Item | Value |
---|---|
geneid | 7174 |
ensemblid | ENSG00000134900.13 |
hgncid | 12016 |
symbol | TPP2 |
name | tripeptidyl peptidase 2 |
refseq_nuc | NM_001330588.2 |
refseq_prot | NP_001317517.1 |
ensembl_nuc | ENST00000376052.5 |
ensembl_prot | ENSP00000365220.3 |
mane_status | MANE Select |
chr | chr13 |
start | 102596986 |
end | 102679958 |
strand | + |
ver | v1.2 |
region | chr13:102596986-102679958 |
region5000 | chr13:102591986-102684958 |
regionname0 | TPP2_chr13_102596986_102679958 |
regionname5000 | TPP2_chr13_102591986_102684958 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1262 | 361 | 72 | 74 | 163 | 10 | 40 | 137 | TPP2_chr13_102591986_102684958 | TPP2 | MATAA others(1257): Show |
chr13 | 102591986 | 102684958 |
a0002 | 0/0 | 1262 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | MATAA others(1257): Show |
chr13 | 102591986 | 102684958 |
a0003 | 0/0 | 1262 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | MATAA others(1257): Show |
chr13 | 102591986 | 102684958 |
a0004 | 0/0 | 1262 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | MATAA others(1257): Show |
chr13 | 102591986 | 102684958 |
a0005 | 0/0 | 1262 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | MATAA others(1257): Show |
chr13 | 102591986 | 102684958 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3786 | 182 | 49 | 37 | 68 | 6 | 21 | TPP2_chr13_102591986_102684958 | TPP2 | ATGGC others(3781): Show |
chr13 | 102591986 | 102684958 | ||
a0001c0002 | 1/0 | 3786 | 129 | 12 | 28 | 67 | 3 | 18 | TPP2_chr13_102591986_102684958 | TPP2 | ATGGC others(3781): Show |
chr13 | 102591986 | 102684958 | ||
a0001c0003 | 0/0 | 3786 | 46 | 9 | 8 | 27 | 1 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | ATGGC others(3781): Show |
chr13 | 102591986 | 102684958 | ||
a0001c0004 | 0/0 | 3786 | 2 | 0 | 1 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | ATGGC others(3781): Show |
chr13 | 102591986 | 102684958 | ||
a0001c0006 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | ATGGC others(3781): Show |
chr13 | 102591986 | 102684958 | ||
a0001c0008 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | ATGGC others(3781): Show |
chr13 | 102591986 | 102684958 | ||
a0002c0005 | 0/0 | 3786 | 2 | 2 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | ATGGC others(3781): Show |
chr13 | 102591986 | 102684958 | ||
a0003c0009 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | ATGGC others(3781): Show |
chr13 | 102591986 | 102684958 | ||
a0004c0007 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | ATGGC others(3781): Show |
chr13 | 102591986 | 102684958 | ||
a0005c0010 | 0/0 | 3786 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | ATGGC others(3781): Show |
chr13 | 102591986 | 102684958 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 5474 | 76 | 19 | 4 | 49 | 0 | 4 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5469): Show |
chr13 | 102591986 | 102684958 |
a0001c0001t0003 | 0/0 | 5478 | 70 | 18 | 22 | 17 | 5 | 8 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5473): Show |
chr13 | 102591986 | 102684958 |
a0001c0001t0006 | 0/1 | 5475 | 22 | 6 | 9 | 0 | 1 | 5 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5470): Show |
chr13 | 102591986 | 102684958 |
a0001c0001t0009 | 0/0 | 5479 | 4 | 0 | 2 | 0 | 0 | 2 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5474): Show |
chr13 | 102591986 | 102684958 |
a0001c0001t0010 | 0/0 | 5479 | 3 | 3 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5474): Show |
chr13 | 102591986 | 102684958 |
a0001c0001t0011 | 0/0 | 5484 | 2 | 1 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5479): Show |
chr13 | 102591986 | 102684958 |
a0001c0001t0013 | 0/0 | 5478 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5473): Show |
chr13 | 102591986 | 102684958 |
a0001c0001t0014 | 0/0 | 5478 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5473): Show |
chr13 | 102591986 | 102684958 |
a0001c0001t0015 | 0/0 | 5480 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5475): Show |
chr13 | 102591986 | 102684958 |
a0001c0001t0016 | 0/0 | 5474 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5469): Show |
chr13 | 102591986 | 102684958 |
a0001c0001t0017 | 0/0 | 5474 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5469): Show |
chr13 | 102591986 | 102684958 |
a0001c0002t0001 | 0/0 | 5483 | 81 | 7 | 20 | 39 | 3 | 12 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5478): Show |
chr13 | 102591986 | 102684958 |
a0001c0002t0005 | 1/0 | 5484 | 35 | 2 | 3 | 25 | 0 | 4 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5479): Show |
chr13 | 102591986 | 102684958 |
a0001c0002t0007 | 0/0 | 5480 | 6 | 0 | 4 | 0 | 0 | 2 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5475): Show |
chr13 | 102591986 | 102684958 |
a0001c0002t0008 | 0/0 | 5480 | 3 | 3 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5475): Show |
chr13 | 102591986 | 102684958 |
a0001c0002t0018 | 0/0 | 5483 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5478): Show |
chr13 | 102591986 | 102684958 |
a0001c0002t0019 | 0/0 | 5483 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5478): Show |
chr13 | 102591986 | 102684958 |
a0001c0002t0020 | 0/0 | 5483 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5478): Show |
chr13 | 102591986 | 102684958 |
a0001c0002t0021 | 0/0 | 5484 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5479): Show |
chr13 | 102591986 | 102684958 |
a0001c0003t0004 | 0/0 | 5481 | 43 | 9 | 8 | 24 | 1 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5476): Show |
chr13 | 102591986 | 102684958 |
a0001c0003t0005 | 0/0 | 5484 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5479): Show |
chr13 | 102591986 | 102684958 |
a0001c0003t0008 | 0/0 | 5480 | 2 | 0 | 0 | 2 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5475): Show |
chr13 | 102591986 | 102684958 |
a0001c0004t0004 | 0/0 | 5481 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5476): Show |
chr13 | 102591986 | 102684958 |
a0001c0004t0005 | 0/0 | 5484 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5479): Show |
chr13 | 102591986 | 102684958 |
a0001c0006t0003 | 0/0 | 5478 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5473): Show |
chr13 | 102591986 | 102684958 |
a0001c0008t0012 | 0/0 | 5480 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5475): Show |
chr13 | 102591986 | 102684958 |
a0002c0005t0004 | 0/0 | 5481 | 2 | 2 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5476): Show |
chr13 | 102591986 | 102684958 |
a0003c0009t0012 | 0/0 | 5480 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5475): Show |
chr13 | 102591986 | 102684958 |
a0004c0007t0002 | 0/0 | 5474 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5469): Show |
chr13 | 102591986 | 102684958 |
a0005c0010t0001 | 0/0 | 5483 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | AGTCC others(5478): Show |
chr13 | 102591986 | 102684958 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0001 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0006g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0006g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0006g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0006g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0006g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0006g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0006g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0006g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0006g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0006g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0006g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0006g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0006g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0006g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0006g0258 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0006g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0006g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0006g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0009g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0009g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0009g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0009g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0010g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0010g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0010g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0011g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0011g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0013g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0014g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0015g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0016g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0001t0017g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0161 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0005g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0007g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0007g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0007g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0007g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0007g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0007g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0008g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0008g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0018g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0019g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0020g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0002t0021g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0004g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0005g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0008g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0003t0008g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0004t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0004t0005g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0006t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0001c0008t0012g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0002c0005t0004g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0003c0009t0012g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0004c0007t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
a0005c0010t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0263 | EUR | GBR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0299 | EUR | GBR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG00140 | hp1 | a0001 | c0001 | t0006 | g0255 | EUR | GBR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0066 | EUR | GBR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG00323 | hp1 | a0001 | c0003 | t0004 | g0146 | EUR | FIN | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0324 | EUR | FIN | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | CHS | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | CHS | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG00597 | hp1 | a0001 | c0002 | t0005 | g0035 | EAS | CHS | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | CHS | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0286 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0314 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0050 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG00733 | hp1 | a0001 | c0002 | t0005 | g0166 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0304 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG00735 | hp1 | a0001 | c0001 | t0006 | g0256 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG00735 | hp2 | a0001 | c0003 | t0004 | g0119 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0300 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0313 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0306 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01069 | hp2 | a0001 | c0002 | t0007 | g0102 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01070 | hp1 | a0001 | c0001 | t0006 | g0022 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0264 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01071 | hp2 | a0001 | c0001 | t0006 | g0022 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01099 | hp1 | a0001 | c0003 | t0004 | g0004 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01099 | hp2 | a0001 | c0002 | t0007 | g0104 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0251 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01106 | hp2 | a0001 | c0003 | t0004 | g0127 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01109 | hp1 | a0001 | c0001 | t0006 | g0247 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01109 | hp2 | a0001 | c0002 | t0005 | g0039 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0042 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0312 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0041 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0287 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01175 | hp1 | a0001 | c0004 | t0004 | g0141 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01175 | hp2 | a0001 | c0001 | t0009 | g0307 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01192 | hp1 | a0001 | c0003 | t0004 | g0144 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0285 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01243 | hp2 | a0001 | c0001 | t0009 | g0029 | AMR | PUR | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0303 | AMR | CLM | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0072 | AMR | CLM | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01256 | hp1 | a0001 | c0002 | t0005 | g0080 | AMR | CLM | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01256 | hp2 | a0001 | c0001 | t0006 | g0023 | AMR | CLM | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0091 | AMR | CLM | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01257 | hp2 | a0001 | c0002 | t0007 | g0106 | AMR | CLM | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01258 | hp1 | a0001 | c0002 | t0007 | g0105 | AMR | CLM | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01258 | hp2 | a0001 | c0001 | t0006 | g0023 | AMR | CLM | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0090 | AMR | CLM | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01261 | hp2 | a0001 | c0003 | t0004 | g0140 | AMR | CLM | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01358 | hp1 | a0001 | c0003 | t0004 | g0150 | AMR | CLM | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01358 | hp2 | a0001 | c0001 | t0006 | g0254 | AMR | CLM | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01361 | hp1 | a0001 | c0003 | t0004 | g0131 | AMR | CLM | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01361 | hp2 | a0001 | c0001 | t0006 | g0257 | AMR | CLM | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0319 | AMR | CLM | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0092 | AMR | CLM | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0093 | EUR | IBS | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0026 | EUR | IBS | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0253 | AFR | ACB | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | ACB | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0160 | AMR | PEL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0271 | AMR | PEL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0058 | AMR | PEL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01934 | hp2 | a0001 | c0002 | t0021 | g0118 | AMR | PEL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PEL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01975 | hp2 | a0001 | c0001 | t0006 | g0241 | AMR | PEL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0059 | AMR | PEL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01978 | hp2 | a0001 | c0003 | t0004 | g0137 | AMR | PEL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PEL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | PEL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0275 | AMR | PEL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0292 | AMR | PEL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | PEL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PEL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02015 | hp1 | a0001 | c0003 | t0004 | g0129 | EAS | KHV | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | KHV | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02027 | hp1 | a0001 | c0002 | t0005 | g0115 | EAS | KHV | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | KHV | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02040 | hp1 | a0001 | c0002 | t0005 | g0075 | EAS | KHV | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02040 | hp2 | a0001 | c0003 | t0004 | g0122 | EAS | KHV | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02055 | hp1 | a0001 | c0003 | t0004 | g0148 | AFR | ACB | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0289 | AFR | ACB | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02056 | hp1 | a0001 | c0002 | t0005 | g0168 | EAS | KHV | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | KHV | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | KHV | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02071 | hp2 | a0001 | c0003 | t0004 | g0152 | EAS | KHV | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | KHV | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0280 | EAS | KHV | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02080 | hp1 | a0001 | c0002 | t0005 | g0156 | EAS | KHV | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | KHV | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02083 | hp2 | a0001 | c0003 | t0004 | g0134 | EAS | KHV | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | KHV | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02132 | hp2 | a0001 | c0002 | t0005 | g0182 | EAS | KHV | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0281 | EAS | KHV | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | KHV | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0068 | AMR | PEL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0176 | AMR | PEL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | ACB | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0316 | AFR | ACB | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0096 | AFR | ACB | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0284 | AMR | PEL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0055 | AMR | PEL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0283 | AMR | PEL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0178 | AMR | PEL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0274 | AMR | PEL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0301 | AMR | PEL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02572 | hp1 | a0001 | c0003 | t0004 | g0147 | AFR | GWD | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0294 | AFR | GWD | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0296 | SAS | PJL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02615 | hp1 | a0001 | c0006 | t0003 | g0310 | AFR | GWD | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0290 | AFR | GWD | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0262 | SAS | PJL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0051 | SAS | PJL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0315 | SAS | PJL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0231 | SAS | PJL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02809 | hp1 | a0001 | c0002 | t0008 | g0098 | AFR | GWD | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02809 | hp2 | a0003 | c0009 | t0012 | g0328 | AFR | GWD | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02886 | hp1 | a0001 | c0001 | t0006 | g0250 | AFR | GWD | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02886 | hp2 | a0001 | c0002 | t0008 | g0101 | AFR | GWD | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | GWD | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0245 | AFR | GWD | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02896 | hp1 | a0001 | c0003 | t0004 | g0330 | AFR | GWD | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0297 | AFR | GWD | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | GWD | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0298 | AFR | GWD | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0317 | AFR | ESN | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | ESN | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0318 | AFR | ESN | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | ESN | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02976 | hp1 | a0001 | c0001 | t0006 | g0246 | AFR | ESN | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02976 | hp2 | a0001 | c0003 | t0004 | g0130 | AFR | ESN | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03017 | hp1 | a0001 | c0002 | t0005 | g0037 | SAS | PJL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03017 | hp2 | a0001 | c0001 | t0006 | g0261 | SAS | PJL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03041 | hp1 | a0001 | c0001 | t0011 | g0311 | AFR | GWD | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0291 | AFR | GWD | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03130 | hp1 | a0001 | c0003 | t0004 | g0128 | AFR | ESN | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03130 | hp2 | a0001 | c0001 | t0010 | g0321 | AFR | ESN | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03139 | hp1 | a0001 | c0002 | t0001 | g0040 | AFR | ESN | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03139 | hp2 | a0001 | c0001 | t0010 | g0320 | AFR | ESN | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03209 | hp1 | a0001 | c0003 | t0004 | g0331 | AFR | MSL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03209 | hp2 | a0001 | c0001 | t0016 | g0191 | AFR | MSL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03225 | hp1 | a0001 | c0003 | t0004 | g0143 | AFR | MSL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | MSL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0155 | SAS | PJL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0325 | SAS | PJL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | MSL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0097 | AFR | MSL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03486 | hp1 | a0001 | c0001 | t0006 | g0249 | AFR | MSL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03486 | hp2 | a0001 | c0003 | t0004 | g0125 | AFR | MSL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03490 | hp1 | a0001 | c0002 | t0005 | g0016 | SAS | PJL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0305 | SAS | PJL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0007 | SAS | PJL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03491 | hp2 | a0001 | c0001 | t0006 | g0259 | SAS | PJL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03492 | hp1 | a0001 | c0002 | t0005 | g0016 | SAS | PJL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0007 | SAS | PJL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0094 | AFR | ESN | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | ESN | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | GWD | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03540 | hp2 | a0001 | c0001 | t0010 | g0323 | AFR | GWD | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03579 | hp1 | a0001 | c0001 | t0006 | g0242 | AFR | MSL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0248 | AFR | MSL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03654 | hp1 | a0001 | c0001 | t0006 | g0244 | SAS | PJL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03654 | hp2 | a0001 | c0002 | t0007 | g0107 | SAS | PJL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0083 | SAS | PJL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0234 | SAS | PJL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0077 | SAS | PJL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03710 | hp2 | a0001 | c0001 | t0006 | g0252 | SAS | PJL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03831 | hp1 | a0001 | c0002 | t0005 | g0165 | SAS | BEB | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03831 | hp2 | a0001 | c0002 | t0007 | g0103 | SAS | BEB | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0302 | SAS | BEB | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0082 | SAS | BEB | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0218 | SAS | BEB | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03927 | hp2 | a0001 | c0001 | t0006 | g0260 | SAS | BEB | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0008 | SAS | BEB | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03942 | hp2 | a0001 | c0001 | t0009 | g0269 | SAS | BEB | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0076 | SAS | BEB | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG04184 | hp2 | a0001 | c0001 | t0009 | g0273 | SAS | BEB | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0158 | SAS | STU | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG04199 | hp2 | a0001 | c0003 | t0004 | g0179 | SAS | STU | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG04204 | hp1 | a0001 | c0001 | t0014 | g0001 | SAS | STU | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0163 | SAS | STU | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0162 | SAS | STU | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | STU | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18522 | hp1 | a0002 | c0005 | t0004 | g0015 | AFR | YRI | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | YRI | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | CHB | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | CHB | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18940 | hp2 | a0001 | c0003 | t0004 | g0145 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18943 | hp1 | a0001 | c0002 | t0005 | g0116 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18945 | hp2 | a0001 | c0003 | t0004 | g0132 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18947 | hp1 | a0001 | c0002 | t0005 | g0031 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18949 | hp1 | a0001 | c0002 | t0005 | g0006 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18962 | hp1 | a0001 | c0002 | t0005 | g0111 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18962 | hp2 | a0001 | c0003 | t0005 | g0012 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18965 | hp1 | a0001 | c0003 | t0004 | g0126 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18969 | hp2 | a0001 | c0003 | t0008 | g0120 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18972 | hp1 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18972 | hp2 | a0001 | c0003 | t0004 | g0151 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18974 | hp1 | a0001 | c0002 | t0005 | g0006 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18975 | hp2 | a0001 | c0003 | t0004 | g0014 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18979 | hp1 | a0001 | c0003 | t0004 | g0123 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18980 | hp2 | a0001 | c0002 | t0005 | g0117 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18982 | hp1 | a0001 | c0003 | t0008 | g0013 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18983 | hp2 | a0001 | c0002 | t0018 | g0057 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18984 | hp1 | a0001 | c0003 | t0004 | g0004 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18985 | hp2 | a0001 | c0002 | t0005 | g0109 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18988 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18989 | hp2 | a0001 | c0003 | t0004 | g0135 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18990 | hp1 | a0001 | c0003 | t0004 | g0139 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18991 | hp1 | a0001 | c0003 | t0004 | g0004 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18992 | hp2 | a0001 | c0002 | t0005 | g0112 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18993 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18995 | hp2 | a0001 | c0003 | t0004 | g0011 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18997 | hp1 | a0001 | c0003 | t0004 | g0014 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18998 | hp1 | a0001 | c0002 | t0005 | g0175 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA18998 | hp2 | a0001 | c0003 | t0004 | g0138 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19000 | hp1 | a0001 | c0002 | t0005 | g0053 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19001 | hp2 | a0001 | c0002 | t0005 | g0113 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19003 | hp1 | a0001 | c0002 | t0005 | g0108 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19003 | hp2 | a0001 | c0001 | t0011 | g0278 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19006 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19009 | hp2 | a0001 | c0003 | t0004 | g0013 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19011 | hp2 | a0001 | c0003 | t0004 | g0011 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19030 | hp1 | a0001 | c0001 | t0015 | g0322 | AFR | LWK | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0295 | AFR | LWK | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19043 | hp1 | a0004 | c0007 | t0002 | g0198 | AFR | LWK | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | LWK | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19054 | hp1 | a0001 | c0003 | t0004 | g0136 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19056 | hp2 | a0001 | c0002 | t0005 | g0028 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19058 | hp1 | a0001 | c0003 | t0004 | g0124 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19058 | hp2 | a0001 | c0002 | t0005 | g0034 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19062 | hp1 | a0001 | c0003 | t0004 | g0121 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19062 | hp2 | a0001 | c0002 | t0005 | g0071 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19063 | hp2 | a0001 | c0002 | t0019 | g0052 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19064 | hp1 | a0001 | c0002 | t0020 | g0063 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19065 | hp1 | a0001 | c0002 | t0005 | g0032 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19068 | hp2 | a0001 | c0003 | t0004 | g0133 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19070 | hp2 | a0001 | c0002 | t0005 | g0033 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19075 | hp1 | a0001 | c0002 | t0005 | g0110 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19076 | hp2 | a0001 | c0004 | t0005 | g0012 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19080 | hp1 | a0005 | c0010 | t0001 | g0044 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19080 | hp2 | a0001 | c0001 | t0017 | g0002 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19081 | hp1 | a0001 | c0002 | t0005 | g0114 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19082 | hp1 | a0001 | c0003 | t0004 | g0149 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19086 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19240 | hp1 | a0001 | c0002 | t0005 | g0046 | AFR | YRI | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA19240 | hp2 | a0002 | c0005 | t0004 | g0015 | AFR | YRI | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ASW | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0187 | AFR | ASW | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0060 | EUR | TSI | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0026 | EUR | TSI | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0308 | SAS | GIH | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA20905 | hp2 | a0001 | c0001 | t0013 | g0309 | SAS | GIH | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0100 | AMR | CLM | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | ACB | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02486 | hp1 | a0001 | c0008 | t0012 | g0329 | AFR | ACB | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0180 | AFR | ACB | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0095 | AFR | MSL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | MSL | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0181 | AFR | USA | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
HG06807 | hp2 | a0001 | c0003 | t0004 | g0142 | AFR | USA | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA20300 | hp1 | a0001 | c0002 | t0008 | g0099 | AFR | USA | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | USA | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | LWK | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
NA21309 | hp2 | a0001 | c0002 | t0005 | g0084 | AFR | LWK | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
homoSapiens | chm13v2 | a0001 | c0001 | t0006 | g0258 | REF | REF | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
homoSapiens | grch38p0 | a0001 | c0002 | t0005 | g0161 | REF | REF | TPP2_chr13_102591986_102684958 | TPP2 | chr13 | 102591986 | 102684958 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:102636248 | G | A | 1 | a0002 | 2 | NA18522.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.1534G>A | p.Val512Ile | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 13/30 | 1587/5484 | 1534/3789 | 512/1262 | chr13 | 102636248 | |||
chr13:102636284 | A | G | 1 | a0005 | 1 | NA19080.hp1 | missense_variant | MODERATE | c.1570A>G | p.Thr524Ala | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 13/30 | 1623/5484 | 1570/3789 | 524/1262 | chr13 | 102636284 | |||
chr13:102646349 | C | T | 1 | a0004 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.2449C>T | p.Arg817Cys | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 20/30 | 2502/5484 | 2449/3789 | 817/1262 | chr13 | 102646349 | |||
chr13:102664889 | A | G | 1 | a0003 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.3335A>G | p.Lys1112Arg | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/30 | 3388/5484 | 3335/3789 | 1112/1262 | chr13 | 102664889 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:102623036 | T | C | 3 | a0001c0001 a0001c0006 a0004c0007 |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
synonymous_variant | LOW | c.780T>C | p.Ser260Ser | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/30 | 833/5484 | 780/3789 | 260/1262 | chr13 | 102623036 | |||
chr13:102627055 | T | C | 1 | a0001c0004 | 2 | HG01175.hp1 NA19076.hp2 |
synonymous_variant | LOW | c.828T>C | p.Phe276Phe | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 7/30 | 881/5484 | 828/3789 | 276/1262 | chr13 | 102627055 | |||
chr13:102638304 | T | C | 2 | a0001c0008 a0003c0009 |
2 | HG02486.hp1 HG02809.hp2 |
synonymous_variant | LOW | c.1902T>C | p.Val634Val | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 15/30 | 1955/5484 | 1902/3789 | 634/1262 | chr13 | 102638304 | |||
chr13:102663726 | T | C | 1 | a0001c0006 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.3222T>C | p.His1074His | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 26/30 | 3275/5484 | 3222/3789 | 1074/1262 | chr13 | 102663726 | |||
chr13:102676310 | A | G | 3 | a0001c0003 a0001c0004 a0002c0005 |
50 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(47): Show |
synonymous_variant | LOW | c.3594A>G | p.Ala1198Ala | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 29/30 | 3647/5484 | 3594/3789 | 1198/1262 | chr13 | 102676310 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:102597026 | C | G | 1 | a0001c0002t0021 | 1 | HG01934.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-13C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/30 | chr13 | 102597026 | |||||||
chr13:102678368 | G | A | 13 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(10): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*52G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 30/30 | 52 | chr13 | 102678368 | ||||||
chr13:102678480 | AATAC | A | 5 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0016 others(2): Show |
100 | HG00140.hp1 HG00597.hp2 HG00735.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*167_*170delACAT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 30/30 | 167 | INFO_REALIGN_3_PRIME | chr13 | 102678480 | |||||
chr13:102678684 | C | T | 1 | a0001c0002t0020 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*368C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 30/30 | 368 | chr13 | 102678684 | ||||||
chr13:102678741 | C | A | 2 | a0001c0008t0012 a0003c0009t0012 |
2 | HG02486.hp1 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*425C>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 30/30 | 425 | chr13 | 102678741 | ||||||
chr13:102678793 | AT | A | 5 | a0001c0002t0001 a0001c0002t0018 a0001c0002t0019 others(2): Show |
85 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*501delT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 30/30 | 501 | INFO_REALIGN_3_PRIME | chr13 | 102678793 | |||||
chr13:102678793 | ATTT | A | 3 | a0001c0003t0004 a0001c0004t0004 a0002c0005t0004 |
46 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*499_*501delTTT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 30/30 | 499 | INFO_REALIGN_3_PRIME | chr13 | 102678793 | |||||
chr13:102678793 | ATTTT | A | 6 | a0001c0001t0015 a0001c0002t0007 a0001c0002t0008 others(3): Show |
14 | HG01069.hp2 HG01099.hp2 HG01257.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*498_*501delTTTT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 30/30 | 498 | INFO_REALIGN_3_PRIME | chr13 | 102678793 | |||||
chr13:102678793 | ATTTTT | A | 3 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0010 |
28 | HG00140.hp1 HG00735.hp1 HG01070.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*497_*501delTTTTT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 30/30 | 497 | INFO_REALIGN_3_PRIME | chr13 | 102678793 | |||||
chr13:102678793 | ATTTTTT | A | 8 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0013 others(5): Show |
152 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*496_*501delTTTTTT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 30/30 | 496 | INFO_REALIGN_3_PRIME | chr13 | 102678793 | |||||
chr13:102678854 | A | G | 1 | a0001c0002t0019 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*538A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 30/30 | 538 | chr13 | 102678854 | ||||||
chr13:102679046 | T | G | 2 | a0001c0001t0010 a0001c0001t0015 |
4 | HG03130.hp2 HG03139.hp2 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*730T>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 30/30 | 730 | chr13 | 102679046 | ||||||
chr13:102679260 | G | T | 1 | a0001c0001t0017 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*944G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 30/30 | 944 | chr13 | 102679260 | ||||||
chr13:102679299 | A | C | 1 | a0001c0002t0007 | 6 | HG01069.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*983A>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 30/30 | 983 | chr13 | 102679299 | ||||||
chr13:102679468 | G | A | 1 | a0001c0001t0016 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1152G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 30/30 | 1152 | chr13 | 102679468 | ||||||
chr13:102679581 | C | T | 1 | a0001c0002t0018 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1265C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 30/30 | 1265 | chr13 | 102679581 | ||||||
chr13:102679582 | G | A | 13 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(10): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*1266G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 30/30 | 1266 | chr13 | 102679582 | ||||||
chr13:102679635 | T | C | 13 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(10): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*1319T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 30/30 | 1319 | chr13 | 102679635 | ||||||
chr13:102679642 | G | A | 13 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(10): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*1326G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 30/30 | 1326 | chr13 | 102679642 | ||||||
chr13:102679778 | G | A | 1 | a0001c0001t0013 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1462G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 30/30 | 1462 | chr13 | 102679778 | ||||||
chr13:102679893 | C | T | 1 | a0001c0001t0014 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1577C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 30/30 | 1577 | chr13 | 102679893 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:102597240 | G | C | 1 | a0001c0001t0003g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.165+37G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102597240 | |||||||
chr13:102597257 | G | T | 2 | a0001c0003t0004g0330 a0001c0003t0004g0331 |
2 | HG02896.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.165+54G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102597257 | |||||||
chr13:102597261 | G | T | 2 | a0001c0008t0012g0329 a0003c0009t0012g0328 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.165+58G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102597261 | |||||||
chr13:102597277 | G | A | 1 | a0001c0002t0005g0028 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.165+74G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102597277 | |||||||
chr13:102597356 | A | G | 161 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(158): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.165+153A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102597356 | |||||||
chr13:102597381 | C | T | 1 | a0001c0002t0001g0180 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.165+178C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102597381 | |||||||
chr13:102597595 | C | T | 1 | a0001c0003t0004g0179 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.165+392C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102597595 | |||||||
chr13:102597618 | C | G | 1 | a0001c0002t0001g0178 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.165+415C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102597618 | |||||||
chr13:102597665 | T | A | 2 | a0001c0001t0003g0181 a0001c0001t0009g0029 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.165+462T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102597665 | |||||||
chr13:102597666 | T | G | 2 | a0001c0001t0003g0181 a0001c0001t0009g0029 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.165+463T>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102597666 | |||||||
chr13:102597668 | TATCATTG others(13): Show |
T | 2 | a0001c0001t0003g0181 a0001c0001t0009g0029 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.165+467_165+486del others(20): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 102597668 | ||||||
chr13:102597870 | G | A | 99 | a0001c0001t0002g0036 a0001c0001t0003g0030 a0001c0002t0001g0007 others(96): Show |
104 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.165+667G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102597870 | |||||||
chr13:102597895 | T | G | 10 | a0001c0001t0002g0036 a0001c0001t0003g0030 a0001c0002t0005g0006 others(7): Show |
11 | HG00597.hp1 HG03017.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.165+692T>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102597895 | |||||||
chr13:102597978 | CT | C | 50 | a0001c0001t0002g0183 a0001c0001t0002g0184 a0001c0001t0002g0185 others(47): Show |
55 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(52): Show |
intron_variant | MODIFIER | c.165+787delT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 102597978 | ||||||
chr13:102597990 | T | A | 44 | a0001c0003t0004g0004 a0001c0003t0004g0011 a0001c0003t0004g0013 others(41): Show |
49 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.165+787T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102597990 | |||||||
chr13:102598065 | C | T | 2 | a0001c0001t0002g0326 a0001c0001t0002g0327 |
2 | NA18747.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.165+862C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102598065 | |||||||
chr13:102598215 | C | G | 1 | a0001c0001t0003g0325 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.165+1012C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102598215 | |||||||
chr13:102598474 | T | C | 286 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(283): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.165+1271T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102598474 | |||||||
chr13:102598661 | T | A | 1 | a0001c0003t0004g0119 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.165+1458T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102598661 | |||||||
chr13:102598673 | A | C | 1 | a0001c0001t0003g0324 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.165+1470A>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102598673 | |||||||
chr13:102598694 | G | A | 2 | a0001c0008t0012g0329 a0003c0009t0012g0328 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.165+1491G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102598694 | |||||||
chr13:102598706 | A | G | 2 | a0001c0001t0003g0181 a0001c0001t0009g0029 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.165+1503A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102598706 | |||||||
chr13:102598836 | C | G | 217 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(214): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.165+1633C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102598836 | |||||||
chr13:102598840 | T | C | 157 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(154): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.165+1637T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102598840 | |||||||
chr13:102598892 | T | C | 1 | a0001c0003t0004g0119 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.165+1689T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102598892 | |||||||
chr13:102598969 | G | A | 1 | a0001c0002t0008g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.165+1766G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102598969 | |||||||
chr13:102598998 | A | T | 1 | a0001c0003t0004g0330 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.165+1795A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102598998 | |||||||
chr13:102599006 | G | A | 174 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(171): Show |
189 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.165+1803G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102599006 | |||||||
chr13:102599029 | G | C | 6 | a0001c0003t0004g0011 a0001c0003t0004g0121 a0001c0003t0004g0122 others(3): Show |
7 | HG02040.hp2 NA18969.hp2 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.165+1826G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102599029 | |||||||
chr13:102599173 | A | T | 1 | a0001c0001t0002g0293 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.165+1970A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102599173 | |||||||
chr13:102599223 | G | A | 1 | a0001c0002t0005g0108 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.165+2020G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102599223 | |||||||
chr13:102599306 | T | A | 1 | a0001c0001t0003g0294 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.165+2103T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102599306 | |||||||
chr13:102599457 | T | C | 1 | a0001c0001t0002g0188 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.165+2254T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102599457 | |||||||
chr13:102599717 | A | G | 1 | a0001c0002t0001g0100 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.165+2514A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102599717 | |||||||
chr13:102599986 | TA | T | 213 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(210): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.165+2798delA | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 102599986 | ||||||
chr13:102600067 | TA | T | 168 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(165): Show |
182 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.165+2875delA | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 102600067 | ||||||
chr13:102600087 | T | C | 1 | a0001c0002t0008g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.165+2884T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102600087 | |||||||
chr13:102600104 | G | A | 1 | a0001c0002t0005g0039 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.165+2901G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102600104 | |||||||
chr13:102600154 | T | C | 38 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0019 others(35): Show |
47 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.165+2951T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102600154 | |||||||
chr13:102600260 | A | G | 220 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(217): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.165+3057A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102600260 | |||||||
chr13:102600269 | G | A | 1 | a0001c0002t0001g0040 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.165+3066G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102600269 | |||||||
chr13:102600302 | A | G | 1 | a0001c0002t0008g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.165+3099A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102600302 | |||||||
chr13:102600501 | C | G | 4 | a0001c0001t0002g0289 a0001c0001t0002g0290 a0001c0001t0002g0291 others(1): Show |
4 | HG01993.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+3298C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102600501 | |||||||
chr13:102600514 | T | C | 1 | a0001c0003t0004g0125 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.165+3311T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102600514 | |||||||
chr13:102600866 | G | C | 45 | a0001c0003t0004g0004 a0001c0003t0004g0011 a0001c0003t0004g0013 others(42): Show |
50 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.165+3663G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102600866 | |||||||
chr13:102600951 | C | T | 2 | a0001c0002t0008g0098 a0001c0002t0008g0099 |
2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.165+3748C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102600951 | |||||||
chr13:102601030 | A | G | 4 | a0001c0002t0001g0094 a0001c0002t0001g0095 a0001c0002t0001g0096 others(1): Show |
4 | HG02258.hp2 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-3763A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102601030 | |||||||
chr13:102601049 | C | T | 1 | a0001c0002t0001g0093 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.166-3744C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102601049 | |||||||
chr13:102601222 | A | G | 1 | a0001c0001t0009g0029 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.166-3571A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102601222 | |||||||
chr13:102601361 | ATTTGTTC others(26): Show |
A | 1 | a0001c0001t0002g0293 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.166-3405_166-3373d others(35): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 102601361 | ||||||
chr13:102601807 | T | C | 2 | a0001c0002t0008g0098 a0001c0002t0008g0099 |
2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.166-2986T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102601807 | |||||||
chr13:102601835 | T | C | 2 | a0001c0001t0003g0181 a0001c0001t0009g0029 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.166-2958T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102601835 | |||||||
chr13:102602065 | A | G | 2 | a0001c0008t0012g0329 a0003c0009t0012g0328 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.166-2728A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102602065 | |||||||
chr13:102602140 | C | T | 11 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(8): Show |
11 | HG01069.hp2 HG01099.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.166-2653C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102602140 | |||||||
chr13:102602141 | A | G | 149 | a0001c0001t0002g0243 a0001c0001t0002g0248 a0001c0001t0002g0277 others(146): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.166-2652A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102602141 | |||||||
chr13:102602162 | T | C | 1 | a0001c0002t0001g0155 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.166-2631T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102602162 | |||||||
chr13:102602230 | A | T | 221 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(218): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.166-2563A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102602230 | |||||||
chr13:102602265 | T | C | 1 | a0001c0002t0008g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.166-2528T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102602265 | |||||||
chr13:102602297 | G | A | 1 | a0001c0002t0005g0109 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.166-2496G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102602297 | |||||||
chr13:102602303 | T | C | 1 | a0001c0001t0002g0189 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.166-2490T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102602303 | |||||||
chr13:102602441 | G | C | 6 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(3): Show |
6 | HG01069.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-2352G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102602441 | |||||||
chr13:102602502 | G | A | 22 | a0001c0001t0002g0243 a0001c0001t0002g0248 a0001c0001t0003g0251 others(19): Show |
24 | HG00140.hp1 HG00735.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.166-2291G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102602502 | |||||||
chr13:102602520 | A | C | 1 | a0001c0001t0003g0288 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.166-2273A>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102602520 | |||||||
chr13:102602691 | A | C | 5 | a0001c0002t0001g0010 a0001c0002t0001g0090 a0001c0002t0001g0091 others(2): Show |
6 | HG00741.hp2 HG01257.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.166-2102A>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102602691 | |||||||
chr13:102602699 | G | A | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.166-2094G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102602699 | |||||||
chr13:102602731 | G | T | 1 | a0001c0001t0002g0036 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.166-2062G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102602731 | |||||||
chr13:102602763 | C | T | 1 | a0001c0001t0002g0240 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.166-2030C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102602763 | |||||||
chr13:102602923 | C | T | 4 | a0001c0001t0010g0320 a0001c0001t0010g0321 a0001c0001t0010g0323 others(1): Show |
4 | HG03130.hp2 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-1870C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102602923 | |||||||
chr13:102602931 | G | GT | 54 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0036 others(51): Show |
57 | HG00597.hp2 HG01981.hp2 HG02027.hp2 others(54): Show |
intron_variant | MODIFIER | c.166-1853dupT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 102602931 | ||||||
chr13:102603358 | G | C | 2 | a0001c0001t0002g0326 a0001c0001t0002g0327 |
2 | NA18747.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.166-1435G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102603358 | |||||||
chr13:102603622 | G | A | 2 | a0001c0001t0003g0181 a0001c0001t0009g0029 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.166-1171G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102603622 | |||||||
chr13:102603654 | A | T | 1 | a0001c0002t0001g0089 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.166-1139A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102603654 | |||||||
chr13:102603875 | T | TAGG | 221 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(218): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.166-917_166-915dup others(3): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 102603875 | ||||||
chr13:102603946 | A | G | 221 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(218): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.166-847A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102603946 | |||||||
chr13:102604085 | A | T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.166-708A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102604085 | |||||||
chr13:102604134 | A | G | 1 | a0001c0001t0002g0239 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.166-659A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102604134 | |||||||
chr13:102604165 | T | A | 1 | a0001c0001t0003g0295 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.166-628T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102604165 | |||||||
chr13:102604206 | AT | A | 71 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(68): Show |
77 | HG00597.hp2 HG01243.hp1 HG01884.hp2 others(74): Show |
intron_variant | MODIFIER | c.166-581delT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 102604206 | ||||||
chr13:102604261 | T | A | 4 | a0001c0001t0010g0320 a0001c0001t0010g0321 a0001c0001t0010g0323 others(1): Show |
4 | HG03130.hp2 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-532T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102604261 | |||||||
chr13:102604330 | A | G | 1 | a0001c0002t0001g0176 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.166-463A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102604330 | |||||||
chr13:102604393 | C | G | 4 | a0001c0001t0010g0320 a0001c0001t0010g0321 a0001c0001t0010g0323 others(1): Show |
4 | HG03130.hp2 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-400C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102604393 | |||||||
chr13:102604590 | A | G | 2 | a0001c0001t0003g0286 a0001c0001t0003g0287 |
2 | HG00639.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.166-203A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102604590 | |||||||
chr13:102604602 | A | T | 1 | a0001c0001t0009g0029 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.166-191A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102604602 | |||||||
chr13:102604667 | G | A | 129 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.166-126G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102604667 | |||||||
chr13:102604691 | T | C | 2 | a0001c0001t0003g0181 a0001c0001t0009g0029 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.166-102T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | chr13 | 102604691 | |||||||
chr13:102604714 | CAT | C | 35 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0019 others(32): Show |
44 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.166-72_166-71delAT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 102604714 | ||||||
chr13:102605127 | C | CCAGTAGT others(3): Show |
89 | a0001c0001t0002g0190 a0001c0001t0003g0001 a0001c0001t0003g0003 others(86): Show |
103 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.294+210_294+211ins others(10): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr13 | 102605127 | ||||||
chr13:102605144 | T | C | 1 | a0001c0001t0016g0191 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.294+223T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102605144 | |||||||
chr13:102605192 | GAGA | G | 6 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(3): Show |
6 | HG01069.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+277_294+279del others(3): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr13 | 102605192 | ||||||
chr13:102605269 | C | T | 1 | a0001c0001t0003g0285 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.294+348C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102605269 | |||||||
chr13:102605381 | A | C | 1 | a0001c0001t0002g0238 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.294+460A>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102605381 | |||||||
chr13:102605728 | C | CT | 37 | a0001c0001t0002g0237 a0001c0001t0003g0001 a0001c0001t0003g0003 others(34): Show |
46 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.294+817dupT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr13 | 102605728 | ||||||
chr13:102605866 | G | A | 1 | a0001c0003t0004g0126 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.294+945G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102605866 | |||||||
chr13:102605943 | C | T | 2 | a0001c0001t0003g0316 a0001c0001t0003g0317 |
2 | HG02258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.294+1022C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102605943 | |||||||
chr13:102606018 | G | A | 2 | a0001c0002t0008g0098 a0001c0002t0008g0099 |
2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.294+1097G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102606018 | |||||||
chr13:102606038 | T | C | 2 | a0001c0008t0012g0329 a0003c0009t0012g0328 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.294+1117T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102606038 | |||||||
chr13:102606075 | C | T | 21 | a0001c0002t0005g0006 a0001c0002t0005g0028 a0001c0002t0005g0031 others(18): Show |
22 | HG00597.hp1 HG01934.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.294+1154C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102606075 | |||||||
chr13:102606250 | T | C | 161 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(158): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.294+1329T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102606250 | |||||||
chr13:102606352 | T | C | 44 | a0001c0003t0004g0004 a0001c0003t0004g0011 a0001c0003t0004g0013 others(41): Show |
49 | HG00323.hp1 HG01099.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.294+1431T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102606352 | |||||||
chr13:102606416 | G | A | 1 | a0001c0001t0002g0189 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.294+1495G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102606416 | |||||||
chr13:102606422 | C | G | 22 | a0001c0001t0002g0243 a0001c0001t0002g0248 a0001c0001t0003g0251 others(19): Show |
24 | HG00140.hp1 HG00735.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.294+1501C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102606422 | |||||||
chr13:102606539 | C | G | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.294+1618C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102606539 | |||||||
chr13:102606679 | C | T | 6 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(3): Show |
6 | HG01069.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+1758C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102606679 | |||||||
chr13:102606769 | G | A | 1 | a0001c0001t0003g0296 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.294+1848G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102606769 | |||||||
chr13:102606894 | G | A | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.294+1973G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102606894 | |||||||
chr13:102606953 | G | T | 2 | a0001c0001t0010g0320 a0001c0001t0010g0321 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.294+2032G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102606953 | |||||||
chr13:102606975 | T | C | 1 | a0001c0001t0003g0295 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.294+2054T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102606975 | |||||||
chr13:102607110 | A | T | 2 | a0001c0002t0001g0087 a0001c0002t0001g0088 |
2 | NA18959.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.294+2189A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102607110 | |||||||
chr13:102607140 | A | G | 2 | a0001c0001t0003g0286 a0001c0001t0003g0287 |
2 | HG00639.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.294+2219A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102607140 | |||||||
chr13:102607146 | C | T | 1 | a0001c0003t0004g0331 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.294+2225C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102607146 | |||||||
chr13:102607201 | G | A | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.294+2280G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102607201 | |||||||
chr13:102607205 | C | T | 1 | a0001c0002t0001g0097 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.294+2284C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102607205 | |||||||
chr13:102607223 | T | C | 2 | a0001c0002t0001g0043 a0005c0010t0001g0044 |
2 | NA18993.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.294+2302T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102607223 | |||||||
chr13:102607375 | A | G | 20 | a0001c0001t0002g0248 a0001c0001t0003g0251 a0001c0001t0006g0022 others(17): Show |
22 | HG00140.hp1 HG00735.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.294+2454A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102607375 | |||||||
chr13:102607394 | C | T | 6 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(3): Show |
6 | HG01069.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+2473C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102607394 | |||||||
chr13:102607430 | A | T | 1 | a0001c0001t0003g0284 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.294+2509A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102607430 | |||||||
chr13:102607529 | A | G | 1 | a0001c0001t0003g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.294+2608A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102607529 | |||||||
chr13:102607536 | C | G | 11 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0169 others(8): Show |
13 | HG00408.hp1 HG00738.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.294+2615C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102607536 | |||||||
chr13:102607655 | C | T | 1 | a0001c0002t0001g0086 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.294+2734C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102607655 | |||||||
chr13:102608013 | A | G | 1 | a0001c0002t0001g0174 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.294+3092A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102608013 | |||||||
chr13:102608360 | G | A | 22 | a0001c0002t0001g0045 a0001c0002t0005g0006 a0001c0002t0005g0028 others(19): Show |
23 | HG00597.hp1 HG01934.hp2 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.294+3439G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102608360 | |||||||
chr13:102608905 | T | A | 1 | a0001c0001t0006g0244 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.294+3984T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102608905 | |||||||
chr13:102609093 | G | A | 31 | a0001c0001t0002g0277 a0001c0001t0003g0024 a0001c0001t0003g0030 others(28): Show |
32 | HG00099.hp1 HG00639.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.294+4172G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102609093 | |||||||
chr13:102609311 | G | GT | 308 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(305): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.294+4390_294+4391i others(3): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102609311 | |||||||
chr13:102609345 | A | G | 1 | a0001c0002t0007g0107 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.294+4424A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102609345 | |||||||
chr13:102609379 | G | A | 2 | a0001c0001t0003g0297 a0001c0001t0003g0298 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.294+4458G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102609379 | |||||||
chr13:102609390 | T | C | 3 | a0001c0001t0003g0262 a0001c0001t0003g0263 a0001c0001t0003g0264 |
3 | HG00099.hp1 HG01070.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.294+4469T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102609390 | |||||||
chr13:102609392 | C | CT | 158 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(155): Show |
172 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.294+4493dupT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr13 | 102609392 | ||||||
chr13:102609392 | C | CTT | 15 | a0001c0001t0002g0154 a0001c0001t0002g0189 a0001c0001t0002g0199 others(12): Show |
15 | HG01358.hp1 HG02056.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.294+4492_294+4493d others(4): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr13 | 102609392 | ||||||
chr13:102609392 | C | CTTT | 32 | a0001c0001t0002g0240 a0001c0001t0003g0001 a0001c0001t0003g0003 others(29): Show |
40 | HG00323.hp2 HG00642.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.294+4491_294+4493d others(5): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr13 | 102609392 | ||||||
chr13:102609392 | C | CTTTT | 12 | a0001c0001t0003g0312 a0001c0001t0003g0313 a0001c0001t0003g0314 others(9): Show |
12 | HG00639.hp2 HG00741.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.294+4490_294+4493d others(6): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr13 | 102609392 | ||||||
chr13:102609459 | G | A | 2 | a0001c0001t0002g0201 a0001c0002t0001g0094 |
2 | HG03516.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.294+4538G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102609459 | |||||||
chr13:102609482 | C | A | 1 | a0001c0001t0006g0242 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.294+4561C>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102609482 | |||||||
chr13:102609571 | A | G | 1 | a0001c0002t0005g0175 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.295-4530A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102609571 | |||||||
chr13:102609805 | G | T | 1 | a0001c0001t0002g0235 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.295-4296G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102609805 | |||||||
chr13:102609809 | C | T | 129 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.295-4292C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102609809 | |||||||
chr13:102609860 | T | C | 1 | a0001c0001t0002g0192 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.295-4241T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102609860 | |||||||
chr13:102609956 | G | T | 1 | a0001c0002t0021g0118 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.295-4145G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102609956 | |||||||
chr13:102609967 | A | C | 2 | a0001c0001t0011g0311 a0001c0006t0003g0310 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.295-4134A>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102609967 | |||||||
chr13:102610001 | T | C | 14 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0153 others(11): Show |
17 | HG01243.hp1 HG01884.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.295-4100T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102610001 | |||||||
chr13:102610207 | G | A | 129 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.295-3894G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102610207 | |||||||
chr13:102610255 | G | A | 3 | a0001c0002t0001g0094 a0001c0002t0001g0095 a0001c0002t0001g0097 |
3 | HG03453.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.295-3846G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102610255 | |||||||
chr13:102610359 | G | T | 9 | a0001c0001t0002g0277 a0001c0001t0003g0024 a0001c0001t0003g0030 others(6): Show |
10 | HG02074.hp2 HG02135.hp1 NA18948.hp2 others(7): Show |
intron_variant | MODIFIER | c.295-3742G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102610359 | |||||||
chr13:102610388 | C | T | 44 | a0001c0003t0004g0004 a0001c0003t0004g0011 a0001c0003t0004g0013 others(41): Show |
49 | HG00323.hp1 HG01099.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.295-3713C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102610388 | |||||||
chr13:102610389 | C | T | 44 | a0001c0003t0004g0004 a0001c0003t0004g0011 a0001c0003t0004g0013 others(41): Show |
49 | HG00323.hp1 HG01099.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.295-3712C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102610389 | |||||||
chr13:102610474 | C | T | 1 | a0001c0003t0004g0125 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.295-3627C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102610474 | |||||||
chr13:102610519 | C | T | 1 | a0001c0001t0003g0300 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.295-3582C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102610519 | |||||||
chr13:102610521 | C | T | 1 | a0001c0002t0001g0167 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.295-3580C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102610521 | |||||||
chr13:102610529 | T | C | 129 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.295-3572T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102610529 | |||||||
chr13:102610576 | A | T | 1 | a0001c0001t0002g0189 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.295-3525A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102610576 | |||||||
chr13:102610607 | T | C | 4 | a0001c0001t0010g0320 a0001c0001t0010g0321 a0001c0001t0010g0323 others(1): Show |
4 | HG03130.hp2 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-3494T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102610607 | |||||||
chr13:102610684 | C | A | 5 | a0001c0001t0002g0248 a0001c0001t0006g0246 a0001c0001t0006g0247 others(2): Show |
5 | HG01109.hp1 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.295-3417C>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102610684 | |||||||
chr13:102610803 | T | G | 1 | a0001c0001t0003g0251 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.295-3298T>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102610803 | |||||||
chr13:102610808 | TACATAAA others(2): Show |
T | 4 | a0001c0002t0007g0102 a0001c0002t0007g0105 a0001c0002t0007g0106 others(1): Show |
4 | HG01069.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.295-3287_295-3279d others(11): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr13 | 102610808 | ||||||
chr13:102610835 | T | G | 1 | a0001c0001t0003g0294 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.295-3266T>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102610835 | |||||||
chr13:102610883 | G | A | 128 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(125): Show |
137 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.295-3218G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102610883 | |||||||
chr13:102610890 | C | A | 1 | a0001c0003t0004g0119 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.295-3211C>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102610890 | |||||||
chr13:102610919 | A | G | 1 | a0001c0003t0004g0119 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.295-3182A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102610919 | |||||||
chr13:102611067 | C | T | 129 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.295-3034C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102611067 | |||||||
chr13:102611181 | C | G | 91 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0025 others(88): Show |
104 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.295-2920C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102611181 | |||||||
chr13:102611208 | A | T | 1 | a0001c0001t0003g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.295-2893A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102611208 | |||||||
chr13:102611220 | C | G | 2 | a0001c0001t0003g0181 a0001c0001t0009g0029 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.295-2881C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102611220 | |||||||
chr13:102611261 | G | A | 1 | a0001c0001t0003g0324 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.295-2840G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102611261 | |||||||
chr13:102611289 | T | C | 1 | a0001c0001t0010g0320 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.295-2812T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102611289 | |||||||
chr13:102611377 | A | G | 2 | a0001c0003t0004g0147 a0001c0003t0004g0148 |
2 | HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.295-2724A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102611377 | |||||||
chr13:102611511 | G | A | 221 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(218): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.295-2590G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102611511 | |||||||
chr13:102611611 | A | G | 1 | a0001c0002t0008g0099 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.295-2490A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102611611 | |||||||
chr13:102611653 | C | T | 1 | a0001c0002t0001g0082 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.295-2448C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102611653 | |||||||
chr13:102611763 | T | G | 1 | a0001c0003t0004g0125 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.295-2338T>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102611763 | |||||||
chr13:102611810 | C | T | 1 | a0001c0002t0001g0173 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.295-2291C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102611810 | |||||||
chr13:102611865 | C | A | 1 | a0001c0002t0001g0047 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.295-2236C>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102611865 | |||||||
chr13:102611964 | C | G | 2 | a0001c0002t0008g0098 a0001c0002t0008g0099 |
2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.295-2137C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102611964 | |||||||
chr13:102612118 | A | T | 2 | a0001c0001t0003g0308 a0001c0001t0013g0309 |
2 | NA20905.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.295-1983A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102612118 | |||||||
chr13:102612212 | C | T | 4 | a0001c0001t0002g0005 a0001c0001t0002g0195 a0001c0001t0002g0196 others(1): Show |
6 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.295-1889C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102612212 | |||||||
chr13:102612324 | G | C | 1 | a0001c0002t0001g0048 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.295-1777G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102612324 | |||||||
chr13:102612363 | A | G | 1 | a0001c0001t0003g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.295-1738A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102612363 | |||||||
chr13:102612585 | A | G | 1 | a0001c0002t0001g0172 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.295-1516A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102612585 | |||||||
chr13:102612965 | T | A | 1 | a0001c0001t0003g0296 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.295-1136T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102612965 | |||||||
chr13:102613034 | G | A | 1 | a0001c0002t0005g0156 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.295-1067G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102613034 | |||||||
chr13:102613065 | T | G | 1 | a0001c0002t0001g0049 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.295-1036T>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102613065 | |||||||
chr13:102613242 | A | G | 1 | a0001c0001t0003g0276 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.295-859A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102613242 | |||||||
chr13:102613412 | C | T | 3 | a0001c0001t0002g0201 a0001c0001t0002g0232 a0001c0001t0002g0233 |
3 | NA18971.hp2 NA18973.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.295-689C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102613412 | |||||||
chr13:102613442 | T | C | 130 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(127): Show |
140 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.295-659T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102613442 | |||||||
chr13:102613751 | T | C | 9 | a0001c0001t0002g0277 a0001c0001t0003g0024 a0001c0001t0003g0030 others(6): Show |
10 | HG02074.hp2 HG02135.hp1 NA18948.hp2 others(7): Show |
intron_variant | MODIFIER | c.295-350T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102613751 | |||||||
chr13:102613783 | C | T | 129 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.295-318C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102613783 | |||||||
chr13:102613795 | G | A | 2 | a0001c0003t0004g0147 a0001c0003t0004g0148 |
2 | HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.295-306G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102613795 | |||||||
chr13:102613905 | A | G | 1 | a0001c0001t0003g0282 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.295-196A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 2/29 | chr13 | 102613905 | |||||||
chr13:102614232 | T | A | 1 | a0001c0002t0001g0007 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.390+36T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 3/29 | chr13 | 102614232 | |||||||
chr13:102614433 | C | T | 129 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.390+237C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 3/29 | chr13 | 102614433 | |||||||
chr13:102614451 | A | G | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.390+255A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 3/29 | chr13 | 102614451 | |||||||
chr13:102614540 | T | A | 1 | a0001c0001t0016g0191 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.390+344T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 3/29 | chr13 | 102614540 | |||||||
chr13:102614546 | A | G | 129 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.390+350A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 3/29 | chr13 | 102614546 | |||||||
chr13:102614562 | C | T | 1 | a0001c0003t0004g0124 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.390+366C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 3/29 | chr13 | 102614562 | |||||||
chr13:102614587 | A | C | 4 | a0001c0001t0010g0320 a0001c0001t0010g0321 a0001c0001t0010g0323 others(1): Show |
4 | HG03130.hp2 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+391A>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 3/29 | chr13 | 102614587 | |||||||
chr13:102614644 | G | A | 221 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(218): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.390+448G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 3/29 | chr13 | 102614644 | |||||||
chr13:102614649 | G | A | 1 | a0001c0003t0004g0126 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.390+453G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 3/29 | chr13 | 102614649 | |||||||
chr13:102614660 | AT | A | 129 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.390+466delT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 102614660 | ||||||
chr13:102614895 | A | AC | 129 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.390+699_390+700ins others(1): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 3/29 | chr13 | 102614895 | |||||||
chr13:102614914 | A | T | 1 | a0001c0002t0001g0081 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.390+718A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 3/29 | chr13 | 102614914 | |||||||
chr13:102614930 | T | C | 1 | a0001c0003t0004g0127 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.390+734T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 3/29 | chr13 | 102614930 | |||||||
chr13:102615001 | G | A | 2 | a0001c0002t0008g0098 a0001c0002t0008g0099 |
2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.390+805G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 3/29 | chr13 | 102615001 | |||||||
chr13:102615246 | A | C | 1 | a0001c0001t0003g0283 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.390+1050A>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 3/29 | chr13 | 102615246 | |||||||
chr13:102615481 | G | A | 2 | a0001c0008t0012g0329 a0003c0009t0012g0328 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.391-915G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 3/29 | chr13 | 102615481 | |||||||
chr13:102615494 | G | A | 129 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.391-902G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 3/29 | chr13 | 102615494 | |||||||
chr13:102615503 | T | C | 45 | a0001c0003t0004g0004 a0001c0003t0004g0011 a0001c0003t0004g0013 others(42): Show |
50 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.391-893T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 3/29 | chr13 | 102615503 | |||||||
chr13:102615547 | G | A | 129 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.391-849G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 3/29 | chr13 | 102615547 | |||||||
chr13:102615589 | A | G | 45 | a0001c0003t0004g0004 a0001c0003t0004g0011 a0001c0003t0004g0013 others(42): Show |
50 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.391-807A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 3/29 | chr13 | 102615589 | |||||||
chr13:102615734 | T | C | 129 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.391-662T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 3/29 | chr13 | 102615734 | |||||||
chr13:102615902 | T | C | 36 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0019 others(33): Show |
45 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.391-494T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 3/29 | chr13 | 102615902 | |||||||
chr13:102615955 | C | CT | 129 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(126): Show |
138 | HG00140.hp1 HG00597.hp2 HG00639.hp1 others(135): Show |
intron_variant | MODIFIER | c.391-428dupT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 102615955 | ||||||
chr13:102615971 | C | T | 129 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(126): Show |
138 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.391-425C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 3/29 | chr13 | 102615971 | |||||||
chr13:102616276 | C | T | 2 | a0001c0008t0012g0329 a0003c0009t0012g0328 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.391-120C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 3/29 | chr13 | 102616276 | |||||||
chr13:102616307 | G | C | 3 | a0001c0002t0005g0110 a0001c0002t0005g0175 a0001c0002t0005g0182 |
3 | HG02132.hp2 NA18998.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.391-89G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 3/29 | chr13 | 102616307 | |||||||
chr13:102616725 | A | G | 5 | a0001c0001t0003g0274 a0001c0001t0003g0275 a0001c0001t0003g0283 others(2): Show |
5 | HG01993.hp1 HG02273.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.495+225A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 4/29 | chr13 | 102616725 | |||||||
chr13:102616754 | G | A | 1 | a0001c0001t0003g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.495+254G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 4/29 | chr13 | 102616754 | |||||||
chr13:102616891 | A | G | 183 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(180): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.495+391A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 4/29 | chr13 | 102616891 | |||||||
chr13:102616911 | G | GT | 4 | a0001c0001t0010g0320 a0001c0001t0010g0321 a0001c0001t0010g0323 others(1): Show |
4 | HG03130.hp2 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+417dupT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 102616911 | ||||||
chr13:102616911 | GT | G | 19 | a0001c0002t0001g0050 a0001c0002t0007g0102 a0001c0002t0007g0103 others(16): Show |
19 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.495+417delT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 102616911 | ||||||
chr13:102616918 | GT | G | 19 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0153 others(16): Show |
23 | HG00099.hp2 HG00639.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.495+430delT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 102616918 | ||||||
chr13:102617075 | G | GT | 8 | a0001c0001t0003g0315 a0001c0001t0006g0261 a0001c0002t0001g0177 others(5): Show |
8 | HG00733.hp1 HG02738.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.495+587dupT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 102617075 | ||||||
chr13:102617075 | GT | G | 19 | a0001c0001t0002g0243 a0001c0001t0003g0027 a0001c0001t0009g0029 others(16): Show |
19 | HG00642.hp1 HG01099.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.495+587delT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 102617075 | ||||||
chr13:102617116 | G | A | 133 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(130): Show |
142 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.495+616G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 4/29 | chr13 | 102617116 | |||||||
chr13:102617158 | C | T | 1 | a0001c0001t0006g0023 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.495+658C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 4/29 | chr13 | 102617158 | |||||||
chr13:102617165 | T | C | 1 | a0001c0003t0004g0130 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.495+665T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 4/29 | chr13 | 102617165 | |||||||
chr13:102617211 | G | A | 1 | a0001c0001t0003g0025 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.495+711G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 4/29 | chr13 | 102617211 | |||||||
chr13:102617215 | A | G | 1 | a0001c0001t0002g0228 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.495+715A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 4/29 | chr13 | 102617215 | |||||||
chr13:102617257 | G | C | 2 | a0001c0001t0006g0256 a0001c0001t0006g0257 |
2 | HG00735.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.495+757G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 4/29 | chr13 | 102617257 | |||||||
chr13:102617397 | G | A | 1 | a0001c0002t0005g0046 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.495+897G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 4/29 | chr13 | 102617397 | |||||||
chr13:102617458 | A | C | 2 | a0001c0001t0003g0316 a0001c0001t0003g0317 |
2 | HG02258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.495+958A>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 4/29 | chr13 | 102617458 | |||||||
chr13:102617817 | G | T | 6 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(3): Show |
6 | HG01069.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.496-905G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 4/29 | chr13 | 102617817 | |||||||
chr13:102617856 | A | G | 1 | a0001c0002t0005g0080 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.496-866A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 4/29 | chr13 | 102617856 | |||||||
chr13:102617883 | A | G | 6 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(3): Show |
6 | HG01069.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.496-839A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 4/29 | chr13 | 102617883 | |||||||
chr13:102617976 | G | A | 1 | a0001c0001t0003g0318 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.496-746G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 4/29 | chr13 | 102617976 | |||||||
chr13:102618074 | A | T | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.496-648A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 4/29 | chr13 | 102618074 | |||||||
chr13:102618079 | C | T | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.496-643C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 4/29 | chr13 | 102618079 | |||||||
chr13:102618153 | G | A | 4 | a0001c0001t0010g0320 a0001c0001t0010g0321 a0001c0001t0010g0323 others(1): Show |
4 | HG03130.hp2 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.496-569G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 4/29 | chr13 | 102618153 | |||||||
chr13:102618225 | T | G | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.496-497T>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 4/29 | chr13 | 102618225 | |||||||
chr13:102618415 | G | A | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.496-307G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 4/29 | chr13 | 102618415 | |||||||
chr13:102618446 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0193 |
3 | HG02615.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.496-276G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 4/29 | chr13 | 102618446 | |||||||
chr13:102618692 | C | G | 4 | a0001c0001t0010g0320 a0001c0001t0010g0321 a0001c0001t0010g0323 others(1): Show |
4 | HG03130.hp2 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.496-30C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 4/29 | chr13 | 102618692 | |||||||
chr13:102618856 | G | A | 164 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(161): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.620+10G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102618856 | |||||||
chr13:102618893 | T | C | 1 | a0001c0001t0002g0243 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.620+47T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102618893 | |||||||
chr13:102619107 | C | T | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.620+261C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102619107 | |||||||
chr13:102619147 | G | A | 45 | a0001c0003t0004g0004 a0001c0003t0004g0011 a0001c0003t0004g0013 others(42): Show |
50 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.620+301G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102619147 | |||||||
chr13:102619195 | T | C | 1 | a0001c0001t0003g0266 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.620+349T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102619195 | |||||||
chr13:102619257 | A | C | 1 | a0001c0002t0005g0071 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.620+411A>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102619257 | |||||||
chr13:102619413 | C | T | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.620+567C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102619413 | |||||||
chr13:102619437 | C | CA | 32 | a0001c0001t0002g0189 a0001c0001t0002g0229 a0001c0001t0002g0277 others(29): Show |
33 | HG00099.hp1 HG00639.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.620+601dupA | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr13 | 102619437 | ||||||
chr13:102619437 | C | CAAA | 51 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(48): Show |
56 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.620+599_620+601dup others(3): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr13 | 102619437 | ||||||
chr13:102619448 | C | A | 11 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(8): Show |
11 | HG01069.hp2 HG01099.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.620+602C>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102619448 | |||||||
chr13:102619502 | C | T | 1 | a0001c0003t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.620+656C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102619502 | |||||||
chr13:102619661 | A | T | 1 | a0001c0001t0006g0241 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.620+815A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102619661 | |||||||
chr13:102619667 | G | A | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.620+821G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102619667 | |||||||
chr13:102619710 | TG | T | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.620+868delG | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr13 | 102619710 | ||||||
chr13:102619820 | G | A | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.620+974G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102619820 | |||||||
chr13:102619822 | A | G | 3 | a0001c0003t0004g0143 a0001c0003t0004g0144 a0002c0005t0004g0015 |
4 | HG01192.hp1 HG03225.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.620+976A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102619822 | |||||||
chr13:102619906 | C | T | 44 | a0001c0003t0004g0004 a0001c0003t0004g0011 a0001c0003t0004g0013 others(41): Show |
49 | HG00323.hp1 HG01099.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.620+1060C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102619906 | |||||||
chr13:102620355 | A | T | 1 | a0001c0002t0001g0082 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.620+1509A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102620355 | |||||||
chr13:102620371 | A | G | 1 | a0001c0002t0008g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.620+1525A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102620371 | |||||||
chr13:102620627 | A | G | 1 | a0001c0002t0001g0164 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.620+1781A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102620627 | |||||||
chr13:102620900 | G | A | 1 | a0001c0003t0004g0131 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.621-1977G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102620900 | |||||||
chr13:102620917 | C | T | 170 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(167): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.621-1960C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102620917 | |||||||
chr13:102620956 | TAAAAC | T | 6 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(3): Show |
6 | HG01069.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.621-1916_621-1912d others(7): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr13 | 102620956 | ||||||
chr13:102620957 | A | G | 1 | a0001c0001t0002g0201 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.621-1920A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102620957 | |||||||
chr13:102621019 | C | T | 1 | a0001c0001t0002g0227 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.621-1858C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102621019 | |||||||
chr13:102621115 | C | T | 158 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(155): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.621-1762C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102621115 | |||||||
chr13:102621143 | A | T | 4 | a0001c0001t0003g0024 a0001c0001t0003g0280 a0001c0001t0003g0281 others(1): Show |
5 | HG02074.hp2 HG02135.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.621-1734A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102621143 | |||||||
chr13:102621381 | C | T | 1 | a0001c0002t0001g0070 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.621-1496C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102621381 | |||||||
chr13:102621489 | A | G | 164 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(161): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.621-1388A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102621489 | |||||||
chr13:102621719 | G | C | 1 | a0001c0002t0005g0168 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.621-1158G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102621719 | |||||||
chr13:102621762 | G | T | 1 | a0001c0003t0004g0127 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.621-1115G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102621762 | |||||||
chr13:102622405 | C | T | 4 | a0001c0001t0002g0224 a0001c0001t0002g0225 a0001c0001t0002g0226 others(1): Show |
4 | HG02027.hp2 HG02056.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.621-472C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102622405 | |||||||
chr13:102622558 | C | T | 1 | a0001c0002t0008g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.621-319C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102622558 | |||||||
chr13:102622851 | T | C | 1 | a0001c0002t0008g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.621-26T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 5/29 | chr13 | 102622851 | |||||||
chr13:102623145 | C | T | 31 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0025 others(28): Show |
39 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.784+105C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102623145 | |||||||
chr13:102623166 | A | G | 4 | a0001c0002t0001g0047 a0001c0002t0001g0078 a0001c0002t0001g0079 others(1): Show |
4 | NA18965.hp2 NA19055.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.784+126A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102623166 | |||||||
chr13:102623282 | G | A | 1 | a0001c0001t0002g0204 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.784+242G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102623282 | |||||||
chr13:102623424 | G | A | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.784+384G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102623424 | |||||||
chr13:102623550 | C | T | 1 | a0001c0001t0003g0317 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.784+510C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102623550 | |||||||
chr13:102623606 | T | C | 1 | a0001c0001t0016g0191 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.784+566T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102623606 | |||||||
chr13:102623626 | T | G | 1 | a0001c0001t0002g0183 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.784+586T>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102623626 | |||||||
chr13:102623708 | A | G | 1 | a0001c0002t0001g0077 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.784+668A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102623708 | |||||||
chr13:102623765 | C | T | 164 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(161): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.784+725C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102623765 | |||||||
chr13:102623803 | G | A | 64 | a0001c0001t0002g0277 a0001c0001t0003g0001 a0001c0001t0003g0003 others(61): Show |
73 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.784+763G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102623803 | |||||||
chr13:102623990 | G | A | 2 | a0001c0001t0003g0181 a0001c0001t0009g0029 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.784+950G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102623990 | |||||||
chr13:102624042 | C | T | 1 | a0001c0001t0003g0318 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.784+1002C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102624042 | |||||||
chr13:102624047 | G | A | 164 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(161): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.784+1007G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102624047 | |||||||
chr13:102624113 | T | C | 1 | a0001c0002t0001g0008 | 2 | HG02004.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.784+1073T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102624113 | |||||||
chr13:102624180 | T | C | 7 | a0001c0001t0003g0003 a0001c0001t0003g0019 a0001c0001t0003g0297 others(4): Show |
11 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.784+1140T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102624180 | |||||||
chr13:102624191 | A | G | 1 | a0001c0002t0001g0047 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.784+1151A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102624191 | |||||||
chr13:102624272 | C | T | 1 | a0001c0003t0004g0128 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.784+1232C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102624272 | |||||||
chr13:102624492 | C | G | 4 | a0001c0001t0010g0320 a0001c0001t0010g0321 a0001c0001t0010g0323 others(1): Show |
4 | HG03130.hp2 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.784+1452C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102624492 | |||||||
chr13:102624496 | C | T | 62 | a0001c0001t0003g0181 a0001c0001t0009g0029 a0001c0001t0010g0320 others(59): Show |
67 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.784+1456C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102624496 | |||||||
chr13:102624745 | G | A | 1 | a0001c0001t0003g0181 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.784+1705G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102624745 | |||||||
chr13:102624811 | C | T | 1 | a0001c0001t0002g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.784+1771C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102624811 | |||||||
chr13:102624840 | T | C | 2 | a0001c0008t0012g0329 a0003c0009t0012g0328 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.784+1800T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102624840 | |||||||
chr13:102624850 | T | C | 170 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(167): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.784+1810T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102624850 | |||||||
chr13:102624851 | CCTTTTT | C | 10 | a0001c0001t0002g0185 a0001c0001t0002g0221 a0001c0001t0002g0222 others(7): Show |
10 | HG01175.hp2 HG02056.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.784+1812_784+1817d others(8): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102624851 | |||||||
chr13:102624851 | CCTTTTTT | C | 155 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(152): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.784+1812_784+1818d others(9): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102624851 | |||||||
chr13:102624852 | C | CT | 20 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0017 others(17): Show |
20 | HG00597.hp1 HG00642.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.784+1836dupT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr13 | 102624852 | ||||||
chr13:102624852 | C | T | 5 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(2): Show |
5 | HG01069.hp2 HG01099.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.784+1812C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102624852 | |||||||
chr13:102624852 | CT | C | 40 | a0001c0003t0004g0004 a0001c0003t0004g0011 a0001c0003t0004g0013 others(37): Show |
43 | HG00323.hp1 HG00735.hp2 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.784+1836delT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr13 | 102624852 | ||||||
chr13:102624852 | CTTTTTTT others(5): Show |
C | 9 | a0001c0002t0001g0038 a0001c0002t0001g0047 a0001c0002t0001g0073 others(6): Show |
9 | HG00408.hp1 HG00408.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.784+1825_784+1836d others(14): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr13 | 102624852 | ||||||
chr13:102624930 | G | A | 1 | a0001c0002t0019g0052 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.784+1890G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102624930 | |||||||
chr13:102624963 | G | T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.784+1923G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102624963 | |||||||
chr13:102625083 | T | C | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.785-1929T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102625083 | |||||||
chr13:102625105 | G | A | 1 | a0001c0002t0005g0111 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.785-1907G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102625105 | |||||||
chr13:102625109 | C | T | 164 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(161): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.785-1903C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102625109 | |||||||
chr13:102625118 | A | G | 1 | a0001c0002t0001g0176 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.785-1894A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102625118 | |||||||
chr13:102625164 | C | CT | 161 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(158): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.785-1830dupT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr13 | 102625164 | ||||||
chr13:102625164 | C | CTT | 6 | a0001c0001t0002g0184 a0001c0001t0002g0185 a0001c0001t0002g0220 others(3): Show |
6 | HG00733.hp2 HG02572.hp2 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.785-1831_785-1830d others(4): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr13 | 102625164 | ||||||
chr13:102625234 | G | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.785-1778G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102625234 | |||||||
chr13:102625251 | G | A | 1 | a0001c0001t0006g0252 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.785-1761G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102625251 | |||||||
chr13:102625258 | G | A | 45 | a0001c0003t0004g0004 a0001c0003t0004g0011 a0001c0003t0004g0013 others(42): Show |
50 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.785-1754G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102625258 | |||||||
chr13:102625275 | T | C | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.785-1737T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102625275 | |||||||
chr13:102625304 | G | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.785-1708G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102625304 | |||||||
chr13:102625346 | A | G | 1 | a0001c0002t0005g0109 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.785-1666A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102625346 | |||||||
chr13:102625389 | C | A | 2 | a0001c0002t0008g0098 a0001c0002t0008g0099 |
2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.785-1623C>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102625389 | |||||||
chr13:102625448 | G | A | 2 | a0001c0001t0003g0305 a0001c0001t0003g0319 |
2 | HG01433.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.785-1564G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102625448 | |||||||
chr13:102625459 | C | T | 1 | a0001c0002t0001g0163 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.785-1553C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102625459 | |||||||
chr13:102625621 | A | G | 1 | a0001c0001t0006g0257 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.785-1391A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102625621 | |||||||
chr13:102625641 | T | A | 2 | a0001c0001t0003g0181 a0001c0001t0009g0029 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.785-1371T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102625641 | |||||||
chr13:102625651 | A | G | 2 | a0001c0001t0002g0202 a0001c0001t0002g0203 |
2 | NA19004.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.785-1361A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102625651 | |||||||
chr13:102625729 | T | C | 3 | a0001c0002t0001g0094 a0001c0002t0001g0095 a0001c0002t0001g0097 |
3 | HG03453.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.785-1283T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102625729 | |||||||
chr13:102625865 | T | C | 1 | a0001c0002t0001g0172 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.785-1147T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102625865 | |||||||
chr13:102625973 | A | G | 1 | a0001c0001t0003g0284 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.785-1039A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102625973 | |||||||
chr13:102625978 | A | C | 1 | a0001c0003t0004g0330 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.785-1034A>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102625978 | |||||||
chr13:102626181 | A | G | 1 | a0001c0003t0004g0125 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.785-831A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102626181 | |||||||
chr13:102626274 | C | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.785-738C>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102626274 | |||||||
chr13:102626418 | G | T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.785-594G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102626418 | |||||||
chr13:102626431 | T | A | 2 | a0001c0001t0010g0320 a0001c0001t0010g0321 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.785-581T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102626431 | |||||||
chr13:102626500 | G | T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.785-512G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102626500 | |||||||
chr13:102626519 | G | A | 1 | a0001c0002t0005g0112 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.785-493G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102626519 | |||||||
chr13:102626612 | G | T | 1 | a0001c0002t0001g0180 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.785-400G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 6/29 | chr13 | 102626612 | |||||||
chr13:102627239 | C | G | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.939+73C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 7/29 | chr13 | 102627239 | |||||||
chr13:102627305 | T | G | 1 | a0001c0002t0005g0053 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.939+139T>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 7/29 | chr13 | 102627305 | |||||||
chr13:102627312 | A | G | 2 | a0001c0002t0008g0098 a0001c0002t0008g0099 |
2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.939+146A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 7/29 | chr13 | 102627312 | |||||||
chr13:102627454 | C | T | 2 | a0001c0001t0002g0020 a0001c0001t0002g0193 |
3 | HG02615.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.939+288C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 7/29 | chr13 | 102627454 | |||||||
chr13:102627508 | G | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.940-340G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 7/29 | chr13 | 102627508 | |||||||
chr13:102627629 | TG | T | 50 | a0001c0002t0007g0106 a0001c0002t0008g0098 a0001c0002t0008g0099 others(47): Show |
55 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(52): Show |
intron_variant | MODIFIER | c.940-218delG | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 7/29 | chr13 | 102627629 | |||||||
chr13:102627630 | G | T | 5 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(2): Show |
5 | HG01069.hp2 HG01099.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.940-218G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 7/29 | chr13 | 102627630 | |||||||
chr13:102627724 | G | A | 1 | a0001c0003t0004g0119 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.940-124G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 7/29 | chr13 | 102627724 | |||||||
chr13:102627782 | T | C | 1 | a0001c0002t0005g0080 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.940-66T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 7/29 | chr13 | 102627782 | |||||||
chr13:102627787 | T | G | 52 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0036 others(49): Show |
55 | HG00597.hp2 HG01981.hp2 HG02027.hp2 others(52): Show |
intron_variant | MODIFIER | c.940-61T>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 7/29 | chr13 | 102627787 | |||||||
chr13:102628070 | C | T | 11 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(8): Show |
11 | HG01069.hp2 HG01099.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1016+146C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 8/29 | chr13 | 102628070 | |||||||
chr13:102628100 | G | A | 2 | a0001c0002t0008g0098 a0001c0002t0008g0099 |
2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1016+176G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 8/29 | chr13 | 102628100 | |||||||
chr13:102628187 | G | A | 62 | a0001c0001t0003g0181 a0001c0001t0009g0029 a0001c0001t0010g0320 others(59): Show |
67 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.1016+263G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 8/29 | chr13 | 102628187 | |||||||
chr13:102628326 | A | G | 58 | a0001c0001t0010g0320 a0001c0001t0010g0321 a0001c0002t0007g0102 others(55): Show |
63 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(60): Show |
intron_variant | MODIFIER | c.1016+402A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 8/29 | chr13 | 102628326 | |||||||
chr13:102628414 | C | T | 1 | a0001c0003t0004g0150 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1016+490C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 8/29 | chr13 | 102628414 | |||||||
chr13:102628476 | G | A | 1 | a0001c0001t0003g0271 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1016+552G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 8/29 | chr13 | 102628476 | |||||||
chr13:102628745 | C | T | 6 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(3): Show |
6 | HG01069.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1017-737C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 8/29 | chr13 | 102628745 | |||||||
chr13:102628900 | C | A | 1 | a0001c0001t0002g0197 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1017-582C>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 8/29 | chr13 | 102628900 | |||||||
chr13:102629099 | T | A | 222 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(219): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1017-383T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 8/29 | chr13 | 102629099 | |||||||
chr13:102629102 | C | G | 1 | a0001c0001t0016g0191 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1017-380C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 8/29 | chr13 | 102629102 | |||||||
chr13:102629170 | A | G | 7 | a0001c0001t0003g0003 a0001c0001t0003g0019 a0001c0001t0003g0297 others(4): Show |
11 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1017-312A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 8/29 | chr13 | 102629170 | |||||||
chr13:102629170 | A | T | 1 | a0001c0002t0001g0162 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1017-312A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 8/29 | chr13 | 102629170 | |||||||
chr13:102629233 | C | T | 1 | a0001c0001t0003g0285 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1017-249C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 8/29 | chr13 | 102629233 | |||||||
chr13:102629275 | C | T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1017-207C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 8/29 | chr13 | 102629275 | |||||||
chr13:102629285 | G | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1017-197G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 8/29 | chr13 | 102629285 | |||||||
chr13:102629731 | A | G | 1 | a0001c0001t0002g0219 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1144+122A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 9/29 | chr13 | 102629731 | |||||||
chr13:102629929 | A | C | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1145-167A>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 9/29 | chr13 | 102629929 | |||||||
chr13:102629949 | C | A | 3 | a0001c0001t0002g0192 a0001c0001t0002g0197 a0004c0007t0002g0198 |
3 | HG02965.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1145-147C>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 9/29 | chr13 | 102629949 | |||||||
chr13:102629949 | C | G | 162 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(159): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1145-147C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 9/29 | chr13 | 102629949 | |||||||
chr13:102629980 | C | T | 1 | a0001c0001t0009g0029 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1145-116C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 9/29 | chr13 | 102629980 | |||||||
chr13:102630234 | G | A | 2 | a0001c0008t0012g0329 a0003c0009t0012g0328 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1244+39G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102630234 | |||||||
chr13:102630293 | TGTTG | T | 45 | a0001c0003t0004g0004 a0001c0003t0004g0011 a0001c0003t0004g0013 others(42): Show |
50 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.1244+102_1244+105d others(6): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr13 | 102630293 | ||||||
chr13:102630302 | T | C | 1 | a0001c0001t0009g0029 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1244+107T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102630302 | |||||||
chr13:102630424 | T | C | 1 | a0001c0001t0003g0019 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1244+229T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102630424 | |||||||
chr13:102630588 | C | T | 1 | a0001c0001t0002g0218 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1244+393C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102630588 | |||||||
chr13:102630589 | G | A | 6 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(3): Show |
6 | HG01069.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1244+394G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102630589 | |||||||
chr13:102630682 | C | T | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.1244+487C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102630682 | |||||||
chr13:102630684 | A | G | 1 | a0001c0001t0002g0239 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1244+489A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102630684 | |||||||
chr13:102630797 | C | T | 1 | a0001c0001t0009g0029 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1244+602C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102630797 | |||||||
chr13:102630925 | C | T | 1 | a0001c0001t0006g0244 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1244+730C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102630925 | |||||||
chr13:102631060 | C | A | 1 | a0001c0001t0002g0224 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1244+865C>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102631060 | |||||||
chr13:102631097 | A | G | 1 | a0001c0003t0004g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1244+902A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102631097 | |||||||
chr13:102631213 | T | A | 2 | a0001c0001t0003g0181 a0001c0001t0009g0029 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1244+1018T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102631213 | |||||||
chr13:102631245 | C | T | 6 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(3): Show |
6 | HG01069.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1244+1050C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102631245 | |||||||
chr13:102631420 | T | C | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.1244+1225T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102631420 | |||||||
chr13:102631568 | A | G | 20 | a0001c0001t0003g0251 a0001c0001t0006g0022 a0001c0001t0006g0023 others(17): Show |
22 | HG00140.hp1 HG00735.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.1244+1373A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102631568 | |||||||
chr13:102631665 | C | T | 6 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(3): Show |
6 | HG01069.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1244+1470C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102631665 | |||||||
chr13:102631898 | C | G | 5 | a0001c0002t0005g0006 a0001c0002t0005g0031 a0001c0002t0005g0032 others(2): Show |
6 | NA18947.hp1 NA18949.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.1244+1703C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102631898 | |||||||
chr13:102632156 | G | A | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.1245-1794G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102632156 | |||||||
chr13:102632243 | C | CT | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.1245-1695dupT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr13 | 102632243 | ||||||
chr13:102632313 | C | T | 1 | a0001c0002t0001g0008 | 2 | HG02004.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1245-1637C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102632313 | |||||||
chr13:102632401 | C | T | 2 | a0001c0001t0003g0270 a0001c0001t0003g0272 |
2 | NA18979.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1245-1549C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102632401 | |||||||
chr13:102632417 | T | A | 65 | a0001c0001t0002g0277 a0001c0001t0003g0001 a0001c0001t0003g0003 others(62): Show |
74 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.1245-1533T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102632417 | |||||||
chr13:102632434 | G | C | 2 | a0001c0008t0012g0329 a0003c0009t0012g0328 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1245-1516G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102632434 | |||||||
chr13:102632548 | T | C | 20 | a0001c0001t0003g0251 a0001c0001t0006g0022 a0001c0001t0006g0023 others(17): Show |
22 | HG00140.hp1 HG00735.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.1245-1402T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102632548 | |||||||
chr13:102632673 | A | T | 2 | a0001c0008t0012g0329 a0003c0009t0012g0328 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1245-1277A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102632673 | |||||||
chr13:102633000 | TA | T | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.1245-944delA | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr13 | 102633000 | ||||||
chr13:102633056 | A | T | 1 | a0001c0003t0004g0014 | 2 | NA18975.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.1245-894A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102633056 | |||||||
chr13:102633083 | G | A | 8 | a0001c0002t0001g0054 a0001c0002t0001g0055 a0001c0002t0001g0056 others(5): Show |
8 | HG01934.hp1 HG01978.hp1 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.1245-867G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102633083 | |||||||
chr13:102633140 | T | C | 1 | a0001c0001t0002g0205 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1245-810T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102633140 | |||||||
chr13:102633207 | G | T | 1 | a0001c0001t0002g0220 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1245-743G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102633207 | |||||||
chr13:102633230 | C | T | 1 | a0001c0002t0008g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1245-720C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102633230 | |||||||
chr13:102633269 | G | A | 1 | a0001c0003t0004g0331 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1245-681G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102633269 | |||||||
chr13:102633345 | G | A | 62 | a0001c0001t0003g0181 a0001c0001t0009g0029 a0001c0001t0010g0320 others(59): Show |
67 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.1245-605G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102633345 | |||||||
chr13:102633354 | C | T | 1 | a0001c0001t0003g0294 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1245-596C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102633354 | |||||||
chr13:102633375 | C | CA | 5 | a0001c0001t0002g0184 a0001c0001t0002g0221 a0001c0001t0003g0262 others(2): Show |
5 | HG02074.hp2 HG02698.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.1245-567dupA | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr13 | 102633375 | ||||||
chr13:102633760 | T | A | 1 | a0001c0001t0009g0273 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1245-190T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102633760 | |||||||
chr13:102633922 | A | G | 1 | a0001c0002t0001g0051 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1245-28A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102633922 | |||||||
chr13:102633930 | T | A | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.1245-20T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 10/29 | chr13 | 102633930 | |||||||
chr13:102634124 | C | T | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.1393+26C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 11/29 | chr13 | 102634124 | |||||||
chr13:102634223 | C | T | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.1393+125C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 11/29 | chr13 | 102634223 | |||||||
chr13:102634234 | T | A | 2 | a0001c0008t0012g0329 a0003c0009t0012g0328 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1393+136T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 11/29 | chr13 | 102634234 | |||||||
chr13:102634357 | G | A | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.1393+259G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 11/29 | chr13 | 102634357 | |||||||
chr13:102634362 | C | T | 1 | a0001c0001t0003g0318 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1393+264C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 11/29 | chr13 | 102634362 | |||||||
chr13:102634413 | T | A | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.1393+315T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 11/29 | chr13 | 102634413 | |||||||
chr13:102634415 | A | T | 1 | a0001c0001t0003g0181 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1393+317A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 11/29 | chr13 | 102634415 | |||||||
chr13:102634462 | C | A | 2 | a0001c0002t0008g0098 a0001c0002t0008g0099 |
2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1393+364C>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 11/29 | chr13 | 102634462 | |||||||
chr13:102634464 | G | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1393+366G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 11/29 | chr13 | 102634464 | |||||||
chr13:102634639 | G | A | 1 | a0001c0002t0008g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1393+541G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 11/29 | chr13 | 102634639 | |||||||
chr13:102634639 | G | C | 59 | a0001c0001t0010g0320 a0001c0001t0010g0321 a0001c0001t0010g0323 others(56): Show |
64 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.1393+541G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 11/29 | chr13 | 102634639 | |||||||
chr13:102634809 | T | C | 1 | a0001c0001t0003g0308 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1393+711T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 11/29 | chr13 | 102634809 | |||||||
chr13:102635019 | A | G | 1 | a0001c0001t0003g0025 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1394-568A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 11/29 | chr13 | 102635019 | |||||||
chr13:102635238 | C | A | 2 | a0001c0002t0001g0157 a0001c0002t0001g0167 |
2 | HG02135.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.1394-349C>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 11/29 | chr13 | 102635238 | |||||||
chr13:102635834 | A | G | 2 | a0001c0002t0005g0108 a0001c0002t0005g0117 |
2 | NA18980.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1509+132A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 12/29 | chr13 | 102635834 | |||||||
chr13:102635909 | A | G | 1 | a0001c0001t0003g0187 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1509+207A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 12/29 | chr13 | 102635909 | |||||||
chr13:102635940 | G | A | 1 | a0001c0002t0005g0039 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1509+238G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 12/29 | chr13 | 102635940 | |||||||
chr13:102636440 | GAATGAGT others(8): Show |
G | 2 | a0001c0003t0005g0012 a0001c0004t0005g0012 |
2 | NA18962.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1678+52_1678+66del others(15): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr13 | 102636440 | ||||||
chr13:102636764 | G | T | 8 | a0001c0002t0005g0006 a0001c0002t0005g0028 a0001c0002t0005g0031 others(5): Show |
9 | HG00597.hp1 HG03017.hp1 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.1679-318G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 13/29 | chr13 | 102636764 | |||||||
chr13:102636947 | A | G | 1 | a0001c0001t0009g0029 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1679-135A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 13/29 | chr13 | 102636947 | |||||||
chr13:102636988 | C | T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1679-94C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 13/29 | chr13 | 102636988 | |||||||
chr13:102636996 | T | C | 1 | a0001c0002t0008g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1679-86T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 13/29 | chr13 | 102636996 | |||||||
chr13:102637059 | A | G | 36 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0009 others(33): Show |
40 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.1679-23A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 13/29 | chr13 | 102637059 | |||||||
chr13:102637505 | G | A | 2 | a0001c0002t0008g0098 a0001c0002t0008g0099 |
2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1836+266G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 14/29 | chr13 | 102637505 | |||||||
chr13:102637541 | C | CTTGTTGT others(2): Show |
67 | a0001c0001t0002g0183 a0001c0001t0002g0277 a0001c0001t0003g0001 others(64): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.1836+317_1836+325d others(11): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr13 | 102637541 | ||||||
chr13:102637541 | C | CTTGTTGT others(5): Show |
26 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0153 others(23): Show |
30 | HG01243.hp1 HG01884.hp2 HG01981.hp1 others(27): Show |
intron_variant | MODIFIER | c.1836+314_1836+325d others(14): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr13 | 102637541 | ||||||
chr13:102637541 | C | CTTGTTGT others(8): Show |
69 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0036 others(66): Show |
74 | HG00140.hp1 HG00597.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.1836+311_1836+325d others(17): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr13 | 102637541 | ||||||
chr13:102637541 | C | CTTGTTGT others(11): Show |
1 | a0001c0001t0002g0206 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1836+308_1836+325d others(20): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr13 | 102637541 | ||||||
chr13:102637541 | C | CTTGTTGT others(14): Show |
1 | a0001c0001t0006g0244 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1836+305_1836+325d others(23): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr13 | 102637541 | ||||||
chr13:102637564 | T | TGTTGTTG others(6): Show |
1 | a0001c0001t0003g0230 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1836+325_1836+326i others(15): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 14/29 | chr13 | 102637564 | |||||||
chr13:102637583 | C | T | 4 | a0001c0001t0010g0320 a0001c0001t0010g0321 a0001c0001t0010g0323 others(1): Show |
4 | HG03130.hp2 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1836+344C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 14/29 | chr13 | 102637583 | |||||||
chr13:102637625 | G | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1836+386G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 14/29 | chr13 | 102637625 | |||||||
chr13:102637655 | A | G | 1 | a0001c0002t0008g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1836+416A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 14/29 | chr13 | 102637655 | |||||||
chr13:102637758 | C | T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1837-481C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 14/29 | chr13 | 102637758 | |||||||
chr13:102637880 | A | C | 1 | a0001c0002t0001g0100 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1837-359A>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 14/29 | chr13 | 102637880 | |||||||
chr13:102638009 | T | C | 3 | a0001c0002t0001g0054 a0001c0002t0001g0069 a0001c0002t0005g0053 |
3 | NA18941.hp2 NA18994.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1837-230T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 14/29 | chr13 | 102638009 | |||||||
chr13:102638091 | G | A | 1 | a0001c0001t0003g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1837-148G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 14/29 | chr13 | 102638091 | |||||||
chr13:102638185 | G | C | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1837-54G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 14/29 | chr13 | 102638185 | |||||||
chr13:102638224 | G | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1837-15G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 14/29 | chr13 | 102638224 | |||||||
chr13:102638617 | G | A | 1 | a0001c0001t0003g0283 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1913+302G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 15/29 | chr13 | 102638617 | |||||||
chr13:102638627 | T | C | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1913+312T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 15/29 | chr13 | 102638627 | |||||||
chr13:102638761 | T | G | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1913+446T>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 15/29 | chr13 | 102638761 | |||||||
chr13:102638783 | TGGAACCA others(1): Show |
T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1913+473_1913+480d others(10): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr13 | 102638783 | ||||||
chr13:102638928 | G | A | 1 | a0001c0002t0001g0086 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1913+613G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 15/29 | chr13 | 102638928 | |||||||
chr13:102638937 | A | G | 1 | a0001c0002t0008g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1913+622A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 15/29 | chr13 | 102638937 | |||||||
chr13:102638974 | G | T | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.1913+659G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 15/29 | chr13 | 102638974 | |||||||
chr13:102639036 | C | T | 1 | a0001c0002t0005g0112 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1913+721C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 15/29 | chr13 | 102639036 | |||||||
chr13:102639333 | T | G | 34 | a0001c0003t0004g0004 a0001c0003t0004g0011 a0001c0003t0004g0013 others(31): Show |
38 | HG00323.hp1 HG01099.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.1914-937T>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 15/29 | chr13 | 102639333 | |||||||
chr13:102639370 | G | C | 1 | a0001c0003t0004g0148 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1914-900G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 15/29 | chr13 | 102639370 | |||||||
chr13:102639383 | A | T | 2 | a0001c0002t0008g0098 a0001c0002t0008g0099 |
2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1914-887A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 15/29 | chr13 | 102639383 | |||||||
chr13:102639385 | A | G | 1 | a0001c0004t0004g0141 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1914-885A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 15/29 | chr13 | 102639385 | |||||||
chr13:102639398 | T | C | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1914-872T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 15/29 | chr13 | 102639398 | |||||||
chr13:102639506 | C | G | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1914-764C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 15/29 | chr13 | 102639506 | |||||||
chr13:102639660 | CAG | C | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1914-609_1914-608d others(4): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 15/29 | chr13 | 102639660 | |||||||
chr13:102639787 | A | C | 1 | a0001c0001t0006g0255 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1914-483A>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 15/29 | chr13 | 102639787 | |||||||
chr13:102639789 | G | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1914-481G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 15/29 | chr13 | 102639789 | |||||||
chr13:102640100 | C | A | 2 | a0001c0001t0003g0181 a0001c0001t0009g0029 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1914-170C>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 15/29 | chr13 | 102640100 | |||||||
chr13:102640101 | TAACCTAC others(98): Show |
T | 2 | a0001c0001t0003g0181 a0001c0001t0009g0029 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1914-166_1914-62de others(1): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr13 | 102640101 | ||||||
chr13:102640208 | A | T | 2 | a0001c0001t0003g0181 a0001c0001t0009g0029 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1914-62A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 15/29 | chr13 | 102640208 | |||||||
chr13:102640230 | T | C | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.1914-40T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 15/29 | chr13 | 102640230 | |||||||
chr13:102640407 | T | C | 2 | a0001c0001t0002g0207 a0001c0001t0002g0238 |
2 | NA18963.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.2020+31T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102640407 | |||||||
chr13:102640460 | G | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2020+84G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102640460 | |||||||
chr13:102640525 | G | A | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.2020+149G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102640525 | |||||||
chr13:102640641 | A | AT | 49 | a0001c0002t0001g0010 a0001c0002t0001g0040 a0001c0002t0001g0041 others(46): Show |
55 | HG00408.hp1 HG00741.hp2 HG01099.hp1 others(52): Show |
intron_variant | MODIFIER | c.2020+293dupT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr13 | 102640641 | ||||||
chr13:102640641 | A | ATT | 13 | a0001c0002t0008g0101 a0001c0003t0004g0138 a0001c0003t0004g0139 others(10): Show |
13 | HG01175.hp1 HG01192.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.2020+292_2020+293d others(4): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr13 | 102640641 | ||||||
chr13:102640641 | A | ATTTTTTT others(3): Show |
2 | a0001c0002t0007g0102 a0001c0002t0007g0104 |
2 | HG01069.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.2020+284_2020+293d others(12): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr13 | 102640641 | ||||||
chr13:102640641 | ATT | A | 10 | a0001c0001t0002g0189 a0001c0001t0002g0192 a0001c0001t0002g0248 others(7): Show |
11 | HG01175.hp2 HG01243.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.2020+292_2020+293d others(4): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr13 | 102640641 | ||||||
chr13:102640641 | ATTT | A | 100 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0153 others(97): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.2020+291_2020+293d others(5): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr13 | 102640641 | ||||||
chr13:102640641 | ATTTT | A | 53 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0036 others(50): Show |
56 | HG00323.hp2 HG00597.hp2 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.2020+290_2020+293d others(6): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr13 | 102640641 | ||||||
chr13:102640647 | T | A | 1 | a0001c0001t0003g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2020+271T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102640647 | |||||||
chr13:102640659 | T | C | 2 | a0001c0001t0002g0205 a0001c0001t0002g0206 |
2 | NA18959.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2020+283T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102640659 | |||||||
chr13:102640697 | C | CTGGA | 4 | a0001c0001t0010g0320 a0001c0001t0010g0321 a0001c0001t0010g0323 others(1): Show |
4 | HG03130.hp2 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2020+322_2020+325d others(6): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr13 | 102640697 | ||||||
chr13:102640719 | C | T | 48 | a0001c0002t0008g0101 a0001c0003t0004g0004 a0001c0003t0004g0011 others(45): Show |
53 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(50): Show |
intron_variant | MODIFIER | c.2020+343C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102640719 | |||||||
chr13:102640738 | C | T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2020+362C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102640738 | |||||||
chr13:102640874 | T | C | 1 | a0001c0002t0001g0072 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2020+498T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102640874 | |||||||
chr13:102640897 | G | A | 27 | a0001c0002t0001g0038 a0001c0002t0001g0040 a0001c0002t0001g0043 others(24): Show |
27 | HG00408.hp2 HG01123.hp1 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.2020+521G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102640897 | |||||||
chr13:102640945 | C | T | 1 | a0001c0002t0001g0180 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2020+569C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102640945 | |||||||
chr13:102640946 | G | A | 48 | a0001c0002t0008g0101 a0001c0003t0004g0004 a0001c0003t0004g0011 others(45): Show |
53 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(50): Show |
intron_variant | MODIFIER | c.2020+570G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102640946 | |||||||
chr13:102641150 | G | T | 42 | a0001c0003t0004g0004 a0001c0003t0004g0011 a0001c0003t0004g0013 others(39): Show |
47 | HG00323.hp1 HG01099.hp1 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.2020+774G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102641150 | |||||||
chr13:102641175 | T | A | 56 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(53): Show |
61 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.2020+799T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102641175 | |||||||
chr13:102641414 | C | T | 1 | a0001c0001t0006g0242 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2020+1038C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102641414 | |||||||
chr13:102641565 | T | C | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2020+1189T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102641565 | |||||||
chr13:102641669 | G | A | 6 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(3): Show |
6 | HG01069.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.2020+1293G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102641669 | |||||||
chr13:102641778 | T | G | 173 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(170): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.2020+1402T>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102641778 | |||||||
chr13:102641939 | G | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2021-1283G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102641939 | |||||||
chr13:102641984 | A | G | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2021-1238A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102641984 | |||||||
chr13:102642042 | T | C | 1 | a0001c0002t0001g0176 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2021-1180T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102642042 | |||||||
chr13:102642065 | G | A | 221 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(218): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.2021-1157G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102642065 | |||||||
chr13:102642072 | G | A | 8 | a0001c0002t0005g0006 a0001c0002t0005g0028 a0001c0002t0005g0031 others(5): Show |
9 | HG00597.hp1 HG03017.hp1 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.2021-1150G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102642072 | |||||||
chr13:102642084 | C | T | 2 | a0001c0008t0012g0329 a0003c0009t0012g0328 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2021-1138C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102642084 | |||||||
chr13:102642130 | C | T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2021-1092C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102642130 | |||||||
chr13:102642421 | A | G | 2 | a0001c0001t0002g0020 a0001c0001t0002g0193 |
3 | HG02615.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2021-801A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102642421 | |||||||
chr13:102642544 | A | G | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2021-678A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102642544 | |||||||
chr13:102642601 | C | T | 1 | a0001c0002t0001g0050 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2021-621C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102642601 | |||||||
chr13:102642666 | T | G | 1 | a0001c0002t0005g0156 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2021-556T>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102642666 | |||||||
chr13:102642749 | G | C | 1 | a0001c0002t0001g0162 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2021-473G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102642749 | |||||||
chr13:102642797 | A | C | 1 | a0001c0002t0008g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2021-425A>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102642797 | |||||||
chr13:102642956 | C | G | 1 | a0001c0001t0016g0191 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2021-266C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102642956 | |||||||
chr13:102643135 | A | AT | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2021-86dupT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr13 | 102643135 | ||||||
chr13:102643141 | A | G | 1 | a0001c0002t0005g0115 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2021-81A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102643141 | |||||||
chr13:102643201 | CTTCT | C | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
splice_region_variant&intron_variant | LOW | c.2021-11_2021-8delT others(3): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr13 | 102643201 | ||||||
chr13:102643210 | T | G | 2 | a0001c0001t0006g0246 a0001c0001t0006g0247 |
2 | HG01109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2021-12T>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 16/29 | chr13 | 102643210 | |||||||
chr13:102643516 | A | T | 2 | a0001c0002t0008g0098 a0001c0002t0008g0099 |
2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2175+140A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 17/29 | chr13 | 102643516 | |||||||
chr13:102643893 | A | G | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2175+517A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 17/29 | chr13 | 102643893 | |||||||
chr13:102644022 | C | T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2176-535C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 17/29 | chr13 | 102644022 | |||||||
chr13:102644201 | G | A | 1 | a0001c0002t0001g0081 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2176-356G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 17/29 | chr13 | 102644201 | |||||||
chr13:102644260 | A | G | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2176-297A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 17/29 | chr13 | 102644260 | |||||||
chr13:102644469 | C | CAT | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2176-87_2176-86ins others(2): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr13 | 102644469 | ||||||
chr13:102644529 | G | A | 1 | a0003c0009t0012g0328 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2176-28G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 17/29 | chr13 | 102644529 | |||||||
chr13:102644717 | G | A | 1 | a0001c0003t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2292+44G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 18/29 | chr13 | 102644717 | |||||||
chr13:102645085 | CT | C | 173 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(170): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.2393+88delT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr13 | 102645085 | ||||||
chr13:102645250 | G | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2393+241G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 19/29 | chr13 | 102645250 | |||||||
chr13:102645655 | A | G | 1 | a0001c0001t0002g0236 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2394-639A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 19/29 | chr13 | 102645655 | |||||||
chr13:102645895 | G | A | 1 | a0001c0002t0001g0050 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2394-399G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 19/29 | chr13 | 102645895 | |||||||
chr13:102645956 | A | G | 1 | a0001c0002t0001g0058 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2394-338A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 19/29 | chr13 | 102645956 | |||||||
chr13:102645983 | AGTT | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2394-308_2394-306d others(5): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr13 | 102645983 | ||||||
chr13:102646733 | G | A | 1 | a0001c0002t0001g0158 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2490+343G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 20/29 | chr13 | 102646733 | |||||||
chr13:102646832 | G | T | 2 | a0001c0008t0012g0329 a0003c0009t0012g0328 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2491-375G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 20/29 | chr13 | 102646832 | |||||||
chr13:102646839 | G | A | 6 | a0001c0001t0002g0208 a0001c0001t0002g0209 a0001c0001t0002g0210 others(3): Show |
6 | HG00597.hp2 HG02132.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.2491-368G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 20/29 | chr13 | 102646839 | |||||||
chr13:102646882 | G | A | 221 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(218): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.2491-325G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 20/29 | chr13 | 102646882 | |||||||
chr13:102647050 | G | T | 1 | a0001c0001t0002g0220 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2491-157G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 20/29 | chr13 | 102647050 | |||||||
chr13:102647051 | C | T | 1 | a0001c0001t0002g0220 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2491-156C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 20/29 | chr13 | 102647051 | |||||||
chr13:102647167 | A | G | 15 | a0001c0001t0003g0251 a0001c0001t0003g0319 a0001c0001t0006g0022 others(12): Show |
17 | HG00140.hp1 HG00735.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.2491-40A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 20/29 | chr13 | 102647167 | |||||||
chr13:102647530 | A | G | 1 | a0001c0002t0001g0066 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2628+186A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 21/29 | chr13 | 102647530 | |||||||
chr13:102647561 | A | G | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2628+217A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 21/29 | chr13 | 102647561 | |||||||
chr13:102647657 | A | G | 2 | a0001c0002t0001g0087 a0001c0002t0001g0088 |
2 | NA18959.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.2628+313A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 21/29 | chr13 | 102647657 | |||||||
chr13:102647680 | G | A | 1 | a0001c0002t0001g0180 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2628+336G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 21/29 | chr13 | 102647680 | |||||||
chr13:102647944 | C | A | 1 | a0001c0002t0001g0083 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2628+600C>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 21/29 | chr13 | 102647944 | |||||||
chr13:102648063 | T | C | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2628+719T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 21/29 | chr13 | 102648063 | |||||||
chr13:102648234 | G | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2629-673G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 21/29 | chr13 | 102648234 | |||||||
chr13:102648336 | C | T | 1 | a0001c0001t0002g0293 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2629-571C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 21/29 | chr13 | 102648336 | |||||||
chr13:102648429 | C | CGT | 12 | a0001c0002t0001g0043 a0001c0002t0001g0050 a0001c0002t0001g0061 others(9): Show |
12 | HG00140.hp2 HG00642.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.2629-441_2629-440d others(4): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr13 | 102648429 | ||||||
chr13:102648429 | C | CGTGT | 39 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0009 others(36): Show |
45 | HG00738.hp1 HG00741.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.2629-443_2629-440d others(6): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr13 | 102648429 | ||||||
chr13:102648429 | C | CGTGTGT | 16 | a0001c0002t0001g0064 a0001c0002t0001g0065 a0001c0002t0001g0068 others(13): Show |
16 | HG00735.hp2 HG01069.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.2629-445_2629-440d others(8): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr13 | 102648429 | ||||||
chr13:102648429 | C | CGTGTGTG others(1): Show |
17 | a0001c0002t0001g0093 a0001c0002t0007g0103 a0001c0002t0008g0099 others(14): Show |
18 | HG00323.hp1 HG01515.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.2629-447_2629-440d others(10): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr13 | 102648429 | ||||||
chr13:102648429 | C | CGTGTGTG others(3): Show |
16 | a0001c0002t0007g0104 a0001c0003t0004g0004 a0001c0003t0004g0013 others(13): Show |
18 | HG01099.hp1 HG01099.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.2629-449_2629-440d others(12): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr13 | 102648429 | ||||||
chr13:102648429 | C | CGTGTGTG others(5): Show |
5 | a0001c0002t0008g0101 a0001c0003t0004g0127 a0001c0003t0004g0140 others(2): Show |
5 | HG01106.hp2 HG01175.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.2629-451_2629-440d others(14): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr13 | 102648429 | ||||||
chr13:102648429 | C | CGTGTGTG others(7): Show |
3 | a0001c0003t0004g0125 a0001c0003t0004g0131 a0001c0003t0004g0132 |
3 | HG01361.hp1 HG03486.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.2629-453_2629-440d others(16): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr13 | 102648429 | ||||||
chr13:102648429 | CGTGTGTG others(5): Show |
C | 23 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0021 others(20): Show |
28 | HG01243.hp1 HG01975.hp2 HG01981.hp1 others(25): Show |
intron_variant | MODIFIER | c.2629-451_2629-440d others(14): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr13 | 102648429 | ||||||
chr13:102648429 | CGTGTGTG others(7): Show |
C | 139 | a0001c0001t0002g0002 a0001c0001t0002g0036 a0001c0001t0002g0184 others(136): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.2629-453_2629-440d others(16): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr13 | 102648429 | ||||||
chr13:102648429 | CGTGTGTG others(9): Show |
C | 3 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0002g0215 |
3 | NA18943.hp2 NA18985.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.2629-455_2629-440d others(18): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr13 | 102648429 | ||||||
chr13:102648444 | G | A | 1 | a0001c0001t0002g0205 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2629-463G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 21/29 | chr13 | 102648444 | |||||||
chr13:102648605 | T | C | 10 | a0001c0001t0003g0025 a0001c0001t0003g0274 a0001c0001t0003g0286 others(7): Show |
11 | HG00099.hp2 HG00639.hp1 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.2629-302T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 21/29 | chr13 | 102648605 | |||||||
chr13:102648661 | T | C | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2629-246T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 21/29 | chr13 | 102648661 | |||||||
chr13:102648697 | C | G | 1 | a0001c0002t0001g0100 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2629-210C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 21/29 | chr13 | 102648697 | |||||||
chr13:102648749 | T | C | 3 | a0001c0002t0007g0102 a0001c0002t0007g0105 a0001c0002t0007g0106 |
3 | HG01069.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2629-158T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 21/29 | chr13 | 102648749 | |||||||
chr13:102648765 | G | T | 2 | a0001c0001t0002g0202 a0001c0001t0002g0203 |
2 | NA19004.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.2629-142G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 21/29 | chr13 | 102648765 | |||||||
chr13:102648780 | T | G | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2629-127T>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 21/29 | chr13 | 102648780 | |||||||
chr13:102649187 | G | T | 287 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(284): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.2873+36G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 22/29 | chr13 | 102649187 | |||||||
chr13:102649269 | G | A | 1 | a0001c0002t0001g0072 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2873+118G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 22/29 | chr13 | 102649269 | |||||||
chr13:102649269 | G | GT | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2873+119dupT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 22/29 | INFO_REALIGN_3_PRIME | chr13 | 102649269 | ||||||
chr13:102649275 | C | T | 2 | a0001c0001t0003g0287 a0001c0001t0003g0314 |
2 | HG00639.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2873+124C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 22/29 | chr13 | 102649275 | |||||||
chr13:102649496 | A | G | 1 | a0001c0002t0008g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2952+10A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 23/29 | chr13 | 102649496 | |||||||
chr13:102649674 | G | C | 221 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(218): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.2952+188G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 23/29 | chr13 | 102649674 | |||||||
chr13:102649766 | T | TTCCTGTG others(17): Show |
2 | a0001c0002t0008g0098 a0001c0002t0008g0099 |
2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2952+293_2952+294i others(26): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr13 | 102649766 | ||||||
chr13:102649947 | C | T | 1 | a0001c0001t0009g0269 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2952+461C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 23/29 | chr13 | 102649947 | |||||||
chr13:102650017 | G | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2952+531G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 23/29 | chr13 | 102650017 | |||||||
chr13:102650097 | T | C | 3 | a0001c0001t0002g0192 a0001c0001t0002g0197 a0004c0007t0002g0198 |
3 | HG02965.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2952+611T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 23/29 | chr13 | 102650097 | |||||||
chr13:102650263 | C | A | 6 | a0001c0001t0003g0003 a0001c0001t0003g0297 a0001c0001t0003g0298 others(3): Show |
9 | HG02109.hp2 HG02615.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.2952+777C>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 23/29 | chr13 | 102650263 | |||||||
chr13:102650382 | A | G | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2952+896A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 23/29 | chr13 | 102650382 | |||||||
chr13:102650521 | A | G | 1 | a0001c0002t0001g0155 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2953-838A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 23/29 | chr13 | 102650521 | |||||||
chr13:102650611 | C | T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2953-748C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 23/29 | chr13 | 102650611 | |||||||
chr13:102650739 | T | C | 1 | a0001c0001t0002g0232 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2953-620T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 23/29 | chr13 | 102650739 | |||||||
chr13:102650803 | G | A | 1 | a0001c0003t0004g0119 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2953-556G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 23/29 | chr13 | 102650803 | |||||||
chr13:102651010 | C | T | 4 | a0001c0001t0006g0022 a0001c0001t0006g0254 a0001c0001t0006g0256 others(1): Show |
5 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.2953-349C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 23/29 | chr13 | 102651010 | |||||||
chr13:102651094 | C | T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2953-265C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 23/29 | chr13 | 102651094 | |||||||
chr13:102651166 | C | T | 1 | a0001c0001t0003g0301 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2953-193C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 23/29 | chr13 | 102651166 | |||||||
chr13:102651579 | G | GT | 7 | a0001c0002t0001g0061 a0001c0002t0001g0065 a0001c0002t0001g0070 others(4): Show |
7 | HG02055.hp1 HG02293.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.2991+195dupT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr13 | 102651579 | ||||||
chr13:102651579 | GT | G | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2991+195delT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr13 | 102651579 | ||||||
chr13:102651608 | C | T | 1 | a0001c0001t0003g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2991+211C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102651608 | |||||||
chr13:102651630 | G | C | 1 | a0001c0001t0016g0191 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2991+233G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102651630 | |||||||
chr13:102651693 | G | A | 4 | a0001c0001t0002g0189 a0001c0001t0002g0192 a0001c0001t0002g0197 others(1): Show |
4 | HG02965.hp2 HG03540.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2991+296G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102651693 | |||||||
chr13:102651735 | TA | T | 44 | a0001c0003t0004g0004 a0001c0003t0004g0011 a0001c0003t0004g0013 others(41): Show |
49 | HG00323.hp1 HG01099.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.2991+340delA | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr13 | 102651735 | ||||||
chr13:102651737 | A | AT | 157 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(154): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.2991+352dupT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr13 | 102651737 | ||||||
chr13:102651737 | A | T | 1 | a0001c0003t0004g0119 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2991+340A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102651737 | |||||||
chr13:102651929 | G | A | 1 | a0001c0001t0006g0023 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2991+532G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102651929 | |||||||
chr13:102651965 | A | G | 4 | a0001c0001t0010g0320 a0001c0001t0010g0321 a0001c0001t0010g0323 others(1): Show |
4 | HG03130.hp2 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2991+568A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102651965 | |||||||
chr13:102652097 | C | T | 2 | a0001c0001t0002g0202 a0001c0001t0002g0203 |
2 | NA19004.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.2991+700C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102652097 | |||||||
chr13:102652192 | A | G | 2 | a0001c0003t0004g0147 a0001c0003t0004g0148 |
2 | HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2991+795A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102652192 | |||||||
chr13:102652397 | C | CAT | 4 | a0001c0002t0001g0045 a0001c0002t0001g0070 a0001c0002t0001g0090 others(1): Show |
4 | HG00597.hp1 HG01261.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.2991+1056_2991+105 others(6): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr13 | 102652397 | ||||||
chr13:102652397 | C | CATAT | 5 | a0001c0002t0001g0061 a0001c0002t0001g0064 a0001c0002t0001g0178 others(2): Show |
5 | HG02293.hp2 NA18947.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.2991+1054_2991+105 others(8): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr13 | 102652397 | ||||||
chr13:102652397 | C | CATATAT | 3 | a0001c0002t0001g0048 a0001c0002t0005g0114 a0001c0002t0005g0115 |
3 | HG02027.hp1 HG02083.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2991+1052_2991+105 others(10): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr13 | 102652397 | ||||||
chr13:102652397 | C | CATATATA others(3): Show |
3 | a0001c0002t0001g0081 a0001c0002t0001g0089 a0001c0002t0005g0166 |
3 | HG00733.hp1 NA18964.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.2991+1048_2991+105 others(14): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr13 | 102652397 | ||||||
chr13:102652397 | CAT | C | 3 | a0001c0002t0001g0050 a0001c0002t0005g0165 a0001c0002t0018g0057 |
3 | HG00642.hp1 HG03831.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.2991+1056_2991+105 others(6): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr13 | 102652397 | ||||||
chr13:102652397 | CATAT | C | 15 | a0001c0002t0001g0009 a0001c0002t0001g0010 a0001c0002t0001g0041 others(12): Show |
17 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.2991+1054_2991+105 others(8): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr13 | 102652397 | ||||||
chr13:102652397 | CATATATA others(1): Show |
C | 5 | a0001c0002t0001g0043 a0001c0002t0001g0170 a0001c0002t0005g0016 others(2): Show |
6 | HG03490.hp1 HG03492.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.2991+1050_2991+105 others(12): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr13 | 102652397 | ||||||
chr13:102652397 | CATATATA others(3): Show |
C | 12 | a0001c0002t0001g0049 a0001c0002t0001g0056 a0001c0002t0001g0066 others(9): Show |
12 | HG00140.hp2 HG00408.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.2991+1048_2991+105 others(14): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr13 | 102652397 | ||||||
chr13:102652397 | CATATATA others(5): Show |
C | 10 | a0001c0002t0001g0059 a0001c0002t0001g0067 a0001c0002t0001g0072 others(7): Show |
10 | HG01255.hp2 HG01978.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.2991+1046_2991+105 others(16): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr13 | 102652397 | ||||||
chr13:102652397 | CATATATA others(7): Show |
C | 12 | a0001c0002t0001g0017 a0001c0002t0001g0040 a0001c0002t0001g0054 others(9): Show |
13 | HG02074.hp1 HG02148.hp2 HG02273.hp2 others(10): Show |
intron_variant | MODIFIER | c.2991+1044_2991+105 others(18): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr13 | 102652397 | ||||||
chr13:102652397 | CATATATA others(9): Show |
C | 10 | a0001c0002t0001g0038 a0001c0002t0001g0047 a0001c0002t0001g0073 others(7): Show |
10 | HG00408.hp2 HG02015.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.2991+1042_2991+105 others(20): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr13 | 102652397 | ||||||
chr13:102652397 | CATATATA others(11): Show |
C | 1 | a0001c0002t0001g0164 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2991+1040_2991+105 others(22): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr13 | 102652397 | ||||||
chr13:102652397 | CATATATA others(13): Show |
C | 4 | a0001c0002t0005g0006 a0001c0002t0005g0033 a0001c0002t0005g0039 others(1): Show |
5 | HG01109.hp2 NA18949.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.2991+1038_2991+105 others(24): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr13 | 102652397 | ||||||
chr13:102652397 | CATATATA others(15): Show |
C | 4 | a0001c0002t0005g0110 a0001c0002t0005g0182 a0001c0002t0008g0101 others(1): Show |
4 | HG02132.hp2 HG02886.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.2991+1036_2991+105 others(26): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr13 | 102652397 | ||||||
chr13:102652397 | CATATATA others(17): Show |
C | 7 | a0001c0002t0005g0032 a0001c0002t0005g0034 a0001c0002t0005g0111 others(4): Show |
7 | HG01934.hp2 NA18943.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.2991+1034_2991+105 others(28): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr13 | 102652397 | ||||||
chr13:102652397 | CATATATA others(19): Show |
C | 3 | a0001c0002t0005g0108 a0001c0002t0005g0109 a0001c0002t0005g0117 |
3 | NA18980.hp2 NA18985.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.2991+1032_2991+105 others(30): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr13 | 102652397 | ||||||
chr13:102652397 | CATATATA others(21): Show |
C | 1 | a0001c0002t0005g0046 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2991+1030_2991+105 others(32): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr13 | 102652397 | ||||||
chr13:102652397 | CATATATA others(27): Show |
C | 6 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(3): Show |
6 | HG01069.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.2991+1024_2991+105 others(38): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr13 | 102652397 | ||||||
chr13:102652397 | CATATATA others(29): Show |
C | 4 | a0001c0001t0003g0026 a0001c0001t0003g0181 a0001c0001t0009g0029 others(1): Show |
5 | HG01175.hp2 HG01243.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.2991+1022_2991+105 others(40): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr13 | 102652397 | ||||||
chr13:102652397 | CATATATA others(31): Show |
C | 161 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(158): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.2991+1020_2991+105 others(42): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr13 | 102652397 | ||||||
chr13:102652397 | CATATATA others(33): Show |
C | 1 | a0001c0002t0001g0058 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2991+1018_2991+105 others(44): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr13 | 102652397 | ||||||
chr13:102652397 | CATATATA others(37): Show |
C | 47 | a0001c0003t0004g0004 a0001c0003t0004g0011 a0001c0003t0004g0013 others(44): Show |
52 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(49): Show |
intron_variant | MODIFIER | c.2991+1014_2991+105 others(48): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr13 | 102652397 | ||||||
chr13:102652397 | CATATATA others(43): Show |
C | 1 | a0001c0002t0001g0163 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2991+1008_2991+105 others(54): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr13 | 102652397 | ||||||
chr13:102652437 | T | C | 4 | a0001c0001t0003g0026 a0001c0001t0003g0181 a0001c0001t0009g0029 others(1): Show |
5 | HG01175.hp2 HG01243.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.2991+1040T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102652437 | |||||||
chr13:102652439 | T | C | 161 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(158): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.2991+1042T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102652439 | |||||||
chr13:102652629 | A | AAAT | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2991+1232_2991+123 others(7): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102652629 | |||||||
chr13:102652809 | T | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2991+1412T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102652809 | |||||||
chr13:102652836 | C | T | 1 | a0001c0001t0009g0029 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2991+1439C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102652836 | |||||||
chr13:102653055 | A | G | 1 | a0001c0002t0005g0117 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2991+1658A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102653055 | |||||||
chr13:102653259 | C | T | 4 | a0001c0001t0003g0025 a0001c0001t0003g0274 a0001c0001t0003g0299 others(1): Show |
5 | HG00099.hp2 HG00738.hp2 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.2991+1862C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102653259 | |||||||
chr13:102653265 | A | T | 159 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(156): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.2991+1868A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102653265 | |||||||
chr13:102653271 | A | G | 1 | a0001c0001t0006g0241 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2991+1874A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102653271 | |||||||
chr13:102653287 | A | G | 67 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0019 others(64): Show |
77 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.2991+1890A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102653287 | |||||||
chr13:102653311 | C | G | 4 | a0001c0001t0010g0320 a0001c0001t0010g0321 a0001c0001t0010g0323 others(1): Show |
4 | HG03130.hp2 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2991+1914C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102653311 | |||||||
chr13:102653339 | C | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2991+1942C>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102653339 | |||||||
chr13:102653389 | C | T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2991+1992C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102653389 | |||||||
chr13:102653428 | T | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2991+2031T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102653428 | |||||||
chr13:102653593 | C | T | 1 | a0001c0002t0001g0072 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2991+2196C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102653593 | |||||||
chr13:102653594 | G | A | 2 | a0001c0001t0003g0181 a0001c0001t0009g0029 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2991+2197G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102653594 | |||||||
chr13:102653627 | C | T | 1 | a0001c0003t0004g0143 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2991+2230C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102653627 | |||||||
chr13:102653744 | T | G | 66 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0019 others(63): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.2991+2347T>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102653744 | |||||||
chr13:102653921 | C | G | 1 | a0001c0002t0001g0158 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2991+2524C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102653921 | |||||||
chr13:102653977 | T | G | 1 | a0001c0002t0005g0031 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2991+2580T>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102653977 | |||||||
chr13:102654037 | T | G | 1 | a0001c0002t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2991+2640T>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102654037 | |||||||
chr13:102654326 | C | T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2992-2730C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102654326 | |||||||
chr13:102654381 | A | C | 8 | a0001c0002t0001g0038 a0001c0002t0001g0047 a0001c0002t0001g0073 others(5): Show |
8 | HG00408.hp2 HG02040.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2992-2675A>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102654381 | |||||||
chr13:102654637 | C | T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2992-2419C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102654637 | |||||||
chr13:102654838 | C | G | 14 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0153 others(11): Show |
17 | HG01243.hp1 HG01884.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.2992-2218C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102654838 | |||||||
chr13:102654841 | G | C | 1 | a0001c0001t0011g0311 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2992-2215G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102654841 | |||||||
chr13:102654868 | C | T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2992-2188C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102654868 | |||||||
chr13:102654892 | C | T | 1 | a0001c0002t0008g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2992-2164C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102654892 | |||||||
chr13:102654972 | A | G | 221 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(218): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.2992-2084A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102654972 | |||||||
chr13:102655010 | G | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2992-2046G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102655010 | |||||||
chr13:102655133 | G | A | 221 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(218): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.2992-1923G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102655133 | |||||||
chr13:102655162 | A | T | 1 | a0001c0001t0002g0216 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2992-1894A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102655162 | |||||||
chr13:102655363 | G | A | 6 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(3): Show |
6 | HG01069.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.2992-1693G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102655363 | |||||||
chr13:102655500 | C | T | 4 | a0001c0001t0002g0005 a0001c0001t0002g0195 a0001c0001t0002g0196 others(1): Show |
6 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.2992-1556C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102655500 | |||||||
chr13:102655641 | A | G | 45 | a0001c0003t0004g0004 a0001c0003t0004g0011 a0001c0003t0004g0013 others(42): Show |
50 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.2992-1415A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102655641 | |||||||
chr13:102655750 | G | T | 2 | a0001c0008t0012g0329 a0003c0009t0012g0328 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2992-1306G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102655750 | |||||||
chr13:102655754 | G | A | 1 | a0001c0001t0009g0273 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2992-1302G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102655754 | |||||||
chr13:102655776 | G | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2992-1280G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102655776 | |||||||
chr13:102655842 | C | G | 1 | a0001c0002t0001g0007 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2992-1214C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102655842 | |||||||
chr13:102655859 | T | C | 1 | a0001c0002t0008g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2992-1197T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102655859 | |||||||
chr13:102655937 | T | C | 221 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(218): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.2992-1119T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102655937 | |||||||
chr13:102656133 | T | G | 8 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(5): Show |
8 | HG01069.hp2 HG01099.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2992-923T>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102656133 | |||||||
chr13:102656670 | C | T | 6 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(3): Show |
6 | HG01069.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.2992-386C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102656670 | |||||||
chr13:102656886 | A | G | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2992-170A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102656886 | |||||||
chr13:102657007 | T | C | 1 | a0001c0002t0001g0100 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2992-49T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 24/29 | chr13 | 102657007 | |||||||
chr13:102657427 | C | T | 6 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(3): Show |
6 | HG01069.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.3143+220C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102657427 | |||||||
chr13:102657479 | A | C | 66 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0019 others(63): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.3143+272A>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102657479 | |||||||
chr13:102657753 | G | C | 1 | a0001c0003t0004g0140 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3143+546G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102657753 | |||||||
chr13:102657804 | C | T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3143+597C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102657804 | |||||||
chr13:102657808 | G | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3143+601G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102657808 | |||||||
chr13:102657965 | C | T | 4 | a0001c0001t0010g0320 a0001c0001t0010g0321 a0001c0001t0010g0323 others(1): Show |
4 | HG03130.hp2 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.3143+758C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102657965 | |||||||
chr13:102658051 | T | C | 1 | a0001c0001t0003g0266 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.3143+844T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102658051 | |||||||
chr13:102658148 | C | T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3143+941C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102658148 | |||||||
chr13:102658261 | G | C | 1 | a0001c0002t0001g0089 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.3143+1054G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102658261 | |||||||
chr13:102658271 | G | T | 1 | a0001c0002t0001g0059 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.3143+1064G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102658271 | |||||||
chr13:102658522 | C | T | 1 | a0001c0001t0003g0181 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3143+1315C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102658522 | |||||||
chr13:102658600 | T | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3143+1393T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102658600 | |||||||
chr13:102658613 | A | G | 1 | a0001c0001t0006g0245 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3143+1406A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102658613 | |||||||
chr13:102658704 | C | T | 4 | a0001c0001t0002g0185 a0001c0001t0002g0200 a0001c0001t0002g0214 others(1): Show |
4 | NA18974.hp2 NA19001.hp1 NA19075.hp2 others(1): Show |
intron_variant | MODIFIER | c.3143+1497C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102658704 | |||||||
chr13:102658711 | A | G | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3143+1504A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102658711 | |||||||
chr13:102658760 | T | TG | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3143+1558dupG | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 102658760 | ||||||
chr13:102658866 | GTAGGGGC others(5): Show |
G | 2 | a0001c0001t0002g0190 a0001c0001t0003g0019 |
3 | HG01981.hp1 HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3143+1661_3143+167 others(16): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 102658866 | ||||||
chr13:102658868 | A | G | 162 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(159): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.3143+1661A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102658868 | |||||||
chr13:102658873 | C | G | 1 | a0001c0001t0002g0290 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3143+1666C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102658873 | |||||||
chr13:102658904 | G | C | 1 | a0001c0002t0001g0172 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.3143+1697G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102658904 | |||||||
chr13:102658967 | G | A | 6 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(3): Show |
6 | HG01069.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.3143+1760G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102658967 | |||||||
chr13:102659035 | A | G | 30 | a0001c0001t0003g0024 a0001c0001t0003g0030 a0001c0001t0003g0186 others(27): Show |
31 | HG00099.hp1 HG00639.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.3143+1828A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102659035 | |||||||
chr13:102659339 | A | G | 1 | a0001c0003t0004g0128 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3143+2132A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102659339 | |||||||
chr13:102659348 | A | T | 34 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0009 others(31): Show |
38 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.3143+2141A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102659348 | |||||||
chr13:102659371 | A | G | 1 | a0001c0002t0008g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3143+2164A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102659371 | |||||||
chr13:102659411 | T | C | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3143+2204T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102659411 | |||||||
chr13:102659530 | A | G | 1 | a0001c0002t0001g0083 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3143+2323A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102659530 | |||||||
chr13:102659535 | G | T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3143+2328G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102659535 | |||||||
chr13:102659599 | A | G | 1 | a0001c0002t0005g0016 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.3143+2392A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102659599 | |||||||
chr13:102659626 | T | C | 43 | a0001c0003t0004g0004 a0001c0003t0004g0011 a0001c0003t0004g0013 others(40): Show |
48 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.3143+2419T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102659626 | |||||||
chr13:102659733 | T | C | 1 | a0001c0001t0002g0224 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3143+2526T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102659733 | |||||||
chr13:102659876 | G | A | 2 | a0001c0001t0002g0243 a0001c0001t0002g0248 |
2 | HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3143+2669G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102659876 | |||||||
chr13:102659981 | TAGTAA | T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3143+2780_3143+278 others(9): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 102659981 | ||||||
chr13:102660003 | GTTAA | G | 30 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0025 others(27): Show |
38 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.3143+2803_3143+280 others(8): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 102660003 | ||||||
chr13:102660019 | A | G | 1 | a0001c0001t0002g0234 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3143+2812A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102660019 | |||||||
chr13:102660038 | CAGAT | C | 6 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(3): Show |
6 | HG01069.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.3143+2835_3143+283 others(8): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 102660038 | ||||||
chr13:102660140 | A | G | 45 | a0001c0003t0004g0004 a0001c0003t0004g0011 a0001c0003t0004g0013 others(42): Show |
50 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.3143+2933A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102660140 | |||||||
chr13:102660151 | T | G | 3 | a0001c0001t0002g0201 a0001c0001t0002g0232 a0001c0001t0002g0233 |
3 | NA18971.hp2 NA18973.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.3143+2944T>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102660151 | |||||||
chr13:102660195 | A | C | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3143+2988A>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102660195 | |||||||
chr13:102660267 | G | A | 1 | a0001c0001t0002g0204 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3143+3060G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102660267 | |||||||
chr13:102660390 | C | T | 1 | a0001c0001t0002g0234 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3143+3183C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102660390 | |||||||
chr13:102660438 | C | CAA | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3144-3209_3144-320 others(6): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 102660438 | ||||||
chr13:102660458 | C | T | 1 | a0001c0002t0005g0046 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3144-3190C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102660458 | |||||||
chr13:102660716 | A | T | 1 | a0001c0003t0004g0137 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3144-2932A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102660716 | |||||||
chr13:102660898 | T | C | 1 | a0001c0001t0003g0324 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3144-2750T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102660898 | |||||||
chr13:102661058 | T | C | 221 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(218): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.3144-2590T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102661058 | |||||||
chr13:102661105 | GA | G | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3144-2534delA | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 102661105 | ||||||
chr13:102661138 | A | G | 1 | a0001c0002t0005g0156 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3144-2510A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102661138 | |||||||
chr13:102661211 | G | T | 221 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(218): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.3144-2437G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102661211 | |||||||
chr13:102661250 | C | CT | 115 | a0001c0001t0002g0205 a0001c0001t0003g0001 a0001c0001t0003g0003 others(112): Show |
129 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.3144-2380dupT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 102661250 | ||||||
chr13:102661250 | C | CTT | 101 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(98): Show |
110 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(107): Show |
intron_variant | MODIFIER | c.3144-2381_3144-238 others(6): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 102661250 | ||||||
chr13:102661532 | C | T | 1 | a0001c0001t0002g0292 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3144-2116C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102661532 | |||||||
chr13:102661556 | A | G | 4 | a0001c0001t0010g0320 a0001c0001t0010g0321 a0001c0001t0010g0323 others(1): Show |
4 | HG03130.hp2 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.3144-2092A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102661556 | |||||||
chr13:102661599 | A | T | 2 | a0001c0001t0003g0287 a0001c0001t0003g0314 |
2 | HG00639.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.3144-2049A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102661599 | |||||||
chr13:102661720 | A | G | 1 | a0001c0003t0004g0146 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3144-1928A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102661720 | |||||||
chr13:102661889 | T | G | 1 | a0001c0001t0002g0218 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3144-1759T>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102661889 | |||||||
chr13:102661950 | A | G | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3144-1698A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102661950 | |||||||
chr13:102662066 | G | C | 163 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(160): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.3144-1582G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102662066 | |||||||
chr13:102662066 | G | T | 2 | a0001c0001t0002g0205 a0001c0001t0002g0206 |
2 | NA18959.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.3144-1582G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102662066 | |||||||
chr13:102662149 | C | T | 1 | a0001c0001t0006g0250 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3144-1499C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102662149 | |||||||
chr13:102662173 | A | G | 2 | a0001c0002t0008g0098 a0001c0002t0008g0099 |
2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3144-1475A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102662173 | |||||||
chr13:102662222 | T | C | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3144-1426T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102662222 | |||||||
chr13:102662400 | T | A | 3 | a0001c0001t0003g0267 a0001c0001t0003g0270 a0001c0001t0003g0272 |
3 | NA18964.hp1 NA18979.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.3144-1248T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102662400 | |||||||
chr13:102662523 | T | A | 1 | a0001c0002t0001g0100 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3144-1125T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102662523 | |||||||
chr13:102662537 | G | T | 163 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(160): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.3144-1111G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102662537 | |||||||
chr13:102662860 | G | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3144-788G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102662860 | |||||||
chr13:102662864 | G | A | 2 | a0001c0002t0008g0098 a0001c0002t0008g0099 |
2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3144-784G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102662864 | |||||||
chr13:102663064 | A | G | 1 | a0001c0002t0008g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3144-584A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102663064 | |||||||
chr13:102663099 | T | C | 1 | a0001c0001t0003g0268 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.3144-549T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102663099 | |||||||
chr13:102663117 | G | T | 45 | a0001c0003t0004g0004 a0001c0003t0004g0011 a0001c0003t0004g0013 others(42): Show |
50 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.3144-531G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102663117 | |||||||
chr13:102663127 | TTTA | T | 51 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(48): Show |
56 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.3144-518_3144-516d others(5): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 102663127 | ||||||
chr13:102663130 | A | T | 2 | a0001c0008t0012g0329 a0003c0009t0012g0328 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.3144-518A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102663130 | |||||||
chr13:102663132 | T | TTATTTA | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3144-515_3144-514i others(8): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 102663132 | ||||||
chr13:102663136 | T | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3144-512T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102663136 | |||||||
chr13:102663139 | A | T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3144-509A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102663139 | |||||||
chr13:102663140 | A | T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3144-508A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102663140 | |||||||
chr13:102663151 | A | T | 18 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0045 others(15): Show |
20 | HG00408.hp1 HG00738.hp1 HG02004.hp1 others(17): Show |
intron_variant | MODIFIER | c.3144-497A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102663151 | |||||||
chr13:102663155 | T | A | 170 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(167): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.3144-493T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102663155 | |||||||
chr13:102663159 | T | A | 1 | a0001c0001t0009g0273 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3144-489T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102663159 | |||||||
chr13:102663217 | G | A | 1 | a0001c0002t0005g0080 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3144-431G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102663217 | |||||||
chr13:102663233 | T | C | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3144-415T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102663233 | |||||||
chr13:102663274 | A | G | 2 | a0001c0001t0003g0181 a0001c0001t0009g0029 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3144-374A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102663274 | |||||||
chr13:102663362 | G | A | 1 | a0001c0001t0002g0036 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.3144-286G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102663362 | |||||||
chr13:102663476 | C | T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3144-172C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102663476 | |||||||
chr13:102663526 | G | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3144-122G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102663526 | |||||||
chr13:102663598 | G | C | 173 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(170): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.3144-50G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 25/29 | chr13 | 102663598 | |||||||
chr13:102663763 | G | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3240+19G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 26/29 | chr13 | 102663763 | |||||||
chr13:102663901 | A | G | 2 | a0001c0002t0005g0006 a0001c0002t0005g0033 |
3 | NA18949.hp1 NA18974.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.3240+157A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 26/29 | chr13 | 102663901 | |||||||
chr13:102663915 | C | G | 1 | a0001c0003t0004g0119 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3240+171C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 26/29 | chr13 | 102663915 | |||||||
chr13:102663988 | G | A | 45 | a0001c0003t0004g0004 a0001c0003t0004g0011 a0001c0003t0004g0013 others(42): Show |
50 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.3240+244G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 26/29 | chr13 | 102663988 | |||||||
chr13:102664008 | C | T | 1 | a0001c0002t0008g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3240+264C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 26/29 | chr13 | 102664008 | |||||||
chr13:102664030 | G | A | 1 | a0001c0002t0001g0082 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3240+286G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 26/29 | chr13 | 102664030 | |||||||
chr13:102664155 | C | T | 1 | a0001c0001t0002g0189 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3240+411C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 26/29 | chr13 | 102664155 | |||||||
chr13:102664264 | C | G | 1 | a0001c0002t0001g0067 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.3240+520C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 26/29 | chr13 | 102664264 | |||||||
chr13:102664375 | T | C | 1 | a0001c0003t0004g0125 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3241-420T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 26/29 | chr13 | 102664375 | |||||||
chr13:102664539 | T | C | 1 | a0001c0002t0008g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3241-256T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 26/29 | chr13 | 102664539 | |||||||
chr13:102664588 | T | C | 1 | a0001c0001t0002g0217 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3241-207T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 26/29 | chr13 | 102664588 | |||||||
chr13:102664592 | G | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3241-203G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 26/29 | chr13 | 102664592 | |||||||
chr13:102664655 | G | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3241-140G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 26/29 | chr13 | 102664655 | |||||||
chr13:102664675 | C | T | 1 | a0001c0002t0001g0045 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3241-120C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 26/29 | chr13 | 102664675 | |||||||
chr13:102664745 | G | A | 1 | a0001c0002t0005g0156 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3241-50G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 26/29 | chr13 | 102664745 | |||||||
chr13:102664774 | T | C | 1 | a0001c0001t0016g0191 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3241-21T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 26/29 | chr13 | 102664774 | |||||||
chr13:102665361 | A | C | 1 | a0001c0001t0002g0189 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3371+436A>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102665361 | |||||||
chr13:102665432 | G | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3371+507G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102665432 | |||||||
chr13:102665682 | T | A | 1 | a0001c0003t0004g0138 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3371+757T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102665682 | |||||||
chr13:102665683 | A | T | 1 | a0001c0003t0004g0138 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3371+758A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102665683 | |||||||
chr13:102665771 | A | G | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3371+846A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102665771 | |||||||
chr13:102666154 | G | A | 2 | a0001c0008t0012g0329 a0003c0009t0012g0328 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.3371+1229G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102666154 | |||||||
chr13:102666487 | A | G | 1 | a0001c0001t0009g0029 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3371+1562A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102666487 | |||||||
chr13:102666544 | C | A | 2 | a0001c0002t0008g0098 a0001c0002t0008g0099 |
2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3371+1619C>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102666544 | |||||||
chr13:102666626 | G | A | 2 | a0001c0002t0008g0098 a0001c0002t0008g0099 |
2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3371+1701G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102666626 | |||||||
chr13:102666719 | G | A | 79 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0036 others(76): Show |
84 | HG00140.hp1 HG00597.hp2 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.3371+1794G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102666719 | |||||||
chr13:102666745 | C | CTTTT | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3371+1823_3371+182 others(8): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr13 | 102666745 | ||||||
chr13:102666766 | C | CT | 10 | a0001c0001t0002g0289 a0001c0001t0003g0027 a0001c0001t0003g0030 others(7): Show |
10 | HG01069.hp1 HG01070.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.3371+1866dupT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr13 | 102666766 | ||||||
chr13:102666766 | C | CTT | 75 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0153 others(72): Show |
88 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.3371+1865_3371+186 others(6): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr13 | 102666766 | ||||||
chr13:102666766 | C | CTTT | 61 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0036 others(58): Show |
64 | HG00597.hp2 HG01109.hp1 HG01243.hp1 others(61): Show |
intron_variant | MODIFIER | c.3371+1864_3371+186 others(7): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr13 | 102666766 | ||||||
chr13:102666766 | C | CTTTT | 16 | a0001c0001t0002g0188 a0001c0001t0002g0212 a0001c0001t0002g0226 others(13): Show |
18 | HG00140.hp1 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.3371+1863_3371+186 others(8): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr13 | 102666766 | ||||||
chr13:102666766 | CT | C | 131 | a0001c0002t0001g0007 a0001c0002t0001g0009 a0001c0002t0001g0010 others(128): Show |
140 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.3371+1866delT | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr13 | 102666766 | ||||||
chr13:102666766 | CTT | C | 10 | a0001c0002t0001g0041 a0001c0002t0001g0054 a0001c0002t0001g0081 others(7): Show |
10 | HG00323.hp1 HG01069.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.3371+1865_3371+186 others(6): Show |
TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr13 | 102666766 | ||||||
chr13:102666834 | C | T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3371+1909C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102666834 | |||||||
chr13:102666874 | A | G | 1 | a0001c0002t0008g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3371+1949A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102666874 | |||||||
chr13:102666920 | C | T | 1 | a0001c0001t0002g0183 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.3371+1995C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102666920 | |||||||
chr13:102667092 | C | T | 1 | a0001c0001t0016g0191 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3371+2167C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102667092 | |||||||
chr13:102667129 | C | G | 4 | a0001c0001t0010g0320 a0001c0001t0010g0321 a0001c0001t0010g0323 others(1): Show |
4 | HG03130.hp2 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.3371+2204C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102667129 | |||||||
chr13:102667173 | G | C | 287 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(284): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.3371+2248G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102667173 | |||||||
chr13:102667219 | T | C | 47 | a0001c0003t0004g0004 a0001c0003t0004g0011 a0001c0003t0004g0013 others(44): Show |
52 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(49): Show |
intron_variant | MODIFIER | c.3371+2294T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102667219 | |||||||
chr13:102667267 | T | C | 1 | a0001c0002t0001g0164 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.3371+2342T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102667267 | |||||||
chr13:102667371 | A | G | 15 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0153 others(12): Show |
19 | HG01243.hp1 HG01884.hp2 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.3371+2446A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102667371 | |||||||
chr13:102667434 | T | G | 258 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(255): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.3371+2509T>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102667434 | |||||||
chr13:102667577 | G | A | 1 | a0001c0002t0001g0086 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.3371+2652G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102667577 | |||||||
chr13:102667602 | A | G | 201 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(198): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.3371+2677A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102667602 | |||||||
chr13:102667808 | T | C | 6 | a0001c0001t0006g0242 a0001c0001t0006g0246 a0001c0001t0006g0247 others(3): Show |
6 | HG01109.hp1 HG01884.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3371+2883T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102667808 | |||||||
chr13:102667928 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3371+3003C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102667928 | |||||||
chr13:102668025 | A | G | 1 | a0001c0003t0004g0126 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3371+3100A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102668025 | |||||||
chr13:102668066 | T | C | 2 | a0001c0002t0005g0114 a0001c0002t0005g0115 |
2 | HG02027.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.3371+3141T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102668066 | |||||||
chr13:102668095 | A | G | 1 | a0001c0003t0004g0126 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3371+3170A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102668095 | |||||||
chr13:102668103 | T | A | 308 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(305): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.3371+3178T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102668103 | |||||||
chr13:102668111 | G | A | 257 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(254): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.3371+3186G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102668111 | |||||||
chr13:102668268 | G | T | 1 | a0001c0001t0002g0184 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.3371+3343G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102668268 | |||||||
chr13:102668328 | T | C | 201 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(198): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.3371+3403T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102668328 | |||||||
chr13:102668338 | T | C | 201 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(198): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.3371+3413T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102668338 | |||||||
chr13:102668413 | G | A | 30 | a0001c0001t0003g0024 a0001c0001t0003g0030 a0001c0001t0003g0186 others(27): Show |
31 | HG00099.hp1 HG00639.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.3371+3488G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102668413 | |||||||
chr13:102668424 | C | T | 6 | a0001c0002t0007g0102 a0001c0002t0007g0103 a0001c0002t0007g0104 others(3): Show |
6 | HG01069.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.3371+3499C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102668424 | |||||||
chr13:102668477 | A | G | 1 | a0001c0001t0003g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3371+3552A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102668477 | |||||||
chr13:102668593 | G | A | 1 | a0001c0003t0004g0011 | 2 | NA18995.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.3371+3668G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102668593 | |||||||
chr13:102668782 | A | G | 2 | a0001c0001t0003g0299 a0001c0001t0003g0300 |
2 | HG00099.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.3371+3857A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102668782 | |||||||
chr13:102668820 | T | C | 67 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0019 others(64): Show |
77 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.3371+3895T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102668820 | |||||||
chr13:102668861 | A | G | 200 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(197): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.3371+3936A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102668861 | |||||||
chr13:102668927 | C | T | 200 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(197): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.3371+4002C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102668927 | |||||||
chr13:102668976 | C | T | 2 | a0001c0002t0008g0098 a0001c0002t0008g0099 |
2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3371+4051C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102668976 | |||||||
chr13:102668999 | C | T | 69 | a0001c0001t0002g0192 a0001c0001t0002g0197 a0001c0001t0003g0001 others(66): Show |
79 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.3371+4074C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102668999 | |||||||
chr13:102669023 | G | C | 1 | a0001c0003t0004g0139 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3371+4098G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102669023 | |||||||
chr13:102669023 | G | T | 1 | a0001c0002t0001g0091 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3371+4098G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102669023 | |||||||
chr13:102669087 | C | T | 2 | a0001c0001t0003g0296 a0001c0001t0003g0324 |
2 | HG00323.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.3371+4162C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102669087 | |||||||
chr13:102669088 | A | G | 1 | a0001c0003t0008g0120 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.3371+4163A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102669088 | |||||||
chr13:102669335 | G | A | 200 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(197): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.3371+4410G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102669335 | |||||||
chr13:102669358 | A | G | 200 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(197): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.3371+4433A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102669358 | |||||||
chr13:102669426 | G | A | 1 | a0001c0001t0016g0191 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3371+4501G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102669426 | |||||||
chr13:102669642 | G | C | 256 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(253): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.3372-4641G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102669642 | |||||||
chr13:102669706 | T | A | 45 | a0001c0003t0004g0004 a0001c0003t0004g0011 a0001c0003t0004g0013 others(42): Show |
50 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.3372-4577T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102669706 | |||||||
chr13:102669718 | G | C | 256 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(253): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.3372-4565G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102669718 | |||||||
chr13:102669748 | TG | T | 47 | a0001c0003t0004g0004 a0001c0003t0004g0011 a0001c0003t0004g0013 others(44): Show |
52 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(49): Show |
intron_variant | MODIFIER | c.3372-4532delG | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr13 | 102669748 | ||||||
chr13:102669847 | G | T | 1 | a0001c0002t0001g0077 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3372-4436G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102669847 | |||||||
chr13:102669879 | C | T | 12 | a0001c0001t0003g0265 a0001c0001t0003g0266 a0001c0001t0003g0267 others(9): Show |
12 | HG01993.hp1 HG02273.hp1 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.3372-4404C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102669879 | |||||||
chr13:102669959 | A | G | 45 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0019 others(42): Show |
54 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.3372-4324A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102669959 | |||||||
chr13:102670024 | G | C | 2 | a0001c0001t0002g0208 a0001c0001t0002g0209 |
2 | HG00597.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.3372-4259G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102670024 | |||||||
chr13:102670111 | C | T | 200 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(197): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.3372-4172C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102670111 | |||||||
chr13:102670112 | A | G | 1 | a0001c0002t0005g0039 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3372-4171A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102670112 | |||||||
chr13:102670151 | A | G | 1 | a0001c0003t0004g0135 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3372-4132A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102670151 | |||||||
chr13:102670171 | T | G | 2 | a0001c0001t0010g0323 a0001c0001t0015g0322 |
2 | HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3372-4112T>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102670171 | |||||||
chr13:102670171 | T | TG | 192 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(189): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.3372-4105dupG | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr13 | 102670171 | ||||||
chr13:102670185 | G | A | 1 | a0001c0001t0009g0029 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3372-4098G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102670185 | |||||||
chr13:102670245 | T | C | 200 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(197): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.3372-4038T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102670245 | |||||||
chr13:102670253 | A | G | 1 | a0001c0002t0008g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3372-4030A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102670253 | |||||||
chr13:102670274 | T | G | 200 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(197): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.3372-4009T>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102670274 | |||||||
chr13:102670312 | G | A | 200 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(197): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.3372-3971G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102670312 | |||||||
chr13:102670354 | G | A | 45 | a0001c0003t0004g0004 a0001c0003t0004g0011 a0001c0003t0004g0013 others(42): Show |
50 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.3372-3929G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102670354 | |||||||
chr13:102670364 | C | T | 199 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(196): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.3372-3919C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102670364 | |||||||
chr13:102670378 | C | A | 200 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(197): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.3372-3905C>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102670378 | |||||||
chr13:102670397 | C | T | 35 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0019 others(32): Show |
44 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.3372-3886C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102670397 | |||||||
chr13:102670412 | G | A | 200 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(197): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.3372-3871G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102670412 | |||||||
chr13:102670436 | G | A | 2 | a0001c0002t0001g0089 a0001c0002t0020g0063 |
2 | NA18964.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.3372-3847G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102670436 | |||||||
chr13:102670586 | A | G | 1 | a0001c0001t0010g0323 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3372-3697A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102670586 | |||||||
chr13:102670688 | G | A | 1 | a0001c0001t0003g0299 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3372-3595G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102670688 | |||||||
chr13:102670757 | A | T | 2 | a0001c0008t0012g0329 a0003c0009t0012g0328 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.3372-3526A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102670757 | |||||||
chr13:102670842 | C | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3372-3441C>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102670842 | |||||||
chr13:102671010 | T | C | 4 | a0001c0001t0010g0320 a0001c0001t0010g0321 a0001c0001t0010g0323 others(1): Show |
4 | HG03130.hp2 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.3372-3273T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102671010 | |||||||
chr13:102671066 | A | G | 200 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(197): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.3372-3217A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102671066 | |||||||
chr13:102671092 | C | G | 1 | a0001c0001t0009g0273 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3372-3191C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102671092 | |||||||
chr13:102671173 | G | A | 200 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(197): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.3372-3110G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102671173 | |||||||
chr13:102671276 | G | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3372-3007G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102671276 | |||||||
chr13:102671313 | G | C | 1 | a0001c0003t0004g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3372-2970G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102671313 | |||||||
chr13:102671423 | A | G | 1 | a0001c0003t0004g0139 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3372-2860A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102671423 | |||||||
chr13:102671461 | C | T | 2 | a0001c0002t0008g0098 a0001c0002t0008g0099 |
2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3372-2822C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102671461 | |||||||
chr13:102671483 | C | T | 256 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(253): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.3372-2800C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102671483 | |||||||
chr13:102671768 | T | C | 1 | a0001c0003t0004g0122 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3372-2515T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102671768 | |||||||
chr13:102671882 | C | CA | 2 | a0001c0001t0003g0026 a0001c0001t0009g0307 |
3 | HG01175.hp2 HG01515.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.3372-2400dupA | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr13 | 102671882 | ||||||
chr13:102671927 | G | C | 11 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0169 others(8): Show |
13 | HG00408.hp1 HG00738.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.3372-2356G>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102671927 | |||||||
chr13:102672016 | C | A | 1 | a0001c0003t0004g0150 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3372-2267C>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102672016 | |||||||
chr13:102672094 | C | T | 1 | a0001c0002t0001g0164 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.3372-2189C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102672094 | |||||||
chr13:102672261 | A | T | 256 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(253): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.3372-2022A>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102672261 | |||||||
chr13:102672323 | G | A | 200 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(197): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.3372-1960G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102672323 | |||||||
chr13:102672355 | G | A | 199 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(196): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.3372-1928G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102672355 | |||||||
chr13:102672356 | G | A | 4 | a0001c0001t0010g0320 a0001c0001t0010g0321 a0001c0001t0010g0323 others(1): Show |
4 | HG03130.hp2 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.3372-1927G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102672356 | |||||||
chr13:102672512 | A | G | 2 | a0001c0002t0008g0098 a0001c0002t0008g0099 |
2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3372-1771A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102672512 | |||||||
chr13:102672847 | A | G | 2 | a0001c0001t0010g0320 a0001c0001t0010g0321 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3372-1436A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102672847 | |||||||
chr13:102672957 | A | G | 194 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(191): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.3372-1326A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102672957 | |||||||
chr13:102672974 | G | A | 200 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(197): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.3372-1309G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102672974 | |||||||
chr13:102673048 | C | T | 1 | a0001c0002t0001g0051 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3372-1235C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102673048 | |||||||
chr13:102673214 | G | A | 1 | a0001c0002t0001g0100 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3372-1069G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102673214 | |||||||
chr13:102673261 | C | T | 43 | a0001c0003t0004g0004 a0001c0003t0004g0011 a0001c0003t0004g0013 others(40): Show |
48 | HG00323.hp1 HG01099.hp1 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.3372-1022C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102673261 | |||||||
chr13:102673281 | A | G | 1 | a0001c0002t0008g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3372-1002A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102673281 | |||||||
chr13:102673299 | A | C | 1 | a0001c0003t0004g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3372-984A>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102673299 | |||||||
chr13:102673545 | C | T | 1 | a0001c0001t0003g0324 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3372-738C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102673545 | |||||||
chr13:102673564 | G | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3372-719G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102673564 | |||||||
chr13:102673648 | C | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3372-635C>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102673648 | |||||||
chr13:102673692 | A | C | 200 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(197): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.3372-591A>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102673692 | |||||||
chr13:102673963 | G | A | 256 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(253): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.3372-320G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102673963 | |||||||
chr13:102673997 | T | A | 1 | a0001c0003t0004g0134 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3372-286T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102673997 | |||||||
chr13:102674139 | C | G | 32 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0025 others(29): Show |
40 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.3372-144C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102674139 | |||||||
chr13:102674156 | C | A | 1 | a0001c0002t0001g0083 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3372-127C>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102674156 | |||||||
chr13:102674179 | T | G | 1 | a0001c0001t0002g0229 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3372-104T>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 27/29 | chr13 | 102674179 | |||||||
chr13:102674552 | G | A | 21 | a0001c0002t0005g0006 a0001c0002t0005g0028 a0001c0002t0005g0031 others(18): Show |
22 | HG00597.hp1 HG01934.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.3579+62G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 28/29 | chr13 | 102674552 | |||||||
chr13:102674600 | G | A | 164 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(161): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.3579+110G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 28/29 | chr13 | 102674600 | |||||||
chr13:102674916 | C | A | 221 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(218): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.3579+426C>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 28/29 | chr13 | 102674916 | |||||||
chr13:102675055 | G | A | 2 | a0001c0008t0012g0329 a0003c0009t0012g0328 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.3579+565G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 28/29 | chr13 | 102675055 | |||||||
chr13:102675089 | A | G | 3 | a0001c0002t0005g0028 a0001c0002t0005g0035 a0001c0002t0005g0037 |
3 | HG00597.hp1 HG03017.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.3579+599A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 28/29 | chr13 | 102675089 | |||||||
chr13:102675547 | A | G | 221 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(218): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.3580-749A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 28/29 | chr13 | 102675547 | |||||||
chr13:102675646 | A | G | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3580-650A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 28/29 | chr13 | 102675646 | |||||||
chr13:102675736 | T | C | 200 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(197): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.3580-560T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 28/29 | chr13 | 102675736 | |||||||
chr13:102675774 | A | G | 1 | a0001c0002t0001g0068 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.3580-522A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 28/29 | chr13 | 102675774 | |||||||
chr13:102676144 | T | C | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3580-152T>C | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 28/29 | chr13 | 102676144 | |||||||
chr13:102676172 | A | G | 1 | a0001c0002t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3580-124A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 28/29 | chr13 | 102676172 | |||||||
chr13:102676229 | G | T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3580-67G>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 28/29 | chr13 | 102676229 | |||||||
chr13:102676269 | C | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3580-27C>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 28/29 | chr13 | 102676269 | |||||||
chr13:102676503 | A | G | 1 | a0001c0002t0008g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3699+88A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 29/29 | chr13 | 102676503 | |||||||
chr13:102676577 | G | A | 1 | a0001c0001t0002g0227 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3699+162G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 29/29 | chr13 | 102676577 | |||||||
chr13:102677046 | T | G | 4 | a0001c0001t0010g0320 a0001c0001t0010g0321 a0001c0001t0010g0323 others(1): Show |
4 | HG03130.hp2 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.3699+631T>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 29/29 | chr13 | 102677046 | |||||||
chr13:102677155 | C | G | 1 | a0001c0001t0002g0289 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3699+740C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 29/29 | chr13 | 102677155 | |||||||
chr13:102677371 | G | GC | 49 | a0001c0002t0001g0038 a0001c0002t0001g0040 a0001c0002t0001g0043 others(46): Show |
50 | HG00408.hp2 HG00597.hp1 HG01255.hp2 others(47): Show |
intron_variant | MODIFIER | c.3700-848dupC | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 29/29 | INFO_REALIGN_3_PRIME | chr13 | 102677371 | ||||||
chr13:102677371 | GC | G | 213 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(210): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.3700-848delC | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 29/29 | INFO_REALIGN_3_PRIME | chr13 | 102677371 | ||||||
chr13:102677372 | C | T | 2 | a0001c0001t0003g0181 a0001c0001t0009g0029 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3700-855C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 29/29 | chr13 | 102677372 | |||||||
chr13:102677374 | C | G | 1 | a0001c0001t0003g0295 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3700-853C>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 29/29 | chr13 | 102677374 | |||||||
chr13:102677379 | C | T | 1 | a0001c0001t0003g0267 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3700-848C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 29/29 | chr13 | 102677379 | |||||||
chr13:102677432 | T | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(162): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3700-795T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 29/29 | chr13 | 102677432 | |||||||
chr13:102677490 | C | T | 1 | a0001c0002t0005g0033 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.3700-737C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 29/29 | chr13 | 102677490 | |||||||
chr13:102677601 | G | A | 6 | a0001c0001t0003g0003 a0001c0001t0003g0297 a0001c0001t0003g0298 others(3): Show |
9 | HG02109.hp2 HG02615.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.3700-626G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 29/29 | chr13 | 102677601 | |||||||
chr13:102677652 | G | A | 4 | a0001c0001t0002g0194 a0001c0001t0002g0289 a0001c0001t0002g0291 others(1): Show |
4 | HG01993.hp2 HG02055.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.3700-575G>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 29/29 | chr13 | 102677652 | |||||||
chr13:102677662 | C | T | 35 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0009 others(32): Show |
39 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.3700-565C>T | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 29/29 | chr13 | 102677662 | |||||||
chr13:102677688 | T | A | 67 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0019 others(64): Show |
77 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.3700-539T>A | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 29/29 | chr13 | 102677688 | |||||||
chr13:102677906 | A | G | 4 | a0001c0002t0007g0102 a0001c0002t0007g0105 a0001c0002t0007g0106 others(1): Show |
4 | HG01069.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.3700-321A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 29/29 | chr13 | 102677906 | |||||||
chr13:102677953 | A | G | 1 | a0001c0003t0004g0136 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.3700-274A>G | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 29/29 | chr13 | 102677953 | |||||||
chr13:102678035 | AG | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0193 |
3 | HG02615.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3700-190delG | TPP2 | ENSG00000134900.13 | transcript | ENST00000376052.5 | protein_coding | 29/29 | INFO_REALIGN_3_PRIME | chr13 | 102678035 |