chr2:230436949 | T | TGTGTATA others(7): Show |
14 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0283 others(11): Show |
14 | HG00280.hp1 HG01074.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.108-5975_108-5974i others(16): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230436949 | ||||||
chr2:230436961 | CACATATA others(1): Show |
C | 25 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(22): Show |
25 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.108-5974_108-5967d others(10): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230436961 | ||||||
chr2:230436964 | A | G | 17 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0283 others(14): Show |
18 | HG00280.hp1 HG01074.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.108-5973A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230436964 | |||||||
chr2:230436965 | T | C | 17 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0283 others(14): Show |
18 | HG00280.hp1 HG01074.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.108-5972T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230436965 | |||||||
chr2:230436971 | T | A | 25 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(22): Show |
25 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.108-5966T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230436971 | |||||||
chr2:230436986 | A | G | 27 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(24): Show |
28 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.108-5951A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230436986 | |||||||
chr2:230436987 | T | C | 27 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(24): Show |
28 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.108-5950T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230436987 | |||||||
chr2:230437220 | C | T | 1 | a0001c0001t0004g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.108-5717C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230437220 | |||||||
chr2:230437419 | T | C | 4 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(1): Show |
4 | HG02630.hp2 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.108-5518T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230437419 | |||||||
chr2:230437504 | T | C | 2 | a0001c0003t0008g0002 a0002c0005t0001g0256 |
3 | HG02257.hp2 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.108-5433T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230437504 | |||||||
chr2:230437653 | G | A | 2 | a0001c0019t0015g0035 a0002c0020t0022g0036 |
2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.108-5284G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230437653 | |||||||
chr2:230437750 | A | G | 160 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(157): Show |
161 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.108-5187A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230437750 | |||||||
chr2:230437798 | C | T | 1 | a0001c0001t0004g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.108-5139C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230437798 | |||||||
chr2:230437803 | G | A | 4 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(1): Show |
4 | HG02630.hp2 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.108-5134G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230437803 | |||||||
chr2:230438077 | C | G | 1 | a0001c0003t0007g0115 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.108-4860C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230438077 | |||||||
chr2:230438113 | T | C | 1 | a0001c0003t0005g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.108-4824T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230438113 | |||||||
chr2:230438223 | T | A | 1 | a0001c0003t0012g0247 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.108-4714T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230438223 | |||||||
chr2:230438277 | G | C | 16 | a0001c0001t0005g0124 a0001c0001t0010g0120 a0001c0003t0005g0047 others(13): Show |
16 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.108-4660G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230438277 | |||||||
chr2:230438328 | A | G | 158 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(155): Show |
159 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.108-4609A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230438328 | |||||||
chr2:230438635 | T | C | 2 | a0001c0003t0008g0002 a0002c0005t0001g0256 |
3 | HG02257.hp2 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.108-4302T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230438635 | |||||||
chr2:230438639 | G | GTA | 5 | a0001c0001t0004g0096 a0001c0001t0005g0095 a0001c0003t0002g0100 others(2): Show |
5 | HG02809.hp1 HG03041.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.108-4289_108-4288d others(4): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230438639 | ||||||
chr2:230438639 | G | GTATA | 7 | a0001c0001t0010g0120 a0001c0003t0004g0099 a0002c0002t0011g0119 others(4): Show |
7 | HG01109.hp1 HG01243.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.108-4291_108-4288d others(6): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230438639 | ||||||
chr2:230438639 | G | GTATATA | 11 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0005g0124 others(8): Show |
11 | HG00673.hp2 HG00738.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.108-4293_108-4288d others(8): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230438639 | ||||||
chr2:230438639 | G | GTATATAT others(1): Show |
9 | a0001c0003t0008g0002 a0001c0003t0012g0042 a0001c0003t0012g0045 others(6): Show |
10 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.108-4295_108-4288d others(10): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230438639 | ||||||
chr2:230438639 | G | GTATATAT others(7): Show |
1 | a0001c0001t0007g0258 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.108-4288_108-4287i others(16): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230438639 | ||||||
chr2:230438639 | G | GTGTATAT others(1): Show |
24 | a0001c0001t0002g0067 a0001c0001t0002g0071 a0001c0001t0002g0072 others(21): Show |
24 | HG00408.hp1 HG00544.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.108-4297_108-4296i others(10): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230438639 | ||||||
chr2:230438639 | G | GTGTATAT others(5): Show |
1 | a0001c0009t0002g0082 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.108-4297_108-4296i others(14): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230438639 | ||||||
chr2:230438639 | GTA | G | 21 | a0001c0001t0002g0105 a0001c0001t0002g0274 a0001c0003t0002g0108 others(18): Show |
21 | HG00323.hp1 HG00408.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.108-4289_108-4288d others(4): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230438639 | ||||||
chr2:230438641 | A | G | 8 | a0001c0001t0002g0065 a0001c0001t0018g0066 a0001c0001t0025g0060 others(5): Show |
8 | HG01496.hp2 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.108-4296A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230438641 | |||||||
chr2:230438648 | T | C | 32 | a0001c0001t0002g0067 a0001c0001t0002g0071 a0001c0001t0002g0072 others(29): Show |
32 | HG00408.hp1 HG00544.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.108-4289T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230438648 | |||||||
chr2:230438648 | T | TAC | 22 | a0001c0001t0002g0148 a0001c0001t0002g0196 a0001c0001t0002g0200 others(19): Show |
22 | HG01943.hp2 HG01981.hp1 HG02132.hp1 others(19): Show |
intron_variant | MODIFIER | c.108-4251_108-4250d others(4): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230438648 | ||||||
chr2:230438648 | T | TATACACA others(3): Show |
1 | a0001c0001t0010g0260 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.108-4288_108-4287i others(12): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230438648 | ||||||
chr2:230438648 | T | TATACACA others(5): Show |
1 | a0001c0003t0004g0125 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.108-4288_108-4287i others(14): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230438648 | ||||||
chr2:230438648 | T | TATATAC | 10 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0284 others(7): Show |
10 | HG00280.hp1 HG01192.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.108-4288_108-4287i others(8): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230438648 | ||||||
chr2:230438648 | T | TATATACA others(1): Show |
15 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(12): Show |
15 | HG00738.hp1 HG01074.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.108-4288_108-4287i others(10): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230438648 | ||||||
chr2:230438648 | T | TATATACA others(3): Show |
13 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0002g0268 others(10): Show |
13 | HG00733.hp2 HG01071.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.108-4288_108-4287i others(12): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230438648 | ||||||
chr2:230438648 | T | TATATACA others(5): Show |
9 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0002c0002t0001g0005 others(6): Show |
9 | HG00280.hp2 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.108-4288_108-4287i others(14): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230438648 | ||||||
chr2:230438648 | T | TATATACA others(7): Show |
2 | a0002c0005t0013g0037 a0003c0004t0003g0261 |
2 | HG06807.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.108-4288_108-4287i others(16): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230438648 | ||||||
chr2:230438648 | T | TATATATA others(3): Show |
11 | a0001c0001t0002g0065 a0001c0001t0010g0130 a0001c0001t0018g0066 others(8): Show |
11 | HG02109.hp2 HG02280.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.108-4288_108-4287i others(12): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230438648 | ||||||
chr2:230438648 | T | TATATATA others(5): Show |
1 | a0003c0004t0003g0271 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.108-4288_108-4287i others(14): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230438648 | ||||||
chr2:230438648 | T | TATATATA others(7): Show |
1 | a0001c0007t0016g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.108-4288_108-4287i others(16): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230438648 | ||||||
chr2:230438648 | T | TATATATA others(5): Show |
1 | a0003c0004t0003g0081 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.108-4288_108-4287i others(14): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230438648 | ||||||
chr2:230438648 | TAC | T | 28 | a0001c0001t0002g0102 a0001c0001t0004g0049 a0001c0001t0004g0050 others(25): Show |
28 | HG00673.hp1 HG01106.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.108-4251_108-4250d others(4): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230438648 | ||||||
chr2:230438648 | TACAC | T | 4 | a0001c0001t0007g0173 a0002c0002t0001g0190 a0002c0002t0001g0191 others(1): Show |
4 | HG00140.hp1 HG01192.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.108-4253_108-4250d others(6): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230438648 | ||||||
chr2:230438648 | TACACACA others(3): Show |
T | 1 | a0002c0005t0001g0141 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.108-4259_108-4250d others(12): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230438648 | ||||||
chr2:230438650 | C | T | 36 | a0001c0001t0002g0167 a0001c0001t0002g0171 a0001c0001t0002g0174 others(33): Show |
36 | HG01109.hp1 HG01243.hp1 HG01255.hp2 others(33): Show |
intron_variant | MODIFIER | c.108-4287C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230438650 | |||||||
chr2:230438652 | C | T | 23 | a0001c0001t0002g0171 a0001c0001t0002g0174 a0001c0001t0005g0124 others(20): Show |
23 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.108-4285C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230438652 | |||||||
chr2:230438654 | C | T | 14 | a0001c0001t0007g0258 a0001c0001t0010g0120 a0001c0003t0005g0047 others(11): Show |
14 | HG01109.hp1 HG01243.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.108-4283C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230438654 | |||||||
chr2:230438660 | C | T | 1 | a0002c0005t0001g0141 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.108-4277C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230438660 | |||||||
chr2:230438688 | T | C | 5 | a0001c0001t0018g0066 a0001c0019t0015g0035 a0002c0020t0022g0036 others(2): Show |
5 | HG01891.hp2 HG01978.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.108-4249T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230438688 | |||||||
chr2:230438693 | T | G | 158 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(155): Show |
159 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.108-4244T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230438693 | |||||||
chr2:230438704 | G | A | 2 | a0001c0003t0008g0002 a0002c0005t0001g0256 |
3 | HG02257.hp2 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.108-4233G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230438704 | |||||||
chr2:230438706 | G | A | 1 | a0001c0003t0005g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.108-4231G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230438706 | |||||||
chr2:230438968 | A | G | 10 | a0001c0001t0005g0124 a0001c0001t0010g0120 a0002c0002t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.108-3969A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230438968 | |||||||
chr2:230439550 | T | TTTG | 45 | a0001c0001t0002g0102 a0001c0001t0002g0105 a0001c0001t0002g0266 others(42): Show |
46 | HG00323.hp1 HG00408.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.108-3363_108-3361d others(5): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230439550 | ||||||
chr2:230439590 | T | G | 38 | a0001c0001t0002g0254 a0001c0001t0002g0266 a0001c0001t0002g0267 others(35): Show |
38 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.108-3347T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230439590 | |||||||
chr2:230439639 | T | C | 9 | a0001c0001t0005g0252 a0001c0003t0015g0170 a0001c0003t0016g0138 others(6): Show |
9 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.108-3298T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230439639 | |||||||
chr2:230439811 | T | C | 28 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(25): Show |
28 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.108-3126T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230439811 | |||||||
chr2:230439947 | G | A | 6 | a0001c0003t0012g0042 a0001c0003t0012g0045 a0001c0003t0012g0046 others(3): Show |
6 | HG02258.hp1 HG02922.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.108-2990G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230439947 | |||||||
chr2:230439998 | C | A | 144 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(141): Show |
144 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.108-2939C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230439998 | |||||||
chr2:230440019 | G | A | 4 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(1): Show |
4 | HG02630.hp2 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.108-2918G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230440019 | |||||||
chr2:230440024 | G | A | 4 | a0001c0001t0005g0124 a0002c0002t0001g0118 a0005c0008t0002g0122 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-2913G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230440024 | |||||||
chr2:230440187 | A | G | 2 | a0001c0003t0008g0002 a0002c0005t0001g0256 |
3 | HG02257.hp2 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.108-2750A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230440187 | |||||||
chr2:230440191 | A | G | 125 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(122): Show |
125 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.108-2746A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230440191 | |||||||
chr2:230440476 | G | T | 27 | a0001c0001t0002g0102 a0001c0001t0002g0105 a0001c0001t0002g0274 others(24): Show |
27 | HG00323.hp1 HG00408.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.108-2461G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230440476 | |||||||
chr2:230440516 | C | T | 2 | a0001c0003t0008g0002 a0002c0005t0001g0256 |
3 | HG02257.hp2 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.108-2421C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230440516 | |||||||
chr2:230440546 | A | T | 1 | a0003c0004t0003g0255 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.108-2391A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230440546 | |||||||
chr2:230440573 | G | A | 2 | a0001c0019t0015g0035 a0002c0020t0022g0036 |
2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.108-2364G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230440573 | |||||||
chr2:230440958 | GA | G | 6 | a0001c0001t0003g0094 a0001c0001t0018g0066 a0001c0003t0008g0002 others(3): Show |
7 | HG02155.hp1 HG02155.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.108-1970delA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230440958 | ||||||
chr2:230441346 | T | C | 2 | a0001c0001t0020g0286 a0002c0005t0013g0287 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.108-1591T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230441346 | |||||||
chr2:230441358 | C | T | 117 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(114): Show |
117 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.108-1579C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230441358 | |||||||
chr2:230441375 | A | T | 1 | a0005c0008t0005g0004 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.108-1562A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230441375 | |||||||
chr2:230441496 | T | C | 1 | a0003c0004t0003g0208 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.108-1441T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230441496 | |||||||
chr2:230441553 | A | G | 1 | a0001c0001t0010g0169 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.108-1384A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230441553 | |||||||
chr2:230441577 | T | C | 2 | a0001c0003t0008g0002 a0002c0005t0001g0256 |
3 | HG02257.hp2 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.108-1360T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230441577 | |||||||
chr2:230441645 | T | G | 1 | a0001c0003t0003g0063 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.108-1292T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230441645 | |||||||
chr2:230441670 | G | GT | 18 | a0001c0001t0005g0124 a0001c0001t0007g0258 a0001c0001t0010g0120 others(15): Show |
18 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.108-1266dupT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230441670 | ||||||
chr2:230441748 | T | C | 27 | a0001c0001t0002g0102 a0001c0001t0002g0105 a0001c0001t0002g0274 others(24): Show |
27 | HG00323.hp1 HG00408.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.108-1189T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230441748 | |||||||
chr2:230441774 | G | A | 2 | a0001c0003t0008g0002 a0002c0005t0001g0256 |
3 | HG02257.hp2 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.108-1163G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230441774 | |||||||
chr2:230441901 | T | G | 1 | a0001c0001t0004g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.108-1036T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230441901 | |||||||
chr2:230442036 | A | G | 27 | a0001c0001t0002g0102 a0001c0001t0002g0105 a0001c0001t0002g0274 others(24): Show |
27 | HG00323.hp1 HG00408.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.108-901A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230442036 | |||||||
chr2:230442041 | C | CT | 58 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(55): Show |
59 | HG00323.hp1 HG00408.hp2 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.108-889dupT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr2 | 230442041 | ||||||
chr2:230442090 | C | T | 1 | a0001c0001t0005g0127 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.108-847C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230442090 | |||||||
chr2:230442359 | G | A | 71 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0071 others(68): Show |
71 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.108-578G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230442359 | |||||||
chr2:230442869 | C | T | 31 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(28): Show |
32 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.108-68C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230442869 | |||||||
chr2:230442927 | T | C | 2 | a0001c0003t0008g0002 a0002c0005t0001g0256 |
3 | HG02257.hp2 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.108-10T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 2/28 | chr2 | 230442927 | |||||||
chr2:230443121 | A | T | 3 | a0001c0001t0007g0258 a0001c0019t0015g0035 a0002c0020t0022g0036 |
3 | HG01891.hp2 HG02572.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.270+22A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 3/28 | chr2 | 230443121 | |||||||
chr2:230443145 | A | G | 31 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(28): Show |
32 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.270+46A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 3/28 | chr2 | 230443145 | |||||||
chr2:230443197 | C | G | 3 | a0001c0003t0002g0100 a0002c0002t0001g0034 a0002c0002t0001g0118 |
3 | HG02055.hp2 HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.270+98C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 3/28 | chr2 | 230443197 | |||||||
chr2:230443332 | T | C | 31 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(28): Show |
32 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.270+233T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 3/28 | chr2 | 230443332 | |||||||
chr2:230443372 | C | T | 4 | a0001c0001t0004g0176 a0001c0001t0017g0177 a0001c0001t0017g0178 others(1): Show |
4 | HG02257.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+273C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 3/28 | chr2 | 230443372 | |||||||
chr2:230443482 | T | C | 1 | a0002c0002t0011g0157 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.270+383T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 3/28 | chr2 | 230443482 | |||||||
chr2:230443611 | A | T | 31 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(28): Show |
32 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.270+512A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 3/28 | chr2 | 230443611 | |||||||
chr2:230443665 | A | G | 2 | a0001c0003t0008g0002 a0002c0005t0001g0256 |
3 | HG02257.hp2 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.271-513A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 3/28 | chr2 | 230443665 | |||||||
chr2:230443949 | A | G | 2 | a0001c0003t0008g0002 a0002c0005t0001g0256 |
3 | HG02257.hp2 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.271-229A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 3/28 | chr2 | 230443949 | |||||||
chr2:230444424 | A | T | 57 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(54): Show |
58 | HG00280.hp1 HG00673.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.439+78A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230444424 | |||||||
chr2:230444502 | C | A | 24 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0283 others(21): Show |
24 | HG00280.hp1 HG00738.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.439+156C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230444502 | |||||||
chr2:230444503 | G | A | 2 | a0001c0003t0008g0002 a0002c0005t0001g0256 |
3 | HG02257.hp2 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.439+157G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230444503 | |||||||
chr2:230444603 | G | A | 2 | a0001c0003t0008g0002 a0002c0005t0001g0256 |
3 | HG02257.hp2 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.439+257G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230444603 | |||||||
chr2:230444636 | G | A | 1 | a0001c0001t0002g0254 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.439+290G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230444636 | |||||||
chr2:230444689 | T | G | 30 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(27): Show |
31 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.439+343T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230444689 | |||||||
chr2:230444704 | C | T | 2 | a0001c0003t0008g0002 a0002c0005t0001g0256 |
3 | HG02257.hp2 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.439+358C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230444704 | |||||||
chr2:230444811 | T | C | 30 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(27): Show |
31 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.439+465T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230444811 | |||||||
chr2:230445031 | G | A | 30 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(27): Show |
31 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.439+685G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230445031 | |||||||
chr2:230445171 | A | G | 2 | a0001c0003t0008g0002 a0002c0005t0001g0256 |
3 | HG02257.hp2 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.439+825A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230445171 | |||||||
chr2:230445251 | C | G | 30 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(27): Show |
31 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.439+905C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230445251 | |||||||
chr2:230445255 | G | A | 30 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(27): Show |
31 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.439+909G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230445255 | |||||||
chr2:230445431 | A | G | 1 | a0001c0001t0025g0060 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.439+1085A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230445431 | |||||||
chr2:230445463 | C | T | 3 | a0001c0003t0002g0100 a0001c0003t0004g0099 a0002c0002t0001g0034 |
3 | HG03139.hp1 HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.439+1117C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230445463 | |||||||
chr2:230445477 | T | C | 3 | a0001c0003t0002g0100 a0001c0003t0004g0099 a0002c0002t0001g0034 |
3 | HG03139.hp1 HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.439+1131T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230445477 | |||||||
chr2:230445530 | A | G | 1 | a0001c0003t0012g0048 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.439+1184A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230445530 | |||||||
chr2:230445592 | CT | C | 3 | a0001c0001t0010g0130 a0001c0009t0007g0272 a0003c0004t0003g0271 |
3 | HG00738.hp2 HG03017.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.440-1225delT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr2 | 230445592 | ||||||
chr2:230445722 | C | T | 5 | a0003c0004t0002g0265 a0003c0004t0003g0261 a0003c0004t0003g0262 others(2): Show |
5 | HG00280.hp2 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.440-1097C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230445722 | |||||||
chr2:230445767 | G | A | 3 | a0001c0003t0002g0100 a0001c0003t0004g0099 a0002c0002t0001g0034 |
3 | HG03139.hp1 HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.440-1052G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230445767 | |||||||
chr2:230445838 | T | C | 6 | a0001c0001t0005g0088 a0001c0001t0005g0091 a0001c0001t0005g0097 others(3): Show |
6 | HG02486.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.440-981T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230445838 | |||||||
chr2:230445846 | G | A | 1 | a0001c0003t0007g0115 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.440-973G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230445846 | |||||||
chr2:230445905 | A | G | 40 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(37): Show |
40 | HG00280.hp2 HG00673.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.440-914A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230445905 | |||||||
chr2:230445924 | A | G | 28 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(25): Show |
28 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.440-895A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230445924 | |||||||
chr2:230445928 | C | G | 6 | a0001c0003t0012g0042 a0001c0003t0012g0045 a0001c0003t0012g0046 others(3): Show |
6 | HG02258.hp1 HG02922.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.440-891C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230445928 | |||||||
chr2:230446069 | G | A | 2 | a0001c0003t0002g0100 a0002c0002t0001g0034 |
2 | HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.440-750G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230446069 | |||||||
chr2:230446085 | T | C | 1 | a0001c0001t0007g0258 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.440-734T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230446085 | |||||||
chr2:230446176 | T | C | 28 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(25): Show |
28 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.440-643T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230446176 | |||||||
chr2:230446195 | G | A | 28 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(25): Show |
28 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.440-624G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230446195 | |||||||
chr2:230446214 | T | G | 28 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(25): Show |
28 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.440-605T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230446214 | |||||||
chr2:230446221 | C | A | 28 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(25): Show |
28 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.440-598C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230446221 | |||||||
chr2:230446261 | A | C | 1 | a0001c0001t0007g0258 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.440-558A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230446261 | |||||||
chr2:230446274 | A | T | 28 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(25): Show |
28 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.440-545A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230446274 | |||||||
chr2:230446360 | C | T | 1 | a0003c0004t0004g0104 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.440-459C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230446360 | |||||||
chr2:230446681 | C | T | 1 | a0003c0004t0002g0265 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.440-138C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230446681 | |||||||
chr2:230446780 | G | A | 1 | a0001c0001t0007g0173 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.440-39G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 4/28 | chr2 | 230446780 | |||||||
chr2:230446994 | G | A | 2 | a0001c0019t0015g0035 a0002c0020t0022g0036 |
2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.523+92G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 5/28 | chr2 | 230446994 | |||||||
chr2:230447039 | G | A | 1 | a0003c0004t0003g0146 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.523+137G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 5/28 | chr2 | 230447039 | |||||||
chr2:230447158 | T | C | 1 | a0001c0001t0008g0172 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.523+256T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 5/28 | chr2 | 230447158 | |||||||
chr2:230447204 | G | A | 2 | a0005c0008t0003g0003 a0005c0008t0005g0004 |
2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.523+302G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 5/28 | chr2 | 230447204 | |||||||
chr2:230447302 | C | T | 2 | a0001c0001t0002g0027 a0001c0001t0003g0029 |
2 | NA18981.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.523+400C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 5/28 | chr2 | 230447302 | |||||||
chr2:230447425 | G | A | 113 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0071 others(110): Show |
113 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.523+523G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 5/28 | chr2 | 230447425 | |||||||
chr2:230447432 | G | A | 1 | a0001c0001t0007g0258 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.523+530G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 5/28 | chr2 | 230447432 | |||||||
chr2:230447648 | T | A | 1 | a0001c0017t0002g0018 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.523+746T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 5/28 | chr2 | 230447648 | |||||||
chr2:230447702 | G | A | 1 | a0001c0001t0006g0230 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.523+800G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 5/28 | chr2 | 230447702 | |||||||
chr2:230447840 | C | T | 24 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(21): Show |
24 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.523+938C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 5/28 | chr2 | 230447840 | |||||||
chr2:230447902 | G | A | 1 | a0001c0001t0002g0196 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.523+1000G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 5/28 | chr2 | 230447902 | |||||||
chr2:230447903 | T | G | 1 | a0001c0001t0002g0196 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.523+1001T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 5/28 | chr2 | 230447903 | |||||||
chr2:230447904 | T | A | 1 | a0001c0001t0002g0196 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.523+1002T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 5/28 | chr2 | 230447904 | |||||||
chr2:230447905 | C | G | 1 | a0001c0001t0002g0196 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.523+1003C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 5/28 | chr2 | 230447905 | |||||||
chr2:230447908 | C | G | 1 | a0001c0001t0002g0196 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.523+1006C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 5/28 | chr2 | 230447908 | |||||||
chr2:230447910 | C | A | 1 | a0001c0001t0002g0196 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.523+1008C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 5/28 | chr2 | 230447910 | |||||||
chr2:230447911 | C | T | 1 | a0001c0001t0002g0196 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.523+1009C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 5/28 | chr2 | 230447911 | |||||||
chr2:230447912 | C | T | 1 | a0001c0001t0002g0196 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.523+1010C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 5/28 | chr2 | 230447912 | |||||||
chr2:230447914 | T | G | 1 | a0002c0005t0001g0164 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.523+1012T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 5/28 | chr2 | 230447914 | |||||||
chr2:230448538 | T | A | 2 | a0001c0003t0008g0002 a0002c0005t0001g0256 |
3 | HG02257.hp2 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.524-550T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 5/28 | chr2 | 230448538 | |||||||
chr2:230448590 | A | T | 1 | a0002c0005t0006g0012 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.524-498A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 5/28 | chr2 | 230448590 | |||||||
chr2:230448612 | A | T | 12 | a0001c0001t0002g0254 a0001c0001t0002g0266 a0001c0001t0002g0267 others(9): Show |
12 | HG00280.hp2 HG00733.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.524-476A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 5/28 | chr2 | 230448612 | |||||||
chr2:230448787 | G | A | 1 | a0001c0003t0012g0042 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.524-301G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 5/28 | chr2 | 230448787 | |||||||
chr2:230449217 | G | C | 2 | a0003c0004t0003g0016 a0003c0004t0003g0255 |
2 | HG02258.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.586+67G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 6/28 | chr2 | 230449217 | |||||||
chr2:230449378 | G | A | 45 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0071 others(42): Show |
45 | HG00408.hp1 HG00544.hp1 HG01123.hp1 others(42): Show |
intron_variant | MODIFIER | c.587-183G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 6/28 | chr2 | 230449378 | |||||||
chr2:230449419 | T | G | 1 | a0001c0003t0002g0013 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.587-142T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 6/28 | chr2 | 230449419 | |||||||
chr2:230449475 | A | G | 4 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(1): Show |
4 | HG00738.hp1 HG01074.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-86A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 6/28 | chr2 | 230449475 | |||||||
chr2:230449965 | G | C | 20 | a0001c0001t0005g0124 a0001c0001t0010g0120 a0001c0003t0008g0002 others(17): Show |
21 | HG01109.hp1 HG01243.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.737-207G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 7/28 | chr2 | 230449965 | |||||||
chr2:230450039 | G | A | 1 | a0001c0001t0007g0258 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.737-133G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 7/28 | chr2 | 230450039 | |||||||
chr2:230450159 | C | T | 1 | a0002c0002t0009g0207 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.737-13C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 7/28 | chr2 | 230450159 | |||||||
chr2:230450347 | C | T | 1 | a0001c0001t0006g0156 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.820+92C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230450347 | |||||||
chr2:230450354 | A | G | 4 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(1): Show |
4 | HG02630.hp2 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.820+99A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230450354 | |||||||
chr2:230450469 | C | T | 4 | a0001c0001t0003g0094 a0001c0001t0018g0066 a0002c0005t0001g0080 others(1): Show |
4 | HG02155.hp1 HG02155.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.820+214C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230450469 | |||||||
chr2:230450543 | A | G | 5 | a0001c0001t0014g0149 a0001c0001t0014g0206 a0001c0001t0014g0229 others(2): Show |
5 | HG00558.hp1 HG02129.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.820+288A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230450543 | |||||||
chr2:230450629 | C | T | 1 | a0004c0006t0004g0238 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.820+374C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230450629 | |||||||
chr2:230450683 | A | G | 1 | a0001c0001t0006g0240 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.820+428A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230450683 | |||||||
chr2:230450701 | C | T | 5 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(2): Show |
5 | HG02486.hp1 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.820+446C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230450701 | |||||||
chr2:230451108 | T | G | 12 | a0001c0001t0002g0254 a0001c0001t0002g0266 a0001c0001t0002g0267 others(9): Show |
12 | HG00280.hp2 HG00733.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.820+853T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230451108 | |||||||
chr2:230451276 | T | C | 3 | a0001c0001t0002g0067 a0002c0005t0001g0068 a0002c0005t0001g0069 |
3 | HG00408.hp1 NA19005.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.820+1021T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230451276 | |||||||
chr2:230451299 | T | C | 2 | a0001c0003t0008g0002 a0002c0005t0001g0256 |
3 | HG02257.hp2 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.820+1044T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230451299 | |||||||
chr2:230451390 | C | T | 162 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(159): Show |
163 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.820+1135C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230451390 | |||||||
chr2:230451797 | A | G | 2 | a0001c0001t0004g0098 a0004c0006t0004g0153 |
2 | HG00099.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.820+1542A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230451797 | |||||||
chr2:230451804 | GTTAAT | G | 108 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0071 others(105): Show |
108 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.820+1552_820+1556d others(7): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr2 | 230451804 | ||||||
chr2:230451943 | A | G | 6 | a0001c0003t0012g0042 a0001c0003t0012g0045 a0001c0003t0012g0046 others(3): Show |
6 | HG02258.hp1 HG02922.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.820+1688A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230451943 | |||||||
chr2:230451990 | T | C | 5 | a0001c0001t0005g0095 a0001c0001t0005g0127 a0001c0001t0019g0126 others(2): Show |
5 | HG02145.hp1 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.820+1735T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230451990 | |||||||
chr2:230452034 | A | G | 3 | a0001c0001t0014g0149 a0001c0001t0014g0206 a0001c0001t0014g0229 |
3 | NA18939.hp1 NA18948.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.820+1779A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230452034 | |||||||
chr2:230452287 | C | T | 2 | a0001c0003t0004g0125 a0003c0004t0002g0269 |
2 | HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.820+2032C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230452287 | |||||||
chr2:230452305 | G | C | 2 | a0001c0019t0015g0035 a0002c0020t0022g0036 |
2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.820+2050G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230452305 | |||||||
chr2:230452455 | C | T | 8 | a0001c0001t0002g0102 a0001c0001t0004g0049 a0001c0001t0004g0050 others(5): Show |
8 | HG01106.hp1 HG02572.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.820+2200C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230452455 | |||||||
chr2:230452456 | G | A | 41 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0071 others(38): Show |
41 | HG00408.hp1 HG00544.hp1 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.820+2201G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230452456 | |||||||
chr2:230452475 | C | A | 4 | a0001c0009t0002g0082 a0001c0009t0010g0064 a0003c0004t0003g0062 others(1): Show |
4 | HG01167.hp2 HG01255.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.820+2220C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230452475 | |||||||
chr2:230452594 | T | G | 1 | a0001c0001t0005g0093 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.820+2339T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230452594 | |||||||
chr2:230452617 | C | T | 1 | a0003c0004t0004g0104 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.820+2362C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230452617 | |||||||
chr2:230452622 | G | A | 4 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(1): Show |
4 | HG02630.hp2 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.820+2367G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230452622 | |||||||
chr2:230452812 | C | G | 62 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0071 others(59): Show |
62 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.820+2557C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230452812 | |||||||
chr2:230452812 | C | T | 1 | a0006c0014t0004g0205 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.820+2557C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230452812 | |||||||
chr2:230452818 | G | GT | 70 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(67): Show |
70 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.820+2582dupT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr2 | 230452818 | ||||||
chr2:230452818 | G | GTT | 16 | a0001c0001t0002g0102 a0001c0001t0004g0049 a0001c0001t0004g0050 others(13): Show |
16 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.820+2581_820+2582d others(4): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr2 | 230452818 | ||||||
chr2:230453126 | A | C | 1 | a0001c0001t0004g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.820+2871A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230453126 | |||||||
chr2:230453188 | G | C | 7 | a0001c0001t0007g0258 a0001c0003t0012g0042 a0001c0003t0012g0045 others(4): Show |
7 | HG02258.hp1 HG02922.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.820+2933G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230453188 | |||||||
chr2:230453218 | T | C | 1 | a0003c0004t0002g0151 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.820+2963T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230453218 | |||||||
chr2:230453479 | T | C | 4 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(1): Show |
4 | HG02630.hp2 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.820+3224T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230453479 | |||||||
chr2:230453530 | T | G | 1 | a0004c0015t0004g0154 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.820+3275T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230453530 | |||||||
chr2:230453574 | A | G | 36 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0071 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.820+3319A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230453574 | |||||||
chr2:230453792 | C | T | 36 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0071 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.820+3537C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230453792 | |||||||
chr2:230453834 | C | T | 1 | a0002c0002t0001g0015 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.820+3579C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230453834 | |||||||
chr2:230453857 | G | A | 4 | a0001c0009t0002g0082 a0001c0009t0010g0064 a0003c0004t0003g0062 others(1): Show |
4 | HG01167.hp2 HG01255.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.820+3602G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230453857 | |||||||
chr2:230453895 | T | C | 60 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0071 others(57): Show |
60 | HG00408.hp1 HG00544.hp1 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.820+3640T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230453895 | |||||||
chr2:230453997 | T | C | 2 | a0001c0001t0020g0286 a0002c0005t0013g0287 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.820+3742T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230453997 | |||||||
chr2:230454388 | ATCTTTCT | A | 2 | a0001c0003t0008g0002 a0002c0005t0001g0256 |
3 | HG02257.hp2 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.820+4142_820+4148d others(9): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr2 | 230454388 | ||||||
chr2:230454465 | A | G | 36 | a0001c0001t0002g0254 a0001c0001t0002g0266 a0001c0001t0002g0267 others(33): Show |
36 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.820+4210A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230454465 | |||||||
chr2:230454517 | A | T | 1 | a0001c0017t0002g0018 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.820+4262A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230454517 | |||||||
chr2:230454540 | T | C | 1 | a0001c0001t0003g0070 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.820+4285T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230454540 | |||||||
chr2:230454706 | T | G | 28 | a0001c0001t0002g0102 a0001c0001t0002g0105 a0001c0001t0002g0274 others(25): Show |
28 | HG00323.hp1 HG00408.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.820+4451T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230454706 | |||||||
chr2:230454783 | A | G | 1 | a0001c0001t0002g0285 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.820+4528A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230454783 | |||||||
chr2:230454936 | A | G | 1 | a0002c0002t0001g0225 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.820+4681A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230454936 | |||||||
chr2:230455119 | G | C | 87 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0071 others(84): Show |
87 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.820+4864G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230455119 | |||||||
chr2:230455229 | T | A | 36 | a0001c0001t0002g0254 a0001c0001t0002g0266 a0001c0001t0002g0267 others(33): Show |
36 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.820+4974T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230455229 | |||||||
chr2:230455262 | T | C | 147 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(144): Show |
147 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.820+5007T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230455262 | |||||||
chr2:230455451 | C | T | 9 | a0001c0001t0005g0252 a0001c0003t0015g0170 a0001c0003t0016g0138 others(6): Show |
9 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.820+5196C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230455451 | |||||||
chr2:230455527 | G | A | 22 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0283 others(19): Show |
22 | HG00280.hp1 HG00738.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.820+5272G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230455527 | |||||||
chr2:230455561 | T | C | 9 | a0001c0001t0005g0124 a0001c0001t0010g0120 a0002c0002t0011g0119 others(6): Show |
9 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.820+5306T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230455561 | |||||||
chr2:230455752 | C | A | 1 | a0002c0002t0001g0193 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.820+5497C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230455752 | |||||||
chr2:230455872 | A | G | 29 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(26): Show |
29 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.821-5390A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230455872 | |||||||
chr2:230456010 | T | G | 146 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(143): Show |
146 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.821-5252T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230456010 | |||||||
chr2:230456056 | T | G | 1 | a0001c0001t0005g0088 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.821-5206T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230456056 | |||||||
chr2:230456088 | G | T | 4 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0003g0114 others(1): Show |
4 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.821-5174G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230456088 | |||||||
chr2:230456120 | T | A | 36 | a0001c0001t0002g0254 a0001c0001t0002g0266 a0001c0001t0002g0267 others(33): Show |
36 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.821-5142T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230456120 | |||||||
chr2:230456125 | C | T | 8 | a0001c0001t0005g0252 a0001c0003t0015g0170 a0001c0003t0016g0138 others(5): Show |
8 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.821-5137C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230456125 | |||||||
chr2:230456193 | A | G | 3 | a0001c0003t0002g0100 a0002c0002t0001g0034 a0002c0002t0001g0118 |
3 | HG02055.hp2 HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.821-5069A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230456193 | |||||||
chr2:230456206 | T | C | 2 | a0002c0002t0001g0131 a0002c0002t0001g0194 |
2 | HG03239.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.821-5056T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230456206 | |||||||
chr2:230456228 | T | C | 2 | a0002c0005t0001g0057 a0002c0005t0001g0058 |
2 | HG02109.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.821-5034T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230456228 | |||||||
chr2:230456245 | T | G | 148 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(145): Show |
148 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.821-5017T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230456245 | |||||||
chr2:230456393 | G | A | 141 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(138): Show |
141 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.821-4869G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230456393 | |||||||
chr2:230456400 | C | T | 1 | a0001c0003t0002g0109 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.821-4862C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230456400 | |||||||
chr2:230456698 | C | G | 1 | a0003c0004t0003g0062 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.821-4564C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230456698 | |||||||
chr2:230457029 | A | T | 3 | a0001c0003t0002g0100 a0002c0002t0001g0034 a0002c0002t0001g0118 |
3 | HG02055.hp2 HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.821-4233A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230457029 | |||||||
chr2:230457151 | A | G | 2 | a0001c0003t0008g0002 a0002c0005t0001g0256 |
3 | HG02257.hp2 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.821-4111A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230457151 | |||||||
chr2:230457288 | G | A | 4 | a0002c0002t0001g0209 a0002c0002t0001g0210 a0002c0002t0001g0231 others(1): Show |
4 | HG00733.hp1 HG01099.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-3974G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230457288 | |||||||
chr2:230457342 | C | T | 1 | a0001c0001t0002g0171 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.821-3920C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230457342 | |||||||
chr2:230457380 | A | G | 2 | a0001c0003t0008g0002 a0002c0005t0001g0256 |
3 | HG02257.hp2 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.821-3882A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230457380 | |||||||
chr2:230457410 | C | T | 12 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0283 others(9): Show |
12 | HG00280.hp1 HG01074.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.821-3852C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230457410 | |||||||
chr2:230457428 | T | C | 2 | a0001c0001t0004g0096 a0005c0013t0024g0161 |
2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.821-3834T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230457428 | |||||||
chr2:230457594 | T | C | 2 | a0003c0004t0003g0142 a0003c0004t0003g0162 |
2 | HG01358.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.821-3668T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230457594 | |||||||
chr2:230457685 | T | C | 4 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(1): Show |
4 | HG02630.hp2 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-3577T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230457685 | |||||||
chr2:230457753 | T | G | 7 | a0001c0001t0007g0258 a0001c0003t0012g0042 a0001c0003t0012g0045 others(4): Show |
7 | HG02258.hp1 HG02922.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.821-3509T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230457753 | |||||||
chr2:230457762 | C | T | 11 | a0001c0001t0004g0096 a0001c0001t0005g0124 a0001c0001t0010g0120 others(8): Show |
11 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.821-3500C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230457762 | |||||||
chr2:230457969 | G | A | 1 | a0001c0003t0003g0110 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.821-3293G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230457969 | |||||||
chr2:230458112 | AG | A | 28 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(25): Show |
28 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.821-3146delG | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr2 | 230458112 | ||||||
chr2:230458116 | G | T | 29 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(26): Show |
29 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.821-3146G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230458116 | |||||||
chr2:230458337 | A | G | 4 | a0001c0003t0002g0100 a0001c0003t0012g0048 a0002c0002t0001g0034 others(1): Show |
4 | HG02055.hp2 HG02615.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.821-2925A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230458337 | |||||||
chr2:230458587 | T | C | 4 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(1): Show |
4 | HG02630.hp2 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-2675T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230458587 | |||||||
chr2:230458620 | C | T | 1 | a0001c0003t0004g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.821-2642C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230458620 | |||||||
chr2:230458888 | A | C | 1 | a0002c0005t0001g0256 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.821-2374A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230458888 | |||||||
chr2:230458947 | A | T | 1 | a0007c0010t0001g0121 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.821-2315A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230458947 | |||||||
chr2:230459298 | T | C | 1 | a0002c0002t0001g0209 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.821-1964T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230459298 | |||||||
chr2:230459530 | G | A | 4 | a0001c0001t0005g0127 a0001c0001t0007g0258 a0002c0005t0001g0256 others(1): Show |
4 | HG02145.hp1 HG02257.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.821-1732G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230459530 | |||||||
chr2:230459589 | A | G | 1 | a0001c0001t0002g0184 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.821-1673A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230459589 | |||||||
chr2:230459690 | C | G | 2 | a0002c0005t0001g0083 a0002c0005t0001g0084 |
2 | HG00544.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.821-1572C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230459690 | |||||||
chr2:230460155 | C | T | 1 | a0001c0001t0007g0173 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.821-1107C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230460155 | |||||||
chr2:230460281 | G | A | 3 | a0002c0005t0001g0010 a0002c0005t0001g0011 a0002c0005t0006g0012 |
3 | NA18978.hp1 NA18994.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.821-981G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230460281 | |||||||
chr2:230460356 | C | T | 2 | a0001c0003t0007g0250 a0001c0003t0007g0251 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.821-906C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230460356 | |||||||
chr2:230460421 | GAGAA | G | 26 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(23): Show |
26 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.821-833_821-830del others(4): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr2 | 230460421 | ||||||
chr2:230460425 | A | G | 15 | a0001c0001t0005g0124 a0001c0001t0020g0286 a0001c0003t0002g0100 others(12): Show |
16 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.821-837A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230460425 | |||||||
chr2:230460454 | C | A | 1 | a0004c0006t0004g0180 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.821-808C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230460454 | |||||||
chr2:230460517 | G | A | 1 | a0001c0001t0006g0230 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.821-745G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230460517 | |||||||
chr2:230460554 | T | C | 1 | a0003c0004t0004g0051 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.821-708T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230460554 | |||||||
chr2:230460579 | TGGTAATC others(336): Show |
T | 161 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(158): Show |
162 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.821-667_821-325del | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr2 | 230460579 | ||||||
chr2:230460592 | C | CT | 18 | a0001c0001t0002g0167 a0001c0001t0003g0199 a0001c0003t0003g0227 others(15): Show |
18 | HG00544.hp2 HG00735.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.821-628dupT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr2 | 230460592 | ||||||
chr2:230460592 | C | CTT | 6 | a0001c0001t0006g0240 a0002c0002t0001g0015 a0002c0002t0001g0216 others(3): Show |
6 | HG02040.hp2 HG02071.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.821-629_821-628dup others(2): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr2 | 230460592 | ||||||
chr2:230460592 | CT | C | 16 | a0001c0001t0005g0088 a0001c0001t0005g0091 a0001c0001t0005g0093 others(13): Show |
16 | HG00323.hp2 HG01884.hp1 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.821-628delT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr2 | 230460592 | ||||||
chr2:230460592 | CTTTTTTT others(3): Show |
C | 2 | a0001c0003t0003g0063 a0002c0002t0001g0235 |
2 | HG02523.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.821-637_821-628del others(10): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr2 | 230460592 | ||||||
chr2:230460592 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0002g0171 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.821-641_821-628del others(14): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr2 | 230460592 | ||||||
chr2:230460592 | CTTTTTTT others(13): Show |
C | 1 | a0001c0001t0014g0229 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.821-647_821-628del others(20): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr2 | 230460592 | ||||||
chr2:230460592 | CTTTTTTT others(14): Show |
C | 26 | a0001c0001t0002g0148 a0001c0001t0004g0098 a0001c0001t0014g0149 others(23): Show |
26 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.821-648_821-628del others(21): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr2 | 230460592 | ||||||
chr2:230460592 | CTTTTTTT others(15): Show |
C | 2 | a0001c0001t0006g0223 a0003c0004t0003g0189 |
2 | HG04199.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.821-649_821-628del others(22): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr2 | 230460592 | ||||||
chr2:230460960 | C | T | 1 | a0005c0008t0003g0003 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.821-302C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230460960 | |||||||
chr2:230461017 | A | AT | 283 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(280): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.821-237dupT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr2 | 230461017 | ||||||
chr2:230461026 | A | T | 5 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(2): Show |
5 | HG02486.hp1 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.821-236A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230461026 | |||||||
chr2:230461047 | C | T | 1 | a0001c0003t0005g0092 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.821-215C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230461047 | |||||||
chr2:230461059 | C | A | 5 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(2): Show |
5 | HG02486.hp1 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.821-203C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230461059 | |||||||
chr2:230461145 | G | A | 7 | a0001c0001t0005g0252 a0001c0003t0015g0170 a0002c0002t0011g0145 others(4): Show |
7 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.821-117G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230461145 | |||||||
chr2:230461207 | A | G | 1 | a0001c0001t0007g0079 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.821-55A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230461207 | |||||||
chr2:230461229 | C | G | 5 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(2): Show |
5 | HG02486.hp1 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.821-33C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 8/28 | chr2 | 230461229 | |||||||
chr2:230461433 | G | A | 5 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(2): Show |
5 | HG02486.hp1 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.973+19G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 9/28 | chr2 | 230461433 | |||||||
chr2:230461473 | A | G | 43 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(40): Show |
44 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.973+59A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 9/28 | chr2 | 230461473 | |||||||
chr2:230461486 | C | G | 43 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(40): Show |
44 | HG00673.hp2 HG00738.hp1 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.973+72C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 9/28 | chr2 | 230461486 | |||||||
chr2:230461693 | A | G | 6 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(3): Show |
6 | HG02486.hp1 HG03041.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.973+279A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 9/28 | chr2 | 230461693 | |||||||
chr2:230461906 | G | A | 35 | a0001c0001t0002g0148 a0001c0001t0014g0149 a0001c0001t0014g0206 others(32): Show |
36 | HG00140.hp2 HG00558.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.973+492G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 9/28 | chr2 | 230461906 | |||||||
chr2:230461955 | G | A | 2 | a0001c0003t0002g0100 a0002c0002t0001g0118 |
2 | HG02055.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.974-480G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 9/28 | chr2 | 230461955 | |||||||
chr2:230461955 | G | GA | 10 | a0001c0001t0004g0096 a0001c0001t0005g0124 a0001c0001t0019g0126 others(7): Show |
10 | HG02145.hp2 HG02486.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.974-470dupA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 9/28 | INFO_REALIGN_3_PRIME | chr2 | 230461955 | ||||||
chr2:230461990 | A | G | 3 | a0001c0003t0004g0249 a0001c0003t0005g0092 a0001c0003t0012g0247 |
3 | HG02055.hp1 HG02897.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.974-445A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 9/28 | chr2 | 230461990 | |||||||
chr2:230462011 | G | A | 2 | a0001c0003t0012g0048 a0002c0002t0013g0038 |
2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.974-424G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 9/28 | chr2 | 230462011 | |||||||
chr2:230462228 | A | T | 1 | a0001c0001t0002g0065 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.974-207A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 9/28 | chr2 | 230462228 | |||||||
chr2:230462229 | C | A | 1 | a0001c0001t0002g0065 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.974-206C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 9/28 | chr2 | 230462229 | |||||||
chr2:230462230 | A | C | 1 | a0001c0001t0002g0065 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.974-205A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 9/28 | chr2 | 230462230 | |||||||
chr2:230462234 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.974-201G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 9/28 | chr2 | 230462234 | |||||||
chr2:230462235 | C | G | 1 | a0001c0001t0002g0065 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.974-200C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 9/28 | chr2 | 230462235 | |||||||
chr2:230462236 | C | A | 1 | a0001c0001t0002g0065 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.974-199C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 9/28 | chr2 | 230462236 | |||||||
chr2:230462238 | T | C | 1 | a0001c0001t0002g0065 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.974-197T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 9/28 | chr2 | 230462238 | |||||||
chr2:230462239 | C | G | 1 | a0001c0001t0002g0065 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.974-196C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 9/28 | chr2 | 230462239 | |||||||
chr2:230462240 | T | C | 1 | a0001c0001t0002g0065 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.974-195T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 9/28 | chr2 | 230462240 | |||||||
chr2:230462245 | G | T | 1 | a0001c0001t0002g0065 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.974-190G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 9/28 | chr2 | 230462245 | |||||||
chr2:230462576 | A | G | 60 | a0001c0001t0002g0167 a0001c0001t0002g0203 a0001c0001t0002g0204 others(57): Show |
60 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.1057+58A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230462576 | |||||||
chr2:230462630 | C | A | 1 | a0003c0004t0004g0051 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1057+112C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230462630 | |||||||
chr2:230462631 | T | C | 1 | a0008c0022t0006g0014 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1057+113T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230462631 | |||||||
chr2:230462715 | G | A | 41 | a0001c0003t0008g0002 a0003c0004t0002g0113 a0003c0004t0002g0117 others(38): Show |
42 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(39): Show |
intron_variant | MODIFIER | c.1057+197G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230462715 | |||||||
chr2:230462807 | T | G | 2 | a0002c0002t0001g0034 a0005c0013t0024g0161 |
2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1057+289T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230462807 | |||||||
chr2:230462831 | T | C | 1 | a0001c0001t0002g0175 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1057+313T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230462831 | |||||||
chr2:230462863 | T | G | 9 | a0001c0001t0005g0252 a0001c0003t0012g0042 a0001c0003t0012g0045 others(6): Show |
9 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1057+345T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230462863 | |||||||
chr2:230462907 | G | C | 45 | a0001c0001t0010g0260 a0001c0003t0008g0002 a0003c0004t0002g0113 others(42): Show |
46 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(43): Show |
intron_variant | MODIFIER | c.1057+389G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230462907 | |||||||
chr2:230462972 | T | A | 6 | a0001c0001t0005g0095 a0001c0001t0020g0286 a0002c0005t0001g0052 others(3): Show |
6 | HG02809.hp1 HG03041.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1057+454T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230462972 | |||||||
chr2:230462973 | G | A | 44 | a0001c0003t0008g0002 a0003c0004t0002g0113 a0003c0004t0002g0117 others(41): Show |
45 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(42): Show |
intron_variant | MODIFIER | c.1057+455G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230462973 | |||||||
chr2:230463141 | C | T | 44 | a0001c0003t0008g0002 a0003c0004t0002g0113 a0003c0004t0002g0117 others(41): Show |
45 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(42): Show |
intron_variant | MODIFIER | c.1057+623C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230463141 | |||||||
chr2:230463307 | A | G | 5 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(2): Show |
5 | HG02572.hp1 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1058-760A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230463307 | |||||||
chr2:230463363 | A | G | 44 | a0001c0003t0008g0002 a0003c0004t0002g0113 a0003c0004t0002g0117 others(41): Show |
45 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(42): Show |
intron_variant | MODIFIER | c.1058-704A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230463363 | |||||||
chr2:230463446 | T | C | 1 | a0005c0008t0005g0004 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1058-621T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230463446 | |||||||
chr2:230463459 | G | A | 2 | a0001c0003t0003g0110 a0001c0003t0007g0111 |
2 | HG00408.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1058-608G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230463459 | |||||||
chr2:230463569 | A | C | 1 | a0001c0003t0005g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1058-498A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230463569 | |||||||
chr2:230463697 | C | G | 44 | a0001c0003t0008g0002 a0003c0004t0002g0113 a0003c0004t0002g0117 others(41): Show |
45 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(42): Show |
intron_variant | MODIFIER | c.1058-370C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230463697 | |||||||
chr2:230463711 | G | C | 44 | a0001c0003t0008g0002 a0003c0004t0002g0113 a0003c0004t0002g0117 others(41): Show |
45 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(42): Show |
intron_variant | MODIFIER | c.1058-356G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230463711 | |||||||
chr2:230463747 | G | A | 1 | a0002c0020t0022g0036 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1058-320G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230463747 | |||||||
chr2:230463865 | T | G | 45 | a0001c0003t0008g0002 a0003c0004t0002g0113 a0003c0004t0002g0117 others(42): Show |
46 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(43): Show |
intron_variant | MODIFIER | c.1058-202T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230463865 | |||||||
chr2:230463927 | A | G | 1 | a0001c0001t0005g0095 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1058-140A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230463927 | |||||||
chr2:230463951 | C | T | 2 | a0001c0001t0007g0173 a0001c0001t0025g0060 |
2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1058-116C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230463951 | |||||||
chr2:230463963 | C | T | 1 | a0001c0001t0019g0126 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1058-104C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230463963 | |||||||
chr2:230463965 | G | A | 1 | a0001c0001t0002g0195 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1058-102G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230463965 | |||||||
chr2:230463965 | G | T | 1 | a0003c0004t0003g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1058-102G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230463965 | |||||||
chr2:230463981 | C | T | 85 | a0001c0001t0005g0252 a0001c0001t0007g0173 a0001c0001t0025g0060 others(82): Show |
86 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.1058-86C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230463981 | |||||||
chr2:230464005 | C | T | 28 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(25): Show |
intron_variant | MODIFIER | c.1058-62C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230464005 | |||||||
chr2:230464013 | C | T | 45 | a0001c0003t0008g0002 a0003c0004t0002g0113 a0003c0004t0002g0117 others(42): Show |
46 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(43): Show |
intron_variant | MODIFIER | c.1058-54C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230464013 | |||||||
chr2:230464015 | G | T | 1 | a0001c0003t0004g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1058-52G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 10/28 | chr2 | 230464015 | |||||||
chr2:230464334 | T | C | 1 | a0001c0001t0002g0195 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1141+184T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | chr2 | 230464334 | |||||||
chr2:230464335 | G | A | 45 | a0001c0003t0008g0002 a0003c0004t0002g0113 a0003c0004t0002g0117 others(42): Show |
46 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(43): Show |
intron_variant | MODIFIER | c.1141+185G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | chr2 | 230464335 | |||||||
chr2:230464519 | A | G | 1 | a0003c0004t0002g0259 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1141+369A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | chr2 | 230464519 | |||||||
chr2:230464608 | T | C | 73 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(70): Show |
73 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.1141+458T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | chr2 | 230464608 | |||||||
chr2:230464611 | CA | C | 46 | a0001c0003t0008g0002 a0003c0004t0002g0113 a0003c0004t0002g0117 others(43): Show |
47 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(44): Show |
intron_variant | MODIFIER | c.1141+470delA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr2 | 230464611 | ||||||
chr2:230464685 | C | T | 4 | a0001c0001t0005g0127 a0001c0001t0007g0258 a0002c0005t0001g0256 others(1): Show |
4 | HG02145.hp1 HG02257.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1141+535C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | chr2 | 230464685 | |||||||
chr2:230464802 | G | A | 45 | a0001c0003t0008g0002 a0003c0004t0002g0113 a0003c0004t0002g0117 others(42): Show |
46 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(43): Show |
intron_variant | MODIFIER | c.1141+652G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | chr2 | 230464802 | |||||||
chr2:230464810 | T | C | 1 | a0003c0004t0004g0104 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1141+660T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | chr2 | 230464810 | |||||||
chr2:230464853 | G | A | 1 | a0007c0010t0001g0168 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1141+703G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | chr2 | 230464853 | |||||||
chr2:230464922 | C | T | 45 | a0001c0003t0008g0002 a0003c0004t0002g0113 a0003c0004t0002g0117 others(42): Show |
46 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(43): Show |
intron_variant | MODIFIER | c.1141+772C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | chr2 | 230464922 | |||||||
chr2:230465005 | G | A | 45 | a0001c0003t0008g0002 a0003c0004t0002g0113 a0003c0004t0002g0117 others(42): Show |
46 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(43): Show |
intron_variant | MODIFIER | c.1141+855G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | chr2 | 230465005 | |||||||
chr2:230465034 | G | C | 2 | a0001c0001t0007g0173 a0001c0001t0025g0060 |
2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1141+884G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | chr2 | 230465034 | |||||||
chr2:230465142 | C | A | 45 | a0001c0003t0008g0002 a0003c0004t0002g0113 a0003c0004t0002g0117 others(42): Show |
46 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(43): Show |
intron_variant | MODIFIER | c.1141+992C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | chr2 | 230465142 | |||||||
chr2:230465178 | G | T | 45 | a0001c0003t0008g0002 a0003c0004t0002g0113 a0003c0004t0002g0117 others(42): Show |
46 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(43): Show |
intron_variant | MODIFIER | c.1141+1028G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | chr2 | 230465178 | |||||||
chr2:230465193 | A | G | 86 | a0001c0001t0005g0252 a0001c0003t0002g0100 a0001c0003t0002g0108 others(83): Show |
87 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.1141+1043A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | chr2 | 230465193 | |||||||
chr2:230465256 | A | C | 45 | a0001c0003t0008g0002 a0003c0004t0002g0113 a0003c0004t0002g0117 others(42): Show |
46 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(43): Show |
intron_variant | MODIFIER | c.1142-1045A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | chr2 | 230465256 | |||||||
chr2:230465485 | C | G | 6 | a0002c0002t0011g0119 a0002c0002t0011g0145 a0002c0002t0011g0157 others(3): Show |
6 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1142-816C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | chr2 | 230465485 | |||||||
chr2:230465731 | C | T | 45 | a0001c0003t0008g0002 a0003c0004t0002g0113 a0003c0004t0002g0117 others(42): Show |
46 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(43): Show |
intron_variant | MODIFIER | c.1142-570C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | chr2 | 230465731 | |||||||
chr2:230465805 | A | G | 45 | a0001c0003t0008g0002 a0003c0004t0002g0113 a0003c0004t0002g0117 others(42): Show |
46 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(43): Show |
intron_variant | MODIFIER | c.1142-496A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | chr2 | 230465805 | |||||||
chr2:230465823 | C | T | 45 | a0001c0003t0008g0002 a0003c0004t0002g0113 a0003c0004t0002g0117 others(42): Show |
46 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(43): Show |
intron_variant | MODIFIER | c.1142-478C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | chr2 | 230465823 | |||||||
chr2:230465852 | T | C | 1 | a0001c0001t0002g0006 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1142-449T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | chr2 | 230465852 | |||||||
chr2:230465923 | G | T | 2 | a0001c0001t0007g0173 a0001c0001t0025g0060 |
2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1142-378G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | chr2 | 230465923 | |||||||
chr2:230466042 | G | T | 1 | a0001c0001t0019g0126 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1142-259G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | chr2 | 230466042 | |||||||
chr2:230466111 | G | A | 45 | a0001c0003t0008g0002 a0003c0004t0002g0113 a0003c0004t0002g0117 others(42): Show |
46 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(43): Show |
intron_variant | MODIFIER | c.1142-190G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | chr2 | 230466111 | |||||||
chr2:230466184 | C | CAAAA | 44 | a0001c0003t0008g0002 a0003c0004t0002g0113 a0003c0004t0002g0117 others(41): Show |
45 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(42): Show |
intron_variant | MODIFIER | c.1142-101_1142-98du others(5): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr2 | 230466184 | ||||||
chr2:230466184 | C | CAAAAAA | 81 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(78): Show |
81 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1142-103_1142-98du others(7): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr2 | 230466184 | ||||||
chr2:230466184 | C | CAAAAAAA | 15 | a0001c0001t0002g0105 a0001c0001t0002g0195 a0001c0001t0002g0200 others(12): Show |
15 | HG01123.hp2 HG01346.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.1142-104_1142-98du others(8): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr2 | 230466184 | ||||||
chr2:230466184 | CA | C | 44 | a0001c0001t0005g0252 a0001c0003t0002g0013 a0001c0003t0002g0100 others(41): Show |
44 | HG00408.hp2 HG00733.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.1142-98delA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr2 | 230466184 | ||||||
chr2:230466201 | A | AAAAAAC | 38 | a0001c0001t0002g0027 a0001c0001t0002g0102 a0001c0001t0003g0029 others(35): Show |
38 | HG00544.hp1 HG00558.hp1 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.1142-98_1142-97ins others(6): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr2 | 230466201 | ||||||
chr2:230466207 | T | A | 1 | a0001c0003t0008g0002 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1142-94T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 11/28 | chr2 | 230466207 | |||||||
chr2:230466664 | G | A | 1 | a0002c0005t0001g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1195+310G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 12/28 | chr2 | 230466664 | |||||||
chr2:230466979 | A | G | 179 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(176): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.1196-141A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 12/28 | chr2 | 230466979 | |||||||
chr2:230466986 | A | AG | 179 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(176): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.1196-132dupG | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 12/28 | INFO_REALIGN_3_PRIME | chr2 | 230466986 | ||||||
chr2:230466991 | C | T | 42 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(39): Show |
42 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(39): Show |
intron_variant | MODIFIER | c.1196-129C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 12/28 | chr2 | 230466991 | |||||||
chr2:230467084 | T | C | 183 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(180): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1196-36T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 12/28 | chr2 | 230467084 | |||||||
chr2:230467367 | C | T | 2 | a0001c0001t0020g0286 a0002c0005t0013g0287 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1291+152C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | chr2 | 230467367 | |||||||
chr2:230467480 | G | A | 43 | a0001c0001t0002g0019 a0001c0001t0002g0027 a0001c0001t0002g0102 others(40): Show |
43 | HG00544.hp1 HG00558.hp1 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.1291+265G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | chr2 | 230467480 | |||||||
chr2:230467503 | G | A | 43 | a0001c0001t0002g0019 a0001c0001t0002g0027 a0001c0001t0002g0102 others(40): Show |
43 | HG00544.hp1 HG00558.hp1 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.1291+288G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | chr2 | 230467503 | |||||||
chr2:230467503 | G | T | 45 | a0001c0001t0010g0169 a0003c0004t0002g0113 a0003c0004t0002g0117 others(42): Show |
45 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(42): Show |
intron_variant | MODIFIER | c.1291+288G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | chr2 | 230467503 | |||||||
chr2:230467564 | G | C | 28 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(25): Show |
intron_variant | MODIFIER | c.1291+349G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | chr2 | 230467564 | |||||||
chr2:230467579 | T | C | 225 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(222): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1291+364T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | chr2 | 230467579 | |||||||
chr2:230467602 | C | G | 194 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(191): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1291+387C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | chr2 | 230467602 | |||||||
chr2:230467623 | T | C | 4 | a0001c0003t0002g0100 a0001c0003t0012g0048 a0002c0002t0001g0118 others(1): Show |
4 | HG02055.hp2 HG02486.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1291+408T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | chr2 | 230467623 | |||||||
chr2:230467628 | C | T | 228 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(225): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1291+413C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | chr2 | 230467628 | |||||||
chr2:230467690 | A | G | 42 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(39): Show |
42 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(39): Show |
intron_variant | MODIFIER | c.1291+475A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | chr2 | 230467690 | |||||||
chr2:230467834 | T | C | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1291+619T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | chr2 | 230467834 | |||||||
chr2:230468094 | T | C | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1291+879T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | chr2 | 230468094 | |||||||
chr2:230468095 | G | A | 1 | a0003c0004t0003g0189 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1291+880G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | chr2 | 230468095 | |||||||
chr2:230468134 | C | G | 10 | a0001c0003t0012g0042 a0001c0003t0012g0045 a0001c0003t0012g0046 others(7): Show |
10 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1292-909C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | chr2 | 230468134 | |||||||
chr2:230468192 | G | A | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1292-851G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | chr2 | 230468192 | |||||||
chr2:230468338 | T | C | 227 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(224): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1292-705T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | chr2 | 230468338 | |||||||
chr2:230468437 | C | T | 1 | a0011c0011t0003g0086 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1292-606C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | chr2 | 230468437 | |||||||
chr2:230468440 | A | G | 1 | a0001c0001t0004g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1292-603A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | chr2 | 230468440 | |||||||
chr2:230468464 | T | G | 6 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(3): Show |
6 | HG01884.hp1 HG02572.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1292-579T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | chr2 | 230468464 | |||||||
chr2:230468491 | G | C | 2 | a0001c0007t0005g0032 a0001c0007t0005g0033 |
2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1292-552G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | chr2 | 230468491 | |||||||
chr2:230468491 | GAAA | G | 42 | a0001c0001t0002g0027 a0001c0001t0002g0102 a0001c0001t0003g0029 others(39): Show |
42 | HG00544.hp1 HG00558.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.1292-550_1292-548d others(5): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr2 | 230468491 | ||||||
chr2:230468542 | C | T | 147 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(144): Show |
147 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.1292-501C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | chr2 | 230468542 | |||||||
chr2:230468566 | AGGCTGAG others(1): Show |
A | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1292-468_1292-461d others(10): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr2 | 230468566 | ||||||
chr2:230468570 | T | C | 34 | a0001c0003t0002g0100 a0001c0003t0002g0108 a0001c0003t0002g0109 others(31): Show |
35 | HG00408.hp2 HG00733.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.1292-473T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | chr2 | 230468570 | |||||||
chr2:230468701 | C | T | 73 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(70): Show |
73 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.1292-342C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | chr2 | 230468701 | |||||||
chr2:230468790 | C | T | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1292-253C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | chr2 | 230468790 | |||||||
chr2:230468794 | G | A | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1292-249G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | chr2 | 230468794 | |||||||
chr2:230468817 | C | CA | 36 | a0001c0001t0002g0254 a0001c0001t0002g0266 a0001c0001t0002g0268 others(33): Show |
36 | HG00408.hp2 HG01074.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.1292-202dupA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr2 | 230468817 | ||||||
chr2:230468817 | C | CAA | 9 | a0001c0001t0002g0195 a0001c0001t0008g0039 a0001c0001t0008g0040 others(6): Show |
9 | HG00733.hp2 HG01884.hp1 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.1292-203_1292-202d others(4): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr2 | 230468817 | ||||||
chr2:230468817 | C | CAAA | 62 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(59): Show |
62 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.1292-204_1292-202d others(5): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr2 | 230468817 | ||||||
chr2:230468817 | C | CAAAA | 8 | a0001c0001t0002g0167 a0001c0001t0002g0174 a0001c0001t0002g0200 others(5): Show |
8 | HG01361.hp1 HG01981.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1292-205_1292-202d others(6): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr2 | 230468817 | ||||||
chr2:230468817 | CAAAAAAA | C | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1292-208_1292-202d others(9): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr2 | 230468817 | ||||||
chr2:230468817 | CAAAAAAA others(3): Show |
C | 1 | a0002c0002t0001g0244 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1292-211_1292-202d others(12): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr2 | 230468817 | ||||||
chr2:230468817 | CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0007g0173 a0001c0001t0025g0060 |
2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1292-213_1292-202d others(14): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr2 | 230468817 | ||||||
chr2:230468821 | A | AG | 41 | a0001c0001t0002g0027 a0001c0001t0002g0102 a0001c0001t0003g0029 others(38): Show |
41 | HG00544.hp1 HG00558.hp1 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.1292-222_1292-221i others(3): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | chr2 | 230468821 | |||||||
chr2:230468824 | A | AAAT | 10 | a0001c0003t0012g0042 a0001c0003t0012g0045 a0001c0003t0012g0046 others(7): Show |
10 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1292-217_1292-216i others(5): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr2 | 230468824 | ||||||
chr2:230468830 | A | G | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1292-213A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | chr2 | 230468830 | |||||||
chr2:230468889 | A | C | 10 | a0001c0003t0012g0042 a0001c0003t0012g0045 a0001c0003t0012g0046 others(7): Show |
10 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1292-154A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 13/28 | chr2 | 230468889 | |||||||
chr2:230469119 | G | A | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1345+23G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 14/28 | chr2 | 230469119 | |||||||
chr2:230469137 | A | C | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1345+41A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 14/28 | chr2 | 230469137 | |||||||
chr2:230469175 | C | T | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1345+79C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 14/28 | chr2 | 230469175 | |||||||
chr2:230469278 | C | G | 1 | a0001c0001t0003g0077 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1345+182C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 14/28 | chr2 | 230469278 | |||||||
chr2:230469282 | G | A | 2 | a0001c0001t0007g0173 a0001c0001t0025g0060 |
2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1345+186G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 14/28 | chr2 | 230469282 | |||||||
chr2:230469295 | C | T | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1345+199C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 14/28 | chr2 | 230469295 | |||||||
chr2:230469296 | A | G | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1345+200A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 14/28 | chr2 | 230469296 | |||||||
chr2:230469501 | T | C | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1345+405T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 14/28 | chr2 | 230469501 | |||||||
chr2:230469584 | G | A | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1346-431G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 14/28 | chr2 | 230469584 | |||||||
chr2:230469706 | A | C | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1346-309A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 14/28 | chr2 | 230469706 | |||||||
chr2:230469789 | AAAAG | A | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1346-223_1346-220d others(6): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr2 | 230469789 | ||||||
chr2:230469817 | G | A | 5 | a0001c0001t0002g0105 a0001c0001t0002g0254 a0001c0001t0002g0266 others(2): Show |
5 | HG01123.hp2 HG01243.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.1346-198G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 14/28 | chr2 | 230469817 | |||||||
chr2:230469865 | G | C | 1 | a0001c0001t0010g0260 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1346-150G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 14/28 | chr2 | 230469865 | |||||||
chr2:230469898 | G | A | 6 | a0001c0001t0002g0105 a0001c0001t0002g0254 a0001c0001t0002g0266 others(3): Show |
6 | HG01123.hp2 HG01243.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346-117G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 14/28 | chr2 | 230469898 | |||||||
chr2:230469964 | A | G | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1346-51A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 14/28 | chr2 | 230469964 | |||||||
chr2:230470379 | C | A | 2 | a0001c0003t0003g0110 a0001c0003t0007g0111 |
2 | HG00408.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1429+281C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230470379 | |||||||
chr2:230470396 | A | G | 2 | a0002c0005t0001g0068 a0002c0005t0001g0069 |
2 | NA19005.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1429+298A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230470396 | |||||||
chr2:230470444 | A | G | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1429+346A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230470444 | |||||||
chr2:230470532 | G | A | 2 | a0001c0001t0002g0065 a0001c0001t0002g0071 |
2 | HG02129.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1429+434G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230470532 | |||||||
chr2:230470597 | C | A | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1429+499C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230470597 | |||||||
chr2:230470655 | A | G | 1 | a0001c0001t0002g0008 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1429+557A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230470655 | |||||||
chr2:230470672 | G | A | 1 | a0001c0001t0002g0019 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1429+574G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230470672 | |||||||
chr2:230470714 | A | G | 1 | a0001c0001t0005g0124 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1429+616A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230470714 | |||||||
chr2:230470741 | G | C | 2 | a0001c0003t0004g0249 a0001c0003t0012g0247 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1429+643G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230470741 | |||||||
chr2:230470751 | G | A | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1429+653G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230470751 | |||||||
chr2:230470857 | A | G | 1 | a0001c0003t0003g0183 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1429+759A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230470857 | |||||||
chr2:230470894 | C | CTGTG | 3 | a0001c0001t0007g0173 a0001c0001t0025g0060 a0002c0020t0022g0036 |
3 | HG01891.hp2 HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1429+812_1429+815d others(6): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | INFO_REALIGN_3_PRIME | chr2 | 230470894 | ||||||
chr2:230470945 | TATAC | T | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1429+855_1429+858d others(6): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | INFO_REALIGN_3_PRIME | chr2 | 230470945 | ||||||
chr2:230470965 | CAT | C | 73 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(70): Show |
73 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.1429+870_1429+871d others(4): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | INFO_REALIGN_3_PRIME | chr2 | 230470965 | ||||||
chr2:230470968 | A | G | 147 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(144): Show |
147 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.1429+870A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230470968 | |||||||
chr2:230471133 | C | G | 1 | a0002c0005t0013g0106 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1429+1035C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230471133 | |||||||
chr2:230471141 | C | T | 4 | a0002c0002t0001g0209 a0002c0002t0001g0210 a0002c0002t0001g0231 others(1): Show |
4 | HG00733.hp1 HG01099.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1429+1043C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230471141 | |||||||
chr2:230471179 | T | A | 195 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(192): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1429+1081T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230471179 | |||||||
chr2:230471220 | G | A | 1 | a0001c0001t0002g0184 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1429+1122G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230471220 | |||||||
chr2:230471405 | C | T | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1429+1307C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230471405 | |||||||
chr2:230471479 | C | T | 1 | a0001c0003t0005g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1429+1381C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230471479 | |||||||
chr2:230471530 | G | A | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1429+1432G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230471530 | |||||||
chr2:230471545 | T | C | 2 | a0003c0004t0003g0062 a0003c0004t0003g0081 |
2 | HG01496.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1429+1447T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230471545 | |||||||
chr2:230471584 | G | C | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1429+1486G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230471584 | |||||||
chr2:230471590 | T | C | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1429+1492T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230471590 | |||||||
chr2:230471628 | G | A | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1429+1530G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230471628 | |||||||
chr2:230471686 | G | A | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1429+1588G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230471686 | |||||||
chr2:230471703 | G | A | 1 | a0002c0020t0022g0036 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1429+1605G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230471703 | |||||||
chr2:230471883 | G | A | 1 | a0003c0004t0004g0104 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1430-1441G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230471883 | |||||||
chr2:230472029 | T | A | 49 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(46): Show |
49 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.1430-1295T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230472029 | |||||||
chr2:230472166 | T | C | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1430-1158T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230472166 | |||||||
chr2:230472204 | G | A | 2 | a0001c0003t0004g0249 a0001c0003t0012g0247 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1430-1120G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230472204 | |||||||
chr2:230472263 | C | T | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1430-1061C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230472263 | |||||||
chr2:230472279 | T | C | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1430-1045T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230472279 | |||||||
chr2:230472342 | G | T | 3 | a0001c0003t0002g0100 a0001c0003t0012g0048 a0002c0002t0013g0038 |
3 | HG02486.hp1 HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1430-982G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230472342 | |||||||
chr2:230472382 | C | T | 2 | a0001c0003t0004g0249 a0001c0003t0012g0247 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1430-942C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230472382 | |||||||
chr2:230472427 | C | CA | 24 | a0001c0001t0002g0105 a0001c0001t0002g0174 a0001c0001t0002g0195 others(21): Show |
25 | HG00738.hp2 HG01109.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.1430-872dupA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | INFO_REALIGN_3_PRIME | chr2 | 230472427 | ||||||
chr2:230472427 | C | CAA | 21 | a0001c0003t0002g0013 a0001c0003t0002g0108 a0001c0003t0002g0109 others(18): Show |
21 | HG00733.hp2 HG01074.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.1430-873_1430-872d others(4): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | INFO_REALIGN_3_PRIME | chr2 | 230472427 | ||||||
chr2:230472427 | CA | C | 67 | a0001c0001t0002g0027 a0001c0001t0002g0102 a0001c0001t0002g0175 others(64): Show |
67 | HG00544.hp1 HG00558.hp1 HG01123.hp1 others(64): Show |
intron_variant | MODIFIER | c.1430-872delA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | INFO_REALIGN_3_PRIME | chr2 | 230472427 | ||||||
chr2:230472427 | CAAAAAAA others(2): Show |
C | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1430-880_1430-872d others(11): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | INFO_REALIGN_3_PRIME | chr2 | 230472427 | ||||||
chr2:230472550 | G | T | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1430-774G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230472550 | |||||||
chr2:230472651 | A | G | 4 | a0001c0003t0015g0170 a0001c0019t0015g0035 a0002c0002t0001g0005 others(1): Show |
4 | HG02572.hp2 HG02615.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1430-673A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230472651 | |||||||
chr2:230472772 | C | T | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1430-552C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230472772 | |||||||
chr2:230472783 | A | G | 2 | a0001c0001t0007g0173 a0001c0001t0025g0060 |
2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1430-541A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230472783 | |||||||
chr2:230472831 | A | C | 193 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(190): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1430-493A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230472831 | |||||||
chr2:230472885 | C | T | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1430-439C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230472885 | |||||||
chr2:230472893 | T | C | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1430-431T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230472893 | |||||||
chr2:230472943 | T | C | 2 | a0001c0001t0020g0286 a0002c0005t0013g0287 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1430-381T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230472943 | |||||||
chr2:230472944 | C | T | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1430-380C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230472944 | |||||||
chr2:230472988 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1430-336C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230472988 | |||||||
chr2:230473245 | C | T | 228 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(225): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1430-79C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 15/28 | chr2 | 230473245 | |||||||
chr2:230473496 | T | G | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1546+56T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 16/28 | chr2 | 230473496 | |||||||
chr2:230473599 | A | G | 1 | a0002c0005t0001g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1546+159A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 16/28 | chr2 | 230473599 | |||||||
chr2:230473617 | C | T | 3 | a0001c0001t0007g0173 a0001c0001t0025g0060 a0002c0020t0022g0036 |
3 | HG01891.hp2 HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1546+177C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 16/28 | chr2 | 230473617 | |||||||
chr2:230473881 | C | G | 1 | a0001c0001t0002g0102 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1546+441C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 16/28 | chr2 | 230473881 | |||||||
chr2:230473972 | G | C | 5 | a0001c0001t0005g0095 a0001c0001t0020g0286 a0002c0005t0001g0052 others(2): Show |
5 | HG02809.hp1 HG03041.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1547-422G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 16/28 | chr2 | 230473972 | |||||||
chr2:230474247 | T | C | 2 | a0001c0003t0004g0249 a0001c0003t0012g0247 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1547-147T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 16/28 | chr2 | 230474247 | |||||||
chr2:230474686 | C | T | 1 | a0001c0003t0005g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1600+239C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230474686 | |||||||
chr2:230474782 | G | T | 1 | a0002c0005t0006g0012 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1600+335G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230474782 | |||||||
chr2:230474812 | G | A | 1 | a0001c0001t0004g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1600+365G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230474812 | |||||||
chr2:230474820 | T | A | 73 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(70): Show |
73 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.1600+373T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230474820 | |||||||
chr2:230474830 | C | T | 1 | a0001c0001t0002g0184 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1600+383C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230474830 | |||||||
chr2:230475016 | A | G | 73 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(70): Show |
73 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.1600+569A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230475016 | |||||||
chr2:230475151 | A | G | 2 | a0001c0001t0020g0286 a0002c0005t0013g0287 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1600+704A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230475151 | |||||||
chr2:230475152 | C | G | 1 | a0001c0003t0016g0138 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1600+705C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230475152 | |||||||
chr2:230475190 | A | G | 1 | a0001c0001t0002g0274 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1600+743A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230475190 | |||||||
chr2:230475278 | A | T | 1 | a0001c0003t0008g0002 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1600+831A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230475278 | |||||||
chr2:230475358 | T | C | 1 | a0002c0002t0001g0144 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1600+911T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230475358 | |||||||
chr2:230475388 | G | A | 1 | a0001c0001t0002g0175 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1600+941G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230475388 | |||||||
chr2:230475441 | T | G | 1 | a0001c0003t0004g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1600+994T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230475441 | |||||||
chr2:230475446 | T | C | 11 | a0001c0001t0002g0105 a0001c0001t0002g0254 a0001c0001t0002g0266 others(8): Show |
11 | HG01109.hp1 HG01123.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1600+999T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230475446 | |||||||
chr2:230475495 | T | C | 1 | a0002c0020t0022g0036 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1600+1048T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230475495 | |||||||
chr2:230475621 | G | A | 42 | a0001c0001t0002g0027 a0001c0001t0002g0102 a0001c0001t0003g0029 others(39): Show |
42 | HG00544.hp1 HG00558.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.1600+1174G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230475621 | |||||||
chr2:230475968 | C | T | 227 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(224): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1600+1521C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230475968 | |||||||
chr2:230475970 | C | T | 228 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(225): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1600+1523C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230475970 | |||||||
chr2:230475981 | G | C | 6 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(3): Show |
6 | HG01884.hp1 HG02572.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1600+1534G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230475981 | |||||||
chr2:230476300 | T | C | 1 | a0001c0001t0002g0102 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1600+1853T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230476300 | |||||||
chr2:230476310 | G | A | 12 | a0001c0001t0005g0095 a0001c0001t0008g0039 a0001c0001t0008g0040 others(9): Show |
12 | HG01884.hp1 HG02572.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.1600+1863G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230476310 | |||||||
chr2:230476333 | C | G | 3 | a0001c0001t0005g0124 a0001c0001t0015g0089 a0001c0001t0021g0090 |
3 | HG02145.hp2 HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1600+1886C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230476333 | |||||||
chr2:230476339 | G | C | 7 | a0001c0003t0005g0047 a0002c0002t0011g0119 a0002c0002t0011g0145 others(4): Show |
7 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1600+1892G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230476339 | |||||||
chr2:230476529 | C | T | 10 | a0001c0003t0012g0042 a0001c0003t0012g0045 a0001c0003t0012g0046 others(7): Show |
10 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1600+2082C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230476529 | |||||||
chr2:230476577 | A | G | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1600+2130A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230476577 | |||||||
chr2:230476601 | T | A | 25 | a0001c0003t0002g0100 a0001c0003t0002g0108 a0001c0003t0002g0109 others(22): Show |
26 | HG00408.hp2 HG00733.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1600+2154T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230476601 | |||||||
chr2:230476702 | G | A | 1 | a0001c0001t0002g0102 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1600+2255G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230476702 | |||||||
chr2:230477116 | C | T | 1 | a0002c0002t0001g0236 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1600+2669C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230477116 | |||||||
chr2:230477160 | C | T | 1 | a0001c0009t0007g0272 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1600+2713C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230477160 | |||||||
chr2:230477161 | G | A | 3 | a0001c0003t0002g0100 a0001c0003t0012g0048 a0002c0002t0013g0038 |
3 | HG02486.hp1 HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1600+2714G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230477161 | |||||||
chr2:230477257 | G | A | 42 | a0001c0001t0002g0027 a0001c0001t0002g0102 a0001c0001t0003g0029 others(39): Show |
42 | HG00544.hp1 HG00558.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.1600+2810G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230477257 | |||||||
chr2:230477260 | G | T | 2 | a0001c0003t0007g0250 a0001c0003t0007g0251 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1600+2813G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230477260 | |||||||
chr2:230477286 | T | C | 1 | a0001c0001t0015g0089 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1600+2839T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230477286 | |||||||
chr2:230477311 | T | C | 1 | a0001c0001t0005g0088 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1600+2864T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230477311 | |||||||
chr2:230477632 | C | G | 10 | a0001c0003t0012g0042 a0001c0003t0012g0045 a0001c0003t0012g0046 others(7): Show |
10 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1600+3185C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230477632 | |||||||
chr2:230477687 | C | A | 1 | a0002c0005t0006g0012 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1600+3240C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230477687 | |||||||
chr2:230477706 | G | T | 44 | a0003c0004t0002g0113 a0003c0004t0002g0117 a0003c0004t0002g0134 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1600+3259G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230477706 | |||||||
chr2:230477747 | C | T | 1 | a0001c0001t0007g0079 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1600+3300C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230477747 | |||||||
chr2:230477850 | G | T | 3 | a0001c0001t0007g0173 a0001c0001t0025g0060 a0002c0020t0022g0036 |
3 | HG01891.hp2 HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1600+3403G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230477850 | |||||||
chr2:230477939 | C | A | 1 | a0001c0001t0004g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1600+3492C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230477939 | |||||||
chr2:230477939 | C | CA | 157 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(154): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.1600+3496dupA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr2 | 230477939 | ||||||
chr2:230477939 | C | CAA | 24 | a0001c0001t0002g0027 a0001c0001t0002g0105 a0001c0001t0002g0254 others(21): Show |
24 | HG00735.hp2 HG01109.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.1600+3495_1600+349 others(6): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr2 | 230477939 | ||||||
chr2:230477939 | C | CAAAAA | 5 | a0002c0002t0011g0119 a0002c0002t0011g0157 a0002c0002t0011g0158 others(2): Show |
5 | HG02622.hp2 HG02647.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1600+3496_1600+349 others(9): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr2 | 230477939 | ||||||
chr2:230477942 | A | AG | 3 | a0002c0002t0001g0118 a0005c0008t0002g0122 a0005c0008t0002g0123 |
3 | HG02055.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1600+3495_1600+349 others(5): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230477942 | |||||||
chr2:230477944 | C | A | 199 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(196): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1600+3497C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230477944 | |||||||
chr2:230477948 | C | A | 199 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(196): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1600+3501C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230477948 | |||||||
chr2:230478157 | C | T | 2 | a0001c0001t0007g0173 a0001c0001t0025g0060 |
2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1600+3710C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230478157 | |||||||
chr2:230478221 | A | G | 2 | a0002c0005t0001g0052 a0002c0005t0001g0129 |
2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1600+3774A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230478221 | |||||||
chr2:230478352 | G | C | 2 | a0001c0001t0007g0173 a0001c0001t0025g0060 |
2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1600+3905G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230478352 | |||||||
chr2:230478375 | G | A | 42 | a0001c0001t0002g0027 a0001c0001t0002g0102 a0001c0001t0003g0029 others(39): Show |
42 | HG00544.hp1 HG00558.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.1600+3928G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230478375 | |||||||
chr2:230478419 | C | T | 1 | a0003c0004t0003g0239 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1600+3972C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230478419 | |||||||
chr2:230478431 | C | T | 1 | a0003c0004t0002g0152 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1600+3984C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230478431 | |||||||
chr2:230478762 | G | A | 10 | a0001c0003t0012g0042 a0001c0003t0012g0045 a0001c0003t0012g0046 others(7): Show |
10 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1600+4315G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230478762 | |||||||
chr2:230478796 | A | G | 1 | a0001c0001t0003g0085 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1600+4349A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230478796 | |||||||
chr2:230478883 | C | CA | 6 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(3): Show |
6 | HG01884.hp1 HG02572.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1600+4438dupA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr2 | 230478883 | ||||||
chr2:230478903 | T | C | 227 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(224): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1600+4456T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230478903 | |||||||
chr2:230478914 | G | A | 1 | a0002c0002t0001g0253 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1600+4467G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230478914 | |||||||
chr2:230478988 | T | G | 2 | a0001c0003t0004g0249 a0001c0003t0012g0247 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1600+4541T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230478988 | |||||||
chr2:230479059 | G | A | 10 | a0001c0003t0012g0042 a0001c0003t0012g0045 a0001c0003t0012g0046 others(7): Show |
10 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1600+4612G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230479059 | |||||||
chr2:230479704 | T | C | 4 | a0001c0003t0002g0100 a0001c0003t0012g0048 a0002c0002t0001g0118 others(1): Show |
4 | HG02055.hp2 HG02486.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1600+5257T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230479704 | |||||||
chr2:230479714 | C | T | 6 | a0002c0002t0011g0119 a0002c0002t0011g0145 a0002c0002t0011g0157 others(3): Show |
6 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1600+5267C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230479714 | |||||||
chr2:230479947 | T | C | 10 | a0001c0003t0012g0042 a0001c0003t0012g0045 a0001c0003t0012g0046 others(7): Show |
10 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1600+5500T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230479947 | |||||||
chr2:230480243 | C | T | 2 | a0001c0003t0002g0100 a0002c0002t0001g0118 |
2 | HG02055.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1600+5796C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230480243 | |||||||
chr2:230480349 | G | A | 2 | a0003c0004t0003g0165 a0003c0004t0003g0239 |
2 | HG02074.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1600+5902G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230480349 | |||||||
chr2:230480582 | A | G | 1 | a0002c0005t0001g0010 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1600+6135A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230480582 | |||||||
chr2:230480669 | C | A | 14 | a0001c0001t0002g0102 a0001c0001t0005g0095 a0001c0001t0008g0039 others(11): Show |
14 | HG01884.hp1 HG02109.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1600+6222C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230480669 | |||||||
chr2:230480845 | C | A | 237 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1600+6398C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230480845 | |||||||
chr2:230480994 | A | T | 24 | a0001c0003t0003g0110 a0002c0002t0001g0044 a0003c0004t0002g0117 others(21): Show |
24 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(21): Show |
intron_variant | MODIFIER | c.1600+6547A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230480994 | |||||||
chr2:230481024 | T | TTGG | 57 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(54): Show |
57 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1600+6610_1600+661 others(7): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr2 | 230481024 | ||||||
chr2:230481024 | T | TTGGTGG | 74 | a0001c0001t0002g0167 a0001c0001t0002g0174 a0001c0001t0002g0203 others(71): Show |
74 | HG00099.hp2 HG00544.hp2 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.1600+6607_1600+661 others(10): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr2 | 230481024 | ||||||
chr2:230481024 | T | TTGGTGGT others(2): Show |
3 | a0001c0001t0002g0175 a0001c0003t0004g0125 a0002c0005t0013g0106 |
3 | HG01106.hp1 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1600+6604_1600+661 others(13): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr2 | 230481024 | ||||||
chr2:230481024 | T | TTGGTGGT others(5): Show |
2 | a0002c0005t0001g0256 a0002c0005t0013g0128 |
2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1600+6601_1600+661 others(16): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr2 | 230481024 | ||||||
chr2:230481276 | C | T | 157 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(154): Show |
157 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.1600+6829C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230481276 | |||||||
chr2:230481405 | A | G | 2 | a0002c0002t0001g0044 a0009c0018t0004g0043 |
2 | HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1600+6958A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230481405 | |||||||
chr2:230481693 | T | A | 1 | a0003c0004t0003g0165 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1600+7246T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230481693 | |||||||
chr2:230481887 | A | G | 72 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(69): Show |
72 | HG00544.hp2 HG00735.hp2 HG01070.hp1 others(69): Show |
intron_variant | MODIFIER | c.1600+7440A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230481887 | |||||||
chr2:230482047 | G | A | 1 | a0003c0004t0004g0051 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1600+7600G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230482047 | |||||||
chr2:230482090 | C | A | 21 | a0001c0001t0004g0096 a0001c0003t0003g0110 a0003c0004t0002g0151 others(18): Show |
21 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(18): Show |
intron_variant | MODIFIER | c.1600+7643C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230482090 | |||||||
chr2:230482142 | G | T | 1 | a0001c0003t0016g0138 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1600+7695G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230482142 | |||||||
chr2:230482155 | G | T | 1 | a0001c0003t0004g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1600+7708G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230482155 | |||||||
chr2:230482184 | C | G | 3 | a0002c0002t0001g0044 a0002c0005t0001g0052 a0002c0005t0001g0129 |
3 | HG02965.hp2 HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1600+7737C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230482184 | |||||||
chr2:230482379 | C | T | 7 | a0001c0001t0015g0089 a0001c0003t0012g0042 a0001c0003t0012g0045 others(4): Show |
7 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1600+7932C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230482379 | |||||||
chr2:230482575 | A | AT | 10 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(7): Show |
10 | HG01884.hp1 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1600+8140dupT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr2 | 230482575 | ||||||
chr2:230482575 | AT | A | 65 | a0001c0001t0002g0025 a0001c0001t0003g0029 a0001c0001t0003g0056 others(62): Show |
65 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.1600+8140delT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr2 | 230482575 | ||||||
chr2:230482581 | T | A | 49 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(46): Show |
49 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.1600+8134T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230482581 | |||||||
chr2:230482607 | G | A | 1 | a0001c0001t0003g0073 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1600+8160G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230482607 | |||||||
chr2:230482697 | C | CAT | 75 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(72): Show |
75 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.1600+8264_1600+826 others(6): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr2 | 230482697 | ||||||
chr2:230482697 | C | CATAT | 34 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(31): Show |
34 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1600+8262_1600+826 others(8): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr2 | 230482697 | ||||||
chr2:230482756 | A | G | 2 | a0001c0007t0016g0031 a0002c0002t0001g0034 |
2 | HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1600+8309A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230482756 | |||||||
chr2:230482805 | C | T | 2 | a0001c0001t0005g0093 a0001c0001t0005g0127 |
2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1600+8358C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230482805 | |||||||
chr2:230482892 | A | C | 1 | a0001c0003t0004g0125 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1600+8445A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230482892 | |||||||
chr2:230483345 | A | T | 1 | a0002c0002t0011g0145 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1600+8898A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230483345 | |||||||
chr2:230483431 | A | G | 50 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1600+8984A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230483431 | |||||||
chr2:230483567 | T | A | 229 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(226): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1600+9120T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230483567 | |||||||
chr2:230483606 | C | A | 1 | a0001c0003t0012g0048 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1600+9159C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230483606 | |||||||
chr2:230483647 | G | A | 3 | a0001c0003t0007g0250 a0001c0003t0007g0251 a0001c0009t0007g0272 |
3 | HG00738.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1600+9200G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230483647 | |||||||
chr2:230483733 | T | C | 1 | a0001c0001t0002g0007 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1600+9286T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230483733 | |||||||
chr2:230483766 | C | T | 1 | a0001c0001t0004g0098 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1600+9319C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230483766 | |||||||
chr2:230483864 | C | T | 1 | a0001c0017t0002g0018 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1600+9417C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230483864 | |||||||
chr2:230484173 | A | G | 16 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0270 others(13): Show |
16 | HG00738.hp2 HG01106.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.1600+9726A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230484173 | |||||||
chr2:230484396 | C | T | 229 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(226): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1600+9949C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230484396 | |||||||
chr2:230484680 | A | G | 1 | a0002c0005t0001g0256 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1601-9736A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230484680 | |||||||
chr2:230484698 | T | C | 1 | a0005c0013t0024g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1601-9718T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230484698 | |||||||
chr2:230484937 | G | T | 1 | a0005c0013t0024g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1601-9479G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230484937 | |||||||
chr2:230485035 | T | G | 1 | a0001c0001t0002g0278 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1601-9381T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230485035 | |||||||
chr2:230485060 | G | A | 1 | a0001c0001t0008g0054 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1601-9356G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230485060 | |||||||
chr2:230485070 | A | C | 8 | a0001c0001t0005g0088 a0001c0001t0005g0091 a0001c0001t0005g0093 others(5): Show |
8 | HG02145.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1601-9346A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230485070 | |||||||
chr2:230485092 | ATATTT | A | 9 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(6): Show |
9 | HG01884.hp1 HG02572.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1601-9299_1601-929 others(9): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr2 | 230485092 | ||||||
chr2:230485215 | G | A | 2 | a0001c0001t0002g0006 a0001c0001t0002g0009 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1601-9201G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230485215 | |||||||
chr2:230485257 | C | T | 1 | a0001c0001t0003g0085 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1601-9159C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230485257 | |||||||
chr2:230485327 | T | C | 4 | a0001c0001t0015g0089 a0001c0003t0002g0100 a0001c0003t0015g0170 others(1): Show |
4 | HG02572.hp2 HG02615.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1601-9089T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230485327 | |||||||
chr2:230485348 | C | A | 1 | a0004c0006t0004g0153 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1601-9068C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230485348 | |||||||
chr2:230485380 | T | G | 1 | a0001c0001t0003g0085 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1601-9036T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230485380 | |||||||
chr2:230485427 | A | G | 8 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(5): Show |
8 | HG01884.hp1 HG02572.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1601-8989A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230485427 | |||||||
chr2:230485472 | A | C | 240 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(237): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1601-8944A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230485472 | |||||||
chr2:230485824 | G | A | 1 | a0001c0001t0003g0199 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1601-8592G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230485824 | |||||||
chr2:230485849 | G | C | 66 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(63): Show |
66 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.1601-8567G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230485849 | |||||||
chr2:230485915 | T | C | 1 | a0007c0010t0001g0121 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1601-8501T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230485915 | |||||||
chr2:230485976 | G | A | 1 | a0001c0001t0002g0105 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1601-8440G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230485976 | |||||||
chr2:230486006 | G | A | 8 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(5): Show |
8 | HG01884.hp1 HG02572.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1601-8410G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230486006 | |||||||
chr2:230486071 | TA | T | 284 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(281): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1601-8337delA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr2 | 230486071 | ||||||
chr2:230486085 | A | T | 239 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(236): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1601-8331A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230486085 | |||||||
chr2:230486095 | C | T | 1 | a0001c0003t0016g0138 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1601-8321C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230486095 | |||||||
chr2:230486112 | G | T | 66 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(63): Show |
66 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.1601-8304G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230486112 | |||||||
chr2:230486202 | C | T | 66 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(63): Show |
66 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.1601-8214C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230486202 | |||||||
chr2:230486205 | G | A | 1 | a0004c0006t0004g0153 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1601-8211G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230486205 | |||||||
chr2:230486206 | G | A | 12 | a0002c0002t0011g0119 a0002c0002t0011g0145 a0002c0002t0011g0157 others(9): Show |
12 | HG02145.hp1 HG02486.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1601-8210G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230486206 | |||||||
chr2:230486236 | G | A | 229 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(226): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1601-8180G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230486236 | |||||||
chr2:230486301 | G | T | 66 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(63): Show |
66 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.1601-8115G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230486301 | |||||||
chr2:230486423 | G | T | 50 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1601-7993G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230486423 | |||||||
chr2:230486536 | T | C | 1 | a0001c0001t0002g0025 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1601-7880T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230486536 | |||||||
chr2:230486584 | A | G | 50 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1601-7832A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230486584 | |||||||
chr2:230486677 | C | G | 50 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1601-7739C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230486677 | |||||||
chr2:230486835 | ATCTG | A | 3 | a0001c0001t0007g0258 a0001c0001t0020g0286 a0001c0003t0007g0111 |
3 | HG02559.hp1 HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1601-7579_1601-757 others(8): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr2 | 230486835 | ||||||
chr2:230486911 | C | T | 1 | a0003c0004t0003g0142 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1601-7505C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230486911 | |||||||
chr2:230487100 | A | G | 6 | a0002c0002t0011g0119 a0002c0002t0011g0145 a0002c0002t0011g0157 others(3): Show |
6 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1601-7316A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230487100 | |||||||
chr2:230487195 | T | G | 1 | a0001c0003t0004g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1601-7221T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230487195 | |||||||
chr2:230487486 | A | G | 66 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(63): Show |
66 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.1601-6930A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230487486 | |||||||
chr2:230487490 | G | A | 1 | a0001c0003t0012g0048 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1601-6926G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230487490 | |||||||
chr2:230487556 | G | A | 1 | a0001c0003t0003g0197 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1601-6860G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230487556 | |||||||
chr2:230487585 | G | C | 4 | a0001c0003t0002g0109 a0001c0003t0002g0275 a0001c0003t0002g0276 others(1): Show |
4 | HG01074.hp2 HG01081.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1601-6831G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230487585 | |||||||
chr2:230487596 | C | T | 1 | a0002c0005t0001g0201 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1601-6820C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230487596 | |||||||
chr2:230487696 | TTCTAATT others(3): Show |
T | 9 | a0001c0001t0005g0088 a0001c0001t0005g0091 a0001c0001t0005g0093 others(6): Show |
9 | HG02145.hp2 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1601-6708_1601-669 others(14): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr2 | 230487696 | ||||||
chr2:230487821 | G | A | 1 | a0001c0001t0002g0200 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1601-6595G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230487821 | |||||||
chr2:230488000 | G | A | 1 | a0001c0001t0007g0173 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1601-6416G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230488000 | |||||||
chr2:230488149 | C | G | 14 | a0001c0001t0005g0088 a0001c0001t0005g0091 a0001c0001t0005g0093 others(11): Show |
14 | HG01109.hp1 HG01891.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1601-6267C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230488149 | |||||||
chr2:230488159 | G | A | 8 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(5): Show |
8 | HG01884.hp1 HG02572.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1601-6257G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230488159 | |||||||
chr2:230488212 | C | T | 12 | a0002c0002t0011g0119 a0002c0002t0011g0145 a0002c0002t0011g0157 others(9): Show |
12 | HG02145.hp1 HG02486.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1601-6204C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230488212 | |||||||
chr2:230488244 | G | A | 50 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1601-6172G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230488244 | |||||||
chr2:230488515 | G | A | 4 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(1): Show |
4 | HG00738.hp1 HG01074.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1601-5901G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230488515 | |||||||
chr2:230488549 | G | A | 1 | a0001c0001t0002g0278 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1601-5867G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230488549 | |||||||
chr2:230488586 | A | T | 229 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(226): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1601-5830A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230488586 | |||||||
chr2:230488597 | T | C | 66 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(63): Show |
66 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.1601-5819T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230488597 | |||||||
chr2:230488732 | G | C | 54 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(51): Show |
54 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.1601-5684G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230488732 | |||||||
chr2:230488798 | G | A | 50 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1601-5618G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230488798 | |||||||
chr2:230488951 | A | G | 1 | a0001c0003t0016g0138 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1601-5465A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230488951 | |||||||
chr2:230489339 | T | C | 1 | a0002c0005t0001g0155 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1601-5077T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230489339 | |||||||
chr2:230489444 | C | A | 1 | a0001c0001t0002g0203 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1601-4972C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230489444 | |||||||
chr2:230489561 | G | A | 1 | a0001c0003t0012g0247 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1601-4855G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230489561 | |||||||
chr2:230489628 | C | T | 4 | a0003c0004t0003g0146 a0003c0004t0003g0208 a0003c0004t0003g0222 others(1): Show |
4 | HG00099.hp1 HG00323.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.1601-4788C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230489628 | |||||||
chr2:230489679 | C | A | 2 | a0004c0006t0004g0238 a0004c0006t0004g0282 |
2 | HG00140.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1601-4737C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230489679 | |||||||
chr2:230489692 | C | T | 1 | a0001c0001t0025g0060 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1601-4724C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230489692 | |||||||
chr2:230489787 | G | A | 1 | a0001c0001t0002g0267 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1601-4629G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230489787 | |||||||
chr2:230489797 | G | A | 8 | a0001c0001t0005g0095 a0002c0002t0001g0005 a0002c0002t0001g0044 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1601-4619G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230489797 | |||||||
chr2:230489822 | T | C | 1 | a0001c0001t0007g0079 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1601-4594T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230489822 | |||||||
chr2:230490054 | G | A | 1 | a0001c0003t0016g0138 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1601-4362G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230490054 | |||||||
chr2:230490480 | G | A | 1 | a0001c0001t0025g0060 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1601-3936G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230490480 | |||||||
chr2:230490652 | T | C | 91 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(88): Show |
91 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.1601-3764T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230490652 | |||||||
chr2:230490678 | G | A | 13 | a0001c0001t0006g0135 a0001c0001t0006g0156 a0001c0001t0006g0223 others(10): Show |
13 | HG00673.hp1 HG02040.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1601-3738G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230490678 | |||||||
chr2:230490686 | G | A | 1 | a0005c0013t0024g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1601-3730G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230490686 | |||||||
chr2:230490785 | T | A | 1 | a0001c0003t0012g0048 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1601-3631T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230490785 | |||||||
chr2:230491061 | A | G | 57 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(54): Show |
57 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.1601-3355A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230491061 | |||||||
chr2:230491143 | C | T | 1 | a0004c0006t0004g0153 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1601-3273C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230491143 | |||||||
chr2:230491207 | C | T | 1 | a0001c0009t0010g0064 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1601-3209C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230491207 | |||||||
chr2:230491245 | C | T | 97 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(94): Show |
97 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.1601-3171C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230491245 | |||||||
chr2:230491301 | C | T | 1 | a0001c0001t0002g0274 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1601-3115C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230491301 | |||||||
chr2:230491302 | G | A | 1 | a0001c0003t0012g0247 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1601-3114G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230491302 | |||||||
chr2:230491370 | T | C | 2 | a0001c0001t0002g0025 a0001c0001t0002g0026 |
2 | HG00673.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.1601-3046T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230491370 | |||||||
chr2:230491447 | A | C | 57 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(54): Show |
57 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.1601-2969A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230491447 | |||||||
chr2:230491512 | C | T | 57 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(54): Show |
57 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.1601-2904C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230491512 | |||||||
chr2:230491674 | A | C | 1 | a0001c0001t0002g0019 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1601-2742A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230491674 | |||||||
chr2:230491699 | C | G | 97 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(94): Show |
97 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.1601-2717C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230491699 | |||||||
chr2:230491799 | G | A | 1 | a0001c0003t0007g0055 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1601-2617G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230491799 | |||||||
chr2:230491824 | C | T | 9 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(6): Show |
9 | HG01884.hp1 HG02572.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1601-2592C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230491824 | |||||||
chr2:230491984 | G | A | 9 | a0001c0001t0005g0088 a0001c0001t0005g0091 a0001c0001t0005g0093 others(6): Show |
9 | HG02145.hp2 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1601-2432G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230491984 | |||||||
chr2:230491992 | T | C | 98 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(95): Show |
98 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.1601-2424T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230491992 | |||||||
chr2:230492024 | T | C | 2 | a0001c0001t0004g0176 a0001c0001t0021g0090 |
2 | HG02451.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1601-2392T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230492024 | |||||||
chr2:230492131 | C | T | 2 | a0002c0002t0001g0044 a0002c0002t0001g0118 |
2 | HG02055.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1601-2285C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230492131 | |||||||
chr2:230492138 | C | T | 1 | a0001c0001t0003g0199 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1601-2278C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230492138 | |||||||
chr2:230492265 | A | T | 3 | a0003c0004t0003g0016 a0003c0004t0003g0137 a0003c0004t0003g0255 |
3 | HG00735.hp2 HG02258.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1601-2151A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230492265 | |||||||
chr2:230492340 | A | G | 1 | a0001c0007t0016g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1601-2076A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230492340 | |||||||
chr2:230492538 | T | C | 1 | a0001c0001t0003g0143 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1601-1878T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230492538 | |||||||
chr2:230492539 | C | A | 1 | a0001c0001t0003g0143 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1601-1877C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230492539 | |||||||
chr2:230492541 | A | T | 1 | a0001c0001t0003g0143 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1601-1875A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230492541 | |||||||
chr2:230492544 | G | A | 1 | a0002c0005t0001g0083 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1601-1872G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230492544 | |||||||
chr2:230492564 | C | A | 1 | a0001c0001t0002g0008 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1601-1852C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230492564 | |||||||
chr2:230492624 | A | G | 113 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(110): Show |
114 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.1601-1792A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230492624 | |||||||
chr2:230492658 | T | C | 57 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(54): Show |
57 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.1601-1758T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230492658 | |||||||
chr2:230492675 | T | A | 1 | a0003c0004t0003g0061 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1601-1741T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230492675 | |||||||
chr2:230492703 | C | T | 1 | a0001c0001t0002g0195 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1601-1713C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230492703 | |||||||
chr2:230492988 | A | G | 1 | a0002c0005t0001g0164 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1601-1428A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230492988 | |||||||
chr2:230493015 | T | C | 1 | a0002c0020t0022g0036 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1601-1401T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230493015 | |||||||
chr2:230493026 | T | C | 1 | a0001c0001t0015g0089 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1601-1390T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230493026 | |||||||
chr2:230493156 | G | T | 1 | a0001c0001t0025g0060 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1601-1260G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230493156 | |||||||
chr2:230493409 | G | T | 5 | a0001c0003t0002g0013 a0001c0003t0002g0109 a0001c0003t0002g0275 others(2): Show |
5 | HG01074.hp2 HG01081.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1601-1007G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230493409 | |||||||
chr2:230493468 | C | T | 1 | a0001c0001t0003g0074 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1601-948C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230493468 | |||||||
chr2:230493480 | G | A | 57 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(54): Show |
57 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.1601-936G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230493480 | |||||||
chr2:230493652 | AT | A | 5 | a0001c0001t0015g0089 a0001c0003t0002g0100 a0001c0003t0008g0002 others(2): Show |
6 | HG02559.hp2 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1601-754delT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr2 | 230493652 | ||||||
chr2:230493807 | G | A | 8 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(5): Show |
8 | HG01884.hp1 HG02572.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1601-609G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230493807 | |||||||
chr2:230493921 | A | T | 1 | a0001c0003t0008g0002 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1601-495A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230493921 | |||||||
chr2:230494053 | C | T | 1 | a0001c0003t0007g0055 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1601-363C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230494053 | |||||||
chr2:230494095 | C | G | 1 | a0001c0003t0016g0138 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1601-321C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230494095 | |||||||
chr2:230494258 | C | T | 8 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(5): Show |
8 | HG01884.hp1 HG02572.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1601-158C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230494258 | |||||||
chr2:230494383 | T | G | 58 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(55): Show |
58 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1601-33T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 17/28 | chr2 | 230494383 | |||||||
chr2:230494510 | T | C | 57 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(54): Show |
57 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.1645+50T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230494510 | |||||||
chr2:230494608 | T | C | 5 | a0001c0003t0012g0042 a0001c0003t0012g0045 a0001c0003t0012g0046 others(2): Show |
5 | HG02258.hp1 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1645+148T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230494608 | |||||||
chr2:230494652 | T | C | 16 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0270 others(13): Show |
16 | HG00738.hp2 HG01106.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.1645+192T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230494652 | |||||||
chr2:230494661 | C | G | 1 | a0001c0001t0004g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1645+201C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230494661 | |||||||
chr2:230494804 | A | G | 1 | a0002c0002t0001g0194 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1645+344A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230494804 | |||||||
chr2:230494887 | G | T | 11 | a0001c0001t0007g0079 a0001c0001t0007g0173 a0001c0001t0007g0258 others(8): Show |
11 | HG00738.hp2 HG01256.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1645+427G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230494887 | |||||||
chr2:230495178 | G | A | 1 | a0002c0002t0001g0140 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1645+718G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230495178 | |||||||
chr2:230495259 | T | C | 1 | a0001c0003t0003g0063 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1645+799T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230495259 | |||||||
chr2:230495355 | C | T | 4 | a0001c0001t0015g0089 a0001c0003t0002g0100 a0001c0003t0015g0170 others(1): Show |
4 | HG02572.hp2 HG02615.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1645+895C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230495355 | |||||||
chr2:230495398 | C | T | 1 | a0001c0001t0007g0258 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1645+938C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230495398 | |||||||
chr2:230495444 | C | G | 1 | a0001c0001t0002g0007 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1645+984C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230495444 | |||||||
chr2:230495464 | C | T | 1 | a0001c0007t0016g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1645+1004C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230495464 | |||||||
chr2:230495571 | C | T | 5 | a0001c0003t0002g0108 a0001c0003t0002g0109 a0001c0003t0002g0275 others(2): Show |
5 | HG01074.hp2 HG01081.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1645+1111C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230495571 | |||||||
chr2:230495717 | C | T | 2 | a0002c0005t0001g0057 a0002c0005t0001g0179 |
2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1645+1257C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230495717 | |||||||
chr2:230495774 | G | A | 60 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(57): Show |
61 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1645+1314G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230495774 | |||||||
chr2:230495910 | T | G | 4 | a0001c0001t0015g0089 a0001c0003t0002g0100 a0001c0003t0015g0170 others(1): Show |
4 | HG02572.hp2 HG02615.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1645+1450T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230495910 | |||||||
chr2:230495921 | T | C | 5 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(2): Show |
5 | HG01109.hp1 HG01891.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1645+1461T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230495921 | |||||||
chr2:230496116 | G | T | 229 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(226): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1645+1656G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230496116 | |||||||
chr2:230496166 | T | A | 9 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(6): Show |
9 | HG01884.hp1 HG02572.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1645+1706T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230496166 | |||||||
chr2:230496189 | T | C | 1 | a0001c0003t0012g0048 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1645+1729T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230496189 | |||||||
chr2:230496310 | G | A | 2 | a0002c0005t0001g0052 a0002c0005t0001g0129 |
2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1645+1850G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230496310 | |||||||
chr2:230496414 | A | G | 16 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0270 others(13): Show |
16 | HG00738.hp2 HG01106.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.1645+1954A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230496414 | |||||||
chr2:230496768 | G | T | 1 | a0002c0002t0001g0144 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1646-1693G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230496768 | |||||||
chr2:230496942 | T | C | 60 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(57): Show |
61 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1646-1519T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230496942 | |||||||
chr2:230497467 | A | AGGAGG | 3 | a0001c0001t0003g0073 a0003c0004t0003g0189 a0011c0011t0003g0086 |
3 | HG04199.hp2 NA19002.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1646-973_1646-969d others(7): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497467 | ||||||
chr2:230497483 | G | GGAGGAGA others(3): Show |
2 | a0001c0007t0005g0030 a0005c0008t0005g0004 |
2 | HG01109.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1646-974_1646-973i others(12): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497483 | ||||||
chr2:230497483 | GGAGGGGA others(13): Show |
G | 1 | a0001c0003t0004g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1646-973_1646-954d others(22): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497483 | ||||||
chr2:230497488 | G | A | 4 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1646-973G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230497488 | |||||||
chr2:230497488 | G | GGAGGA | 10 | a0001c0003t0007g0111 a0001c0003t0012g0045 a0001c0003t0012g0046 others(7): Show |
10 | HG01993.hp2 HG02040.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1646-917_1646-913d others(7): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497488 | ||||||
chr2:230497488 | G | GGAGGAGA others(3): Show |
5 | a0001c0001t0004g0270 a0001c0001t0007g0258 a0001c0003t0012g0247 others(2): Show |
5 | HG01884.hp2 HG02965.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1646-922_1646-913d others(12): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497488 | ||||||
chr2:230497488 | G | GGAGGAGA others(8): Show |
5 | a0001c0001t0021g0090 a0004c0006t0004g0153 a0004c0006t0004g0238 others(2): Show |
5 | HG00140.hp1 HG01516.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1646-927_1646-913d others(17): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497488 | ||||||
chr2:230497488 | G | GGAGGAGA others(13): Show |
2 | a0001c0001t0004g0049 a0003c0004t0004g0104 |
2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1646-932_1646-913d others(22): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497488 | ||||||
chr2:230497488 | G | GGAGGAGA others(18): Show |
4 | a0001c0001t0004g0050 a0001c0001t0004g0176 a0002c0005t0013g0106 others(1): Show |
4 | HG01106.hp1 HG02129.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1646-937_1646-913d others(27): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497488 | ||||||
chr2:230497488 | G | GGAGGAGA others(23): Show |
3 | a0001c0003t0004g0249 a0003c0004t0004g0051 a0004c0006t0004g0180 |
3 | HG02055.hp1 HG02886.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1646-942_1646-913d others(32): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497488 | ||||||
chr2:230497488 | G | GGAGGAGA others(28): Show |
1 | a0004c0006t0004g0277 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1646-947_1646-913d others(37): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497488 | ||||||
chr2:230497488 | G | GGAGGAGA others(43): Show |
1 | a0004c0006t0004g0182 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1646-962_1646-913d others(52): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497488 | ||||||
chr2:230497488 | G | GGAGGGGA others(3): Show |
1 | a0003c0004t0003g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1646-969_1646-968i others(12): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497488 | ||||||
chr2:230497488 | GGAGGA | G | 18 | a0001c0001t0003g0070 a0001c0001t0003g0074 a0001c0001t0005g0088 others(15): Show |
18 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1646-917_1646-913d others(7): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497488 | ||||||
chr2:230497488 | GGAGGAGA others(3): Show |
G | 13 | a0001c0001t0003g0085 a0001c0001t0005g0124 a0001c0001t0005g0252 others(10): Show |
13 | HG00323.hp2 HG00733.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1646-922_1646-913d others(12): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497488 | ||||||
chr2:230497488 | GGAGGAGA others(8): Show |
G | 7 | a0001c0001t0005g0093 a0001c0003t0003g0110 a0002c0005t0013g0128 others(4): Show |
7 | HG00408.hp2 HG01256.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.1646-927_1646-913d others(17): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497488 | ||||||
chr2:230497488 | GGAGGAGA others(13): Show |
G | 11 | a0002c0002t0011g0119 a0002c0002t0011g0145 a0002c0002t0011g0157 others(8): Show |
11 | HG02486.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1646-932_1646-913d others(22): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497488 | ||||||
chr2:230497488 | GGAGGAGA others(18): Show |
G | 2 | a0001c0001t0008g0054 a0001c0001t0019g0126 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1646-937_1646-913d others(27): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497488 | ||||||
chr2:230497493 | A | G | 38 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0077 others(35): Show |
39 | HG00544.hp2 HG00735.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1646-968A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230497493 | |||||||
chr2:230497498 | A | G | 7 | a0001c0001t0005g0088 a0001c0001t0005g0097 a0003c0004t0003g0061 others(4): Show |
7 | HG00099.hp1 HG00280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1646-963A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230497498 | |||||||
chr2:230497503 | A | G | 9 | a0001c0001t0005g0124 a0001c0001t0005g0252 a0001c0003t0003g0273 others(6): Show |
9 | HG00323.hp2 HG00733.hp2 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1646-958A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230497503 | |||||||
chr2:230497508 | A | G | 4 | a0001c0001t0005g0093 a0001c0003t0003g0110 a0003c0004t0003g0081 others(1): Show |
4 | HG00408.hp2 HG01256.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.1646-953A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230497508 | |||||||
chr2:230497512 | G | A | 1 | a0003c0004t0002g0117 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1646-949G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230497512 | |||||||
chr2:230497513 | A | G | 1 | a0003c0004t0003g0081 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1646-948A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230497513 | |||||||
chr2:230497519 | GAGGAGAG others(28): Show |
G | 6 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(3): Show |
6 | HG01884.hp1 HG02896.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1646-937_1646-903d others(37): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497519 | ||||||
chr2:230497524 | G | A | 2 | a0005c0008t0003g0003 a0011c0011t0003g0086 |
2 | NA19002.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1646-937G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230497524 | |||||||
chr2:230497524 | G | GAGGAAAG others(3): Show |
3 | a0001c0001t0003g0143 a0003c0004t0003g0262 a0003c0004t0003g0263 |
3 | HG01070.hp1 HG01071.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1646-933_1646-932i others(12): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497524 | ||||||
chr2:230497524 | G | GAGGAAAG others(8): Show |
1 | a0003c0004t0003g0271 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1646-933_1646-932i others(17): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497524 | ||||||
chr2:230497524 | GAGGAGAG others(28): Show |
G | 1 | a0001c0003t0004g0125 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1646-932_1646-898d others(37): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497524 | ||||||
chr2:230497524 | GAGGAGAG others(33): Show |
G | 1 | a0001c0001t0002g0175 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1646-932_1646-893d others(42): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497524 | ||||||
chr2:230497524 | GAGGAGAG others(38): Show |
G | 2 | a0001c0001t0002g0102 a0005c0008t0002g0122 |
2 | HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1646-932_1646-888d others(47): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497524 | ||||||
chr2:230497524 | GAGGAGAG others(43): Show |
G | 1 | a0005c0008t0002g0123 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1646-932_1646-883d others(52): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497524 | ||||||
chr2:230497529 | G | A | 12 | a0001c0001t0003g0073 a0001c0001t0003g0143 a0003c0004t0003g0061 others(9): Show |
12 | HG00280.hp2 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1646-932G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230497529 | |||||||
chr2:230497529 | G | GAGGAAAG others(8): Show |
1 | a0003c0004t0003g0137 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1646-928_1646-927i others(17): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497529 | ||||||
chr2:230497529 | G | GAGGAAAG others(18): Show |
1 | a0001c0003t0003g0139 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1646-928_1646-927i others(27): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497529 | ||||||
chr2:230497529 | GAGGAGAG others(13): Show |
G | 1 | a0001c0001t0005g0127 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1646-927_1646-908d others(22): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497529 | ||||||
chr2:230497529 | GAGGAGAG others(28): Show |
G | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(4): Show |
7 | HG00408.hp1 HG00738.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.1646-927_1646-893d others(37): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497529 | ||||||
chr2:230497529 | GAGGAGAG others(33): Show |
G | 3 | a0001c0003t0002g0109 a0001c0003t0002g0276 a0001c0003t0002g0281 |
3 | HG01081.hp2 HG01109.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1646-927_1646-888d others(42): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497529 | ||||||
chr2:230497534 | G | A | 20 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0143 others(17): Show |
20 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.1646-927G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230497534 | |||||||
chr2:230497534 | G | GAGGAAAG others(3): Show |
3 | a0001c0001t0003g0094 a0001c0001t0003g0199 a0001c0003t0003g0227 |
3 | HG00544.hp2 HG02155.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1646-923_1646-922i others(12): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497534 | ||||||
chr2:230497534 | G | GAGGAAAG others(8): Show |
1 | a0001c0003t0008g0002 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1646-923_1646-922i others(17): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497534 | ||||||
chr2:230497534 | G | GAGGAAAG others(13): Show |
1 | a0001c0003t0008g0002 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1646-923_1646-922i others(22): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497534 | ||||||
chr2:230497534 | G | GAGGAAAG others(18): Show |
2 | a0001c0001t0003g0029 a0001c0001t0003g0056 |
2 | HG04184.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1646-923_1646-922i others(27): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497534 | ||||||
chr2:230497534 | G | GAGGAAAG others(23): Show |
1 | a0001c0003t0003g0212 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1646-923_1646-922i others(32): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497534 | ||||||
chr2:230497534 | G | GAGGAAAG others(33): Show |
2 | a0001c0003t0003g0063 a0001c0003t0003g0188 |
2 | HG02523.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.1646-923_1646-922i others(42): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497534 | ||||||
chr2:230497534 | GAGGAGAG others(18): Show |
G | 11 | a0001c0001t0002g0072 a0001c0001t0002g0200 a0001c0001t0006g0223 others(8): Show |
11 | HG01346.hp1 HG01981.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1646-922_1646-898d others(27): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497534 | ||||||
chr2:230497534 | GAGGAGAG others(23): Show |
G | 14 | a0001c0001t0002g0065 a0001c0001t0002g0071 a0001c0001t0002g0195 others(11): Show |
14 | HG00673.hp1 HG01081.hp1 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.1646-922_1646-893d others(32): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497534 | ||||||
chr2:230497534 | GAGGAGAG others(28): Show |
G | 36 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0148 others(33): Show |
36 | HG00544.hp1 HG00558.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.1646-922_1646-888d others(37): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497534 | ||||||
chr2:230497534 | GAGGAGAG others(43): Show |
G | 1 | a0001c0001t0002g0019 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1646-922_1646-873d others(52): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497534 | ||||||
chr2:230497539 | G | A | 37 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(34): Show |
38 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.1646-922G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230497539 | |||||||
chr2:230497539 | G | GAGGAAAG others(3): Show |
2 | a0001c0003t0003g0022 a0003c0004t0003g0112 |
2 | HG01516.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1646-918_1646-917i others(12): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497539 | ||||||
chr2:230497539 | G | GAGGAAAG others(13): Show |
2 | a0003c0004t0003g0116 a0003c0004t0003g0133 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1646-918_1646-917i others(22): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497539 | ||||||
chr2:230497539 | G | GAGGAAAG others(18): Show |
2 | a0001c0001t0003g0077 a0003c0004t0003g0114 |
2 | HG02148.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1646-918_1646-917i others(27): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497539 | ||||||
chr2:230497539 | G | GAGGAAAG others(28): Show |
1 | a0001c0003t0003g0185 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1646-918_1646-917i others(37): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497539 | ||||||
chr2:230497539 | G | GAGGAAAG others(38): Show |
1 | a0001c0003t0003g0183 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1646-918_1646-917i others(47): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497539 | ||||||
chr2:230497539 | G | GAGGAAAG others(63): Show |
1 | a0001c0003t0003g0202 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1646-918_1646-917i others(72): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497539 | ||||||
chr2:230497539 | GAGGAGAG others(3): Show |
G | 2 | a0001c0001t0002g0266 a0001c0001t0005g0091 |
2 | HG01123.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1646-917_1646-908d others(12): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497539 | ||||||
chr2:230497539 | GAGGAGAG others(8): Show |
G | 1 | a0001c0001t0002g0268 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1646-917_1646-903d others(17): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497539 | ||||||
chr2:230497539 | GAGGAGAG others(13): Show |
G | 2 | a0001c0001t0002g0105 a0001c0001t0002g0184 |
2 | HG02602.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1646-917_1646-898d others(22): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497539 | ||||||
chr2:230497539 | GAGGAGAG others(18): Show |
G | 1 | a0001c0001t0002g0027 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1646-917_1646-893d others(27): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497539 | ||||||
chr2:230497539 | GAGGAGAG others(23): Show |
G | 5 | a0001c0001t0002g0284 a0001c0001t0004g0017 a0001c0001t0004g0098 others(2): Show |
5 | HG00099.hp2 HG00280.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.1646-917_1646-888d others(32): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497539 | ||||||
chr2:230497539 | GAGGAGAG others(28): Show |
G | 5 | a0001c0001t0002g0267 a0001c0001t0002g0283 a0001c0001t0010g0130 others(2): Show |
5 | HG01071.hp1 HG01255.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.1646-917_1646-883d others(37): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497539 | ||||||
chr2:230497544 | G | A | 52 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(49): Show |
53 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.1646-917G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230497544 | |||||||
chr2:230497544 | G | GAGGAA | 15 | a0001c0001t0007g0079 a0001c0003t0004g0249 a0001c0003t0007g0055 others(12): Show |
15 | HG01243.hp1 HG01358.hp1 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.1646-847_1646-843d others(7): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497544 | ||||||
chr2:230497544 | G | GAGGAAAG others(3): Show |
4 | a0001c0001t0004g0176 a0002c0002t0011g0119 a0005c0013t0024g0161 others(1): Show |
4 | HG02451.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1646-852_1646-843d others(12): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497544 | ||||||
chr2:230497544 | G | GAGGAAAG others(8): Show |
1 | a0004c0006t0004g0277 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1646-857_1646-843d others(17): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497544 | ||||||
chr2:230497544 | G | GAGGAAAG others(18): Show |
3 | a0001c0001t0004g0270 a0004c0006t0004g0182 a0004c0006t0004g0238 |
3 | HG00140.hp1 HG01884.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1646-867_1646-843d others(27): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497544 | ||||||
chr2:230497544 | G | GAGGAAAG others(23): Show |
2 | a0002c0005t0013g0106 a0004c0006t0004g0180 |
2 | HG01106.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1646-872_1646-843d others(32): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497544 | ||||||
chr2:230497544 | G | GAGGAAAG others(28): Show |
2 | a0004c0006t0004g0282 a0004c0015t0004g0154 |
2 | HG02129.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1646-877_1646-843d others(37): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497544 | ||||||
chr2:230497544 | G | GAGGAAAG others(33): Show |
1 | a0004c0006t0004g0153 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1646-882_1646-843d others(42): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497544 | ||||||
chr2:230497544 | G | GAGGAAAG others(53): Show |
1 | a0001c0003t0003g0197 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1646-902_1646-843d others(62): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497544 | ||||||
chr2:230497544 | G | GAGGAAAG others(58): Show |
1 | a0001c0003t0003g0288 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1646-907_1646-843d others(67): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497544 | ||||||
chr2:230497544 | G | GAGGAGAG others(3): Show |
1 | a0007c0010t0001g0168 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1646-913_1646-912i others(12): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497544 | ||||||
chr2:230497544 | G | GAGGAGAG others(8): Show |
1 | a0003c0004t0003g0103 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1646-913_1646-912i others(17): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497544 | ||||||
chr2:230497544 | G | GAGGAGAG others(33): Show |
1 | a0002c0005t0001g0256 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1646-913_1646-912i others(42): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497544 | ||||||
chr2:230497544 | G | GAGGAGAG others(38): Show |
1 | a0006c0016t0004g0280 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1646-913_1646-912i others(47): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497544 | ||||||
chr2:230497544 | GAGGAA | G | 24 | a0001c0001t0007g0258 a0001c0001t0021g0090 a0001c0003t0007g0250 others(21): Show |
25 | HG00738.hp2 HG01099.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.1646-847_1646-843d others(7): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497544 | ||||||
chr2:230497544 | GAGGAAAG others(3): Show |
G | 18 | a0001c0001t0005g0095 a0001c0001t0020g0286 a0001c0003t0007g0111 others(15): Show |
18 | HG00323.hp1 HG00735.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.1646-852_1646-843d others(12): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497544 | ||||||
chr2:230497544 | GAGGAAAG others(8): Show |
G | 10 | a0001c0001t0004g0050 a0001c0001t0004g0096 a0001c0001t0006g0240 others(7): Show |
10 | HG01943.hp2 HG02071.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1646-857_1646-843d others(17): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497544 | ||||||
chr2:230497544 | GAGGAAAG others(13): Show |
G | 2 | a0001c0003t0012g0247 a0002c0002t0001g0236 |
2 | HG02965.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1646-862_1646-843d others(22): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497544 | ||||||
chr2:230497544 | GAGGAAAG others(23): Show |
G | 4 | a0003c0004t0002g0151 a0003c0004t0002g0152 a0003c0004t0002g0163 others(1): Show |
4 | HG00140.hp2 HG01255.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.1646-872_1646-843d others(32): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr2 | 230497544 | ||||||
chr2:230497549 | A | G | 18 | a0001c0003t0004g0099 a0001c0003t0012g0048 a0001c0007t0016g0031 others(15): Show |
18 | HG00558.hp2 HG00733.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1646-912A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230497549 | |||||||
chr2:230497554 | A | G | 20 | a0001c0007t0016g0031 a0002c0002t0001g0028 a0002c0002t0001g0144 others(17): Show |
21 | HG00733.hp1 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.1646-907A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230497554 | |||||||
chr2:230497559 | A | G | 13 | a0001c0001t0005g0095 a0001c0007t0016g0031 a0002c0002t0001g0078 others(10): Show |
13 | HG00323.hp1 HG00735.hp1 HG02293.hp2 others(10): Show |
intron_variant | MODIFIER | c.1646-902A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230497559 | |||||||
chr2:230497564 | A | G | 10 | a0001c0001t0005g0095 a0001c0001t0006g0240 a0002c0002t0001g0107 others(7): Show |
10 | HG00323.hp1 HG00735.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.1646-897A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230497564 | |||||||
chr2:230497569 | A | G | 1 | a0002c0002t0001g0236 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1646-892A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230497569 | |||||||
chr2:230498208 | G | A | 1 | a0002c0005t0001g0256 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1646-253G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230498208 | |||||||
chr2:230498265 | C | T | 1 | a0001c0003t0005g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1646-196C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 18/28 | chr2 | 230498265 | |||||||
chr2:230498537 | T | TA | 8 | a0001c0001t0003g0073 a0001c0007t0005g0030 a0001c0007t0005g0032 others(5): Show |
8 | HG01109.hp1 HG02630.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1720+15dupA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chr2 | 230498537 | ||||||
chr2:230498537 | TA | T | 164 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(161): Show |
164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1720+15delA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chr2 | 230498537 | ||||||
chr2:230498648 | T | C | 1 | a0002c0002t0001g0194 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1720+113T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230498648 | |||||||
chr2:230498657 | T | C | 1 | a0001c0003t0004g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1720+122T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230498657 | |||||||
chr2:230499045 | C | T | 2 | a0002c0005t0006g0012 a0002c0005t0006g0198 |
2 | NA18975.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1720+510C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230499045 | |||||||
chr2:230499075 | G | A | 51 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(48): Show |
52 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1720+540G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230499075 | |||||||
chr2:230499351 | C | T | 1 | a0001c0003t0012g0048 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1720+816C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230499351 | |||||||
chr2:230499467 | A | ACT | 20 | a0001c0001t0002g0065 a0001c0001t0002g0071 a0001c0001t0002g0195 others(17): Show |
20 | HG00673.hp1 HG01081.hp1 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.1720+954_1720+955d others(4): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chr2 | 230499467 | ||||||
chr2:230499467 | A | ACTCTCT | 9 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(6): Show |
9 | HG01884.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1720+950_1720+955d others(8): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chr2 | 230499467 | ||||||
chr2:230499489 | T | C | 2 | a0001c0001t0020g0286 a0002c0020t0022g0036 |
2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1720+954T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230499489 | |||||||
chr2:230499491 | C | T | 137 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(134): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1720+956C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230499491 | |||||||
chr2:230499495 | T | C | 137 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(134): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1720+960T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230499495 | |||||||
chr2:230499496 | A | C | 137 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(134): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1720+961A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230499496 | |||||||
chr2:230499509 | T | A | 24 | a0001c0001t0002g0065 a0001c0001t0002g0071 a0001c0001t0002g0195 others(21): Show |
24 | HG00673.hp1 HG01081.hp1 HG02040.hp1 others(21): Show |
intron_variant | MODIFIER | c.1720+974T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230499509 | |||||||
chr2:230499510 | A | ATAAATAT others(214): Show |
1 | a0006c0016t0004g0280 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1720+975_1720+976i others(223): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230499510 | |||||||
chr2:230499510 | A | ATAAATAT others(214): Show |
6 | a0004c0006t0004g0153 a0004c0006t0004g0182 a0004c0006t0004g0238 others(3): Show |
6 | HG00140.hp1 HG01516.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.1720+975_1720+976i others(223): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230499510 | |||||||
chr2:230499510 | A | ATAAATAT others(214): Show |
13 | a0002c0002t0011g0119 a0002c0002t0011g0145 a0002c0002t0011g0157 others(10): Show |
13 | HG02145.hp1 HG02486.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1720+975_1720+976i others(223): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230499510 | |||||||
chr2:230499510 | A | ATAAATAT others(218): Show |
1 | a0001c0001t0025g0060 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1720+975_1720+976i others(227): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230499510 | |||||||
chr2:230499510 | A | ATATATAT others(208): Show |
1 | a0001c0001t0005g0097 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1720+975_1720+976i others(217): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230499510 | |||||||
chr2:230499510 | A | ATATATAT others(208): Show |
5 | a0001c0001t0005g0088 a0001c0001t0005g0091 a0001c0001t0005g0124 others(2): Show |
5 | HG02145.hp2 HG02647.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1720+975_1720+976i others(217): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230499510 | |||||||
chr2:230499510 | A | ATATATAT others(210): Show |
1 | a0001c0003t0005g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1720+975_1720+976i others(219): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230499510 | |||||||
chr2:230499510 | A | ATATATAT others(208): Show |
2 | a0001c0001t0005g0093 a0001c0001t0005g0127 |
2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1720+975_1720+976i others(217): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230499510 | |||||||
chr2:230499510 | A | ATATATAT others(214): Show |
2 | a0001c0001t0002g0196 a0001c0001t0002g0285 |
2 | HG02148.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1720+975_1720+976i others(223): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230499510 | |||||||
chr2:230499510 | A | ATATATAT others(214): Show |
11 | a0001c0001t0002g0195 a0001c0001t0006g0135 a0001c0001t0006g0156 others(8): Show |
11 | HG00673.hp1 HG01081.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.1720+975_1720+976i others(223): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230499510 | |||||||
chr2:230499510 | A | ATATATAT others(166): Show |
2 | a0001c0001t0002g0065 a0001c0001t0002g0071 |
2 | HG02129.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1720+975_1720+976i others(175): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230499510 | |||||||
chr2:230499512 | A | ATATATAT others(204): Show |
2 | a0001c0007t0005g0032 a0001c0007t0005g0033 |
2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1720+978_1720+979i others(213): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chr2 | 230499512 | ||||||
chr2:230499512 | A | ATATATAT others(216): Show |
2 | a0001c0007t0005g0030 a0005c0008t0005g0004 |
2 | HG01109.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1720+978_1720+979i others(225): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chr2 | 230499512 | ||||||
chr2:230499512 | A | ATATATAT others(212): Show |
51 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(48): Show |
52 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1720+978_1720+979i others(221): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chr2 | 230499512 | ||||||
chr2:230499512 | A | ATATATAT others(216): Show |
4 | a0001c0001t0002g0027 a0001c0001t0002g0072 a0001c0001t0002g0184 others(1): Show |
4 | HG01981.hp1 NA18612.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+978_1720+979i others(225): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chr2 | 230499512 | ||||||
chr2:230499512 | A | ATATATAT others(215): Show |
1 | a0003c0004t0002g0117 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1720+978_1720+979i others(224): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chr2 | 230499512 | ||||||
chr2:230499512 | A | ATATATAT others(216): Show |
80 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(77): Show |
80 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.1720+978_1720+979i others(225): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chr2 | 230499512 | ||||||
chr2:230499512 | A | ATATATAT others(172): Show |
1 | a0001c0003t0004g0125 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1720+978_1720+979i others(181): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chr2 | 230499512 | ||||||
chr2:230499512 | A | ATATATAT others(260): Show |
1 | a0003c0004t0004g0104 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1720+978_1720+979i others(269): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chr2 | 230499512 | ||||||
chr2:230499512 | A | ATATATAT others(212): Show |
29 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(26): Show |
29 | HG00738.hp2 HG01106.hp1 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.1720+978_1720+979i others(221): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chr2 | 230499512 | ||||||
chr2:230499512 | A | ATATATAT others(216): Show |
12 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(9): Show |
12 | HG01884.hp1 HG02572.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1720+978_1720+979i others(225): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chr2 | 230499512 | ||||||
chr2:230499512 | A | ATATATAT others(216): Show |
1 | a0001c0001t0019g0126 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1720+978_1720+979i others(225): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chr2 | 230499512 | ||||||
chr2:230499512 | A | G | 45 | a0001c0001t0002g0065 a0001c0001t0002g0071 a0001c0001t0002g0195 others(42): Show |
45 | HG00140.hp1 HG00673.hp1 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.1720+977A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230499512 | |||||||
chr2:230499643 | T | G | 1 | a0001c0001t0019g0126 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1720+1108T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230499643 | |||||||
chr2:230499744 | G | A | 1 | a0001c0001t0002g0171 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1720+1209G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230499744 | |||||||
chr2:230499760 | A | T | 4 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1720+1225A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230499760 | |||||||
chr2:230499793 | C | T | 1 | a0001c0001t0025g0060 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1720+1258C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230499793 | |||||||
chr2:230499824 | G | C | 4 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1720+1289G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230499824 | |||||||
chr2:230499905 | C | T | 11 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(8): Show |
11 | HG01884.hp1 HG02572.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1720+1370C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230499905 | |||||||
chr2:230500123 | T | A | 1 | a0001c0003t0012g0247 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1720+1588T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230500123 | |||||||
chr2:230500124 | T | A | 1 | a0001c0003t0012g0247 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1720+1589T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230500124 | |||||||
chr2:230500126 | G | A | 1 | a0001c0003t0012g0247 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1720+1591G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230500126 | |||||||
chr2:230500128 | C | A | 1 | a0001c0003t0012g0247 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1720+1593C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230500128 | |||||||
chr2:230500128 | C | T | 1 | a0001c0003t0012g0048 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1720+1593C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230500128 | |||||||
chr2:230500129 | C | T | 1 | a0001c0003t0012g0247 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1720+1594C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230500129 | |||||||
chr2:230500130 | C | A | 1 | a0001c0003t0012g0247 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1720+1595C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230500130 | |||||||
chr2:230500253 | A | G | 1 | a0007c0010t0001g0168 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1720+1718A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230500253 | |||||||
chr2:230500373 | T | C | 229 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(226): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1720+1838T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230500373 | |||||||
chr2:230500426 | G | T | 4 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1720+1891G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230500426 | |||||||
chr2:230500759 | C | T | 7 | a0002c0002t0001g0107 a0002c0002t0001g0193 a0002c0002t0001g0209 others(4): Show |
7 | HG00323.hp1 HG00733.hp1 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.1720+2224C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230500759 | |||||||
chr2:230500763 | A | G | 229 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(226): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1720+2228A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230500763 | |||||||
chr2:230500804 | C | G | 51 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(48): Show |
52 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1721-2262C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230500804 | |||||||
chr2:230500814 | A | T | 51 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(48): Show |
52 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1721-2252A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230500814 | |||||||
chr2:230501174 | G | A | 1 | a0001c0003t0016g0138 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1721-1892G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230501174 | |||||||
chr2:230501335 | T | A | 1 | a0002c0005t0006g0012 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1721-1731T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230501335 | |||||||
chr2:230501353 | A | T | 1 | a0002c0005t0001g0155 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1721-1713A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230501353 | |||||||
chr2:230501588 | C | G | 38 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(35): Show |
38 | HG00140.hp1 HG00738.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1721-1478C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230501588 | |||||||
chr2:230501625 | A | G | 18 | a0001c0001t0005g0088 a0001c0001t0005g0091 a0001c0001t0005g0093 others(15): Show |
18 | HG01884.hp1 HG02145.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.1721-1441A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230501625 | |||||||
chr2:230501627 | G | C | 1 | a0001c0001t0002g0285 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1721-1439G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230501627 | |||||||
chr2:230501655 | G | GAGGAGTT others(1): Show |
101 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(98): Show |
101 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.1721-1410_1721-140 others(12): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chr2 | 230501655 | ||||||
chr2:230501660 | G | T | 51 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(48): Show |
52 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1721-1406G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230501660 | |||||||
chr2:230501691 | C | T | 1 | a0003c0004t0004g0051 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1721-1375C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230501691 | |||||||
chr2:230501693 | A | G | 229 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(226): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1721-1373A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230501693 | |||||||
chr2:230501730 | G | A | 1 | a0001c0003t0016g0138 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1721-1336G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230501730 | |||||||
chr2:230501847 | C | T | 30 | a0001c0001t0004g0050 a0001c0001t0004g0096 a0001c0001t0004g0176 others(27): Show |
30 | HG00140.hp1 HG00738.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1721-1219C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230501847 | |||||||
chr2:230501864 | C | T | 8 | a0001c0001t0005g0088 a0001c0001t0005g0091 a0001c0001t0005g0093 others(5): Show |
8 | HG02145.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1721-1202C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230501864 | |||||||
chr2:230502017 | T | C | 1 | a0001c0003t0012g0048 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1721-1049T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230502017 | |||||||
chr2:230502032 | C | CT | 22 | a0001c0001t0004g0096 a0001c0001t0004g0176 a0001c0001t0021g0090 others(19): Show |
22 | HG00140.hp1 HG01243.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.1721-1016dupT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chr2 | 230502032 | ||||||
chr2:230502032 | CT | C | 7 | a0001c0001t0008g0040 a0002c0002t0001g0140 a0002c0002t0001g0233 others(4): Show |
7 | HG01169.hp1 HG02897.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1721-1016delT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chr2 | 230502032 | ||||||
chr2:230502050 | T | A | 1 | a0001c0001t0004g0270 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1721-1016T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230502050 | |||||||
chr2:230502050 | T | TA | 14 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0007g0079 others(11): Show |
14 | HG00738.hp2 HG01106.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.1721-1014dupA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chr2 | 230502050 | ||||||
chr2:230502076 | C | G | 1 | a0002c0002t0001g0244 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1721-990C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230502076 | |||||||
chr2:230502327 | G | A | 3 | a0001c0001t0015g0089 a0001c0003t0015g0170 a0001c0019t0015g0035 |
3 | HG02572.hp2 HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1721-739G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230502327 | |||||||
chr2:230502448 | ATTTATAT others(7): Show |
A | 1 | a0001c0001t0025g0060 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1721-616_1721-603d others(16): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chr2 | 230502448 | ||||||
chr2:230502463 | T | A | 1 | a0001c0001t0025g0060 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1721-603T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230502463 | |||||||
chr2:230502561 | T | A | 2 | a0002c0002t0001g0078 a0002c0002t0001g0242 |
2 | NA18984.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1721-505T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230502561 | |||||||
chr2:230502707 | A | G | 38 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(35): Show |
38 | HG00140.hp1 HG00738.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1721-359A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230502707 | |||||||
chr2:230502710 | T | A | 4 | a0001c0003t0012g0042 a0001c0003t0012g0045 a0001c0003t0012g0046 others(1): Show |
4 | HG02258.hp1 HG03195.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1721-356T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230502710 | |||||||
chr2:230502731 | G | A | 1 | a0001c0003t0016g0138 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1721-335G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230502731 | |||||||
chr2:230502787 | T | G | 1 | a0006c0014t0004g0205 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1721-279T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230502787 | |||||||
chr2:230502907 | A | G | 2 | a0002c0005t0001g0052 a0002c0005t0001g0129 |
2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1721-159A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230502907 | |||||||
chr2:230502958 | T | C | 1 | a0005c0013t0024g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1721-108T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 19/28 | chr2 | 230502958 | |||||||
chr2:230503214 | G | C | 2 | a0001c0001t0007g0079 a0001c0003t0007g0055 |
2 | HG01943.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1765+104G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 20/28 | chr2 | 230503214 | |||||||
chr2:230503229 | C | T | 1 | a0001c0001t0002g0102 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1765+119C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 20/28 | chr2 | 230503229 | |||||||
chr2:230503260 | A | G | 2 | a0001c0001t0020g0286 a0002c0020t0022g0036 |
2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1765+150A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 20/28 | chr2 | 230503260 | |||||||
chr2:230503334 | C | T | 8 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(5): Show |
8 | HG00738.hp1 HG01074.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.1765+224C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 20/28 | chr2 | 230503334 | |||||||
chr2:230503413 | G | A | 1 | a0002c0005t0001g0256 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1765+303G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 20/28 | chr2 | 230503413 | |||||||
chr2:230503556 | T | C | 1 | a0001c0001t0003g0074 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1765+446T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 20/28 | chr2 | 230503556 | |||||||
chr2:230503762 | C | T | 2 | a0002c0002t0001g0078 a0002c0002t0001g0242 |
2 | NA18984.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1766-424C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 20/28 | chr2 | 230503762 | |||||||
chr2:230504182 | G | T | 33 | a0001c0001t0004g0096 a0001c0001t0004g0176 a0001c0001t0007g0079 others(30): Show |
33 | HG00140.hp1 HG00738.hp2 HG01243.hp1 others(30): Show |
splice_region_variant&intron_variant | LOW | c.1766-4G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 20/28 | chr2 | 230504182 | |||||||
chr2:230504394 | C | T | 1 | a0001c0001t0003g0056 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1870+104C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 21/28 | chr2 | 230504394 | |||||||
chr2:230504464 | T | C | 1 | a0001c0001t0020g0286 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1870+174T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 21/28 | chr2 | 230504464 | |||||||
chr2:230504503 | A | G | 5 | a0001c0003t0012g0042 a0001c0003t0012g0045 a0001c0003t0012g0046 others(2): Show |
5 | HG02258.hp1 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1870+213A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 21/28 | chr2 | 230504503 | |||||||
chr2:230504593 | C | G | 8 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(5): Show |
8 | HG01884.hp1 HG02572.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1870+303C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 21/28 | chr2 | 230504593 | |||||||
chr2:230504756 | C | T | 2 | a0001c0003t0015g0170 a0002c0002t0001g0150 |
2 | HG02615.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1870+466C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 21/28 | chr2 | 230504756 | |||||||
chr2:230504968 | G | T | 3 | a0001c0001t0002g0105 a0001c0001t0002g0266 a0001c0001t0002g0268 |
3 | HG01123.hp2 HG01433.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1870+678G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 21/28 | chr2 | 230504968 | |||||||
chr2:230505697 | T | C | 18 | a0001c0001t0004g0049 a0001c0001t0005g0088 a0001c0001t0005g0091 others(15): Show |
18 | HG02145.hp2 HG02622.hp2 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.1871-606T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 21/28 | chr2 | 230505697 | |||||||
chr2:230505731 | T | A | 1 | a0001c0003t0004g0249 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1871-572T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 21/28 | chr2 | 230505731 | |||||||
chr2:230505849 | G | A | 7 | a0001c0003t0012g0048 a0002c0002t0013g0038 a0002c0002t0013g0059 others(4): Show |
7 | HG01106.hp1 HG02145.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1871-454G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 21/28 | chr2 | 230505849 | |||||||
chr2:230505867 | G | A | 2 | a0002c0005t0001g0058 a0002c0005t0001g0256 |
2 | HG02257.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1871-436G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 21/28 | chr2 | 230505867 | |||||||
chr2:230505868 | C | T | 1 | a0001c0003t0012g0247 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1871-435C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 21/28 | chr2 | 230505868 | |||||||
chr2:230505915 | T | C | 1 | a0002c0005t0013g0106 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1871-388T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 21/28 | chr2 | 230505915 | |||||||
chr2:230506050 | G | T | 2 | a0001c0003t0016g0138 a0001c0007t0016g0031 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1871-253G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 21/28 | chr2 | 230506050 | |||||||
chr2:230506702 | T | G | 4 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2013+257T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 22/28 | chr2 | 230506702 | |||||||
chr2:230506762 | C | T | 1 | a0002c0005t0001g0076 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2013+317C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 22/28 | chr2 | 230506762 | |||||||
chr2:230506782 | T | TAC | 6 | a0002c0002t0001g0194 a0002c0002t0001g0210 a0002c0002t0001g0220 others(3): Show |
7 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2013+379_2013+380d others(4): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 22/28 | INFO_REALIGN_3_PRIME | chr2 | 230506782 | ||||||
chr2:230506782 | T | TACAC | 3 | a0002c0002t0001g0228 a0002c0002t0009g0226 a0002c0005t0006g0198 |
3 | NA18975.hp1 NA19082.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2013+377_2013+380d others(6): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 22/28 | INFO_REALIGN_3_PRIME | chr2 | 230506782 | ||||||
chr2:230506782 | TAC | T | 36 | a0001c0001t0002g0065 a0001c0001t0002g0071 a0001c0001t0002g0072 others(33): Show |
36 | HG00140.hp2 HG00733.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.2013+379_2013+380d others(4): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 22/28 | INFO_REALIGN_3_PRIME | chr2 | 230506782 | ||||||
chr2:230506782 | TACAC | T | 26 | a0001c0001t0002g0027 a0001c0001t0002g0196 a0001c0001t0003g0070 others(23): Show |
26 | HG00280.hp2 HG00738.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.2013+377_2013+380d others(6): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 22/28 | INFO_REALIGN_3_PRIME | chr2 | 230506782 | ||||||
chr2:230506782 | TACACAC | T | 54 | a0001c0001t0003g0029 a0001c0001t0003g0073 a0001c0001t0003g0077 others(51): Show |
54 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.2013+375_2013+380d others(8): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 22/28 | INFO_REALIGN_3_PRIME | chr2 | 230506782 | ||||||
chr2:230506782 | TACACACA others(1): Show |
T | 37 | a0001c0001t0003g0056 a0001c0001t0004g0049 a0001c0001t0004g0050 others(34): Show |
38 | HG00140.hp1 HG01243.hp1 HG01261.hp2 others(35): Show |
intron_variant | MODIFIER | c.2013+373_2013+380d others(10): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 22/28 | INFO_REALIGN_3_PRIME | chr2 | 230506782 | ||||||
chr2:230506782 | TACACACA others(3): Show |
T | 6 | a0001c0001t0020g0286 a0001c0003t0012g0042 a0001c0003t0012g0045 others(3): Show |
6 | HG02258.hp1 HG03098.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2013+371_2013+380d others(12): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 22/28 | INFO_REALIGN_3_PRIME | chr2 | 230506782 | ||||||
chr2:230506782 | TACACACA others(5): Show |
T | 5 | a0001c0003t0005g0047 a0002c0002t0013g0059 a0002c0005t0013g0037 others(2): Show |
5 | HG01106.hp1 HG02922.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.2013+369_2013+380d others(14): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 22/28 | INFO_REALIGN_3_PRIME | chr2 | 230506782 | ||||||
chr2:230506782 | TACACACA others(7): Show |
T | 1 | a0001c0001t0019g0126 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2013+367_2013+380d others(16): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 22/28 | INFO_REALIGN_3_PRIME | chr2 | 230506782 | ||||||
chr2:230506824 | C | CACACAT | 9 | a0001c0001t0006g0240 a0001c0001t0010g0120 a0001c0001t0010g0187 others(6): Show |
9 | HG02040.hp1 HG02071.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2013+380_2013+381i others(8): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 22/28 | INFO_REALIGN_3_PRIME | chr2 | 230506824 | ||||||
chr2:230506824 | C | CACAT | 7 | a0001c0001t0006g0223 a0001c0001t0006g0237 a0001c0001t0010g0260 others(4): Show |
7 | HG01255.hp2 HG01346.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2013+380_2013+381i others(6): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 22/28 | INFO_REALIGN_3_PRIME | chr2 | 230506824 | ||||||
chr2:230506824 | C | CAT | 9 | a0001c0001t0002g0102 a0001c0001t0002g0204 a0001c0001t0010g0130 others(6): Show |
9 | HG01109.hp1 HG01433.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2013+382_2013+383d others(4): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 22/28 | INFO_REALIGN_3_PRIME | chr2 | 230506824 | ||||||
chr2:230506824 | C | T | 209 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(206): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.2013+379C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 22/28 | chr2 | 230506824 | |||||||
chr2:230506970 | A | G | 2 | a0002c0002t0009g0213 a0002c0002t0009g0246 |
2 | NA18973.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.2013+525A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 22/28 | chr2 | 230506970 | |||||||
chr2:230506994 | T | C | 10 | a0001c0001t0007g0079 a0001c0001t0007g0173 a0001c0001t0007g0258 others(7): Show |
10 | HG00738.hp2 HG01256.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2013+549T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 22/28 | chr2 | 230506994 | |||||||
chr2:230507043 | G | A | 103 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(100): Show |
103 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.2013+598G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 22/28 | chr2 | 230507043 | |||||||
chr2:230507409 | C | T | 1 | a0001c0001t0010g0245 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2014-584C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 22/28 | chr2 | 230507409 | |||||||
chr2:230507470 | G | A | 4 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2014-523G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 22/28 | chr2 | 230507470 | |||||||
chr2:230507545 | T | C | 8 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(5): Show |
9 | HG01884.hp1 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2014-448T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 22/28 | chr2 | 230507545 | |||||||
chr2:230507681 | C | T | 1 | a0001c0001t0007g0173 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2014-312C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 22/28 | chr2 | 230507681 | |||||||
chr2:230508036 | T | C | 14 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(11): Show |
14 | HG01106.hp1 HG01884.hp1 HG02145.hp1 others(11): Show |
splice_region_variant&intron_variant | LOW | c.2052+5T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230508036 | |||||||
chr2:230508069 | T | C | 14 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(11): Show |
14 | HG01106.hp1 HG01884.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.2052+38T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230508069 | |||||||
chr2:230508097 | A | C | 15 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(12): Show |
16 | HG01106.hp1 HG01884.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.2052+66A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230508097 | |||||||
chr2:230508159 | A | C | 1 | a0003c0004t0004g0248 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2052+128A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230508159 | |||||||
chr2:230508246 | C | T | 2 | a0002c0002t0001g0166 a0002c0002t0001g0235 |
2 | HG02074.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.2052+215C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230508246 | |||||||
chr2:230508304 | T | A | 6 | a0002c0002t0011g0119 a0002c0002t0011g0145 a0002c0002t0011g0157 others(3): Show |
6 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2052+273T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230508304 | |||||||
chr2:230508306 | C | T | 7 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(4): Show |
7 | HG01884.hp1 HG02572.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2052+275C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230508306 | |||||||
chr2:230508311 | C | CATT | 5 | a0004c0006t0004g0238 a0004c0006t0004g0277 a0004c0006t0004g0282 others(2): Show |
5 | HG00140.hp1 HG02922.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.2052+280_2052+281i others(5): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230508311 | |||||||
chr2:230508311 | C | CATTT | 12 | a0001c0001t0004g0096 a0001c0001t0004g0176 a0001c0001t0021g0090 others(9): Show |
13 | HG01243.hp1 HG01261.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.2052+280_2052+281i others(6): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230508311 | |||||||
chr2:230508311 | C | CT | 6 | a0001c0001t0005g0093 a0001c0001t0005g0127 a0001c0001t0020g0286 others(3): Show |
6 | HG02970.hp1 HG03130.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2052+300dupT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230508311 | ||||||
chr2:230508311 | C | CTT | 13 | a0001c0001t0005g0088 a0001c0001t0005g0091 a0001c0001t0005g0097 others(10): Show |
13 | HG00323.hp2 HG01070.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.2052+299_2052+300d others(4): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230508311 | ||||||
chr2:230508311 | C | CTTT | 73 | a0001c0001t0002g0072 a0001c0001t0003g0029 a0001c0001t0003g0056 others(70): Show |
73 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.2052+298_2052+300d others(5): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230508311 | ||||||
chr2:230508311 | C | CTTTT | 120 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(117): Show |
120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.2052+297_2052+300d others(6): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230508311 | ||||||
chr2:230508311 | C | CTTTTTTT others(3): Show |
1 | a0001c0003t0004g0125 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2052+291_2052+300d others(12): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230508311 | ||||||
chr2:230508419 | G | T | 1 | a0002c0002t0001g0078 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2052+388G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230508419 | |||||||
chr2:230508481 | A | AT | 7 | a0001c0003t0012g0048 a0002c0002t0013g0038 a0002c0002t0013g0059 others(4): Show |
7 | HG01106.hp1 HG02145.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2052+458dupT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230508481 | ||||||
chr2:230508596 | G | C | 1 | a0002c0020t0022g0036 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2052+565G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230508596 | |||||||
chr2:230508617 | G | A | 1 | a0001c0001t0020g0286 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2052+586G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230508617 | |||||||
chr2:230508652 | C | A | 1 | a0007c0010t0001g0168 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2052+621C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230508652 | |||||||
chr2:230508653 | A | G | 1 | a0001c0001t0003g0056 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2052+622A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230508653 | |||||||
chr2:230508745 | G | A | 1 | a0001c0001t0019g0126 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2052+714G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230508745 | |||||||
chr2:230508750 | T | G | 1 | a0001c0001t0006g0135 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2052+719T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230508750 | |||||||
chr2:230508810 | C | T | 5 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0270 others(2): Show |
5 | HG01884.hp2 HG02055.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2052+779C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230508810 | |||||||
chr2:230508917 | CCACA | C | 4 | a0001c0001t0002g0284 a0001c0001t0003g0056 a0002c0005t0001g0010 others(1): Show |
4 | HG00280.hp1 HG04184.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.2052+913_2052+916d others(6): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230508917 | ||||||
chr2:230508917 | CCACACA | C | 145 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(142): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.2052+911_2052+916d others(8): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230508917 | ||||||
chr2:230508936 | CACACACA others(5): Show |
C | 2 | a0001c0001t0002g0019 a0001c0001t0019g0126 |
2 | HG01106.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2052+917_2052+928d others(14): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230508936 | ||||||
chr2:230508938 | CACACACA others(3): Show |
C | 1 | a0001c0001t0004g0270 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2052+917_2052+926d others(12): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230508938 | ||||||
chr2:230508942 | C | T | 1 | a0001c0001t0015g0089 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2052+911C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230508942 | |||||||
chr2:230508942 | CACACAT | C | 5 | a0001c0001t0004g0049 a0001c0007t0005g0030 a0001c0007t0005g0032 others(2): Show |
5 | HG01109.hp1 HG02630.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2052+917_2052+922d others(8): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230508942 | ||||||
chr2:230508944 | CACAT | C | 3 | a0001c0001t0004g0176 a0001c0001t0015g0089 a0002c0002t0001g0034 |
3 | HG02451.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2052+917_2052+920d others(6): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230508944 | ||||||
chr2:230508946 | CAT | C | 7 | a0001c0003t0007g0055 a0002c0002t0011g0119 a0002c0002t0011g0145 others(4): Show |
7 | HG01943.hp1 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2052+917_2052+918d others(4): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230508946 | ||||||
chr2:230508948 | T | C | 34 | a0001c0001t0004g0096 a0001c0001t0008g0039 a0001c0001t0008g0040 others(31): Show |
35 | HG00140.hp1 HG01106.hp1 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.2052+917T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230508948 | |||||||
chr2:230508948 | TAC | T | 7 | a0002c0002t0001g0005 a0002c0002t0001g0044 a0002c0002t0001g0118 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2052+937_2052+938d others(4): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230508948 | ||||||
chr2:230508948 | TACAC | T | 25 | a0001c0001t0004g0050 a0001c0001t0005g0088 a0001c0001t0005g0091 others(22): Show |
25 | HG00738.hp2 HG01256.hp2 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.2052+935_2052+938d others(6): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230508948 | ||||||
chr2:230508950 | C | T | 1 | a0002c0002t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2052+919C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230508950 | |||||||
chr2:230508952 | C | CACACAT | 13 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(10): Show |
13 | HG01106.hp1 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.2052+926_2052+927i others(8): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230508952 | ||||||
chr2:230508952 | C | CAT | 10 | a0003c0004t0004g0051 a0003c0004t0004g0104 a0004c0006t0004g0180 others(7): Show |
10 | HG00140.hp1 HG01243.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.2052+922_2052+923i others(4): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230508952 | ||||||
chr2:230508952 | C | T | 24 | a0001c0001t0004g0049 a0001c0001t0004g0096 a0001c0001t0004g0270 others(21): Show |
25 | HG01109.hp1 HG01884.hp2 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.2052+921C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230508952 | |||||||
chr2:230508954 | C | T | 2 | a0001c0001t0002g0019 a0004c0006t0004g0153 |
2 | HG01106.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.2052+923C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230508954 | |||||||
chr2:230508956 | CACACACA others(7): Show |
C | 1 | a0002c0002t0001g0233 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2052+938_2052+951d others(16): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230508956 | ||||||
chr2:230508966 | C | T | 1 | a0001c0003t0004g0125 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2052+935C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230508966 | |||||||
chr2:230508970 | T | C | 14 | a0001c0001t0004g0176 a0001c0001t0021g0090 a0003c0004t0004g0051 others(11): Show |
14 | HG00140.hp1 HG01243.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.2052+939T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230508970 | |||||||
chr2:230508982 | C | T | 1 | a0001c0001t0002g0008 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2052+951C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230508982 | |||||||
chr2:230508983 | G | A | 1 | a0001c0001t0020g0286 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2052+952G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230508983 | |||||||
chr2:230509045 | A | G | 230 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(227): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.2052+1014A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230509045 | |||||||
chr2:230509419 | T | A | 1 | a0002c0005t0001g0141 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2052+1388T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230509419 | |||||||
chr2:230509746 | A | C | 7 | a0001c0003t0012g0048 a0002c0002t0013g0038 a0002c0002t0013g0059 others(4): Show |
7 | HG01106.hp1 HG02145.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2053-1379A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230509746 | |||||||
chr2:230509873 | A | G | 1 | a0001c0003t0005g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2053-1252A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230509873 | |||||||
chr2:230509903 | A | G | 229 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(226): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.2053-1222A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230509903 | |||||||
chr2:230509927 | G | A | 1 | a0001c0001t0002g0284 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2053-1198G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230509927 | |||||||
chr2:230509955 | G | C | 1 | a0001c0001t0004g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2053-1170G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230509955 | |||||||
chr2:230509987 | C | A | 1 | a0001c0003t0005g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2053-1138C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230509987 | |||||||
chr2:230510377 | A | C | 1 | a0003c0004t0004g0051 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2053-748A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230510377 | |||||||
chr2:230510377 | A | G | 43 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(40): Show |
44 | HG00140.hp1 HG00738.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.2053-748A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230510377 | |||||||
chr2:230510435 | G | A | 1 | a0002c0020t0022g0036 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2053-690G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230510435 | |||||||
chr2:230510473 | CTTTTTTT others(2): Show |
C | 10 | a0001c0001t0007g0079 a0001c0003t0004g0099 a0001c0003t0004g0249 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2053-601_2053-593d others(11): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230510473 | ||||||
chr2:230510473 | CTTTTTTT others(3): Show |
C | 7 | a0001c0001t0004g0049 a0001c0001t0007g0173 a0001c0003t0004g0125 others(4): Show |
7 | HG01258.hp1 HG01978.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.2053-602_2053-593d others(12): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230510473 | ||||||
chr2:230510473 | CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0007g0258 a0001c0003t0007g0055 a0001c0003t0007g0250 others(1): Show |
4 | HG00738.hp2 HG01256.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.2053-603_2053-593d others(13): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230510473 | ||||||
chr2:230510473 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0025g0060 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2053-604_2053-593d others(14): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230510473 | ||||||
chr2:230510473 | CTTTTTTT others(6): Show |
C | 1 | a0002c0002t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2053-605_2053-593d others(15): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230510473 | ||||||
chr2:230510473 | CTTTTTTT others(8): Show |
C | 3 | a0001c0001t0002g0203 a0001c0003t0002g0100 a0002c0005t0001g0256 |
3 | HG02257.hp2 HG02683.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2053-607_2053-593d others(17): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230510473 | ||||||
chr2:230510473 | CTTTTTTT others(9): Show |
C | 2 | a0001c0001t0005g0124 a0005c0013t0024g0161 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2053-608_2053-593d others(18): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230510473 | ||||||
chr2:230510473 | CTTTTTTT others(10): Show |
C | 23 | a0001c0001t0002g0102 a0001c0001t0002g0175 a0001c0001t0002g0274 others(20): Show |
23 | HG00735.hp1 HG01192.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.2053-609_2053-593d others(19): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230510473 | ||||||
chr2:230510473 | CTTTTTTT others(11): Show |
C | 24 | a0001c0001t0004g0098 a0001c0001t0005g0093 a0001c0001t0005g0127 others(21): Show |
24 | HG00099.hp2 HG00323.hp1 HG01943.hp2 others(21): Show |
intron_variant | MODIFIER | c.2053-610_2053-593d others(20): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230510473 | ||||||
chr2:230510473 | CTTTTTTT others(12): Show |
C | 29 | a0001c0001t0002g0105 a0001c0001t0002g0184 a0001c0001t0002g0254 others(26): Show |
30 | HG00558.hp2 HG00733.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.2053-611_2053-593d others(21): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230510473 | ||||||
chr2:230510473 | CTTTTTTT others(13): Show |
C | 35 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0019 others(32): Show |
35 | HG00544.hp1 HG00673.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.2053-612_2053-593d others(22): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230510473 | ||||||
chr2:230510473 | CTTTTTTT others(14): Show |
C | 41 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0026 others(38): Show |
41 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.2053-613_2053-593d others(23): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230510473 | ||||||
chr2:230510473 | CTTTTTTT others(15): Show |
C | 4 | a0001c0001t0002g0279 a0001c0001t0004g0270 a0001c0001t0014g0149 others(1): Show |
4 | HG01884.hp2 HG03654.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.2053-614_2053-593d others(24): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230510473 | ||||||
chr2:230510473 | CTTTTTTT others(16): Show |
C | 1 | a0001c0001t0008g0054 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2053-615_2053-593d others(25): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230510473 | ||||||
chr2:230510473 | CTTTTTTT others(17): Show |
C | 6 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(3): Show |
6 | HG01884.hp1 HG02896.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2053-616_2053-593d others(26): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230510473 | ||||||
chr2:230510473 | CTTTTTTT others(19): Show |
C | 1 | a0001c0001t0004g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2053-618_2053-593d others(28): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230510473 | ||||||
chr2:230510473 | CTTTTTTT others(22): Show |
C | 1 | a0001c0003t0012g0247 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2053-621_2053-593d others(31): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230510473 | ||||||
chr2:230510473 | CTTTTTTT others(23): Show |
C | 5 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(2): Show |
5 | HG01109.hp1 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2053-622_2053-593d others(32): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230510473 | ||||||
chr2:230510473 | CTTTTTTT others(24): Show |
C | 7 | a0001c0003t0005g0047 a0001c0003t0012g0048 a0002c0002t0013g0059 others(4): Show |
7 | HG01106.hp1 HG02145.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2053-623_2053-593d others(33): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230510473 | ||||||
chr2:230510473 | CTTTTTTT others(25): Show |
C | 1 | a0003c0004t0004g0051 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2053-624_2053-593d others(34): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230510473 | ||||||
chr2:230510473 | CTTTTTTT others(27): Show |
C | 1 | a0006c0014t0004g0205 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2053-626_2053-593d others(36): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230510473 | ||||||
chr2:230510473 | CTTTTTTT others(28): Show |
C | 9 | a0001c0003t0016g0138 a0004c0006t0004g0153 a0004c0006t0004g0180 others(6): Show |
9 | HG00140.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.2053-627_2053-593d others(37): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230510473 | ||||||
chr2:230510473 | CTTTTTTT others(29): Show |
C | 6 | a0002c0002t0011g0119 a0002c0002t0011g0145 a0002c0002t0011g0157 others(3): Show |
6 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2053-628_2053-593d others(38): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230510473 | ||||||
chr2:230510473 | CTTTTTTT others(30): Show |
C | 1 | a0003c0004t0002g0269 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2053-629_2053-593d others(39): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230510473 | ||||||
chr2:230510473 | CTTTTTTT others(32): Show |
C | 4 | a0001c0001t0003g0029 a0001c0001t0003g0143 a0001c0003t0003g0188 others(1): Show |
4 | NA18974.hp1 NA18975.hp2 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.2053-631_2053-593d others(41): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230510473 | ||||||
chr2:230510473 | CTTTTTTT others(33): Show |
C | 46 | a0001c0001t0003g0056 a0001c0001t0003g0070 a0001c0001t0003g0073 others(43): Show |
46 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.2053-632_2053-593d others(42): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230510473 | ||||||
chr2:230510473 | CTTTTTTT others(34): Show |
C | 1 | a0003c0004t0003g0116 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2053-633_2053-593d others(43): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr2 | 230510473 | ||||||
chr2:230510479 | T | C | 1 | a0003c0004t0004g0104 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2053-646T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230510479 | |||||||
chr2:230510486 | T | G | 1 | a0001c0003t0004g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2053-639T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230510486 | |||||||
chr2:230510604 | G | A | 1 | a0001c0001t0003g0199 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2053-521G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230510604 | |||||||
chr2:230510631 | C | CTCCCAAG others(7): Show |
230 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(227): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.2053-494_2053-493i others(16): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230510631 | |||||||
chr2:230510632 | C | G | 230 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(227): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.2053-493C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230510632 | |||||||
chr2:230510656 | T | C | 15 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(12): Show |
16 | HG01106.hp1 HG01884.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.2053-469T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230510656 | |||||||
chr2:230510822 | C | A | 3 | a0001c0001t0005g0093 a0001c0001t0005g0095 a0001c0001t0005g0127 |
3 | HG02809.hp1 HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2053-303C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230510822 | |||||||
chr2:230510968 | T | A | 7 | a0001c0003t0012g0048 a0002c0002t0013g0038 a0002c0002t0013g0059 others(4): Show |
7 | HG01106.hp1 HG02145.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2053-157T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230510968 | |||||||
chr2:230511111 | G | T | 2 | a0001c0001t0017g0177 a0001c0001t0017g0178 |
2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2053-14G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230511111 | |||||||
chr2:230511120 | A | C | 2 | a0001c0001t0017g0177 a0001c0001t0017g0178 |
2 | HG02257.hp1 HG02970.hp2 |
splice_region_variant&intron_variant | LOW | c.2053-5A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 23/28 | chr2 | 230511120 | |||||||
chr2:230511259 | G | A | 18 | a0001c0001t0004g0096 a0001c0001t0004g0176 a0001c0001t0021g0090 others(15): Show |
19 | HG00140.hp1 HG01243.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.2094+93G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230511259 | |||||||
chr2:230511275 | G | A | 1 | a0005c0008t0003g0003 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2094+109G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230511275 | |||||||
chr2:230511385 | C | T | 1 | a0001c0003t0016g0138 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2094+219C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230511385 | |||||||
chr2:230511527 | G | A | 3 | a0001c0003t0007g0250 a0001c0003t0007g0251 a0001c0009t0007g0272 |
3 | HG00738.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2094+361G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230511527 | |||||||
chr2:230511605 | C | T | 229 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(226): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.2094+439C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230511605 | |||||||
chr2:230511625 | G | A | 1 | a0002c0005t0001g0155 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2094+459G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230511625 | |||||||
chr2:230511649 | CT | C | 44 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(41): Show |
45 | HG00140.hp1 HG00738.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.2094+484delT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230511649 | |||||||
chr2:230511669 | G | A | 1 | a0001c0003t0005g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2094+503G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230511669 | |||||||
chr2:230512012 | G | A | 1 | a0001c0003t0004g0249 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2094+846G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230512012 | |||||||
chr2:230512186 | C | T | 229 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(226): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.2094+1020C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230512186 | |||||||
chr2:230512276 | C | CT | 13 | a0001c0001t0025g0060 a0002c0002t0001g0005 a0002c0002t0001g0118 others(10): Show |
13 | HG01943.hp2 HG02055.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.2094+1141dupT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230512276 | ||||||
chr2:230512276 | CT | C | 89 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(86): Show |
89 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.2094+1141delT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230512276 | ||||||
chr2:230512276 | CTT | C | 31 | a0001c0001t0002g0026 a0001c0001t0005g0088 a0001c0001t0005g0091 others(28): Show |
31 | HG00140.hp1 HG01243.hp1 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.2094+1140_2094+114 others(6): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230512276 | ||||||
chr2:230512276 | CTTT | C | 12 | a0001c0001t0004g0176 a0001c0001t0004g0270 a0001c0001t0005g0252 others(9): Show |
12 | HG00738.hp2 HG01256.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.2094+1139_2094+114 others(7): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230512276 | ||||||
chr2:230512276 | CTTTTTTT others(2): Show |
C | 19 | a0001c0003t0003g0110 a0001c0003t0003g0188 a0001c0003t0003g0273 others(16): Show |
19 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.2094+1133_2094+114 others(13): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230512276 | ||||||
chr2:230512276 | CTTTTTTT others(3): Show |
C | 34 | a0001c0001t0003g0056 a0001c0001t0003g0070 a0001c0001t0003g0073 others(31): Show |
34 | HG00544.hp2 HG00735.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.2094+1132_2094+114 others(14): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230512276 | ||||||
chr2:230512276 | CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0003g0029 a0001c0003t0016g0138 a0002c0005t0013g0128 |
3 | HG02145.hp1 HG03225.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.2094+1131_2094+114 others(15): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230512276 | ||||||
chr2:230512276 | CTTTTTTT others(5): Show |
C | 14 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(11): Show |
15 | HG01106.hp1 HG01884.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.2094+1130_2094+114 others(16): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230512276 | ||||||
chr2:230512320 | C | T | 1 | a0001c0003t0005g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2094+1154C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230512320 | |||||||
chr2:230512365 | C | G | 1 | a0002c0020t0022g0036 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2094+1199C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230512365 | |||||||
chr2:230512420 | G | C | 9 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(6): Show |
9 | HG01884.hp1 HG02109.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2094+1254G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230512420 | |||||||
chr2:230512490 | A | G | 1 | a0001c0001t0002g0008 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2094+1324A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230512490 | |||||||
chr2:230512577 | C | T | 50 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.2094+1411C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230512577 | |||||||
chr2:230512578 | G | A | 1 | a0006c0016t0004g0280 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2094+1412G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230512578 | |||||||
chr2:230512649 | T | C | 153 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(150): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.2094+1483T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230512649 | |||||||
chr2:230512673 | G | A | 7 | a0001c0001t0002g0065 a0001c0001t0002g0071 a0001c0001t0002g0195 others(4): Show |
7 | HG02129.hp1 NA18939.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.2094+1507G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230512673 | |||||||
chr2:230512910 | G | A | 1 | a0001c0001t0002g0105 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2094+1744G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230512910 | |||||||
chr2:230512961 | CT | C | 6 | a0002c0002t0001g0078 a0002c0002t0001g0131 a0002c0002t0001g0147 others(3): Show |
6 | HG01943.hp2 HG03239.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.2094+1796delT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230512961 | |||||||
chr2:230513009 | G | A | 4 | a0001c0001t0002g0027 a0001c0001t0002g0072 a0001c0001t0002g0184 others(1): Show |
4 | NA18612.hp1 NA18981.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.2094+1843G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230513009 | |||||||
chr2:230513012 | G | A | 2 | a0001c0003t0016g0138 a0001c0007t0016g0031 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2094+1846G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230513012 | |||||||
chr2:230513280 | C | A | 39 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(36): Show |
39 | HG00140.hp1 HG00738.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.2094+2114C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230513280 | |||||||
chr2:230513280 | C | T | 17 | a0001c0001t0005g0088 a0001c0001t0005g0091 a0001c0001t0005g0093 others(14): Show |
17 | HG02145.hp2 HG02622.hp2 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.2094+2114C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230513280 | |||||||
chr2:230513314 | G | A | 1 | a0002c0020t0022g0036 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2094+2148G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230513314 | |||||||
chr2:230513518 | T | TA | 8 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(5): Show |
8 | HG01109.hp1 HG01943.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2094+2367dupA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230513518 | ||||||
chr2:230513518 | TA | T | 153 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(150): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.2094+2367delA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230513518 | ||||||
chr2:230513632 | C | T | 1 | a0001c0001t0025g0060 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2094+2466C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230513632 | |||||||
chr2:230513636 | G | A | 4 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2094+2470G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230513636 | |||||||
chr2:230513867 | C | T | 15 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(12): Show |
16 | HG01106.hp1 HG01884.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.2094+2701C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230513867 | |||||||
chr2:230513907 | C | T | 1 | a0002c0020t0022g0036 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2094+2741C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230513907 | |||||||
chr2:230513910 | T | G | 1 | a0001c0001t0002g0067 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2094+2744T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230513910 | |||||||
chr2:230513961 | A | AAAAGAAA others(93): Show |
50 | a0001c0001t0003g0056 a0001c0001t0003g0070 a0001c0001t0003g0073 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.2094+2957_2094+305 others(104): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230513961 | ||||||
chr2:230513961 | A | AAAAGAAA others(92): Show |
1 | a0001c0001t0003g0029 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2094+2811_2094+281 others(103): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230513961 | ||||||
chr2:230513964 | A | G | 8 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(5): Show |
9 | HG01884.hp1 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2094+2798A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230513964 | |||||||
chr2:230514115 | C | T | 2 | a0001c0001t0017g0177 a0001c0001t0017g0178 |
2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2094+2949C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230514115 | |||||||
chr2:230514153 | C | T | 4 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2094+2987C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230514153 | |||||||
chr2:230514160 | A | C | 1 | a0004c0006t0004g0282 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2094+2994A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230514160 | |||||||
chr2:230514269 | A | T | 1 | a0005c0013t0024g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2094+3103A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230514269 | |||||||
chr2:230514337 | A | G | 1 | a0001c0001t0010g0187 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2094+3171A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230514337 | |||||||
chr2:230514362 | GA | G | 43 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(40): Show |
43 | HG00140.hp1 HG00738.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.2094+3204delA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230514362 | ||||||
chr2:230514803 | C | T | 9 | a0004c0006t0004g0153 a0004c0006t0004g0180 a0004c0006t0004g0182 others(6): Show |
9 | HG00140.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.2094+3637C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230514803 | |||||||
chr2:230514900 | A | G | 8 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(5): Show |
9 | HG01884.hp1 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2094+3734A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230514900 | |||||||
chr2:230514902 | G | A | 1 | a0002c0002t0001g0005 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2094+3736G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230514902 | |||||||
chr2:230514944 | A | G | 4 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2094+3778A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230514944 | |||||||
chr2:230515012 | A | C | 6 | a0002c0002t0011g0119 a0002c0002t0011g0145 a0002c0002t0011g0157 others(3): Show |
6 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2094+3846A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230515012 | |||||||
chr2:230515074 | T | G | 1 | a0001c0001t0004g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2094+3908T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230515074 | |||||||
chr2:230515096 | A | G | 5 | a0001c0003t0012g0042 a0001c0003t0012g0045 a0001c0003t0012g0046 others(2): Show |
5 | HG02258.hp1 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2094+3930A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230515096 | |||||||
chr2:230515430 | C | T | 1 | a0002c0002t0001g0028 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2094+4264C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230515430 | |||||||
chr2:230515431 | G | A | 2 | a0001c0003t0016g0138 a0001c0007t0016g0031 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2094+4265G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230515431 | |||||||
chr2:230515502 | T | G | 15 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(12): Show |
16 | HG01106.hp1 HG01884.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.2094+4336T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230515502 | |||||||
chr2:230515728 | C | T | 2 | a0001c0003t0016g0138 a0001c0007t0016g0031 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2094+4562C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230515728 | |||||||
chr2:230515812 | C | T | 1 | a0002c0002t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2094+4646C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230515812 | |||||||
chr2:230515857 | A | G | 1 | a0003c0004t0003g0255 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2094+4691A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230515857 | |||||||
chr2:230515863 | G | T | 1 | a0004c0006t0004g0182 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2094+4697G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230515863 | |||||||
chr2:230515999 | C | G | 6 | a0002c0002t0011g0119 a0002c0002t0011g0145 a0002c0002t0011g0157 others(3): Show |
6 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2094+4833C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230515999 | |||||||
chr2:230516020 | C | CA | 99 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(96): Show |
99 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.2094+4866dupA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230516020 | ||||||
chr2:230516020 | C | CAA | 28 | a0001c0001t0002g0105 a0001c0001t0002g0167 a0001c0001t0002g0267 others(25): Show |
28 | HG00280.hp1 HG00738.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.2094+4865_2094+486 others(6): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230516020 | ||||||
chr2:230516020 | C | CAAA | 19 | a0001c0001t0004g0049 a0001c0001t0004g0096 a0001c0001t0004g0176 others(16): Show |
19 | HG00140.hp1 HG01243.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.2094+4864_2094+486 others(7): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230516020 | ||||||
chr2:230516020 | CA | C | 10 | a0001c0001t0020g0286 a0001c0003t0005g0047 a0001c0003t0016g0138 others(7): Show |
10 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2094+4866delA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230516020 | ||||||
chr2:230516439 | AGTTT | A | 5 | a0001c0003t0012g0042 a0001c0003t0012g0045 a0001c0003t0012g0046 others(2): Show |
5 | HG02258.hp1 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2094+5274_2094+527 others(8): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230516439 | |||||||
chr2:230516556 | G | A | 1 | a0001c0003t0004g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2094+5390G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230516556 | |||||||
chr2:230516771 | T | G | 3 | a0002c0002t0013g0059 a0002c0005t0013g0106 a0002c0005t0013g0287 |
3 | HG01106.hp1 HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2094+5605T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230516771 | |||||||
chr2:230516782 | T | C | 1 | a0001c0001t0020g0286 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2094+5616T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230516782 | |||||||
chr2:230516928 | G | A | 4 | a0003c0004t0003g0146 a0003c0004t0003g0208 a0003c0004t0003g0222 others(1): Show |
4 | HG00099.hp1 HG00323.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.2094+5762G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230516928 | |||||||
chr2:230517113 | T | C | 2 | a0001c0003t0012g0045 a0001c0003t0012g0257 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2094+5947T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230517113 | |||||||
chr2:230517219 | A | G | 39 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(36): Show |
39 | HG00140.hp1 HG00738.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.2094+6053A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230517219 | |||||||
chr2:230517764 | C | CA | 214 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(211): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.2094+6611dupA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230517764 | ||||||
chr2:230517979 | A | T | 43 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(40): Show |
43 | HG00140.hp1 HG00738.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.2094+6813A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230517979 | |||||||
chr2:230518109 | C | T | 2 | a0001c0003t0016g0138 a0001c0007t0016g0031 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2094+6943C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230518109 | |||||||
chr2:230518110 | T | TTACCA | 118 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(115): Show |
119 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.2094+6947_2094+694 others(9): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230518110 | ||||||
chr2:230518257 | A | T | 1 | a0001c0003t0003g0273 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2094+7091A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230518257 | |||||||
chr2:230518502 | T | C | 1 | a0001c0001t0002g0065 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2094+7336T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230518502 | |||||||
chr2:230518512 | A | G | 1 | a0009c0018t0004g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2094+7346A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230518512 | |||||||
chr2:230518733 | C | T | 101 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(98): Show |
101 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.2094+7567C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230518733 | |||||||
chr2:230518878 | T | A | 101 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(98): Show |
101 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.2094+7712T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230518878 | |||||||
chr2:230519136 | G | T | 50 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.2094+7970G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230519136 | |||||||
chr2:230519406 | T | G | 6 | a0002c0002t0011g0119 a0002c0002t0011g0145 a0002c0002t0011g0157 others(3): Show |
6 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2094+8240T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230519406 | |||||||
chr2:230519424 | T | C | 1 | a0001c0001t0005g0095 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2094+8258T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230519424 | |||||||
chr2:230519455 | C | T | 230 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(227): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.2094+8289C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230519455 | |||||||
chr2:230519635 | A | G | 1 | a0001c0003t0016g0138 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2094+8469A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230519635 | |||||||
chr2:230519705 | A | AT | 7 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(4): Show |
7 | HG01884.hp1 HG02572.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2094+8547dupT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230519705 | ||||||
chr2:230519713 | T | C | 103 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(100): Show |
103 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.2094+8547T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230519713 | |||||||
chr2:230519751 | G | C | 6 | a0002c0002t0011g0119 a0002c0002t0011g0145 a0002c0002t0011g0157 others(3): Show |
6 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2094+8585G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230519751 | |||||||
chr2:230519871 | G | T | 2 | a0003c0004t0002g0117 a0003c0004t0002g0134 |
2 | HG01070.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.2094+8705G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230519871 | |||||||
chr2:230519887 | T | G | 1 | a0001c0003t0005g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2094+8721T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230519887 | |||||||
chr2:230519889 | T | C | 55 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(52): Show |
55 | HG00140.hp1 HG00738.hp2 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.2094+8723T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230519889 | |||||||
chr2:230520023 | G | A | 1 | a0002c0020t0022g0036 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2094+8857G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230520023 | |||||||
chr2:230520071 | A | G | 215 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(212): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2094+8905A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230520071 | |||||||
chr2:230520080 | A | G | 2 | a0001c0007t0005g0032 a0001c0007t0005g0033 |
2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2094+8914A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230520080 | |||||||
chr2:230520114 | A | G | 1 | a0001c0003t0002g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2094+8948A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230520114 | |||||||
chr2:230520150 | G | C | 4 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2094+8984G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230520150 | |||||||
chr2:230520183 | C | T | 1 | a0001c0003t0016g0138 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2094+9017C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230520183 | |||||||
chr2:230520184 | G | A | 1 | a0009c0018t0004g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2094+9018G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230520184 | |||||||
chr2:230520226 | T | C | 2 | a0001c0001t0010g0260 a0001c0009t0010g0064 |
2 | HG01255.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2094+9060T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230520226 | |||||||
chr2:230520232 | T | C | 103 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(100): Show |
103 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.2094+9066T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230520232 | |||||||
chr2:230520254 | C | T | 230 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(227): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.2094+9088C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230520254 | |||||||
chr2:230520516 | G | A | 103 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(100): Show |
103 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.2094+9350G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230520516 | |||||||
chr2:230520534 | C | A | 230 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(227): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.2094+9368C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230520534 | |||||||
chr2:230520539 | G | C | 50 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.2094+9373G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230520539 | |||||||
chr2:230520587 | G | A | 6 | a0002c0002t0011g0119 a0002c0002t0011g0145 a0002c0002t0011g0157 others(3): Show |
6 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2094+9421G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230520587 | |||||||
chr2:230520662 | C | T | 1 | a0002c0002t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2094+9496C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230520662 | |||||||
chr2:230520978 | T | A | 4 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(1): Show |
4 | HG00738.hp1 HG01074.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2094+9812T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230520978 | |||||||
chr2:230521054 | T | C | 5 | a0001c0001t0002g0102 a0001c0001t0002g0175 a0003c0004t0002g0269 others(2): Show |
5 | HG02896.hp2 HG02897.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.2094+9888T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230521054 | |||||||
chr2:230521130 | G | C | 38 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(35): Show |
38 | HG00140.hp1 HG00738.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.2094+9964G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230521130 | |||||||
chr2:230521159 | T | C | 110 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(107): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.2094+9993T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230521159 | |||||||
chr2:230521211 | G | C | 1 | a0002c0002t0001g0220 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2094+10045G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230521211 | |||||||
chr2:230521449 | C | A | 3 | a0001c0001t0003g0070 a0001c0001t0003g0074 a0001c0001t0003g0085 |
3 | HG01123.hp1 HG01981.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.2094+10283C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230521449 | |||||||
chr2:230521534 | T | C | 2 | a0001c0001t0003g0143 a0011c0011t0003g0086 |
2 | NA19002.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.2094+10368T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230521534 | |||||||
chr2:230521627 | G | T | 1 | a0001c0003t0004g0125 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2094+10461G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230521627 | |||||||
chr2:230521628 | C | T | 1 | a0001c0003t0004g0125 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2094+10462C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230521628 | |||||||
chr2:230521682 | TG | T | 6 | a0002c0002t0011g0119 a0002c0002t0011g0145 a0002c0002t0011g0157 others(3): Show |
6 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2094+10518delG | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230521682 | ||||||
chr2:230521776 | C | G | 1 | a0001c0001t0004g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2094+10610C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230521776 | |||||||
chr2:230521815 | C | T | 6 | a0002c0002t0011g0119 a0002c0002t0011g0145 a0002c0002t0011g0157 others(3): Show |
6 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2094+10649C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230521815 | |||||||
chr2:230521827 | A | G | 8 | a0003c0004t0003g0103 a0003c0004t0003g0112 a0003c0004t0003g0114 others(5): Show |
8 | HG01168.hp2 HG01169.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.2094+10661A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230521827 | |||||||
chr2:230521839 | G | T | 1 | a0001c0001t0008g0039 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2094+10673G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230521839 | |||||||
chr2:230521844 | G | T | 6 | a0002c0002t0011g0119 a0002c0002t0011g0145 a0002c0002t0011g0157 others(3): Show |
6 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2094+10678G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230521844 | |||||||
chr2:230522109 | G | A | 1 | a0002c0005t0013g0287 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2094+10943G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230522109 | |||||||
chr2:230522197 | G | C | 1 | a0001c0001t0002g0067 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2094+11031G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230522197 | |||||||
chr2:230522242 | G | T | 1 | a0003c0004t0004g0051 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2094+11076G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230522242 | |||||||
chr2:230522246 | T | TTTGGTGA others(11): Show |
4 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2094+11084_2094+11 others(24): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230522246 | ||||||
chr2:230522258 | G | A | 8 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(5): Show |
9 | HG01884.hp1 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2094+11092G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230522258 | |||||||
chr2:230522326 | C | A | 115 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(112): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.2094+11160C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230522326 | |||||||
chr2:230522476 | C | CT | 55 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(52): Show |
55 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.2094+11332dupT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230522476 | ||||||
chr2:230522476 | C | CTTT | 26 | a0001c0001t0004g0096 a0001c0001t0004g0176 a0001c0001t0005g0088 others(23): Show |
26 | HG00140.hp1 HG01243.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.2094+11330_2094+11 others(9): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230522476 | ||||||
chr2:230522476 | C | CTTTT | 38 | a0001c0001t0002g0200 a0001c0001t0002g0279 a0001c0001t0004g0049 others(35): Show |
39 | HG00099.hp2 HG00738.hp2 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.2094+11329_2094+11 others(10): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230522476 | ||||||
chr2:230522476 | C | CTTTTT | 83 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(80): Show |
83 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.2094+11328_2094+11 others(11): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230522476 | ||||||
chr2:230522476 | C | CTTTTTT | 17 | a0001c0001t0002g0027 a0001c0001t0002g0196 a0001c0001t0002g0285 others(14): Show |
17 | HG00140.hp2 HG01070.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.2094+11327_2094+11 others(12): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230522476 | ||||||
chr2:230522509 | CTTGCACT others(1): Show |
C | 9 | a0001c0001t0020g0286 a0001c0003t0016g0138 a0001c0007t0016g0031 others(6): Show |
9 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.2094+11345_2094+11 others(14): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230522509 | ||||||
chr2:230522520 | A | G | 9 | a0001c0001t0020g0286 a0001c0003t0016g0138 a0001c0007t0016g0031 others(6): Show |
9 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.2094+11354A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230522520 | |||||||
chr2:230522645 | C | T | 1 | a0003c0004t0002g0113 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2094+11479C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230522645 | |||||||
chr2:230522789 | C | T | 3 | a0001c0001t0002g0105 a0001c0001t0002g0266 a0001c0001t0002g0268 |
3 | HG01123.hp2 HG01433.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.2094+11623C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230522789 | |||||||
chr2:230522790 | C | T | 2 | a0001c0003t0016g0138 a0001c0007t0016g0031 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2094+11624C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230522790 | |||||||
chr2:230522982 | T | C | 7 | a0001c0003t0012g0048 a0002c0002t0013g0038 a0002c0002t0013g0059 others(4): Show |
7 | HG01106.hp1 HG02145.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2094+11816T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230522982 | |||||||
chr2:230523335 | A | G | 8 | a0001c0003t0016g0138 a0001c0007t0016g0031 a0002c0002t0011g0119 others(5): Show |
8 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.2094+12169A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230523335 | |||||||
chr2:230523374 | A | T | 39 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(36): Show |
39 | HG00140.hp1 HG00738.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.2094+12208A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230523374 | |||||||
chr2:230523387 | C | G | 39 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(36): Show |
39 | HG00140.hp1 HG00738.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.2094+12221C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230523387 | |||||||
chr2:230523404 | C | T | 9 | a0001c0001t0020g0286 a0001c0003t0016g0138 a0001c0007t0016g0031 others(6): Show |
9 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.2094+12238C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230523404 | |||||||
chr2:230523461 | G | A | 4 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2094+12295G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230523461 | |||||||
chr2:230523512 | A | AAAAT | 9 | a0001c0001t0020g0286 a0001c0003t0016g0138 a0001c0007t0016g0031 others(6): Show |
9 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.2094+12354_2094+12 others(10): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230523512 | ||||||
chr2:230523537 | T | G | 9 | a0001c0001t0020g0286 a0001c0003t0016g0138 a0001c0007t0016g0031 others(6): Show |
9 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.2094+12371T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230523537 | |||||||
chr2:230523669 | G | A | 1 | a0002c0002t0009g0001 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2094+12503G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230523669 | |||||||
chr2:230523689 | G | A | 1 | a0001c0001t0006g0230 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2094+12523G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230523689 | |||||||
chr2:230523735 | C | A | 9 | a0004c0006t0004g0153 a0004c0006t0004g0180 a0004c0006t0004g0182 others(6): Show |
9 | HG00140.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.2094+12569C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230523735 | |||||||
chr2:230523766 | A | C | 8 | a0001c0003t0016g0138 a0001c0007t0016g0031 a0002c0002t0011g0119 others(5): Show |
8 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.2094+12600A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230523766 | |||||||
chr2:230523766 | A | T | 1 | a0001c0001t0020g0286 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2094+12600A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230523766 | |||||||
chr2:230523778 | G | A | 1 | a0001c0003t0005g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2094+12612G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230523778 | |||||||
chr2:230523823 | C | T | 2 | a0004c0006t0004g0182 a0004c0006t0004g0277 |
2 | HG03491.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.2094+12657C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230523823 | |||||||
chr2:230523850 | A | G | 2 | a0001c0003t0016g0138 a0001c0007t0016g0031 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2094+12684A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230523850 | |||||||
chr2:230524063 | G | T | 39 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(36): Show |
39 | HG00140.hp1 HG00738.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.2094+12897G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230524063 | |||||||
chr2:230524073 | C | T | 1 | a0001c0003t0012g0247 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2094+12907C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230524073 | |||||||
chr2:230524176 | A | G | 1 | a0001c0003t0004g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2094+13010A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230524176 | |||||||
chr2:230524179 | C | CA | 109 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(106): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.2094+13035dupA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230524179 | ||||||
chr2:230524179 | C | CAA | 16 | a0001c0001t0002g0067 a0001c0001t0002g0171 a0001c0001t0002g0278 others(13): Show |
16 | HG00408.hp1 HG01261.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2094+13034_2094+13 others(8): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230524179 | ||||||
chr2:230524179 | CA | C | 9 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0270 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.2094+13035delA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230524179 | ||||||
chr2:230524195 | A | AG | 48 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(45): Show |
48 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.2094+13029_2094+13 others(7): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230524195 | |||||||
chr2:230524195 | A | G | 2 | a0003c0004t0003g0264 a0005c0008t0003g0003 |
2 | HG00280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2094+13029A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230524195 | |||||||
chr2:230524196 | A | AG | 9 | a0001c0001t0005g0088 a0001c0001t0005g0091 a0001c0001t0005g0093 others(6): Show |
9 | HG02145.hp2 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2094+13030_2094+13 others(7): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230524196 | |||||||
chr2:230524196 | A | G | 17 | a0001c0001t0004g0096 a0001c0001t0004g0176 a0001c0001t0021g0090 others(14): Show |
17 | HG00140.hp1 HG01243.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.2094+13030A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230524196 | |||||||
chr2:230524197 | A | G | 2 | a0002c0002t0001g0015 a0002c0002t0001g0218 |
2 | HG02071.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2094+13031A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230524197 | |||||||
chr2:230524217 | G | A | 1 | a0002c0002t0001g0015 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2094+13051G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230524217 | |||||||
chr2:230524263 | G | A | 4 | a0002c0002t0001g0044 a0002c0002t0001g0118 a0002c0005t0001g0052 others(1): Show |
4 | HG02055.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2094+13097G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230524263 | |||||||
chr2:230524286 | G | A | 50 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.2094+13120G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230524286 | |||||||
chr2:230524352 | A | G | 1 | a0001c0003t0005g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2094+13186A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230524352 | |||||||
chr2:230524356 | C | CA | 117 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(114): Show |
118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.2094+13205dupA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230524356 | ||||||
chr2:230524362 | A | C | 17 | a0001c0001t0004g0096 a0001c0001t0004g0176 a0001c0001t0021g0090 others(14): Show |
17 | HG00140.hp1 HG01243.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.2094+13196A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230524362 | |||||||
chr2:230524364 | AAAAAAAA others(1): Show |
A | 6 | a0002c0002t0011g0119 a0002c0002t0011g0145 a0002c0002t0011g0157 others(3): Show |
6 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2094+13204_2094+13 others(14): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230524364 | ||||||
chr2:230524372 | G | A | 3 | a0001c0001t0020g0286 a0001c0003t0016g0138 a0001c0007t0016g0031 |
3 | HG03130.hp1 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2094+13206G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230524372 | |||||||
chr2:230524398 | C | T | 10 | a0001c0001t0007g0258 a0001c0003t0007g0111 a0001c0003t0016g0138 others(7): Show |
10 | HG02559.hp1 HG02622.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2094+13232C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230524398 | |||||||
chr2:230524512 | C | T | 39 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(36): Show |
39 | HG00140.hp1 HG00738.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.2094+13346C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230524512 | |||||||
chr2:230524589 | TAAAG | T | 8 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(5): Show |
9 | HG01884.hp1 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2094+13426_2094+13 others(10): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230524589 | ||||||
chr2:230524626 | T | C | 2 | a0001c0001t0019g0126 a0001c0001t0025g0060 |
2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2094+13460T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230524626 | |||||||
chr2:230524715 | A | G | 9 | a0001c0001t0005g0088 a0001c0001t0005g0091 a0001c0001t0005g0093 others(6): Show |
9 | HG02145.hp2 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2094+13549A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230524715 | |||||||
chr2:230524736 | G | C | 7 | a0002c0002t0001g0005 a0002c0002t0001g0044 a0002c0002t0001g0118 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2094+13570G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230524736 | |||||||
chr2:230524859 | A | C | 50 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.2094+13693A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230524859 | |||||||
chr2:230524900 | G | A | 11 | a0001c0001t0005g0088 a0001c0001t0005g0091 a0001c0001t0005g0093 others(8): Show |
11 | HG02145.hp2 HG02630.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.2094+13734G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230524900 | |||||||
chr2:230525125 | T | C | 6 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0073 others(3): Show |
6 | HG02148.hp2 HG02155.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.2094+13959T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230525125 | |||||||
chr2:230525190 | C | T | 1 | a0009c0018t0004g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2094+14024C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230525190 | |||||||
chr2:230525213 | C | T | 1 | a0003c0004t0002g0265 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2094+14047C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230525213 | |||||||
chr2:230525244 | T | C | 1 | a0002c0002t0001g0235 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2095-14023T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230525244 | |||||||
chr2:230525281 | G | A | 6 | a0002c0002t0011g0119 a0002c0002t0011g0145 a0002c0002t0011g0157 others(3): Show |
6 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2095-13986G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230525281 | |||||||
chr2:230525412 | C | T | 9 | a0001c0001t0020g0286 a0001c0003t0016g0138 a0001c0007t0016g0031 others(6): Show |
9 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.2095-13855C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230525412 | |||||||
chr2:230525417 | A | G | 7 | a0001c0003t0003g0110 a0003c0004t0003g0062 a0003c0004t0003g0081 others(4): Show |
7 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(4): Show |
intron_variant | MODIFIER | c.2095-13850A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230525417 | |||||||
chr2:230525586 | G | A | 1 | a0005c0013t0024g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2095-13681G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230525586 | |||||||
chr2:230525664 | G | C | 1 | a0001c0001t0019g0126 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2095-13603G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230525664 | |||||||
chr2:230525854 | A | AC | 4 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2095-13411dupC | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230525854 | ||||||
chr2:230525917 | G | A | 1 | a0001c0001t0020g0286 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2095-13350G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230525917 | |||||||
chr2:230525968 | G | A | 50 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.2095-13299G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230525968 | |||||||
chr2:230525970 | G | A | 6 | a0002c0002t0011g0119 a0002c0002t0011g0145 a0002c0002t0011g0157 others(3): Show |
6 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2095-13297G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230525970 | |||||||
chr2:230526053 | G | T | 1 | a0003c0004t0004g0104 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2095-13214G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230526053 | |||||||
chr2:230526175 | C | T | 2 | a0001c0003t0016g0138 a0001c0007t0016g0031 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2095-13092C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230526175 | |||||||
chr2:230526203 | T | C | 1 | a0001c0003t0007g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2095-13064T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230526203 | |||||||
chr2:230526260 | C | T | 1 | a0001c0001t0020g0286 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2095-13007C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230526260 | |||||||
chr2:230526316 | A | T | 9 | a0001c0001t0020g0286 a0001c0003t0016g0138 a0001c0007t0016g0031 others(6): Show |
9 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.2095-12951A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230526316 | |||||||
chr2:230526322 | C | T | 4 | a0001c0001t0015g0089 a0001c0003t0002g0100 a0001c0003t0015g0170 others(1): Show |
4 | HG02572.hp2 HG02615.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2095-12945C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230526322 | |||||||
chr2:230526392 | C | T | 39 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(36): Show |
39 | HG00140.hp1 HG00738.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.2095-12875C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230526392 | |||||||
chr2:230526496 | C | T | 45 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(42): Show |
45 | HG00140.hp1 HG00738.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.2095-12771C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230526496 | |||||||
chr2:230526620 | C | T | 1 | a0001c0001t0020g0286 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2095-12647C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230526620 | |||||||
chr2:230526625 | A | G | 1 | a0001c0001t0020g0286 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2095-12642A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230526625 | |||||||
chr2:230526796 | G | A | 2 | a0001c0003t0016g0138 a0001c0007t0016g0031 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2095-12471G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230526796 | |||||||
chr2:230526843 | A | G | 9 | a0004c0006t0004g0153 a0004c0006t0004g0180 a0004c0006t0004g0182 others(6): Show |
9 | HG00140.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.2095-12424A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230526843 | |||||||
chr2:230526968 | C | T | 1 | a0001c0001t0003g0077 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2095-12299C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230526968 | |||||||
chr2:230527033 | T | C | 1 | a0002c0002t0001g0236 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2095-12234T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230527033 | |||||||
chr2:230527100 | A | G | 1 | a0002c0005t0001g0164 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2095-12167A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230527100 | |||||||
chr2:230527187 | T | A | 7 | a0001c0003t0012g0048 a0002c0002t0013g0038 a0002c0002t0013g0059 others(4): Show |
7 | HG01106.hp1 HG02145.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2095-12080T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230527187 | |||||||
chr2:230527245 | G | A | 1 | a0002c0002t0001g0228 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2095-12022G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230527245 | |||||||
chr2:230527246 | C | G | 1 | a0001c0001t0010g0245 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2095-12021C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230527246 | |||||||
chr2:230527260 | C | T | 2 | a0001c0001t0019g0126 a0001c0001t0025g0060 |
2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2095-12007C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230527260 | |||||||
chr2:230527393 | C | T | 1 | a0003c0004t0002g0151 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2095-11874C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230527393 | |||||||
chr2:230527555 | G | C | 39 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(36): Show |
39 | HG00140.hp1 HG00738.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.2095-11712G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230527555 | |||||||
chr2:230527691 | A | G | 1 | a0001c0001t0008g0039 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2095-11576A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230527691 | |||||||
chr2:230527862 | G | A | 9 | a0001c0001t0020g0286 a0001c0003t0016g0138 a0001c0007t0016g0031 others(6): Show |
9 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.2095-11405G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230527862 | |||||||
chr2:230527975 | A | T | 9 | a0001c0001t0020g0286 a0001c0003t0016g0138 a0001c0007t0016g0031 others(6): Show |
9 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.2095-11292A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230527975 | |||||||
chr2:230528139 | C | G | 2 | a0002c0005t0001g0057 a0002c0005t0001g0179 |
2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2095-11128C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230528139 | |||||||
chr2:230528168 | C | A | 108 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(105): Show |
109 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.2095-11099C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230528168 | |||||||
chr2:230528186 | G | A | 1 | a0001c0001t0019g0126 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2095-11081G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230528186 | |||||||
chr2:230528395 | G | A | 211 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(208): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.2095-10872G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230528395 | |||||||
chr2:230528433 | T | G | 6 | a0001c0003t0012g0042 a0001c0003t0012g0045 a0001c0003t0012g0046 others(3): Show |
6 | HG02258.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2095-10834T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230528433 | |||||||
chr2:230528470 | A | C | 2 | a0002c0002t0013g0059 a0002c0005t0013g0287 |
2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2095-10797A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230528470 | |||||||
chr2:230528526 | GC | G | 38 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(35): Show |
38 | HG00140.hp1 HG00738.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.2095-10740delC | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230528526 | |||||||
chr2:230528613 | C | T | 1 | a0002c0005t0001g0075 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2095-10654C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230528613 | |||||||
chr2:230528666 | T | C | 7 | a0001c0003t0012g0048 a0002c0002t0013g0038 a0002c0002t0013g0059 others(4): Show |
7 | HG01106.hp1 HG02145.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2095-10601T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230528666 | |||||||
chr2:230528864 | A | C | 9 | a0001c0001t0005g0088 a0001c0001t0005g0091 a0001c0001t0005g0093 others(6): Show |
9 | HG02145.hp2 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2095-10403A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230528864 | |||||||
chr2:230528876 | A | G | 2 | a0001c0003t0016g0138 a0001c0007t0016g0031 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2095-10391A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230528876 | |||||||
chr2:230528902 | C | A | 1 | a0001c0003t0004g0125 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2095-10365C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230528902 | |||||||
chr2:230528984 | A | G | 2 | a0002c0002t0001g0216 a0002c0002t0001g0225 |
2 | HG02040.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.2095-10283A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230528984 | |||||||
chr2:230529243 | T | A | 9 | a0004c0006t0004g0153 a0004c0006t0004g0180 a0004c0006t0004g0182 others(6): Show |
9 | HG00140.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.2095-10024T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230529243 | |||||||
chr2:230529277 | G | A | 39 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0096 others(36): Show |
39 | HG00140.hp1 HG00738.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.2095-9990G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230529277 | |||||||
chr2:230529453 | C | T | 2 | a0001c0001t0007g0079 a0001c0003t0007g0055 |
2 | HG01943.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2095-9814C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230529453 | |||||||
chr2:230529607 | G | A | 1 | a0003c0004t0002g0152 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2095-9660G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230529607 | |||||||
chr2:230529637 | T | C | 1 | a0001c0001t0004g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2095-9630T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230529637 | |||||||
chr2:230529642 | T | C | 7 | a0001c0003t0012g0048 a0002c0002t0013g0038 a0002c0002t0013g0059 others(4): Show |
7 | HG01106.hp1 HG02145.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2095-9625T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230529642 | |||||||
chr2:230529684 | C | T | 1 | a0002c0002t0009g0207 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2095-9583C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230529684 | |||||||
chr2:230529712 | A | T | 1 | a0002c0002t0011g0160 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2095-9555A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230529712 | |||||||
chr2:230529720 | A | C | 1 | a0002c0002t0011g0160 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2095-9547A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230529720 | |||||||
chr2:230529723 | T | C | 1 | a0002c0002t0011g0160 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2095-9544T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230529723 | |||||||
chr2:230529775 | T | C | 11 | a0001c0001t0005g0088 a0001c0001t0005g0091 a0001c0001t0005g0093 others(8): Show |
11 | HG02145.hp2 HG02630.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.2095-9492T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230529775 | |||||||
chr2:230529817 | C | T | 100 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(97): Show |
100 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.2095-9450C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230529817 | |||||||
chr2:230529868 | G | T | 1 | a0005c0008t0003g0003 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2095-9399G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230529868 | |||||||
chr2:230529875 | A | T | 1 | a0002c0002t0001g0150 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2095-9392A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230529875 | |||||||
chr2:230529971 | G | A | 1 | a0001c0001t0019g0126 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2095-9296G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230529971 | |||||||
chr2:230529995 | C | A | 1 | a0001c0001t0019g0126 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2095-9272C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230529995 | |||||||
chr2:230530092 | A | G | 1 | a0001c0009t0007g0272 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2095-9175A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230530092 | |||||||
chr2:230530211 | G | A | 1 | a0001c0001t0010g0187 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2095-9056G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230530211 | |||||||
chr2:230530250 | G | A | 49 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(46): Show |
49 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.2095-9017G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230530250 | |||||||
chr2:230530411 | C | T | 1 | a0002c0002t0011g0145 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2095-8856C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230530411 | |||||||
chr2:230530564 | G | A | 1 | a0001c0001t0025g0060 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2095-8703G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230530564 | |||||||
chr2:230530583 | T | A | 8 | a0001c0003t0016g0138 a0001c0007t0016g0031 a0002c0002t0011g0119 others(5): Show |
8 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.2095-8684T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230530583 | |||||||
chr2:230530586 | T | C | 1 | a0002c0005t0001g0011 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2095-8681T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230530586 | |||||||
chr2:230530669 | C | T | 6 | a0002c0002t0011g0119 a0002c0002t0011g0145 a0002c0002t0011g0157 others(3): Show |
6 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2095-8598C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230530669 | |||||||
chr2:230530772 | A | G | 10 | a0001c0001t0005g0088 a0001c0001t0005g0091 a0001c0001t0005g0093 others(7): Show |
10 | HG02145.hp2 HG02630.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2095-8495A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230530772 | |||||||
chr2:230530880 | C | T | 9 | a0001c0003t0002g0013 a0001c0003t0016g0138 a0001c0007t0016g0031 others(6): Show |
9 | HG01261.hp1 HG02622.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2095-8387C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230530880 | |||||||
chr2:230530886 | G | T | 8 | a0001c0003t0016g0138 a0001c0007t0016g0031 a0002c0002t0011g0119 others(5): Show |
8 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.2095-8381G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230530886 | |||||||
chr2:230530923 | A | G | 7 | a0001c0003t0012g0048 a0002c0002t0013g0038 a0002c0002t0013g0059 others(4): Show |
7 | HG01106.hp1 HG02145.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2095-8344A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230530923 | |||||||
chr2:230531054 | C | T | 1 | a0001c0003t0003g0110 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2095-8213C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230531054 | |||||||
chr2:230531120 | G | A | 6 | a0002c0002t0011g0119 a0002c0002t0011g0145 a0002c0002t0011g0157 others(3): Show |
6 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2095-8147G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230531120 | |||||||
chr2:230531274 | A | G | 124 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(121): Show |
125 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2095-7993A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230531274 | |||||||
chr2:230531369 | G | A | 2 | a0002c0005t0001g0057 a0002c0005t0001g0179 |
2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2095-7898G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230531369 | |||||||
chr2:230531417 | G | T | 48 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(45): Show |
48 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.2095-7850G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230531417 | |||||||
chr2:230531434 | G | A | 4 | a0001c0001t0010g0130 a0001c0001t0010g0260 a0001c0003t0010g0020 others(1): Show |
4 | HG01255.hp2 HG01346.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.2095-7833G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230531434 | |||||||
chr2:230531576 | A | T | 2 | a0002c0005t0001g0052 a0002c0005t0001g0129 |
2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2095-7691A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230531576 | |||||||
chr2:230531605 | T | G | 127 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(124): Show |
128 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.2095-7662T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230531605 | |||||||
chr2:230532111 | C | A | 2 | a0001c0001t0019g0126 a0001c0001t0025g0060 |
2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2095-7156C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230532111 | |||||||
chr2:230532182 | C | T | 8 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(5): Show |
9 | HG01884.hp1 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2095-7085C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230532182 | |||||||
chr2:230532217 | GA | G | 3 | a0002c0002t0001g0140 a0002c0002t0001g0236 a0002c0021t0001g0101 |
3 | NA18950.hp2 NA18974.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.2095-7043delA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230532217 | ||||||
chr2:230532224 | A | AT | 48 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(45): Show |
48 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.2095-7042dupT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230532224 | ||||||
chr2:230532225 | T | A | 4 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2095-7042T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230532225 | |||||||
chr2:230532536 | T | TA | 124 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(121): Show |
125 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2095-6719dupA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230532536 | ||||||
chr2:230532536 | TA | T | 8 | a0001c0003t0016g0138 a0001c0007t0016g0031 a0002c0002t0011g0119 others(5): Show |
8 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.2095-6719delA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230532536 | ||||||
chr2:230532539 | A | G | 48 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(45): Show |
48 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.2095-6728A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230532539 | |||||||
chr2:230532690 | T | A | 5 | a0001c0001t0002g0102 a0001c0001t0002g0175 a0003c0004t0002g0269 others(2): Show |
5 | HG02896.hp2 HG02897.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.2095-6577T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230532690 | |||||||
chr2:230532795 | T | C | 1 | a0002c0002t0001g0005 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2095-6472T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230532795 | |||||||
chr2:230532804 | G | A | 8 | a0001c0003t0016g0138 a0001c0007t0016g0031 a0002c0002t0011g0119 others(5): Show |
8 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.2095-6463G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230532804 | |||||||
chr2:230532862 | C | A | 1 | a0002c0020t0022g0036 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2095-6405C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230532862 | |||||||
chr2:230532866 | T | C | 1 | a0001c0003t0008g0002 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2095-6401T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230532866 | |||||||
chr2:230532983 | G | A | 2 | a0001c0003t0016g0138 a0001c0007t0016g0031 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2095-6284G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230532983 | |||||||
chr2:230533071 | G | A | 1 | a0002c0002t0001g0228 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2095-6196G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230533071 | |||||||
chr2:230533090 | T | C | 1 | a0001c0001t0002g0171 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2095-6177T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230533090 | |||||||
chr2:230533221 | T | A | 10 | a0001c0001t0005g0088 a0001c0001t0005g0091 a0001c0001t0005g0093 others(7): Show |
10 | HG02145.hp2 HG02630.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2095-6046T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230533221 | |||||||
chr2:230533406 | C | T | 3 | a0001c0001t0002g0267 a0001c0001t0002g0283 a0001c0001t0002g0284 |
3 | HG00280.hp1 HG01071.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.2095-5861C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230533406 | |||||||
chr2:230533461 | T | C | 50 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.2095-5806T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230533461 | |||||||
chr2:230533789 | A | T | 1 | a0002c0002t0001g0210 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2095-5478A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230533789 | |||||||
chr2:230534065 | T | C | 2 | a0001c0001t0002g0065 a0001c0001t0002g0071 |
2 | HG02129.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.2095-5202T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230534065 | |||||||
chr2:230534299 | G | A | 4 | a0004c0006t0004g0153 a0004c0006t0004g0238 a0004c0006t0004g0282 others(1): Show |
4 | HG00140.hp1 HG01516.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.2095-4968G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230534299 | |||||||
chr2:230534400 | C | T | 10 | a0001c0003t0003g0063 a0001c0003t0003g0139 a0001c0003t0003g0183 others(7): Show |
10 | HG00544.hp2 HG02132.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.2095-4867C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230534400 | |||||||
chr2:230534401 | G | A | 1 | a0001c0017t0002g0018 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2095-4866G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230534401 | |||||||
chr2:230534604 | C | T | 1 | a0002c0020t0022g0036 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2095-4663C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230534604 | |||||||
chr2:230534707 | G | T | 1 | a0001c0001t0005g0095 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2095-4560G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230534707 | |||||||
chr2:230534747 | T | C | 1 | a0001c0003t0008g0002 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2095-4520T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230534747 | |||||||
chr2:230534842 | T | C | 203 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(200): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.2095-4425T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230534842 | |||||||
chr2:230534919 | G | A | 1 | a0001c0001t0020g0286 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2095-4348G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230534919 | |||||||
chr2:230534968 | G | A | 2 | a0001c0001t0004g0017 a0001c0001t0004g0098 |
2 | HG00099.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.2095-4299G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230534968 | |||||||
chr2:230534970 | G | A | 6 | a0002c0002t0011g0119 a0002c0002t0011g0145 a0002c0002t0011g0157 others(3): Show |
6 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2095-4297G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230534970 | |||||||
chr2:230534971 | T | G | 2 | a0002c0002t0001g0209 a0002c0002t0001g0253 |
2 | HG00733.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2095-4296T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230534971 | |||||||
chr2:230534972 | G | A | 7 | a0001c0003t0012g0042 a0001c0003t0012g0045 a0001c0003t0012g0046 others(4): Show |
7 | HG02258.hp1 HG02615.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2095-4295G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230534972 | |||||||
chr2:230535053 | G | A | 6 | a0002c0002t0013g0038 a0002c0002t0013g0059 a0002c0005t0013g0037 others(3): Show |
6 | HG01106.hp1 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2095-4214G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230535053 | |||||||
chr2:230535063 | G | A | 6 | a0002c0002t0013g0038 a0002c0002t0013g0059 a0002c0005t0013g0037 others(3): Show |
6 | HG01106.hp1 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2095-4204G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230535063 | |||||||
chr2:230535089 | G | A | 1 | a0005c0008t0003g0003 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2095-4178G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230535089 | |||||||
chr2:230535195 | C | CA | 113 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(110): Show |
114 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.2095-4060dupA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230535195 | ||||||
chr2:230535359 | T | C | 1 | a0009c0018t0004g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2095-3908T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230535359 | |||||||
chr2:230535360 | C | A | 1 | a0009c0018t0004g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2095-3907C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230535360 | |||||||
chr2:230535361 | A | T | 1 | a0009c0018t0004g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2095-3906A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230535361 | |||||||
chr2:230535454 | T | G | 9 | a0004c0006t0004g0153 a0004c0006t0004g0180 a0004c0006t0004g0182 others(6): Show |
9 | HG00140.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.2095-3813T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230535454 | |||||||
chr2:230535502 | T | C | 2 | a0002c0005t0001g0068 a0002c0005t0001g0069 |
2 | NA19005.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2095-3765T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230535502 | |||||||
chr2:230535779 | T | C | 96 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(93): Show |
97 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.2095-3488T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230535779 | |||||||
chr2:230535780 | G | A | 1 | a0001c0001t0006g0135 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2095-3487G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230535780 | |||||||
chr2:230535870 | C | G | 206 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(203): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.2095-3397C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230535870 | |||||||
chr2:230535906 | C | CA | 18 | a0001c0001t0004g0050 a0001c0001t0025g0060 a0001c0003t0007g0136 others(15): Show |
18 | HG00735.hp1 HG01192.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2095-3332dupA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230535906 | ||||||
chr2:230535906 | C | CAAAAAAA others(4): Show |
2 | a0001c0003t0012g0042 a0001c0003t0012g0045 |
2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2095-3342_2095-333 others(15): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230535906 | ||||||
chr2:230535906 | C | CAAAAAAA others(5): Show |
2 | a0001c0003t0012g0046 a0001c0003t0012g0257 |
2 | HG02258.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2095-3343_2095-333 others(16): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230535906 | ||||||
chr2:230535906 | C | CAAAAAAA others(7): Show |
1 | a0001c0003t0012g0048 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2095-3345_2095-333 others(18): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230535906 | ||||||
chr2:230535906 | C | CAAAAAAA others(9): Show |
1 | a0005c0013t0024g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2095-3347_2095-333 others(20): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230535906 | ||||||
chr2:230535906 | CA | C | 38 | a0001c0001t0002g0285 a0001c0001t0003g0056 a0001c0001t0003g0070 others(35): Show |
39 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.2095-3332delA | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230535906 | ||||||
chr2:230535906 | CAA | C | 54 | a0001c0001t0002g0102 a0001c0001t0002g0174 a0001c0001t0002g0195 others(51): Show |
54 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.2095-3333_2095-333 others(6): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230535906 | ||||||
chr2:230535906 | CAAA | C | 84 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(81): Show |
84 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.2095-3334_2095-333 others(7): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230535906 | ||||||
chr2:230535906 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0019g0126 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2095-3346_2095-333 others(19): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230535906 | ||||||
chr2:230535906 | CAAAAAAA others(9): Show |
C | 2 | a0004c0006t0004g0182 a0004c0006t0004g0277 |
2 | HG03491.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.2095-3347_2095-333 others(20): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230535906 | ||||||
chr2:230535906 | CAAAAAAA others(10): Show |
C | 2 | a0002c0005t0001g0164 a0010c0012t0009g0087 |
2 | NA18970.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.2095-3348_2095-333 others(21): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230535906 | ||||||
chr2:230535997 | G | A | 1 | a0001c0003t0012g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2095-3270G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230535997 | |||||||
chr2:230536086 | A | G | 1 | a0004c0006t0004g0282 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2095-3181A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230536086 | |||||||
chr2:230536206 | T | C | 2 | a0005c0008t0002g0122 a0005c0008t0002g0123 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2095-3061T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230536206 | |||||||
chr2:230536223 | AT | A | 6 | a0002c0002t0011g0119 a0002c0002t0011g0145 a0002c0002t0011g0157 others(3): Show |
6 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2095-3039delT | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230536223 | ||||||
chr2:230536268 | C | T | 3 | a0001c0001t0002g0019 a0001c0001t0002g0148 a0001c0001t0002g0278 |
3 | HG01106.hp2 HG03491.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2095-2999C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230536268 | |||||||
chr2:230536429 | G | A | 1 | a0001c0001t0020g0286 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2095-2838G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230536429 | |||||||
chr2:230536605 | A | T | 1 | a0009c0018t0004g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2095-2662A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230536605 | |||||||
chr2:230536609 | A | G | 122 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(119): Show |
123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.2095-2658A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230536609 | |||||||
chr2:230536621 | C | A | 1 | a0009c0018t0004g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2095-2646C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230536621 | |||||||
chr2:230536749 | CCTTCTTG others(49): Show |
C | 88 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(85): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.2095-2516_2095-246 others(60): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr2 | 230536749 | ||||||
chr2:230537004 | T | G | 1 | a0009c0018t0004g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2095-2263T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230537004 | |||||||
chr2:230537233 | G | A | 3 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0270 |
3 | HG01884.hp2 HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2095-2034G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230537233 | |||||||
chr2:230537267 | A | C | 1 | a0001c0003t0004g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2095-2000A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230537267 | |||||||
chr2:230537514 | C | T | 50 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.2095-1753C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230537514 | |||||||
chr2:230537546 | C | A | 1 | a0009c0018t0004g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2095-1721C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230537546 | |||||||
chr2:230537697 | T | A | 1 | a0002c0002t0001g0107 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2095-1570T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230537697 | |||||||
chr2:230537739 | G | A | 1 | a0001c0001t0025g0060 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2095-1528G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230537739 | |||||||
chr2:230537920 | T | A | 9 | a0001c0001t0020g0286 a0001c0003t0016g0138 a0001c0007t0016g0031 others(6): Show |
9 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.2095-1347T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230537920 | |||||||
chr2:230537931 | T | C | 1 | a0001c0003t0012g0048 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2095-1336T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230537931 | |||||||
chr2:230538038 | T | G | 1 | a0009c0018t0004g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2095-1229T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230538038 | |||||||
chr2:230538132 | G | A | 2 | a0002c0005t0001g0057 a0002c0005t0001g0179 |
2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2095-1135G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230538132 | |||||||
chr2:230538175 | A | G | 1 | a0002c0002t0001g0150 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2095-1092A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230538175 | |||||||
chr2:230538176 | G | C | 49 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(46): Show |
49 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.2095-1091G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230538176 | |||||||
chr2:230538200 | G | A | 119 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(116): Show |
120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.2095-1067G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230538200 | |||||||
chr2:230538202 | A | C | 50 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.2095-1065A>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230538202 | |||||||
chr2:230538205 | A | G | 50 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.2095-1062A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230538205 | |||||||
chr2:230538244 | C | T | 9 | a0001c0001t0020g0286 a0001c0003t0016g0138 a0001c0007t0016g0031 others(6): Show |
9 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.2095-1023C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230538244 | |||||||
chr2:230538266 | C | T | 1 | a0004c0006t0004g0277 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2095-1001C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230538266 | |||||||
chr2:230538313 | T | C | 1 | a0001c0001t0025g0060 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2095-954T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230538313 | |||||||
chr2:230538382 | T | C | 96 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(93): Show |
97 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.2095-885T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230538382 | |||||||
chr2:230538391 | T | G | 4 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2095-876T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230538391 | |||||||
chr2:230538409 | T | C | 14 | a0001c0003t0012g0042 a0001c0003t0012g0045 a0001c0003t0012g0046 others(11): Show |
14 | HG01106.hp1 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.2095-858T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230538409 | |||||||
chr2:230538470 | T | G | 1 | a0009c0018t0004g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2095-797T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230538470 | |||||||
chr2:230538479 | G | A | 2 | a0001c0001t0002g0171 a0001c0001t0026g0021 |
2 | HG03654.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2095-788G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230538479 | |||||||
chr2:230538492 | C | A | 1 | a0009c0018t0004g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2095-775C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230538492 | |||||||
chr2:230538702 | C | A | 1 | a0001c0001t0002g0196 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2095-565C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230538702 | |||||||
chr2:230538702 | C | G | 50 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.2095-565C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230538702 | |||||||
chr2:230538729 | C | T | 1 | a0001c0001t0018g0066 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2095-538C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230538729 | |||||||
chr2:230538747 | G | A | 8 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(5): Show |
9 | HG01884.hp1 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2095-520G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230538747 | |||||||
chr2:230538844 | G | C | 1 | a0001c0001t0020g0286 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2095-423G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230538844 | |||||||
chr2:230538853 | T | C | 1 | a0002c0002t0023g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2095-414T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230538853 | |||||||
chr2:230539018 | C | A | 3 | a0002c0002t0001g0140 a0002c0002t0001g0236 a0002c0021t0001g0101 |
3 | NA18950.hp2 NA18974.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.2095-249C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 24/28 | chr2 | 230539018 | |||||||
chr2:230539500 | G | A | 4 | a0001c0007t0005g0030 a0001c0007t0005g0032 a0001c0007t0005g0033 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2210+118G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 25/28 | chr2 | 230539500 | |||||||
chr2:230539685 | ATACACTG others(17): Show |
A | 6 | a0002c0002t0011g0119 a0002c0002t0011g0145 a0002c0002t0011g0157 others(3): Show |
6 | HG02622.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2210+309_2210+332d others(26): Show |
SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr2 | 230539685 | ||||||
chr2:230539759 | A | T | 1 | a0002c0002t0001g0225 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2210+377A>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 25/28 | chr2 | 230539759 | |||||||
chr2:230539811 | G | A | 2 | a0001c0001t0004g0049 a0001c0001t0004g0050 |
2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2210+429G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 25/28 | chr2 | 230539811 | |||||||
chr2:230539881 | G | A | 8 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(5): Show |
9 | HG01884.hp1 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2210+499G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 25/28 | chr2 | 230539881 | |||||||
chr2:230539898 | G | A | 1 | a0001c0001t0020g0286 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2210+516G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 25/28 | chr2 | 230539898 | |||||||
chr2:230540015 | G | A | 3 | a0001c0001t0020g0286 a0001c0003t0016g0138 a0001c0007t0016g0031 |
3 | HG03130.hp1 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2210+633G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 25/28 | chr2 | 230540015 | |||||||
chr2:230540032 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2210+650C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 25/28 | chr2 | 230540032 | |||||||
chr2:230540079 | G | T | 13 | a0001c0003t0012g0042 a0001c0003t0012g0045 a0001c0003t0012g0046 others(10): Show |
13 | HG02258.hp1 HG02615.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.2210+697G>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 25/28 | chr2 | 230540079 | |||||||
chr2:230540360 | C | A | 2 | a0002c0002t0013g0059 a0002c0005t0013g0287 |
2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2211-516C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 25/28 | chr2 | 230540360 | |||||||
chr2:230540504 | G | A | 217 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(214): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.2211-372G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 25/28 | chr2 | 230540504 | |||||||
chr2:230540521 | T | C | 14 | a0001c0003t0012g0042 a0001c0003t0012g0045 a0001c0003t0012g0046 others(11): Show |
14 | HG01891.hp2 HG02258.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.2211-355T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 25/28 | chr2 | 230540521 | |||||||
chr2:230540857 | T | G | 50 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.2211-19T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 25/28 | chr2 | 230540857 | |||||||
chr2:230541134 | G | A | 1 | a0001c0001t0020g0286 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2331+138G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 26/28 | chr2 | 230541134 | |||||||
chr2:230541222 | G | A | 8 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(5): Show |
9 | HG01884.hp1 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2332-79G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 26/28 | chr2 | 230541222 | |||||||
chr2:230541251 | T | A | 7 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(4): Show |
7 | HG01884.hp1 HG02572.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2332-50T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 26/28 | chr2 | 230541251 | |||||||
chr2:230541410 | T | C | 1 | a0001c0003t0004g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2403+38T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 27/28 | chr2 | 230541410 | |||||||
chr2:230541455 | A | G | 2 | a0001c0003t0016g0138 a0001c0007t0016g0031 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2403+83A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 27/28 | chr2 | 230541455 | |||||||
chr2:230541479 | G | A | 50 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.2403+107G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 27/28 | chr2 | 230541479 | |||||||
chr2:230541539 | C | T | 1 | a0001c0001t0020g0286 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2403+167C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 27/28 | chr2 | 230541539 | |||||||
chr2:230541550 | G | A | 2 | a0002c0002t0009g0001 a0002c0002t0023g0219 |
3 | HG01167.hp1 HG01169.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.2403+178G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 27/28 | chr2 | 230541550 | |||||||
chr2:230541589 | G | A | 1 | a0002c0020t0022g0036 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2403+217G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 27/28 | chr2 | 230541589 | |||||||
chr2:230541594 | T | C | 1 | a0003c0004t0003g0255 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2403+222T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 27/28 | chr2 | 230541594 | |||||||
chr2:230541617 | T | G | 147 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(144): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.2403+245T>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 27/28 | chr2 | 230541617 | |||||||
chr2:230541722 | C | T | 50 | a0001c0001t0003g0029 a0001c0001t0003g0056 a0001c0001t0003g0070 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.2404-170C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 27/28 | chr2 | 230541722 | |||||||
chr2:230541734 | T | A | 1 | a0001c0003t0003g0110 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2404-158T>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 27/28 | chr2 | 230541734 | |||||||
chr2:230541777 | AG | A | 5 | a0001c0001t0002g0167 a0001c0001t0002g0174 a0001c0001t0002g0203 others(2): Show |
5 | HG02683.hp1 HG03831.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.2404-109delG | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr2 | 230541777 | ||||||
chr2:230541814 | T | C | 51 | a0001c0001t0004g0017 a0001c0001t0004g0049 a0001c0001t0004g0050 others(48): Show |
51 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.2404-78T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 27/28 | chr2 | 230541814 | |||||||
chr2:230541854 | C | T | 2 | a0001c0003t0016g0138 a0001c0007t0016g0031 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2404-38C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 27/28 | chr2 | 230541854 | |||||||
chr2:230542046 | C | G | 2 | a0001c0001t0017g0177 a0001c0001t0017g0178 |
2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2547+11C>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 28/28 | chr2 | 230542046 | |||||||
chr2:230542116 | G | C | 4 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(1): Show |
4 | HG00738.hp1 HG01074.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2547+81G>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 28/28 | chr2 | 230542116 | |||||||
chr2:230542131 | G | A | 86 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(83): Show |
86 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.2547+96G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 28/28 | chr2 | 230542131 | |||||||
chr2:230542189 | T | C | 1 | a0001c0003t0004g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2547+154T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 28/28 | chr2 | 230542189 | |||||||
chr2:230542252 | A | G | 9 | a0001c0003t0016g0138 a0001c0007t0016g0031 a0002c0002t0011g0119 others(6): Show |
9 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2547+217A>G | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 28/28 | chr2 | 230542252 | |||||||
chr2:230542256 | C | T | 1 | a0002c0020t0022g0036 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2547+221C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 28/28 | chr2 | 230542256 | |||||||
chr2:230542291 | C | T | 11 | a0001c0001t0005g0088 a0001c0001t0005g0091 a0001c0001t0005g0093 others(8): Show |
11 | HG00733.hp2 HG02145.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.2547+256C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 28/28 | chr2 | 230542291 | |||||||
chr2:230542378 | T | C | 1 | a0002c0020t0022g0036 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2547+343T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 28/28 | chr2 | 230542378 | |||||||
chr2:230542468 | T | C | 3 | a0001c0003t0016g0138 a0001c0007t0016g0031 a0002c0020t0022g0036 |
3 | HG01891.hp2 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2548-368T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 28/28 | chr2 | 230542468 | |||||||
chr2:230542627 | C | A | 86 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(83): Show |
86 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.2548-209C>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 28/28 | chr2 | 230542627 | |||||||
chr2:230542657 | T | C | 211 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(208): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.2548-179T>C | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 28/28 | chr2 | 230542657 | |||||||
chr2:230542658 | G | A | 10 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(7): Show |
11 | HG01884.hp1 HG02559.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2548-178G>A | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 28/28 | chr2 | 230542658 | |||||||
chr2:230542804 | C | T | 205 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(202): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.2548-32C>T | SP100 | ENSG00000067066.17 | transcript | ENST00000340126.9 | protein_coding | 28/28 | chr2 | 230542804 |