Item | Value |
---|---|
geneid | 441631 |
ensemblid | ENSG00000110900.16 |
hgncid | 30795 |
symbol | TSPAN11 |
name | tetraspanin 11 |
refseq_nuc | NM_001370302.1 |
refseq_prot | NP_001357231.1 |
ensembl_nuc | ENST00000546076.6 |
ensembl_prot | ENSP00000437403.1 |
mane_status | MANE Select |
chr | chr12 |
start | 30926748 |
end | 30996599 |
strand | + |
ver | v1.2 |
region | chr12:30926748-30996599 |
region5000 | chr12:30921748-31001599 |
regionname0 | TSPAN11_chr12_30926748_30996599 |
regionname5000 | TSPAN11_chr12_30921748_31001599 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 253 | 245 | 59 | 55 | 89 | 9 | 32 | 66 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | MAHYK others(248): Show |
chr12 | 30921748 | 31001599 |
a0002 | 1/0 | 253 | 120 | 33 | 17 | 57 | 2 | 10 | 40 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | MAHYK others(248): Show |
chr12 | 30921748 | 31001599 |
a0003 | 0/0 | 253 | 17 | 0 | 1 | 11 | 1 | 4 | 8 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | MAHYK others(248): Show |
chr12 | 30921748 | 31001599 |
a0004 | 0/0 | 253 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | MAHYK others(248): Show |
chr12 | 30921748 | 31001599 |
a0005 | 0/0 | 253 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | MAHYK others(248): Show |
chr12 | 30921748 | 31001599 |
a0006 | 0/0 | 253 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | MAHYK others(248): Show |
chr12 | 30921748 | 31001599 |
a0007 | 0/0 | 253 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | MAHYK others(248): Show |
chr12 | 30921748 | 31001599 |
a0008 | 0/0 | 253 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | MAHYK others(248): Show |
chr12 | 30921748 | 31001599 |
a0009 | 0/0 | 253 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | MAHYK others(248): Show |
chr12 | 30921748 | 31001599 |
a0010 | 0/0 | 253 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | MAHYK others(248): Show |
chr12 | 30921748 | 31001599 |
a0011 | 0/0 | 253 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | MAHYK others(248): Show |
chr12 | 30921748 | 31001599 |
a0012 | 0/0 | 253 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | MAHYK others(248): Show |
chr12 | 30921748 | 31001599 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 759 | 241 | 57 | 55 | 87 | 9 | 32 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | ATGGC others(754): Show |
chr12 | 30921748 | 31001599 | ||
a0001c0007 | 0/0 | 759 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | ATGGC others(754): Show |
chr12 | 30921748 | 31001599 | ||
a0001c0008 | 0/0 | 759 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | ATGGC others(754): Show |
chr12 | 30921748 | 31001599 | ||
a0002c0002 | 0/0 | 759 | 102 | 29 | 12 | 52 | 1 | 8 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | ATGGC others(754): Show |
chr12 | 30921748 | 31001599 | ||
a0002c0004 | 1/0 | 759 | 15 | 1 | 5 | 5 | 1 | 2 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | ATGGC others(754): Show |
chr12 | 30921748 | 31001599 | ||
a0002c0005 | 0/0 | 759 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | ATGGC others(754): Show |
chr12 | 30921748 | 31001599 | ||
a0003c0003 | 0/0 | 759 | 17 | 0 | 1 | 11 | 1 | 4 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | ATGGC others(754): Show |
chr12 | 30921748 | 31001599 | ||
a0004c0006 | 0/0 | 759 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | ATGGC others(754): Show |
chr12 | 30921748 | 31001599 | ||
a0004c0016 | 0/0 | 759 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | ATGGC others(754): Show |
chr12 | 30921748 | 31001599 | ||
a0005c0011 | 0/0 | 759 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | ATGGC others(754): Show |
chr12 | 30921748 | 31001599 | ||
a0006c0010 | 0/0 | 759 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | ATGGC others(754): Show |
chr12 | 30921748 | 31001599 | ||
a0007c0013 | 0/0 | 759 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | ATGGC others(754): Show |
chr12 | 30921748 | 31001599 | ||
a0008c0015 | 0/0 | 759 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | ATGGC others(754): Show |
chr12 | 30921748 | 31001599 | ||
a0009c0014 | 0/0 | 759 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | ATGGC others(754): Show |
chr12 | 30921748 | 31001599 | ||
a0010c0012 | 0/0 | 759 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | ATGGC others(754): Show |
chr12 | 30921748 | 31001599 | ||
a0011c0009 | 0/0 | 759 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | ATGGC others(754): Show |
chr12 | 30921748 | 31001599 | ||
a0012c0017 | 0/0 | 759 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | ATGGC others(754): Show |
chr12 | 30921748 | 31001599 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5505 | 34 | 6 | 2 | 21 | 1 | 4 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0002 | 0/1 | 5509 | 41 | 3 | 20 | 3 | 3 | 11 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5504): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0003 | 0/0 | 5505 | 25 | 0 | 0 | 23 | 0 | 2 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0004 | 0/0 | 5509 | 8 | 6 | 2 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5504): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0005 | 0/0 | 5505 | 12 | 0 | 5 | 3 | 1 | 3 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0006 | 0/0 | 5505 | 12 | 2 | 0 | 9 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0007 | 0/0 | 5505 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0008 | 0/0 | 5505 | 12 | 0 | 0 | 12 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0009 | 0/0 | 5509 | 10 | 2 | 7 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5504): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0010 | 0/0 | 5506 | 9 | 3 | 5 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5501): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0011 | 0/0 | 5505 | 7 | 0 | 5 | 2 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0012 | 0/0 | 5505 | 5 | 0 | 0 | 5 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0014 | 0/0 | 5506 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5501): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0015 | 0/0 | 5509 | 4 | 3 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5504): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0016 | 0/0 | 5507 | 5 | 5 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5502): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0017 | 0/0 | 5502 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5497): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0018 | 0/0 | 5508 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5503): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0019 | 0/0 | 5505 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0020 | 0/0 | 5505 | 3 | 1 | 2 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0021 | 0/0 | 5505 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0022 | 0/0 | 5505 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0023 | 0/0 | 5506 | 3 | 0 | 1 | 0 | 2 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5501): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0024 | 0/0 | 5505 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0025 | 0/0 | 5505 | 2 | 0 | 1 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0027 | 0/0 | 5505 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0028 | 0/0 | 5510 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5505): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0029 | 0/0 | 5506 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5501): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0031 | 0/0 | 5510 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5505): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0032 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0033 | 0/0 | 5505 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0034 | 0/0 | 5505 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0036 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0037 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0039 | 0/0 | 5509 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5504): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0040 | 0/0 | 5509 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5504): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0042 | 0/0 | 5509 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5504): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0043 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0047 | 0/0 | 5505 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0048 | 0/0 | 5509 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5504): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0050 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0054 | 0/0 | 5509 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5504): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0055 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0056 | 0/0 | 5509 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5504): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0057 | 0/0 | 5509 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5504): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0058 | 0/0 | 5509 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5504): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0062 | 0/0 | 5509 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5504): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0063 | 0/0 | 5510 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5505): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0064 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0066 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0068 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0069 | 0/0 | 5505 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0070 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0001t0075 | 0/0 | 5508 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5503): Show |
chr12 | 30921748 | 31001599 |
a0001c0007t0013 | 0/0 | 5505 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0001c0008t0001 | 0/0 | 5505 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0001 | 0/0 | 5505 | 27 | 0 | 1 | 24 | 0 | 2 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0002 | 0/0 | 5509 | 5 | 4 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5504): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0003 | 0/0 | 5505 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0004 | 0/0 | 5509 | 11 | 4 | 6 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5504): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0005 | 0/0 | 5505 | 5 | 0 | 0 | 3 | 0 | 2 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0006 | 0/0 | 5505 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0007 | 0/0 | 5505 | 14 | 0 | 0 | 13 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0012 | 0/0 | 5505 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0013 | 0/0 | 5505 | 5 | 5 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0014 | 0/0 | 5506 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5501): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0015 | 0/0 | 5509 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5504): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0018 | 0/0 | 5508 | 4 | 4 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5503): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0021 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0024 | 0/0 | 5505 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0025 | 0/0 | 5505 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0026 | 0/0 | 5505 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0030 | 0/0 | 5509 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5504): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0038 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0041 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0044 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0045 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0046 | 0/0 | 5507 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5502): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0059 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0060 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0065 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0071 | 0/0 | 5509 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5504): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0072 | 0/0 | 5505 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0073 | 0/0 | 5505 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0002c0002t0074 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0002c0004t0001 | 0/0 | 5505 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0002c0004t0004 | 0/0 | 5509 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5504): Show |
chr12 | 30921748 | 31001599 |
a0002c0004t0005 | 0/0 | 5505 | 2 | 0 | 0 | 1 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0002c0004t0014 | 0/0 | 5506 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5501): Show |
chr12 | 30921748 | 31001599 |
a0002c0004t0017 | 0/0 | 5502 | 4 | 0 | 3 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5497): Show |
chr12 | 30921748 | 31001599 |
a0002c0004t0030 | 0/0 | 5509 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5504): Show |
chr12 | 30921748 | 31001599 |
a0002c0004t0052 | 0/0 | 5502 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5497): Show |
chr12 | 30921748 | 31001599 |
a0002c0004t0053 | 1/0 | 5506 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5501): Show |
chr12 | 30921748 | 31001599 |
a0002c0005t0004 | 0/0 | 5509 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5504): Show |
chr12 | 30921748 | 31001599 |
a0003c0003t0001 | 0/0 | 5505 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0003c0003t0003 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0003c0003t0005 | 0/0 | 5505 | 2 | 0 | 0 | 1 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0003c0003t0006 | 0/0 | 5505 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0003c0003t0008 | 0/0 | 5505 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0003c0003t0009 | 0/0 | 5509 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5504): Show |
chr12 | 30921748 | 31001599 |
a0003c0003t0010 | 0/0 | 5506 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5501): Show |
chr12 | 30921748 | 31001599 |
a0003c0003t0012 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0003c0003t0032 | 0/0 | 5505 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0003c0003t0035 | 0/0 | 5509 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5504): Show |
chr12 | 30921748 | 31001599 |
a0003c0003t0051 | 0/0 | 5506 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5501): Show |
chr12 | 30921748 | 31001599 |
a0003c0003t0061 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0003c0003t0067 | 0/0 | 5509 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5504): Show |
chr12 | 30921748 | 31001599 |
a0004c0006t0001 | 0/0 | 5505 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0004c0006t0007 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0004c0016t0007 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0005c0011t0002 | 0/0 | 5509 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5504): Show |
chr12 | 30921748 | 31001599 |
a0006c0010t0022 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0007c0013t0011 | 0/0 | 5505 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0008c0015t0019 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0009c0014t0019 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0010c0012t0049 | 0/0 | 5509 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5504): Show |
chr12 | 30921748 | 31001599 |
a0011c0009t0001 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
a0012c0017t0011 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | AGTCT others(5500): Show |
chr12 | 30921748 | 31001599 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0002g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0003g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0003g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0004g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0004g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0004g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0005g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0005g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0005g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0005g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0005g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0005g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0005g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0005g0378 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0006g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0006g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0006g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0006g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0006g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0006g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0006g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0006g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0006g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0006g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0007g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0007g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0008g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0008g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0008g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0008g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0008g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0008g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0008g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0008g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0008g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0008g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0008g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0008g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0009g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0009g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0009g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0009g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0009g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0009g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0009g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0009g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0009g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0009g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0010g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0010g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0010g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0010g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0010g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0010g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0010g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0010g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0010g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0011g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0011g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0011g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0011g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0011g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0011g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0012g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0012g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0012g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0012g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0012g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0014g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0014g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0015g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0015g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0015g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0015g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0016g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0016g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0016g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0016g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0016g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0017g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0018g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0019g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0019g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0020g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0020g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0020g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0021g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0021g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0022g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0022g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0023g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0023g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0023g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0024g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0024g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0025g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0025g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0027g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0027g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0028g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0028g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0029g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0029g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0031g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0031g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0032g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0033g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0033g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0034g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0034g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0036g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0037g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0039g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0040g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0042g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0043g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0047g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0048g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0050g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0054g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0055g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0056g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0057g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0058g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0062g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0063g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0064g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0066g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0068g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0069g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0070g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0001t0075g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0007t0013g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0007t0013g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0008t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0001c0008t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0004g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0004g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0004g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0004g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0004g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0005g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0005g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0005g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0006g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0006g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0007g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0007g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0007g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0007g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0007g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0007g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0007g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0007g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0007g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0007g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0007g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0007g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0012g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0012g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0013g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0013g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0013g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0013g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0014g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0014g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0015g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0018g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0018g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0018g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0018g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0021g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0024g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0025g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0026g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0026g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0026g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0030g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0038g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0041g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0044g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0045g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0046g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0059g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0060g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0065g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0071g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0072g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0073g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0002t0074g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0004t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0004t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0004t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0004t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0004t0004g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0004t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0004t0005g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0004t0014g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0004t0017g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0004t0017g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0004t0017g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0004t0030g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0004t0052g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0004t0053g0311 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0005t0004g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0002c0005t0004g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0003c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0003c0003t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0003c0003t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0003c0003t0005g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0003c0003t0006g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0003c0003t0006g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0003c0003t0006g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0003c0003t0008g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0003c0003t0008g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0003c0003t0009g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0003c0003t0010g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0003c0003t0012g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0003c0003t0032g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0003c0003t0035g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0003c0003t0051g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0003c0003t0061g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0003c0003t0067g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0004c0006t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0004c0006t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0004c0006t0007g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0004c0016t0007g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0005c0011t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0006c0010t0022g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0007c0013t0011g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0008c0015t0019g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0009c0014t0019g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0010c0012t0049g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0011c0009t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
a0012c0017t0011g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0003 | c0003 | t0010 | g0161 | EUR | GBR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00140 | hp2 | a0001 | c0001 | t0009 | g0290 | EUR | GBR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00280 | hp1 | a0001 | c0001 | t0042 | g0256 | EUR | FIN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0220 | EUR | FIN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0244 | EUR | FIN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00323 | hp2 | a0002 | c0002 | t0007 | g0078 | EUR | FIN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00408 | hp2 | a0001 | c0001 | t0032 | g0268 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00423 | hp1 | a0005 | c0011 | t0002 | g0260 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0224 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0372 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00438 | hp2 | a0002 | c0002 | t0007 | g0150 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00544 | hp2 | a0001 | c0001 | t0066 | g0305 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00558 | hp2 | a0001 | c0001 | t0006 | g0159 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00621 | hp1 | a0001 | c0001 | t0006 | g0032 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0274 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00639 | hp2 | a0003 | c0003 | t0009 | g0162 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00642 | hp1 | a0001 | c0001 | t0009 | g0329 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00642 | hp2 | a0001 | c0001 | t0010 | g0273 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00673 | hp1 | a0003 | c0003 | t0012 | g0216 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00673 | hp2 | a0002 | c0002 | t0007 | g0251 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00733 | hp1 | a0001 | c0001 | t0009 | g0346 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0277 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0325 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0339 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00738 | hp1 | a0002 | c0004 | t0014 | g0195 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00738 | hp2 | a0002 | c0002 | t0004 | g0300 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00741 | hp1 | a0001 | c0001 | t0010 | g0052 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG00741 | hp2 | a0002 | c0002 | t0004 | g0323 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01069 | hp2 | a0002 | c0004 | t0004 | g0283 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01070 | hp1 | a0002 | c0002 | t0030 | g0308 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01070 | hp2 | a0002 | c0004 | t0017 | g0005 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01071 | hp1 | a0002 | c0004 | t0017 | g0005 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01074 | hp1 | a0002 | c0002 | t0004 | g0370 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01074 | hp2 | a0001 | c0001 | t0009 | g0303 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0307 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0157 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01106 | hp1 | a0001 | c0001 | t0009 | g0204 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01109 | hp1 | a0002 | c0002 | t0024 | g0155 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0344 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01167 | hp1 | a0002 | c0002 | t0014 | g0124 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01167 | hp2 | a0001 | c0001 | t0020 | g0019 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01168 | hp1 | a0001 | c0001 | t0010 | g0335 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01169 | hp2 | a0001 | c0001 | t0020 | g0020 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01192 | hp1 | a0001 | c0001 | t0015 | g0363 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01243 | hp2 | a0001 | c0001 | t0009 | g0231 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01255 | hp1 | a0002 | c0002 | t0004 | g0098 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01255 | hp2 | a0002 | c0002 | t0071 | g0153 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01257 | hp1 | a0001 | c0001 | t0009 | g0369 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01257 | hp2 | a0001 | c0001 | t0005 | g0374 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0343 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01258 | hp2 | a0001 | c0001 | t0005 | g0375 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01358 | hp1 | a0001 | c0001 | t0054 | g0172 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01358 | hp2 | a0001 | c0001 | t0009 | g0271 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0291 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01361 | hp2 | a0002 | c0002 | t0004 | g0376 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01433 | hp1 | a0001 | c0001 | t0004 | g0081 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01433 | hp2 | a0001 | c0001 | t0023 | g0170 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0373 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01496 | hp2 | a0001 | c0001 | t0005 | g0342 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01516 | hp1 | a0001 | c0001 | t0023 | g0337 | EUR | IBS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01516 | hp2 | a0002 | c0004 | t0030 | g0206 | EUR | IBS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01517 | hp1 | a0001 | c0001 | t0023 | g0336 | EUR | IBS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0163 | EUR | IBS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01884 | hp1 | a0001 | c0001 | t0034 | g0010 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01884 | hp2 | a0002 | c0002 | t0041 | g0014 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01891 | hp1 | a0006 | c0010 | t0022 | g0185 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01891 | hp2 | a0002 | c0002 | t0018 | g0201 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01928 | hp2 | a0001 | c0001 | t0031 | g0207 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01934 | hp1 | a0001 | c0001 | t0005 | g0377 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01934 | hp2 | a0002 | c0002 | t0004 | g0023 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0030 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01943 | hp2 | a0001 | c0001 | t0010 | g0209 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01952 | hp2 | a0001 | c0001 | t0011 | g0006 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01975 | hp1 | a0001 | c0001 | t0011 | g0006 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0340 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01978 | hp1 | a0001 | c0001 | t0063 | g0208 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01978 | hp2 | a0007 | c0013 | t0011 | g0338 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01981 | hp1 | a0002 | c0004 | t0017 | g0152 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01981 | hp2 | a0001 | c0001 | t0005 | g0050 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02004 | hp1 | a0001 | c0001 | t0031 | g0104 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02004 | hp2 | a0001 | c0001 | t0011 | g0221 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02015 | hp2 | a0001 | c0001 | t0006 | g0285 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0202 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02027 | hp2 | a0001 | c0001 | t0006 | g0328 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02040 | hp2 | a0001 | c0001 | t0006 | g0158 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02055 | hp1 | a0001 | c0001 | t0021 | g0198 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02055 | hp2 | a0001 | c0001 | t0022 | g0179 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02056 | hp2 | a0002 | c0004 | t0001 | g0227 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02071 | hp1 | a0003 | c0003 | t0051 | g0347 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02074 | hp1 | a0002 | c0004 | t0001 | g0234 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02080 | hp2 | a0002 | c0002 | t0007 | g0128 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02083 | hp1 | a0001 | c0008 | t0001 | g0048 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02083 | hp2 | a0001 | c0001 | t0006 | g0222 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02132 | hp1 | a0003 | c0003 | t0003 | g0080 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02132 | hp2 | a0002 | c0002 | t0007 | g0144 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02135 | hp1 | a0001 | c0008 | t0001 | g0047 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0360 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02145 | hp2 | a0002 | c0005 | t0004 | g0001 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0345 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02148 | hp2 | a0001 | c0001 | t0011 | g0099 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | CDX | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02165 | hp2 | a0001 | c0001 | t0005 | g0106 | EAS | CDX | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02257 | hp1 | a0001 | c0001 | t0028 | g0181 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0351 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02258 | hp2 | a0001 | c0001 | t0021 | g0212 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02280 | hp1 | a0002 | c0005 | t0004 | g0359 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02280 | hp2 | a0001 | c0001 | t0009 | g0156 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02293 | hp1 | a0001 | c0001 | t0011 | g0087 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0341 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0269 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02523 | hp1 | a0002 | c0002 | t0003 | g0121 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0355 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02572 | hp2 | a0001 | c0001 | t0043 | g0317 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0357 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02615 | hp1 | a0001 | c0001 | t0015 | g0364 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02615 | hp2 | a0001 | c0007 | t0013 | g0243 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02622 | hp1 | a0002 | c0002 | t0004 | g0295 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02622 | hp2 | a0001 | c0001 | t0034 | g0228 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02630 | hp2 | a0001 | c0001 | t0010 | g0319 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02647 | hp1 | a0002 | c0002 | t0004 | g0182 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02647 | hp2 | a0001 | c0001 | t0024 | g0180 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02683 | hp1 | a0003 | c0003 | t0001 | g0114 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02683 | hp2 | a0002 | c0002 | t0004 | g0239 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02717 | hp1 | a0001 | c0001 | t0010 | g0031 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02717 | hp2 | a0002 | c0002 | t0018 | g0352 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02723 | hp1 | a0001 | c0001 | t0020 | g0026 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02723 | hp2 | a0002 | c0002 | t0014 | g0279 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0120 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02735 | hp2 | a0001 | c0001 | t0006 | g0258 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02738 | hp1 | a0002 | c0002 | t0005 | g0322 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02738 | hp2 | a0003 | c0003 | t0035 | g0321 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02809 | hp1 | a0001 | c0001 | t0022 | g0053 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02809 | hp2 | a0002 | c0002 | t0004 | g0176 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02818 | hp1 | a0001 | c0001 | t0028 | g0316 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02818 | hp2 | a0002 | c0002 | t0044 | g0039 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02886 | hp1 | a0001 | c0001 | t0050 | g0177 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02886 | hp2 | a0002 | c0002 | t0045 | g0188 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02895 | hp1 | a0002 | c0002 | t0026 | g0027 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02895 | hp2 | a0001 | c0001 | t0029 | g0193 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02896 | hp1 | a0001 | c0001 | t0006 | g0189 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02897 | hp1 | a0001 | c0001 | t0006 | g0190 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02897 | hp2 | a0001 | c0001 | t0029 | g0192 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02922 | hp1 | a0001 | c0001 | t0036 | g0009 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02922 | hp2 | a0002 | c0002 | t0013 | g0018 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02965 | hp1 | a0001 | c0001 | t0016 | g0178 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02965 | hp2 | a0002 | c0002 | t0002 | g0315 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02970 | hp1 | a0002 | c0002 | t0059 | g0138 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0349 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02976 | hp1 | a0002 | c0002 | t0026 | g0299 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02976 | hp2 | a0001 | c0001 | t0015 | g0367 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0361 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03017 | hp2 | a0001 | c0001 | t0005 | g0122 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03041 | hp1 | a0001 | c0001 | t0016 | g0353 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03041 | hp2 | a0002 | c0002 | t0004 | g0318 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03098 | hp1 | a0001 | c0001 | t0018 | g0350 | AFR | MSL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03098 | hp2 | a0001 | c0001 | t0016 | g0362 | AFR | MSL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0354 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03139 | hp1 | a0002 | c0002 | t0026 | g0281 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0214 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03195 | hp1 | a0001 | c0001 | t0015 | g0365 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03195 | hp2 | a0008 | c0015 | t0019 | g0001 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03209 | hp1 | a0001 | c0001 | t0056 | g0213 | AFR | MSL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03209 | hp2 | a0002 | c0002 | t0002 | g0174 | AFR | MSL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03225 | hp1 | a0002 | c0004 | t0052 | g0021 | AFR | MSL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03225 | hp2 | a0001 | c0001 | t0014 | g0366 | AFR | MSL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03239 | hp1 | a0002 | c0002 | t0073 | g0368 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03239 | hp2 | a0002 | c0004 | t0017 | g0217 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03453 | hp1 | a0002 | c0002 | t0015 | g0382 | AFR | MSL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03453 | hp2 | a0001 | c0001 | t0075 | g0383 | AFR | MSL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03486 | hp1 | a0009 | c0014 | t0019 | g0125 | AFR | MSL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03486 | hp2 | a0001 | c0001 | t0010 | g0324 | AFR | MSL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03491 | hp1 | a0001 | c0001 | t0027 | g0024 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0286 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03492 | hp2 | a0001 | c0001 | t0027 | g0025 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03516 | hp1 | a0002 | c0002 | t0002 | g0184 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03516 | hp2 | a0001 | c0001 | t0014 | g0384 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0296 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03540 | hp2 | a0002 | c0002 | t0013 | g0002 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03579 | hp1 | a0001 | c0001 | t0058 | g0332 | AFR | MSL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03579 | hp2 | a0001 | c0007 | t0013 | g0249 | AFR | MSL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0199 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03669 | hp1 | a0001 | c0001 | t0010 | g0127 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03669 | hp2 | a0001 | c0001 | t0057 | g0108 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03688 | hp1 | a0001 | c0001 | t0039 | g0004 | SAS | STU | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03688 | hp2 | a0003 | c0003 | t0005 | g0242 | SAS | STU | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03704 | hp2 | a0001 | c0001 | t0040 | g0255 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0287 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03710 | hp2 | a0001 | c0001 | t0017 | g0302 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0223 | SAS | BEB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03831 | hp2 | a0001 | c0001 | t0005 | g0313 | SAS | BEB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03834 | hp1 | a0002 | c0002 | t0025 | g0139 | SAS | BEB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03834 | hp2 | a0002 | c0002 | t0005 | g0312 | SAS | BEB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03927 | hp1 | a0001 | c0001 | t0069 | g0119 | SAS | BEB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03927 | hp2 | a0001 | c0001 | t0062 | g0133 | SAS | BEB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03942 | hp1 | a0001 | c0001 | t0005 | g0301 | SAS | BEB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03942 | hp2 | a0003 | c0003 | t0032 | g0241 | SAS | BEB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | STU | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG04115 | hp2 | a0001 | c0001 | t0025 | g0219 | SAS | STU | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0238 | SAS | BEB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0282 | SAS | BEB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | STU | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG04199 | hp2 | a0001 | c0001 | t0047 | g0259 | SAS | STU | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0123 | SAS | STU | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG04204 | hp2 | a0002 | c0004 | t0005 | g0272 | SAS | STU | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG04228 | hp1 | a0002 | c0002 | t0072 | g0160 | SAS | STU | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0126 | SAS | STU | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18522 | hp1 | a0001 | c0001 | t0019 | g0385 | AFR | YRI | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18522 | hp2 | a0001 | c0001 | t0048 | g0012 | AFR | YRI | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CHB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18612 | hp2 | a0002 | c0002 | t0006 | g0035 | EAS | CHB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | CHB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18747 | hp2 | a0001 | c0001 | t0033 | g0191 | EAS | CHB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18906 | hp1 | a0001 | c0001 | t0016 | g0331 | AFR | YRI | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18906 | hp2 | a0002 | c0002 | t0018 | g0040 | AFR | YRI | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18940 | hp1 | a0002 | c0002 | t0007 | g0358 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18940 | hp2 | a0001 | c0001 | t0068 | g0304 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18941 | hp1 | a0004 | c0016 | t0007 | g0135 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18941 | hp2 | a0001 | c0001 | t0012 | g0147 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18942 | hp1 | a0002 | c0002 | t0001 | g0293 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18943 | hp1 | a0002 | c0002 | t0003 | g0093 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18945 | hp1 | a0002 | c0002 | t0012 | g0381 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18946 | hp2 | a0001 | c0001 | t0008 | g0049 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18947 | hp1 | a0001 | c0001 | t0011 | g0077 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18947 | hp2 | a0001 | c0001 | t0008 | g0306 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18949 | hp1 | a0002 | c0002 | t0007 | g0029 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0309 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18950 | hp2 | a0002 | c0002 | t0060 | g0252 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18951 | hp1 | a0003 | c0003 | t0006 | g0166 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18951 | hp2 | a0002 | c0002 | t0007 | g0007 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18953 | hp1 | a0002 | c0002 | t0005 | g0143 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18954 | hp1 | a0001 | c0001 | t0008 | g0069 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18954 | hp2 | a0002 | c0002 | t0003 | g0168 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18956 | hp2 | a0003 | c0003 | t0061 | g0265 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18957 | hp1 | a0004 | c0006 | t0001 | g0136 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18957 | hp2 | a0001 | c0001 | t0008 | g0092 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18959 | hp1 | a0001 | c0001 | t0012 | g0034 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18959 | hp2 | a0002 | c0002 | t0007 | g0007 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18960 | hp2 | a0001 | c0001 | t0008 | g0086 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18962 | hp1 | a0002 | c0004 | t0001 | g0046 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18964 | hp1 | a0002 | c0002 | t0006 | g0132 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0334 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18970 | hp2 | a0002 | c0002 | t0007 | g0097 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18971 | hp2 | a0002 | c0002 | t0006 | g0254 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0371 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18977 | hp2 | a0002 | c0002 | t0005 | g0131 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18978 | hp1 | a0002 | c0002 | t0007 | g0140 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18979 | hp1 | a0003 | c0003 | t0006 | g0232 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18980 | hp2 | a0001 | c0001 | t0006 | g0173 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18981 | hp1 | a0001 | c0001 | t0008 | g0065 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18981 | hp2 | a0003 | c0003 | t0008 | g0264 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18984 | hp1 | a0002 | c0004 | t0001 | g0247 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18984 | hp2 | a0001 | c0001 | t0070 | g0297 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18985 | hp1 | a0002 | c0002 | t0007 | g0055 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18986 | hp1 | a0002 | c0004 | t0005 | g0246 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18990 | hp1 | a0001 | c0001 | t0008 | g0129 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18990 | hp2 | a0001 | c0001 | t0011 | g0067 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18991 | hp1 | a0001 | c0001 | t0008 | g0107 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18991 | hp2 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18993 | hp1 | a0001 | c0001 | t0006 | g0284 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18994 | hp2 | a0002 | c0002 | t0005 | g0130 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0326 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19005 | hp1 | a0002 | c0002 | t0074 | g0149 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19005 | hp2 | a0003 | c0003 | t0006 | g0270 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19007 | hp2 | a0002 | c0002 | t0065 | g0167 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19009 | hp2 | a0001 | c0001 | t0008 | g0060 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19010 | hp2 | a0001 | c0001 | t0005 | g0118 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19012 | hp1 | a0004 | c0006 | t0007 | g0137 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19012 | hp2 | a0002 | c0002 | t0007 | g0102 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19030 | hp1 | a0010 | c0012 | t0049 | g0248 | AFR | LWK | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19030 | hp2 | a0001 | c0001 | t0019 | g0386 | AFR | LWK | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19043 | hp1 | a0002 | c0002 | t0038 | g0194 | AFR | LWK | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | LWK | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19054 | hp1 | a0002 | c0002 | t0012 | g0237 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0380 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19057 | hp1 | a0001 | c0001 | t0008 | g0105 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19057 | hp2 | a0001 | c0001 | t0012 | g0164 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19063 | hp1 | a0001 | c0001 | t0008 | g0091 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0379 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19064 | hp2 | a0002 | c0002 | t0007 | g0141 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19065 | hp1 | a0003 | c0003 | t0008 | g0263 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19065 | hp2 | a0001 | c0001 | t0007 | g0094 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19078 | hp1 | a0001 | c0001 | t0012 | g0145 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19078 | hp2 | a0001 | c0001 | t0008 | g0095 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19079 | hp1 | a0001 | c0001 | t0012 | g0148 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19079 | hp2 | a0003 | c0003 | t0067 | g0226 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19081 | hp1 | a0001 | c0001 | t0006 | g0261 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19081 | hp2 | a0003 | c0003 | t0005 | g0056 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19082 | hp1 | a0011 | c0009 | t0001 | g0057 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19085 | hp1 | a0012 | c0017 | t0011 | g0171 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19086 | hp2 | a0002 | c0002 | t0001 | g0314 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19087 | hp2 | a0001 | c0001 | t0033 | g0253 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19088 | hp1 | a0004 | c0006 | t0001 | g0134 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19088 | hp2 | a0002 | c0002 | t0006 | g0250 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19090 | hp2 | a0001 | c0001 | t0064 | g0066 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19240 | hp1 | a0002 | c0005 | t0004 | g0001 | AFR | YRI | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0186 | AFR | YRI | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA20129 | hp1 | a0001 | c0001 | t0037 | g0016 | AFR | ASW | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA20129 | hp2 | a0002 | c0002 | t0013 | g0015 | AFR | ASW | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA20805 | hp1 | a0001 | c0001 | t0005 | g0378 | EUR | TSI | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0298 | EUR | TSI | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0348 | SAS | GIH | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0333 | SAS | GIH | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01123 | hp1 | a0001 | c0001 | t0010 | g0294 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG01123 | hp2 | a0001 | c0001 | t0025 | g0205 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02109 | hp1 | a0002 | c0002 | t0002 | g0175 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02109 | hp2 | a0002 | c0002 | t0018 | g0183 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0330 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG02559 | hp2 | a0002 | c0002 | t0013 | g0280 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03471 | hp1 | a0001 | c0001 | t0024 | g0017 | AFR | MSL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG06807 | hp1 | a0002 | c0002 | t0021 | g0036 | AFR | USA | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
HG06807 | hp2 | a0001 | c0001 | t0016 | g0187 | AFR | USA | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18955 | hp1 | a0001 | c0001 | t0007 | g0200 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA18955 | hp2 | a0001 | c0001 | t0005 | g0278 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA20300 | hp1 | a0001 | c0001 | t0055 | g0356 | AFR | USA | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA20300 | hp2 | a0001 | c0001 | t0009 | g0229 | AFR | USA | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA21309 | hp1 | a0002 | c0002 | t0013 | g0002 | AFR | LWK | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
NA21309 | hp2 | a0002 | c0002 | t0046 | g0310 | AFR | LWK | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0089 | REF | REF | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
homoSapiens | grch38p0 | a0002 | c0004 | t0053 | g0311 | REF | REF | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:30954007 | A | C | 3 | a0003 a0004 a0012 |
22 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(19): Show |
missense_variant | MODERATE | c.16A>C | p.Thr6Pro | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/8 | 76/5506 | 16/762 | 6/253 | chr12 | 30954007 | |||
chr12:30963892 | G | T | 1 | a0007 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.151G>T | p.Val51Phe | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/8 | 211/5506 | 151/762 | 51/253 | chr12 | 30963892 | |||
chr12:30978613 | T | C | 1 | a0009 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.329T>C | p.Leu110Pro | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/8 | 389/5506 | 329/762 | 110/253 | chr12 | 30978613 | |||
chr12:30979597 | G | A | 1 | a0011 | 1 | NA19082.hp1 | missense_variant | MODERATE | c.383G>A | p.Arg128Gln | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/8 | 443/5506 | 383/762 | 128/253 | chr12 | 30979597 | |||
chr12:30982598 | G | A | 1 | a0006 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.523G>A | p.Ala175Thr | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/8 | 583/5506 | 523/762 | 175/253 | chr12 | 30982598 | |||
chr12:30982644 | T | C | 8 | a0001 a0003 a0005 others(5): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
missense_variant | MODERATE | c.569T>C | p.Val190Ala | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/8 | 629/5506 | 569/762 | 190/253 | chr12 | 30982644 | |||
chr12:30982680 | A | G | 1 | a0012 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.605A>G | p.Tyr202Cys | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/8 | 665/5506 | 605/762 | 202/253 | chr12 | 30982680 | |||
chr12:30983100 | G | A | 1 | a0005 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.652G>A | p.Asp218Asn | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/8 | 712/5506 | 652/762 | 218/253 | chr12 | 30983100 | |||
chr12:30991875 | C | A | 1 | a0008 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.722C>A | p.Thr241Asn | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 782/5506 | 722/762 | 241/253 | chr12 | 30991875 | |||
chr12:30991902 | G | A | 1 | a0010 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.749G>A | p.Arg250Gln | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 809/5506 | 749/762 | 250/253 | chr12 | 30991902 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:30954018 | C | T | 1 | a0001c0008 | 2 | HG02083.hp1 HG02135.hp1 |
synonymous_variant | LOW | c.27C>T | p.Asp9Asp | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/8 | 87/5506 | 27/762 | 9/253 | chr12 | 30954018 | |||
chr12:30963888 | C | G | 3 | a0002c0005 a0008c0015 a0009c0014 |
5 | HG02145.hp2 HG02280.hp1 HG03195.hp2 others(2): Show |
synonymous_variant | LOW | c.147C>G | p.Leu49Leu | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/8 | 207/5506 | 147/762 | 49/253 | chr12 | 30963888 | |||
chr12:30982543 | T | C | 14 | a0001c0001 a0001c0007 a0001c0008 others(11): Show |
374 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(371): Show |
synonymous_variant | LOW | c.468T>C | p.Cys156Cys | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/8 | 528/5506 | 468/762 | 156/253 | chr12 | 30982543 | |||
chr12:30982579 | G | A | 1 | a0004c0016 | 1 | NA18941.hp1 | synonymous_variant | LOW | c.504G>A | p.Thr168Thr | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/8 | 564/5506 | 504/762 | 168/253 | chr12 | 30982579 | |||
chr12:30982651 | C | T | 1 | a0001c0007 | 2 | HG02615.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.576C>T | p.Cys192Cys | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/8 | 636/5506 | 576/762 | 192/253 | chr12 | 30982651 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:30991949 | A | G | 74 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(71): Show |
263 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(260): Show |
3_prime_UTR_variant | MODIFIER | c.*34A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 34 | chr12 | 30991949 | ||||||
chr12:30991971 | A | G | 2 | a0001c0001t0055 a0001c0001t0056 |
2 | HG03209.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*56A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 56 | chr12 | 30991971 | ||||||
chr12:30992037 | A | G | 1 | a0001c0001t0054 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*122A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 122 | chr12 | 30992037 | ||||||
chr12:30992075 | T | TCTA | 113 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(110): Show |
386 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(383): Show |
3_prime_UTR_variant | MODIFIER | c.*162_*163insACT | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 163 | INFO_REALIGN_3_PRIME | chr12 | 30992075 | |||||
chr12:30992094 | A | G | 68 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(65): Show |
251 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(248): Show |
3_prime_UTR_variant | MODIFIER | c.*179A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 179 | chr12 | 30992094 | ||||||
chr12:30992101 | C | T | 3 | a0001c0001t0016 a0001c0001t0055 a0001c0001t0056 |
7 | HG02965.hp1 HG03041.hp1 HG03098.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*186C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 186 | chr12 | 30992101 | ||||||
chr12:30992149 | G | A | 10 | a0001c0001t0006 a0001c0001t0028 a0001c0001t0029 others(7): Show |
28 | HG00558.hp2 HG00621.hp1 HG01070.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*234G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 234 | chr12 | 30992149 | ||||||
chr12:30992151 | G | A | 1 | a0003c0003t0035 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*236G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 236 | chr12 | 30992151 | ||||||
chr12:30992234 | C | A | 3 | a0001c0001t0011 a0007c0013t0011 a0012c0017t0011 |
9 | HG01952.hp2 HG01975.hp1 HG01978.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*319C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 319 | chr12 | 30992234 | ||||||
chr12:30992270 | G | C | 3 | a0001c0001t0016 a0001c0001t0055 a0001c0001t0056 |
7 | HG02965.hp1 HG03041.hp1 HG03098.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*355G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 355 | chr12 | 30992270 | ||||||
chr12:30992370 | G | C | 12 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0018 others(9): Show |
28 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*455G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 455 | chr12 | 30992370 | ||||||
chr12:30992590 | G | A | 1 | a0001c0001t0037 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*675G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 675 | chr12 | 30992590 | ||||||
chr12:30992698 | G | A | 3 | a0001c0001t0008 a0001c0001t0064 a0003c0003t0008 |
15 | NA18946.hp2 NA18947.hp2 NA18954.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*783G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 783 | chr12 | 30992698 | ||||||
chr12:30992739 | A | G | 11 | a0001c0001t0007 a0001c0001t0018 a0001c0001t0034 others(8): Show |
31 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*824A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 824 | chr12 | 30992739 | ||||||
chr12:30992791 | A | C | 46 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(43): Show |
161 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*876A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 876 | chr12 | 30992791 | ||||||
chr12:30992981 | A | T | 12 | a0001c0001t0004 a0001c0001t0047 a0001c0001t0048 others(9): Show |
31 | HG00733.hp2 HG00738.hp2 HG00741.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1066A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 1066 | chr12 | 30992981 | ||||||
chr12:30992989 | G | A | 3 | a0001c0001t0020 a0001c0001t0036 a0002c0002t0038 |
5 | HG01167.hp2 HG01169.hp2 HG02723.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1074G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 1074 | chr12 | 30992989 | ||||||
chr12:30993113 | A | AC | 14 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0018 others(11): Show |
32 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1205dupC | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 1206 | INFO_REALIGN_3_PRIME | chr12 | 30993113 | |||||
chr12:30993125 | G | A | 56 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(53): Show |
212 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*1210G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 1210 | chr12 | 30993125 | ||||||
chr12:30993204 | C | T | 1 | a0001c0001t0033 | 2 | NA18747.hp2 NA19087.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1289C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 1289 | chr12 | 30993204 | ||||||
chr12:30993266 | C | G | 3 | a0001c0001t0015 a0001c0001t0043 a0002c0002t0015 |
6 | HG01192.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1351C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 1351 | chr12 | 30993266 | ||||||
chr12:30993522 | T | C | 1 | a0002c0002t0065 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1607T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 1607 | chr12 | 30993522 | ||||||
chr12:30993599 | G | A | 10 | a0001c0001t0004 a0001c0001t0047 a0001c0001t0048 others(7): Show |
29 | HG00733.hp2 HG00738.hp2 HG00741.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1684G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 1684 | chr12 | 30993599 | ||||||
chr12:30993700 | A | G | 60 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(57): Show |
219 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*1785A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 1785 | chr12 | 30993700 | ||||||
chr12:30993758 | C | T | 1 | a0001c0001t0048 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1843C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 1843 | chr12 | 30993758 | ||||||
chr12:30993782 | G | A | 1 | a0001c0001t0039 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1867G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 1867 | chr12 | 30993782 | ||||||
chr12:30993821 | C | T | 8 | a0001c0001t0007 a0001c0001t0034 a0002c0002t0007 others(5): Show |
25 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1906C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 1906 | chr12 | 30993821 | ||||||
chr12:30993822 | G | A | 1 | a0001c0001t0040 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1907G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 1907 | chr12 | 30993822 | ||||||
chr12:30993939 | G | A | 56 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(53): Show |
212 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*2024G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 2024 | chr12 | 30993939 | ||||||
chr12:30994013 | A | C | 2 | a0001c0001t0055 a0001c0001t0056 |
2 | HG03209.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2098A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 2098 | chr12 | 30994013 | ||||||
chr12:30994200 | G | T | 1 | a0003c0003t0061 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2285G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 2285 | chr12 | 30994200 | ||||||
chr12:30994248 | G | A | 1 | a0001c0001t0034 | 2 | HG01884.hp1 HG02622.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2333G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 2333 | chr12 | 30994248 | ||||||
chr12:30994294 | A | G | 1 | a0002c0002t0072 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2379A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 2379 | chr12 | 30994294 | ||||||
chr12:30994364 | G | A | 1 | a0002c0002t0060 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2449G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 2449 | chr12 | 30994364 | ||||||
chr12:30994477 | C | T | 1 | a0001c0001t0047 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2562C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 2562 | chr12 | 30994477 | ||||||
chr12:30994500 | G | A | 90 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(87): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
3_prime_UTR_variant | MODIFIER | c.*2585G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 2585 | chr12 | 30994500 | ||||||
chr12:30994506 | G | A | 7 | a0001c0001t0005 a0001c0001t0043 a0001c0001t0069 others(4): Show |
24 | HG01257.hp2 HG01258.hp2 HG01496.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2591G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 2591 | chr12 | 30994506 | ||||||
chr12:30994540 | G | T | 33 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0015 others(30): Show |
105 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*2625G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 2625 | chr12 | 30994540 | ||||||
chr12:30994602 | G | C | 1 | a0001c0001t0070 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2687G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 2687 | chr12 | 30994602 | ||||||
chr12:30994677 | C | T | 3 | a0001c0001t0036 a0002c0002t0026 a0002c0002t0038 |
5 | HG02895.hp1 HG02922.hp1 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2762C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 2762 | chr12 | 30994677 | ||||||
chr12:30994940 | C | T | 4 | a0001c0001t0016 a0001c0001t0018 a0001c0001t0075 others(1): Show |
11 | HG01891.hp2 HG02109.hp2 HG02717.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3025C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 3025 | chr12 | 30994940 | ||||||
chr12:30994997 | CAG | C | 5 | a0001c0001t0016 a0001c0001t0018 a0001c0001t0075 others(2): Show |
12 | HG01891.hp2 HG02109.hp2 HG02717.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3083_*3084delAG | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 3083 | chr12 | 30994997 | ||||||
chr12:30995252 | G | A | 21 | a0001c0001t0001 a0001c0001t0017 a0001c0001t0019 others(18): Show |
91 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*3337G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 3337 | chr12 | 30995252 | ||||||
chr12:30995414 | G | C | 1 | a0010c0012t0049 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3499G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 3499 | chr12 | 30995414 | ||||||
chr12:30995446 | A | C | 32 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0017 others(29): Show |
113 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*3531A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 3531 | chr12 | 30995446 | ||||||
chr12:30995480 | C | T | 1 | a0001c0001t0069 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3565C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 3565 | chr12 | 30995480 | ||||||
chr12:30995483 | G | A | 2 | a0002c0002t0041 a0010c0012t0049 |
2 | HG01884.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3568G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 3568 | chr12 | 30995483 | ||||||
chr12:30995498 | G | C | 1 | a0001c0001t0002 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3583G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 3583 | chr12 | 30995498 | ||||||
chr12:30995700 | C | T | 1 | a0010c0012t0049 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3785C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 3785 | chr12 | 30995700 | ||||||
chr12:30995727 | G | A | 82 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(79): Show |
275 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*3812G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 3812 | chr12 | 30995727 | ||||||
chr12:30995740 | G | A | 1 | a0010c0012t0049 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3825G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 3825 | chr12 | 30995740 | ||||||
chr12:30995784 | TACAA | T | 82 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(79): Show |
275 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*3873_*3876delAACA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 3873 | INFO_REALIGN_3_PRIME | chr12 | 30995784 | |||||
chr12:30995857 | G | A | 83 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(80): Show |
276 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(273): Show |
3_prime_UTR_variant | MODIFIER | c.*3942G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 3942 | chr12 | 30995857 | ||||||
chr12:30995867 | C | T | 82 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(79): Show |
275 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*3952C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 3952 | chr12 | 30995867 | ||||||
chr12:30995921 | C | A | 1 | a0001c0001t0042 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4006C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 4006 | chr12 | 30995921 | ||||||
chr12:30995935 | A | C | 2 | a0002c0002t0030 a0002c0004t0030 |
2 | HG01070.hp1 HG01516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4020A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 4020 | chr12 | 30995935 | ||||||
chr12:30995957 | C | T | 1 | a0010c0012t0049 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4042C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 4042 | chr12 | 30995957 | ||||||
chr12:30995983 | G | C | 1 | a0001c0001t0016 | 5 | HG02965.hp1 HG03041.hp1 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4068G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 4068 | chr12 | 30995983 | ||||||
chr12:30996009 | C | T | 4 | a0001c0001t0016 a0001c0001t0018 a0001c0001t0075 others(1): Show |
11 | HG01891.hp2 HG02109.hp2 HG02717.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4094C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 4094 | chr12 | 30996009 | ||||||
chr12:30996097 | G | A | 1 | a0010c0012t0049 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4182G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 4182 | chr12 | 30996097 | ||||||
chr12:30996274 | T | G | 2 | a0001c0001t0022 a0006c0010t0022 |
3 | HG01891.hp1 HG02055.hp2 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4359T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 4359 | chr12 | 30996274 | ||||||
chr12:30996485 | C | T | 1 | a0010c0012t0049 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4570C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 4570 | chr12 | 30996485 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:30927105 | G | C | 1 | a0001c0001t0004g0008 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-12+309G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30927105 | |||||||
chr12:30927131 | C | T | 5 | a0001c0001t0014g0384 a0001c0001t0019g0385 a0001c0001t0019g0386 others(2): Show |
5 | HG03453.hp1 HG03453.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+335C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30927131 | |||||||
chr12:30927393 | G | T | 1 | a0002c0002t0012g0381 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-12+597G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30927393 | |||||||
chr12:30927460 | T | C | 1 | a0001c0001t0036g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-12+664T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30927460 | |||||||
chr12:30927473 | G | A | 18 | a0001c0001t0004g0011 a0001c0001t0004g0013 a0001c0001t0014g0384 others(15): Show |
19 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.-12+677G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30927473 | |||||||
chr12:30927516 | G | C | 2 | a0001c0001t0001g0022 a0002c0002t0004g0023 |
2 | HG01106.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-12+720G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30927516 | |||||||
chr12:30927597 | G | A | 2 | a0001c0001t0027g0024 a0001c0001t0027g0025 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-12+801G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30927597 | |||||||
chr12:30927802 | G | T | 1 | a0001c0001t0004g0008 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-12+1006G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30927802 | |||||||
chr12:30927923 | T | A | 3 | a0001c0001t0014g0384 a0001c0001t0075g0383 a0002c0002t0015g0382 |
3 | HG03453.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-12+1127T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30927923 | |||||||
chr12:30928005 | C | T | 2 | a0001c0001t0001g0379 a0001c0001t0003g0380 |
2 | NA19054.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-12+1209C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30928005 | |||||||
chr12:30928006 | G | A | 2 | a0001c0001t0020g0026 a0002c0002t0026g0027 |
2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-12+1210G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30928006 | |||||||
chr12:30928019 | G | A | 31 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0379 others(28): Show |
31 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.-12+1223G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30928019 | |||||||
chr12:30928196 | G | A | 70 | a0001c0001t0001g0059 a0001c0001t0001g0082 a0001c0001t0001g0088 others(67): Show |
71 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.-12+1400G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30928196 | |||||||
chr12:30928301 | G | A | 1 | a0002c0002t0014g0124 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-12+1505G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30928301 | |||||||
chr12:30928450 | G | A | 1 | a0009c0014t0019g0125 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-12+1654G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30928450 | |||||||
chr12:30928628 | C | T | 1 | a0002c0002t0007g0007 | 2 | NA18951.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.-12+1832C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30928628 | |||||||
chr12:30928734 | A | G | 2 | a0001c0001t0002g0123 a0001c0001t0005g0122 |
2 | HG03017.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-12+1938A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30928734 | |||||||
chr12:30928794 | A | G | 18 | a0001c0001t0002g0371 a0001c0001t0002g0372 a0001c0001t0002g0373 others(15): Show |
18 | HG00438.hp1 HG01074.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12+1998A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30928794 | |||||||
chr12:30928901 | G | A | 1 | a0001c0001t0002g0126 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-12+2105G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30928901 | |||||||
chr12:30928981 | G | C | 1 | a0001c0001t0034g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-12+2185G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30928981 | |||||||
chr12:30929098 | C | G | 1 | a0001c0001t0002g0360 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-12+2302C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30929098 | |||||||
chr12:30929156 | A | G | 4 | a0002c0005t0004g0001 a0002c0005t0004g0359 a0008c0015t0019g0001 others(1): Show |
5 | HG02145.hp2 HG02280.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+2360A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30929156 | |||||||
chr12:30929192 | C | T | 1 | a0002c0002t0003g0121 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-12+2396C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30929192 | |||||||
chr12:30929193 | G | A | 18 | a0001c0001t0002g0371 a0001c0001t0002g0372 a0001c0001t0002g0373 others(15): Show |
18 | HG00438.hp1 HG01074.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12+2397G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30929193 | |||||||
chr12:30929265 | C | T | 1 | a0002c0002t0007g0055 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-12+2469C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30929265 | |||||||
chr12:30929270 | T | G | 1 | a0001c0001t0010g0127 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-12+2474T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30929270 | |||||||
chr12:30929306 | A | G | 6 | a0001c0001t0002g0373 a0001c0001t0005g0374 a0001c0001t0005g0375 others(3): Show |
6 | HG01257.hp2 HG01258.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+2510A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30929306 | |||||||
chr12:30929339 | T | C | 61 | a0001c0001t0001g0146 a0001c0001t0001g0154 a0001c0001t0001g0165 others(58): Show |
62 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-12+2543T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30929339 | |||||||
chr12:30929390 | T | C | 61 | a0001c0001t0001g0146 a0001c0001t0001g0154 a0001c0001t0001g0165 others(58): Show |
62 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-12+2594T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30929390 | |||||||
chr12:30929420 | G | T | 1 | a0002c0002t0007g0358 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-12+2624G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30929420 | |||||||
chr12:30929436 | C | A | 1 | a0002c0002t0007g0128 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-12+2640C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30929436 | |||||||
chr12:30929646 | A | G | 1 | a0002c0002t0002g0184 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-12+2850A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30929646 | |||||||
chr12:30929667 | T | C | 1 | a0006c0010t0022g0185 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-12+2871T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30929667 | |||||||
chr12:30929819 | A | G | 1 | a0001c0001t0002g0357 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-12+3023A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30929819 | |||||||
chr12:30930022 | A | T | 1 | a0001c0001t0055g0356 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-12+3226A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930022 | |||||||
chr12:30930073 | A | G | 1 | a0001c0001t0004g0355 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-12+3277A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930073 | |||||||
chr12:30930098 | G | A | 55 | a0001c0001t0001g0146 a0001c0001t0001g0154 a0001c0001t0001g0165 others(52): Show |
56 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.-12+3302G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930098 | |||||||
chr12:30930143 | A | T | 1 | a0002c0002t0001g0054 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-12+3347A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930143 | |||||||
chr12:30930170 | C | G | 6 | a0001c0001t0001g0349 a0001c0001t0001g0351 a0001c0001t0001g0354 others(3): Show |
6 | HG02258.hp1 HG02717.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+3374C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930170 | |||||||
chr12:30930173 | C | T | 1 | a0001c0001t0022g0053 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-12+3377C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930173 | |||||||
chr12:30930391 | G | A | 3 | a0001c0001t0004g0186 a0001c0001t0016g0187 a0002c0002t0045g0188 |
3 | HG02886.hp2 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-12+3595G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930391 | |||||||
chr12:30930590 | C | A | 1 | a0011c0009t0001g0057 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-12+3794C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930590 | |||||||
chr12:30930698 | T | C | 2 | a0001c0001t0006g0189 a0001c0001t0006g0190 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-12+3902T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930698 | |||||||
chr12:30930711 | G | A | 69 | a0001c0001t0001g0059 a0001c0001t0001g0082 a0001c0001t0001g0088 others(66): Show |
70 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.-12+3915G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930711 | |||||||
chr12:30930760 | C | A | 4 | a0001c0001t0029g0192 a0001c0001t0029g0193 a0002c0002t0038g0194 others(1): Show |
4 | HG00738.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+3964C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930760 | |||||||
chr12:30930826 | TTTCTCCC others(21): Show |
T | 1 | a0001c0001t0003g0196 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-12+4031_-12+4058d others(30): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930826 | |||||||
chr12:30930848 | A | G | 61 | a0001c0001t0001g0146 a0001c0001t0001g0154 a0001c0001t0001g0165 others(58): Show |
62 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-12+4052A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930848 | |||||||
chr12:30930852 | G | A | 13 | a0001c0001t0004g0011 a0001c0001t0004g0013 a0001c0001t0020g0019 others(10): Show |
14 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12+4056G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930852 | |||||||
chr12:30930929 | C | T | 55 | a0001c0001t0001g0146 a0001c0001t0001g0154 a0001c0001t0001g0165 others(52): Show |
56 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.-12+4133C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930929 | |||||||
chr12:30931088 | A | G | 2 | a0001c0001t0002g0348 a0002c0002t0001g0120 |
2 | HG02735.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-12+4292A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931088 | |||||||
chr12:30931105 | C | G | 19 | a0001c0001t0001g0109 a0001c0001t0001g0112 a0001c0001t0001g0113 others(16): Show |
19 | HG02165.hp2 HG02602.hp2 HG02683.hp1 others(16): Show |
intron_variant | MODIFIER | c.-12+4309C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931105 | |||||||
chr12:30931109 | T | C | 73 | a0001c0001t0001g0146 a0001c0001t0001g0154 a0001c0001t0001g0165 others(70): Show |
74 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.-12+4313T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931109 | |||||||
chr12:30931121 | C | T | 1 | a0003c0003t0051g0347 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-12+4325C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931121 | |||||||
chr12:30931159 | A | G | 56 | a0001c0001t0001g0146 a0001c0001t0001g0154 a0001c0001t0001g0165 others(53): Show |
57 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.-12+4363A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931159 | |||||||
chr12:30931297 | G | C | 18 | a0001c0001t0002g0371 a0001c0001t0002g0372 a0001c0001t0002g0373 others(15): Show |
18 | HG00438.hp1 HG01074.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12+4501G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931297 | |||||||
chr12:30931311 | G | A | 18 | a0001c0001t0002g0371 a0001c0001t0002g0372 a0001c0001t0002g0373 others(15): Show |
18 | HG00438.hp1 HG01074.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12+4515G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931311 | |||||||
chr12:30931498 | T | TAA | 307 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(304): Show |
310 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.-12+4703_-12+4704i others(4): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30931498 | ||||||
chr12:30931517 | G | A | 56 | a0001c0001t0001g0146 a0001c0001t0001g0154 a0001c0001t0001g0165 others(53): Show |
57 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.-12+4721G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931517 | |||||||
chr12:30931605 | C | T | 1 | a0002c0002t0026g0281 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-12+4809C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931605 | |||||||
chr12:30931606 | G | A | 37 | a0001c0001t0001g0022 a0001c0001t0001g0197 a0001c0001t0001g0203 others(34): Show |
37 | HG00280.hp2 HG00609.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.-12+4810G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931606 | |||||||
chr12:30931614 | T | C | 1 | a0001c0001t0002g0360 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-12+4818T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931614 | |||||||
chr12:30931739 | G | A | 6 | a0001c0001t0001g0059 a0001c0001t0003g0058 a0001c0001t0003g0061 others(3): Show |
6 | HG00609.hp2 HG02040.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+4943G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931739 | |||||||
chr12:30931761 | T | A | 104 | a0001c0001t0001g0022 a0001c0001t0001g0197 a0001c0001t0001g0203 others(101): Show |
104 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.-12+4965T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931761 | |||||||
chr12:30931828 | C | T | 1 | a0001c0001t0006g0222 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-12+5032C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931828 | |||||||
chr12:30931879 | C | CAAAA | 45 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0379 others(42): Show |
46 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.-12+5100_-12+5103d others(6): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30931879 | ||||||
chr12:30931879 | C | CAAAAA | 13 | a0001c0001t0002g0028 a0001c0001t0002g0360 a0001c0001t0004g0011 others(10): Show |
13 | HG01192.hp1 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-12+5099_-12+5103d others(7): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30931879 | ||||||
chr12:30931879 | C | CAAAAAAA others(1): Show |
45 | a0001c0001t0001g0257 a0001c0001t0001g0262 a0001c0001t0001g0267 others(42): Show |
45 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.-12+5096_-12+5103d others(10): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30931879 | ||||||
chr12:30931879 | C | CAAAAAAA others(2): Show |
152 | a0001c0001t0001g0022 a0001c0001t0001g0082 a0001c0001t0001g0088 others(149): Show |
154 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.-12+5095_-12+5103d others(11): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30931879 | ||||||
chr12:30931879 | C | CAAAAAAA others(3): Show |
31 | a0001c0001t0001g0059 a0001c0001t0001g0197 a0001c0001t0002g0223 others(28): Show |
31 | HG00423.hp2 HG01891.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.-12+5094_-12+5103d others(12): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30931879 | ||||||
chr12:30931879 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0008g0129 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-12+5093_-12+5103d others(13): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30931879 | ||||||
chr12:30931879 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0354 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-12+5092_-12+5103d others(14): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30931879 | ||||||
chr12:30931879 | C | CAAAAAAA others(6): Show |
3 | a0001c0001t0001g0351 a0001c0001t0016g0353 a0002c0002t0018g0352 |
3 | HG02258.hp1 HG02717.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-12+5091_-12+5103d others(15): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30931879 | ||||||
chr12:30931879 | C | CAAAAAAA others(7): Show |
2 | a0001c0001t0001g0349 a0001c0001t0018g0350 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-12+5090_-12+5103d others(16): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30931879 | ||||||
chr12:30931879 | CAAA | C | 6 | a0001c0001t0029g0192 a0001c0001t0029g0193 a0001c0001t0055g0356 others(3): Show |
6 | HG00738.hp1 HG02559.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+5101_-12+5103d others(5): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30931879 | ||||||
chr12:30931999 | G | A | 1 | a0001c0001t0002g0282 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-12+5203G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931999 | |||||||
chr12:30932237 | T | C | 69 | a0001c0001t0001g0059 a0001c0001t0001g0082 a0001c0001t0001g0088 others(66): Show |
69 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.-12+5441T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30932237 | |||||||
chr12:30932375 | C | T | 1 | a0001c0001t0069g0119 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-12+5579C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30932375 | |||||||
chr12:30932407 | G | A | 66 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0379 others(63): Show |
67 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.-12+5611G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30932407 | |||||||
chr12:30932465 | C | T | 72 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(69): Show |
74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.-12+5669C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30932465 | |||||||
chr12:30932471 | G | A | 160 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0082 others(157): Show |
162 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.-12+5675G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30932471 | |||||||
chr12:30932503 | A | G | 5 | a0001c0001t0022g0179 a0001c0001t0024g0180 a0001c0001t0028g0181 others(2): Show |
5 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+5707A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30932503 | |||||||
chr12:30932516 | C | T | 2 | a0001c0001t0023g0336 a0001c0001t0023g0337 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-12+5720C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30932516 | |||||||
chr12:30932561 | G | T | 9 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0016g0178 others(6): Show |
9 | HG02109.hp1 HG02809.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12+5765G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30932561 | |||||||
chr12:30932616 | G | A | 65 | a0001c0001t0001g0082 a0001c0001t0001g0088 a0001c0001t0001g0101 others(62): Show |
65 | HG00323.hp2 HG00544.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.-12+5820G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30932616 | |||||||
chr12:30932747 | A | G | 1 | a0001c0001t0006g0173 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-12+5951A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30932747 | |||||||
chr12:30933167 | C | T | 10 | a0001c0001t0004g0008 a0001c0001t0006g0189 a0001c0001t0006g0190 others(7): Show |
10 | HG02109.hp1 HG02809.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12+6371C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30933167 | |||||||
chr12:30933225 | A | G | 19 | a0001c0001t0001g0109 a0001c0001t0001g0112 a0001c0001t0001g0113 others(16): Show |
19 | HG02165.hp2 HG02602.hp2 HG02683.hp1 others(16): Show |
intron_variant | MODIFIER | c.-12+6429A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30933225 | |||||||
chr12:30933285 | C | G | 1 | a0001c0001t0036g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-12+6489C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30933285 | |||||||
chr12:30933300 | T | TGACATTA others(92): Show |
91 | a0001c0001t0001g0146 a0001c0001t0001g0154 a0001c0001t0001g0165 others(88): Show |
92 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.-12+6538_-12+6636d others(101): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30933300 | ||||||
chr12:30933519 | G | T | 1 | a0001c0001t0019g0386 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-12+6723G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30933519 | |||||||
chr12:30933546 | C | T | 38 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0002g0028 others(35): Show |
38 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.-12+6750C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30933546 | |||||||
chr12:30933620 | C | A | 1 | a0002c0002t0025g0139 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-12+6824C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30933620 | |||||||
chr12:30933673 | TTGCAGCT others(8): Show |
T | 1 | a0001c0001t0055g0356 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-12+6900_-12+6914d others(17): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30933673 | ||||||
chr12:30933732 | C | T | 1 | a0001c0001t0005g0378 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-12+6936C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30933732 | |||||||
chr12:30933876 | C | T | 1 | a0002c0002t0001g0041 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-12+7080C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30933876 | |||||||
chr12:30933949 | C | A | 1 | a0001c0001t0016g0362 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-12+7153C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30933949 | |||||||
chr12:30933957 | G | A | 258 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0082 others(255): Show |
260 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.-12+7161G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30933957 | |||||||
chr12:30934001 | C | A | 2 | a0001c0001t0002g0286 a0001c0001t0002g0287 |
2 | HG03491.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-12+7205C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30934001 | |||||||
chr12:30934085 | C | T | 1 | a0001c0001t0010g0335 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-12+7289C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30934085 | |||||||
chr12:30934165 | G | A | 1 | a0001c0001t0002g0360 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-12+7369G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30934165 | |||||||
chr12:30934172 | C | A | 8 | a0001c0001t0001g0203 a0001c0001t0001g0349 a0001c0001t0001g0351 others(5): Show |
8 | HG02258.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12+7376C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30934172 | |||||||
chr12:30934268 | T | C | 10 | a0001c0001t0004g0008 a0001c0001t0006g0189 a0001c0001t0006g0190 others(7): Show |
10 | HG02109.hp1 HG02809.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12+7472T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30934268 | |||||||
chr12:30934297 | T | A | 1 | a0001c0001t0036g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-12+7501T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30934297 | |||||||
chr12:30934402 | G | A | 52 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0146 others(49): Show |
53 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.-12+7606G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30934402 | |||||||
chr12:30934422 | T | A | 103 | a0001c0001t0001g0059 a0001c0001t0001g0154 a0001c0001t0001g0165 others(100): Show |
103 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.-12+7626T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30934422 | |||||||
chr12:30934632 | A | AT | 78 | a0001c0001t0001g0082 a0001c0001t0001g0088 a0001c0001t0001g0109 others(75): Show |
79 | HG00323.hp2 HG00544.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.-12+7851dupT | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30934632 | ||||||
chr12:30934632 | A | ATT | 6 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0005g0118 others(3): Show |
6 | NA18967.hp1 NA18991.hp1 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+7850_-12+7851d others(4): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30934632 | ||||||
chr12:30934632 | AT | A | 7 | a0001c0001t0002g0360 a0001c0001t0003g0042 a0001c0001t0004g0011 others(4): Show |
7 | HG00408.hp1 HG01884.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12+7851delT | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30934632 | ||||||
chr12:30934632 | ATTT | A | 10 | a0001c0001t0004g0008 a0001c0001t0006g0189 a0001c0001t0006g0190 others(7): Show |
10 | HG02109.hp1 HG02809.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12+7849_-12+7851d others(5): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30934632 | ||||||
chr12:30934653 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-12+7857T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30934653 | |||||||
chr12:30934669 | G | A | 3 | a0002c0002t0006g0250 a0002c0002t0007g0251 a0002c0002t0060g0252 |
3 | HG00673.hp2 NA18950.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-12+7873G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30934669 | |||||||
chr12:30934818 | T | C | 1 | a0002c0002t0002g0174 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-12+8022T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30934818 | |||||||
chr12:30934823 | A | G | 242 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0082 others(239): Show |
243 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.-12+8027A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30934823 | |||||||
chr12:30934954 | G | A | 1 | a0001c0001t0036g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-12+8158G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30934954 | |||||||
chr12:30935052 | C | G | 4 | a0002c0005t0004g0001 a0002c0005t0004g0359 a0008c0015t0019g0001 others(1): Show |
5 | HG02145.hp2 HG02280.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+8256C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30935052 | |||||||
chr12:30935138 | C | T | 9 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0016g0178 others(6): Show |
9 | HG02109.hp1 HG02809.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12+8342C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30935138 | |||||||
chr12:30935198 | G | T | 242 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0082 others(239): Show |
243 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.-12+8402G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30935198 | |||||||
chr12:30935356 | T | C | 2 | a0002c0002t0001g0068 a0002c0002t0001g0072 |
2 | NA18991.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.-12+8560T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30935356 | |||||||
chr12:30935373 | G | GT | 29 | a0001c0001t0001g0327 a0001c0001t0002g0282 a0001c0001t0002g0287 others(26): Show |
29 | HG00408.hp1 HG00621.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-12+8603dupT | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30935373 | ||||||
chr12:30935373 | GT | G | 249 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0059 others(246): Show |
251 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.-12+8603delT | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30935373 | ||||||
chr12:30935381 | T | G | 24 | a0001c0001t0001g0022 a0001c0001t0001g0169 a0001c0001t0002g0123 others(21): Show |
24 | HG00438.hp1 HG00733.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.-12+8585T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30935381 | |||||||
chr12:30935382 | T | G | 215 | a0001c0001t0001g0059 a0001c0001t0001g0082 a0001c0001t0001g0088 others(212): Show |
216 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.-12+8586T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30935382 | |||||||
chr12:30935383 | T | G | 1 | a0002c0002t0002g0030 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-12+8587T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30935383 | |||||||
chr12:30935422 | C | A | 1 | a0001c0001t0004g0355 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-12+8626C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30935422 | |||||||
chr12:30935558 | A | G | 1 | a0001c0001t0014g0366 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-12+8762A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30935558 | |||||||
chr12:30935661 | C | T | 2 | a0001c0001t0008g0129 a0002c0002t0006g0132 |
2 | NA18964.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-12+8865C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30935661 | |||||||
chr12:30935717 | T | C | 1 | a0001c0001t0001g0022 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-12+8921T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30935717 | |||||||
chr12:30935920 | G | T | 44 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0146 others(41): Show |
45 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.-12+9124G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30935920 | |||||||
chr12:30936160 | C | T | 7 | a0001c0001t0029g0192 a0001c0001t0029g0193 a0001c0001t0055g0356 others(4): Show |
7 | HG00738.hp1 HG01167.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12+9364C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30936160 | |||||||
chr12:30936184 | G | GCTTAATT others(14): Show |
12 | a0001c0001t0004g0011 a0001c0001t0004g0013 a0001c0001t0029g0192 others(9): Show |
12 | HG00738.hp1 HG01167.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.-12+9389_-12+9409d others(23): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30936184 | ||||||
chr12:30936405 | G | A | 313 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(310): Show |
316 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(313): Show |
intron_variant | MODIFIER | c.-12+9609G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30936405 | |||||||
chr12:30936603 | T | A | 1 | a0001c0001t0002g0345 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-12+9807T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30936603 | |||||||
chr12:30936612 | G | A | 3 | a0001c0001t0004g0186 a0001c0001t0016g0187 a0002c0002t0045g0188 |
3 | HG02886.hp2 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-12+9816G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30936612 | |||||||
chr12:30936648 | C | T | 1 | a0001c0001t0016g0178 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12+9852C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30936648 | |||||||
chr12:30936668 | C | T | 250 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0082 others(247): Show |
251 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.-12+9872C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30936668 | |||||||
chr12:30936738 | G | A | 249 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0082 others(246): Show |
250 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.-12+9942G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30936738 | |||||||
chr12:30936824 | G | C | 3 | a0002c0002t0001g0064 a0002c0002t0001g0073 a0002c0002t0001g0074 |
3 | HG02056.hp1 NA18747.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-12+10028G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30936824 | |||||||
chr12:30936830 | G | T | 1 | a0002c0002t0065g0167 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-12+10034G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30936830 | |||||||
chr12:30936843 | G | A | 1 | a0001c0001t0003g0196 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-12+10047G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30936843 | |||||||
chr12:30936859 | C | A | 1 | a0001c0001t0055g0356 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-12+10063C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30936859 | |||||||
chr12:30936942 | C | T | 1 | a0001c0001t0002g0360 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-12+10146C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30936942 | |||||||
chr12:30936945 | T | A | 1 | a0001c0001t0010g0319 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-12+10149T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30936945 | |||||||
chr12:30937017 | G | A | 1 | a0001c0001t0016g0362 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-12+10221G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30937017 | |||||||
chr12:30937117 | A | G | 150 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0154 others(147): Show |
150 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-12+10321A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30937117 | |||||||
chr12:30937171 | T | A | 242 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0082 others(239): Show |
243 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.-12+10375T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30937171 | |||||||
chr12:30937182 | G | T | 1 | a0002c0002t0013g0280 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-12+10386G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30937182 | |||||||
chr12:30937348 | C | G | 1 | a0001c0001t0032g0268 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-12+10552C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30937348 | |||||||
chr12:30937361 | C | T | 21 | a0001c0001t0001g0109 a0001c0001t0001g0112 a0001c0001t0001g0113 others(18): Show |
21 | HG02015.hp2 HG02165.hp2 HG02602.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12+10565C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30937361 | |||||||
chr12:30937383 | C | A | 1 | a0002c0002t0013g0015 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-12+10587C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30937383 | |||||||
chr12:30937432 | G | T | 1 | a0001c0001t0002g0028 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-12+10636G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30937432 | |||||||
chr12:30937434 | G | T | 1 | a0001c0001t0002g0220 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-12+10638G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30937434 | |||||||
chr12:30937669 | G | A | 1 | a0002c0002t0014g0279 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-12+10873G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30937669 | |||||||
chr12:30937683 | C | A | 41 | a0001c0001t0001g0022 a0001c0001t0001g0197 a0001c0001t0002g0210 others(38): Show |
41 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.-12+10887C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30937683 | |||||||
chr12:30937756 | T | C | 71 | a0001c0001t0001g0082 a0001c0001t0001g0088 a0001c0001t0001g0101 others(68): Show |
72 | HG00323.hp2 HG00544.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.-12+10960T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30937756 | |||||||
chr12:30937821 | T | C | 50 | a0001c0001t0001g0082 a0001c0001t0001g0088 a0001c0001t0001g0101 others(47): Show |
51 | HG00323.hp2 HG00544.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.-12+11025T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30937821 | |||||||
chr12:30938036 | A | G | 3 | a0001c0001t0002g0274 a0001c0001t0002g0275 a0001c0001t0002g0276 |
3 | HG00639.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-12+11240A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30938036 | |||||||
chr12:30938098 | T | C | 44 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0146 others(41): Show |
45 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.-12+11302T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30938098 | |||||||
chr12:30938214 | A | T | 1 | a0003c0003t0006g0166 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-12+11418A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30938214 | |||||||
chr12:30938334 | C | A | 242 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0082 others(239): Show |
243 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.-12+11538C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30938334 | |||||||
chr12:30938353 | C | T | 7 | a0001c0001t0029g0192 a0001c0001t0029g0193 a0001c0001t0055g0356 others(4): Show |
7 | HG00738.hp1 HG01167.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12+11557C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30938353 | |||||||
chr12:30938727 | C | T | 1 | a0001c0001t0036g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-12+11931C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30938727 | |||||||
chr12:30938748 | G | C | 9 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0016g0178 others(6): Show |
9 | HG02109.hp1 HG02809.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12+11952G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30938748 | |||||||
chr12:30938991 | G | T | 1 | a0001c0001t0001g0165 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-12+12195G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30938991 | |||||||
chr12:30938994 | A | G | 242 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0082 others(239): Show |
243 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.-12+12198A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30938994 | |||||||
chr12:30939182 | A | G | 3 | a0001c0001t0003g0096 a0001c0001t0003g0100 a0002c0002t0007g0097 |
3 | NA18970.hp2 NA18971.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-12+12386A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939182 | |||||||
chr12:30939212 | G | T | 7 | a0001c0001t0029g0192 a0001c0001t0029g0193 a0001c0001t0055g0356 others(4): Show |
7 | HG00738.hp1 HG01167.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12+12416G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939212 | |||||||
chr12:30939238 | C | CA | 153 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0112 others(150): Show |
153 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.-12+12458dupA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30939238 | ||||||
chr12:30939238 | C | CAA | 82 | a0001c0001t0001g0082 a0001c0001t0001g0088 a0001c0001t0001g0101 others(79): Show |
83 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.-12+12457_-12+1245 others(6): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30939238 | ||||||
chr12:30939238 | C | CAAAAA | 11 | a0001c0001t0001g0203 a0001c0001t0001g0349 a0001c0001t0001g0351 others(8): Show |
11 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12+12454_-12+1245 others(9): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30939238 | ||||||
chr12:30939238 | C | CAAAAAA | 32 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0002g0028 others(29): Show |
33 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.-12+12453_-12+1245 others(10): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30939238 | ||||||
chr12:30939238 | C | CAAAAAAA | 10 | a0001c0001t0001g0146 a0001c0001t0012g0145 a0001c0001t0015g0363 others(7): Show |
10 | HG01192.hp1 HG02135.hp1 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12+12452_-12+1245 others(11): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30939238 | ||||||
chr12:30939378 | TG | T | 3 | a0001c0001t0001g0235 a0002c0002t0001g0236 a0002c0002t0012g0237 |
3 | NA18945.hp2 NA18998.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.-12+12585delG | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30939378 | ||||||
chr12:30939380 | G | C | 3 | a0001c0001t0001g0235 a0002c0002t0001g0236 a0002c0002t0012g0237 |
3 | NA18945.hp2 NA18998.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.-12+12584G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939380 | |||||||
chr12:30939440 | T | C | 53 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0146 others(50): Show |
54 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.-12+12644T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939440 | |||||||
chr12:30939476 | C | T | 10 | a0001c0001t0004g0008 a0001c0001t0006g0189 a0001c0001t0006g0190 others(7): Show |
10 | HG02109.hp1 HG02809.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12+12680C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939476 | |||||||
chr12:30939536 | T | C | 71 | a0001c0001t0001g0082 a0001c0001t0001g0088 a0001c0001t0001g0101 others(68): Show |
72 | HG00323.hp2 HG00544.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.-12+12740T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939536 | |||||||
chr12:30939546 | C | G | 1 | a0002c0002t0003g0093 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-12+12750C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939546 | |||||||
chr12:30939570 | T | G | 53 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0146 others(50): Show |
54 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.-12+12774T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939570 | |||||||
chr12:30939617 | A | G | 295 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(292): Show |
297 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.-12+12821A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939617 | |||||||
chr12:30939722 | G | A | 1 | a0002c0002t0073g0368 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-12+12926G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939722 | |||||||
chr12:30939762 | A | G | 1 | a0001c0001t0055g0356 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-12+12966A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939762 | |||||||
chr12:30939839 | A | C | 53 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0146 others(50): Show |
54 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.-12+13043A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939839 | |||||||
chr12:30939854 | C | T | 1 | a0002c0002t0004g0182 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-12+13058C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939854 | |||||||
chr12:30939859 | A | G | 1 | a0001c0001t0002g0360 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-12+13063A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939859 | |||||||
chr12:30939866 | T | G | 1 | a0001c0001t0036g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-12+13070T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939866 | |||||||
chr12:30939894 | G | T | 1 | a0002c0002t0004g0318 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-12+13098G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939894 | |||||||
chr12:30939963 | G | A | 143 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0154 others(140): Show |
143 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.-12+13167G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939963 | |||||||
chr12:30940032 | G | A | 144 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0154 others(141): Show |
144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.-12+13236G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940032 | |||||||
chr12:30940135 | G | A | 1 | a0001c0001t0037g0016 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-12+13339G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940135 | |||||||
chr12:30940160 | G | A | 15 | a0001c0001t0004g0008 a0001c0001t0006g0189 a0001c0001t0006g0190 others(12): Show |
15 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-12+13364G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940160 | |||||||
chr12:30940161 | C | A | 15 | a0001c0001t0004g0008 a0001c0001t0006g0189 a0001c0001t0006g0190 others(12): Show |
15 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-12+13365C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940161 | |||||||
chr12:30940298 | A | G | 295 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(292): Show |
297 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.-12+13502A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940298 | |||||||
chr12:30940314 | A | C | 1 | a0004c0006t0007g0137 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-12+13518A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940314 | |||||||
chr12:30940333 | A | G | 3 | a0001c0001t0005g0374 a0001c0001t0005g0375 a0002c0002t0004g0376 |
3 | HG01257.hp2 HG01258.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.-12+13537A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940333 | |||||||
chr12:30940337 | G | A | 1 | a0001c0001t0024g0017 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-12+13541G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940337 | |||||||
chr12:30940355 | A | G | 1 | a0002c0002t0018g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-12+13559A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940355 | |||||||
chr12:30940482 | GAGAAATA others(3): Show |
G | 1 | a0001c0001t0008g0092 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-11-13495_-11-1348 others(14): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30940482 | ||||||
chr12:30940511 | G | A | 1 | a0002c0004t0017g0152 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-11-13470G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940511 | |||||||
chr12:30940600 | G | T | 1 | a0001c0001t0002g0371 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-11-13381G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940600 | |||||||
chr12:30940702 | C | T | 7 | a0001c0001t0029g0192 a0001c0001t0029g0193 a0001c0001t0055g0356 others(4): Show |
7 | HG00738.hp1 HG01167.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-13279C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940702 | |||||||
chr12:30940739 | G | T | 1 | a0001c0001t0014g0384 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-11-13242G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940739 | |||||||
chr12:30940837 | C | T | 1 | a0001c0001t0036g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11-13144C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940837 | |||||||
chr12:30940958 | C | G | 1 | a0001c0001t0001g0165 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-11-13023C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940958 | |||||||
chr12:30941039 | G | A | 44 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0146 others(41): Show |
45 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.-11-12942G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30941039 | |||||||
chr12:30941283 | G | T | 1 | a0001c0001t0008g0091 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-11-12698G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30941283 | |||||||
chr12:30941356 | A | G | 1 | a0001c0001t0005g0278 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-11-12625A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30941356 | |||||||
chr12:30941428 | C | T | 144 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0154 others(141): Show |
144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.-11-12553C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30941428 | |||||||
chr12:30941519 | G | C | 6 | a0001c0001t0002g0210 a0001c0001t0002g0211 a0001c0001t0010g0209 others(3): Show |
6 | HG01243.hp1 HG01928.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11-12462G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30941519 | |||||||
chr12:30941626 | G | T | 20 | a0001c0001t0002g0210 a0001c0001t0002g0211 a0001c0001t0002g0220 others(17): Show |
20 | HG00280.hp2 HG00609.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.-11-12355G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30941626 | |||||||
chr12:30941751 | G | A | 44 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0146 others(41): Show |
45 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.-11-12230G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30941751 | |||||||
chr12:30941939 | C | T | 2 | a0001c0001t0006g0222 a0001c0001t0007g0200 |
2 | HG02083.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.-11-12042C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30941939 | |||||||
chr12:30942038 | G | A | 2 | a0001c0001t0001g0197 a0001c0001t0021g0212 |
2 | HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-11-11943G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30942038 | |||||||
chr12:30942102 | G | A | 294 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(291): Show |
296 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.-11-11879G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30942102 | |||||||
chr12:30942110 | C | T | 1 | a0002c0002t0004g0318 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-11-11871C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30942110 | |||||||
chr12:30942307 | A | G | 64 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0146 others(61): Show |
66 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.-11-11674A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30942307 | |||||||
chr12:30942572 | C | A | 1 | a0001c0001t0004g0355 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-11-11409C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30942572 | |||||||
chr12:30942689 | T | C | 1 | a0002c0002t0013g0015 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-11-11292T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30942689 | |||||||
chr12:30942727 | T | TA | 277 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(274): Show |
279 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.-11-11239dupA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30942727 | ||||||
chr12:30942727 | T | TAA | 23 | a0001c0001t0001g0203 a0001c0001t0001g0349 a0001c0001t0001g0351 others(20): Show |
24 | HG01167.hp2 HG01169.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.-11-11240_-11-1123 others(6): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30942727 | ||||||
chr12:30942832 | C | T | 1 | a0001c0001t0002g0211 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-11-11149C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30942832 | |||||||
chr12:30942847 | T | C | 64 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0146 others(61): Show |
66 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.-11-11134T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30942847 | |||||||
chr12:30942890 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-11-11091A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30942890 | |||||||
chr12:30942949 | G | A | 144 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0154 others(141): Show |
144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.-11-11032G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30942949 | |||||||
chr12:30942984 | T | C | 1 | a0001c0001t0036g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11-10997T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30942984 | |||||||
chr12:30943193 | C | T | 1 | a0002c0002t0001g0054 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-11-10788C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30943193 | |||||||
chr12:30943217 | G | A | 307 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(304): Show |
310 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.-11-10764G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30943217 | |||||||
chr12:30943369 | C | A | 1 | a0001c0001t0006g0189 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-11-10612C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30943369 | |||||||
chr12:30943518 | C | T | 2 | a0001c0007t0013g0243 a0001c0007t0013g0249 |
2 | HG02615.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-11-10463C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30943518 | |||||||
chr12:30943584 | T | C | 1 | a0001c0001t0003g0266 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-11-10397T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30943584 | |||||||
chr12:30943585 | G | T | 1 | a0001c0001t0003g0266 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-11-10396G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30943585 | |||||||
chr12:30943586 | C | G | 1 | a0001c0001t0003g0266 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-11-10395C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30943586 | |||||||
chr12:30943795 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-11-10186G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30943795 | |||||||
chr12:30943835 | C | T | 20 | a0001c0001t0001g0203 a0001c0001t0001g0349 a0001c0001t0001g0351 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.-11-10146C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30943835 | |||||||
chr12:30943883 | T | C | 1 | a0002c0002t0001g0293 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-11-10098T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30943883 | |||||||
chr12:30944044 | G | C | 3 | a0001c0001t0001g0235 a0002c0002t0001g0236 a0002c0002t0012g0237 |
3 | NA18945.hp2 NA18998.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.-11-9937G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30944044 | |||||||
chr12:30944131 | C | T | 12 | a0001c0001t0019g0385 a0001c0001t0019g0386 a0001c0001t0020g0019 others(9): Show |
13 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11-9850C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30944131 | |||||||
chr12:30944195 | C | G | 1 | a0001c0001t0036g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11-9786C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30944195 | |||||||
chr12:30944219 | T | C | 2 | a0001c0001t0029g0192 a0001c0001t0029g0193 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-11-9762T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30944219 | |||||||
chr12:30944451 | A | G | 49 | a0001c0001t0001g0082 a0001c0001t0001g0088 a0001c0001t0002g0079 others(46): Show |
50 | HG00323.hp2 HG00544.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.-11-9530A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30944451 | |||||||
chr12:30944572 | C | T | 3 | a0001c0001t0003g0096 a0001c0001t0003g0100 a0002c0002t0007g0097 |
3 | NA18970.hp2 NA18971.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-11-9409C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30944572 | |||||||
chr12:30944577 | AT | A | 63 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0146 others(60): Show |
65 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.-11-9403delT | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30944577 | |||||||
chr12:30944621 | A | C | 6 | a0001c0001t0014g0366 a0001c0001t0015g0363 a0001c0001t0015g0364 others(3): Show |
6 | HG01192.hp1 HG02615.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11-9360A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30944621 | |||||||
chr12:30944901 | T | C | 3 | a0001c0001t0004g0186 a0001c0001t0016g0187 a0002c0002t0045g0188 |
3 | HG02886.hp2 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-11-9080T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30944901 | |||||||
chr12:30944904 | G | A | 1 | a0006c0010t0022g0185 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-11-9077G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30944904 | |||||||
chr12:30944937 | A | T | 1 | a0002c0002t0004g0318 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-11-9044A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30944937 | |||||||
chr12:30945069 | G | C | 22 | a0001c0001t0001g0103 a0001c0001t0001g0109 a0001c0001t0001g0112 others(19): Show |
22 | HG02015.hp2 HG02165.hp2 HG02602.hp2 others(19): Show |
intron_variant | MODIFIER | c.-11-8912G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30945069 | |||||||
chr12:30945087 | C | A | 63 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0146 others(60): Show |
65 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.-11-8894C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30945087 | |||||||
chr12:30945306 | A | G | 63 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0146 others(60): Show |
65 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.-11-8675A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30945306 | |||||||
chr12:30945447 | A | G | 1 | a0002c0002t0002g0030 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-11-8534A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30945447 | |||||||
chr12:30945534 | C | T | 1 | a0001c0001t0011g0221 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-11-8447C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30945534 | |||||||
chr12:30945650 | C | T | 63 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0146 others(60): Show |
65 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.-11-8331C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30945650 | |||||||
chr12:30945698 | G | A | 1 | a0011c0009t0001g0057 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-11-8283G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30945698 | |||||||
chr12:30945813 | TGTC | T | 3 | a0001c0001t0008g0069 a0002c0002t0001g0070 a0002c0002t0001g0071 |
3 | NA18954.hp1 NA18977.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-11-8165_-11-8163d others(5): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30945813 | ||||||
chr12:30945834 | T | C | 63 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0146 others(60): Show |
65 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.-11-8147T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30945834 | |||||||
chr12:30945869 | C | A | 1 | a0001c0001t0040g0255 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-11-8112C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30945869 | |||||||
chr12:30945948 | T | C | 1 | a0002c0002t0003g0121 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-11-8033T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30945948 | |||||||
chr12:30946028 | G | A | 16 | a0001c0001t0002g0360 a0001c0001t0004g0008 a0001c0001t0006g0189 others(13): Show |
16 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-11-7953G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30946028 | |||||||
chr12:30946121 | T | C | 1 | a0002c0002t0018g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-11-7860T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30946121 | |||||||
chr12:30946169 | C | T | 7 | a0001c0001t0016g0331 a0001c0001t0028g0316 a0001c0001t0043g0317 others(4): Show |
7 | HG02572.hp2 HG02818.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-7812C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30946169 | |||||||
chr12:30946262 | A | G | 7 | a0001c0001t0029g0192 a0001c0001t0029g0193 a0001c0001t0055g0356 others(4): Show |
7 | HG00738.hp1 HG01167.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-7719A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30946262 | |||||||
chr12:30946406 | G | A | 64 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0146 others(61): Show |
66 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.-11-7575G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30946406 | |||||||
chr12:30946529 | A | G | 7 | a0001c0001t0016g0331 a0001c0001t0028g0316 a0001c0001t0043g0317 others(4): Show |
7 | HG02572.hp2 HG02818.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-7452A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30946529 | |||||||
chr12:30946602 | A | G | 71 | a0001c0001t0001g0082 a0001c0001t0001g0088 a0001c0001t0001g0103 others(68): Show |
72 | HG00323.hp2 HG00544.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.-11-7379A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30946602 | |||||||
chr12:30946607 | G | A | 1 | a0002c0002t0005g0322 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-11-7374G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30946607 | |||||||
chr12:30946833 | G | A | 43 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0146 others(40): Show |
44 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.-11-7148G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30946833 | |||||||
chr12:30946853 | C | T | 1 | a0001c0001t0002g0330 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-11-7128C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30946853 | |||||||
chr12:30947107 | C | T | 3 | a0001c0001t0014g0384 a0001c0001t0075g0383 a0002c0002t0015g0382 |
3 | HG03453.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-11-6874C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30947107 | |||||||
chr12:30947261 | G | T | 7 | a0001c0001t0001g0203 a0001c0001t0001g0349 a0001c0001t0001g0351 others(4): Show |
7 | HG02258.hp1 HG02717.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-6720G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30947261 | |||||||
chr12:30947541 | C | T | 1 | a0001c0001t0002g0163 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-11-6440C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30947541 | |||||||
chr12:30947572 | G | T | 1 | a0001c0001t0004g0355 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-11-6409G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30947572 | |||||||
chr12:30947603 | C | T | 1 | a0001c0001t0011g0087 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-11-6378C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30947603 | |||||||
chr12:30947695 | C | T | 58 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0146 others(55): Show |
60 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.-11-6286C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30947695 | |||||||
chr12:30947730 | C | G | 60 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0146 others(57): Show |
62 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.-11-6251C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30947730 | |||||||
chr12:30947802 | C | T | 45 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0146 others(42): Show |
46 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.-11-6179C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30947802 | |||||||
chr12:30947899 | C | T | 5 | a0001c0001t0004g0011 a0001c0001t0004g0013 a0001c0001t0034g0010 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-6082C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30947899 | |||||||
chr12:30947962 | T | C | 9 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0016g0178 others(6): Show |
9 | HG02109.hp1 HG02809.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11-6019T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30947962 | |||||||
chr12:30948037 | A | C | 1 | a0001c0001t0001g0354 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-11-5944A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30948037 | |||||||
chr12:30948067 | C | T | 215 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(212): Show |
218 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.-11-5914C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30948067 | |||||||
chr12:30948073 | T | C | 58 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0146 others(55): Show |
60 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.-11-5908T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30948073 | |||||||
chr12:30948105 | C | T | 1 | a0002c0002t0045g0188 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-11-5876C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30948105 | |||||||
chr12:30948400 | A | G | 44 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0146 others(41): Show |
45 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.-11-5581A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30948400 | |||||||
chr12:30948406 | C | G | 1 | a0001c0001t0003g0196 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-11-5575C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30948406 | |||||||
chr12:30948411 | G | A | 1 | a0001c0001t0010g0335 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-11-5570G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30948411 | |||||||
chr12:30948558 | G | A | 50 | a0001c0001t0001g0059 a0001c0001t0001g0088 a0001c0001t0001g0235 others(47): Show |
50 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.-11-5423G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30948558 | |||||||
chr12:30949267 | T | A | 12 | a0001c0001t0001g0354 a0001c0001t0004g0355 a0001c0001t0014g0366 others(9): Show |
12 | HG01167.hp1 HG01192.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11-4714T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30949267 | |||||||
chr12:30949297 | C | G | 1 | a0002c0002t0005g0322 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-11-4684C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30949297 | |||||||
chr12:30949348 | T | A | 83 | a0001c0001t0001g0059 a0001c0001t0001g0154 a0001c0001t0001g0165 others(80): Show |
84 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.-11-4633T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30949348 | |||||||
chr12:30949348 | T | C | 207 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0082 others(204): Show |
212 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.-11-4633T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30949348 | |||||||
chr12:30949431 | G | A | 339 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0059 others(336): Show |
345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.-11-4550G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30949431 | |||||||
chr12:30949446 | T | C | 20 | a0001c0001t0003g0042 a0001c0001t0004g0186 a0001c0001t0007g0094 others(17): Show |
21 | HG00408.hp1 HG01943.hp1 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.-11-4535T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30949446 | |||||||
chr12:30949565 | A | G | 1 | a0002c0002t0007g0007 | 2 | NA18951.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.-11-4416A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30949565 | |||||||
chr12:30949581 | G | A | 10 | a0001c0001t0004g0011 a0001c0001t0004g0013 a0001c0001t0014g0366 others(7): Show |
10 | HG01192.hp1 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-11-4400G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30949581 | |||||||
chr12:30949748 | G | C | 31 | a0001c0001t0001g0288 a0001c0001t0002g0282 a0001c0001t0002g0286 others(28): Show |
33 | HG00140.hp2 HG00735.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.-11-4233G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30949748 | |||||||
chr12:30949763 | C | T | 1 | a0001c0001t0006g0285 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-11-4218C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30949763 | |||||||
chr12:30949816 | C | T | 1 | a0003c0003t0001g0114 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-11-4165C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30949816 | |||||||
chr12:30949841 | C | G | 69 | a0001c0001t0001g0045 a0001c0001t0001g0059 a0001c0001t0001g0088 others(66): Show |
69 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-11-4140C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30949841 | |||||||
chr12:30949965 | C | T | 7 | a0001c0001t0014g0384 a0001c0001t0043g0317 a0001c0001t0058g0332 others(4): Show |
7 | HG02572.hp2 HG02886.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-4016C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30949965 | |||||||
chr12:30950019 | C | T | 12 | a0001c0001t0002g0220 a0001c0001t0002g0360 a0001c0001t0006g0222 others(9): Show |
12 | HG00280.hp2 HG01069.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11-3962C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30950019 | |||||||
chr12:30950068 | G | C | 2 | a0001c0001t0001g0349 a0001c0001t0001g0351 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-11-3913G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30950068 | |||||||
chr12:30950276 | G | T | 1 | a0001c0001t0002g0345 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-11-3705G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30950276 | |||||||
chr12:30950426 | G | A | 6 | a0001c0001t0001g0101 a0001c0001t0003g0289 a0001c0001t0003g0320 others(3): Show |
6 | HG00544.hp2 NA18967.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11-3555G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30950426 | |||||||
chr12:30950840 | A | G | 6 | a0001c0001t0008g0065 a0001c0001t0008g0091 a0001c0001t0008g0095 others(3): Show |
6 | NA18981.hp1 NA18990.hp1 NA19057.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11-3141A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30950840 | |||||||
chr12:30950984 | T | G | 1 | a0001c0001t0001g0244 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-11-2997T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30950984 | |||||||
chr12:30951028 | G | A | 90 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0103 others(87): Show |
91 | HG00558.hp1 HG00609.hp1 HG00738.hp1 others(88): Show |
intron_variant | MODIFIER | c.-11-2953G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30951028 | |||||||
chr12:30951059 | A | G | 1 | a0001c0001t0010g0052 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-11-2922A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30951059 | |||||||
chr12:30951088 | C | T | 20 | a0001c0001t0001g0146 a0001c0001t0012g0034 a0002c0002t0001g0037 others(17): Show |
21 | HG00438.hp2 HG02080.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.-11-2893C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30951088 | |||||||
chr12:30951089 | G | A | 3 | a0001c0001t0055g0356 a0002c0002t0013g0280 a0002c0004t0014g0195 |
3 | HG00738.hp1 HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-11-2892G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30951089 | |||||||
chr12:30951553 | G | A | 1 | a0007c0013t0011g0338 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-11-2428G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30951553 | |||||||
chr12:30951679 | A | AC | 3 | a0001c0001t0003g0289 a0001c0001t0003g0320 a0001c0001t0006g0284 |
3 | NA18985.hp2 NA18993.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.-11-2301dupC | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30951679 | ||||||
chr12:30951988 | T | C | 184 | a0001c0001t0001g0045 a0001c0001t0001g0059 a0001c0001t0001g0088 others(181): Show |
185 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.-11-1993T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30951988 | |||||||
chr12:30952037 | A | G | 1 | a0002c0002t0065g0167 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-11-1944A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30952037 | |||||||
chr12:30952056 | C | G | 1 | a0002c0002t0005g0322 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-11-1925C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30952056 | |||||||
chr12:30952060 | G | A | 1 | a0001c0001t0009g0369 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-11-1921G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30952060 | |||||||
chr12:30952109 | C | G | 11 | a0001c0001t0002g0220 a0001c0001t0006g0222 a0001c0001t0007g0200 others(8): Show |
11 | HG00280.hp2 HG01069.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11-1872C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30952109 | |||||||
chr12:30952149 | T | C | 258 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0059 others(255): Show |
260 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.-11-1832T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30952149 | |||||||
chr12:30952315 | C | A | 6 | a0001c0001t0008g0065 a0001c0001t0008g0091 a0001c0001t0008g0095 others(3): Show |
6 | NA18981.hp1 NA18990.hp1 NA19057.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11-1666C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30952315 | |||||||
chr12:30952327 | C | T | 1 | a0007c0013t0011g0338 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-11-1654C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30952327 | |||||||
chr12:30952336 | G | A | 51 | a0001c0001t0001g0113 a0001c0001t0001g0230 a0001c0001t0001g0257 others(48): Show |
52 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.-11-1645G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30952336 | |||||||
chr12:30952369 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-11-1612C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30952369 | |||||||
chr12:30952471 | C | T | 1 | a0002c0002t0065g0167 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-11-1510C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30952471 | |||||||
chr12:30952506 | C | T | 256 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0059 others(253): Show |
259 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.-11-1475C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30952506 | |||||||
chr12:30952634 | G | A | 2 | a0001c0001t0032g0268 a0002c0002t0071g0153 |
2 | HG00408.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.-11-1347G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30952634 | |||||||
chr12:30952641 | C | A | 339 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0059 others(336): Show |
344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.-11-1340C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30952641 | |||||||
chr12:30952986 | C | T | 1 | a0002c0004t0004g0283 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-11-995C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30952986 | |||||||
chr12:30953100 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-11-881G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30953100 | |||||||
chr12:30953241 | A | G | 1 | a0002c0002t0018g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-11-740A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30953241 | |||||||
chr12:30953362 | T | C | 1 | a0001c0001t0002g0126 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-11-619T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30953362 | |||||||
chr12:30953365 | C | G | 2 | a0002c0002t0021g0036 a0002c0002t0044g0039 |
2 | HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-11-616C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30953365 | |||||||
chr12:30953376 | G | A | 1 | a0001c0001t0009g0204 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-11-605G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30953376 | |||||||
chr12:30953595 | T | C | 3 | a0001c0001t0016g0178 a0001c0001t0016g0331 a0002c0002t0002g0315 |
3 | HG02965.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-11-386T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30953595 | |||||||
chr12:30953666 | T | C | 1 | a0001c0001t0009g0346 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-11-315T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30953666 | |||||||
chr12:30953707 | C | T | 4 | a0001c0001t0055g0356 a0002c0002t0013g0280 a0002c0002t0015g0382 others(1): Show |
4 | HG00738.hp1 HG02559.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11-274C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30953707 | |||||||
chr12:30953716 | T | C | 78 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0103 others(75): Show |
79 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.-11-265T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30953716 | |||||||
chr12:30953852 | A | G | 77 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0103 others(74): Show |
78 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.-11-129A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30953852 | |||||||
chr12:30953869 | C | A | 77 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0103 others(74): Show |
78 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.-11-112C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30953869 | |||||||
chr12:30953913 | T | G | 1 | a0002c0002t0006g0254 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-11-68T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30953913 | |||||||
chr12:30953922 | G | A | 22 | a0003c0003t0001g0114 a0003c0003t0003g0080 a0003c0003t0005g0056 others(19): Show |
22 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.-11-59G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30953922 | |||||||
chr12:30954197 | A | G | 98 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0103 others(95): Show |
99 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.84+122A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30954197 | |||||||
chr12:30954238 | G | T | 1 | a0001c0001t0014g0366 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.84+163G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30954238 | |||||||
chr12:30954389 | T | G | 21 | a0003c0003t0001g0114 a0003c0003t0003g0080 a0003c0003t0005g0056 others(18): Show |
21 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.84+314T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30954389 | |||||||
chr12:30954638 | C | T | 10 | a0001c0001t0001g0203 a0001c0001t0001g0349 a0001c0001t0001g0351 others(7): Show |
10 | HG01167.hp1 HG02258.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.84+563C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30954638 | |||||||
chr12:30954725 | A | G | 3 | a0001c0001t0029g0192 a0001c0001t0029g0193 a0002c0002t0004g0295 |
3 | HG02622.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.84+650A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30954725 | |||||||
chr12:30954931 | C | A | 1 | a0001c0001t0002g0371 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.84+856C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30954931 | |||||||
chr12:30955021 | G | A | 313 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0059 others(310): Show |
318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.84+946G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30955021 | |||||||
chr12:30955410 | C | A | 4 | a0002c0005t0004g0001 a0002c0005t0004g0359 a0008c0015t0019g0001 others(1): Show |
5 | HG02145.hp2 HG02280.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+1335C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30955410 | |||||||
chr12:30955434 | G | A | 350 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0059 others(347): Show |
355 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.84+1359G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30955434 | |||||||
chr12:30955503 | G | A | 75 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0103 others(72): Show |
76 | HG00558.hp1 HG00609.hp1 HG01255.hp1 others(73): Show |
intron_variant | MODIFIER | c.84+1428G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30955503 | |||||||
chr12:30955853 | A | G | 2 | a0001c0007t0013g0243 a0001c0007t0013g0249 |
2 | HG02615.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.84+1778A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30955853 | |||||||
chr12:30955937 | C | T | 1 | a0001c0001t0025g0219 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.84+1862C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30955937 | |||||||
chr12:30956145 | A | C | 1 | a0002c0002t0001g0054 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.84+2070A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956145 | |||||||
chr12:30956263 | G | A | 8 | a0001c0001t0002g0360 a0001c0001t0029g0192 a0001c0001t0029g0193 others(5): Show |
8 | HG00738.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.84+2188G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956263 | |||||||
chr12:30956438 | T | G | 6 | a0001c0001t0004g0355 a0001c0007t0013g0243 a0001c0007t0013g0249 others(3): Show |
6 | HG02572.hp1 HG02615.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.84+2363T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956438 | |||||||
chr12:30956549 | CT | C | 26 | a0001c0001t0002g0220 a0001c0001t0006g0189 a0001c0001t0006g0190 others(23): Show |
26 | HG00280.hp2 HG01069.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.84+2475delT | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956549 | |||||||
chr12:30956591 | T | G | 2 | a0001c0001t0010g0031 a0001c0001t0010g0324 |
2 | HG02717.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.84+2516T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956591 | |||||||
chr12:30956666 | A | G | 36 | a0001c0001t0001g0203 a0001c0001t0001g0349 a0001c0001t0001g0351 others(33): Show |
36 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.84+2591A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956666 | |||||||
chr12:30956716 | TA | T | 172 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0103 others(169): Show |
175 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.84+2642delA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956716 | |||||||
chr12:30956720 | A | G | 172 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0103 others(169): Show |
175 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.84+2645A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956720 | |||||||
chr12:30956764 | G | A | 23 | a0001c0001t0002g0004 a0001c0001t0039g0004 a0003c0003t0001g0114 others(20): Show |
23 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.84+2689G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956764 | |||||||
chr12:30956827 | C | T | 26 | a0001c0001t0002g0163 a0001c0001t0002g0333 a0001c0001t0002g0360 others(23): Show |
26 | HG00438.hp1 HG00738.hp1 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.84+2752C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956827 | |||||||
chr12:30956928 | G | C | 23 | a0001c0001t0002g0004 a0001c0001t0039g0004 a0003c0003t0001g0114 others(20): Show |
23 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.84+2853G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956928 | |||||||
chr12:30956946 | G | T | 1 | a0002c0002t0001g0314 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.84+2871G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956946 | |||||||
chr12:30956947 | T | A | 1 | a0002c0002t0001g0314 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.84+2872T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956947 | |||||||
chr12:30956948 | A | T | 1 | a0002c0002t0001g0314 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.84+2873A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956948 | |||||||
chr12:30956962 | C | A | 4 | a0001c0001t0001g0203 a0001c0001t0016g0353 a0001c0001t0018g0350 others(1): Show |
4 | HG02717.hp2 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.84+2887C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956962 | |||||||
chr12:30957120 | A | G | 61 | a0001c0001t0001g0146 a0001c0001t0001g0288 a0001c0001t0002g0210 others(58): Show |
63 | HG00140.hp2 HG00438.hp2 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.84+3045A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957120 | |||||||
chr12:30957122 | A | G | 61 | a0001c0001t0001g0146 a0001c0001t0001g0288 a0001c0001t0002g0210 others(58): Show |
63 | HG00140.hp2 HG00438.hp2 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.84+3047A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957122 | |||||||
chr12:30957225 | G | A | 1 | a0001c0001t0022g0053 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.84+3150G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957225 | |||||||
chr12:30957228 | A | AC | 66 | a0001c0001t0001g0045 a0001c0001t0001g0059 a0001c0001t0001g0088 others(63): Show |
66 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.84+3167dupC | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957228 | ||||||
chr12:30957228 | A | ACC | 34 | a0001c0001t0001g0101 a0001c0001t0001g0113 a0001c0001t0001g0230 others(31): Show |
35 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.84+3166_84+3167dup others(2): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957228 | ||||||
chr12:30957228 | AC | A | 53 | a0001c0001t0001g0203 a0001c0001t0001g0327 a0001c0001t0001g0351 others(50): Show |
54 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.84+3167delC | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957228 | ||||||
chr12:30957228 | ACC | A | 58 | a0001c0001t0001g0103 a0001c0001t0001g0197 a0001c0001t0001g0240 others(55): Show |
58 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.84+3166_84+3167del others(2): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957228 | ||||||
chr12:30957228 | ACCC | A | 52 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0146 others(49): Show |
53 | HG00558.hp1 HG00738.hp2 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.84+3165_84+3167del others(3): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957228 | ||||||
chr12:30957228 | ACCCC | A | 54 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0169 others(51): Show |
56 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.84+3164_84+3167del others(4): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957228 | ||||||
chr12:30957240 | C | G | 1 | a0001c0001t0002g0348 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.84+3165C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957240 | |||||||
chr12:30957241 | C | A | 1 | a0001c0001t0062g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.84+3166C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957241 | |||||||
chr12:30957335 | G | A | 3 | a0001c0001t0001g0197 a0001c0001t0004g0186 a0001c0001t0021g0212 |
3 | HG02258.hp2 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.84+3260G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957335 | |||||||
chr12:30957369 | A | T | 1 | a0001c0001t0006g0261 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.84+3294A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957369 | |||||||
chr12:30957407 | T | C | 1 | a0002c0002t0001g0054 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.84+3332T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957407 | |||||||
chr12:30957446 | G | A | 14 | a0001c0001t0001g0146 a0001c0001t0040g0255 a0002c0002t0001g0142 others(11): Show |
15 | HG00438.hp2 HG02080.hp2 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.84+3371G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957446 | |||||||
chr12:30957479 | A | G | 1 | a0003c0003t0035g0321 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.84+3404A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957479 | |||||||
chr12:30957514 | T | C | 2 | a0001c0001t0001g0288 a0001c0001t0002g0296 |
2 | HG03540.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.84+3439T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957514 | |||||||
chr12:30957525 | G | A | 1 | a0001c0001t0002g0287 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.84+3450G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957525 | |||||||
chr12:30957541 | T | C | 21 | a0003c0003t0001g0114 a0003c0003t0003g0080 a0003c0003t0005g0056 others(18): Show |
21 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.84+3466T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957541 | |||||||
chr12:30957560 | A | G | 29 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0002g0163 others(26): Show |
29 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.84+3485A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957560 | |||||||
chr12:30957596 | C | T | 3 | a0001c0001t0029g0192 a0001c0001t0029g0193 a0002c0002t0004g0295 |
3 | HG02622.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.84+3521C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957596 | |||||||
chr12:30957629 | ATCCC | A | 11 | a0001c0001t0001g0197 a0001c0001t0004g0186 a0001c0001t0004g0214 others(8): Show |
11 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.84+3576_84+3579del others(4): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957629 | ||||||
chr12:30957629 | ATCCCTCC others(5): Show |
A | 31 | a0001c0001t0002g0360 a0001c0001t0006g0189 a0001c0001t0006g0190 others(28): Show |
31 | HG00738.hp1 HG01192.hp1 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.84+3568_84+3579del others(12): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957629 | ||||||
chr12:30957638 | T | C | 1 | a0002c0002t0001g0314 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.84+3563T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957638 | |||||||
chr12:30957703 | CCCT | C | 53 | a0001c0001t0002g0360 a0001c0001t0006g0189 a0001c0001t0006g0190 others(50): Show |
53 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.84+3632_84+3634del others(3): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957703 | ||||||
chr12:30957705 | CTCCT | C | 11 | a0001c0001t0004g0008 a0001c0001t0006g0284 a0001c0001t0019g0385 others(8): Show |
12 | HG01167.hp2 HG01169.hp2 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.84+3650_84+3653del others(4): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957705 | ||||||
chr12:30957707 | C | T | 3 | a0001c0001t0001g0288 a0001c0001t0002g0296 a0001c0001t0034g0228 |
3 | HG02622.hp2 HG03540.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.84+3632C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957707 | |||||||
chr12:30957707 | CCTT | C | 132 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0103 others(129): Show |
135 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.84+3634_84+3636del others(3): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957707 | ||||||
chr12:30957710 | TCCTTCCT others(68): Show |
T | 3 | a0001c0001t0001g0288 a0001c0001t0002g0296 a0001c0001t0034g0228 |
3 | HG02622.hp2 HG03540.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.84+3636_84+3710del others(75): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957710 | |||||||
chr12:30957712 | C | T | 54 | a0001c0001t0002g0360 a0001c0001t0006g0189 a0001c0001t0006g0190 others(51): Show |
54 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.84+3637C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957712 | |||||||
chr12:30957713 | TTCCTTCC others(81): Show |
T | 1 | a0002c0004t0001g0247 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.84+3726_84+3813del others(88): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957713 | ||||||
chr12:30957716 | C | T | 132 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0103 others(129): Show |
135 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.84+3641C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957716 | |||||||
chr12:30957721 | TTCCTTCC others(61): Show |
T | 132 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0103 others(129): Show |
135 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.84+3654_84+3721del others(68): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957721 | ||||||
chr12:30957725 | TTCCCTCC others(53): Show |
T | 3 | a0001c0001t0029g0192 a0001c0001t0029g0193 a0001c0001t0037g0016 |
3 | HG02895.hp2 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.84+3662_84+3721del others(60): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957725 | ||||||
chr12:30957729 | CTCCTTCC others(17): Show |
C | 4 | a0001c0001t0002g0360 a0002c0002t0013g0280 a0002c0002t0015g0382 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.84+3662_84+3685del others(24): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957729 | ||||||
chr12:30957729 | CTCCTTCC others(57): Show |
C | 27 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0022g0053 others(24): Show |
27 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.84+3666_84+3729del others(64): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957729 | ||||||
chr12:30957733 | TTCCCTCC others(49): Show |
T | 3 | a0001c0001t0055g0356 a0002c0002t0004g0295 a0002c0004t0052g0021 |
3 | HG02622.hp1 HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.84+3662_84+3717del others(56): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957733 | ||||||
chr12:30957741 | C | T | 1 | a0001c0001t0005g0377 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.84+3666C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957741 | |||||||
chr12:30957745 | CTCCCTCC others(69): Show |
C | 1 | a0001c0001t0005g0377 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.84+3678_84+3753del others(76): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957745 | ||||||
chr12:30957759 | C | T | 1 | a0001c0001t0020g0026 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.84+3684C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957759 | |||||||
chr12:30957761 | TTCCTTCC others(69): Show |
T | 1 | a0001c0001t0014g0366 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.84+3702_84+3777del others(76): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957761 | ||||||
chr12:30957765 | TTCCTTCC others(65): Show |
T | 5 | a0001c0001t0015g0363 a0001c0001t0015g0364 a0001c0001t0015g0365 others(2): Show |
5 | HG01192.hp1 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+3702_84+3773del others(72): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957765 | ||||||
chr12:30957769 | T | C | 4 | a0001c0001t0002g0360 a0002c0002t0013g0280 a0002c0002t0015g0382 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.84+3694T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957769 | |||||||
chr12:30957769 | TTCCTTCC others(61): Show |
T | 8 | a0001c0001t0014g0384 a0001c0001t0016g0178 a0001c0001t0016g0331 others(5): Show |
8 | HG02809.hp2 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.84+3702_84+3769del others(68): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957769 | ||||||
chr12:30957773 | TTCCCTCC others(49): Show |
T | 1 | a0002c0002t0002g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.84+3710_84+3765del others(56): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957773 | ||||||
chr12:30957773 | TTCCCTCC others(57): Show |
T | 2 | a0002c0002t0002g0184 a0002c0004t0014g0195 |
2 | HG00738.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.84+3702_84+3765del others(64): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957773 | ||||||
chr12:30957777 | CTCCCTCC others(77): Show |
C | 13 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0002g0220 others(10): Show |
13 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.84+3718_84+3801del others(84): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957777 | ||||||
chr12:30957789 | C | T | 3 | a0001c0001t0001g0288 a0001c0001t0002g0296 a0001c0001t0034g0228 |
3 | HG02622.hp2 HG03540.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.84+3714C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957789 | |||||||
chr12:30957793 | T | C | 1 | a0001c0001t0002g0360 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.84+3718T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957793 | |||||||
chr12:30957793 | TTCCTTCC others(77): Show |
T | 13 | a0001c0001t0002g0163 a0001c0001t0002g0333 a0001c0001t0002g0371 others(10): Show |
13 | HG00438.hp1 HG01257.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.84+3726_84+3809del others(84): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957793 | ||||||
chr12:30957801 | C | T | 34 | a0001c0001t0002g0360 a0001c0001t0006g0189 a0001c0001t0006g0190 others(31): Show |
34 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.84+3726C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957801 | |||||||
chr12:30957805 | T | C | 3 | a0001c0001t0029g0192 a0001c0001t0029g0193 a0001c0001t0037g0016 |
3 | HG02895.hp2 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.84+3730T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957805 | |||||||
chr12:30957809 | T | C | 30 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0022g0053 others(27): Show |
30 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.84+3734T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957809 | |||||||
chr12:30957809 | TTCCTTCC others(21): Show |
T | 1 | a0002c0002t0018g0040 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.84+3742_84+3769del others(28): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957809 | ||||||
chr12:30957813 | T | C | 6 | a0001c0001t0029g0192 a0001c0001t0029g0193 a0001c0001t0037g0016 others(3): Show |
6 | HG02622.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.84+3738T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957813 | |||||||
chr12:30957813 | TTCCCTCC others(13): Show |
T | 1 | a0002c0002t0013g0280 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.84+3750_84+3769del others(20): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957813 | ||||||
chr12:30957813 | TTCCCTCC others(17): Show |
T | 2 | a0001c0001t0002g0360 a0002c0002t0015g0382 |
2 | HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.84+3742_84+3765del others(24): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957813 | ||||||
chr12:30957821 | T | C | 33 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0022g0053 others(30): Show |
33 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.84+3746T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957821 | |||||||
chr12:30957825 | C | T | 2 | a0001c0001t0055g0356 a0002c0004t0052g0021 |
2 | HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.84+3750C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957825 | |||||||
chr12:30957829 | C | T | 6 | a0001c0001t0029g0192 a0001c0001t0029g0193 a0001c0001t0037g0016 others(3): Show |
6 | HG02622.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.84+3754C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957829 | |||||||
chr12:30957833 | C | T | 34 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0022g0053 others(31): Show |
34 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.84+3758C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957833 | |||||||
chr12:30957837 | C | T | 37 | a0001c0001t0001g0262 a0001c0001t0005g0377 a0001c0001t0006g0189 others(34): Show |
37 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.84+3762C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957837 | |||||||
chr12:30957837 | CTCCT | C | 57 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0103 others(54): Show |
58 | HG00558.hp1 HG00609.hp1 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.84+3786_84+3789del others(4): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957837 | ||||||
chr12:30957857 | T | C | 1 | a0001c0001t0037g0016 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.84+3782T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957857 | |||||||
chr12:30957857 | TTCCTTCC others(1): Show |
T | 8 | a0001c0001t0003g0096 a0001c0001t0003g0100 a0001c0001t0003g0110 others(5): Show |
8 | HG04184.hp1 NA18956.hp1 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.84+3786_84+3793del others(8): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957857 | ||||||
chr12:30957861 | T | C | 75 | a0001c0001t0001g0197 a0001c0001t0001g0262 a0001c0001t0001g0354 others(72): Show |
75 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.84+3786T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957861 | |||||||
chr12:30957861 | T | TTCCC | 179 | a0001c0001t0001g0045 a0001c0001t0001g0059 a0001c0001t0001g0088 others(176): Show |
183 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.84+3802_84+3805dup others(4): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957861 | ||||||
chr12:30957861 | T | TTCCTTCC others(1): Show |
3 | a0002c0002t0021g0036 a0002c0002t0044g0039 a0002c0004t0017g0152 |
3 | HG01981.hp1 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.84+3789_84+3790ins others(8): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957861 | ||||||
chr12:30957877 | C | T | 16 | a0001c0001t0001g0197 a0001c0001t0001g0354 a0001c0001t0004g0186 others(13): Show |
16 | HG01167.hp1 HG01891.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.84+3802C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957877 | |||||||
chr12:30957881 | T | C | 8 | a0001c0001t0003g0096 a0001c0001t0003g0100 a0001c0001t0003g0110 others(5): Show |
8 | HG04184.hp1 NA18956.hp1 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.84+3806T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957881 | |||||||
chr12:30958007 | C | T | 15 | a0001c0001t0001g0197 a0001c0001t0001g0354 a0001c0001t0004g0186 others(12): Show |
15 | HG01167.hp1 HG01891.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.84+3932C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958007 | |||||||
chr12:30958028 | G | C | 1 | a0002c0002t0030g0308 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.84+3953G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958028 | |||||||
chr12:30958207 | G | A | 1 | a0001c0001t0037g0016 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.84+4132G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958207 | |||||||
chr12:30958366 | G | A | 20 | a0001c0001t0014g0366 a0001c0001t0014g0384 a0001c0001t0015g0363 others(17): Show |
20 | HG00738.hp1 HG01192.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.84+4291G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958366 | |||||||
chr12:30958410 | C | A | 4 | a0001c0001t0001g0354 a0001c0001t0034g0228 a0002c0002t0014g0124 others(1): Show |
4 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.84+4335C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958410 | |||||||
chr12:30958446 | C | T | 1 | a0001c0001t0002g0126 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.84+4371C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958446 | |||||||
chr12:30958454 | T | C | 82 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0002g0163 others(79): Show |
82 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.84+4379T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958454 | |||||||
chr12:30958492 | C | G | 1 | a0001c0001t0001g0022 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.84+4417C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958492 | |||||||
chr12:30958548 | G | A | 1 | a0002c0002t0001g0071 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.84+4473G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958548 | |||||||
chr12:30958658 | C | G | 2 | a0002c0002t0018g0040 a0002c0004t0052g0021 |
2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.84+4583C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958658 | |||||||
chr12:30958683 | C | T | 82 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0002g0163 others(79): Show |
82 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.84+4608C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958683 | |||||||
chr12:30958695 | A | T | 1 | a0001c0001t0037g0016 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.84+4620A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958695 | |||||||
chr12:30958702 | C | T | 14 | a0001c0001t0001g0082 a0001c0001t0001g0112 a0001c0001t0001g0146 others(11): Show |
14 | HG00609.hp1 HG02015.hp2 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.84+4627C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958702 | |||||||
chr12:30958856 | T | C | 1 | a0001c0001t0002g0360 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.84+4781T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958856 | |||||||
chr12:30958915 | C | A | 5 | a0001c0001t0001g0203 a0001c0001t0004g0355 a0001c0001t0016g0353 others(2): Show |
5 | HG02572.hp1 HG02717.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.84+4840C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958915 | |||||||
chr12:30959076 | G | A | 2 | a0001c0001t0031g0104 a0001c0001t0031g0207 |
2 | HG01928.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.85-4750G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959076 | |||||||
chr12:30959161 | G | A | 1 | a0002c0002t0001g0309 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.85-4665G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959161 | |||||||
chr12:30959191 | C | T | 1 | a0002c0002t0001g0054 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.85-4635C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959191 | |||||||
chr12:30959192 | G | A | 1 | a0001c0001t0062g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.85-4634G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959192 | |||||||
chr12:30959237 | G | C | 1 | a0001c0001t0001g0115 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.85-4589G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959237 | |||||||
chr12:30959350 | T | C | 1 | a0002c0002t0007g0097 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.85-4476T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959350 | |||||||
chr12:30959362 | G | A | 4 | a0001c0001t0024g0180 a0001c0001t0028g0181 a0001c0001t0028g0316 others(1): Show |
4 | HG02257.hp1 HG02647.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.85-4464G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959362 | |||||||
chr12:30959418 | C | G | 84 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0002g0163 others(81): Show |
84 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.85-4408C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959418 | |||||||
chr12:30959482 | T | G | 16 | a0001c0001t0014g0366 a0001c0001t0014g0384 a0001c0001t0015g0363 others(13): Show |
16 | HG01192.hp1 HG02109.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.85-4344T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959482 | |||||||
chr12:30959538 | T | C | 5 | a0001c0001t0001g0203 a0001c0001t0004g0355 a0001c0001t0016g0353 others(2): Show |
5 | HG02572.hp1 HG02717.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.85-4288T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959538 | |||||||
chr12:30959614 | G | GA | 63 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0002g0163 others(60): Show |
63 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.85-4204dupA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30959614 | ||||||
chr12:30959614 | G | GAA | 21 | a0003c0003t0001g0114 a0003c0003t0003g0080 a0003c0003t0005g0056 others(18): Show |
21 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.85-4205_85-4204dup others(2): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30959614 | ||||||
chr12:30959648 | C | T | 21 | a0003c0003t0001g0114 a0003c0003t0003g0080 a0003c0003t0005g0056 others(18): Show |
21 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.85-4178C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959648 | |||||||
chr12:30959719 | G | T | 41 | a0001c0001t0001g0203 a0001c0001t0001g0288 a0001c0001t0002g0210 others(38): Show |
42 | HG00738.hp2 HG01074.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.85-4107G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959719 | |||||||
chr12:30959735 | A | G | 96 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0002g0163 others(93): Show |
97 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.85-4091A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959735 | |||||||
chr12:30959779 | C | CA | 73 | a0001c0001t0001g0022 a0001c0001t0001g0045 a0001c0001t0001g0082 others(70): Show |
73 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.85-4027dupA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30959779 | ||||||
chr12:30959779 | CA | C | 9 | a0001c0001t0001g0197 a0001c0001t0004g0186 a0001c0001t0004g0214 others(6): Show |
9 | HG01167.hp1 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.85-4027delA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30959779 | ||||||
chr12:30959795 | A | AAC | 30 | a0001c0001t0002g0163 a0001c0001t0002g0333 a0001c0001t0002g0372 others(27): Show |
30 | HG00438.hp1 HG00673.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.85-4030_85-4029ins others(2): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30959795 | ||||||
chr12:30959795 | A | AC | 51 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0002g0220 others(48): Show |
51 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.85-4031_85-4030ins others(1): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959795 | |||||||
chr12:30959802 | G | A | 1 | a0002c0002t0018g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.85-4024G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959802 | |||||||
chr12:30959874 | G | A | 11 | a0001c0001t0001g0197 a0001c0001t0004g0186 a0001c0001t0004g0214 others(8): Show |
11 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.85-3952G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959874 | |||||||
chr12:30959884 | A | G | 1 | a0001c0001t0002g0287 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.85-3942A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959884 | |||||||
chr12:30959999 | C | T | 1 | a0002c0002t0044g0039 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.85-3827C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959999 | |||||||
chr12:30960030 | C | T | 1 | a0001c0001t0002g0296 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.85-3796C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960030 | |||||||
chr12:30960063 | G | C | 1 | a0002c0002t0018g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.85-3763G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960063 | |||||||
chr12:30960082 | A | G | 84 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0002g0163 others(81): Show |
84 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.85-3744A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960082 | |||||||
chr12:30960121 | T | TGTGG | 5 | a0001c0001t0004g0011 a0001c0001t0004g0013 a0001c0001t0034g0010 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.85-3685_85-3682dup others(4): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30960121 | ||||||
chr12:30960129 | G | A | 4 | a0001c0001t0055g0356 a0002c0002t0013g0280 a0002c0002t0015g0382 others(1): Show |
4 | HG00738.hp1 HG02559.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.85-3697G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960129 | |||||||
chr12:30960178 | A | G | 1 | a0001c0001t0055g0356 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.85-3648A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960178 | |||||||
chr12:30960199 | T | A | 1 | a0001c0001t0002g0371 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-3627T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960199 | |||||||
chr12:30960316 | A | G | 20 | a0003c0003t0001g0114 a0003c0003t0003g0080 a0003c0003t0005g0056 others(17): Show |
20 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.85-3510A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960316 | |||||||
chr12:30960464 | T | C | 1 | a0001c0001t0003g0111 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.85-3362T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960464 | |||||||
chr12:30960466 | T | C | 140 | a0001c0001t0001g0203 a0001c0001t0001g0244 a0001c0001t0001g0245 others(137): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.85-3360T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960466 | |||||||
chr12:30960529 | G | A | 67 | a0001c0001t0001g0101 a0001c0001t0001g0257 a0001c0001t0001g0340 others(64): Show |
69 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.85-3297G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960529 | |||||||
chr12:30960542 | T | TTTCTCTC others(32): Show |
1 | a0001c0001t0023g0336 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.85-3283_85-3245dup others(39): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30960542 | ||||||
chr12:30960564 | G | A | 2 | a0001c0001t0008g0049 a0001c0001t0008g0086 |
2 | NA18946.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.85-3262G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960564 | |||||||
chr12:30960615 | C | T | 21 | a0003c0003t0001g0114 a0003c0003t0003g0080 a0003c0003t0005g0056 others(18): Show |
21 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.85-3211C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960615 | |||||||
chr12:30960655 | C | T | 1 | a0002c0002t0007g0078 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.85-3171C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960655 | |||||||
chr12:30960676 | A | G | 181 | a0001c0001t0001g0101 a0001c0001t0001g0203 a0001c0001t0001g0244 others(178): Show |
185 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.85-3150A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960676 | |||||||
chr12:30960679 | C | T | 3 | a0003c0003t0006g0232 a0003c0003t0006g0270 a0003c0003t0061g0265 |
3 | NA18956.hp2 NA18979.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.85-3147C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960679 | |||||||
chr12:30960685 | G | A | 1 | a0002c0002t0001g0157 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.85-3141G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960685 | |||||||
chr12:30960808 | G | C | 1 | a0002c0002t0046g0310 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.85-3018G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960808 | |||||||
chr12:30960912 | A | G | 21 | a0003c0003t0001g0114 a0003c0003t0003g0080 a0003c0003t0005g0056 others(18): Show |
21 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.85-2914A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960912 | |||||||
chr12:30960965 | G | A | 3 | a0001c0001t0034g0228 a0002c0002t0014g0124 a0006c0010t0022g0185 |
3 | HG01167.hp1 HG01891.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.85-2861G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960965 | |||||||
chr12:30961017 | C | T | 1 | a0001c0001t0037g0016 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.85-2809C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961017 | |||||||
chr12:30961029 | G | GA | 133 | a0001c0001t0001g0101 a0001c0001t0001g0165 a0001c0001t0001g0244 others(130): Show |
135 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.85-2783dupA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30961029 | ||||||
chr12:30961029 | GA | G | 6 | a0001c0001t0008g0306 a0001c0001t0016g0187 a0001c0001t0034g0228 others(3): Show |
6 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.85-2783delA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30961029 | ||||||
chr12:30961029 | GAA | G | 20 | a0003c0003t0001g0114 a0003c0003t0003g0080 a0003c0003t0005g0056 others(17): Show |
20 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.85-2784_85-2783del others(2): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30961029 | ||||||
chr12:30961096 | C | A | 1 | a0002c0004t0005g0272 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.85-2730C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961096 | |||||||
chr12:30961174 | G | A | 126 | a0001c0001t0001g0101 a0001c0001t0001g0244 a0001c0001t0001g0245 others(123): Show |
128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.85-2652G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961174 | |||||||
chr12:30961213 | A | C | 1 | a0001c0001t0002g0371 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2613A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961213 | |||||||
chr12:30961214 | G | T | 1 | a0001c0001t0002g0371 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2612G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961214 | |||||||
chr12:30961216 | C | A | 1 | a0001c0001t0002g0371 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2610C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961216 | |||||||
chr12:30961217 | A | C | 1 | a0001c0001t0002g0371 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2609A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961217 | |||||||
chr12:30961218 | G | C | 1 | a0001c0001t0002g0371 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2608G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961218 | |||||||
chr12:30961220 | T | C | 1 | a0001c0001t0002g0371 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2606T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961220 | |||||||
chr12:30961222 | C | G | 1 | a0001c0001t0002g0371 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2604C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961222 | |||||||
chr12:30961224 | A | T | 1 | a0001c0001t0002g0371 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2602A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961224 | |||||||
chr12:30961226 | G | A | 1 | a0001c0001t0002g0371 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2600G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961226 | |||||||
chr12:30961228 | G | T | 1 | a0001c0001t0002g0371 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2598G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961228 | |||||||
chr12:30961229 | G | A | 1 | a0001c0001t0002g0371 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2597G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961229 | |||||||
chr12:30961230 | C | T | 1 | a0001c0001t0002g0371 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2596C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961230 | |||||||
chr12:30961232 | T | C | 1 | a0001c0001t0002g0371 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2594T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961232 | |||||||
chr12:30961233 | G | A | 1 | a0001c0001t0002g0371 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2593G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961233 | |||||||
chr12:30961235 | G | T | 1 | a0001c0001t0002g0371 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2591G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961235 | |||||||
chr12:30961241 | G | A | 1 | a0001c0001t0002g0371 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2585G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961241 | |||||||
chr12:30961244 | A | T | 1 | a0001c0001t0002g0371 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2582A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961244 | |||||||
chr12:30961298 | T | C | 21 | a0003c0003t0001g0114 a0003c0003t0003g0080 a0003c0003t0005g0056 others(18): Show |
21 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.85-2528T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961298 | |||||||
chr12:30961347 | T | C | 128 | a0001c0001t0001g0101 a0001c0001t0001g0244 a0001c0001t0001g0245 others(125): Show |
130 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.85-2479T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961347 | |||||||
chr12:30961440 | A | T | 45 | a0001c0001t0001g0044 a0001c0001t0001g0103 a0001c0001t0001g0240 others(42): Show |
46 | HG00558.hp1 HG01928.hp2 HG01943.hp1 others(43): Show |
intron_variant | MODIFIER | c.85-2386A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961440 | |||||||
chr12:30961620 | G | T | 3 | a0001c0001t0034g0228 a0002c0002t0014g0124 a0006c0010t0022g0185 |
3 | HG01167.hp1 HG01891.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.85-2206G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961620 | |||||||
chr12:30961636 | G | A | 54 | a0001c0001t0001g0203 a0001c0001t0001g0288 a0001c0001t0002g0210 others(51): Show |
56 | HG00438.hp2 HG00738.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.85-2190G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961636 | |||||||
chr12:30961727 | A | T | 21 | a0003c0003t0001g0114 a0003c0003t0003g0080 a0003c0003t0005g0056 others(18): Show |
21 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.85-2099A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961727 | |||||||
chr12:30961824 | C | G | 1 | a0001c0001t0001g0169 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.85-2002C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961824 | |||||||
chr12:30961849 | G | A | 6 | a0001c0001t0001g0059 a0001c0001t0003g0042 a0001c0001t0003g0058 others(3): Show |
6 | HG00408.hp1 HG00609.hp2 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-1977G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961849 | |||||||
chr12:30961961 | A | G | 66 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0103 others(63): Show |
67 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.85-1865A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961961 | |||||||
chr12:30962036 | C | T | 21 | a0003c0003t0001g0114 a0003c0003t0003g0080 a0003c0003t0005g0056 others(18): Show |
21 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.85-1790C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962036 | |||||||
chr12:30962043 | T | C | 2 | a0001c0001t0029g0192 a0001c0001t0029g0193 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.85-1783T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962043 | |||||||
chr12:30962076 | A | G | 11 | a0001c0001t0001g0197 a0001c0001t0004g0186 a0001c0001t0004g0214 others(8): Show |
11 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.85-1750A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962076 | |||||||
chr12:30962170 | G | A | 14 | a0001c0001t0002g0163 a0001c0001t0002g0333 a0001c0001t0002g0371 others(11): Show |
14 | HG00438.hp1 HG01257.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.85-1656G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962170 | |||||||
chr12:30962220 | G | A | 1 | a0004c0006t0001g0134 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.85-1606G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962220 | |||||||
chr12:30962347 | A | C | 1 | a0001c0001t0001g0045 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.85-1479A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962347 | |||||||
chr12:30962411 | A | C | 280 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0101 others(277): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.85-1415A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962411 | |||||||
chr12:30962494 | A | G | 1 | a0001c0001t0001g0235 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.85-1332A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962494 | |||||||
chr12:30962558 | G | A | 11 | a0001c0001t0001g0197 a0001c0001t0004g0186 a0001c0001t0004g0214 others(8): Show |
11 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.85-1268G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962558 | |||||||
chr12:30962611 | A | G | 108 | a0001c0001t0001g0101 a0001c0001t0001g0244 a0001c0001t0001g0245 others(105): Show |
110 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.85-1215A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962611 | |||||||
chr12:30962641 | C | T | 16 | a0001c0001t0002g0163 a0001c0001t0002g0333 a0001c0001t0002g0371 others(13): Show |
16 | HG00438.hp1 HG01257.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.85-1185C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962641 | |||||||
chr12:30962712 | A | G | 1 | a0001c0001t0043g0317 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.85-1114A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962712 | |||||||
chr12:30962727 | A | G | 280 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0101 others(277): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.85-1099A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962727 | |||||||
chr12:30962783 | C | T | 84 | a0001c0001t0001g0197 a0001c0001t0001g0203 a0001c0001t0001g0288 others(81): Show |
86 | HG00438.hp1 HG00438.hp2 HG00738.hp2 others(83): Show |
intron_variant | MODIFIER | c.85-1043C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962783 | |||||||
chr12:30962798 | A | C | 348 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0059 others(345): Show |
353 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.85-1028A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962798 | |||||||
chr12:30962829 | A | G | 109 | a0001c0001t0001g0101 a0001c0001t0001g0244 a0001c0001t0001g0245 others(106): Show |
111 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.85-997A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962829 | |||||||
chr12:30962868 | C | G | 21 | a0003c0003t0001g0114 a0003c0003t0003g0080 a0003c0003t0005g0056 others(18): Show |
21 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.85-958C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962868 | |||||||
chr12:30962944 | A | T | 5 | a0001c0001t0002g0210 a0001c0001t0002g0343 a0001c0001t0010g0209 others(2): Show |
5 | HG01243.hp1 HG01258.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.85-882A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962944 | |||||||
chr12:30962972 | A | G | 1 | a0003c0003t0003g0080 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.85-854A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962972 | |||||||
chr12:30962996 | G | C | 109 | a0001c0001t0001g0101 a0001c0001t0001g0244 a0001c0001t0001g0245 others(106): Show |
111 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.85-830G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962996 | |||||||
chr12:30963077 | C | G | 14 | a0001c0001t0020g0026 a0002c0002t0001g0142 a0002c0002t0005g0130 others(11): Show |
15 | HG00438.hp2 HG02080.hp2 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.85-749C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30963077 | |||||||
chr12:30963102 | GA | G | 65 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0103 others(62): Show |
66 | HG00558.hp1 HG00609.hp1 HG01928.hp2 others(63): Show |
intron_variant | MODIFIER | c.85-722delA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30963102 | ||||||
chr12:30963110 | C | A | 1 | a0001c0001t0033g0191 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.85-716C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30963110 | |||||||
chr12:30963270 | G | C | 65 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0103 others(62): Show |
66 | HG00558.hp1 HG00609.hp1 HG01928.hp2 others(63): Show |
intron_variant | MODIFIER | c.85-556G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30963270 | |||||||
chr12:30963371 | A | T | 65 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0103 others(62): Show |
66 | HG00558.hp1 HG00609.hp1 HG01928.hp2 others(63): Show |
intron_variant | MODIFIER | c.85-455A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30963371 | |||||||
chr12:30963552 | C | T | 8 | a0001c0001t0001g0288 a0001c0001t0002g0296 a0001c0001t0005g0301 others(5): Show |
8 | HG00738.hp2 HG01074.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.85-274C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30963552 | |||||||
chr12:30963622 | G | T | 3 | a0001c0001t0034g0228 a0002c0002t0014g0124 a0006c0010t0022g0185 |
3 | HG01167.hp1 HG01891.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.85-204G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30963622 | |||||||
chr12:30963663 | G | A | 1 | a0001c0001t0037g0016 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.85-163G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30963663 | |||||||
chr12:30963743 | G | T | 2 | a0001c0001t0031g0104 a0001c0001t0031g0207 |
2 | HG01928.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.85-83G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30963743 | |||||||
chr12:30963795 | C | A | 5 | a0001c0001t0004g0011 a0001c0001t0004g0013 a0001c0001t0034g0010 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.85-31C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30963795 | |||||||
chr12:30963804 | C | G | 1 | a0001c0001t0016g0362 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.85-22C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30963804 | |||||||
chr12:30963810 | C | T | 21 | a0001c0001t0001g0045 a0001c0001t0001g0154 a0001c0001t0001g0169 others(18): Show |
21 | HG00558.hp2 HG01099.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.85-16C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30963810 | |||||||
chr12:30964106 | AGTGGGAG others(11): Show |
A | 59 | a0001c0001t0001g0203 a0001c0001t0001g0288 a0001c0001t0002g0210 others(56): Show |
61 | HG00438.hp2 HG00738.hp2 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.276+97_276+114delG others(17): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30964106 | ||||||
chr12:30964374 | C | T | 66 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0103 others(63): Show |
67 | HG00558.hp1 HG00609.hp1 HG01928.hp2 others(64): Show |
intron_variant | MODIFIER | c.276+357C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30964374 | |||||||
chr12:30964380 | CT | C | 14 | a0001c0001t0014g0366 a0001c0001t0015g0363 a0001c0001t0015g0364 others(11): Show |
14 | HG01192.hp1 HG02109.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.276+365delT | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30964380 | ||||||
chr12:30964424 | C | G | 1 | a0002c0002t0001g0075 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.276+407C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30964424 | |||||||
chr12:30964426 | C | CCCTCTTC others(5): Show |
54 | a0001c0001t0001g0288 a0001c0001t0002g0210 a0001c0001t0002g0287 others(51): Show |
56 | HG00438.hp2 HG00738.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.276+420_276+431dup others(12): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30964426 | ||||||
chr12:30964604 | A | C | 2 | a0001c0001t0034g0228 a0006c0010t0022g0185 |
2 | HG01891.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.276+587A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30964604 | |||||||
chr12:30964611 | A | C | 3 | a0001c0001t0022g0053 a0002c0002t0004g0318 a0002c0002t0045g0188 |
3 | HG02809.hp1 HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.276+594A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30964611 | |||||||
chr12:30964661 | G | C | 1 | a0001c0001t0011g0067 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.276+644G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30964661 | |||||||
chr12:30964785 | A | G | 5 | a0001c0001t0005g0050 a0001c0001t0011g0006 a0001c0001t0011g0087 others(2): Show |
6 | HG01952.hp2 HG01975.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.276+768A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30964785 | |||||||
chr12:30964865 | T | C | 2 | a0001c0001t0002g0371 a0001c0001t0002g0372 |
2 | HG00438.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.276+848T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30964865 | |||||||
chr12:30964913 | G | A | 1 | a0001c0001t0002g0269 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.276+896G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30964913 | |||||||
chr12:30964924 | C | A | 1 | a0001c0001t0002g0123 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.276+907C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30964924 | |||||||
chr12:30965126 | G | A | 1 | a0001c0001t0055g0356 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.276+1109G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965126 | |||||||
chr12:30965132 | C | T | 2 | a0001c0001t0001g0288 a0001c0001t0002g0296 |
2 | HG03540.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.276+1115C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965132 | |||||||
chr12:30965160 | C | A | 6 | a0001c0001t0010g0127 a0001c0001t0010g0273 a0001c0001t0027g0024 others(3): Show |
6 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.276+1143C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965160 | |||||||
chr12:30965172 | C | T | 2 | a0001c0001t0007g0094 a0002c0002t0007g0102 |
2 | NA19012.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.276+1155C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965172 | |||||||
chr12:30965253 | G | A | 1 | a0002c0002t0004g0176 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.276+1236G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965253 | |||||||
chr12:30965262 | C | A | 10 | a0001c0001t0001g0197 a0001c0001t0004g0214 a0001c0001t0016g0362 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.276+1245C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965262 | |||||||
chr12:30965360 | C | T | 28 | a0001c0001t0001g0197 a0001c0001t0002g0163 a0001c0001t0002g0333 others(25): Show |
28 | HG00438.hp1 HG01257.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.276+1343C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965360 | |||||||
chr12:30965395 | A | T | 5 | a0001c0001t0001g0327 a0001c0001t0003g0196 a0001c0001t0008g0306 others(2): Show |
5 | NA18946.hp1 NA18947.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.276+1378A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965395 | |||||||
chr12:30965440 | A | G | 254 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0088 others(251): Show |
258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.276+1423A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965440 | |||||||
chr12:30965459 | C | G | 5 | a0001c0001t0012g0034 a0002c0002t0001g0037 a0002c0002t0001g0038 others(2): Show |
5 | HG02080.hp1 HG02523.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.276+1442C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965459 | |||||||
chr12:30965459 | C | T | 2 | a0001c0001t0005g0301 a0001c0001t0017g0302 |
2 | HG03710.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.276+1442C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965459 | |||||||
chr12:30965461 | A | C | 1 | a0001c0001t0003g0117 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.276+1444A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965461 | |||||||
chr12:30965463 | C | CGCCTTCC others(11): Show |
11 | a0001c0001t0001g0197 a0001c0001t0004g0186 a0001c0001t0004g0214 others(8): Show |
11 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.276+1450_276+1467d others(20): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30965463 | ||||||
chr12:30965536 | T | A | 1 | a0002c0002t0003g0093 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.276+1519T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965536 | |||||||
chr12:30965570 | A | G | 72 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0088 others(69): Show |
73 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.276+1553A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965570 | |||||||
chr12:30965591 | A | G | 6 | a0001c0001t0001g0203 a0001c0001t0004g0355 a0001c0001t0016g0353 others(3): Show |
6 | HG02572.hp1 HG02717.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.276+1574A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965591 | |||||||
chr12:30965662 | C | T | 1 | a0001c0001t0011g0099 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.276+1645C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965662 | |||||||
chr12:30965675 | C | CACA | 3 | a0001c0001t0003g0380 a0001c0001t0006g0032 a0002c0004t0001g0234 |
3 | HG00621.hp1 HG02074.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.276+1660_276+1661i others(5): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30965675 | ||||||
chr12:30965675 | C | T | 60 | a0001c0001t0001g0203 a0001c0001t0001g0288 a0001c0001t0002g0210 others(57): Show |
62 | HG00438.hp2 HG00738.hp2 HG01074.hp1 others(59): Show |
intron_variant | MODIFIER | c.276+1658C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965675 | |||||||
chr12:30965679 | T | C | 100 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0088 others(97): Show |
101 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.276+1662T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965679 | |||||||
chr12:30965717 | G | A | 8 | a0001c0001t0001g0240 a0001c0001t0008g0065 a0001c0001t0008g0069 others(5): Show |
8 | NA18942.hp2 NA18954.hp1 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.276+1700G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965717 | |||||||
chr12:30965940 | G | A | 2 | a0001c0001t0008g0049 a0001c0001t0008g0086 |
2 | NA18946.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.276+1923G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965940 | |||||||
chr12:30966002 | TTA | T | 56 | a0001c0001t0001g0101 a0001c0001t0001g0257 a0001c0001t0001g0340 others(53): Show |
57 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.276+1987_276+1988d others(4): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30966002 | ||||||
chr12:30966021 | A | AT | 129 | a0001c0001t0001g0101 a0001c0001t0001g0244 a0001c0001t0001g0245 others(126): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.276+2018dupT | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30966021 | ||||||
chr12:30966021 | AT | A | 7 | a0001c0001t0006g0190 a0001c0001t0024g0180 a0001c0001t0028g0181 others(4): Show |
7 | HG01891.hp1 HG02027.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.276+2018delT | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30966021 | ||||||
chr12:30966021 | ATT | A | 71 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0088 others(68): Show |
72 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.276+2017_276+2018d others(4): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30966021 | ||||||
chr12:30966081 | G | T | 14 | a0001c0001t0002g0163 a0001c0001t0002g0333 a0001c0001t0002g0371 others(11): Show |
14 | HG00438.hp1 HG01257.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.276+2064G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966081 | |||||||
chr12:30966104 | C | T | 1 | a0001c0001t0022g0179 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.276+2087C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966104 | |||||||
chr12:30966106 | A | G | 5 | a0001c0001t0004g0011 a0001c0001t0004g0013 a0001c0001t0034g0010 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.276+2089A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966106 | |||||||
chr12:30966117 | C | A | 1 | a0001c0001t0009g0229 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.276+2100C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966117 | |||||||
chr12:30966137 | T | C | 178 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0088 others(175): Show |
181 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.276+2120T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966137 | |||||||
chr12:30966189 | G | C | 28 | a0001c0001t0001g0197 a0001c0001t0002g0163 a0001c0001t0002g0333 others(25): Show |
28 | HG00438.hp1 HG01257.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.276+2172G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966189 | |||||||
chr12:30966261 | C | T | 1 | a0012c0017t0011g0171 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.276+2244C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966261 | |||||||
chr12:30966262 | G | A | 1 | a0002c0004t0052g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.276+2245G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966262 | |||||||
chr12:30966371 | G | A | 11 | a0001c0001t0001g0197 a0001c0001t0004g0186 a0001c0001t0004g0214 others(8): Show |
11 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.276+2354G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966371 | |||||||
chr12:30966533 | A | G | 72 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0088 others(69): Show |
73 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.276+2516A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966533 | |||||||
chr12:30966589 | G | A | 29 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0002g0220 others(26): Show |
29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.276+2572G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966589 | |||||||
chr12:30966613 | T | TAAG | 5 | a0001c0001t0004g0011 a0001c0001t0004g0013 a0001c0001t0034g0010 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.276+2598_276+2600d others(5): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30966613 | ||||||
chr12:30966661 | G | A | 1 | a0001c0001t0002g0360 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.276+2644G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966661 | |||||||
chr12:30966677 | G | C | 1 | a0001c0001t0005g0050 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.276+2660G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966677 | |||||||
chr12:30966688 | G | A | 1 | a0002c0002t0021g0036 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.276+2671G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966688 | |||||||
chr12:30966861 | G | A | 2 | a0001c0001t0050g0177 a0002c0002t0004g0295 |
2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.276+2844G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966861 | |||||||
chr12:30966867 | C | T | 6 | a0001c0001t0001g0203 a0001c0001t0004g0355 a0001c0001t0016g0353 others(3): Show |
6 | HG02572.hp1 HG02717.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.276+2850C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966867 | |||||||
chr12:30966937 | C | T | 1 | a0002c0002t0001g0199 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.276+2920C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966937 | |||||||
chr12:30967001 | G | A | 14 | a0001c0001t0001g0327 a0001c0001t0003g0196 a0001c0001t0008g0060 others(11): Show |
14 | HG02056.hp1 HG02165.hp1 NA18747.hp1 others(11): Show |
intron_variant | MODIFIER | c.276+2984G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30967001 | |||||||
chr12:30967055 | G | C | 1 | a0001c0001t0019g0385 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.276+3038G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30967055 | |||||||
chr12:30967208 | G | A | 1 | a0001c0001t0006g0328 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.276+3191G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30967208 | |||||||
chr12:30967227 | G | T | 11 | a0001c0001t0001g0197 a0001c0001t0004g0186 a0001c0001t0004g0214 others(8): Show |
11 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.276+3210G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30967227 | |||||||
chr12:30967412 | C | T | 1 | a0001c0001t0023g0170 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.276+3395C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30967412 | |||||||
chr12:30967661 | C | T | 99 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0088 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.276+3644C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30967661 | |||||||
chr12:30967674 | GTGCACAC others(13): Show |
G | 104 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0088 others(101): Show |
105 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.276+3678_276+3697d others(22): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967674 | ||||||
chr12:30967678 | ACACACAT others(31): Show |
A | 103 | a0001c0001t0001g0101 a0001c0001t0001g0244 a0001c0001t0001g0245 others(100): Show |
104 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.276+3672_276+3709d others(40): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967678 | ||||||
chr12:30967695 | T | C | 1 | a0001c0001t0003g0117 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.276+3678T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30967695 | |||||||
chr12:30967695 | TGCACACA others(13): Show |
T | 5 | a0001c0001t0004g0011 a0001c0001t0004g0013 a0001c0001t0034g0010 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.276+3686_276+3705d others(22): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967695 | ||||||
chr12:30967699 | CACACATG others(14): Show |
C | 1 | a0001c0001t0003g0117 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.276+3683_276+3703d others(23): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30967699 | |||||||
chr12:30967722 | A | C | 1 | a0001c0001t0003g0117 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.276+3705A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30967722 | |||||||
chr12:30967773 | C | T | 1 | a0001c0001t0003g0116 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.276+3756C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30967773 | |||||||
chr12:30967774 | G | A | 1 | a0002c0002t0026g0299 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.276+3757G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30967774 | |||||||
chr12:30967795 | T | TGGCCTAG others(302): Show |
1 | a0002c0002t0007g0141 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.276+3799_276+3800i others(311): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | ||||||
chr12:30967795 | T | TGGCCTAG others(305): Show |
1 | a0001c0001t0016g0187 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.276+3799_276+3800i others(314): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | ||||||
chr12:30967795 | T | TGGCCTAG others(307): Show |
1 | a0002c0002t0074g0149 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.276+3799_276+3800i others(316): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | ||||||
chr12:30967795 | T | TGGCCTAG others(310): Show |
1 | a0001c0001t0004g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.276+3799_276+3800i others(319): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | ||||||
chr12:30967795 | T | TGGCCTAG others(311): Show |
4 | a0001c0001t0004g0013 a0001c0001t0034g0010 a0001c0001t0048g0012 others(1): Show |
4 | HG01884.hp1 HG02257.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.276+3799_276+3800i others(320): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | ||||||
chr12:30967795 | T | TGGCCTAG others(311): Show |
17 | a0001c0001t0001g0288 a0001c0001t0002g0296 a0001c0001t0005g0301 others(14): Show |
18 | HG01074.hp1 HG01123.hp1 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.276+3799_276+3800i others(320): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | ||||||
chr12:30967795 | T | TGGCCTAG others(312): Show |
1 | a0002c0002t0004g0300 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.276+3799_276+3800i others(321): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | ||||||
chr12:30967795 | T | TGGCCTAG others(315): Show |
1 | a0002c0004t0017g0152 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.276+3799_276+3800i others(324): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | ||||||
chr12:30967795 | T | TGGCCTAG others(317): Show |
4 | a0001c0001t0001g0203 a0001c0001t0016g0353 a0002c0002t0018g0352 others(1): Show |
4 | HG02717.hp2 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.276+3799_276+3800i others(326): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | ||||||
chr12:30967795 | T | TGGCCTAG others(318): Show |
2 | a0001c0001t0004g0355 a0001c0001t0018g0350 |
2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.276+3799_276+3800i others(327): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | ||||||
chr12:30967795 | T | TGGCCTAG others(323): Show |
1 | a0001c0001t0002g0343 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.276+3799_276+3800i others(332): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | ||||||
chr12:30967795 | T | TGGCCTAG others(324): Show |
2 | a0001c0001t0006g0190 a0002c0002t0007g0140 |
2 | HG02897.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.276+3799_276+3800i others(333): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | ||||||
chr12:30967795 | T | TGGCCTAG others(325): Show |
1 | a0001c0001t0006g0189 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.276+3799_276+3800i others(334): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | ||||||
chr12:30967795 | T | TGGCCTAG others(326): Show |
1 | a0001c0001t0058g0332 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.276+3799_276+3800i others(335): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | ||||||
chr12:30967795 | T | TGGCCTAG others(334): Show |
1 | a0001c0001t0002g0298 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.276+3799_276+3800i others(343): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | ||||||
chr12:30967795 | T | TGGCCTAG others(335): Show |
1 | a0002c0002t0007g0144 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.276+3799_276+3800i others(344): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | ||||||
chr12:30967795 | T | TGGCCTAG others(335): Show |
5 | a0001c0001t0002g0287 a0001c0001t0002g0330 a0001c0001t0010g0209 others(2): Show |
5 | HG01943.hp2 HG01978.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.276+3799_276+3800i others(344): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | ||||||
chr12:30967795 | T | TGGCCTAG others(336): Show |
3 | a0002c0002t0006g0132 a0002c0002t0007g0128 a0002c0002t0026g0027 |
3 | HG02080.hp2 HG02895.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.276+3799_276+3800i others(345): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | ||||||
chr12:30967795 | T | TGGCCTAG others(336): Show |
2 | a0001c0001t0002g0210 a0002c0002t0041g0014 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.276+3799_276+3800i others(345): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | ||||||
chr12:30967795 | T | TGGCCTAG others(337): Show |
1 | a0001c0001t0020g0026 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.276+3799_276+3800i others(346): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | ||||||
chr12:30967795 | T | TGGCCTAG others(340): Show |
1 | a0001c0001t0023g0336 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.276+3799_276+3800i others(349): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | ||||||
chr12:30967795 | T | TGGCCTAG others(341): Show |
1 | a0002c0002t0005g0143 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.276+3799_276+3800i others(350): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | ||||||
chr12:30967795 | T | TGGCCTAG others(341): Show |
1 | a0001c0001t0023g0337 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.276+3799_276+3800i others(350): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | ||||||
chr12:30967795 | T | TGGCCTAG others(342): Show |
2 | a0002c0002t0005g0131 a0002c0002t0007g0007 |
3 | NA18951.hp2 NA18959.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.276+3799_276+3800i others(351): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | ||||||
chr12:30967795 | T | TGGCCTAG others(343): Show |
3 | a0002c0002t0001g0142 a0002c0002t0005g0130 a0002c0002t0007g0150 |
3 | HG00438.hp2 NA18994.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.276+3799_276+3800i others(352): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | ||||||
chr12:30967970 | A | G | 71 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0088 others(68): Show |
72 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.276+3953A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30967970 | |||||||
chr12:30967986 | C | T | 4 | a0001c0001t0024g0180 a0001c0001t0028g0181 a0001c0001t0028g0316 others(1): Show |
4 | HG02257.hp1 HG02647.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.276+3969C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30967986 | |||||||
chr12:30968126 | G | A | 1 | a0002c0002t0018g0183 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.276+4109G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30968126 | |||||||
chr12:30968314 | T | A | 1 | a0002c0002t0004g0239 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.276+4297T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30968314 | |||||||
chr12:30968333 | C | A | 5 | a0001c0001t0004g0011 a0001c0001t0004g0013 a0001c0001t0004g0214 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.276+4316C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30968333 | |||||||
chr12:30968411 | C | T | 1 | a0001c0001t0004g0186 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.276+4394C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30968411 | |||||||
chr12:30968415 | G | A | 60 | a0001c0001t0001g0203 a0001c0001t0001g0288 a0001c0001t0002g0210 others(57): Show |
62 | HG00438.hp2 HG00738.hp2 HG01074.hp1 others(59): Show |
intron_variant | MODIFIER | c.276+4398G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30968415 | |||||||
chr12:30968637 | G | A | 54 | a0001c0001t0001g0288 a0001c0001t0002g0210 a0001c0001t0002g0287 others(51): Show |
56 | HG00438.hp2 HG00738.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.276+4620G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30968637 | |||||||
chr12:30968661 | T | G | 29 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0002g0220 others(26): Show |
29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.276+4644T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30968661 | |||||||
chr12:30968806 | C | T | 10 | a0001c0001t0001g0340 a0001c0001t0002g0003 a0001c0001t0002g0079 others(7): Show |
11 | HG00733.hp1 HG00735.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.276+4789C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30968806 | |||||||
chr12:30968928 | G | A | 17 | a0001c0001t0002g0163 a0001c0001t0002g0333 a0001c0001t0002g0371 others(14): Show |
17 | HG00438.hp1 HG01257.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.276+4911G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30968928 | |||||||
chr12:30968933 | A | G | 72 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0088 others(69): Show |
73 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.276+4916A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30968933 | |||||||
chr12:30968958 | T | A | 1 | a0002c0002t0003g0168 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.276+4941T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30968958 | |||||||
chr12:30969044 | A | G | 1 | a0002c0002t0007g0141 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.276+5027A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969044 | |||||||
chr12:30969095 | C | A | 10 | a0001c0001t0001g0197 a0001c0001t0004g0186 a0001c0001t0016g0362 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.276+5078C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969095 | |||||||
chr12:30969112 | T | A | 10 | a0001c0001t0001g0197 a0001c0001t0004g0186 a0001c0001t0016g0362 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.276+5095T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969112 | |||||||
chr12:30969149 | G | C | 19 | a0002c0002t0018g0183 a0003c0003t0001g0114 a0003c0003t0003g0080 others(16): Show |
19 | HG00673.hp1 HG02109.hp2 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.276+5132G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969149 | |||||||
chr12:30969152 | A | G | 104 | a0001c0001t0001g0101 a0001c0001t0001g0244 a0001c0001t0001g0245 others(101): Show |
105 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.276+5135A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969152 | |||||||
chr12:30969214 | G | C | 4 | a0001c0001t0008g0060 a0001c0001t0012g0164 a0002c0002t0001g0033 others(1): Show |
4 | HG02165.hp1 NA18985.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.276+5197G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969214 | |||||||
chr12:30969281 | T | C | 54 | a0001c0001t0001g0288 a0001c0001t0002g0210 a0001c0001t0002g0287 others(51): Show |
56 | HG00438.hp2 HG00738.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.276+5264T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969281 | |||||||
chr12:30969314 | T | C | 27 | a0001c0001t0001g0197 a0001c0001t0002g0163 a0001c0001t0002g0333 others(24): Show |
27 | HG00438.hp1 HG01257.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.276+5297T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969314 | |||||||
chr12:30969366 | A | G | 1 | a0001c0001t0009g0369 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.276+5349A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969366 | |||||||
chr12:30969477 | G | A | 1 | a0002c0002t0001g0083 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.276+5460G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969477 | |||||||
chr12:30969534 | C | T | 18 | a0003c0003t0001g0114 a0003c0003t0003g0080 a0003c0003t0005g0056 others(15): Show |
18 | HG00673.hp1 HG02132.hp1 HG02683.hp1 others(15): Show |
intron_variant | MODIFIER | c.276+5517C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969534 | |||||||
chr12:30969539 | T | C | 177 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0088 others(174): Show |
180 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.276+5522T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969539 | |||||||
chr12:30969555 | C | T | 4 | a0001c0001t0001g0197 a0001c0001t0021g0198 a0001c0001t0021g0212 others(1): Show |
4 | HG02055.hp1 HG02258.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.276+5538C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969555 | |||||||
chr12:30969594 | C | T | 10 | a0001c0001t0001g0197 a0001c0001t0004g0186 a0001c0001t0016g0362 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.276+5577C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969594 | |||||||
chr12:30969631 | C | G | 60 | a0001c0001t0001g0203 a0001c0001t0001g0288 a0001c0001t0002g0210 others(57): Show |
62 | HG00438.hp2 HG00738.hp2 HG01074.hp1 others(59): Show |
intron_variant | MODIFIER | c.276+5614C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969631 | |||||||
chr12:30969669 | C | T | 1 | a0001c0001t0006g0328 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.276+5652C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969669 | |||||||
chr12:30969690 | G | A | 17 | a0001c0001t0002g0163 a0001c0001t0002g0333 a0001c0001t0002g0371 others(14): Show |
17 | HG00438.hp1 HG01257.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.276+5673G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969690 | |||||||
chr12:30969771 | C | T | 103 | a0001c0001t0001g0101 a0001c0001t0001g0244 a0001c0001t0001g0245 others(100): Show |
104 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.276+5754C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969771 | |||||||
chr12:30969872 | G | A | 10 | a0001c0001t0001g0197 a0001c0001t0004g0186 a0001c0001t0016g0362 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.276+5855G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969872 | |||||||
chr12:30970022 | C | T | 1 | a0001c0001t0068g0304 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.276+6005C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30970022 | |||||||
chr12:30970107 | A | C | 1 | a0001c0001t0001g0082 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.276+6090A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30970107 | |||||||
chr12:30970463 | A | G | 2 | a0003c0003t0001g0114 a0003c0003t0032g0241 |
2 | HG02683.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.276+6446A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30970463 | |||||||
chr12:30970622 | A | T | 81 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0088 others(78): Show |
82 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.276+6605A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30970622 | |||||||
chr12:30970641 | C | T | 81 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0088 others(78): Show |
82 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.276+6624C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30970641 | |||||||
chr12:30970737 | C | T | 116 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0088 others(113): Show |
117 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.276+6720C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30970737 | |||||||
chr12:30970915 | T | C | 1 | a0002c0002t0001g0074 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.276+6898T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30970915 | |||||||
chr12:30970985 | C | A | 20 | a0002c0002t0018g0040 a0002c0002t0018g0183 a0003c0003t0001g0114 others(17): Show |
20 | HG00673.hp1 HG02109.hp2 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.276+6968C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30970985 | |||||||
chr12:30971433 | A | G | 69 | a0001c0001t0001g0101 a0001c0001t0001g0257 a0001c0001t0001g0340 others(66): Show |
70 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.277-7128A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30971433 | |||||||
chr12:30971447 | C | A | 15 | a0001c0001t0002g0163 a0001c0001t0002g0371 a0001c0001t0002g0372 others(12): Show |
15 | HG00438.hp1 HG01257.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.277-7114C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30971447 | |||||||
chr12:30971553 | G | A | 72 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0088 others(69): Show |
73 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.277-7008G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30971553 | |||||||
chr12:30971633 | C | T | 18 | a0003c0003t0001g0114 a0003c0003t0003g0080 a0003c0003t0005g0056 others(15): Show |
18 | HG00673.hp1 HG02132.hp1 HG02683.hp1 others(15): Show |
intron_variant | MODIFIER | c.277-6928C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30971633 | |||||||
chr12:30971655 | T | G | 68 | a0001c0001t0001g0045 a0001c0001t0001g0059 a0001c0001t0001g0113 others(65): Show |
68 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.277-6906T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30971655 | |||||||
chr12:30971682 | C | T | 130 | a0001c0001t0001g0045 a0001c0001t0001g0059 a0001c0001t0001g0113 others(127): Show |
133 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.277-6879C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30971682 | |||||||
chr12:30971724 | A | T | 1 | a0002c0002t0014g0124 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.277-6837A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30971724 | |||||||
chr12:30971749 | CA | C | 91 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0088 others(88): Show |
92 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.277-6801delA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30971749 | ||||||
chr12:30971843 | T | TA | 131 | a0001c0001t0001g0045 a0001c0001t0001g0059 a0001c0001t0001g0113 others(128): Show |
134 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.277-6705dupA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30971843 | ||||||
chr12:30971843 | TA | T | 155 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0088 others(152): Show |
157 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.277-6705delA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30971843 | ||||||
chr12:30971880 | T | C | 1 | a0002c0004t0014g0195 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.277-6681T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30971880 | |||||||
chr12:30972064 | T | C | 3 | a0001c0001t0002g0233 a0001c0001t0004g0277 a0001c0001t0009g0271 |
3 | HG00733.hp2 HG01192.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.277-6497T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30972064 | |||||||
chr12:30972768 | C | T | 1 | a0002c0002t0001g0041 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.277-5793C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30972768 | |||||||
chr12:30972795 | C | T | 15 | a0003c0003t0001g0114 a0003c0003t0003g0080 a0003c0003t0005g0056 others(12): Show |
15 | HG00673.hp1 HG02132.hp1 HG02683.hp1 others(12): Show |
intron_variant | MODIFIER | c.277-5766C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30972795 | |||||||
chr12:30972807 | G | A | 2 | a0001c0001t0019g0385 a0001c0001t0019g0386 |
2 | NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.277-5754G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30972807 | |||||||
chr12:30972899 | G | A | 77 | a0001c0001t0001g0101 a0001c0001t0001g0257 a0001c0001t0001g0340 others(74): Show |
78 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.277-5662G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30972899 | |||||||
chr12:30972910 | C | T | 1 | a0002c0004t0005g0246 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.277-5651C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30972910 | |||||||
chr12:30972916 | G | A | 2 | a0001c0001t0001g0022 a0002c0002t0018g0201 |
2 | HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.277-5645G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30972916 | |||||||
chr12:30972997 | C | T | 14 | a0001c0001t0020g0026 a0002c0002t0001g0142 a0002c0002t0005g0130 others(11): Show |
15 | HG00438.hp2 HG02080.hp2 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.277-5564C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30972997 | |||||||
chr12:30973055 | T | C | 1 | a0002c0002t0001g0142 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.277-5506T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30973055 | |||||||
chr12:30973085 | C | T | 1 | a0001c0001t0002g0123 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.277-5476C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30973085 | |||||||
chr12:30973248 | G | A | 1 | a0002c0002t0004g0098 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.277-5313G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30973248 | |||||||
chr12:30973280 | T | A | 2 | a0001c0001t0050g0177 a0002c0002t0004g0295 |
2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.277-5281T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30973280 | |||||||
chr12:30973305 | C | T | 16 | a0001c0001t0001g0045 a0001c0001t0001g0154 a0001c0001t0001g0169 others(13): Show |
16 | HG00558.hp2 HG01099.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.277-5256C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30973305 | |||||||
chr12:30973499 | G | A | 1 | a0001c0001t0010g0127 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.277-5062G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30973499 | |||||||
chr12:30973524 | C | T | 8 | a0001c0001t0014g0366 a0001c0001t0014g0384 a0001c0001t0050g0177 others(5): Show |
9 | HG02622.hp1 HG02886.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.277-5037C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30973524 | |||||||
chr12:30973590 | T | TG | 5 | a0001c0001t0003g0100 a0001c0001t0008g0095 a0001c0001t0011g0099 others(2): Show |
5 | HG02148.hp2 NA18998.hp1 NA19078.hp1 others(2): Show |
intron_variant | MODIFIER | c.277-4967dupG | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30973590 | ||||||
chr12:30973667 | C | T | 3 | a0002c0002t0004g0023 a0002c0002t0030g0308 a0002c0004t0017g0005 |
4 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.277-4894C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30973667 | |||||||
chr12:30973745 | T | C | 84 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0088 others(81): Show |
85 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.277-4816T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30973745 | |||||||
chr12:30973860 | C | T | 3 | a0001c0001t0001g0197 a0001c0001t0001g0203 a0001c0001t0018g0350 |
3 | HG03098.hp1 HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.277-4701C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30973860 | |||||||
chr12:30973982 | G | C | 3 | a0001c0001t0010g0209 a0001c0001t0031g0104 a0001c0001t0031g0207 |
3 | HG01928.hp2 HG01943.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.277-4579G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30973982 | |||||||
chr12:30974016 | C | T | 2 | a0001c0001t0025g0205 a0001c0001t0025g0219 |
2 | HG01123.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.277-4545C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974016 | |||||||
chr12:30974164 | C | T | 50 | a0001c0001t0001g0044 a0001c0001t0001g0059 a0001c0001t0001g0082 others(47): Show |
51 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.277-4397C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974164 | |||||||
chr12:30974170 | C | T | 51 | a0001c0001t0001g0044 a0001c0001t0001g0059 a0001c0001t0001g0082 others(48): Show |
52 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.277-4391C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974170 | |||||||
chr12:30974225 | A | G | 83 | a0001c0001t0001g0197 a0001c0001t0001g0203 a0001c0001t0001g0349 others(80): Show |
84 | HG00140.hp1 HG00642.hp2 HG00738.hp2 others(81): Show |
intron_variant | MODIFIER | c.277-4336A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974225 | |||||||
chr12:30974228 | C | T | 14 | a0002c0002t0001g0142 a0002c0002t0003g0121 a0002c0002t0005g0130 others(11): Show |
15 | HG00438.hp2 HG02080.hp2 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.277-4333C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974228 | |||||||
chr12:30974229 | G | A | 14 | a0001c0001t0024g0180 a0001c0001t0028g0181 a0001c0001t0028g0316 others(11): Show |
15 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.277-4332G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974229 | |||||||
chr12:30974256 | G | A | 3 | a0002c0002t0004g0318 a0002c0002t0026g0281 a0002c0002t0045g0188 |
3 | HG02886.hp2 HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.277-4305G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974256 | |||||||
chr12:30974309 | A | G | 65 | a0001c0001t0001g0101 a0001c0001t0001g0112 a0001c0001t0002g0051 others(62): Show |
66 | HG00544.hp2 HG00558.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.277-4252A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974309 | |||||||
chr12:30974336 | G | A | 1 | a0001c0001t0011g0067 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.277-4225G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974336 | |||||||
chr12:30974380 | C | T | 3 | a0002c0005t0004g0001 a0002c0005t0004g0359 a0008c0015t0019g0001 |
4 | HG02145.hp2 HG02280.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.277-4181C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974380 | |||||||
chr12:30974385 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.277-4176C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974385 | |||||||
chr12:30974559 | A | G | 1 | a0001c0001t0004g0081 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.277-4002A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974559 | |||||||
chr12:30974592 | G | A | 2 | a0001c0001t0005g0301 a0001c0001t0017g0302 |
2 | HG03710.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.277-3969G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974592 | |||||||
chr12:30974598 | A | G | 6 | a0001c0001t0001g0349 a0001c0001t0001g0351 a0001c0001t0004g0011 others(3): Show |
6 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.277-3963A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974598 | |||||||
chr12:30974718 | G | A | 1 | a0002c0002t0004g0239 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.277-3843G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974718 | |||||||
chr12:30974786 | G | A | 1 | a0002c0002t0015g0382 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.277-3775G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974786 | |||||||
chr12:30974809 | C | T | 1 | a0001c0001t0002g0360 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.277-3752C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974809 | |||||||
chr12:30974823 | A | G | 1 | a0002c0002t0001g0236 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.277-3738A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974823 | |||||||
chr12:30974824 | G | A | 1 | a0002c0002t0001g0236 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.277-3737G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974824 | |||||||
chr12:30974865 | G | A | 1 | a0002c0002t0046g0310 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.277-3696G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974865 | |||||||
chr12:30974909 | C | T | 1 | a0010c0012t0049g0248 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.277-3652C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974909 | |||||||
chr12:30974986 | C | T | 2 | a0001c0001t0002g0371 a0001c0001t0002g0372 |
2 | HG00438.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.277-3575C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974986 | |||||||
chr12:30975081 | G | A | 63 | a0001c0001t0001g0257 a0001c0001t0001g0288 a0001c0001t0001g0340 others(60): Show |
64 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.277-3480G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975081 | |||||||
chr12:30975155 | G | A | 1 | a0002c0002t0038g0194 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.277-3406G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975155 | |||||||
chr12:30975164 | G | A | 1 | a0002c0002t0001g0120 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.277-3397G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975164 | |||||||
chr12:30975397 | G | A | 1 | a0001c0001t0034g0228 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.277-3164G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975397 | |||||||
chr12:30975493 | G | A | 1 | a0001c0001t0028g0181 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.277-3068G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975493 | |||||||
chr12:30975496 | A | G | 1 | a0001c0001t0002g0345 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.277-3065A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975496 | |||||||
chr12:30975656 | C | T | 3 | a0001c0001t0019g0385 a0001c0001t0019g0386 a0009c0014t0019g0125 |
3 | HG03486.hp1 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.277-2905C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975656 | |||||||
chr12:30975658 | A | C | 46 | a0001c0001t0001g0044 a0001c0001t0001g0059 a0001c0001t0001g0082 others(43): Show |
47 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.277-2903A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975658 | |||||||
chr12:30975663 | G | A | 1 | a0002c0002t0001g0071 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.277-2898G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975663 | |||||||
chr12:30975671 | T | C | 372 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(369): Show |
377 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.277-2890T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975671 | |||||||
chr12:30975742 | C | G | 7 | a0001c0001t0001g0109 a0001c0001t0002g0348 a0001c0001t0012g0034 others(4): Show |
7 | HG02083.hp1 HG02135.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.277-2819C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975742 | |||||||
chr12:30975884 | G | A | 1 | a0002c0002t0001g0236 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.277-2677G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975884 | |||||||
chr12:30975885 | A | G | 1 | a0002c0002t0001g0236 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.277-2676A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975885 | |||||||
chr12:30975886 | G | C | 1 | a0002c0002t0001g0236 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.277-2675G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975886 | |||||||
chr12:30975913 | T | C | 2 | a0001c0001t0002g0220 a0001c0001t0002g0269 |
2 | HG00280.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.277-2648T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975913 | |||||||
chr12:30975985 | G | A | 64 | a0001c0001t0001g0257 a0001c0001t0001g0288 a0001c0001t0001g0340 others(61): Show |
65 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.277-2576G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975985 | |||||||
chr12:30976011 | A | G | 132 | a0001c0001t0001g0197 a0001c0001t0001g0203 a0001c0001t0001g0257 others(129): Show |
134 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.277-2550A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976011 | |||||||
chr12:30976024 | G | A | 2 | a0001c0001t0003g0266 a0005c0011t0002g0260 |
2 | HG00423.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.277-2537G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976024 | |||||||
chr12:30976037 | G | C | 14 | a0001c0001t0001g0197 a0001c0001t0001g0203 a0001c0001t0001g0349 others(11): Show |
14 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.277-2524G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976037 | |||||||
chr12:30976053 | G | A | 120 | a0001c0001t0001g0022 a0001c0001t0001g0045 a0001c0001t0001g0103 others(117): Show |
121 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.277-2508G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976053 | |||||||
chr12:30976195 | G | A | 21 | a0001c0001t0002g0373 a0001c0001t0004g0186 a0001c0001t0005g0313 others(18): Show |
21 | HG01167.hp2 HG01169.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.277-2366G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976195 | |||||||
chr12:30976232 | G | A | 1 | a0002c0002t0072g0160 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.277-2329G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976232 | |||||||
chr12:30976240 | C | T | 43 | a0001c0001t0001g0022 a0001c0001t0001g0045 a0001c0001t0001g0103 others(40): Show |
43 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.277-2321C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976240 | |||||||
chr12:30976245 | T | G | 1 | a0002c0002t0026g0281 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.277-2316T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976245 | |||||||
chr12:30976302 | C | T | 1 | a0001c0001t0037g0016 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.277-2259C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976302 | |||||||
chr12:30976424 | G | T | 15 | a0002c0002t0001g0142 a0002c0002t0003g0121 a0002c0002t0005g0130 others(12): Show |
16 | HG00438.hp2 HG02080.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.277-2137G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976424 | |||||||
chr12:30976509 | A | G | 374 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(371): Show |
379 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(376): Show |
intron_variant | MODIFIER | c.277-2052A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976509 | |||||||
chr12:30976636 | A | G | 1 | a0001c0001t0001g0022 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.277-1925A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976636 | |||||||
chr12:30976658 | C | T | 295 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(292): Show |
299 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(296): Show |
intron_variant | MODIFIER | c.277-1903C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976658 | |||||||
chr12:30976659 | A | G | 374 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(371): Show |
379 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(376): Show |
intron_variant | MODIFIER | c.277-1902A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976659 | |||||||
chr12:30976689 | G | A | 6 | a0001c0001t0002g0360 a0001c0001t0022g0053 a0001c0001t0055g0356 others(3): Show |
6 | HG02145.hp1 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.277-1872G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976689 | |||||||
chr12:30976740 | G | A | 4 | a0001c0001t0001g0288 a0001c0001t0002g0286 a0001c0001t0002g0296 others(1): Show |
4 | HG00735.hp1 HG03491.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.277-1821G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976740 | |||||||
chr12:30976961 | T | C | 75 | a0001c0001t0001g0101 a0001c0001t0001g0112 a0001c0001t0001g0197 others(72): Show |
76 | HG00544.hp2 HG00558.hp1 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.277-1600T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976961 | |||||||
chr12:30976969 | G | A | 1 | a0001c0001t0002g0296 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.277-1592G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976969 | |||||||
chr12:30977098 | A | T | 2 | a0001c0001t0022g0053 a0001c0001t0055g0356 |
2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.277-1463A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977098 | |||||||
chr12:30977164 | G | A | 1 | a0002c0002t0071g0153 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.277-1397G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977164 | |||||||
chr12:30977232 | A | G | 1 | a0002c0002t0045g0188 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.277-1329A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977232 | |||||||
chr12:30977291 | G | A | 1 | a0002c0002t0026g0299 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.277-1270G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977291 | |||||||
chr12:30977296 | G | GCCGCCAC | 8 | a0001c0001t0002g0373 a0001c0001t0005g0313 a0001c0001t0005g0374 others(5): Show |
8 | HG01257.hp2 HG01258.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.277-1256_277-1250d others(9): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30977296 | ||||||
chr12:30977314 | A | G | 36 | a0001c0001t0002g0123 a0001c0001t0002g0357 a0001c0001t0005g0122 others(33): Show |
37 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.277-1247A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977314 | |||||||
chr12:30977319 | C | T | 375 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(372): Show |
380 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(377): Show |
intron_variant | MODIFIER | c.277-1242C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977319 | |||||||
chr12:30977370 | C | T | 1 | a0002c0002t0001g0037 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.277-1191C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977370 | |||||||
chr12:30977406 | C | T | 1 | a0002c0002t0001g0070 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.277-1155C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977406 | |||||||
chr12:30977415 | C | T | 213 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(210): Show |
216 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.277-1146C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977415 | |||||||
chr12:30977440 | G | A | 1 | a0002c0002t0026g0027 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.277-1121G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977440 | |||||||
chr12:30977472 | G | T | 1 | a0001c0001t0058g0332 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.277-1089G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977472 | |||||||
chr12:30977502 | C | A | 9 | a0002c0002t0002g0174 a0002c0002t0002g0175 a0002c0002t0002g0184 others(6): Show |
9 | HG01167.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.277-1059C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977502 | |||||||
chr12:30977506 | C | T | 1 | a0002c0002t0044g0039 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.277-1055C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977506 | |||||||
chr12:30977532 | G | GCTCCCCC others(3): Show |
8 | a0001c0001t0002g0373 a0001c0001t0005g0313 a0001c0001t0005g0374 others(5): Show |
8 | HG01257.hp2 HG01258.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.277-1024_277-1015d others(12): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30977532 | ||||||
chr12:30977566 | C | T | 118 | a0001c0001t0001g0022 a0001c0001t0001g0045 a0001c0001t0001g0103 others(115): Show |
119 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.277-995C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977566 | |||||||
chr12:30977745 | G | A | 1 | a0001c0001t0010g0127 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.277-816G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977745 | |||||||
chr12:30977868 | T | C | 1 | a0002c0002t0038g0194 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.277-693T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977868 | |||||||
chr12:30977897 | A | C | 1 | a0001c0001t0005g0378 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.277-664A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977897 | |||||||
chr12:30977937 | C | G | 9 | a0002c0002t0002g0174 a0002c0002t0002g0175 a0002c0002t0002g0184 others(6): Show |
9 | HG01167.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.277-624C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977937 | |||||||
chr12:30977969 | G | A | 8 | a0001c0001t0002g0373 a0001c0001t0005g0313 a0001c0001t0005g0374 others(5): Show |
8 | HG01257.hp2 HG01258.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.277-592G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977969 | |||||||
chr12:30978047 | G | A | 1 | a0002c0004t0001g0234 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.277-514G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30978047 | |||||||
chr12:30978104 | T | C | 1 | a0002c0002t0002g0030 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.277-457T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30978104 | |||||||
chr12:30978137 | G | A | 1 | a0010c0012t0049g0248 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.277-424G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30978137 | |||||||
chr12:30978137 | G | C | 72 | a0001c0001t0001g0101 a0001c0001t0001g0109 a0001c0001t0001g0112 others(69): Show |
73 | HG00544.hp2 HG00558.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.277-424G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30978137 | |||||||
chr12:30978277 | G | C | 1 | a0001c0001t0004g0186 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.277-284G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30978277 | |||||||
chr12:30978388 | G | C | 1 | a0010c0012t0049g0248 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.277-173G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30978388 | |||||||
chr12:30978414 | C | T | 1 | a0007c0013t0011g0338 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.277-147C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30978414 | |||||||
chr12:30978689 | G | A | 1 | a0002c0004t0014g0195 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.351+54G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30978689 | |||||||
chr12:30978777 | T | C | 346 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(343): Show |
350 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.351+142T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30978777 | |||||||
chr12:30978782 | G | A | 3 | a0002c0002t0014g0279 a0002c0002t0021g0036 a0002c0002t0044g0039 |
3 | HG02723.hp2 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.351+147G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30978782 | |||||||
chr12:30978863 | C | T | 23 | a0001c0001t0001g0044 a0001c0001t0001g0059 a0001c0001t0001g0082 others(20): Show |
23 | HG00408.hp2 HG00438.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.351+228C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30978863 | |||||||
chr12:30978918 | G | T | 1 | a0010c0012t0049g0248 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.351+283G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30978918 | |||||||
chr12:30978941 | A | G | 15 | a0002c0002t0001g0142 a0002c0002t0003g0121 a0002c0002t0005g0130 others(12): Show |
16 | HG00438.hp2 HG02080.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.351+306A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30978941 | |||||||
chr12:30979081 | G | A | 1 | a0002c0002t0007g0251 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.351+446G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30979081 | |||||||
chr12:30979089 | G | A | 54 | a0001c0001t0001g0109 a0001c0001t0001g0112 a0001c0001t0002g0051 others(51): Show |
55 | HG00544.hp2 HG00558.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.351+454G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30979089 | |||||||
chr12:30979125 | C | G | 30 | a0001c0001t0001g0044 a0001c0001t0001g0059 a0001c0001t0001g0082 others(27): Show |
30 | HG00408.hp2 HG00438.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.352-441C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30979125 | |||||||
chr12:30979131 | G | A | 63 | a0001c0001t0001g0257 a0001c0001t0001g0288 a0001c0001t0001g0340 others(60): Show |
64 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.352-435G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30979131 | |||||||
chr12:30979248 | T | G | 2 | a0002c0002t0001g0083 a0002c0002t0001g0084 |
2 | NA18946.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.352-318T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30979248 | |||||||
chr12:30979308 | T | A | 64 | a0001c0001t0001g0257 a0001c0001t0001g0288 a0001c0001t0001g0340 others(61): Show |
65 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.352-258T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30979308 | |||||||
chr12:30979356 | G | A | 1 | a0001c0001t0014g0366 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.352-210G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30979356 | |||||||
chr12:30979422 | T | TA | 30 | a0001c0001t0001g0044 a0001c0001t0001g0059 a0001c0001t0001g0082 others(27): Show |
30 | HG00408.hp2 HG00438.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.352-143dupA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 30979422 | ||||||
chr12:30979450 | C | A | 12 | a0001c0001t0004g0186 a0001c0001t0015g0363 a0001c0001t0015g0364 others(9): Show |
12 | HG01167.hp2 HG01169.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.352-116C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30979450 | |||||||
chr12:30979462 | C | T | 3 | a0001c0001t0015g0363 a0001c0001t0015g0364 a0001c0001t0015g0367 |
3 | HG01192.hp1 HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.352-104C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30979462 | |||||||
chr12:30979484 | G | T | 2 | a0001c0001t0001g0197 a0001c0001t0001g0203 |
2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.352-82G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30979484 | |||||||
chr12:30979526 | C | T | 2 | a0001c0007t0013g0243 a0001c0007t0013g0249 |
2 | HG02615.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.352-40C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30979526 | |||||||
chr12:30979544 | A | C | 358 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(355): Show |
362 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.352-22A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30979544 | |||||||
chr12:30979549 | G | C | 1 | a0001c0001t0001g0257 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.352-17G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30979549 | |||||||
chr12:30979725 | G | A | 9 | a0002c0002t0002g0174 a0002c0002t0002g0175 a0002c0002t0002g0184 others(6): Show |
9 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.456+55G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30979725 | |||||||
chr12:30979940 | G | T | 155 | a0001c0001t0001g0101 a0001c0001t0001g0109 a0001c0001t0001g0112 others(152): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.456+270G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30979940 | |||||||
chr12:30979957 | G | T | 12 | a0001c0001t0002g0360 a0002c0002t0002g0174 a0002c0002t0002g0175 others(9): Show |
12 | HG01167.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.456+287G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30979957 | |||||||
chr12:30979967 | C | T | 4 | a0001c0001t0015g0363 a0001c0001t0015g0364 a0001c0001t0015g0365 others(1): Show |
4 | HG01192.hp1 HG02615.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.456+297C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30979967 | |||||||
chr12:30980039 | C | T | 73 | a0001c0001t0043g0317 a0002c0002t0001g0033 a0002c0002t0001g0037 others(70): Show |
74 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.456+369C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980039 | |||||||
chr12:30980108 | C | T | 170 | a0001c0001t0001g0022 a0001c0001t0001g0045 a0001c0001t0001g0101 others(167): Show |
173 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(170): Show |
intron_variant | MODIFIER | c.456+438C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980108 | |||||||
chr12:30980130 | C | T | 165 | a0001c0001t0001g0022 a0001c0001t0001g0045 a0001c0001t0001g0101 others(162): Show |
167 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(164): Show |
intron_variant | MODIFIER | c.456+460C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980130 | |||||||
chr12:30980204 | C | A | 11 | a0002c0002t0002g0174 a0002c0002t0002g0175 a0002c0002t0002g0184 others(8): Show |
11 | HG01167.hp1 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.456+534C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980204 | |||||||
chr12:30980287 | C | T | 1 | a0002c0002t0046g0310 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.456+617C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980287 | |||||||
chr12:30980316 | T | C | 374 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(371): Show |
379 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(376): Show |
intron_variant | MODIFIER | c.456+646T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980316 | |||||||
chr12:30980484 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.456+814C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980484 | |||||||
chr12:30980485 | G | A | 223 | a0001c0001t0001g0022 a0001c0001t0001g0045 a0001c0001t0001g0101 others(220): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.456+815G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980485 | |||||||
chr12:30980552 | C | T | 15 | a0002c0002t0001g0142 a0002c0002t0003g0121 a0002c0002t0005g0130 others(12): Show |
16 | HG00438.hp2 HG02080.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.456+882C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980552 | |||||||
chr12:30980565 | C | T | 1 | a0002c0002t0046g0310 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.456+895C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980565 | |||||||
chr12:30980590 | G | A | 1 | a0001c0001t0005g0301 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.456+920G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980590 | |||||||
chr12:30980719 | T | G | 258 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(255): Show |
261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.456+1049T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980719 | |||||||
chr12:30980720 | C | A | 258 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(255): Show |
261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.456+1050C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980720 | |||||||
chr12:30980729 | T | C | 224 | a0001c0001t0001g0022 a0001c0001t0001g0045 a0001c0001t0001g0101 others(221): Show |
227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.456+1059T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980729 | |||||||
chr12:30980814 | A | G | 1 | a0002c0002t0024g0155 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.456+1144A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980814 | |||||||
chr12:30980885 | C | T | 222 | a0001c0001t0001g0022 a0001c0001t0001g0045 a0001c0001t0001g0101 others(219): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.456+1215C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980885 | |||||||
chr12:30980961 | G | A | 1 | a0001c0001t0020g0026 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.456+1291G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980961 | |||||||
chr12:30980966 | G | A | 6 | a0001c0001t0001g0109 a0001c0001t0001g0112 a0001c0001t0002g0348 others(3): Show |
6 | HG00673.hp1 HG02602.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.456+1296G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980966 | |||||||
chr12:30980993 | CAG | C | 14 | a0001c0001t0002g0373 a0001c0001t0005g0106 a0001c0001t0005g0118 others(11): Show |
14 | HG01257.hp2 HG01258.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.456+1325_456+1326d others(4): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 30980993 | ||||||
chr12:30981040 | G | A | 1 | a0001c0001t0008g0092 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.456+1370G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981040 | |||||||
chr12:30981128 | A | G | 268 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(265): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.457-1404A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981128 | |||||||
chr12:30981133 | C | T | 84 | a0001c0001t0043g0317 a0002c0002t0001g0033 a0002c0002t0001g0037 others(81): Show |
85 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.457-1399C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981133 | |||||||
chr12:30981167 | G | C | 3 | a0001c0001t0004g0008 a0001c0001t0014g0366 a0001c0001t0014g0384 |
3 | HG02896.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.457-1365G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981167 | |||||||
chr12:30981208 | A | G | 369 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(366): Show |
373 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.457-1324A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981208 | |||||||
chr12:30981230 | G | A | 219 | a0001c0001t0001g0022 a0001c0001t0001g0045 a0001c0001t0001g0101 others(216): Show |
221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.457-1302G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981230 | |||||||
chr12:30981236 | G | T | 73 | a0001c0001t0043g0317 a0002c0002t0001g0033 a0002c0002t0001g0037 others(70): Show |
74 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.457-1296G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981236 | |||||||
chr12:30981251 | C | T | 1 | a0002c0002t0025g0139 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.457-1281C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981251 | |||||||
chr12:30981367 | T | C | 254 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(251): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.457-1165T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981367 | |||||||
chr12:30981501 | CAG | C | 3 | a0001c0001t0010g0209 a0001c0001t0031g0104 a0001c0001t0031g0207 |
3 | HG01928.hp2 HG01943.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.457-1028_457-1027d others(4): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 30981501 | ||||||
chr12:30981536 | CCTT | C | 11 | a0002c0002t0002g0174 a0002c0002t0002g0175 a0002c0002t0002g0184 others(8): Show |
11 | HG01167.hp1 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.457-993_457-991del others(3): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 30981536 | ||||||
chr12:30981546 | G | A | 3 | a0001c0001t0004g0008 a0001c0001t0014g0366 a0001c0001t0014g0384 |
3 | HG02896.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.457-986G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981546 | |||||||
chr12:30981573 | GTCATGCT others(4): Show |
G | 48 | a0002c0002t0001g0033 a0002c0002t0001g0037 a0002c0002t0001g0038 others(45): Show |
48 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.457-956_457-946del others(11): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 30981573 | ||||||
chr12:30981579 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.457-953C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981579 | |||||||
chr12:30981623 | C | T | 1 | a0002c0002t0004g0239 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.457-909C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981623 | |||||||
chr12:30981691 | C | T | 370 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(367): Show |
374 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(371): Show |
intron_variant | MODIFIER | c.457-841C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981691 | |||||||
chr12:30981696 | G | A | 1 | a0002c0002t0015g0382 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.457-836G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981696 | |||||||
chr12:30981767 | T | C | 1 | a0001c0001t0014g0366 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.457-765T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981767 | |||||||
chr12:30981897 | C | T | 1 | a0002c0002t0030g0308 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.457-635C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981897 | |||||||
chr12:30981974 | C | T | 1 | a0002c0004t0017g0152 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.457-558C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981974 | |||||||
chr12:30982019 | C | T | 2 | a0001c0001t0029g0192 a0001c0001t0029g0193 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.457-513C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30982019 | |||||||
chr12:30982244 | G | A | 36 | a0001c0001t0001g0044 a0001c0001t0001g0059 a0001c0001t0001g0082 others(33): Show |
36 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.457-288G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30982244 | |||||||
chr12:30982250 | C | T | 2 | a0001c0001t0020g0019 a0001c0001t0020g0020 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.457-282C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30982250 | |||||||
chr12:30982469 | C | G | 1 | a0001c0001t0005g0122 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.457-63C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30982469 | |||||||
chr12:30982483 | C | A | 51 | a0001c0001t0001g0044 a0001c0001t0001g0059 a0001c0001t0001g0082 others(48): Show |
51 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.457-49C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30982483 | |||||||
chr12:30982487 | C | T | 6 | a0001c0001t0001g0109 a0001c0001t0001g0112 a0001c0001t0002g0348 others(3): Show |
6 | HG00673.hp1 HG02602.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.457-45C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30982487 | |||||||
chr12:30982740 | C | T | 1 | a0002c0004t0052g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.615+50C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/7 | chr12 | 30982740 | |||||||
chr12:30982778 | G | A | 1 | a0001c0001t0037g0016 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.615+88G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/7 | chr12 | 30982778 | |||||||
chr12:30982781 | T | C | 2 | a0001c0007t0013g0243 a0001c0007t0013g0249 |
2 | HG02615.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.615+91T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/7 | chr12 | 30982781 | |||||||
chr12:30982814 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0235 |
2 | NA18945.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.615+124C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/7 | chr12 | 30982814 | |||||||
chr12:30982832 | G | T | 1 | a0012c0017t0011g0171 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.615+142G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/7 | chr12 | 30982832 | |||||||
chr12:30982871 | T | C | 20 | a0002c0002t0001g0142 a0002c0002t0003g0121 a0002c0002t0005g0130 others(17): Show |
21 | HG00438.hp2 HG02080.hp2 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.615+181T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/7 | chr12 | 30982871 | |||||||
chr12:30982970 | A | T | 251 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(248): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.616-94A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/7 | chr12 | 30982970 | |||||||
chr12:30982990 | G | A | 33 | a0001c0001t0001g0044 a0001c0001t0001g0059 a0001c0001t0001g0082 others(30): Show |
33 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.616-74G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/7 | chr12 | 30982990 | |||||||
chr12:30983000 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0022g0179 |
2 | HG02055.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.616-64G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/7 | chr12 | 30983000 | |||||||
chr12:30983165 | G | A | 2 | a0001c0001t0003g0043 a0001c0001t0003g0085 |
2 | HG00558.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.702+15G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983165 | |||||||
chr12:30983217 | C | T | 1 | a0001c0001t0005g0118 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.702+67C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983217 | |||||||
chr12:30983259 | C | A | 1 | a0002c0004t0005g0246 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.702+109C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983259 | |||||||
chr12:30983261 | C | G | 1 | a0002c0004t0005g0246 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.702+111C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983261 | |||||||
chr12:30983262 | G | C | 1 | a0002c0004t0005g0246 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.702+112G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983262 | |||||||
chr12:30983292 | C | T | 1 | a0002c0004t0005g0246 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.702+142C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983292 | |||||||
chr12:30983321 | C | T | 84 | a0002c0002t0001g0033 a0002c0002t0001g0037 a0002c0002t0001g0038 others(81): Show |
85 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.702+171C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983321 | |||||||
chr12:30983384 | A | G | 37 | a0001c0001t0001g0044 a0001c0001t0001g0059 a0001c0001t0001g0082 others(34): Show |
37 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.702+234A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983384 | |||||||
chr12:30983433 | C | A | 48 | a0002c0002t0001g0033 a0002c0002t0001g0037 a0002c0002t0001g0038 others(45): Show |
48 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.702+283C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983433 | |||||||
chr12:30983480 | C | T | 34 | a0001c0001t0002g0373 a0001c0001t0005g0106 a0001c0001t0005g0118 others(31): Show |
35 | HG00438.hp2 HG01257.hp2 HG01258.hp2 others(32): Show |
intron_variant | MODIFIER | c.702+330C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983480 | |||||||
chr12:30983521 | A | G | 1 | a0010c0012t0049g0248 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.702+371A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983521 | |||||||
chr12:30983755 | C | T | 3 | a0001c0001t0005g0374 a0001c0001t0005g0375 a0001c0001t0005g0377 |
3 | HG01257.hp2 HG01258.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.702+605C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983755 | |||||||
chr12:30983763 | T | C | 3 | a0001c0001t0004g0008 a0001c0001t0014g0366 a0001c0001t0014g0384 |
3 | HG02896.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.702+613T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983763 | |||||||
chr12:30983815 | A | T | 14 | a0001c0001t0001g0197 a0001c0001t0001g0203 a0001c0001t0001g0349 others(11): Show |
14 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.702+665A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983815 | |||||||
chr12:30983825 | T | A | 37 | a0001c0001t0001g0044 a0001c0001t0001g0059 a0001c0001t0001g0082 others(34): Show |
37 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.702+675T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983825 | |||||||
chr12:30983898 | T | C | 1 | a0001c0001t0002g0360 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.702+748T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983898 | |||||||
chr12:30983936 | A | T | 1 | a0002c0004t0005g0246 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.702+786A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983936 | |||||||
chr12:30983983 | T | G | 3 | a0001c0001t0004g0008 a0001c0001t0014g0366 a0001c0001t0014g0384 |
3 | HG02896.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.702+833T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983983 | |||||||
chr12:30984068 | G | A | 1 | a0002c0002t0001g0199 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.702+918G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984068 | |||||||
chr12:30984089 | G | T | 1 | a0002c0004t0005g0246 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.702+939G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984089 | |||||||
chr12:30984094 | G | A | 214 | a0001c0001t0001g0022 a0001c0001t0001g0045 a0001c0001t0001g0101 others(211): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.702+944G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984094 | |||||||
chr12:30984116 | C | T | 73 | a0001c0001t0001g0022 a0001c0001t0001g0045 a0001c0001t0001g0103 others(70): Show |
73 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.702+966C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984116 | |||||||
chr12:30984123 | G | A | 20 | a0002c0002t0001g0142 a0002c0002t0003g0121 a0002c0002t0005g0130 others(17): Show |
21 | HG00438.hp2 HG02080.hp2 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.702+973G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984123 | |||||||
chr12:30984124 | C | T | 8 | a0001c0001t0003g0096 a0001c0001t0003g0100 a0001c0001t0003g0110 others(5): Show |
8 | HG04184.hp1 NA18956.hp1 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.702+974C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984124 | |||||||
chr12:30984132 | C | T | 50 | a0001c0001t0001g0109 a0001c0001t0001g0112 a0001c0001t0002g0051 others(47): Show |
51 | HG00544.hp2 HG00558.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.702+982C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984132 | |||||||
chr12:30984205 | G | A | 214 | a0001c0001t0001g0022 a0001c0001t0001g0045 a0001c0001t0001g0101 others(211): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.702+1055G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984205 | |||||||
chr12:30984261 | T | G | 252 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(249): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.702+1111T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984261 | |||||||
chr12:30984377 | C | A | 29 | a0001c0001t0002g0123 a0001c0001t0002g0357 a0001c0001t0005g0301 others(26): Show |
29 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.702+1227C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984377 | |||||||
chr12:30984544 | G | A | 1 | a0001c0001t0005g0377 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.702+1394G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984544 | |||||||
chr12:30984552 | C | CT | 72 | a0001c0001t0002g0051 a0001c0001t0002g0360 a0001c0001t0003g0096 others(69): Show |
72 | HG00642.hp2 HG00673.hp2 HG00741.hp1 others(69): Show |
intron_variant | MODIFIER | c.702+1426dupT | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 30984552 | ||||||
chr12:30984552 | C | CTT | 37 | a0001c0001t0001g0113 a0001c0001t0001g0240 a0001c0001t0001g0262 others(34): Show |
38 | HG00438.hp2 HG02015.hp1 HG02015.hp2 others(35): Show |
intron_variant | MODIFIER | c.702+1425_702+1426d others(4): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 30984552 | ||||||
chr12:30984552 | C | CTTT | 49 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(46): Show |
49 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.702+1424_702+1426d others(5): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 30984552 | ||||||
chr12:30984552 | C | CTTTT | 21 | a0001c0001t0001g0059 a0001c0001t0001g0146 a0001c0001t0001g0292 others(18): Show |
21 | HG00438.hp1 HG00673.hp1 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.702+1423_702+1426d others(6): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 30984552 | ||||||
chr12:30984552 | CT | C | 54 | a0001c0001t0001g0288 a0001c0001t0001g0340 a0001c0001t0002g0003 others(51): Show |
55 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.702+1426delT | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 30984552 | ||||||
chr12:30984552 | CTTT | C | 11 | a0002c0002t0002g0174 a0002c0002t0002g0175 a0002c0002t0002g0184 others(8): Show |
11 | HG01167.hp1 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.702+1424_702+1426d others(5): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 30984552 | ||||||
chr12:30984833 | T | C | 370 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(367): Show |
374 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(371): Show |
intron_variant | MODIFIER | c.702+1683T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984833 | |||||||
chr12:30984873 | C | T | 1 | a0010c0012t0049g0248 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.702+1723C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984873 | |||||||
chr12:30984907 | A | C | 1 | a0001c0001t0001g0115 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.702+1757A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984907 | |||||||
chr12:30984967 | C | T | 43 | a0001c0001t0001g0022 a0001c0001t0001g0045 a0001c0001t0001g0103 others(40): Show |
43 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.702+1817C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984967 | |||||||
chr12:30984968 | C | T | 19 | a0002c0002t0001g0142 a0002c0002t0003g0121 a0002c0002t0005g0130 others(16): Show |
20 | HG00438.hp2 HG02080.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.702+1818C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984968 | |||||||
chr12:30985070 | T | A | 1 | a0001c0001t0003g0320 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.702+1920T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30985070 | |||||||
chr12:30985132 | G | C | 20 | a0002c0002t0001g0142 a0002c0002t0003g0121 a0002c0002t0005g0130 others(17): Show |
21 | HG00438.hp2 HG02080.hp2 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.702+1982G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30985132 | |||||||
chr12:30985145 | C | T | 1 | a0002c0002t0018g0040 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.702+1995C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30985145 | |||||||
chr12:30985194 | C | G | 1 | a0001c0001t0055g0356 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.702+2044C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30985194 | |||||||
chr12:30985242 | T | C | 5 | a0001c0001t0001g0109 a0001c0001t0001g0112 a0001c0001t0002g0348 others(2): Show |
5 | HG02602.hp2 HG02683.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.702+2092T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30985242 | |||||||
chr12:30985383 | G | A | 220 | a0001c0001t0001g0022 a0001c0001t0001g0045 a0001c0001t0001g0103 others(217): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.702+2233G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30985383 | |||||||
chr12:30985522 | T | C | 1 | a0001c0001t0002g0360 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.702+2372T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30985522 | |||||||
chr12:30985662 | G | A | 4 | a0001c0001t0001g0197 a0001c0001t0001g0203 a0001c0001t0001g0354 others(1): Show |
4 | HG03130.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.702+2512G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30985662 | |||||||
chr12:30985777 | G | A | 1 | a0001c0001t0003g0225 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.702+2627G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30985777 | |||||||
chr12:30985874 | A | C | 368 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(365): Show |
372 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.702+2724A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30985874 | |||||||
chr12:30985932 | C | T | 1 | a0001c0001t0011g0067 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.702+2782C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30985932 | |||||||
chr12:30985999 | G | T | 2 | a0002c0002t0004g0182 a0002c0002t0004g0295 |
2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.702+2849G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30985999 | |||||||
chr12:30986282 | T | C | 1 | a0002c0002t0026g0281 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.702+3132T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30986282 | |||||||
chr12:30986325 | G | A | 14 | a0001c0001t0002g0373 a0001c0001t0005g0106 a0001c0001t0005g0118 others(11): Show |
14 | HG01257.hp2 HG01258.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.702+3175G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30986325 | |||||||
chr12:30986334 | C | T | 35 | a0001c0001t0001g0044 a0001c0001t0001g0059 a0001c0001t0001g0082 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.702+3184C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30986334 | |||||||
chr12:30986366 | T | C | 188 | a0001c0001t0001g0022 a0001c0001t0001g0045 a0001c0001t0001g0101 others(185): Show |
190 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.702+3216T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30986366 | |||||||
chr12:30986447 | T | C | 1 | a0001c0001t0002g0123 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.702+3297T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30986447 | |||||||
chr12:30986489 | C | T | 4 | a0002c0004t0014g0195 a0002c0005t0004g0001 a0002c0005t0004g0359 others(1): Show |
5 | HG00738.hp1 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.702+3339C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30986489 | |||||||
chr12:30986514 | G | C | 1 | a0002c0002t0005g0312 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.702+3364G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30986514 | |||||||
chr12:30986662 | C | T | 15 | a0001c0001t0002g0373 a0001c0001t0005g0106 a0001c0001t0005g0118 others(12): Show |
15 | HG01257.hp2 HG01258.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+3512C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30986662 | |||||||
chr12:30986751 | A | G | 86 | a0001c0001t0001g0044 a0001c0001t0001g0059 a0001c0001t0001g0082 others(83): Show |
87 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.702+3601A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30986751 | |||||||
chr12:30986759 | A | G | 1 | a0001c0001t0002g0357 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.702+3609A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30986759 | |||||||
chr12:30986784 | G | C | 15 | a0001c0001t0002g0373 a0001c0001t0005g0106 a0001c0001t0005g0118 others(12): Show |
15 | HG01257.hp2 HG01258.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+3634G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30986784 | |||||||
chr12:30986876 | G | A | 2 | a0001c0008t0001g0047 a0001c0008t0001g0048 |
2 | HG02083.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.702+3726G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30986876 | |||||||
chr12:30986892 | C | T | 1 | a0002c0002t0044g0039 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.702+3742C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30986892 | |||||||
chr12:30986968 | A | G | 3 | a0001c0001t0004g0008 a0001c0001t0014g0366 a0001c0001t0014g0384 |
3 | HG02896.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.702+3818A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30986968 | |||||||
chr12:30987030 | G | A | 15 | a0001c0001t0002g0373 a0001c0001t0005g0106 a0001c0001t0005g0118 others(12): Show |
15 | HG01257.hp2 HG01258.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+3880G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30987030 | |||||||
chr12:30987031 | T | C | 9 | a0002c0002t0002g0174 a0002c0002t0002g0175 a0002c0002t0002g0184 others(6): Show |
9 | HG01167.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.702+3881T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30987031 | |||||||
chr12:30987180 | G | A | 175 | a0001c0001t0001g0022 a0001c0001t0001g0045 a0001c0001t0001g0101 others(172): Show |
177 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.702+4030G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30987180 | |||||||
chr12:30987267 | C | T | 15 | a0001c0001t0002g0373 a0001c0001t0005g0106 a0001c0001t0005g0118 others(12): Show |
15 | HG01257.hp2 HG01258.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+4117C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30987267 | |||||||
chr12:30987272 | G | A | 4 | a0002c0002t0001g0070 a0002c0002t0001g0071 a0002c0002t0001g0075 others(1): Show |
4 | HG01943.hp1 NA18977.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+4122G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30987272 | |||||||
chr12:30987283 | G | C | 1 | a0001c0001t0004g0214 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.702+4133G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30987283 | |||||||
chr12:30987344 | C | A | 1 | a0001c0001t0002g0360 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.702+4194C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30987344 | |||||||
chr12:30987383 | T | C | 2 | a0002c0002t0012g0237 a0002c0002t0012g0381 |
2 | NA18945.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.702+4233T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30987383 | |||||||
chr12:30987623 | A | G | 1 | a0001c0001t0001g0245 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.703-4233A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30987623 | |||||||
chr12:30987688 | A | C | 1 | a0002c0002t0001g0083 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.703-4168A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30987688 | |||||||
chr12:30987861 | C | T | 1 | a0011c0009t0001g0057 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.703-3995C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30987861 | |||||||
chr12:30987910 | C | CA | 274 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(271): Show |
277 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(274): Show |
intron_variant | MODIFIER | c.703-3945dupA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 30987910 | ||||||
chr12:30987953 | A | G | 1 | a0001c0001t0040g0255 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.703-3903A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30987953 | |||||||
chr12:30987985 | C | T | 20 | a0002c0002t0001g0142 a0002c0002t0003g0121 a0002c0002t0005g0130 others(17): Show |
21 | HG00438.hp2 HG02080.hp2 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.703-3871C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30987985 | |||||||
chr12:30988075 | A | C | 1 | a0002c0002t0014g0124 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.703-3781A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30988075 | |||||||
chr12:30988141 | A | G | 3 | a0001c0001t0004g0008 a0001c0001t0014g0366 a0001c0001t0014g0384 |
3 | HG02896.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.703-3715A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30988141 | |||||||
chr12:30988210 | C | A | 3 | a0002c0002t0005g0130 a0002c0002t0005g0131 a0002c0002t0005g0143 |
3 | NA18953.hp1 NA18977.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.703-3646C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30988210 | |||||||
chr12:30988212 | A | C | 1 | a0001c0001t0005g0122 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.703-3644A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30988212 | |||||||
chr12:30988270 | T | C | 67 | a0001c0001t0001g0044 a0001c0001t0001g0059 a0001c0001t0001g0082 others(64): Show |
67 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.703-3586T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30988270 | |||||||
chr12:30988278 | T | C | 254 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(251): Show |
256 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.703-3578T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30988278 | |||||||
chr12:30988339 | C | G | 1 | a0001c0001t0014g0366 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.703-3517C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30988339 | |||||||
chr12:30988461 | C | T | 39 | a0001c0001t0001g0044 a0001c0001t0001g0059 a0001c0001t0001g0082 others(36): Show |
39 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.703-3395C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30988461 | |||||||
chr12:30988513 | C | T | 5 | a0001c0001t0008g0065 a0001c0001t0008g0069 a0001c0001t0008g0091 others(2): Show |
5 | NA18947.hp2 NA18954.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.703-3343C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30988513 | |||||||
chr12:30988573 | A | G | 368 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(365): Show |
372 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.703-3283A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30988573 | |||||||
chr12:30988605 | A | C | 2 | a0001c0001t0001g0154 a0001c0001t0001g0235 |
2 | NA18945.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.703-3251A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30988605 | |||||||
chr12:30988724 | C | T | 1 | a0001c0001t0002g0333 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.703-3132C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30988724 | |||||||
chr12:30988727 | G | C | 186 | a0001c0001t0001g0022 a0001c0001t0001g0045 a0001c0001t0001g0101 others(183): Show |
188 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.703-3129G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30988727 | |||||||
chr12:30989014 | C | T | 1 | a0001c0001t0002g0360 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.703-2842C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30989014 | |||||||
chr12:30989078 | C | T | 14 | a0001c0001t0002g0373 a0001c0001t0005g0106 a0001c0001t0005g0118 others(11): Show |
14 | HG01257.hp2 HG01258.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.703-2778C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30989078 | |||||||
chr12:30989112 | A | C | 85 | a0001c0001t0001g0044 a0001c0001t0001g0059 a0001c0001t0001g0082 others(82): Show |
85 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.703-2744A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30989112 | |||||||
chr12:30989328 | T | A | 1 | a0001c0001t0002g0360 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.703-2528T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30989328 | |||||||
chr12:30989370 | G | A | 14 | a0001c0001t0002g0373 a0001c0001t0005g0106 a0001c0001t0005g0118 others(11): Show |
14 | HG01257.hp2 HG01258.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.703-2486G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30989370 | |||||||
chr12:30989390 | C | T | 19 | a0001c0001t0001g0044 a0001c0001t0001g0059 a0001c0001t0001g0082 others(16): Show |
19 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(16): Show |
intron_variant | MODIFIER | c.703-2466C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30989390 | |||||||
chr12:30989440 | G | A | 2 | a0001c0001t0037g0016 a0010c0012t0049g0248 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.703-2416G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30989440 | |||||||
chr12:30989680 | A | G | 258 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(255): Show |
260 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.703-2176A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30989680 | |||||||
chr12:30989840 | G | A | 2 | a0001c0001t0037g0016 a0010c0012t0049g0248 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.703-2016G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30989840 | |||||||
chr12:30989915 | G | A | 50 | a0002c0002t0001g0033 a0002c0002t0001g0037 a0002c0002t0001g0038 others(47): Show |
50 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.703-1941G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30989915 | |||||||
chr12:30990008 | C | T | 1 | a0001c0001t0014g0384 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.703-1848C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30990008 | |||||||
chr12:30990031 | G | A | 1 | a0001c0001t0002g0223 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.703-1825G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30990031 | |||||||
chr12:30990137 | C | CGT | 23 | a0001c0001t0002g0360 a0001c0001t0015g0363 a0001c0001t0015g0364 others(20): Show |
23 | HG01167.hp1 HG01192.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.703-1705_703-1704d others(4): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 30990137 | ||||||
chr12:30990137 | C | CGTGT | 69 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0059 others(66): Show |
69 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.703-1707_703-1704d others(6): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 30990137 | ||||||
chr12:30990137 | C | T | 12 | a0001c0001t0002g0373 a0001c0001t0005g0106 a0001c0001t0005g0118 others(9): Show |
12 | HG01257.hp2 HG01258.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.703-1719C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30990137 | |||||||
chr12:30990315 | G | A | 2 | a0001c0001t0002g0274 a0001c0001t0004g0008 |
2 | HG00639.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.703-1541G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30990315 | |||||||
chr12:30990327 | C | T | 1 | a0001c0001t0010g0273 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.703-1529C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30990327 | |||||||
chr12:30990328 | G | A | 1 | a0003c0003t0010g0161 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.703-1528G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30990328 | |||||||
chr12:30990359 | G | A | 1 | a0010c0012t0049g0248 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.703-1497G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30990359 | |||||||
chr12:30990369 | C | T | 2 | a0002c0002t0001g0064 a0002c0002t0001g0236 |
2 | NA18998.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.703-1487C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30990369 | |||||||
chr12:30990450 | A | C | 378 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(375): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.703-1406A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30990450 | |||||||
chr12:30990698 | C | T | 36 | a0002c0002t0001g0033 a0002c0002t0001g0037 a0002c0002t0001g0038 others(33): Show |
36 | HG00423.hp2 HG00609.hp1 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.703-1158C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30990698 | |||||||
chr12:30990816 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.703-1040T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30990816 | |||||||
chr12:30990878 | C | T | 1 | a0001c0001t0002g0126 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.703-978C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30990878 | |||||||
chr12:30991239 | T | A | 1 | a0010c0012t0049g0248 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.703-617T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30991239 | |||||||
chr12:30991442 | C | T | 1 | a0001c0001t0022g0053 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.703-414C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30991442 | |||||||
chr12:30991586 | T | C | 2 | a0001c0001t0029g0192 a0001c0001t0029g0193 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.703-270T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30991586 | |||||||
chr12:30991602 | T | C | 47 | a0001c0001t0003g0043 a0001c0001t0003g0076 a0001c0001t0003g0085 others(44): Show |
48 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.703-254T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30991602 | |||||||
chr12:30991698 | G | A | 2 | a0001c0001t0025g0205 a0001c0001t0025g0219 |
2 | HG01123.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.703-158G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30991698 | |||||||
chr12:30991800 | G | A | 19 | a0001c0001t0005g0301 a0001c0001t0010g0031 a0001c0001t0010g0052 others(16): Show |
19 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.703-56G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30991800 |