Item | Value |
---|---|
geneid | 8295 |
ensemblid | ENSG00000196367.15 |
hgncid | 12347 |
symbol | TRRAP |
name | transformation/transcription domain associated protein |
refseq_nuc | NM_001375524.1 |
refseq_prot | NP_001362453.1 |
ensembl_nuc | ENST00000456197.2 |
ensembl_prot | ENSP00000394645.2 |
mane_status | MANE Select |
chr | chr7 |
start | 98878532 |
end | 99013241 |
strand | + |
ver | v1.2 |
region | chr7:98878532-99013241 |
region5000 | chr7:98873532-99018241 |
regionname0 | TRRAP_chr7_98878532_99013241 |
regionname5000 | TRRAP_chr7_98873532_99018241 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 3873 | 247 | 80 | 40 | 97 | 12 | 16 | 72 | TRRAP_chr7_98873532_99018241 | TRRAP | MAFVA others(3868): Show |
chr7 | 98873532 | 99018241 |
a0002 | 0/0 | 3873 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | MAFVA others(3868): Show |
chr7 | 98873532 | 99018241 |
a0003 | 0/0 | 3873 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TRRAP_chr7_98873532_99018241 | TRRAP | MAFVA others(3868): Show |
chr7 | 98873532 | 99018241 |
a0004 | 0/0 | 3873 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | MAFVA others(3868): Show |
chr7 | 98873532 | 99018241 |
a0005 | 0/0 | 3873 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | MAFVA others(3868): Show |
chr7 | 98873532 | 99018241 |
a0006 | 0/0 | 3873 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | MAFVA others(3868): Show |
chr7 | 98873532 | 99018241 |
a0007 | 0/0 | 3873 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | MAFVA others(3868): Show |
chr7 | 98873532 | 99018241 |
a0008 | 0/0 | 3873 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | MAFVA others(3868): Show |
chr7 | 98873532 | 99018241 |
a0009 | 0/0 | 3873 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | MAFVA others(3868): Show |
chr7 | 98873532 | 99018241 |
a0010 | 0/0 | 3873 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | MAFVA others(3868): Show |
chr7 | 98873532 | 99018241 |
a0011 | 0/0 | 3873 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | MAFVA others(3868): Show |
chr7 | 98873532 | 99018241 |
a0012 | 0/0 | 3873 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | MAFVA others(3868): Show |
chr7 | 98873532 | 99018241 |
a0013 | 0/0 | 3873 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | MAFVA others(3868): Show |
chr7 | 98873532 | 99018241 |
a0014 | 0/0 | 3873 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | MAFVA others(3868): Show |
chr7 | 98873532 | 99018241 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 11619 | 167 | 25 | 30 | 88 | 10 | 12 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0002 | 0/0 | 11619 | 23 | 17 | 5 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0003 | 0/0 | 11619 | 10 | 7 | 3 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0004 | 0/0 | 11619 | 9 | 9 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0005 | 0/0 | 11619 | 6 | 6 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0006 | 0/0 | 11619 | 4 | 4 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0007 | 0/0 | 11619 | 2 | 2 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0009 | 0/0 | 11619 | 2 | 2 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0010 | 0/0 | 11619 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0011 | 0/0 | 11619 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0012 | 0/0 | 11619 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0013 | 0/0 | 11619 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0014 | 0/0 | 11619 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0017 | 0/0 | 11619 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0018 | 0/0 | 11619 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0019 | 0/0 | 11619 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0021 | 0/0 | 11619 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0022 | 0/0 | 11619 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0023 | 0/0 | 11619 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0024 | 0/0 | 11619 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0025 | 0/0 | 11619 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0026 | 0/0 | 11619 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0027 | 0/0 | 11619 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0028 | 0/0 | 11619 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0030 | 0/0 | 11619 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0031 | 0/0 | 11619 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0033 | 0/0 | 11619 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0038 | 0/0 | 11619 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0043 | 0/0 | 11619 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0044 | 0/0 | 11619 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0045 | 0/0 | 11619 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0001c0046 | 0/0 | 11619 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0002c0008 | 0/0 | 11619 | 2 | 2 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0003c0036 | 0/0 | 11619 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0003c0037 | 0/0 | 11619 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0004c0016 | 0/0 | 11619 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0005c0040 | 0/0 | 11619 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0006c0039 | 0/0 | 11619 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0007c0041 | 0/0 | 11619 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0008c0042 | 0/0 | 11619 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0009c0029 | 0/0 | 11619 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0010c0034 | 0/0 | 11619 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0011c0015 | 0/0 | 11619 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0012c0020 | 0/0 | 11619 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0013c0035 | 0/0 | 11619 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 | ||
a0014c0032 | 0/0 | 11619 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | ATGGC others(11614): Show |
chr7 | 98873532 | 99018241 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 12675 | 113 | 14 | 20 | 59 | 6 | 12 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0001t0002 | 0/0 | 12675 | 36 | 7 | 7 | 20 | 2 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0001t0003 | 0/0 | 12675 | 9 | 0 | 0 | 9 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0001t0005 | 0/0 | 12674 | 3 | 3 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12669): Show |
chr7 | 98873532 | 99018241 |
a0001c0001t0006 | 0/0 | 12675 | 5 | 0 | 3 | 0 | 2 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0001t0011 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0002t0002 | 0/0 | 12675 | 17 | 14 | 3 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0002t0007 | 0/0 | 12675 | 3 | 0 | 2 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0002t0009 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0002t0010 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0002t0012 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0003t0002 | 0/0 | 12675 | 10 | 7 | 3 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0004t0002 | 0/0 | 12675 | 9 | 9 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0005t0004 | 0/0 | 12675 | 6 | 6 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0006t0002 | 0/0 | 12675 | 4 | 4 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0007t0001 | 0/0 | 12675 | 2 | 2 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0009t0002 | 0/0 | 12675 | 2 | 2 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0010t0001 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0011t0013 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0012t0001 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0013t0002 | 0/0 | 12675 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0014t0002 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0017t0001 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0018t0002 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0019t0001 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0021t0001 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0022t0001 | 0/0 | 12675 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0023t0002 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0024t0001 | 0/0 | 12675 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0025t0001 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0026t0003 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0027t0001 | 0/0 | 12675 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0028t0002 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0030t0001 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0031t0002 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0033t0001 | 0/0 | 12675 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0038t0001 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0043t0002 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0044t0002 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0045t0001 | 0/0 | 12675 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0001c0046t0001 | 0/0 | 12675 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0002c0008t0008 | 0/0 | 12675 | 2 | 2 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0003c0036t0002 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0003c0037t0002 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0004c0016t0001 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0005c0040t0005 | 0/0 | 12674 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12669): Show |
chr7 | 98873532 | 99018241 |
a0006c0039t0002 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0007c0041t0001 | 0/0 | 12675 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0008c0042t0002 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0009c0029t0001 | 0/0 | 12675 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0010c0034t0003 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0011c0015t0002 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0012c0020t0001 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0013c0035t0002 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12670): Show |
chr7 | 98873532 | 99018241 |
a0014c0032t0005 | 0/0 | 12674 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | AAGCG others(12669): Show |
chr7 | 98873532 | 99018241 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0153 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0218 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0006g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0006g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0006g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0006g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0006g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0001t0011g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0002t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0002t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0002t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0002t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0002t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0002t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0002t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0002t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0002t0007g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0002t0007g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0002t0007g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0002t0009g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0002t0010g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0002t0012g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0003t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0003t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0003t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0003t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0003t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0003t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0003t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0003t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0003t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0004t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0004t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0004t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0004t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0004t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0004t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0004t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0004t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0005t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0005t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0005t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0005t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0005t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0005t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0006t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0006t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0006t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0006t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0007t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0007t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0009t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0009t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0010t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0011t0013g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0012t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0013t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0014t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0017t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0018t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0019t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0021t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0022t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0023t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0024t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0025t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0026t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0027t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0028t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0030t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0031t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0033t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0038t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0043t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0044t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0045t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0001c0046t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0002c0008t0008g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0002c0008t0008g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0003c0036t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0003c0037t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0004c0016t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0005c0040t0005g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0006c0039t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0007c0041t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0008c0042t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0009c0029t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0010c0034t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0011c0015t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0012c0020t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0013c0035t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
a0014c0032t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | GBR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG00140 | hp2 | a0001 | c0002 | t0007 | g0154 | EUR | GBR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG00280 | hp1 | a0001 | c0001 | t0006 | g0251 | EUR | FIN | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | CHS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | CHS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | CHS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | CHS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | CHS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG00621 | hp2 | a0001 | c0030 | t0001 | g0014 | EAS | CHS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG00642 | hp1 | a0001 | c0001 | t0006 | g0254 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0228 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01081 | hp1 | a0001 | c0002 | t0002 | g0187 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01081 | hp2 | a0001 | c0003 | t0002 | g0003 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01106 | hp1 | a0001 | c0001 | t0006 | g0250 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01167 | hp1 | a0001 | c0003 | t0002 | g0201 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01169 | hp1 | a0001 | c0027 | t0001 | g0037 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01169 | hp2 | a0001 | c0003 | t0002 | g0003 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01192 | hp2 | a0001 | c0024 | t0001 | g0048 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0173 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01243 | hp2 | a0001 | c0002 | t0007 | g0155 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0255 | AMR | CLM | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01346 | hp1 | a0001 | c0002 | t0007 | g0156 | AMR | CLM | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01358 | hp2 | a0001 | c0001 | t0006 | g0252 | AMR | CLM | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | CLM | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0219 | EUR | IBS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0058 | EUR | IBS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0217 | EUR | IBS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01884 | hp1 | a0001 | c0002 | t0002 | g0016 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01891 | hp1 | a0001 | c0002 | t0002 | g0180 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01891 | hp2 | a0001 | c0007 | t0001 | g0105 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | PEL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02040 | hp2 | a0004 | c0016 | t0001 | g0229 | EAS | KHV | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02055 | hp1 | a0005 | c0040 | t0005 | g0158 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02055 | hp2 | a0001 | c0038 | t0001 | g0034 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02129 | hp1 | a0001 | c0018 | t0002 | g0245 | EAS | KHV | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PEL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02257 | hp1 | a0001 | c0004 | t0002 | g0170 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02257 | hp2 | a0001 | c0002 | t0002 | g0188 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0162 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02280 | hp1 | a0001 | c0010 | t0001 | g0068 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02280 | hp2 | a0001 | c0003 | t0002 | g0198 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0232 | AMR | PEL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0177 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02451 | hp2 | a0001 | c0003 | t0002 | g0203 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02572 | hp1 | a0001 | c0003 | t0002 | g0199 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02615 | hp1 | a0001 | c0003 | t0002 | g0206 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02622 | hp1 | a0001 | c0005 | t0004 | g0004 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02622 | hp2 | a0001 | c0004 | t0002 | g0183 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02630 | hp1 | a0001 | c0005 | t0004 | g0007 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0160 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02647 | hp1 | a0001 | c0004 | t0002 | g0176 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02647 | hp2 | a0006 | c0039 | t0002 | g0148 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02683 | hp1 | a0007 | c0041 | t0001 | g0065 | SAS | PJL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02723 | hp2 | a0001 | c0006 | t0002 | g0152 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02809 | hp1 | a0001 | c0028 | t0002 | g0207 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02809 | hp2 | a0001 | c0009 | t0002 | g0210 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02818 | hp1 | a0001 | c0044 | t0002 | g0186 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02818 | hp2 | a0001 | c0006 | t0002 | g0149 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02886 | hp1 | a0001 | c0002 | t0002 | g0172 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02886 | hp2 | a0001 | c0004 | t0002 | g0189 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02895 | hp1 | a0001 | c0005 | t0004 | g0008 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02895 | hp2 | a0002 | c0008 | t0008 | g0193 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02896 | hp2 | a0001 | c0002 | t0002 | g0164 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02897 | hp2 | a0001 | c0005 | t0004 | g0009 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02965 | hp1 | a0001 | c0004 | t0002 | g0169 | AFR | ESN | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02970 | hp1 | a0001 | c0006 | t0002 | g0151 | AFR | ESN | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02970 | hp2 | a0001 | c0002 | t0002 | g0017 | AFR | ESN | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03017 | hp1 | a0001 | c0046 | t0001 | g0146 | SAS | PJL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03098 | hp1 | a0001 | c0002 | t0002 | g0182 | AFR | MSL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03098 | hp2 | a0001 | c0011 | t0013 | g0190 | AFR | MSL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03130 | hp2 | a0001 | c0005 | t0004 | g0005 | AFR | ESN | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03139 | hp1 | a0001 | c0004 | t0002 | g0168 | AFR | ESN | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03209 | hp1 | a0001 | c0002 | t0010 | g0179 | AFR | MSL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03225 | hp2 | a0001 | c0002 | t0002 | g0174 | AFR | MSL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03239 | hp1 | a0001 | c0022 | t0001 | g0124 | SAS | PJL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03239 | hp2 | a0001 | c0033 | t0001 | g0020 | SAS | PJL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03486 | hp2 | a0001 | c0002 | t0009 | g0175 | AFR | MSL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03516 | hp1 | a0001 | c0003 | t0002 | g0205 | AFR | ESN | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03540 | hp1 | a0001 | c0002 | t0002 | g0166 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03540 | hp2 | a0001 | c0007 | t0001 | g0081 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03579 | hp2 | a0001 | c0043 | t0002 | g0167 | AFR | MSL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03704 | hp1 | a0009 | c0029 | t0001 | g0018 | SAS | PJL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03942 | hp1 | a0001 | c0045 | t0001 | g0073 | SAS | BEB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | STU | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | STU | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18522 | hp1 | a0001 | c0004 | t0002 | g0002 | AFR | YRI | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18522 | hp2 | a0001 | c0002 | t0002 | g0165 | AFR | YRI | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18747 | hp2 | a0001 | c0017 | t0001 | g0116 | EAS | CHB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18940 | hp2 | a0003 | c0036 | t0002 | g0247 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18944 | hp1 | a0001 | c0025 | t0001 | g0118 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18956 | hp1 | a0010 | c0034 | t0003 | g0024 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18969 | hp1 | a0011 | c0015 | t0002 | g0239 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18970 | hp2 | a0001 | c0021 | t0001 | g0129 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18981 | hp2 | a0012 | c0020 | t0001 | g0097 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18986 | hp2 | a0001 | c0026 | t0003 | g0023 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19000 | hp1 | a0001 | c0031 | t0002 | g0226 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19009 | hp1 | a0013 | c0035 | t0002 | g0224 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19030 | hp1 | a0001 | c0002 | t0002 | g0181 | AFR | LWK | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | LWK | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19043 | hp1 | a0001 | c0004 | t0002 | g0185 | AFR | LWK | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19043 | hp2 | a0001 | c0003 | t0002 | g0202 | AFR | LWK | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19070 | hp1 | a0001 | c0014 | t0002 | g0256 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19070 | hp2 | a0001 | c0019 | t0001 | g0112 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19080 | hp1 | a0003 | c0037 | t0002 | g0242 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19240 | hp1 | a0014 | c0032 | t0005 | g0161 | AFR | YRI | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA19240 | hp2 | a0001 | c0002 | t0002 | g0178 | AFR | YRI | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA20129 | hp1 | a0001 | c0004 | t0002 | g0002 | AFR | ASW | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA20129 | hp2 | a0001 | c0023 | t0002 | g0204 | AFR | ASW | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | TSI | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA20752 | hp2 | a0001 | c0013 | t0002 | g0215 | EUR | TSI | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | TSI | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA20805 | hp2 | a0001 | c0001 | t0006 | g0253 | EUR | TSI | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | GIH | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | GIH | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02109 | hp2 | a0001 | c0003 | t0002 | g0200 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02486 | hp1 | a0001 | c0001 | t0011 | g0209 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02486 | hp2 | a0001 | c0001 | t0005 | g0159 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02559 | hp1 | a0001 | c0006 | t0002 | g0150 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG02559 | hp2 | a0002 | c0008 | t0008 | g0192 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03471 | hp1 | a0001 | c0009 | t0002 | g0163 | AFR | MSL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG03471 | hp2 | a0008 | c0042 | t0002 | g0184 | AFR | MSL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG06807 | hp1 | a0001 | c0002 | t0002 | g0171 | AFR | USA | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
HG06807 | hp2 | a0001 | c0012 | t0001 | g0110 | AFR | USA | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA20300 | hp1 | a0001 | c0002 | t0012 | g0194 | AFR | USA | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | USA | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | LWK | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
NA21309 | hp2 | a0001 | c0005 | t0004 | g0006 | AFR | LWK | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0153 | REF | REF | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0218 | REF | REF | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:98910150 | C | G | 1 | a0007 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.1445C>G | p.Ala482Gly | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 15/73 | 1612/12675 | 1445/11622 | 482/3873 | chr7 | 98910150 | |||
chr7:98910234 | C | T | 1 | a0005 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.1529C>T | p.Pro510Leu | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 15/73 | 1696/12675 | 1529/11622 | 510/3873 | chr7 | 98910234 | |||
chr7:98910275 | G | A | 1 | a0002 | 2 | HG02559.hp2 HG02895.hp2 |
missense_variant | MODERATE | c.1570G>A | p.Val524Met | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 15/73 | 1737/12675 | 1570/11622 | 524/3873 | chr7 | 98910275 | |||
chr7:98925217 | C | A | 1 | a0004 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.2929C>A | p.Leu977Met | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/73 | 3096/12675 | 2929/11622 | 977/3873 | chr7 | 98925217 | |||
chr7:98949523 | G | T | 1 | a0003 | 2 | NA18940.hp2 NA19080.hp1 |
missense_variant | MODERATE | c.4895G>T | p.Arg1632Leu | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 36/73 | 5062/12675 | 4895/11622 | 1632/3873 | chr7 | 98949523 | |||
chr7:98949832 | A | G | 1 | a0013 | 1 | NA19009.hp1 | missense_variant | MODERATE | c.5126A>G | p.Asn1709Ser | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 37/73 | 5293/12675 | 5126/11622 | 1709/3873 | chr7 | 98949832 | |||
chr7:98950138 | C | T | 1 | a0010 | 1 | NA18956.hp1 | missense_variant | MODERATE | c.5210C>T | p.Thr1737Ile | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 38/73 | 5377/12675 | 5210/11622 | 1737/3873 | chr7 | 98950138 | |||
chr7:98956442 | A | G | 1 | a0014 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.6140A>G | p.Asn2047Ser | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/73 | 6307/12675 | 6140/11622 | 2047/3873 | chr7 | 98956442 | |||
chr7:98956447 | G | A | 1 | a0008 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.6145G>A | p.Val2049Ile | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/73 | 6312/12675 | 6145/11622 | 2049/3873 | chr7 | 98956447 | |||
chr7:98964749 | C | T | 1 | a0006 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.6950C>T | p.Ala2317Val | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 48/73 | 7117/12675 | 6950/11622 | 2317/3873 | chr7 | 98964749 | |||
chr7:98976173 | G | A | 1 | a0012 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.7864G>A | p.Val2622Ile | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 54/73 | 8031/12675 | 7864/11622 | 2622/3873 | chr7 | 98976173 | |||
chr7:98976195 | C | T | 1 | a0009 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.7886C>T | p.Thr2629Met | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 54/73 | 8053/12675 | 7886/11622 | 2629/3873 | chr7 | 98976195 | |||
chr7:99012141 | C | T | 1 | a0011 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.11408C>T | p.Thr3803Met | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 11575/12675 | 11408/11622 | 3803/3873 | chr7 | 99012141 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:98897785 | G | C | 1 | a0001c0010 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.552G>C | p.Val184Val | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 8/73 | 719/12675 | 552/11622 | 184/3873 | chr7 | 98897785 | |||
chr7:98897848 | G | A | 1 | a0001c0011 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.615G>A | p.Glu205Glu | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 8/73 | 782/12675 | 615/11622 | 205/3873 | chr7 | 98897848 | |||
chr7:98899744 | C | T | 1 | a0001c0046 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.777C>T | p.Ala259Ala | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 10/73 | 944/12675 | 777/11622 | 259/3873 | chr7 | 98899744 | |||
chr7:98903495 | C | T | 1 | a0001c0045 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.1014C>T | p.Ile338Ile | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/73 | 1181/12675 | 1014/11622 | 338/3873 | chr7 | 98903495 | |||
chr7:98908818 | C | T | 8 | a0001c0002 a0001c0004 a0001c0005 others(5): Show |
45 | HG00140.hp2 HG01081.hp1 HG01243.hp1 others(42): Show |
synonymous_variant | LOW | c.1206C>T | p.Phe402Phe | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 14/73 | 1373/12675 | 1206/11622 | 402/3873 | chr7 | 98908818 | |||
chr7:98910604 | T | C | 1 | a0001c0012 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.1809T>C | p.Tyr603Tyr | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 16/73 | 1976/12675 | 1809/11622 | 603/3873 | chr7 | 98910604 | |||
chr7:98917487 | T | C | 1 | a0001c0013 | 1 | NA20752.hp2 | synonymous_variant | LOW | c.2430T>C | p.Cys810Cys | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/73 | 2597/12675 | 2430/11622 | 810/3873 | chr7 | 98917487 | |||
chr7:98917490 | C | T | 1 | a0002c0008 | 2 | HG02559.hp2 HG02895.hp2 |
synonymous_variant | LOW | c.2433C>T | p.Leu811Leu | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/73 | 2600/12675 | 2433/11622 | 811/3873 | chr7 | 98917490 | |||
chr7:98917673 | C | T | 2 | a0001c0006 a0006c0039 |
5 | HG02559.hp1 HG02647.hp2 HG02723.hp2 others(2): Show |
synonymous_variant | LOW | c.2616C>T | p.Leu872Leu | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/73 | 2783/12675 | 2616/11622 | 872/3873 | chr7 | 98917673 | |||
chr7:98921818 | T | C | 2 | a0001c0014 a0011c0015 |
2 | NA18969.hp1 NA19070.hp1 |
synonymous_variant | LOW | c.2688T>C | p.Gly896Gly | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/73 | 2855/12675 | 2688/11622 | 896/3873 | chr7 | 98921818 | |||
chr7:98930065 | G | A | 2 | a0001c0004 a0008c0042 |
10 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(7): Show |
synonymous_variant | LOW | c.3252G>A | p.Ser1084Ser | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 24/73 | 3419/12675 | 3252/11622 | 1084/3873 | chr7 | 98930065 | |||
chr7:98933261 | C | T | 1 | a0001c0038 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.3873C>T | p.Pro1291Pro | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/73 | 4040/12675 | 3873/11622 | 1291/3873 | chr7 | 98933261 | |||
chr7:98948325 | G | T | 1 | a0001c0007 | 2 | HG01891.hp2 HG03540.hp2 |
synonymous_variant | LOW | c.4653G>T | p.Arg1551Arg | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 34/73 | 4820/12675 | 4653/11622 | 1551/3873 | chr7 | 98948325 | |||
chr7:98950989 | T | C | 1 | a0001c0017 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.5448T>C | p.Ser1816Ser | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/73 | 5615/12675 | 5448/11622 | 1816/3873 | chr7 | 98950989 | |||
chr7:98955127 | A | G | 1 | a0001c0033 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.5760A>G | p.Ala1920Ala | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 41/73 | 5927/12675 | 5760/11622 | 1920/3873 | chr7 | 98955127 | |||
chr7:98956190 | C | T | 1 | a0003c0037 | 1 | NA19080.hp1 | synonymous_variant | LOW | c.5982C>T | p.Ser1994Ser | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 42/73 | 6149/12675 | 5982/11622 | 1994/3873 | chr7 | 98956190 | |||
chr7:98956512 | G | A | 1 | a0001c0018 | 1 | HG02129.hp1 | synonymous_variant | LOW | c.6210G>A | p.Thr2070Thr | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/73 | 6377/12675 | 6210/11622 | 2070/3873 | chr7 | 98956512 | |||
chr7:98958043 | G | A | 1 | a0001c0019 | 1 | NA19070.hp2 | synonymous_variant | LOW | c.6294G>A | p.Lys2098Lys | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/73 | 6461/12675 | 6294/11622 | 2098/3873 | chr7 | 98958043 | |||
chr7:98962357 | C | T | 1 | a0001c0031 | 1 | NA19000.hp1 | synonymous_variant | LOW | c.6759C>T | p.Val2253Val | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/73 | 6926/12675 | 6759/11622 | 2253/3873 | chr7 | 98962357 | |||
chr7:98967563 | A | C | 1 | a0001c0030 | 1 | HG00621.hp2 | synonymous_variant | LOW | c.7377A>C | p.Pro2459Pro | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/73 | 7544/12675 | 7377/11622 | 2459/3873 | chr7 | 98967563 | |||
chr7:98970216 | C | T | 1 | a0001c0044 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.7617C>T | p.Asp2539Asp | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/73 | 7784/12675 | 7617/11622 | 2539/3873 | chr7 | 98970216 | |||
chr7:98976214 | G | A | 1 | a0001c0021 | 1 | NA18970.hp2 | synonymous_variant | LOW | c.7905G>A | p.Thr2635Thr | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 54/73 | 8072/12675 | 7905/11622 | 2635/3873 | chr7 | 98976214 | |||
chr7:98976220 | C | T | 1 | a0001c0043 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.7911C>T | p.Val2637Val | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 54/73 | 8078/12675 | 7911/11622 | 2637/3873 | chr7 | 98976220 | |||
chr7:98976557 | G | A | 1 | a0001c0022 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.8034G>A | p.Ala2678Ala | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 55/73 | 8201/12675 | 8034/11622 | 2678/3873 | chr7 | 98976557 | |||
chr7:98976953 | C | T | 1 | a0001c0011 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.8262C>T | p.Ser2754Ser | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/73 | 8429/12675 | 8262/11622 | 2754/3873 | chr7 | 98976953 | |||
chr7:98978240 | T | C | 1 | a0001c0009 | 2 | HG02809.hp2 HG03471.hp1 |
synonymous_variant | LOW | c.8415T>C | p.Asp2805Asp | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 57/73 | 8582/12675 | 8415/11622 | 2805/3873 | chr7 | 98978240 | |||
chr7:98984169 | A | C | 1 | a0001c0028 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.9099A>C | p.Ser3033Ser | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 61/73 | 9266/12675 | 9099/11622 | 3033/3873 | chr7 | 98984169 | |||
chr7:98984946 | C | A | 2 | a0001c0003 a0001c0023 |
11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
splice_region_variant&synonymous_variant | LOW | c.9291C>A | p.Gly3097Gly | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/73 | 9458/12675 | 9291/11622 | 3097/3873 | chr7 | 98984946 | |||
chr7:98994601 | C | T | 1 | a0001c0023 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.10062C>T | p.Leu3354Leu | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/73 | 10229/12675 | 10062/11622 | 3354/3873 | chr7 | 98994601 | |||
chr7:99008483 | C | T | 1 | a0001c0027 | 1 | HG01169.hp1 | synonymous_variant | LOW | c.10860C>T | p.Ile3620Ile | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/73 | 11027/12675 | 10860/11622 | 3620/3873 | chr7 | 99008483 | |||
chr7:99008537 | G | A | 1 | a0001c0019 | 1 | NA19070.hp2 | synonymous_variant | LOW | c.10914G>A | p.Ala3638Ala | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/73 | 11081/12675 | 10914/11622 | 3638/3873 | chr7 | 99008537 | |||
chr7:99011096 | G | A | 1 | a0001c0024 | 1 | HG01192.hp2 | synonymous_variant | LOW | c.10983G>A | p.Pro3661Pro | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 71/73 | 11150/12675 | 10983/11622 | 3661/3873 | chr7 | 99011096 | |||
chr7:99011352 | A | G | 1 | a0001c0019 | 1 | NA19070.hp2 | synonymous_variant | LOW | c.11154A>G | p.Lys3718Lys | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 72/73 | 11321/12675 | 11154/11622 | 3718/3873 | chr7 | 99011352 | |||
chr7:99011433 | C | G | 1 | a0001c0005 | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
synonymous_variant | LOW | c.11235C>G | p.Leu3745Leu | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 72/73 | 11402/12675 | 11235/11622 | 3745/3873 | chr7 | 99011433 | |||
chr7:99012157 | G | A | 1 | a0001c0025 | 1 | NA18944.hp1 | synonymous_variant | LOW | c.11424G>A | p.Ser3808Ser | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 11591/12675 | 11424/11622 | 3808/3873 | chr7 | 99012157 | |||
chr7:99012220 | C | T | 1 | a0001c0026 | 1 | NA18986.hp2 | synonymous_variant | LOW | c.11487C>T | p.Val3829Val | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 11654/12675 | 11487/11622 | 3829/3873 | chr7 | 99012220 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:99012364 | G | A | 1 | a0002c0008t0008 | 2 | HG02559.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 9 | chr7 | 99012364 | ||||||
chr7:99012369 | G | A | 1 | a0001c0002t0009 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 14 | chr7 | 99012369 | ||||||
chr7:99012409 | G | A | 1 | a0001c0002t0010 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*54G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 54 | chr7 | 99012409 | ||||||
chr7:99012479 | G | A | 1 | a0001c0001t0011 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*124G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 124 | chr7 | 99012479 | ||||||
chr7:99012500 | G | A | 1 | a0002c0008t0008 | 2 | HG02559.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*145G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 145 | chr7 | 99012500 | ||||||
chr7:99012702 | G | A | 1 | a0001c0002t0012 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*347G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 347 | chr7 | 99012702 | ||||||
chr7:99012912 | G | A | 1 | a0001c0005t0004 | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*557G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 557 | chr7 | 99012912 | ||||||
chr7:99012964 | G | A | 1 | a0001c0002t0007 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
3_prime_UTR_variant | MODIFIER | c.*609G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 609 | chr7 | 99012964 | ||||||
chr7:99012972 | T | C | 34 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(31): Show |
128 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*617T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 617 | chr7 | 99012972 | ||||||
chr7:99013059 | C | T | 1 | a0001c0001t0006 | 5 | HG00280.hp1 HG00642.hp1 HG01106.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*704C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 704 | chr7 | 99013059 | ||||||
chr7:99013061 | C | T | 32 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(29): Show |
118 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*706C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 706 | chr7 | 99013061 | ||||||
chr7:99013207 | AT | A | 3 | a0001c0001t0005 a0005c0040t0005 a0014c0032t0005 |
5 | HG02055.hp1 HG02258.hp1 HG02486.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*863delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 863 | INFO_REALIGN_3_PRIME | chr7 | 99013207 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:98878644 | T | TGGCG | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-62+16_-62+19dupGG others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | INFO_REALIGN_3_PRIME | chr7 | 98878644 | ||||||
chr7:98878765 | C | A | 2 | a0001c0001t0002g0010 a0001c0001t0002g0011 |
2 | HG00544.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.-62+128C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98878765 | |||||||
chr7:98878802 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-62+165C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98878802 | |||||||
chr7:98878806 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(205): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.-62+169T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98878806 | |||||||
chr7:98878973 | G | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(1): Show |
4 | HG00621.hp2 HG01993.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.-62+336G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98878973 | |||||||
chr7:98879068 | G | T | 1 | a0001c0009t0002g0210 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-62+431G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98879068 | |||||||
chr7:98879072 | G | C | 2 | a0001c0002t0002g0016 a0001c0002t0002g0017 |
2 | HG01884.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-62+435G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98879072 | |||||||
chr7:98879130 | C | A | 191 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(188): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.-62+493C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98879130 | |||||||
chr7:98879183 | C | T | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-62+546C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98879183 | |||||||
chr7:98879188 | C | T | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-62+551C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98879188 | |||||||
chr7:98879288 | A | G | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | NA18971.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-62+651A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98879288 | |||||||
chr7:98879453 | G | C | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-62+816G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98879453 | |||||||
chr7:98879593 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-62+956C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98879593 | |||||||
chr7:98879807 | A | G | 3 | a0001c0001t0002g0208 a0001c0001t0011g0209 a0001c0028t0002g0207 |
3 | HG02486.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-62+1170A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98879807 | |||||||
chr7:98880092 | A | G | 32 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0164 others(29): Show |
33 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.-61-998A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880092 | |||||||
chr7:98880096 | A | C | 5 | a0001c0001t0005g0159 a0001c0001t0005g0160 a0001c0001t0005g0162 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-61-994A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880096 | |||||||
chr7:98880123 | A | G | 44 | a0001c0001t0002g0157 a0001c0002t0002g0016 a0001c0002t0002g0017 others(41): Show |
45 | HG00140.hp2 HG01081.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.-61-967A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880123 | |||||||
chr7:98880232 | GCCTGCTG others(51): Show |
G | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-61-854_-61-797del others(58): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | INFO_REALIGN_3_PRIME | chr7 | 98880232 | ||||||
chr7:98880259 | G | T | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-61-831G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880259 | |||||||
chr7:98880262 | G | GT | 5 | a0001c0001t0002g0211 a0001c0001t0002g0219 a0001c0031t0002g0226 others(2): Show |
5 | HG01515.hp2 NA18940.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.-61-811dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | INFO_REALIGN_3_PRIME | chr7 | 98880262 | ||||||
chr7:98880262 | G | GTTTTGT | 62 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(59): Show |
62 | HG00408.hp2 HG00621.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.-61-824_-61-823ins others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | INFO_REALIGN_3_PRIME | chr7 | 98880262 | ||||||
chr7:98880262 | G | GTTTTGTT | 5 | a0001c0001t0001g0043 a0001c0001t0001g0053 a0001c0001t0001g0123 others(2): Show |
5 | HG00423.hp1 HG01358.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.-61-824_-61-823ins others(7): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | INFO_REALIGN_3_PRIME | chr7 | 98880262 | ||||||
chr7:98880262 | G | GTTTTT | 45 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0067 others(42): Show |
46 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.-61-815_-61-811dup others(5): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | INFO_REALIGN_3_PRIME | chr7 | 98880262 | ||||||
chr7:98880262 | G | GTTTTTT | 17 | a0001c0001t0001g0066 a0001c0001t0001g0076 a0001c0001t0001g0082 others(14): Show |
17 | HG00438.hp1 HG00621.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-61-816_-61-811dup others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | INFO_REALIGN_3_PRIME | chr7 | 98880262 | ||||||
chr7:98880262 | G | T | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-61-828G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880262 | |||||||
chr7:98880262 | GT | G | 46 | a0001c0001t0002g0147 a0001c0001t0002g0157 a0001c0001t0002g0220 others(43): Show |
47 | HG00438.hp2 HG01081.hp1 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.-61-811delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | INFO_REALIGN_3_PRIME | chr7 | 98880262 | ||||||
chr7:98880265 | T | G | 23 | a0001c0001t0002g0195 a0001c0001t0002g0196 a0001c0001t0002g0197 others(20): Show |
24 | HG00280.hp1 HG00642.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.-61-825T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880265 | |||||||
chr7:98880266 | T | G | 5 | a0001c0001t0002g0157 a0001c0001t0005g0159 a0002c0008t0008g0192 others(2): Show |
5 | HG02486.hp2 HG02559.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-61-824T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880266 | |||||||
chr7:98880267 | T | G | 2 | a0001c0001t0001g0055 a0001c0002t0002g0188 |
2 | HG02257.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.-61-823T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880267 | |||||||
chr7:98880268 | T | G | 3 | a0001c0001t0002g0208 a0001c0001t0011g0209 a0001c0028t0002g0207 |
3 | HG02486.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-61-822T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880268 | |||||||
chr7:98880335 | C | T | 1 | a0001c0004t0002g0189 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-61-755C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880335 | |||||||
chr7:98880436 | G | T | 6 | a0001c0001t0002g0147 a0001c0006t0002g0149 a0001c0006t0002g0150 others(3): Show |
6 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-61-654G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880436 | |||||||
chr7:98880474 | C | T | 1 | a0001c0046t0001g0146 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-61-616C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880474 | |||||||
chr7:98880577 | T | C | 1 | a0009c0029t0001g0018 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-61-513T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880577 | |||||||
chr7:98880585 | A | C | 1 | a0001c0001t0001g0145 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-61-505A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880585 | |||||||
chr7:98880778 | A | G | 1 | a0001c0002t0002g0188 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-61-312A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880778 | |||||||
chr7:98880794 | A | G | 18 | a0001c0001t0001g0128 a0001c0001t0001g0130 a0001c0001t0001g0131 others(15): Show |
18 | HG00738.hp1 HG01192.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.-61-296A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880794 | |||||||
chr7:98880966 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-61-124A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880966 | |||||||
chr7:98880982 | G | A | 2 | a0001c0001t0001g0019 a0001c0033t0001g0020 |
2 | HG03239.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-61-108G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880982 | |||||||
chr7:98881057 | A | G | 43 | a0001c0001t0002g0157 a0001c0002t0002g0016 a0001c0002t0002g0017 others(40): Show |
44 | HG00140.hp2 HG01081.hp1 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.-61-33A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98881057 | |||||||
chr7:98881401 | C | T | 2 | a0001c0002t0002g0187 a0001c0044t0002g0186 |
2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.100+151C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 2/72 | chr7 | 98881401 | |||||||
chr7:98881498 | G | A | 5 | a0001c0002t0002g0164 a0001c0002t0002g0165 a0001c0002t0002g0166 others(2): Show |
5 | HG02809.hp2 HG02896.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+248G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 2/72 | chr7 | 98881498 | |||||||
chr7:98881508 | G | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(123): Show |
127 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.100+258G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 2/72 | chr7 | 98881508 | |||||||
chr7:98881544 | C | T | 11 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(8): Show |
11 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.100+294C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 2/72 | chr7 | 98881544 | |||||||
chr7:98881571 | C | CA | 35 | a0001c0001t0002g0208 a0001c0001t0002g0211 a0001c0001t0011g0209 others(32): Show |
36 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.100+337dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 2/72 | INFO_REALIGN_3_PRIME | chr7 | 98881571 | ||||||
chr7:98881571 | C | CAA | 5 | a0001c0001t0002g0157 a0001c0002t0007g0154 a0001c0002t0007g0155 others(2): Show |
5 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+336_100+337dup others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 2/72 | INFO_REALIGN_3_PRIME | chr7 | 98881571 | ||||||
chr7:98881571 | CA | C | 11 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0259 others(8): Show |
11 | HG01884.hp2 HG02040.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.100+337delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 2/72 | INFO_REALIGN_3_PRIME | chr7 | 98881571 | ||||||
chr7:98881608 | A | G | 1 | a0001c0022t0001g0124 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.100+358A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 2/72 | chr7 | 98881608 | |||||||
chr7:98881610 | A | G | 4 | a0001c0004t0002g0183 a0001c0004t0002g0185 a0001c0004t0002g0189 others(1): Show |
4 | HG02622.hp2 HG02886.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+360A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 2/72 | chr7 | 98881610 | |||||||
chr7:98881835 | C | T | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.101-140C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 2/72 | chr7 | 98881835 | |||||||
chr7:98882032 | C | T | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | splice_region_variant&intron_variant | LOW | c.150+8C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98882032 | |||||||
chr7:98882084 | G | A | 11 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(8): Show |
11 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.150+60G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98882084 | |||||||
chr7:98882200 | C | G | 1 | a0001c0001t0001g0123 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.150+176C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98882200 | |||||||
chr7:98882270 | T | C | 1 | a0001c0001t0002g0212 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.150+246T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98882270 | |||||||
chr7:98882363 | C | CT | 8 | a0001c0001t0006g0250 a0001c0001t0006g0251 a0001c0001t0006g0252 others(5): Show |
8 | HG00280.hp1 HG00642.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.150+355dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98882363 | ||||||
chr7:98882402 | G | A | 2 | a0001c0001t0002g0213 a0001c0001t0002g0214 |
2 | NA18966.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.150+378G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98882402 | |||||||
chr7:98882483 | C | T | 1 | a0001c0001t0002g0249 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.150+459C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98882483 | |||||||
chr7:98882563 | A | G | 3 | a0001c0005t0004g0007 a0001c0005t0004g0008 a0001c0005t0004g0009 |
3 | HG02630.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.150+539A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98882563 | |||||||
chr7:98882636 | T | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(1): Show |
4 | HG00621.hp2 HG01993.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+612T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98882636 | |||||||
chr7:98882777 | G | T | 253 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(250): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.150+753G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98882777 | |||||||
chr7:98882781 | C | A | 5 | a0001c0001t0005g0159 a0001c0001t0005g0160 a0001c0001t0005g0162 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.150+757C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98882781 | |||||||
chr7:98882825 | AT | A | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.150+806delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98882825 | ||||||
chr7:98883099 | A | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(206): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.150+1075A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98883099 | |||||||
chr7:98883158 | A | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(204): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.150+1134A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98883158 | |||||||
chr7:98883217 | G | T | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.150+1193G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98883217 | |||||||
chr7:98883462 | A | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(189): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.150+1438A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98883462 | |||||||
chr7:98883520 | T | C | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.150+1496T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98883520 | |||||||
chr7:98883813 | C | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0066 others(62): Show |
66 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.150+1789C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98883813 | |||||||
chr7:98884177 | C | T | 42 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(39): Show |
43 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(40): Show |
intron_variant | MODIFIER | c.150+2153C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98884177 | |||||||
chr7:98884310 | T | A | 1 | a0001c0004t0002g0183 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.150+2286T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98884310 | |||||||
chr7:98884487 | A | C | 1 | a0007c0041t0001g0065 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.150+2463A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98884487 | |||||||
chr7:98884503 | A | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01167.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.150+2479A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98884503 | |||||||
chr7:98884526 | T | C | 1 | a0001c0001t0001g0012 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.150+2502T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98884526 | |||||||
chr7:98884597 | G | A | 3 | a0001c0001t0002g0195 a0001c0001t0002g0196 a0001c0001t0002g0197 |
3 | HG02258.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.150+2573G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98884597 | |||||||
chr7:98884995 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.150+2971G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98884995 | |||||||
chr7:98885062 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.150+3038A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98885062 | |||||||
chr7:98885254 | A | AT | 132 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(129): Show |
133 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.150+3243dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98885254 | ||||||
chr7:98885306 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.150+3282C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98885306 | |||||||
chr7:98885319 | C | T | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.150+3295C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98885319 | |||||||
chr7:98885350 | G | T | 2 | a0001c0002t0002g0165 a0001c0002t0002g0166 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.150+3326G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98885350 | |||||||
chr7:98885368 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.150+3344C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98885368 | |||||||
chr7:98885385 | A | G | 2 | a0001c0001t0002g0208 a0001c0001t0011g0209 |
2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.150+3361A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98885385 | |||||||
chr7:98885408 | T | C | 1 | a0002c0008t0008g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.150+3384T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98885408 | |||||||
chr7:98885429 | G | A | 205 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(202): Show |
208 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.150+3405G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98885429 | |||||||
chr7:98885449 | C | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0111 others(12): Show |
16 | HG00280.hp2 HG00558.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.150+3425C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98885449 | |||||||
chr7:98885485 | G | A | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0126 |
3 | HG02572.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.150+3461G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98885485 | |||||||
chr7:98885667 | A | AAT | 7 | a0001c0001t0002g0147 a0001c0001t0002g0220 a0001c0001t0002g0221 others(4): Show |
7 | HG00140.hp2 HG00438.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.150+3660_150+3661d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98885667 | ||||||
chr7:98885667 | A | AATATAT | 4 | a0001c0004t0002g0002 a0001c0004t0002g0168 a0001c0004t0002g0169 others(1): Show |
5 | HG02257.hp1 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.150+3656_150+3661d others(8): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98885667 | ||||||
chr7:98885794 | G | C | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.150+3770G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98885794 | |||||||
chr7:98886033 | C | T | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.150+4009C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886033 | |||||||
chr7:98886082 | C | T | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.150+4058C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886082 | |||||||
chr7:98886299 | CATAGATA others(31): Show |
C | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.151-3994_151-3957d others(40): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98886299 | ||||||
chr7:98886313 | T | C | 1 | a0001c0002t0002g0188 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.151-4022T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886313 | |||||||
chr7:98886335 | T | G | 1 | a0001c0001t0001g0032 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.151-4000T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886335 | |||||||
chr7:98886355 | T | G | 1 | a0001c0001t0001g0032 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.151-3980T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886355 | |||||||
chr7:98886357 | T | G | 1 | a0001c0001t0001g0032 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.151-3978T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886357 | |||||||
chr7:98886389 | T | C | 10 | a0001c0003t0002g0003 a0001c0003t0002g0198 a0001c0003t0002g0199 others(7): Show |
11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.151-3946T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886389 | |||||||
chr7:98886437 | T | C | 32 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0164 others(29): Show |
33 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.151-3898T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886437 | |||||||
chr7:98886438 | A | G | 43 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(40): Show |
44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.151-3897A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886438 | |||||||
chr7:98886441 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.151-3894T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886441 | |||||||
chr7:98886449 | T | G | 43 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(40): Show |
44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.151-3886T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886449 | |||||||
chr7:98886595 | A | G | 3 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0145 |
3 | HG02129.hp2 NA18979.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.151-3740A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886595 | |||||||
chr7:98886770 | G | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(132): Show |
136 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.151-3565G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886770 | |||||||
chr7:98886770 | G | T | 1 | a0001c0012t0001g0110 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.151-3565G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886770 | |||||||
chr7:98886796 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0120 a0001c0033t0001g0020 |
3 | HG02698.hp2 HG03239.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.151-3539C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886796 | |||||||
chr7:98886859 | G | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(206): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.151-3476G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886859 | |||||||
chr7:98886912 | A | T | 1 | a0001c0001t0003g0030 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.151-3423A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886912 | |||||||
chr7:98887096 | C | CT | 12 | a0001c0001t0002g0157 a0001c0002t0007g0154 a0001c0002t0007g0155 others(9): Show |
12 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.151-3231dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98887096 | ||||||
chr7:98887143 | C | T | 1 | a0001c0002t0002g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.151-3192C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98887143 | |||||||
chr7:98887166 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.151-3169C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98887166 | |||||||
chr7:98887356 | T | G | 1 | a0001c0001t0002g0208 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.151-2979T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98887356 | |||||||
chr7:98887514 | G | A | 5 | a0001c0001t0005g0159 a0001c0001t0005g0160 a0001c0001t0005g0162 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.151-2821G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98887514 | |||||||
chr7:98887662 | G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.151-2673G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98887662 | |||||||
chr7:98887690 | A | G | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.151-2645A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98887690 | |||||||
chr7:98887729 | C | CA | 67 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(64): Show |
68 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.151-2585dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98887729 | ||||||
chr7:98887729 | C | CAA | 114 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(111): Show |
115 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.151-2586_151-2585d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98887729 | ||||||
chr7:98887729 | C | CAAA | 24 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(21): Show |
24 | HG00423.hp1 HG00738.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.151-2587_151-2585d others(5): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98887729 | ||||||
chr7:98887744 | A | AC | 40 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(37): Show |
41 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.151-2591_151-2590i others(3): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98887744 | |||||||
chr7:98887845 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.151-2490A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98887845 | |||||||
chr7:98887864 | A | G | 1 | a0001c0001t0001g0001 | 2 | HG00280.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.151-2471A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98887864 | |||||||
chr7:98887894 | C | A | 1 | a0001c0001t0001g0070 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.151-2441C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98887894 | |||||||
chr7:98888102 | C | T | 1 | a0001c0001t0003g0028 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.151-2233C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98888102 | |||||||
chr7:98888261 | A | G | 2 | a0001c0002t0002g0187 a0001c0044t0002g0186 |
2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.151-2074A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98888261 | |||||||
chr7:98888375 | T | TA | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.151-1949dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98888375 | ||||||
chr7:98888446 | A | G | 1 | a0001c0001t0002g0248 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.151-1889A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98888446 | |||||||
chr7:98888642 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.151-1693C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98888642 | |||||||
chr7:98888674 | C | G | 1 | a0001c0002t0012g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.151-1661C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98888674 | |||||||
chr7:98888684 | A | G | 6 | a0001c0001t0002g0157 a0001c0002t0007g0154 a0001c0002t0007g0155 others(3): Show |
6 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.151-1651A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98888684 | |||||||
chr7:98888714 | T | C | 32 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0164 others(29): Show |
33 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.151-1621T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98888714 | |||||||
chr7:98889045 | CT | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(171): Show |
176 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.151-1269delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98889045 | ||||||
chr7:98889045 | CTTTTTTT others(4): Show |
C | 1 | a0001c0002t0012g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.151-1279_151-1269d others(13): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98889045 | ||||||
chr7:98889064 | T | C | 1 | a0001c0001t0002g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.151-1271T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889064 | |||||||
chr7:98889076 | T | C | 43 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(40): Show |
44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.151-1259T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889076 | |||||||
chr7:98889230 | A | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.151-1105A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889230 | |||||||
chr7:98889265 | A | G | 2 | a0001c0001t0006g0253 a0001c0001t0006g0254 |
2 | HG00642.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.151-1070A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889265 | |||||||
chr7:98889354 | A | T | 7 | a0001c0002t0002g0177 a0001c0002t0002g0178 a0001c0002t0002g0180 others(4): Show |
7 | HG01257.hp2 HG01891.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.151-981A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889354 | |||||||
chr7:98889386 | A | G | 2 | a0001c0001t0002g0196 a0001c0001t0002g0197 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.151-949A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889386 | |||||||
chr7:98889411 | T | G | 1 | a0001c0001t0001g0123 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.151-924T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889411 | |||||||
chr7:98889538 | CT | C | 59 | a0001c0001t0002g0147 a0001c0001t0002g0157 a0001c0001t0002g0195 others(56): Show |
60 | HG00140.hp2 HG01081.hp1 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.151-780delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98889538 | ||||||
chr7:98889554 | T | A | 4 | a0001c0001t0002g0157 a0001c0002t0007g0154 a0001c0002t0007g0155 others(1): Show |
4 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-781T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889554 | |||||||
chr7:98889555 | T | A | 6 | a0001c0001t0002g0157 a0001c0002t0007g0154 a0001c0002t0007g0155 others(3): Show |
6 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.151-780T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889555 | |||||||
chr7:98889555 | TA | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(118): Show |
122 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.151-772delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98889555 | ||||||
chr7:98889555 | TAA | T | 5 | a0001c0001t0001g0072 a0001c0001t0001g0130 a0001c0001t0001g0140 others(2): Show |
5 | HG01169.hp1 HG03017.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.151-773_151-772del others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98889555 | ||||||
chr7:98889556 | A | T | 7 | a0001c0001t0001g0033 a0001c0001t0001g0142 a0001c0001t0002g0222 others(4): Show |
7 | HG02148.hp2 NA18942.hp2 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.151-779A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889556 | |||||||
chr7:98889557 | A | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(115): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.151-778A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889557 | |||||||
chr7:98889558 | A | T | 1 | a0001c0001t0001g0119 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.151-777A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889558 | |||||||
chr7:98889676 | T | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(123): Show |
127 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.151-659T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889676 | |||||||
chr7:98889731 | T | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(125): Show |
129 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.151-604T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889731 | |||||||
chr7:98889745 | G | T | 4 | a0001c0001t0002g0157 a0001c0002t0007g0154 a0001c0002t0007g0155 others(1): Show |
4 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-590G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889745 | |||||||
chr7:98889810 | C | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.151-525C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889810 | |||||||
chr7:98890580 | C | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.261+135C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98890580 | |||||||
chr7:98890581 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.261+136G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98890581 | |||||||
chr7:98890587 | T | C | 1 | a0001c0001t0001g0038 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.261+142T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98890587 | |||||||
chr7:98890720 | G | C | 1 | a0001c0005t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.261+275G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98890720 | |||||||
chr7:98890781 | C | CT | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
105 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.261+360dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | INFO_REALIGN_3_PRIME | chr7 | 98890781 | ||||||
chr7:98890781 | C | CTT | 8 | a0001c0001t0001g0015 a0001c0001t0001g0061 a0001c0001t0001g0106 others(5): Show |
8 | HG01891.hp2 HG03579.hp1 HG03710.hp1 others(5): Show |
intron_variant | MODIFIER | c.261+359_261+360dup others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | INFO_REALIGN_3_PRIME | chr7 | 98890781 | ||||||
chr7:98890781 | CT | C | 6 | a0001c0001t0006g0250 a0001c0001t0006g0251 a0001c0001t0006g0252 others(3): Show |
6 | HG00280.hp1 HG00642.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.261+360delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | INFO_REALIGN_3_PRIME | chr7 | 98890781 | ||||||
chr7:98890794 | TTTTTTTT others(5): Show |
T | 1 | a0005c0040t0005g0158 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.261+350_261+361del others(12): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98890794 | |||||||
chr7:98890804 | TTA | T | 7 | a0001c0001t0005g0159 a0001c0001t0005g0160 a0001c0001t0005g0162 others(4): Show |
7 | HG01167.hp1 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.261+360_261+361del others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98890804 | |||||||
chr7:98890805 | TA | T | 56 | a0001c0001t0001g0031 a0001c0001t0002g0147 a0001c0001t0002g0157 others(53): Show |
58 | HG00140.hp2 HG01081.hp1 HG01081.hp2 others(55): Show |
intron_variant | MODIFIER | c.261+364delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | INFO_REALIGN_3_PRIME | chr7 | 98890805 | ||||||
chr7:98890806 | A | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(129): Show |
133 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.261+361A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98890806 | |||||||
chr7:98890858 | G | A | 254 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(251): Show |
257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.261+413G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98890858 | |||||||
chr7:98891137 | A | G | 12 | a0001c0001t0002g0157 a0001c0002t0007g0154 a0001c0002t0007g0155 others(9): Show |
12 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.261+692A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891137 | |||||||
chr7:98891145 | C | T | 1 | a0001c0001t0001g0015 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.261+700C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891145 | |||||||
chr7:98891192 | C | CAT | 8 | a0001c0001t0001g0058 a0001c0001t0002g0213 a0001c0001t0002g0214 others(5): Show |
8 | HG01081.hp1 HG01517.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.261+758_261+759dup others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | INFO_REALIGN_3_PRIME | chr7 | 98891192 | ||||||
chr7:98891192 | C | CATAT | 108 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(105): Show |
109 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.261+756_261+759dup others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | INFO_REALIGN_3_PRIME | chr7 | 98891192 | ||||||
chr7:98891192 | C | CATATAT | 10 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0076 others(7): Show |
10 | HG00642.hp2 HG01515.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.261+754_261+759dup others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | INFO_REALIGN_3_PRIME | chr7 | 98891192 | ||||||
chr7:98891204 | T | TA | 51 | a0001c0001t0002g0011 a0001c0001t0002g0147 a0001c0001t0002g0157 others(48): Show |
53 | HG00438.hp2 HG01081.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.261+759_261+760ins others(1): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891204 | |||||||
chr7:98891204 | T | TATA | 10 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0103 others(7): Show |
10 | HG00423.hp2 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.261+759_261+760ins others(3): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891204 | |||||||
chr7:98891205 | T | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(180): Show |
184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.261+760T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891205 | |||||||
chr7:98891206 | T | A | 25 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0103 others(22): Show |
25 | HG00423.hp2 HG01496.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.261+761T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891206 | |||||||
chr7:98891207 | T | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(129): Show |
133 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.261+762T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891207 | |||||||
chr7:98891208 | T | A | 16 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0103 others(13): Show |
16 | HG00423.hp2 HG01496.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.261+763T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891208 | |||||||
chr7:98891209 | T | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(122): Show |
126 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.261+764T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891209 | |||||||
chr7:98891210 | T | A | 13 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0103 others(10): Show |
13 | HG00423.hp2 HG01496.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.261+765T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891210 | |||||||
chr7:98891211 | T | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(120): Show |
124 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.261+766T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891211 | |||||||
chr7:98891212 | T | A | 4 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0120 others(1): Show |
4 | HG02572.hp2 HG02698.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+767T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891212 | |||||||
chr7:98891213 | T | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0111 a0001c0027t0001g0037 |
3 | HG00642.hp2 HG01169.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.261+768T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891213 | |||||||
chr7:98891215 | T | A | 1 | a0001c0001t0001g0031 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.261+770T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891215 | |||||||
chr7:98891238 | G | T | 1 | a0001c0001t0001g0102 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.261+793G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891238 | |||||||
chr7:98891283 | C | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG02109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.261+838C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891283 | |||||||
chr7:98891453 | G | A | 1 | a0001c0013t0002g0215 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.262-971G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891453 | |||||||
chr7:98891462 | A | G | 4 | a0001c0002t0002g0177 a0001c0002t0002g0178 a0001c0002t0010g0179 others(1): Show |
4 | HG02451.hp1 HG03209.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-962A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891462 | |||||||
chr7:98891536 | C | CT | 10 | a0001c0001t0001g0099 a0001c0002t0002g0164 a0001c0002t0002g0165 others(7): Show |
10 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.262-871dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | INFO_REALIGN_3_PRIME | chr7 | 98891536 | ||||||
chr7:98891598 | C | G | 1 | a0001c0006t0002g0152 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.262-826C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891598 | |||||||
chr7:98891630 | G | A | 1 | a0001c0004t0002g0189 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.262-794G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891630 | |||||||
chr7:98891834 | G | A | 1 | a0001c0005t0004g0005 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.262-590G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891834 | |||||||
chr7:98891905 | G | A | 1 | a0001c0038t0001g0034 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.262-519G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891905 | |||||||
chr7:98892050 | T | C | 1 | a0001c0003t0002g0200 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.262-374T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98892050 | |||||||
chr7:98892125 | A | G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0122 |
2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.262-299A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98892125 | |||||||
chr7:98892369 | T | C | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.262-55T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98892369 | |||||||
chr7:98892796 | G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.366+268G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98892796 | |||||||
chr7:98892806 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.366+278C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98892806 | |||||||
chr7:98892890 | G | C | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.366+362G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98892890 | |||||||
chr7:98893045 | G | A | 1 | a0001c0001t0002g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.366+517G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98893045 | |||||||
chr7:98893193 | A | G | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.367-605A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98893193 | |||||||
chr7:98893198 | C | A | 1 | a0001c0002t0002g0188 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.367-600C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98893198 | |||||||
chr7:98893295 | A | C | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.367-503A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98893295 | |||||||
chr7:98893295 | A | G | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.367-503A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98893295 | |||||||
chr7:98893314 | A | G | 43 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(40): Show |
44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.367-484A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98893314 | |||||||
chr7:98893333 | G | A | 9 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(6): Show |
9 | HG00738.hp1 HG01192.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.367-465G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98893333 | |||||||
chr7:98893344 | G | A | 1 | a0001c0021t0001g0129 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.367-454G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98893344 | |||||||
chr7:98893399 | A | T | 1 | a0001c0002t0002g0174 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.367-399A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98893399 | |||||||
chr7:98893428 | A | G | 1 | a0001c0001t0003g0027 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.367-370A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98893428 | |||||||
chr7:98893623 | C | T | 1 | a0001c0002t0002g0255 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.367-175C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98893623 | |||||||
chr7:98893638 | T | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(189): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.367-160T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98893638 | |||||||
chr7:98893929 | T | A | 3 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0026t0003g0023 |
3 | NA18957.hp2 NA18986.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.450+48T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98893929 | |||||||
chr7:98894141 | C | T | 1 | a0001c0025t0001g0118 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.450+260C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98894141 | |||||||
chr7:98894166 | T | C | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.450+285T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98894166 | |||||||
chr7:98894219 | C | A | 1 | a0001c0001t0001g0042 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.450+338C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98894219 | |||||||
chr7:98894404 | A | G | 1 | a0001c0001t0001g0038 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.450+523A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98894404 | |||||||
chr7:98894422 | G | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(199): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.450+541G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98894422 | |||||||
chr7:98894522 | G | T | 1 | a0001c0001t0001g0015 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.450+641G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98894522 | |||||||
chr7:98894567 | A | C | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.450+686A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98894567 | |||||||
chr7:98894623 | G | GT | 137 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(134): Show |
138 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.450+751dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | INFO_REALIGN_3_PRIME | chr7 | 98894623 | ||||||
chr7:98894634 | G | A | 5 | a0001c0001t0005g0159 a0001c0001t0005g0160 a0001c0001t0005g0162 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.450+753G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98894634 | |||||||
chr7:98894715 | C | T | 2 | a0001c0009t0002g0163 a0001c0009t0002g0210 |
2 | HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.450+834C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98894715 | |||||||
chr7:98894779 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.450+898A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98894779 | |||||||
chr7:98894783 | G | GT | 31 | a0001c0001t0001g0258 a0001c0001t0002g0011 a0001c0001t0002g0147 others(28): Show |
31 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.450+927dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | INFO_REALIGN_3_PRIME | chr7 | 98894783 | ||||||
chr7:98894783 | G | GTT | 8 | a0001c0002t0002g0173 a0001c0002t0002g0177 a0001c0002t0002g0178 others(5): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.450+926_450+927dup others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | INFO_REALIGN_3_PRIME | chr7 | 98894783 | ||||||
chr7:98894783 | GT | G | 48 | a0001c0001t0001g0015 a0001c0001t0001g0038 a0001c0001t0001g0057 others(45): Show |
49 | HG00423.hp1 HG00423.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.450+927delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | INFO_REALIGN_3_PRIME | chr7 | 98894783 | ||||||
chr7:98894783 | GTT | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(103): Show |
107 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.450+926_450+927del others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | INFO_REALIGN_3_PRIME | chr7 | 98894783 | ||||||
chr7:98894956 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.451-808G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98894956 | |||||||
chr7:98895087 | G | T | 2 | a0001c0001t0002g0208 a0001c0001t0011g0209 |
2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.451-677G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98895087 | |||||||
chr7:98895164 | C | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.451-600C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98895164 | |||||||
chr7:98895166 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.451-598G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98895166 | |||||||
chr7:98895209 | A | G | 1 | a0001c0001t0003g0098 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.451-555A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98895209 | |||||||
chr7:98895462 | C | T | 2 | a0001c0001t0003g0022 a0001c0001t0003g0025 |
2 | NA18948.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.451-302C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98895462 | |||||||
chr7:98895463 | G | A | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0126 |
3 | HG02572.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.451-301G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98895463 | |||||||
chr7:98895468 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.451-296A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98895468 | |||||||
chr7:98895566 | A | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.451-198A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98895566 | |||||||
chr7:98895659 | C | T | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.451-105C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98895659 | |||||||
chr7:98895913 | G | T | 1 | a0001c0002t0002g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.507+93G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98895913 | |||||||
chr7:98895954 | A | G | 10 | a0001c0003t0002g0003 a0001c0003t0002g0198 a0001c0003t0002g0199 others(7): Show |
11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.507+134A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98895954 | |||||||
chr7:98896224 | A | T | 7 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(4): Show |
7 | HG01169.hp1 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.507+404A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98896224 | |||||||
chr7:98896427 | C | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.507+607C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98896427 | |||||||
chr7:98896435 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.507+615C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98896435 | |||||||
chr7:98896437 | G | A | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.507+617G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98896437 | |||||||
chr7:98896544 | G | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.507+724G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98896544 | |||||||
chr7:98896664 | G | A | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.507+844G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98896664 | |||||||
chr7:98896792 | A | C | 9 | a0001c0003t0002g0003 a0001c0003t0002g0199 a0001c0003t0002g0200 others(6): Show |
10 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.508-949A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98896792 | |||||||
chr7:98896910 | G | C | 1 | a0001c0005t0004g0005 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.508-831G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98896910 | |||||||
chr7:98896942 | TC | T | 43 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(40): Show |
44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.508-797delC | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | INFO_REALIGN_3_PRIME | chr7 | 98896942 | ||||||
chr7:98896971 | A | C | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0126 |
3 | HG02572.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.508-770A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98896971 | |||||||
chr7:98897190 | G | A | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-551G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98897190 | |||||||
chr7:98897327 | G | A | 1 | a0001c0002t0002g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.508-414G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98897327 | |||||||
chr7:98897480 | A | G | 3 | a0001c0004t0002g0183 a0001c0004t0002g0185 a0008c0042t0002g0184 |
3 | HG02622.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.508-261A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98897480 | |||||||
chr7:98897525 | A | G | 2 | a0001c0001t0001g0070 a0001c0001t0003g0028 |
2 | HG00438.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.508-216A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98897525 | |||||||
chr7:98897676 | G | GTT | 123 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(120): Show |
124 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.508-62_508-61dupTT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | INFO_REALIGN_3_PRIME | chr7 | 98897676 | ||||||
chr7:98897676 | G | GTTT | 12 | a0001c0001t0001g0072 a0001c0001t0001g0075 a0001c0001t0001g0077 others(9): Show |
12 | HG00423.hp2 HG01975.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.508-63_508-61dupTT others(1): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | INFO_REALIGN_3_PRIME | chr7 | 98897676 | ||||||
chr7:98897676 | G | T | 1 | a0001c0001t0003g0027 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.508-65G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98897676 | |||||||
chr7:98897681 | G | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(177): Show |
182 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.508-60G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98897681 | |||||||
chr7:98897933 | A | AT | 11 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(8): Show |
11 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.633+76dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 8/72 | INFO_REALIGN_3_PRIME | chr7 | 98897933 | ||||||
chr7:98898331 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(133): Show |
137 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.633+465G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 8/72 | chr7 | 98898331 | |||||||
chr7:98898439 | C | A | 1 | a0001c0001t0001g0035 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.633+573C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 8/72 | chr7 | 98898439 | |||||||
chr7:98898469 | C | A | 1 | a0001c0017t0001g0116 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.633+603C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 8/72 | chr7 | 98898469 | |||||||
chr7:98898707 | G | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(126): Show |
130 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.634-715G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 8/72 | chr7 | 98898707 | |||||||
chr7:98899015 | G | T | 1 | a0001c0002t0010g0179 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.634-407G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 8/72 | chr7 | 98899015 | |||||||
chr7:98899583 | C | G | 25 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0164 others(22): Show |
26 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.711+84C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 9/72 | chr7 | 98899583 | |||||||
chr7:98899884 | T | C | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.800+117T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 10/72 | chr7 | 98899884 | |||||||
chr7:98899970 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.800+203C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 10/72 | chr7 | 98899970 | |||||||
chr7:98900002 | G | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0046 |
3 | HG01346.hp2 HG02145.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.800+235G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 10/72 | chr7 | 98900002 | |||||||
chr7:98900123 | C | T | 4 | a0001c0001t0002g0157 a0001c0002t0007g0154 a0001c0002t0007g0155 others(1): Show |
4 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.800+356C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 10/72 | chr7 | 98900123 | |||||||
chr7:98900268 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.801-356A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 10/72 | chr7 | 98900268 | |||||||
chr7:98900290 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.801-334T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 10/72 | chr7 | 98900290 | |||||||
chr7:98900531 | A | G | 4 | a0001c0001t0005g0159 a0001c0001t0005g0160 a0001c0001t0005g0162 others(1): Show |
4 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.801-93A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 10/72 | chr7 | 98900531 | |||||||
chr7:98900774 | A | G | 1 | a0001c0001t0005g0162 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.897+54A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98900774 | |||||||
chr7:98900846 | C | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0075 |
2 | NA18957.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.897+126C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98900846 | |||||||
chr7:98900883 | T | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(125): Show |
129 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.897+163T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98900883 | |||||||
chr7:98901085 | G | T | 9 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(6): Show |
9 | HG00738.hp1 HG01192.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.897+365G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98901085 | |||||||
chr7:98901337 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.897+617G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98901337 | |||||||
chr7:98901483 | T | A | 3 | a0001c0001t0002g0208 a0001c0001t0011g0209 a0001c0028t0002g0207 |
3 | HG02486.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.897+763T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98901483 | |||||||
chr7:98901613 | A | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0086 |
2 | HG01099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.897+893A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98901613 | |||||||
chr7:98901927 | C | T | 5 | a0001c0004t0002g0002 a0001c0004t0002g0168 a0001c0004t0002g0169 others(2): Show |
6 | HG02257.hp1 HG02647.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.897+1207C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98901927 | |||||||
chr7:98901959 | G | A | 11 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(8): Show |
11 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.897+1239G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98901959 | |||||||
chr7:98901965 | C | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(180): Show |
185 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.897+1245C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98901965 | |||||||
chr7:98902054 | C | G | 1 | a0001c0001t0001g0074 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.898-1325C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98902054 | |||||||
chr7:98902128 | A | C | 1 | a0001c0002t0012g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.898-1251A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98902128 | |||||||
chr7:98902158 | T | A | 10 | a0001c0003t0002g0003 a0001c0003t0002g0198 a0001c0003t0002g0199 others(7): Show |
11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.898-1221T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98902158 | |||||||
chr7:98902227 | T | C | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.898-1152T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98902227 | |||||||
chr7:98902454 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0122 |
2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.898-925G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98902454 | |||||||
chr7:98902546 | T | G | 61 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(58): Show |
61 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.898-833T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98902546 | |||||||
chr7:98902592 | A | ATGGAAC | 61 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(58): Show |
61 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.898-786_898-781dup others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | INFO_REALIGN_3_PRIME | chr7 | 98902592 | ||||||
chr7:98902630 | T | C | 43 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(40): Show |
44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.898-749T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98902630 | |||||||
chr7:98902699 | G | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(180): Show |
185 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.898-680G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98902699 | |||||||
chr7:98902882 | G | A | 1 | a0008c0042t0002g0184 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.898-497G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98902882 | |||||||
chr7:98902906 | T | C | 43 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(40): Show |
44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.898-473T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98902906 | |||||||
chr7:98902908 | T | TA | 21 | a0001c0001t0001g0076 a0001c0001t0001g0259 a0001c0001t0002g0196 others(18): Show |
21 | HG00140.hp2 HG01099.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.898-453dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | INFO_REALIGN_3_PRIME | chr7 | 98902908 | ||||||
chr7:98902908 | T | TAA | 118 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(115): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.898-454_898-453dup others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | INFO_REALIGN_3_PRIME | chr7 | 98902908 | ||||||
chr7:98902908 | T | TAAA | 5 | a0001c0001t0001g0079 a0001c0001t0001g0089 a0001c0001t0001g0091 others(2): Show |
5 | HG00544.hp1 HG00621.hp1 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.898-455_898-453dup others(3): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | INFO_REALIGN_3_PRIME | chr7 | 98902908 | ||||||
chr7:98902908 | TA | T | 11 | a0001c0001t0002g0147 a0001c0001t0002g0246 a0001c0001t0005g0159 others(8): Show |
11 | HG01884.hp2 HG02055.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.898-453delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | INFO_REALIGN_3_PRIME | chr7 | 98902908 | ||||||
chr7:98903001 | G | A | 2 | a0001c0001t0002g0196 a0001c0001t0002g0197 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.898-378G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98903001 | |||||||
chr7:98903033 | G | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(186): Show |
191 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.898-346G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98903033 | |||||||
chr7:98903033 | G | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0191 |
2 | NA18940.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.898-346G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98903033 | |||||||
chr7:98903049 | C | CAA | 191 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(188): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.898-330_898-329ins others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98903049 | |||||||
chr7:98903053 | T | C | 1 | a0001c0002t0012g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.898-326T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98903053 | |||||||
chr7:98903075 | G | T | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.898-304G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98903075 | |||||||
chr7:98903219 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(205): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.898-160A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98903219 | |||||||
chr7:98903333 | C | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(132): Show |
136 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.898-46C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98903333 | |||||||
chr7:98903761 | G | A | 1 | a0001c0001t0001g0032 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1036+244G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98903761 | |||||||
chr7:98903817 | C | T | 4 | a0001c0001t0002g0157 a0001c0002t0007g0154 a0001c0002t0007g0155 others(1): Show |
4 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1036+300C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98903817 | |||||||
chr7:98903846 | G | A | 3 | a0001c0001t0002g0195 a0001c0001t0002g0196 a0001c0001t0002g0197 |
3 | HG02258.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1036+329G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98903846 | |||||||
chr7:98903850 | G | A | 1 | a0001c0001t0002g0195 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1036+333G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98903850 | |||||||
chr7:98903875 | A | T | 6 | a0001c0001t0002g0147 a0001c0006t0002g0149 a0001c0006t0002g0150 others(3): Show |
6 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+358A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98903875 | |||||||
chr7:98903881 | C | T | 1 | a0001c0038t0001g0034 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1036+364C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98903881 | |||||||
chr7:98903912 | C | T | 4 | a0001c0001t0002g0157 a0001c0002t0007g0154 a0001c0002t0007g0155 others(1): Show |
4 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1036+395C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98903912 | |||||||
chr7:98903933 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1036+416C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98903933 | |||||||
chr7:98903966 | C | A | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1036+449C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98903966 | |||||||
chr7:98904087 | G | A | 1 | a0002c0008t0008g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1036+570G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98904087 | |||||||
chr7:98904145 | G | C | 1 | a0001c0001t0001g0043 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1036+628G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98904145 | |||||||
chr7:98904157 | G | A | 2 | a0001c0002t0002g0187 a0001c0044t0002g0186 |
2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1036+640G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98904157 | |||||||
chr7:98904202 | A | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(188): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1036+685A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98904202 | |||||||
chr7:98904265 | C | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1036+748C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98904265 | |||||||
chr7:98904300 | G | A | 2 | a0001c0001t0002g0208 a0001c0001t0011g0209 |
2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1036+783G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98904300 | |||||||
chr7:98904408 | A | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(132): Show |
136 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1036+891A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98904408 | |||||||
chr7:98904483 | C | CA | 45 | a0001c0001t0001g0032 a0001c0001t0001g0045 a0001c0001t0001g0047 others(42): Show |
45 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1036+992dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | INFO_REALIGN_3_PRIME | chr7 | 98904483 | ||||||
chr7:98904483 | C | CAA | 5 | a0001c0001t0001g0038 a0001c0001t0001g0145 a0001c0002t0002g0016 others(2): Show |
5 | HG01081.hp1 HG01884.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1036+991_1036+992d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | INFO_REALIGN_3_PRIME | chr7 | 98904483 | ||||||
chr7:98904483 | CA | C | 21 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0072 others(18): Show |
21 | HG01515.hp1 HG02148.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1036+992delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | INFO_REALIGN_3_PRIME | chr7 | 98904483 | ||||||
chr7:98904483 | CAA | C | 7 | a0001c0003t0002g0003 a0001c0003t0002g0198 a0001c0003t0002g0200 others(4): Show |
8 | HG01081.hp2 HG01169.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1036+991_1036+992d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | INFO_REALIGN_3_PRIME | chr7 | 98904483 | ||||||
chr7:98904483 | CAAAAAAA others(5): Show |
C | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1036+981_1036+992d others(14): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | INFO_REALIGN_3_PRIME | chr7 | 98904483 | ||||||
chr7:98904483 | CAAAAAAA others(6): Show |
C | 10 | a0001c0001t0002g0157 a0001c0002t0007g0154 a0001c0002t0007g0155 others(7): Show |
10 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1036+980_1036+992d others(15): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | INFO_REALIGN_3_PRIME | chr7 | 98904483 | ||||||
chr7:98904566 | C | A | 4 | a0001c0004t0002g0002 a0001c0004t0002g0168 a0001c0004t0002g0169 others(1): Show |
5 | HG02257.hp1 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1036+1049C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98904566 | |||||||
chr7:98904593 | A | G | 5 | a0001c0006t0002g0149 a0001c0006t0002g0150 a0001c0006t0002g0151 others(2): Show |
5 | HG02559.hp1 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1036+1076A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98904593 | |||||||
chr7:98904668 | C | T | 1 | a0001c0009t0002g0163 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1036+1151C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98904668 | |||||||
chr7:98904808 | A | C | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1036+1291A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98904808 | |||||||
chr7:98904878 | A | G | 1 | a0007c0041t0001g0065 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1037-1299A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98904878 | |||||||
chr7:98904921 | G | A | 6 | a0001c0001t0001g0069 a0001c0001t0001g0080 a0001c0001t0001g0086 others(3): Show |
6 | HG00140.hp1 HG01099.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.1037-1256G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98904921 | |||||||
chr7:98905140 | G | A | 1 | a0001c0022t0001g0124 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1037-1037G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98905140 | |||||||
chr7:98905165 | G | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG02109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1037-1012G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98905165 | |||||||
chr7:98905267 | G | A | 4 | a0001c0006t0002g0149 a0001c0006t0002g0150 a0001c0006t0002g0152 others(1): Show |
4 | HG02559.hp1 HG02647.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1037-910G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98905267 | |||||||
chr7:98905552 | A | G | 1 | a0001c0002t0002g0178 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1037-625A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98905552 | |||||||
chr7:98905585 | C | A | 2 | a0001c0001t0002g0208 a0001c0001t0011g0209 |
2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1037-592C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98905585 | |||||||
chr7:98905652 | T | G | 6 | a0001c0001t0002g0147 a0001c0006t0002g0149 a0001c0006t0002g0150 others(3): Show |
6 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-525T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98905652 | |||||||
chr7:98905697 | T | G | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1037-480T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98905697 | |||||||
chr7:98905724 | G | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1037-453G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98905724 | |||||||
chr7:98905814 | C | A | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1037-363C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98905814 | |||||||
chr7:98906043 | C | G | 1 | a0001c0001t0001g0241 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1037-134C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98906043 | |||||||
chr7:98906084 | TG | T | 191 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(188): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1037-91delG | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | INFO_REALIGN_3_PRIME | chr7 | 98906084 | ||||||
chr7:98906099 | T | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1037-78T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98906099 | |||||||
chr7:98906157 | A | G | 1 | a0001c0001t0002g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1037-20A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98906157 | |||||||
chr7:98906396 | TTTTTGTT others(3): Show |
T | 4 | a0001c0001t0001g0042 a0001c0001t0005g0159 a0001c0024t0001g0048 others(1): Show |
4 | HG00741.hp1 HG01192.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1115+145_1115+154d others(12): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | INFO_REALIGN_3_PRIME | chr7 | 98906396 | ||||||
chr7:98906402 | T | TTTTA | 40 | a0001c0001t0001g0240 a0001c0001t0001g0257 a0001c0001t0001g0258 others(37): Show |
40 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.1115+191_1115+194d others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | INFO_REALIGN_3_PRIME | chr7 | 98906402 | ||||||
chr7:98906402 | T | TTTTATTT others(1): Show |
8 | a0001c0001t0001g0241 a0001c0001t0002g0010 a0001c0001t0002g0220 others(5): Show |
8 | HG00544.hp2 NA18969.hp1 NA19009.hp1 others(5): Show |
intron_variant | MODIFIER | c.1115+187_1115+194d others(10): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | INFO_REALIGN_3_PRIME | chr7 | 98906402 | ||||||
chr7:98906402 | T | TTTTATTT others(5): Show |
1 | a0002c0008t0008g0193 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1115+183_1115+194d others(14): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | INFO_REALIGN_3_PRIME | chr7 | 98906402 | ||||||
chr7:98906402 | TTTTA | T | 10 | a0001c0001t0002g0147 a0001c0001t0005g0160 a0001c0001t0005g0162 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1115+191_1115+194d others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | INFO_REALIGN_3_PRIME | chr7 | 98906402 | ||||||
chr7:98906402 | TTTTATTT others(1): Show |
T | 3 | a0001c0001t0001g0050 a0001c0002t0012g0194 a0001c0025t0001g0118 |
3 | HG00408.hp2 NA18944.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1115+187_1115+194d others(10): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | INFO_REALIGN_3_PRIME | chr7 | 98906402 | ||||||
chr7:98906402 | TTTTATTT others(5): Show |
T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(131): Show |
136 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1115+183_1115+194d others(14): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | INFO_REALIGN_3_PRIME | chr7 | 98906402 | ||||||
chr7:98906456 | C | T | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0056 |
3 | HG01358.hp1 HG01943.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1115+201C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98906456 | |||||||
chr7:98906476 | G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1115+221G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98906476 | |||||||
chr7:98906589 | T | C | 3 | a0001c0001t0002g0212 a0001c0001t0002g0227 a0001c0001t0002g0243 |
3 | HG01099.hp2 HG01496.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.1115+334T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98906589 | |||||||
chr7:98906984 | A | C | 2 | a0001c0001t0002g0196 a0001c0001t0002g0197 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1115+729A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98906984 | |||||||
chr7:98906999 | A | C | 1 | a0001c0001t0001g0137 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1115+744A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98906999 | |||||||
chr7:98907046 | A | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(132): Show |
136 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1115+791A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98907046 | |||||||
chr7:98907113 | C | T | 11 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(8): Show |
11 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1115+858C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98907113 | |||||||
chr7:98907323 | C | CA | 5 | a0001c0001t0002g0011 a0001c0002t0002g0177 a0001c0002t0002g0178 others(2): Show |
5 | HG02027.hp1 HG02451.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1115+1080dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | INFO_REALIGN_3_PRIME | chr7 | 98907323 | ||||||
chr7:98907441 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0089 |
2 | HG00544.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1115+1186C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98907441 | |||||||
chr7:98907573 | C | T | 3 | a0001c0001t0002g0195 a0001c0001t0002g0196 a0001c0001t0002g0197 |
3 | HG02258.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1116-1155C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98907573 | |||||||
chr7:98907597 | G | A | 1 | a0001c0002t0002g0188 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1116-1131G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98907597 | |||||||
chr7:98907703 | T | G | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1116-1025T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98907703 | |||||||
chr7:98907779 | C | T | 45 | a0001c0001t0001g0125 a0001c0001t0002g0147 a0001c0001t0005g0159 others(42): Show |
46 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(43): Show |
intron_variant | MODIFIER | c.1116-949C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98907779 | |||||||
chr7:98907796 | ATCCCTGA others(34): Show |
A | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1116-899_1116-859d others(43): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | INFO_REALIGN_3_PRIME | chr7 | 98907796 | ||||||
chr7:98907903 | G | A | 1 | a0001c0001t0001g0013 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1116-825G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98907903 | |||||||
chr7:98908016 | T | C | 14 | a0001c0001t0001g0128 a0001c0001t0001g0130 a0001c0001t0001g0131 others(11): Show |
14 | HG00738.hp1 HG01192.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.1116-712T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98908016 | |||||||
chr7:98908044 | G | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0046 |
3 | HG01346.hp2 HG02145.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1116-684G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98908044 | |||||||
chr7:98908055 | G | A | 1 | a0001c0007t0001g0081 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1116-673G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98908055 | |||||||
chr7:98908163 | G | A | 2 | a0001c0001t0001g0056 a0001c0011t0013g0190 |
2 | HG01943.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1116-565G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98908163 | |||||||
chr7:98908295 | A | T | 1 | a0001c0002t0002g0188 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1116-433A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98908295 | |||||||
chr7:98909019 | A | AT | 17 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0047 others(14): Show |
17 | HG01081.hp1 HG01993.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1350+79dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 14/72 | INFO_REALIGN_3_PRIME | chr7 | 98909019 | ||||||
chr7:98909019 | AT | A | 12 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0077 others(9): Show |
13 | HG01515.hp2 HG01975.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1350+79delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 14/72 | INFO_REALIGN_3_PRIME | chr7 | 98909019 | ||||||
chr7:98909104 | A | G | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1350+142A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 14/72 | chr7 | 98909104 | |||||||
chr7:98909212 | CA | C | 67 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(64): Show |
67 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.1350+251delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 14/72 | chr7 | 98909212 | |||||||
chr7:98909214 | G | T | 67 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(64): Show |
67 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.1350+252G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 14/72 | chr7 | 98909214 | |||||||
chr7:98909319 | G | A | 1 | a0001c0001t0002g0211 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1350+357G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 14/72 | chr7 | 98909319 | |||||||
chr7:98909440 | G | GT | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1350+484dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 14/72 | INFO_REALIGN_3_PRIME | chr7 | 98909440 | ||||||
chr7:98909661 | C | T | 1 | a0001c0001t0003g0027 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1351-395C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 14/72 | chr7 | 98909661 | |||||||
chr7:98909792 | C | CCTTT | 191 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(188): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1351-263_1351-260d others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 14/72 | INFO_REALIGN_3_PRIME | chr7 | 98909792 | ||||||
chr7:98910051 | G | A | 1 | a0001c0017t0001g0116 | 1 | NA18747.hp2 | splice_region_variant&intron_variant | LOW | c.1351-5G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 14/72 | chr7 | 98910051 | |||||||
chr7:98910824 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1812+217C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 16/72 | chr7 | 98910824 | |||||||
chr7:98910900 | T | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1813-177T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 16/72 | chr7 | 98910900 | |||||||
chr7:98910917 | T | G | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1813-160T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 16/72 | chr7 | 98910917 | |||||||
chr7:98910951 | G | A | 43 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(40): Show |
44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.1813-126G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 16/72 | chr7 | 98910951 | |||||||
chr7:98911397 | T | G | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2007+126T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 17/72 | chr7 | 98911397 | |||||||
chr7:98911751 | G | A | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2008-271G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 17/72 | chr7 | 98911751 | |||||||
chr7:98911774 | C | CA | 33 | a0001c0001t0001g0114 a0001c0001t0006g0254 a0001c0002t0002g0016 others(30): Show |
33 | HG00642.hp1 HG01081.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.2008-233dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 17/72 | INFO_REALIGN_3_PRIME | chr7 | 98911774 | ||||||
chr7:98911774 | C | CAA | 6 | a0001c0002t0010g0179 a0001c0004t0002g0002 a0001c0004t0002g0168 others(3): Show |
7 | HG02257.hp1 HG02647.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2008-234_2008-233d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 17/72 | INFO_REALIGN_3_PRIME | chr7 | 98911774 | ||||||
chr7:98911865 | A | G | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2008-157A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 17/72 | chr7 | 98911865 | |||||||
chr7:98911927 | G | C | 15 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0164 others(12): Show |
15 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.2008-95G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 17/72 | chr7 | 98911927 | |||||||
chr7:98912318 | A | G | 1 | a0001c0004t0002g0170 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2199+105A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98912318 | |||||||
chr7:98912610 | A | G | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2199+397A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98912610 | |||||||
chr7:98912931 | G | A | 2 | a0001c0002t0002g0180 a0001c0002t0002g0255 |
2 | HG01257.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.2199+718G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98912931 | |||||||
chr7:98913000 | G | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(127): Show |
131 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.2199+787G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98913000 | |||||||
chr7:98913139 | CGT | C | 31 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0164 others(28): Show |
32 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.2199+930_2199+931d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | INFO_REALIGN_3_PRIME | chr7 | 98913139 | ||||||
chr7:98913145 | C | A | 31 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0164 others(28): Show |
32 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.2199+932C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98913145 | |||||||
chr7:98913175 | C | G | 1 | a0002c0008t0008g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2199+962C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98913175 | |||||||
chr7:98913185 | G | C | 5 | a0001c0001t0005g0159 a0001c0001t0005g0160 a0001c0001t0005g0162 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2199+972G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98913185 | |||||||
chr7:98913309 | G | GT | 12 | a0001c0001t0001g0094 a0001c0001t0003g0025 a0001c0003t0002g0003 others(9): Show |
13 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.2199+1106dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | INFO_REALIGN_3_PRIME | chr7 | 98913309 | ||||||
chr7:98913530 | C | T | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2199+1317C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98913530 | |||||||
chr7:98913547 | C | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(124): Show |
128 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.2199+1334C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98913547 | |||||||
chr7:98913568 | G | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(124): Show |
128 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.2199+1355G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98913568 | |||||||
chr7:98913577 | T | C | 5 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0171 others(2): Show |
5 | HG01243.hp1 HG01884.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2199+1364T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98913577 | |||||||
chr7:98913865 | T | C | 2 | a0001c0001t0001g0092 a0001c0001t0001g0104 |
2 | HG01496.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.2199+1652T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98913865 | |||||||
chr7:98913971 | G | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(179): Show |
184 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.2200-1752G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98913971 | |||||||
chr7:98914173 | T | C | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2200-1550T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98914173 | |||||||
chr7:98914242 | A | T | 61 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(58): Show |
61 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.2200-1481A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98914242 | |||||||
chr7:98914302 | AAG | A | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2200-1414_2200-141 others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | INFO_REALIGN_3_PRIME | chr7 | 98914302 | ||||||
chr7:98914375 | T | G | 1 | a0001c0001t0002g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2200-1348T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98914375 | |||||||
chr7:98914462 | A | G | 3 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0003g0028 |
3 | HG00438.hp1 HG00544.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.2200-1261A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98914462 | |||||||
chr7:98914519 | A | G | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2200-1204A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98914519 | |||||||
chr7:98914559 | T | G | 1 | a0001c0019t0001g0112 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2200-1164T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98914559 | |||||||
chr7:98914718 | C | CA | 109 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(106): Show |
111 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.2200-976dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | INFO_REALIGN_3_PRIME | chr7 | 98914718 | ||||||
chr7:98914718 | C | CAA | 29 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0042 others(26): Show |
29 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.2200-977_2200-976d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | INFO_REALIGN_3_PRIME | chr7 | 98914718 | ||||||
chr7:98914718 | CA | C | 8 | a0001c0001t0002g0157 a0001c0001t0002g0195 a0001c0001t0002g0196 others(5): Show |
8 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.2200-976delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | INFO_REALIGN_3_PRIME | chr7 | 98914718 | ||||||
chr7:98914718 | CAAAA | C | 27 | a0001c0001t0002g0147 a0001c0002t0002g0016 a0001c0002t0002g0017 others(24): Show |
28 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.2200-979_2200-976d others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | INFO_REALIGN_3_PRIME | chr7 | 98914718 | ||||||
chr7:98914718 | CAAAAA | C | 11 | a0001c0001t0005g0159 a0001c0001t0005g0160 a0001c0001t0005g0162 others(8): Show |
11 | HG02055.hp1 HG02258.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2200-980_2200-976d others(7): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | INFO_REALIGN_3_PRIME | chr7 | 98914718 | ||||||
chr7:98914718 | CAAAAAAA others(5): Show |
C | 1 | a0001c0022t0001g0124 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2200-987_2200-976d others(14): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | INFO_REALIGN_3_PRIME | chr7 | 98914718 | ||||||
chr7:98914718 | CAAAAAAA others(10): Show |
C | 1 | a0001c0038t0001g0034 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2200-992_2200-976d others(19): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | INFO_REALIGN_3_PRIME | chr7 | 98914718 | ||||||
chr7:98914744 | A | C | 1 | a0001c0002t0010g0179 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2200-979A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98914744 | |||||||
chr7:98914756 | A | G | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2200-967A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98914756 | |||||||
chr7:98915111 | G | A | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2200-612G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98915111 | |||||||
chr7:98915623 | G | T | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2200-100G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98915623 | |||||||
chr7:98915660 | G | A | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2200-63G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98915660 | |||||||
chr7:98915677 | C | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(130): Show |
134 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.2200-46C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98915677 | |||||||
chr7:98915712 | C | G | 7 | a0001c0002t0002g0187 a0001c0004t0002g0002 a0001c0004t0002g0168 others(4): Show |
8 | HG01081.hp1 HG02257.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2200-11C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98915712 | |||||||
chr7:98916137 | T | C | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2365+249T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 19/72 | chr7 | 98916137 | |||||||
chr7:98916164 | A | G | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG02015.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.2365+276A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 19/72 | chr7 | 98916164 | |||||||
chr7:98916388 | G | A | 1 | a0001c0001t0002g0227 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2365+500G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 19/72 | chr7 | 98916388 | |||||||
chr7:98916419 | T | C | 3 | a0001c0001t0002g0208 a0001c0001t0011g0209 a0001c0028t0002g0207 |
3 | HG02486.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2365+531T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 19/72 | chr7 | 98916419 | |||||||
chr7:98916635 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2365+747C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 19/72 | chr7 | 98916635 | |||||||
chr7:98916662 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2366-761C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 19/72 | chr7 | 98916662 | |||||||
chr7:98916737 | G | A | 1 | a0001c0002t0002g0188 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2366-686G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 19/72 | chr7 | 98916737 | |||||||
chr7:98916811 | G | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0111 |
3 | HG00280.hp2 HG00642.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.2366-612G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 19/72 | chr7 | 98916811 | |||||||
chr7:98916831 | C | T | 6 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0171 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2366-592C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 19/72 | chr7 | 98916831 | |||||||
chr7:98916872 | C | T | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2366-551C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 19/72 | chr7 | 98916872 | |||||||
chr7:98917123 | A | G | 1 | a0001c0028t0002g0207 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2366-300A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 19/72 | chr7 | 98917123 | |||||||
chr7:98917410 | C | T | 14 | a0001c0001t0001g0128 a0001c0001t0001g0130 a0001c0001t0001g0131 others(11): Show |
14 | HG00738.hp1 HG01192.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.2366-13C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 19/72 | chr7 | 98917410 | |||||||
chr7:98917846 | G | T | 7 | a0001c0002t0002g0177 a0001c0002t0002g0178 a0001c0002t0002g0180 others(4): Show |
7 | HG01257.hp2 HG01891.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2622+167G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98917846 | |||||||
chr7:98917877 | T | G | 12 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(9): Show |
12 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.2622+198T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98917877 | |||||||
chr7:98918120 | C | CA | 44 | a0001c0001t0001g0078 a0001c0001t0001g0082 a0001c0001t0002g0147 others(41): Show |
45 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(42): Show |
intron_variant | MODIFIER | c.2622+455dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | INFO_REALIGN_3_PRIME | chr7 | 98918120 | ||||||
chr7:98918214 | C | T | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2622+535C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98918214 | |||||||
chr7:98918227 | C | CT | 29 | a0001c0001t0002g0147 a0001c0001t0002g0211 a0001c0001t0002g0212 others(26): Show |
29 | HG00438.hp1 HG00438.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.2622+569dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | INFO_REALIGN_3_PRIME | chr7 | 98918227 | ||||||
chr7:98918227 | C | CTT | 9 | a0001c0001t0001g0241 a0001c0001t0005g0160 a0001c0001t0005g0162 others(6): Show |
9 | HG02258.hp1 HG02630.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2622+568_2622+569d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | INFO_REALIGN_3_PRIME | chr7 | 98918227 | ||||||
chr7:98918227 | CT | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(127): Show |
131 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.2622+569delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | INFO_REALIGN_3_PRIME | chr7 | 98918227 | ||||||
chr7:98918292 | G | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(123): Show |
127 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.2622+613G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98918292 | |||||||
chr7:98918317 | G | A | 1 | a0007c0041t0001g0065 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2622+638G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98918317 | |||||||
chr7:98918375 | C | T | 1 | a0001c0006t0002g0151 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2622+696C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98918375 | |||||||
chr7:98918451 | A | G | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2622+772A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98918451 | |||||||
chr7:98918509 | C | T | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2622+830C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98918509 | |||||||
chr7:98918624 | A | G | 1 | a0001c0001t0001g0191 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2622+945A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98918624 | |||||||
chr7:98918660 | C | G | 2 | a0001c0001t0001g0074 a0001c0045t0001g0073 |
2 | HG03710.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.2622+981C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98918660 | |||||||
chr7:98918710 | A | G | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2622+1031A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98918710 | |||||||
chr7:98918747 | A | G | 4 | a0001c0001t0002g0157 a0001c0002t0007g0154 a0001c0002t0007g0155 others(1): Show |
4 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.2622+1068A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98918747 | |||||||
chr7:98918905 | A | C | 1 | a0001c0002t0002g0188 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2622+1226A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98918905 | |||||||
chr7:98918984 | C | CA | 6 | a0001c0001t0001g0102 a0001c0001t0001g0106 a0001c0001t0001g0122 others(3): Show |
6 | HG02027.hp1 HG02630.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.2622+1321dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | INFO_REALIGN_3_PRIME | chr7 | 98918984 | ||||||
chr7:98918984 | CA | C | 7 | a0001c0001t0001g0054 a0001c0001t0002g0147 a0001c0001t0002g0208 others(4): Show |
7 | HG01884.hp2 HG02300.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2622+1321delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | INFO_REALIGN_3_PRIME | chr7 | 98918984 | ||||||
chr7:98918996 | A | G | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2622+1317A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98918996 | |||||||
chr7:98919019 | T | C | 5 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 others(2): Show |
5 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.2622+1340T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98919019 | |||||||
chr7:98919178 | G | A | 1 | a0001c0004t0002g0176 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2622+1499G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98919178 | |||||||
chr7:98919494 | C | T | 1 | a0001c0010t0001g0068 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2622+1815C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98919494 | |||||||
chr7:98919517 | C | T | 2 | a0001c0001t0002g0196 a0001c0001t0002g0197 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2622+1838C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98919517 | |||||||
chr7:98919529 | G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2622+1850G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98919529 | |||||||
chr7:98919578 | A | G | 43 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(40): Show |
44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.2622+1899A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98919578 | |||||||
chr7:98920066 | G | A | 6 | a0001c0002t0002g0177 a0001c0002t0002g0178 a0001c0002t0002g0180 others(3): Show |
6 | HG01257.hp2 HG01891.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2623-1687G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98920066 | |||||||
chr7:98920425 | G | T | 1 | a0001c0001t0002g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2623-1328G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98920425 | |||||||
chr7:98920607 | C | T | 4 | a0001c0001t0005g0159 a0001c0001t0005g0160 a0001c0001t0005g0162 others(1): Show |
4 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.2623-1146C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98920607 | |||||||
chr7:98920760 | A | T | 1 | a0001c0038t0001g0034 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2623-993A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98920760 | |||||||
chr7:98920901 | G | A | 44 | a0001c0001t0001g0076 a0001c0001t0002g0147 a0001c0001t0005g0159 others(41): Show |
45 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(42): Show |
intron_variant | MODIFIER | c.2623-852G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98920901 | |||||||
chr7:98921032 | A | G | 1 | a0001c0018t0002g0245 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2623-721A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98921032 | |||||||
chr7:98921065 | G | A | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2623-688G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98921065 | |||||||
chr7:98921086 | C | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG02109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2623-667C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98921086 | |||||||
chr7:98921090 | G | A | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2623-663G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98921090 | |||||||
chr7:98921144 | C | T | 4 | a0001c0004t0002g0002 a0001c0004t0002g0168 a0001c0004t0002g0169 others(1): Show |
5 | HG02257.hp1 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2623-609C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98921144 | |||||||
chr7:98921328 | G | A | 5 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 others(2): Show |
5 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.2623-425G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98921328 | |||||||
chr7:98921396 | A | G | 7 | a0001c0002t0002g0177 a0001c0002t0002g0178 a0001c0002t0002g0180 others(4): Show |
7 | HG01257.hp2 HG01891.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2623-357A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98921396 | |||||||
chr7:98921526 | C | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0062 |
2 | NA19054.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.2623-227C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98921526 | |||||||
chr7:98921607 | G | T | 16 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(13): Show |
16 | HG00558.hp1 HG02015.hp2 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.2623-146G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98921607 | |||||||
chr7:98922354 | T | C | 1 | a0001c0009t0002g0210 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2823+401T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98922354 | |||||||
chr7:98922436 | C | T | 1 | a0001c0002t0007g0156 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2823+483C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98922436 | |||||||
chr7:98922437 | G | A | 3 | a0001c0001t0002g0195 a0001c0001t0002g0196 a0001c0001t0002g0197 |
3 | HG02258.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2823+484G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98922437 | |||||||
chr7:98922460 | T | C | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2823+507T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98922460 | |||||||
chr7:98922508 | G | C | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2823+555G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98922508 | |||||||
chr7:98922573 | T | C | 2 | a0001c0002t0002g0180 a0001c0002t0002g0255 |
2 | HG01257.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.2823+620T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98922573 | |||||||
chr7:98922660 | G | T | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2823+707G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98922660 | |||||||
chr7:98922706 | C | T | 1 | a0001c0022t0001g0124 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2823+753C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98922706 | |||||||
chr7:98922752 | T | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(1): Show |
4 | HG00621.hp2 HG01993.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.2823+799T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98922752 | |||||||
chr7:98922752 | T | G | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | NA18948.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.2823+799T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98922752 | |||||||
chr7:98922880 | T | C | 1 | a0001c0038t0001g0034 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2823+927T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98922880 | |||||||
chr7:98922888 | G | A | 1 | a0001c0002t0002g0187 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2823+935G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98922888 | |||||||
chr7:98922959 | C | T | 1 | a0001c0025t0001g0118 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2823+1006C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98922959 | |||||||
chr7:98922983 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2823+1030C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98922983 | |||||||
chr7:98923119 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2823+1166C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98923119 | |||||||
chr7:98923128 | A | G | 1 | a0001c0001t0002g0232 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2823+1175A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98923128 | |||||||
chr7:98923605 | T | G | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2824-1507T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98923605 | |||||||
chr7:98923612 | G | A | 1 | a0001c0021t0001g0129 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2824-1500G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98923612 | |||||||
chr7:98923655 | G | A | 43 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(40): Show |
44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.2824-1457G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98923655 | |||||||
chr7:98923716 | C | T | 2 | a0001c0001t0002g0228 a0001c0001t0002g0231 |
2 | HG00741.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2824-1396C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98923716 | |||||||
chr7:98923853 | A | C | 43 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(40): Show |
44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.2824-1259A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98923853 | |||||||
chr7:98924040 | G | C | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2824-1072G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98924040 | |||||||
chr7:98924329 | CTATTAAA others(4): Show |
C | 1 | a0001c0019t0001g0112 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2824-767_2824-757d others(13): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | INFO_REALIGN_3_PRIME | chr7 | 98924329 | ||||||
chr7:98924423 | C | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(124): Show |
128 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.2824-689C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98924423 | |||||||
chr7:98924546 | G | A | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2824-566G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98924546 | |||||||
chr7:98924636 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2824-476C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98924636 | |||||||
chr7:98924688 | C | CA | 135 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(132): Show |
136 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.2824-406dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | INFO_REALIGN_3_PRIME | chr7 | 98924688 | ||||||
chr7:98924688 | CA | C | 31 | a0001c0001t0001g0076 a0001c0001t0002g0147 a0001c0001t0005g0159 others(28): Show |
31 | HG01257.hp2 HG01884.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.2824-406delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | INFO_REALIGN_3_PRIME | chr7 | 98924688 | ||||||
chr7:98924688 | CAA | C | 22 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0164 others(19): Show |
23 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.2824-407_2824-406d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | INFO_REALIGN_3_PRIME | chr7 | 98924688 | ||||||
chr7:98924726 | G | T | 2 | a0001c0001t0002g0196 a0001c0001t0002g0197 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2824-386G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98924726 | |||||||
chr7:98924769 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2824-343C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98924769 | |||||||
chr7:98924792 | A | G | 3 | a0001c0001t0002g0208 a0001c0001t0011g0209 a0001c0028t0002g0207 |
3 | HG02486.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2824-320A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98924792 | |||||||
chr7:98924849 | A | G | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2824-263A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98924849 | |||||||
chr7:98924865 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0093 |
2 | HG02015.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.2824-247G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98924865 | |||||||
chr7:98924873 | G | A | 3 | a0001c0001t0001g0083 a0001c0001t0001g0100 a0001c0001t0001g0101 |
3 | HG02109.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2824-239G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98924873 | |||||||
chr7:98924877 | A | G | 3 | a0001c0001t0001g0083 a0001c0001t0001g0100 a0001c0001t0001g0101 |
3 | HG02109.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2824-235A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98924877 | |||||||
chr7:98924957 | T | TA | 11 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0002g0223 others(8): Show |
11 | HG01099.hp2 HG01496.hp1 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.2824-154dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | INFO_REALIGN_3_PRIME | chr7 | 98924957 | ||||||
chr7:98924969 | C | T | 1 | a0001c0030t0001g0014 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2824-143C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98924969 | |||||||
chr7:98924991 | C | T | 1 | a0001c0038t0001g0034 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2824-121C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98924991 | |||||||
chr7:98924999 | C | T | 3 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0046 |
3 | HG01346.hp2 HG02145.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.2824-113C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98924999 | |||||||
chr7:98925004 | CA | C | 5 | a0001c0001t0001g0099 a0001c0001t0001g0106 a0001c0002t0007g0154 others(2): Show |
5 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.2824-95delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | INFO_REALIGN_3_PRIME | chr7 | 98925004 | ||||||
chr7:98925270 | C | T | 38 | a0001c0001t0002g0147 a0001c0002t0002g0016 a0001c0002t0002g0017 others(35): Show |
39 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(36): Show |
splice_region_variant&intron_variant | LOW | c.2975+7C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98925270 | |||||||
chr7:98925285 | G | C | 1 | a0001c0005t0004g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2975+22G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98925285 | |||||||
chr7:98925299 | A | T | 6 | a0001c0001t0002g0147 a0001c0006t0002g0149 a0001c0006t0002g0150 others(3): Show |
6 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2975+36A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98925299 | |||||||
chr7:98925340 | T | G | 40 | a0001c0001t0002g0228 a0001c0001t0002g0231 a0001c0002t0002g0016 others(37): Show |
41 | HG00140.hp2 HG00741.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.2975+77T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98925340 | |||||||
chr7:98925428 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2975+165A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98925428 | |||||||
chr7:98925682 | C | T | 1 | a0001c0004t0002g0189 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2975+419C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98925682 | |||||||
chr7:98925750 | T | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(125): Show |
129 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.2975+487T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98925750 | |||||||
chr7:98925851 | A | T | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2975+588A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98925851 | |||||||
chr7:98925902 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2975+639A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98925902 | |||||||
chr7:98926134 | A | G | 1 | a0001c0001t0002g0230 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2975+871A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98926134 | |||||||
chr7:98926320 | C | A | 1 | a0001c0001t0001g0074 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2976-847C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98926320 | |||||||
chr7:98926371 | T | C | 1 | a0001c0001t0002g0248 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2976-796T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98926371 | |||||||
chr7:98926829 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2976-338A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98926829 | |||||||
chr7:98926888 | G | A | 2 | a0001c0001t0002g0225 a0013c0035t0002g0224 |
2 | NA19009.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2976-279G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98926888 | |||||||
chr7:98927127 | A | G | 7 | a0001c0002t0002g0187 a0001c0004t0002g0002 a0001c0004t0002g0168 others(4): Show |
8 | HG01081.hp1 HG02257.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2976-40A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98927127 | |||||||
chr7:98927718 | T | A | 4 | a0001c0001t0002g0157 a0001c0002t0007g0154 a0001c0002t0007g0155 others(1): Show |
4 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.3175+352T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98927718 | |||||||
chr7:98927784 | C | G | 1 | a0001c0004t0002g0176 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3175+418C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98927784 | |||||||
chr7:98927791 | C | G | 1 | a0001c0001t0001g0103 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3175+425C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98927791 | |||||||
chr7:98927825 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3175+459C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98927825 | |||||||
chr7:98927908 | T | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(143): Show |
148 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.3175+542T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98927908 | |||||||
chr7:98927956 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3175+590T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98927956 | |||||||
chr7:98927976 | C | T | 2 | a0001c0001t0001g0042 a0001c0024t0001g0048 |
2 | HG00741.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.3175+610C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98927976 | |||||||
chr7:98928153 | G | A | 1 | a0001c0021t0001g0129 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3175+787G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98928153 | |||||||
chr7:98928231 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.3175+865C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98928231 | |||||||
chr7:98928579 | C | T | 13 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0164 others(10): Show |
13 | HG01243.hp1 HG01884.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.3175+1213C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98928579 | |||||||
chr7:98928639 | T | C | 3 | a0001c0001t0001g0078 a0001c0001t0001g0088 a0001c0001t0001g0090 |
3 | NA18960.hp2 NA19010.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.3175+1273T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98928639 | |||||||
chr7:98928798 | G | A | 4 | a0001c0001t0002g0157 a0001c0002t0007g0154 a0001c0002t0007g0155 others(1): Show |
4 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.3176-1191G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98928798 | |||||||
chr7:98928834 | C | T | 5 | a0001c0002t0002g0164 a0001c0002t0002g0165 a0001c0002t0002g0181 others(2): Show |
5 | HG02809.hp2 HG02896.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.3176-1155C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98928834 | |||||||
chr7:98928934 | C | T | 5 | a0001c0001t0006g0250 a0001c0001t0006g0251 a0001c0001t0006g0252 others(2): Show |
5 | HG00280.hp1 HG00642.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.3176-1055C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98928934 | |||||||
chr7:98928940 | A | AT | 7 | a0001c0001t0001g0094 a0001c0001t0005g0162 a0001c0006t0002g0149 others(4): Show |
7 | HG02258.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.3176-1034dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | INFO_REALIGN_3_PRIME | chr7 | 98928940 | ||||||
chr7:98928940 | AT | A | 9 | a0001c0001t0002g0208 a0001c0001t0011g0209 a0001c0002t0002g0187 others(6): Show |
10 | HG01081.hp1 HG02257.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.3176-1034delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | INFO_REALIGN_3_PRIME | chr7 | 98928940 | ||||||
chr7:98928991 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3176-998G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98928991 | |||||||
chr7:98929051 | C | T | 1 | a0001c0002t0002g0188 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3176-938C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98929051 | |||||||
chr7:98929101 | G | A | 44 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(41): Show |
45 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(42): Show |
intron_variant | MODIFIER | c.3176-888G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98929101 | |||||||
chr7:98929198 | C | T | 1 | a0001c0004t0002g0189 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3176-791C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98929198 | |||||||
chr7:98929226 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3176-763C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98929226 | |||||||
chr7:98929392 | A | G | 1 | a0001c0001t0002g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3176-597A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98929392 | |||||||
chr7:98929738 | C | T | 1 | a0001c0003t0002g0200 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3176-251C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98929738 | |||||||
chr7:98929870 | G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3176-119G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98929870 | |||||||
chr7:98929972 | C | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG02109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3176-17C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98929972 | |||||||
chr7:98929973 | C | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG02109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3176-16C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98929973 | |||||||
chr7:98930294 | C | G | 1 | a0001c0001t0001g0035 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3393+88C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 24/72 | chr7 | 98930294 | |||||||
chr7:98930295 | G | A | 11 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(8): Show |
11 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.3393+89G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 24/72 | chr7 | 98930295 | |||||||
chr7:98930473 | G | A | 1 | a0001c0001t0002g0233 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.3394-160G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 24/72 | chr7 | 98930473 | |||||||
chr7:98930519 | G | C | 1 | a0001c0001t0001g0041 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3394-114G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 24/72 | chr7 | 98930519 | |||||||
chr7:98930526 | C | T | 1 | a0001c0012t0001g0110 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3394-107C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 24/72 | chr7 | 98930526 | |||||||
chr7:98930578 | C | CA | 5 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0106 others(2): Show |
5 | HG02572.hp2 HG02965.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.3394-47dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 24/72 | INFO_REALIGN_3_PRIME | chr7 | 98930578 | ||||||
chr7:98930629 | C | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | splice_region_variant&intron_variant | LOW | c.3394-4C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 24/72 | chr7 | 98930629 | |||||||
chr7:98931096 | T | G | 4 | a0001c0001t0002g0157 a0001c0002t0007g0154 a0001c0002t0007g0155 others(1): Show |
4 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.3591+266T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 25/72 | chr7 | 98931096 | |||||||
chr7:98931100 | A | G | 6 | a0001c0002t0002g0164 a0001c0002t0002g0165 a0001c0002t0002g0166 others(3): Show |
6 | HG02809.hp2 HG02896.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.3591+270A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 25/72 | chr7 | 98931100 | |||||||
chr7:98931342 | G | A | 1 | a0001c0002t0002g0255 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3592-63G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 25/72 | chr7 | 98931342 | |||||||
chr7:98931697 | T | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0086 |
2 | HG01099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.3852+32T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 26/72 | chr7 | 98931697 | |||||||
chr7:98931703 | A | G | 7 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0166 others(4): Show |
7 | HG01243.hp1 HG01884.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.3852+38A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 26/72 | chr7 | 98931703 | |||||||
chr7:98931718 | T | A | 1 | a0001c0001t0001g0094 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3852+53T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 26/72 | chr7 | 98931718 | |||||||
chr7:98931973 | A | C | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3852+308A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 26/72 | chr7 | 98931973 | |||||||
chr7:98932470 | A | G | 12 | a0001c0001t0002g0157 a0001c0002t0007g0154 a0001c0002t0007g0155 others(9): Show |
12 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.3853-771A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 26/72 | chr7 | 98932470 | |||||||
chr7:98932538 | C | G | 13 | a0001c0001t0001g0128 a0001c0001t0001g0130 a0001c0001t0001g0132 others(10): Show |
13 | HG00738.hp1 HG01192.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.3853-703C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 26/72 | chr7 | 98932538 | |||||||
chr7:98932608 | T | C | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3853-633T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 26/72 | chr7 | 98932608 | |||||||
chr7:98932664 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(195): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.3853-577G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 26/72 | chr7 | 98932664 | |||||||
chr7:98933008 | A | AT | 150 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(147): Show |
152 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.3853-219dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 26/72 | INFO_REALIGN_3_PRIME | chr7 | 98933008 | ||||||
chr7:98933008 | A | ATT | 8 | a0001c0001t0002g0157 a0001c0002t0002g0016 a0001c0002t0002g0017 others(5): Show |
8 | HG01243.hp1 HG01884.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.3853-220_3853-219d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 26/72 | INFO_REALIGN_3_PRIME | chr7 | 98933008 | ||||||
chr7:98933091 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3853-150G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 26/72 | chr7 | 98933091 | |||||||
chr7:98933118 | C | T | 1 | a0001c0001t0002g0246 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3853-123C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 26/72 | chr7 | 98933118 | |||||||
chr7:98933197 | C | G | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.3853-44C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 26/72 | chr7 | 98933197 | |||||||
chr7:98933469 | C | T | 3 | a0001c0001t0002g0195 a0001c0001t0002g0196 a0001c0001t0002g0197 |
3 | HG02258.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4014+67C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98933469 | |||||||
chr7:98933504 | C | T | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4014+102C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98933504 | |||||||
chr7:98933505 | G | A | 1 | a0001c0006t0002g0152 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4014+103G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98933505 | |||||||
chr7:98933799 | ACAT | A | 10 | a0001c0003t0002g0003 a0001c0003t0002g0198 a0001c0003t0002g0199 others(7): Show |
11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.4014+400_4014+402d others(5): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | INFO_REALIGN_3_PRIME | chr7 | 98933799 | ||||||
chr7:98933999 | C | T | 10 | a0001c0003t0002g0003 a0001c0003t0002g0198 a0001c0003t0002g0199 others(7): Show |
11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.4014+597C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98933999 | |||||||
chr7:98934017 | A | G | 1 | a0001c0025t0001g0118 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.4014+615A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98934017 | |||||||
chr7:98934260 | C | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(118): Show |
122 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.4014+858C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98934260 | |||||||
chr7:98934261 | G | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4014+859G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98934261 | |||||||
chr7:98934551 | A | G | 8 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(5): Show |
8 | HG02559.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.4015-1028A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98934551 | |||||||
chr7:98934964 | A | C | 3 | a0001c0001t0002g0208 a0001c0001t0011g0209 a0001c0028t0002g0207 |
3 | HG02486.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.4015-615A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98934964 | |||||||
chr7:98934980 | A | G | 1 | a0001c0004t0002g0189 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4015-599A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98934980 | |||||||
chr7:98935018 | G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4015-561G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98935018 | |||||||
chr7:98935056 | C | T | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.4015-523C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98935056 | |||||||
chr7:98935166 | T | C | 5 | a0001c0001t0002g0157 a0001c0002t0007g0154 a0001c0002t0007g0155 others(2): Show |
5 | HG00140.hp2 HG01243.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.4015-413T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98935166 | |||||||
chr7:98935500 | T | C | 2 | a0001c0001t0002g0228 a0001c0001t0002g0231 |
2 | HG00741.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4015-79T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98935500 | |||||||
chr7:98935564 | T | G | 1 | a0001c0024t0001g0048 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4015-15T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98935564 | |||||||
chr7:98936494 | A | G | 11 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(8): Show |
11 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.4112-662A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 28/72 | chr7 | 98936494 | |||||||
chr7:98936606 | C | T | 10 | a0001c0003t0002g0003 a0001c0003t0002g0198 a0001c0003t0002g0199 others(7): Show |
11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.4112-550C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 28/72 | chr7 | 98936606 | |||||||
chr7:98936730 | G | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(123): Show |
127 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.4112-426G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 28/72 | chr7 | 98936730 | |||||||
chr7:98936790 | G | C | 11 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(8): Show |
11 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.4112-366G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 28/72 | chr7 | 98936790 | |||||||
chr7:98936850 | T | C | 1 | a0001c0001t0002g0234 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.4112-306T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 28/72 | chr7 | 98936850 | |||||||
chr7:98937034 | C | T | 3 | a0001c0001t0006g0250 a0001c0001t0006g0251 a0001c0001t0006g0252 |
3 | HG00280.hp1 HG01106.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.4112-122C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 28/72 | chr7 | 98937034 | |||||||
chr7:98937297 | T | A | 43 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(40): Show |
44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.4233+20T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 29/72 | chr7 | 98937297 | |||||||
chr7:98937323 | CAT | C | 12 | a0001c0001t0001g0070 a0001c0001t0002g0213 a0001c0001t0002g0214 others(9): Show |
12 | HG01257.hp2 HG01891.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.4233+47_4233+48del others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 29/72 | chr7 | 98937323 | |||||||
chr7:98937841 | C | T | 3 | a0001c0001t0002g0208 a0001c0001t0011g0209 a0001c0028t0002g0207 |
3 | HG02486.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.4404+21C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98937841 | |||||||
chr7:98937972 | C | T | 1 | a0001c0031t0002g0226 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.4404+152C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98937972 | |||||||
chr7:98938333 | T | C | 4 | a0001c0001t0002g0157 a0001c0002t0007g0154 a0001c0002t0007g0155 others(1): Show |
4 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.4404+513T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98938333 | |||||||
chr7:98938428 | C | G | 1 | a0001c0001t0001g0143 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.4404+608C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98938428 | |||||||
chr7:98938476 | C | A | 43 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(40): Show |
44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.4404+656C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98938476 | |||||||
chr7:98938510 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(133): Show |
137 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.4404+690A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98938510 | |||||||
chr7:98938558 | A | AAT | 136 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(133): Show |
137 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.4404+748_4404+749d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | INFO_REALIGN_3_PRIME | chr7 | 98938558 | ||||||
chr7:98938578 | T | C | 1 | a0001c0001t0002g0232 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.4404+758T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98938578 | |||||||
chr7:98938844 | T | C | 7 | a0001c0002t0002g0177 a0001c0002t0002g0178 a0001c0002t0002g0180 others(4): Show |
7 | HG01257.hp2 HG01891.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.4404+1024T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98938844 | |||||||
chr7:98939052 | C | T | 5 | a0001c0001t0005g0159 a0001c0001t0005g0160 a0001c0001t0005g0162 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.4404+1232C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98939052 | |||||||
chr7:98939059 | C | G | 1 | a0001c0004t0002g0176 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4404+1239C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98939059 | |||||||
chr7:98939093 | G | A | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.4404+1273G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98939093 | |||||||
chr7:98939321 | G | A | 61 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(58): Show |
61 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.4404+1501G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98939321 | |||||||
chr7:98939474 | T | C | 1 | a0001c0007t0001g0081 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4404+1654T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98939474 | |||||||
chr7:98939537 | G | T | 1 | a0001c0001t0001g0117 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4404+1717G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98939537 | |||||||
chr7:98939609 | C | G | 11 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 others(8): Show |
11 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.4404+1789C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98939609 | |||||||
chr7:98939693 | G | A | 1 | a0001c0005t0004g0007 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4404+1873G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98939693 | |||||||
chr7:98940250 | G | A | 1 | a0001c0002t0002g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4404+2430G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98940250 | |||||||
chr7:98940279 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4404+2459C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98940279 | |||||||
chr7:98940379 | G | A | 43 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(40): Show |
44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.4404+2559G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98940379 | |||||||
chr7:98940422 | T | C | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.4405-2527T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98940422 | |||||||
chr7:98940527 | A | G | 1 | a0001c0001t0001g0114 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.4405-2422A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98940527 | |||||||
chr7:98940548 | C | T | 2 | a0001c0002t0010g0179 a0001c0043t0002g0167 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.4405-2401C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98940548 | |||||||
chr7:98940561 | C | G | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4405-2388C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98940561 | |||||||
chr7:98941060 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.4405-1889C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98941060 | |||||||
chr7:98941256 | A | C | 1 | a0001c0001t0001g0092 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4405-1693A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98941256 | |||||||
chr7:98941337 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4405-1612G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98941337 | |||||||
chr7:98941370 | C | T | 6 | a0001c0001t0002g0147 a0001c0006t0002g0149 a0001c0006t0002g0150 others(3): Show |
6 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.4405-1579C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98941370 | |||||||
chr7:98941466 | G | T | 6 | a0001c0001t0002g0147 a0001c0006t0002g0149 a0001c0006t0002g0150 others(3): Show |
6 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.4405-1483G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98941466 | |||||||
chr7:98941733 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(133): Show |
137 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.4405-1216A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98941733 | |||||||
chr7:98941847 | C | CA | 10 | a0001c0003t0002g0003 a0001c0003t0002g0198 a0001c0003t0002g0199 others(7): Show |
11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.4405-1099dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | INFO_REALIGN_3_PRIME | chr7 | 98941847 | ||||||
chr7:98942243 | A | G | 6 | a0001c0001t0002g0147 a0001c0006t0002g0149 a0001c0006t0002g0150 others(3): Show |
6 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.4405-706A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98942243 | |||||||
chr7:98942283 | C | T | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.4405-666C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98942283 | |||||||
chr7:98942316 | C | G | 70 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(67): Show |
70 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.4405-633C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98942316 | |||||||
chr7:98942347 | C | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4405-602C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98942347 | |||||||
chr7:98942500 | T | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(134): Show |
138 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.4405-449T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98942500 | |||||||
chr7:98942865 | T | C | 2 | a0001c0002t0002g0016 a0001c0002t0002g0017 |
2 | HG01884.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4405-84T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98942865 | |||||||
chr7:98943159 | T | A | 1 | a0001c0001t0001g0144 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.4473+142T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98943159 | |||||||
chr7:98943395 | C | T | 1 | a0005c0040t0005g0158 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4473+378C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98943395 | |||||||
chr7:98943638 | T | A | 185 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(182): Show |
187 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.4473+621T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98943638 | |||||||
chr7:98943753 | G | A | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.4473+736G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98943753 | |||||||
chr7:98944051 | C | T | 1 | a0005c0040t0005g0158 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4473+1034C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98944051 | |||||||
chr7:98944052 | G | A | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.4473+1035G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98944052 | |||||||
chr7:98944110 | G | A | 1 | a0001c0004t0002g0185 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4473+1093G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98944110 | |||||||
chr7:98944146 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.4473+1129C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98944146 | |||||||
chr7:98944171 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.4473+1154G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98944171 | |||||||
chr7:98944281 | T | TA | 9 | a0001c0001t0002g0195 a0001c0001t0005g0159 a0001c0001t0005g0160 others(6): Show |
9 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.4473+1273dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | INFO_REALIGN_3_PRIME | chr7 | 98944281 | ||||||
chr7:98944380 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.4473+1363T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98944380 | |||||||
chr7:98944741 | C | T | 1 | a0001c0002t0012g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4474-1006C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98944741 | |||||||
chr7:98944742 | G | A | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.4474-1005G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98944742 | |||||||
chr7:98944993 | T | C | 44 | a0001c0001t0002g0147 a0001c0001t0002g0195 a0001c0001t0005g0159 others(41): Show |
45 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(42): Show |
intron_variant | MODIFIER | c.4474-754T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98944993 | |||||||
chr7:98945029 | T | G | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4474-718T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98945029 | |||||||
chr7:98945085 | G | A | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.4474-662G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98945085 | |||||||
chr7:98945227 | C | G | 1 | a0001c0002t0012g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4474-520C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98945227 | |||||||
chr7:98945243 | C | A | 1 | a0001c0004t0002g0176 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4474-504C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98945243 | |||||||
chr7:98945264 | A | G | 33 | a0001c0001t0002g0195 a0001c0002t0002g0016 a0001c0002t0002g0017 others(30): Show |
34 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.4474-483A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98945264 | |||||||
chr7:98945485 | A | C | 38 | a0001c0001t0002g0195 a0001c0001t0005g0159 a0001c0001t0005g0160 others(35): Show |
39 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(36): Show |
intron_variant | MODIFIER | c.4474-262A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98945485 | |||||||
chr7:98945629 | T | G | 1 | a0001c0001t0001g0032 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.4474-118T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98945629 | |||||||
chr7:98945989 | C | T | 5 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 others(2): Show |
5 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.4548+39C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98945989 | |||||||
chr7:98946279 | TCA | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(121): Show |
125 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.4548+334_4548+335d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | INFO_REALIGN_3_PRIME | chr7 | 98946279 | ||||||
chr7:98946301 | G | C | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4548+351G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98946301 | |||||||
chr7:98946323 | T | C | 9 | a0001c0004t0002g0002 a0001c0004t0002g0168 a0001c0004t0002g0169 others(6): Show |
10 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.4548+373T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98946323 | |||||||
chr7:98946408 | G | A | 1 | a0001c0045t0001g0073 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4548+458G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98946408 | |||||||
chr7:98946441 | A | ATGCACTC others(27): Show |
1 | a0001c0001t0001g0113 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.4548+502_4548+535d others(36): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | INFO_REALIGN_3_PRIME | chr7 | 98946441 | ||||||
chr7:98946452 | A | G | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4548+502A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98946452 | |||||||
chr7:98946481 | T | TCACACCA others(10): Show |
2 | a0001c0001t0001g0084 a0001c0001t0001g0089 |
2 | HG00544.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.4548+556_4548+572d others(19): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | INFO_REALIGN_3_PRIME | chr7 | 98946481 | ||||||
chr7:98946583 | C | CCACATAT others(8): Show |
3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.4548+648_4548+662d others(17): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | INFO_REALIGN_3_PRIME | chr7 | 98946583 | ||||||
chr7:98946654 | A | G | 1 | a0001c0003t0002g0198 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4548+704A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98946654 | |||||||
chr7:98946705 | T | G | 32 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0164 others(29): Show |
33 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.4548+755T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98946705 | |||||||
chr7:98946719 | T | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(133): Show |
137 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.4548+769T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98946719 | |||||||
chr7:98946751 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.4548+801T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98946751 | |||||||
chr7:98946925 | G | C | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.4548+975G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98946925 | |||||||
chr7:98947113 | G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4549-1108G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98947113 | |||||||
chr7:98947160 | T | C | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.4549-1061T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98947160 | |||||||
chr7:98947276 | C | G | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.4549-945C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98947276 | |||||||
chr7:98947480 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(131): Show |
135 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.4549-741G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98947480 | |||||||
chr7:98947519 | G | A | 1 | a0001c0004t0002g0169 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4549-702G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98947519 | |||||||
chr7:98947558 | C | G | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4549-663C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98947558 | |||||||
chr7:98947581 | G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4549-640G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98947581 | |||||||
chr7:98947671 | G | A | 1 | a0001c0012t0001g0110 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4549-550G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98947671 | |||||||
chr7:98947931 | T | A | 1 | a0001c0001t0001g0084 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.4549-290T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98947931 | |||||||
chr7:98948394 | G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4668+54G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 34/72 | chr7 | 98948394 | |||||||
chr7:98948532 | G | A | 5 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 others(2): Show |
5 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.4669-34G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 34/72 | chr7 | 98948532 | |||||||
chr7:98948730 | T | G | 32 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0164 others(29): Show |
33 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.4788+45T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 35/72 | chr7 | 98948730 | |||||||
chr7:98948806 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4788+121T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 35/72 | chr7 | 98948806 | |||||||
chr7:98948853 | T | G | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4788+168T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 35/72 | chr7 | 98948853 | |||||||
chr7:98948990 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4788+305C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 35/72 | chr7 | 98948990 | |||||||
chr7:98948991 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.4788+306G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 35/72 | chr7 | 98948991 | |||||||
chr7:98949011 | T | C | 1 | a0001c0001t0001g0102 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.4788+326T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 35/72 | chr7 | 98949011 | |||||||
chr7:98949095 | C | T | 5 | a0001c0001t0006g0250 a0001c0001t0006g0251 a0001c0001t0006g0252 others(2): Show |
5 | HG00280.hp1 HG00642.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.4789-322C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 35/72 | chr7 | 98949095 | |||||||
chr7:98949276 | G | C | 33 | a0001c0001t0002g0195 a0001c0002t0002g0016 a0001c0002t0002g0017 others(30): Show |
34 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.4789-141G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 35/72 | chr7 | 98949276 | |||||||
chr7:98949657 | C | T | 1 | a0001c0002t0002g0188 | 1 | HG02257.hp2 | splice_region_variant&intron_variant | LOW | c.4954-3C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 36/72 | chr7 | 98949657 | |||||||
chr7:98949927 | G | A | 1 | a0001c0001t0003g0029 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.5135+86G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 37/72 | chr7 | 98949927 | |||||||
chr7:98950356 | T | C | 3 | a0001c0001t0001g0050 a0002c0008t0008g0192 a0002c0008t0008g0193 |
3 | HG00408.hp2 HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.5334+94T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 38/72 | chr7 | 98950356 | |||||||
chr7:98950531 | A | G | 1 | a0001c0001t0001g0114 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.5334+269A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 38/72 | chr7 | 98950531 | |||||||
chr7:98951059 | C | CTG | 15 | a0001c0001t0001g0109 a0001c0001t0002g0208 a0001c0001t0002g0220 others(12): Show |
15 | HG02055.hp2 HG02083.hp1 HG02148.hp1 others(12): Show |
intron_variant | MODIFIER | c.5463+89_5463+90dup others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98951059 | ||||||
chr7:98951059 | C | CTGTG | 24 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0089 others(21): Show |
25 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.5463+87_5463+90dup others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98951059 | ||||||
chr7:98951059 | C | CTGTGTG | 68 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0042 others(65): Show |
69 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.5463+85_5463+90dup others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98951059 | ||||||
chr7:98951059 | C | CTGTGTGT others(1): Show |
18 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0040 others(15): Show |
18 | HG00423.hp1 HG00423.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.5463+83_5463+90dup others(8): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98951059 | ||||||
chr7:98951059 | C | CTGTGTGT others(3): Show |
24 | a0001c0001t0001g0013 a0001c0001t0001g0031 a0001c0001t0001g0032 others(21): Show |
24 | HG00408.hp2 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.5463+81_5463+90dup others(10): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98951059 | ||||||
chr7:98951059 | C | CTGTGTGT others(5): Show |
5 | a0001c0001t0001g0052 a0001c0001t0001g0060 a0001c0001t0005g0162 others(2): Show |
5 | HG02129.hp2 HG02258.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.5463+79_5463+90dup others(12): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98951059 | ||||||
chr7:98951059 | C | CTGTGTGT others(7): Show |
6 | a0001c0001t0001g0038 a0001c0001t0001g0043 a0001c0001t0001g0044 others(3): Show |
6 | HG02055.hp1 HG03704.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.5463+77_5463+90dup others(14): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98951059 | ||||||
chr7:98951059 | C | CTGTGTGT others(9): Show |
1 | a0001c0001t0001g0062 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.5463+75_5463+90dup others(16): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98951059 | ||||||
chr7:98951059 | C | CTGTGTGT others(11): Show |
1 | a0001c0001t0001g0059 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.5463+73_5463+90dup others(18): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98951059 | ||||||
chr7:98951059 | CTG | C | 32 | a0001c0001t0002g0211 a0001c0001t0003g0021 a0001c0001t0006g0250 others(29): Show |
32 | HG00280.hp1 HG00642.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.5463+89_5463+90del others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98951059 | ||||||
chr7:98951180 | C | T | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.5463+176C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98951180 | |||||||
chr7:98951219 | C | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(125): Show |
129 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.5463+215C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98951219 | |||||||
chr7:98951319 | G | A | 1 | a0001c0002t0007g0154 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.5463+315G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98951319 | |||||||
chr7:98951562 | T | C | 191 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(188): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.5463+558T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98951562 | |||||||
chr7:98951593 | G | A | 13 | a0001c0001t0001g0128 a0001c0001t0001g0130 a0001c0001t0001g0132 others(10): Show |
13 | HG00738.hp1 HG01192.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.5463+589G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98951593 | |||||||
chr7:98951622 | G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5463+618G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98951622 | |||||||
chr7:98951647 | G | A | 5 | a0001c0006t0002g0149 a0001c0006t0002g0150 a0001c0006t0002g0151 others(2): Show |
5 | HG02559.hp1 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.5463+643G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98951647 | |||||||
chr7:98951965 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0051 |
2 | NA18960.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.5463+961C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98951965 | |||||||
chr7:98952312 | C | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(194): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.5464-855C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98952312 | |||||||
chr7:98952386 | A | G | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5464-781A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98952386 | |||||||
chr7:98952567 | C | T | 3 | a0001c0001t0002g0208 a0001c0001t0011g0209 a0001c0028t0002g0207 |
3 | HG02486.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.5464-600C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98952567 | |||||||
chr7:98952698 | C | T | 1 | a0001c0001t0002g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5464-469C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98952698 | |||||||
chr7:98952753 | G | C | 2 | a0001c0001t0002g0196 a0001c0001t0002g0197 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.5464-414G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98952753 | |||||||
chr7:98952780 | C | T | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.5464-387C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98952780 | |||||||
chr7:98952822 | C | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(122): Show |
126 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.5464-345C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98952822 | |||||||
chr7:98952824 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5464-343T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98952824 | |||||||
chr7:98953031 | T | TTG | 6 | a0001c0001t0001g0241 a0001c0001t0001g0257 a0001c0002t0002g0180 others(3): Show |
6 | HG01891.hp1 HG02129.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.5464-88_5464-87dup others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | ||||||
chr7:98953031 | T | TTGTG | 3 | a0001c0001t0002g0230 a0001c0002t0002g0177 a0004c0016t0001g0229 |
3 | HG00408.hp1 HG02040.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.5464-90_5464-87dup others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | ||||||
chr7:98953031 | T | TTGTGTG | 2 | a0001c0001t0002g0221 a0001c0001t0002g0232 |
2 | HG00438.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.5464-92_5464-87dup others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | ||||||
chr7:98953031 | TTG | T | 11 | a0001c0001t0002g0246 a0001c0002t0002g0171 a0001c0002t0002g0173 others(8): Show |
11 | HG01243.hp1 HG01257.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.5464-88_5464-87del others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | ||||||
chr7:98953031 | TTGTG | T | 10 | a0001c0001t0002g0249 a0001c0001t0006g0250 a0001c0001t0006g0252 others(7): Show |
10 | HG00140.hp2 HG00642.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.5464-90_5464-87del others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | ||||||
chr7:98953031 | TTGTGTG | T | 28 | a0001c0001t0002g0195 a0001c0001t0002g0208 a0001c0001t0005g0160 others(25): Show |
29 | HG00280.hp1 HG01081.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.5464-92_5464-87del others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | ||||||
chr7:98953031 | TTGTGTGT others(1): Show |
T | 3 | a0001c0001t0001g0240 a0001c0001t0002g0157 a0001c0004t0002g0176 |
3 | HG02015.hp2 HG02647.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.5464-94_5464-87del others(8): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | ||||||
chr7:98953031 | TTGTGTGT others(3): Show |
T | 2 | a0001c0001t0002g0010 a0001c0001t0002g0011 |
2 | HG00544.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.5464-96_5464-87del others(10): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | ||||||
chr7:98953031 | TTGTGTGT others(5): Show |
T | 4 | a0001c0001t0002g0196 a0001c0001t0002g0197 a0001c0011t0013g0190 others(1): Show |
4 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.5464-98_5464-87del others(12): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | ||||||
chr7:98953031 | TTGTGTGT others(7): Show |
T | 1 | a0001c0001t0003g0028 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.5464-100_5464-87de others(15): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | ||||||
chr7:98953031 | TTGTGTGT others(9): Show |
T | 1 | a0014c0032t0005g0161 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5464-102_5464-87de others(17): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | ||||||
chr7:98953031 | TTGTGTGT others(11): Show |
T | 1 | a0001c0001t0005g0159 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5464-104_5464-87de others(19): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | ||||||
chr7:98953031 | TTGTGTGT others(13): Show |
T | 6 | a0001c0001t0002g0147 a0001c0006t0002g0149 a0001c0006t0002g0150 others(3): Show |
6 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.5464-106_5464-87de others(21): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | ||||||
chr7:98953031 | TTGTGTGT others(23): Show |
T | 1 | a0001c0001t0001g0057 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.5464-116_5464-87de others(31): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | ||||||
chr7:98953031 | TTGTGTGT others(25): Show |
T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(121): Show |
125 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.5464-118_5464-87de others(33): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | ||||||
chr7:98953075 | GTGTGTT | G | 9 | a0001c0003t0002g0003 a0001c0003t0002g0198 a0001c0003t0002g0199 others(6): Show |
10 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.5464-90_5464-85del others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953075 | ||||||
chr7:98953463 | C | T | 1 | a0001c0002t0007g0154 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.5730+30C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98953463 | |||||||
chr7:98953529 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(123): Show |
127 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.5730+96C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98953529 | |||||||
chr7:98953691 | G | C | 1 | a0001c0001t0001g0091 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.5730+258G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98953691 | |||||||
chr7:98953709 | C | T | 2 | a0001c0001t0002g0213 a0001c0001t0002g0214 |
2 | NA18966.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.5730+276C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98953709 | |||||||
chr7:98953752 | G | A | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0056 |
3 | HG01358.hp1 HG01943.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.5730+319G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98953752 | |||||||
chr7:98953769 | G | A | 1 | a0001c0001t0002g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5730+336G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98953769 | |||||||
chr7:98953898 | C | G | 1 | a0001c0001t0001g0071 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.5730+465C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98953898 | |||||||
chr7:98953918 | G | A | 1 | a0001c0002t0002g0188 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.5730+485G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98953918 | |||||||
chr7:98954158 | C | CT | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.5730+726dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | INFO_REALIGN_3_PRIME | chr7 | 98954158 | ||||||
chr7:98954249 | G | T | 1 | a0001c0010t0001g0068 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.5730+816G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98954249 | |||||||
chr7:98954344 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(122): Show |
126 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.5731-754C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98954344 | |||||||
chr7:98954429 | G | A | 1 | a0001c0045t0001g0073 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.5731-669G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98954429 | |||||||
chr7:98954444 | C | T | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5731-654C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98954444 | |||||||
chr7:98954453 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.5731-645A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98954453 | |||||||
chr7:98954803 | C | T | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5731-295C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98954803 | |||||||
chr7:98954852 | C | T | 1 | a0001c0004t0002g0176 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5731-246C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98954852 | |||||||
chr7:98954949 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.5731-149G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98954949 | |||||||
chr7:98954967 | A | G | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5731-131A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98954967 | |||||||
chr7:98955087 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5731-11C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98955087 | |||||||
chr7:98955335 | G | A | 11 | a0001c0001t0002g0222 a0001c0001t0002g0233 a0001c0001t0002g0234 others(8): Show |
11 | HG00558.hp1 HG02129.hp1 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.5937+31G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 41/72 | chr7 | 98955335 | |||||||
chr7:98955738 | G | C | 1 | a0001c0001t0005g0162 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5938-408G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 41/72 | chr7 | 98955738 | |||||||
chr7:98955841 | T | G | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.5938-305T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 41/72 | chr7 | 98955841 | |||||||
chr7:98956079 | G | A | 5 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0171 others(2): Show |
5 | HG01243.hp1 HG01884.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.5938-67G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 41/72 | chr7 | 98956079 | |||||||
chr7:98956087 | G | T | 1 | a0001c0001t0001g0033 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.5938-59G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 41/72 | chr7 | 98956087 | |||||||
chr7:98956116 | T | TC | 193 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(190): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.5938-28dupC | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 41/72 | INFO_REALIGN_3_PRIME | chr7 | 98956116 | ||||||
chr7:98956122 | G | C | 1 | a0001c0001t0001g0057 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.5938-24G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 41/72 | chr7 | 98956122 | |||||||
chr7:98956337 | G | A | 7 | a0001c0001t0001g0084 a0001c0005t0004g0004 a0001c0005t0004g0005 others(4): Show |
7 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.6096+33G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 42/72 | chr7 | 98956337 | |||||||
chr7:98956587 | G | A | 1 | a0001c0002t0010g0179 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.6231+54G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98956587 | |||||||
chr7:98956614 | C | G | 1 | a0001c0001t0001g0125 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.6231+81C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98956614 | |||||||
chr7:98956636 | G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6231+103G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98956636 | |||||||
chr7:98956698 | A | G | 1 | a0001c0001t0001g0141 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.6231+165A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98956698 | |||||||
chr7:98956769 | G | A | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.6231+236G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98956769 | |||||||
chr7:98956961 | G | C | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.6231+428G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98956961 | |||||||
chr7:98956987 | C | T | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.6231+454C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98956987 | |||||||
chr7:98957004 | T | C | 6 | a0001c0001t0002g0147 a0001c0006t0002g0149 a0001c0006t0002g0150 others(3): Show |
6 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.6231+471T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957004 | |||||||
chr7:98957040 | T | C | 1 | a0001c0001t0001g0015 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.6231+507T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957040 | |||||||
chr7:98957075 | C | T | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.6231+542C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957075 | |||||||
chr7:98957227 | G | A | 1 | a0001c0026t0003g0023 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.6231+694G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957227 | |||||||
chr7:98957228 | A | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(189): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.6231+695A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957228 | |||||||
chr7:98957320 | A | G | 5 | a0001c0001t0002g0222 a0001c0001t0002g0238 a0001c0001t0002g0246 others(2): Show |
5 | NA18942.hp2 NA18944.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.6232-661A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957320 | |||||||
chr7:98957357 | A | G | 1 | a0001c0001t0002g0195 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.6232-624A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957357 | |||||||
chr7:98957552 | C | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6232-429C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957552 | |||||||
chr7:98957586 | C | T | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.6232-395C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957586 | |||||||
chr7:98957600 | T | C | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.6232-381T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957600 | |||||||
chr7:98957621 | C | T | 1 | a0001c0002t0002g0017 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.6232-360C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957621 | |||||||
chr7:98957638 | A | G | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.6232-343A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957638 | |||||||
chr7:98957699 | G | A | 11 | a0001c0002t0002g0187 a0001c0004t0002g0002 a0001c0004t0002g0168 others(8): Show |
12 | HG01081.hp1 HG02257.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.6232-282G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957699 | |||||||
chr7:98957853 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.6232-128C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957853 | |||||||
chr7:98957940 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.6232-41G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957940 | |||||||
chr7:98958118 | G | C | 1 | a0001c0001t0002g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.6342+27G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/72 | chr7 | 98958118 | |||||||
chr7:98958309 | G | GT | 5 | a0001c0001t0002g0234 a0001c0001t0002g0235 a0001c0001t0002g0236 others(2): Show |
5 | HG00558.hp1 HG01169.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.6342+229dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/72 | INFO_REALIGN_3_PRIME | chr7 | 98958309 | ||||||
chr7:98958319 | T | C | 1 | a0001c0001t0001g0031 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.6342+228T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/72 | chr7 | 98958319 | |||||||
chr7:98958365 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.6342+274C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/72 | chr7 | 98958365 | |||||||
chr7:98958472 | G | A | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0109 |
3 | HG02083.hp1 NA18948.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.6342+381G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/72 | chr7 | 98958472 | |||||||
chr7:98958497 | A | T | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.6342+406A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/72 | chr7 | 98958497 | |||||||
chr7:98958535 | A | G | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.6342+444A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/72 | chr7 | 98958535 | |||||||
chr7:98958670 | C | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6342+579C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/72 | chr7 | 98958670 | |||||||
chr7:98958671 | A | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(199): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.6342+580A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/72 | chr7 | 98958671 | |||||||
chr7:98958681 | C | T | 2 | a0001c0001t0002g0196 a0001c0001t0002g0197 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.6342+590C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/72 | chr7 | 98958681 | |||||||
chr7:98958711 | G | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(122): Show |
126 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.6342+620G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/72 | chr7 | 98958711 | |||||||
chr7:98958744 | C | T | 1 | a0001c0012t0001g0110 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.6343-600C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/72 | chr7 | 98958744 | |||||||
chr7:98959273 | C | T | 1 | a0001c0002t0002g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.6343-71C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/72 | chr7 | 98959273 | |||||||
chr7:98959339 | C | T | 48 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(45): Show |
48 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(45): Show |
splice_region_variant&intron_variant | LOW | c.6343-5C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/72 | chr7 | 98959339 | |||||||
chr7:98959733 | G | C | 11 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 others(8): Show |
11 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.6489+243G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98959733 | |||||||
chr7:98959754 | A | G | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | NA18971.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.6489+264A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98959754 | |||||||
chr7:98959882 | A | G | 1 | a0001c0019t0001g0112 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.6489+392A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98959882 | |||||||
chr7:98959936 | T | TA | 12 | a0001c0001t0001g0001 a0001c0001t0001g0111 a0001c0001t0001g0142 others(9): Show |
13 | HG00280.hp2 HG00642.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.6489+464dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | INFO_REALIGN_3_PRIME | chr7 | 98959936 | ||||||
chr7:98959936 | TA | T | 10 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0087 others(7): Show |
10 | HG01943.hp1 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.6489+464delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | INFO_REALIGN_3_PRIME | chr7 | 98959936 | ||||||
chr7:98959937 | A | G | 26 | a0001c0001t0002g0195 a0001c0002t0002g0016 a0001c0002t0002g0017 others(23): Show |
27 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.6489+447A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98959937 | |||||||
chr7:98959943 | AAAAAAAA others(5): Show |
A | 5 | a0001c0003t0002g0003 a0001c0003t0002g0199 a0001c0003t0002g0201 others(2): Show |
6 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.6489+459_6489+470d others(14): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | INFO_REALIGN_3_PRIME | chr7 | 98959943 | ||||||
chr7:98959954 | AG | A | 53 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(50): Show |
53 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.6489+465delG | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98959954 | |||||||
chr7:98959955 | G | A | 58 | a0001c0001t0002g0011 a0001c0001t0002g0147 a0001c0001t0002g0195 others(55): Show |
59 | HG00140.hp2 HG00438.hp2 HG01081.hp1 others(56): Show |
intron_variant | MODIFIER | c.6489+465G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98959955 | |||||||
chr7:98960232 | T | C | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.6489+742T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98960232 | |||||||
chr7:98960398 | A | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0115 |
2 | HG00558.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.6490-863A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98960398 | |||||||
chr7:98960562 | A | G | 3 | a0001c0002t0002g0164 a0001c0002t0002g0165 a0001c0002t0002g0166 |
3 | HG02896.hp2 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.6490-699A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98960562 | |||||||
chr7:98960604 | G | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0102 |
2 | NA18982.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.6490-657G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98960604 | |||||||
chr7:98960690 | C | G | 1 | a0001c0001t0001g0082 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.6490-571C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98960690 | |||||||
chr7:98960757 | TTTTG | T | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.6490-502_6490-499d others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | INFO_REALIGN_3_PRIME | chr7 | 98960757 | ||||||
chr7:98960759 | T | TTG | 7 | a0001c0001t0001g0058 a0001c0001t0002g0147 a0001c0001t0005g0159 others(4): Show |
7 | HG01517.hp1 HG01884.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.6490-472_6490-471d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | INFO_REALIGN_3_PRIME | chr7 | 98960759 | ||||||
chr7:98960759 | T | TTGTG | 5 | a0001c0006t0002g0149 a0001c0006t0002g0150 a0001c0006t0002g0151 others(2): Show |
5 | HG02559.hp1 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.6490-474_6490-471d others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | INFO_REALIGN_3_PRIME | chr7 | 98960759 | ||||||
chr7:98960759 | TTG | T | 173 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(170): Show |
175 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.6490-472_6490-471d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | INFO_REALIGN_3_PRIME | chr7 | 98960759 | ||||||
chr7:98960785 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.6490-476G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98960785 | |||||||
chr7:98961059 | A | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6490-202A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98961059 | |||||||
chr7:98961220 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.6490-41T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98961220 | |||||||
chr7:98961257 | G | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(200): Show |
206 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(203): Show |
splice_region_variant&intron_variant | LOW | c.6490-4G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98961257 | |||||||
chr7:98961516 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.6703+42C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 46/72 | chr7 | 98961516 | |||||||
chr7:98961535 | T | C | 4 | a0001c0002t0002g0177 a0001c0002t0002g0178 a0001c0002t0010g0179 others(1): Show |
4 | HG02451.hp1 HG03209.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.6703+61T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 46/72 | chr7 | 98961535 | |||||||
chr7:98961554 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.6703+80C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 46/72 | chr7 | 98961554 | |||||||
chr7:98961582 | A | G | 2 | a0001c0001t0002g0208 a0001c0001t0011g0209 |
2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.6703+108A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 46/72 | chr7 | 98961582 | |||||||
chr7:98961618 | T | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(132): Show |
136 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.6703+144T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 46/72 | chr7 | 98961618 | |||||||
chr7:98961655 | C | T | 1 | a0001c0004t0002g0189 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.6703+181C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 46/72 | chr7 | 98961655 | |||||||
chr7:98961812 | G | A | 1 | a0001c0001t0002g0249 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.6703+338G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 46/72 | chr7 | 98961812 | |||||||
chr7:98961858 | T | A | 1 | a0001c0001t0001g0141 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.6703+384T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 46/72 | chr7 | 98961858 | |||||||
chr7:98961894 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.6704-408T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 46/72 | chr7 | 98961894 | |||||||
chr7:98961957 | G | A | 1 | a0001c0001t0003g0025 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.6704-345G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 46/72 | chr7 | 98961957 | |||||||
chr7:98962056 | A | T | 6 | a0001c0001t0002g0147 a0001c0006t0002g0149 a0001c0006t0002g0150 others(3): Show |
6 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.6704-246A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 46/72 | chr7 | 98962056 | |||||||
chr7:98962454 | G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6829+27G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98962454 | |||||||
chr7:98962587 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.6829+160G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98962587 | |||||||
chr7:98962590 | T | C | 65 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(62): Show |
65 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.6829+163T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98962590 | |||||||
chr7:98962604 | T | C | 132 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(129): Show |
134 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.6829+177T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98962604 | |||||||
chr7:98962620 | C | T | 43 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(40): Show |
44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.6829+193C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98962620 | |||||||
chr7:98962655 | G | T | 1 | a0001c0002t0012g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.6829+228G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98962655 | |||||||
chr7:98962723 | C | T | 10 | a0001c0003t0002g0003 a0001c0003t0002g0198 a0001c0003t0002g0199 others(7): Show |
11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.6829+296C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98962723 | |||||||
chr7:98962811 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0051 |
2 | NA18960.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.6829+384G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98962811 | |||||||
chr7:98963008 | G | A | 122 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(119): Show |
124 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.6829+581G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963008 | |||||||
chr7:98963027 | C | G | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6829+600C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963027 | |||||||
chr7:98963176 | G | A | 12 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0093 others(9): Show |
12 | HG00621.hp1 HG02015.hp1 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.6829+749G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963176 | |||||||
chr7:98963194 | A | G | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.6829+767A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963194 | |||||||
chr7:98963201 | A | G | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.6829+774A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963201 | |||||||
chr7:98963320 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.6829+893G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963320 | |||||||
chr7:98963363 | C | A | 1 | a0001c0002t0002g0164 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.6829+936C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963363 | |||||||
chr7:98963373 | C | T | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.6829+946C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963373 | |||||||
chr7:98963424 | G | A | 1 | a0001c0002t0009g0175 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6829+997G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963424 | |||||||
chr7:98963537 | G | A | 1 | a0001c0001t0002g0147 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6830-1092G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963537 | |||||||
chr7:98963573 | C | T | 2 | a0001c0001t0002g0196 a0001c0001t0002g0197 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.6830-1056C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963573 | |||||||
chr7:98963814 | C | T | 1 | a0001c0001t0002g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.6830-815C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963814 | |||||||
chr7:98963865 | G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6830-764G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963865 | |||||||
chr7:98963908 | C | T | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.6830-721C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963908 | |||||||
chr7:98963919 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.6830-710A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963919 | |||||||
chr7:98963930 | A | G | 76 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(73): Show |
77 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.6830-699A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963930 | |||||||
chr7:98963941 | C | T | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.6830-688C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963941 | |||||||
chr7:98964080 | T | TA | 17 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0077 others(14): Show |
18 | HG00280.hp2 HG00642.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.6830-530dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | INFO_REALIGN_3_PRIME | chr7 | 98964080 | ||||||
chr7:98964080 | TA | T | 12 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0057 others(9): Show |
12 | HG01943.hp1 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.6830-530delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | INFO_REALIGN_3_PRIME | chr7 | 98964080 | ||||||
chr7:98964792 | C | T | 2 | a0001c0001t0002g0196 a0001c0001t0002g0197 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.6976+17C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 48/72 | chr7 | 98964792 | |||||||
chr7:98964898 | G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6976+123G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 48/72 | chr7 | 98964898 | |||||||
chr7:98964924 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.6976+149T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 48/72 | chr7 | 98964924 | |||||||
chr7:98964966 | T | C | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6976+191T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 48/72 | chr7 | 98964966 | |||||||
chr7:98964988 | C | T | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.6976+213C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 48/72 | chr7 | 98964988 | |||||||
chr7:98965026 | G | A | 2 | a0001c0001t0002g0196 a0001c0001t0002g0197 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.6976+251G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 48/72 | chr7 | 98965026 | |||||||
chr7:98965043 | G | C | 74 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(71): Show |
75 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.6976+268G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 48/72 | chr7 | 98965043 | |||||||
chr7:98965132 | A | G | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.6976+357A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 48/72 | chr7 | 98965132 | |||||||
chr7:98965342 | T | C | 44 | a0001c0001t0002g0147 a0001c0001t0002g0195 a0001c0001t0005g0159 others(41): Show |
45 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(42): Show |
intron_variant | MODIFIER | c.6977-354T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 48/72 | chr7 | 98965342 | |||||||
chr7:98965442 | C | G | 131 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(128): Show |
133 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.6977-254C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 48/72 | chr7 | 98965442 | |||||||
chr7:98965521 | T | C | 131 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(128): Show |
133 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.6977-175T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 48/72 | chr7 | 98965521 | |||||||
chr7:98966003 | A | G | 44 | a0001c0001t0002g0147 a0001c0001t0002g0195 a0001c0001t0005g0159 others(41): Show |
45 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(42): Show |
intron_variant | MODIFIER | c.7176+108A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 49/72 | chr7 | 98966003 | |||||||
chr7:98966025 | C | T | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.7176+130C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 49/72 | chr7 | 98966025 | |||||||
chr7:98966456 | A | G | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.7176+561A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 49/72 | chr7 | 98966456 | |||||||
chr7:98966541 | C | T | 1 | a0008c0042t0002g0184 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.7177-500C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 49/72 | chr7 | 98966541 | |||||||
chr7:98966554 | G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7177-487G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 49/72 | chr7 | 98966554 | |||||||
chr7:98966686 | GA | G | 12 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0003t0002g0003 others(9): Show |
13 | HG00544.hp2 HG01081.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.7177-343delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 49/72 | INFO_REALIGN_3_PRIME | chr7 | 98966686 | ||||||
chr7:98966924 | T | C | 1 | a0001c0001t0002g0195 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.7177-117T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 49/72 | chr7 | 98966924 | |||||||
chr7:98966974 | G | C | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.7177-67G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 49/72 | chr7 | 98966974 | |||||||
chr7:98967374 | G | A | 2 | a0001c0001t0001g0074 a0001c0045t0001g0073 |
2 | HG03710.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.7299-111G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 50/72 | chr7 | 98967374 | |||||||
chr7:98967705 | A | G | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.7512+7A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98967705 | |||||||
chr7:98967820 | C | A | 2 | a0001c0002t0007g0154 a0001c0002t0007g0156 |
2 | HG00140.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.7512+122C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98967820 | |||||||
chr7:98967923 | T | A | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.7512+225T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98967923 | |||||||
chr7:98967980 | G | A | 66 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(63): Show |
67 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.7512+282G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98967980 | |||||||
chr7:98968024 | CT | C | 67 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0031 others(64): Show |
67 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.7512+338delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | INFO_REALIGN_3_PRIME | chr7 | 98968024 | ||||||
chr7:98968316 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0111 |
3 | HG00280.hp2 HG00642.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.7512+618G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98968316 | |||||||
chr7:98968336 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.7512+638A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98968336 | |||||||
chr7:98968340 | A | G | 1 | a0001c0010t0001g0068 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.7512+642A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98968340 | |||||||
chr7:98968951 | G | C | 1 | a0001c0001t0001g0113 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.7513-1161G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98968951 | |||||||
chr7:98969006 | G | A | 32 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0164 others(29): Show |
33 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.7513-1106G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98969006 | |||||||
chr7:98969126 | C | T | 1 | a0001c0027t0001g0037 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.7513-986C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98969126 | |||||||
chr7:98969157 | G | A | 1 | a0001c0002t0002g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.7513-955G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98969157 | |||||||
chr7:98969157 | G | T | 1 | a0001c0001t0001g0015 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7513-955G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98969157 | |||||||
chr7:98969578 | G | A | 52 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(49): Show |
52 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.7513-534G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98969578 | |||||||
chr7:98969637 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.7513-475C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98969637 | |||||||
chr7:98969681 | C | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7513-431C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98969681 | |||||||
chr7:98969720 | C | T | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.7513-392C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98969720 | |||||||
chr7:98969732 | C | T | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.7513-380C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98969732 | |||||||
chr7:98970391 | G | C | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.7692+100G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98970391 | |||||||
chr7:98970394 | C | T | 55 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(52): Show |
55 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.7692+103C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98970394 | |||||||
chr7:98970597 | AT | A | 121 | a0001c0001t0001g0036 a0001c0001t0001g0240 a0001c0001t0001g0241 others(118): Show |
123 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.7692+320delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | INFO_REALIGN_3_PRIME | chr7 | 98970597 | ||||||
chr7:98970635 | C | T | 1 | a0001c0002t0002g0188 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.7692+344C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98970635 | |||||||
chr7:98970663 | C | T | 1 | a0001c0001t0011g0209 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.7692+372C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98970663 | |||||||
chr7:98970709 | C | T | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.7692+418C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98970709 | |||||||
chr7:98970739 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.7692+448C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98970739 | |||||||
chr7:98970774 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.7692+483C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98970774 | |||||||
chr7:98970782 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.7692+491C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98970782 | |||||||
chr7:98970838 | C | T | 2 | a0001c0001t0002g0208 a0001c0001t0011g0209 |
2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.7692+547C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98970838 | |||||||
chr7:98970883 | G | A | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.7692+592G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98970883 | |||||||
chr7:98970922 | T | A | 1 | a0001c0001t0001g0106 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.7692+631T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98970922 | |||||||
chr7:98971144 | C | T | 7 | a0001c0002t0002g0177 a0001c0002t0002g0178 a0001c0002t0002g0180 others(4): Show |
7 | HG01257.hp2 HG01891.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.7693-655C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98971144 | |||||||
chr7:98971210 | T | G | 6 | a0001c0002t0002g0164 a0001c0002t0002g0165 a0001c0002t0002g0166 others(3): Show |
6 | HG02809.hp2 HG02896.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.7693-589T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98971210 | |||||||
chr7:98971412 | G | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | NA18982.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.7693-387G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98971412 | |||||||
chr7:98971435 | C | T | 1 | a0001c0004t0002g0189 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.7693-364C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98971435 | |||||||
chr7:98971436 | G | A | 5 | a0001c0001t0006g0250 a0001c0001t0006g0251 a0001c0001t0006g0252 others(2): Show |
5 | HG00280.hp1 HG00642.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.7693-363G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98971436 | |||||||
chr7:98971570 | A | G | 1 | a0001c0019t0001g0112 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.7693-229A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98971570 | |||||||
chr7:98971954 | G | A | 3 | a0001c0001t0002g0212 a0001c0001t0002g0227 a0001c0001t0002g0243 |
3 | HG01099.hp2 HG01496.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.7839+9G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98971954 | |||||||
chr7:98972032 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.7839+87C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98972032 | |||||||
chr7:98972333 | G | A | 5 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0121 others(2): Show |
5 | HG00558.hp2 HG03710.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.7839+388G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98972333 | |||||||
chr7:98972432 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.7839+487T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98972432 | |||||||
chr7:98972569 | G | A | 10 | a0001c0003t0002g0003 a0001c0003t0002g0198 a0001c0003t0002g0199 others(7): Show |
11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.7839+624G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98972569 | |||||||
chr7:98972605 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.7839+660G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98972605 | |||||||
chr7:98973042 | C | G | 1 | a0001c0001t0001g0114 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.7839+1097C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98973042 | |||||||
chr7:98973260 | A | C | 82 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(79): Show |
83 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.7839+1315A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98973260 | |||||||
chr7:98973278 | C | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7839+1333C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98973278 | |||||||
chr7:98973388 | G | C | 121 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(118): Show |
123 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.7839+1443G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98973388 | |||||||
chr7:98973701 | G | A | 122 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(119): Show |
124 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.7839+1756G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98973701 | |||||||
chr7:98973965 | G | A | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.7839+2020G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98973965 | |||||||
chr7:98974004 | A | C | 18 | a0001c0001t0001g0128 a0001c0001t0001g0130 a0001c0001t0001g0131 others(15): Show |
18 | HG00738.hp1 HG01192.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.7839+2059A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98974004 | |||||||
chr7:98974092 | C | T | 2 | a0001c0001t0002g0208 a0001c0001t0011g0209 |
2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.7840-2057C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98974092 | |||||||
chr7:98974159 | A | G | 33 | a0001c0001t0002g0195 a0001c0002t0002g0016 a0001c0002t0002g0017 others(30): Show |
34 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.7840-1990A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98974159 | |||||||
chr7:98974211 | T | A | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.7840-1938T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98974211 | |||||||
chr7:98974558 | C | G | 1 | a0001c0001t0001g0052 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.7840-1591C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98974558 | |||||||
chr7:98974885 | A | AT | 64 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0019 others(61): Show |
65 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.7840-1258dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | INFO_REALIGN_3_PRIME | chr7 | 98974885 | ||||||
chr7:98975030 | A | G | 132 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(129): Show |
134 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.7840-1119A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98975030 | |||||||
chr7:98975098 | G | A | 1 | a0001c0027t0001g0037 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.7840-1051G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98975098 | |||||||
chr7:98975389 | G | A | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.7840-760G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98975389 | |||||||
chr7:98975600 | C | T | 25 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0164 others(22): Show |
26 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.7840-549C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98975600 | |||||||
chr7:98975601 | G | C | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.7840-548G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98975601 | |||||||
chr7:98975672 | C | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0019 others(63): Show |
67 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.7840-477C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98975672 | |||||||
chr7:98975749 | A | G | 6 | a0001c0001t0001g0069 a0001c0001t0001g0080 a0001c0001t0001g0086 others(3): Show |
6 | HG00140.hp1 HG01099.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.7840-400A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98975749 | |||||||
chr7:98975755 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.7840-394G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98975755 | |||||||
chr7:98975937 | G | C | 7 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(4): Show |
7 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.7840-212G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98975937 | |||||||
chr7:98976008 | G | T | 11 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(8): Show |
11 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.7840-141G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98976008 | |||||||
chr7:98976065 | C | G | 2 | a0001c0001t0001g0059 a0001c0001t0001g0062 |
2 | NA19054.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.7840-84C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98976065 | |||||||
chr7:98976106 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.7840-43C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98976106 | |||||||
chr7:98976370 | G | A | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.7959+102G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 54/72 | chr7 | 98976370 | |||||||
chr7:98976374 | C | T | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.7959+106C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 54/72 | chr7 | 98976374 | |||||||
chr7:98976375 | G | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7959+107G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 54/72 | chr7 | 98976375 | |||||||
chr7:98976877 | T | C | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.8248-62T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 55/72 | chr7 | 98976877 | |||||||
chr7:98976888 | GA | G | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.8248-44delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 55/72 | INFO_REALIGN_3_PRIME | chr7 | 98976888 | ||||||
chr7:98977087 | G | A | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.8385+11G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977087 | |||||||
chr7:98977146 | T | C | 1 | a0001c0001t0002g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.8385+70T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977146 | |||||||
chr7:98977185 | G | A | 1 | a0001c0019t0001g0112 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.8385+109G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977185 | |||||||
chr7:98977207 | C | G | 131 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(128): Show |
133 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.8385+131C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977207 | |||||||
chr7:98977224 | C | T | 1 | a0001c0001t0003g0028 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.8385+148C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977224 | |||||||
chr7:98977243 | C | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0075 |
2 | NA18957.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.8385+167C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977243 | |||||||
chr7:98977320 | C | T | 59 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(56): Show |
59 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.8385+244C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977320 | |||||||
chr7:98977434 | C | T | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.8385+358C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977434 | |||||||
chr7:98977504 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01167.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.8385+428G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977504 | |||||||
chr7:98977623 | G | A | 4 | a0001c0001t0001g0047 a0001c0001t0001g0051 a0001c0001t0001g0055 others(1): Show |
4 | HG02683.hp1 HG02683.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.8385+547G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977623 | |||||||
chr7:98977691 | A | C | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.8386-520A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977691 | |||||||
chr7:98977714 | A | T | 1 | a0001c0001t0001g0090 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.8386-497A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977714 | |||||||
chr7:98977750 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.8386-461C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977750 | |||||||
chr7:98977781 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0046 |
2 | HG01346.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.8386-430C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977781 | |||||||
chr7:98977793 | C | T | 1 | a0001c0006t0002g0151 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.8386-418C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977793 | |||||||
chr7:98977860 | G | C | 1 | a0001c0001t0002g0211 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.8386-351G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977860 | |||||||
chr7:98978351 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.8498+28G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 57/72 | chr7 | 98978351 | |||||||
chr7:98978620 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.8499-149G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 57/72 | chr7 | 98978620 | |||||||
chr7:98978994 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.8634+90C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98978994 | |||||||
chr7:98979121 | T | C | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.8634+217T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98979121 | |||||||
chr7:98979210 | C | T | 13 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0164 others(10): Show |
13 | HG01243.hp1 HG01884.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.8634+306C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98979210 | |||||||
chr7:98979418 | A | G | 3 | a0001c0004t0002g0183 a0001c0004t0002g0185 a0008c0042t0002g0184 |
3 | HG02622.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.8634+514A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98979418 | |||||||
chr7:98980356 | A | G | 2 | a0001c0002t0002g0187 a0001c0044t0002g0186 |
2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.8635-1413A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98980356 | |||||||
chr7:98980388 | C | CAA | 130 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(127): Show |
132 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.8635-1380_8635-137 others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | INFO_REALIGN_3_PRIME | chr7 | 98980388 | ||||||
chr7:98980491 | CA | C | 119 | a0001c0001t0001g0039 a0001c0001t0001g0240 a0001c0001t0001g0241 others(116): Show |
121 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.8635-1268delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | INFO_REALIGN_3_PRIME | chr7 | 98980491 | ||||||
chr7:98980571 | A | G | 10 | a0001c0003t0002g0003 a0001c0003t0002g0198 a0001c0003t0002g0199 others(7): Show |
11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.8635-1198A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98980571 | |||||||
chr7:98980574 | G | A | 2 | a0001c0001t0002g0208 a0001c0001t0011g0209 |
2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.8635-1195G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98980574 | |||||||
chr7:98980594 | G | A | 1 | a0001c0001t0002g0011 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.8635-1175G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98980594 | |||||||
chr7:98980625 | A | G | 2 | a0001c0001t0005g0159 a0014c0032t0005g0161 |
2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.8635-1144A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98980625 | |||||||
chr7:98981310 | G | T | 53 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(50): Show |
54 | HG00140.hp2 HG01081.hp1 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.8635-459G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98981310 | |||||||
chr7:98981379 | G | A | 5 | a0001c0001t0006g0250 a0001c0001t0006g0251 a0001c0001t0006g0252 others(2): Show |
5 | HG00280.hp1 HG00642.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.8635-390G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98981379 | |||||||
chr7:98981397 | G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.8635-372G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98981397 | |||||||
chr7:98981412 | T | C | 1 | a0001c0004t0002g0189 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.8635-357T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98981412 | |||||||
chr7:98981416 | A | G | 1 | a0001c0004t0002g0189 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.8635-353A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98981416 | |||||||
chr7:98981696 | T | G | 5 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 others(2): Show |
5 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.8635-73T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98981696 | |||||||
chr7:98981740 | C | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.8635-29C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98981740 | |||||||
chr7:98982147 | G | A | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.8826+187G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 59/72 | chr7 | 98982147 | |||||||
chr7:98982296 | A | G | 11 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0002g0223 others(8): Show |
11 | HG01099.hp2 HG01496.hp1 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.8826+336A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 59/72 | chr7 | 98982296 | |||||||
chr7:98982496 | C | G | 3 | a0001c0001t0002g0208 a0001c0001t0011g0209 a0001c0028t0002g0207 |
3 | HG02486.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.8826+536C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 59/72 | chr7 | 98982496 | |||||||
chr7:98982529 | T | C | 67 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(64): Show |
67 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.8826+569T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 59/72 | chr7 | 98982529 | |||||||
chr7:98982616 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.8827-648A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 59/72 | chr7 | 98982616 | |||||||
chr7:98982630 | C | A | 1 | a0001c0001t0001g0050 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.8827-634C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 59/72 | chr7 | 98982630 | |||||||
chr7:98982647 | G | A | 2 | a0001c0002t0002g0180 a0001c0002t0002g0255 |
2 | HG01257.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.8827-617G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 59/72 | chr7 | 98982647 | |||||||
chr7:98983038 | A | G | 123 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(120): Show |
125 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.8827-226A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 59/72 | chr7 | 98983038 | |||||||
chr7:98983144 | C | A | 1 | a0001c0001t0001g0241 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.8827-120C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 59/72 | chr7 | 98983144 | |||||||
chr7:98983189 | A | G | 5 | a0001c0001t0006g0250 a0001c0001t0006g0251 a0001c0001t0006g0252 others(2): Show |
5 | HG00280.hp1 HG00642.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.8827-75A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 59/72 | chr7 | 98983189 | |||||||
chr7:98983234 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.8827-30C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 59/72 | chr7 | 98983234 | |||||||
chr7:98983555 | G | T | 1 | a0001c0001t0001g0117 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.9022+96G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 60/72 | chr7 | 98983555 | |||||||
chr7:98983564 | T | C | 1 | a0001c0002t0002g0188 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.9022+105T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 60/72 | chr7 | 98983564 | |||||||
chr7:98983570 | A | C | 1 | a0001c0001t0002g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.9022+111A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 60/72 | chr7 | 98983570 | |||||||
chr7:98983572 | G | T | 52 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(49): Show |
52 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.9022+113G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 60/72 | chr7 | 98983572 | |||||||
chr7:98983716 | G | A | 5 | a0001c0004t0002g0002 a0001c0004t0002g0168 a0001c0004t0002g0169 others(2): Show |
6 | HG02257.hp1 HG02647.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.9022+257G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 60/72 | chr7 | 98983716 | |||||||
chr7:98983790 | C | T | 1 | a0001c0002t0012g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.9023-303C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 60/72 | chr7 | 98983790 | |||||||
chr7:98983810 | C | G | 1 | a0001c0001t0003g0028 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.9023-283C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 60/72 | chr7 | 98983810 | |||||||
chr7:98983889 | C | A | 3 | a0001c0001t0001g0039 a0001c0001t0001g0045 a0001c0001t0001g0046 |
3 | HG01346.hp2 HG01515.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.9023-204C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 60/72 | chr7 | 98983889 | |||||||
chr7:98983960 | C | T | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.9023-133C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 60/72 | chr7 | 98983960 | |||||||
chr7:98983996 | CAT | C | 7 | a0001c0001t0001g0076 a0001c0005t0004g0004 a0001c0005t0004g0005 others(4): Show |
7 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.9023-96_9023-95del others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 60/72 | chr7 | 98983996 | |||||||
chr7:98984618 | A | C | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.9288+260A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 61/72 | chr7 | 98984618 | |||||||
chr7:98984667 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.9289-277A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 61/72 | chr7 | 98984667 | |||||||
chr7:98984803 | C | A | 1 | a0001c0002t0002g0188 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.9289-141C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 61/72 | chr7 | 98984803 | |||||||
chr7:98985053 | G | A | 1 | a0001c0006t0002g0151 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.9389+9G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98985053 | |||||||
chr7:98985189 | C | T | 1 | a0001c0027t0001g0037 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.9389+145C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98985189 | |||||||
chr7:98985219 | T | G | 3 | a0001c0001t0002g0195 a0001c0001t0002g0196 a0001c0001t0002g0197 |
3 | HG02258.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.9389+175T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98985219 | |||||||
chr7:98985445 | A | G | 1 | a0001c0002t0007g0156 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.9389+401A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98985445 | |||||||
chr7:98985525 | C | T | 129 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(126): Show |
131 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.9389+481C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98985525 | |||||||
chr7:98985537 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.9389+493A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98985537 | |||||||
chr7:98985607 | G | A | 3 | a0001c0001t0006g0250 a0001c0001t0006g0251 a0001c0001t0006g0252 |
3 | HG00280.hp1 HG01106.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.9389+563G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98985607 | |||||||
chr7:98985623 | T | C | 43 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(40): Show |
44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.9389+579T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98985623 | |||||||
chr7:98985709 | T | C | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.9389+665T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98985709 | |||||||
chr7:98985759 | A | C | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.9389+715A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98985759 | |||||||
chr7:98985899 | T | C | 44 | a0001c0001t0002g0147 a0001c0001t0002g0195 a0001c0001t0005g0159 others(41): Show |
45 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(42): Show |
intron_variant | MODIFIER | c.9389+855T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98985899 | |||||||
chr7:98985954 | C | G | 1 | a0001c0001t0001g0031 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.9389+910C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98985954 | |||||||
chr7:98986006 | C | T | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.9389+962C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98986006 | |||||||
chr7:98986075 | A | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.9389+1031A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98986075 | |||||||
chr7:98986168 | A | C | 44 | a0001c0001t0002g0147 a0001c0001t0002g0195 a0001c0001t0005g0159 others(41): Show |
45 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(42): Show |
intron_variant | MODIFIER | c.9389+1124A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98986168 | |||||||
chr7:98986182 | T | TG | 43 | a0001c0001t0002g0147 a0001c0001t0002g0195 a0001c0001t0005g0159 others(40): Show |
44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.9389+1139dupG | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | INFO_REALIGN_3_PRIME | chr7 | 98986182 | ||||||
chr7:98986558 | G | C | 1 | a0001c0002t0002g0188 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.9389+1514G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98986558 | |||||||
chr7:98986640 | G | A | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.9389+1596G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98986640 | |||||||
chr7:98986752 | G | A | 122 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(119): Show |
124 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.9389+1708G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98986752 | |||||||
chr7:98986849 | C | A | 1 | a0001c0001t0005g0162 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.9389+1805C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98986849 | |||||||
chr7:98986885 | G | T | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.9389+1841G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98986885 | |||||||
chr7:98986953 | T | G | 122 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(119): Show |
123 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.9390-1812T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98986953 | |||||||
chr7:98987041 | T | G | 11 | a0001c0002t0002g0187 a0001c0004t0002g0002 a0001c0004t0002g0168 others(8): Show |
12 | HG01081.hp1 HG02257.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.9390-1724T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98987041 | |||||||
chr7:98987197 | C | G | 1 | a0001c0001t0001g0140 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.9390-1568C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98987197 | |||||||
chr7:98987487 | T | A | 65 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(62): Show |
65 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.9390-1278T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98987487 | |||||||
chr7:98987522 | G | C | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.9390-1243G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98987522 | |||||||
chr7:98987529 | G | T | 43 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(40): Show |
44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.9390-1236G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98987529 | |||||||
chr7:98987692 | G | T | 1 | a0001c0001t0001g0127 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.9390-1073G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98987692 | |||||||
chr7:98987809 | T | C | 1 | a0001c0022t0001g0124 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.9390-956T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98987809 | |||||||
chr7:98988143 | C | T | 1 | a0001c0018t0002g0245 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.9390-622C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98988143 | |||||||
chr7:98988150 | T | A | 2 | a0001c0002t0002g0180 a0001c0002t0002g0255 |
2 | HG01257.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.9390-615T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98988150 | |||||||
chr7:98988561 | A | G | 2 | a0001c0011t0013g0190 a0001c0033t0001g0020 |
2 | HG03098.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.9390-204A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98988561 | |||||||
chr7:98988596 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.9390-169G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98988596 | |||||||
chr7:98988724 | A | G | 10 | a0001c0003t0002g0003 a0001c0003t0002g0198 a0001c0003t0002g0199 others(7): Show |
11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.9390-41A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98988724 | |||||||
chr7:98988969 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG00408.hp2 | splice_region_variant&intron_variant | LOW | c.9591+3G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98988969 | |||||||
chr7:98989056 | G | A | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.9591+90G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98989056 | |||||||
chr7:98989137 | G | A | 3 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0003g0028 |
3 | HG00438.hp1 HG00544.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.9591+171G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98989137 | |||||||
chr7:98989157 | A | G | 3 | a0001c0001t0002g0208 a0001c0001t0011g0209 a0001c0028t0002g0207 |
3 | HG02486.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.9591+191A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98989157 | |||||||
chr7:98989285 | C | G | 5 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0057 others(2): Show |
5 | HG02523.hp1 NA18969.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.9591+319C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98989285 | |||||||
chr7:98989321 | T | C | 132 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(129): Show |
134 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.9591+355T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98989321 | |||||||
chr7:98989329 | AC | A | 5 | a0001c0002t0002g0164 a0001c0002t0002g0165 a0001c0002t0002g0181 others(2): Show |
5 | HG02809.hp2 HG02896.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.9591+364delC | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98989329 | |||||||
chr7:98989420 | C | T | 1 | a0001c0001t0003g0030 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.9591+454C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98989420 | |||||||
chr7:98989499 | A | G | 1 | a0008c0042t0002g0184 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.9591+533A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98989499 | |||||||
chr7:98989666 | C | T | 61 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(58): Show |
61 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.9591+700C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98989666 | |||||||
chr7:98989672 | T | C | 132 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(129): Show |
134 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.9591+706T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98989672 | |||||||
chr7:98990196 | C | T | 1 | a0001c0001t0002g0249 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.9592-259C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98990196 | |||||||
chr7:98990330 | A | G | 1 | a0001c0001t0002g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.9592-125A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98990330 | |||||||
chr7:98990364 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.9592-91T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98990364 | |||||||
chr7:98990367 | A | G | 62 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(59): Show |
62 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.9592-88A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98990367 | |||||||
chr7:98990633 | G | T | 2 | a0001c0001t0001g0119 a0001c0033t0001g0020 |
2 | HG03239.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.9756+14G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 64/72 | chr7 | 98990633 | |||||||
chr7:98990677 | G | A | 4 | a0001c0006t0002g0149 a0001c0006t0002g0150 a0001c0006t0002g0152 others(1): Show |
4 | HG02559.hp1 HG02647.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.9756+58G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 64/72 | chr7 | 98990677 | |||||||
chr7:98990779 | A | G | 77 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(74): Show |
78 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.9756+160A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 64/72 | chr7 | 98990779 | |||||||
chr7:98991054 | G | A | 1 | a0001c0001t0003g0028 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.9756+435G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 64/72 | chr7 | 98991054 | |||||||
chr7:98991068 | A | G | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.9756+449A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 64/72 | chr7 | 98991068 | |||||||
chr7:98991188 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0086 |
2 | HG01099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.9756+569C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 64/72 | chr7 | 98991188 | |||||||
chr7:98991190 | C | T | 10 | a0001c0003t0002g0003 a0001c0003t0002g0198 a0001c0003t0002g0199 others(7): Show |
11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.9756+571C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 64/72 | chr7 | 98991190 | |||||||
chr7:98991378 | C | T | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.9756+759C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 64/72 | chr7 | 98991378 | |||||||
chr7:98991407 | C | T | 2 | a0001c0001t0002g0196 a0001c0001t0002g0197 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.9757-730C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 64/72 | chr7 | 98991407 | |||||||
chr7:98991491 | G | A | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.9757-646G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 64/72 | chr7 | 98991491 | |||||||
chr7:98992236 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.9847+9C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98992236 | |||||||
chr7:98992306 | G | A | 10 | a0001c0003t0002g0003 a0001c0003t0002g0198 a0001c0003t0002g0199 others(7): Show |
11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.9847+79G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98992306 | |||||||
chr7:98992321 | C | G | 1 | a0001c0001t0002g0233 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.9847+94C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98992321 | |||||||
chr7:98992428 | A | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0019 others(186): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.9847+201A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98992428 | |||||||
chr7:98992443 | G | A | 2 | a0001c0017t0001g0116 a0001c0030t0001g0014 |
2 | HG00621.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.9847+216G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98992443 | |||||||
chr7:98992477 | A | C | 1 | a0001c0001t0002g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.9847+250A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98992477 | |||||||
chr7:98992495 | A | G | 1 | a0001c0004t0002g0189 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.9847+268A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98992495 | |||||||
chr7:98992560 | C | CAT | 24 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0166 others(21): Show |
25 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.9847+333_9847+334i others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98992560 | |||||||
chr7:98992560 | C | CGT | 19 | a0001c0001t0001g0038 a0001c0001t0001g0069 a0001c0001t0001g0074 others(16): Show |
19 | HG00140.hp1 HG00544.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.9847+360_9847+361d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | INFO_REALIGN_3_PRIME | chr7 | 98992560 | ||||||
chr7:98992560 | C | CGTGT | 3 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0133 |
3 | HG01192.hp1 HG03017.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.9847+358_9847+361d others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | INFO_REALIGN_3_PRIME | chr7 | 98992560 | ||||||
chr7:98992560 | C | CGTGTGT | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.9847+356_9847+361d others(8): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | INFO_REALIGN_3_PRIME | chr7 | 98992560 | ||||||
chr7:98992560 | C | CGTGTGTG others(13): Show |
1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.9847+342_9847+361d others(22): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | INFO_REALIGN_3_PRIME | chr7 | 98992560 | ||||||
chr7:98992560 | CGT | C | 65 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0258 others(62): Show |
66 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.9847+360_9847+361d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | INFO_REALIGN_3_PRIME | chr7 | 98992560 | ||||||
chr7:98992561 | G | A | 11 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(8): Show |
11 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.9847+334G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98992561 | |||||||
chr7:98992587 | GTT | G | 11 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(8): Show |
11 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.9847+362_9847+363d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | INFO_REALIGN_3_PRIME | chr7 | 98992587 | ||||||
chr7:98992828 | C | T | 4 | a0001c0004t0002g0183 a0001c0004t0002g0185 a0001c0004t0002g0189 others(1): Show |
4 | HG02622.hp2 HG02886.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.9847+601C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98992828 | |||||||
chr7:98993216 | G | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.9848-322G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98993216 | |||||||
chr7:98993229 | G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.9848-309G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98993229 | |||||||
chr7:98993255 | G | A | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.9848-283G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98993255 | |||||||
chr7:98993373 | C | T | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.9848-165C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98993373 | |||||||
chr7:98993457 | G | C | 3 | a0001c0001t0002g0208 a0001c0001t0011g0209 a0001c0028t0002g0207 |
3 | HG02486.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.9848-81G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98993457 | |||||||
chr7:98993497 | C | T | 3 | a0001c0005t0004g0007 a0001c0005t0004g0008 a0001c0005t0004g0009 |
3 | HG02630.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.9848-41C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98993497 | |||||||
chr7:98994002 | A | G | 1 | a0001c0001t0002g0147 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.10047+265A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 66/72 | chr7 | 98994002 | |||||||
chr7:98994076 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.10047+339G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 66/72 | chr7 | 98994076 | |||||||
chr7:98994099 | G | T | 1 | a0001c0002t0012g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.10047+362G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 66/72 | chr7 | 98994099 | |||||||
chr7:98994257 | G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.10048-330G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 66/72 | chr7 | 98994257 | |||||||
chr7:98994312 | G | A | 2 | a0001c0001t0002g0196 a0001c0001t0002g0197 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.10048-275G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 66/72 | chr7 | 98994312 | |||||||
chr7:98994374 | A | G | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.10048-213A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 66/72 | chr7 | 98994374 | |||||||
chr7:98994398 | C | A | 1 | a0001c0001t0001g0241 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10048-189C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 66/72 | chr7 | 98994398 | |||||||
chr7:98994420 | G | A | 1 | a0001c0001t0001g0241 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10048-167G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 66/72 | chr7 | 98994420 | |||||||
chr7:98994471 | C | T | 2 | a0001c0001t0002g0208 a0001c0001t0011g0209 |
2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.10048-116C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 66/72 | chr7 | 98994471 | |||||||
chr7:98994519 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.10048-68C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 66/72 | chr7 | 98994519 | |||||||
chr7:98994530 | G | C | 1 | a0001c0001t0001g0031 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.10048-57G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 66/72 | chr7 | 98994530 | |||||||
chr7:98995188 | A | C | 44 | a0001c0001t0002g0147 a0001c0001t0002g0195 a0001c0001t0005g0159 others(41): Show |
45 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(42): Show |
intron_variant | MODIFIER | c.10309+340A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98995188 | |||||||
chr7:98995269 | C | T | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.10309+421C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98995269 | |||||||
chr7:98995323 | C | T | 1 | a0001c0012t0001g0110 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.10309+475C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98995323 | |||||||
chr7:98995324 | G | A | 66 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(63): Show |
67 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.10309+476G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98995324 | |||||||
chr7:98995574 | G | T | 51 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(48): Show |
51 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.10309+726G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98995574 | |||||||
chr7:98995812 | C | T | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.10309+964C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98995812 | |||||||
chr7:98995869 | ATGTCCCA others(13): Show |
A | 43 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(40): Show |
44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.10309+1031_10309+1 others(26): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98995869 | ||||||
chr7:98995953 | A | G | 43 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(40): Show |
44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.10309+1105A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98995953 | |||||||
chr7:98995995 | A | T | 13 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0164 others(10): Show |
13 | HG01243.hp1 HG01884.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.10309+1147A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98995995 | |||||||
chr7:98996057 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.10309+1209C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98996057 | |||||||
chr7:98996109 | C | T | 10 | a0001c0003t0002g0003 a0001c0003t0002g0198 a0001c0003t0002g0199 others(7): Show |
11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.10309+1261C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98996109 | |||||||
chr7:98996169 | TC | T | 3 | a0001c0001t0002g0195 a0001c0001t0002g0196 a0001c0001t0002g0197 |
3 | HG02258.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.10309+1325delC | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98996169 | ||||||
chr7:98996174 | G | A | 5 | a0001c0001t0001g0128 a0001c0001t0001g0139 a0001c0001t0001g0140 others(2): Show |
5 | NA18966.hp2 NA18970.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.10309+1326G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98996174 | |||||||
chr7:98996696 | C | T | 10 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0002g0223 others(7): Show |
10 | HG01099.hp2 HG01496.hp1 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.10309+1848C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98996696 | |||||||
chr7:98996843 | G | T | 1 | a0001c0001t0001g0053 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.10309+1995G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98996843 | |||||||
chr7:98996866 | C | G | 2 | a0001c0005t0004g0008 a0001c0005t0004g0009 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.10309+2018C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98996866 | |||||||
chr7:98996904 | A | C | 1 | a0001c0002t0002g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.10309+2056A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98996904 | |||||||
chr7:98996955 | A | G | 2 | a0001c0001t0002g0228 a0001c0001t0002g0231 |
2 | HG00741.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.10309+2107A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98996955 | |||||||
chr7:98997017 | A | G | 1 | a0001c0001t0003g0028 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.10309+2169A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98997017 | |||||||
chr7:98997080 | C | T | 7 | a0001c0001t0001g0057 a0001c0005t0004g0004 a0001c0005t0004g0005 others(4): Show |
7 | HG02523.hp1 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.10309+2232C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98997080 | |||||||
chr7:98997122 | A | G | 15 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0164 others(12): Show |
15 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.10309+2274A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98997122 | |||||||
chr7:98997147 | A | C | 67 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(64): Show |
68 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.10309+2299A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98997147 | |||||||
chr7:98997179 | G | A | 4 | a0001c0001t0001g0094 a0001c0002t0002g0182 a0002c0008t0008g0192 others(1): Show |
4 | HG02559.hp2 HG02895.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.10309+2331G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98997179 | |||||||
chr7:98997221 | G | A | 122 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(119): Show |
124 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.10309+2373G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98997221 | |||||||
chr7:98997483 | C | CA | 23 | a0001c0001t0001g0015 a0001c0001t0001g0036 a0001c0001t0001g0039 others(20): Show |
23 | HG00438.hp1 HG00621.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.10309+2664dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98997483 | ||||||
chr7:98997483 | C | CAA | 7 | a0001c0001t0001g0042 a0001c0001t0001g0053 a0001c0001t0001g0056 others(4): Show |
7 | HG00741.hp1 HG01358.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.10309+2663_10309+2 others(8): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98997483 | ||||||
chr7:98997483 | C | CAAAAAAA | 21 | a0001c0001t0001g0241 a0001c0001t0001g0257 a0001c0001t0001g0258 others(18): Show |
21 | HG00558.hp1 HG00642.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.10309+2658_10309+2 others(13): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98997483 | ||||||
chr7:98997483 | C | CAAAAAAA others(1): Show |
16 | a0001c0001t0001g0240 a0001c0001t0002g0211 a0001c0001t0002g0212 others(13): Show |
16 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.10309+2657_10309+2 others(14): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98997483 | ||||||
chr7:98997483 | C | CAAAAAAA others(2): Show |
7 | a0001c0001t0002g0220 a0001c0001t0002g0232 a0001c0001t0002g0244 others(4): Show |
7 | HG01106.hp1 HG02148.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.10309+2656_10309+2 others(15): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98997483 | ||||||
chr7:98997483 | C | CAAAAAAA others(3): Show |
3 | a0001c0001t0002g0221 a0003c0037t0002g0242 a0013c0035t0002g0224 |
3 | HG00438.hp2 NA19009.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.10309+2655_10309+2 others(16): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98997483 | ||||||
chr7:98997483 | C | CAAAAAAA others(4): Show |
3 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0031t0002g0226 |
3 | NA18966.hp1 NA18978.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.10309+2654_10309+2 others(17): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98997483 | ||||||
chr7:98997483 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0002g0011 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.10309+2652_10309+2 others(19): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98997483 | ||||||
chr7:98997483 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0002g0010 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.10309+2651_10309+2 others(20): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98997483 | ||||||
chr7:98997483 | CA | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0019 others(76): Show |
81 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.10309+2664delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98997483 | ||||||
chr7:98997483 | CAA | C | 7 | a0001c0001t0001g0078 a0001c0001t0001g0096 a0001c0001t0003g0030 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.10309+2663_10309+2 others(8): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98997483 | ||||||
chr7:98997483 | CAAAAAAA others(2): Show |
C | 11 | a0001c0001t0002g0147 a0001c0003t0002g0003 a0001c0003t0002g0198 others(8): Show |
12 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.10309+2656_10309+2 others(15): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98997483 | ||||||
chr7:98997483 | CAAAAAAA others(3): Show |
C | 1 | a0002c0008t0008g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.10309+2655_10309+2 others(16): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98997483 | ||||||
chr7:98997483 | CAAAAAAA others(4): Show |
C | 2 | a0001c0021t0001g0129 a0001c0038t0001g0034 |
2 | HG02055.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.10309+2654_10309+2 others(17): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98997483 | ||||||
chr7:98997641 | G | C | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.10309+2793G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98997641 | |||||||
chr7:98997795 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.10309+2947G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98997795 | |||||||
chr7:98997836 | T | G | 131 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(128): Show |
133 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.10309+2988T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98997836 | |||||||
chr7:98997995 | G | A | 5 | a0001c0001t0005g0159 a0001c0001t0005g0160 a0001c0001t0005g0162 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.10309+3147G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98997995 | |||||||
chr7:98998089 | A | G | 3 | a0001c0001t0001g0082 a0002c0008t0008g0192 a0002c0008t0008g0193 |
3 | HG02559.hp2 HG02615.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.10309+3241A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98998089 | |||||||
chr7:98998307 | G | A | 67 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(64): Show |
68 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.10309+3459G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98998307 | |||||||
chr7:98998484 | G | A | 56 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0162 others(53): Show |
57 | HG00140.hp2 HG01081.hp1 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.10309+3636G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98998484 | |||||||
chr7:98998503 | A | G | 3 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0046 |
3 | HG01346.hp2 HG02145.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.10309+3655A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98998503 | |||||||
chr7:98998532 | A | C | 1 | a0001c0001t0001g0141 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.10309+3684A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98998532 | |||||||
chr7:98998564 | C | G | 1 | a0001c0001t0011g0209 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.10309+3716C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98998564 | |||||||
chr7:98998601 | C | T | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.10309+3753C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98998601 | |||||||
chr7:98998659 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.10309+3811G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98998659 | |||||||
chr7:98998700 | A | G | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.10309+3852A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98998700 | |||||||
chr7:98998762 | C | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0099 |
2 | HG00621.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.10309+3914C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98998762 | |||||||
chr7:98998763 | C | A | 2 | a0001c0001t0001g0074 a0001c0045t0001g0073 |
2 | HG03710.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.10309+3915C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98998763 | |||||||
chr7:98998785 | G | A | 121 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(118): Show |
123 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.10309+3937G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98998785 | |||||||
chr7:98998800 | C | T | 3 | a0001c0001t0002g0195 a0001c0001t0002g0196 a0001c0001t0002g0197 |
3 | HG02258.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.10309+3952C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98998800 | |||||||
chr7:98998905 | G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.10309+4057G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98998905 | |||||||
chr7:98999071 | A | T | 1 | a0001c0001t0001g0117 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.10309+4223A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98999071 | |||||||
chr7:98999115 | A | G | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.10309+4267A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98999115 | |||||||
chr7:98999166 | C | T | 1 | a0001c0002t0009g0175 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.10309+4318C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98999166 | |||||||
chr7:98999257 | G | A | 1 | a0001c0004t0002g0183 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.10309+4409G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98999257 | |||||||
chr7:98999516 | G | A | 66 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(63): Show |
67 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.10309+4668G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98999516 | |||||||
chr7:98999676 | G | T | 1 | a0001c0022t0001g0124 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.10310-4514G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98999676 | |||||||
chr7:98999801 | T | G | 1 | a0001c0004t0002g0176 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.10310-4389T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98999801 | |||||||
chr7:98999829 | C | T | 5 | a0001c0004t0002g0002 a0001c0004t0002g0168 a0001c0004t0002g0169 others(2): Show |
6 | HG02257.hp1 HG02647.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.10310-4361C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98999829 | |||||||
chr7:98999963 | A | C | 1 | a0008c0042t0002g0184 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.10310-4227A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98999963 | |||||||
chr7:99000001 | G | GTTTA | 43 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(40): Show |
44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.10310-4169_10310-4 others(10): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 99000001 | ||||||
chr7:99000084 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.10310-4106C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99000084 | |||||||
chr7:99000133 | G | C | 43 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(40): Show |
44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.10310-4057G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99000133 | |||||||
chr7:99000382 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.10310-3808C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99000382 | |||||||
chr7:99000566 | C | T | 1 | a0001c0001t0002g0214 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.10310-3624C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99000566 | |||||||
chr7:99000858 | C | T | 10 | a0001c0003t0002g0003 a0001c0003t0002g0198 a0001c0003t0002g0199 others(7): Show |
11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.10310-3332C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99000858 | |||||||
chr7:99000901 | C | G | 1 | a0009c0029t0001g0018 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.10310-3289C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99000901 | |||||||
chr7:99000994 | A | T | 2 | a0001c0007t0001g0081 a0001c0007t0001g0105 |
2 | HG01891.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.10310-3196A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99000994 | |||||||
chr7:99000995 | A | T | 2 | a0001c0007t0001g0081 a0001c0007t0001g0105 |
2 | HG01891.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.10310-3195A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99000995 | |||||||
chr7:99001003 | A | C | 1 | a0014c0032t0005g0161 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.10310-3187A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99001003 | |||||||
chr7:99001017 | C | T | 129 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(126): Show |
131 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.10310-3173C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99001017 | |||||||
chr7:99001273 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.10310-2917C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99001273 | |||||||
chr7:99001516 | G | C | 2 | a0001c0003t0002g0003 a0001c0003t0002g0201 |
3 | HG01081.hp2 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.10310-2674G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99001516 | |||||||
chr7:99001535 | T | TA | 32 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0164 others(29): Show |
33 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.10310-2646dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 99001535 | ||||||
chr7:99001805 | A | T | 1 | a0001c0002t0002g0178 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.10310-2385A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99001805 | |||||||
chr7:99001911 | C | T | 128 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(125): Show |
130 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.10310-2279C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99001911 | |||||||
chr7:99001976 | A | G | 1 | a0001c0001t0002g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.10310-2214A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99001976 | |||||||
chr7:99002135 | TGGTGGGG others(3): Show |
T | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.10310-2049_10310-2 others(16): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 99002135 | ||||||
chr7:99002527 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.10310-1663C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99002527 | |||||||
chr7:99002607 | T | C | 10 | a0001c0003t0002g0003 a0001c0003t0002g0198 a0001c0003t0002g0199 others(7): Show |
11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.10310-1583T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99002607 | |||||||
chr7:99002639 | G | C | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.10310-1551G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99002639 | |||||||
chr7:99002731 | A | C | 2 | a0001c0001t0001g0040 a0001c0001t0001g0133 |
2 | HG01192.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.10310-1459A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99002731 | |||||||
chr7:99002836 | T | C | 1 | a0001c0025t0001g0118 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.10310-1354T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99002836 | |||||||
chr7:99002847 | C | T | 1 | a0001c0001t0006g0251 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.10310-1343C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99002847 | |||||||
chr7:99002850 | G | A | 2 | a0001c0002t0002g0016 a0001c0002t0002g0017 |
2 | HG01884.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.10310-1340G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99002850 | |||||||
chr7:99002927 | C | A | 1 | a0001c0001t0001g0039 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.10310-1263C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99002927 | |||||||
chr7:99002938 | T | G | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.10310-1252T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99002938 | |||||||
chr7:99002999 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.10310-1191C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99002999 | |||||||
chr7:99003055 | T | C | 2 | a0001c0001t0001g0085 a0001c0001t0001g0102 |
2 | NA18982.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.10310-1135T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003055 | |||||||
chr7:99003104 | C | G | 1 | a0001c0002t0002g0174 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.10310-1086C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003104 | |||||||
chr7:99003208 | G | T | 1 | a0001c0001t0001g0115 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.10310-982G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003208 | |||||||
chr7:99003216 | C | G | 75 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(72): Show |
76 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.10310-974C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003216 | |||||||
chr7:99003402 | T | C | 57 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(54): Show |
57 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.10310-788T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003402 | |||||||
chr7:99003429 | A | G | 4 | a0001c0001t0005g0159 a0001c0001t0005g0160 a0001c0001t0005g0162 others(1): Show |
4 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.10310-761A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003429 | |||||||
chr7:99003621 | T | C | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.10310-569T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003621 | |||||||
chr7:99003697 | C | T | 1 | a0001c0045t0001g0073 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.10310-493C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003697 | |||||||
chr7:99003782 | G | A | 3 | a0001c0001t0006g0250 a0001c0001t0006g0251 a0001c0001t0006g0252 |
3 | HG00280.hp1 HG01106.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.10310-408G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003782 | |||||||
chr7:99003821 | T | C | 1 | a0001c0001t0002g0147 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.10310-369T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003821 | |||||||
chr7:99003854 | G | A | 2 | a0001c0002t0002g0180 a0001c0002t0002g0255 |
2 | HG01257.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.10310-336G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003854 | |||||||
chr7:99003858 | G | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0046 |
3 | HG01346.hp2 HG02145.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.10310-332G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003858 | |||||||
chr7:99003893 | G | C | 1 | a0001c0004t0002g0183 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.10310-297G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003893 | |||||||
chr7:99003941 | C | T | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.10310-249C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003941 | |||||||
chr7:99003965 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.10310-225C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003965 | |||||||
chr7:99003998 | G | A | 1 | a0012c0020t0001g0097 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.10310-192G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003998 | |||||||
chr7:99004005 | G | A | 2 | a0001c0001t0002g0208 a0001c0001t0011g0209 |
2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.10310-185G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99004005 | |||||||
chr7:99004009 | G | A | 66 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(63): Show |
67 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.10310-181G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99004009 | |||||||
chr7:99004147 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.10310-43C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99004147 | |||||||
chr7:99004588 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.10535+173G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 68/72 | chr7 | 99004588 | |||||||
chr7:99004700 | C | T | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.10535+285C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 68/72 | chr7 | 99004700 | |||||||
chr7:99004732 | T | C | 4 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0001t0003g0098 others(1): Show |
4 | NA18941.hp1 NA18957.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.10535+317T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 68/72 | chr7 | 99004732 | |||||||
chr7:99004973 | C | T | 1 | a0001c0002t0002g0180 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.10536-158C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 68/72 | chr7 | 99004973 | |||||||
chr7:99004974 | G | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0111 |
3 | HG00280.hp2 HG00642.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.10536-157G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 68/72 | chr7 | 99004974 | |||||||
chr7:99005016 | G | A | 43 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(40): Show |
44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.10536-115G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 68/72 | chr7 | 99005016 | |||||||
chr7:99005037 | T | TC | 3 | a0001c0001t0001g0062 a0001c0001t0001g0141 a0001c0001t0002g0213 |
3 | NA18978.hp2 NA18982.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.10536-91dupC | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 68/72 | INFO_REALIGN_3_PRIME | chr7 | 99005037 | ||||||
chr7:99005091 | G | T | 6 | a0001c0001t0002g0147 a0001c0006t0002g0149 a0001c0006t0002g0150 others(3): Show |
6 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.10536-40G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 68/72 | chr7 | 99005091 | |||||||
chr7:99005367 | G | C | 122 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(119): Show |
124 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.10753+19G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99005367 | |||||||
chr7:99005472 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.10753+124A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99005472 | |||||||
chr7:99005487 | G | A | 4 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0219 others(1): Show |
4 | HG00738.hp2 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.10753+139G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99005487 | |||||||
chr7:99005636 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.10753+288C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99005636 | |||||||
chr7:99005662 | G | A | 121 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(118): Show |
123 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.10753+314G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99005662 | |||||||
chr7:99005673 | ATTTCTT | A | 3 | a0001c0004t0002g0183 a0001c0004t0002g0185 a0008c0042t0002g0184 |
3 | HG02622.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.10753+335_10753+34 others(10): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | INFO_REALIGN_3_PRIME | chr7 | 99005673 | ||||||
chr7:99005843 | C | T | 57 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(54): Show |
57 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.10753+495C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99005843 | |||||||
chr7:99005854 | G | A | 1 | a0001c0017t0001g0116 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.10753+506G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99005854 | |||||||
chr7:99005880 | G | A | 6 | a0001c0002t0002g0164 a0001c0002t0002g0165 a0001c0002t0002g0166 others(3): Show |
6 | HG02809.hp2 HG02896.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.10753+532G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99005880 | |||||||
chr7:99005933 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.10753+585G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99005933 | |||||||
chr7:99006041 | G | A | 1 | a0009c0029t0001g0018 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.10753+693G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99006041 | |||||||
chr7:99006154 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.10753+806T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99006154 | |||||||
chr7:99006160 | G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.10753+812G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99006160 | |||||||
chr7:99006233 | C | G | 1 | a0001c0001t0001g0083 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.10753+885C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99006233 | |||||||
chr7:99006248 | C | T | 1 | a0001c0038t0001g0034 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.10753+900C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99006248 | |||||||
chr7:99006301 | C | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG02109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.10753+953C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99006301 | |||||||
chr7:99006442 | T | TGTAGTGT others(12): Show |
1 | a0001c0001t0001g0141 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.10753+1095_10753+1 others(25): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | INFO_REALIGN_3_PRIME | chr7 | 99006442 | ||||||
chr7:99006443 | G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.10753+1095G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99006443 | |||||||
chr7:99006493 | T | A | 1 | a0001c0022t0001g0124 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.10753+1145T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99006493 | |||||||
chr7:99006503 | A | G | 132 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(129): Show |
134 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.10753+1155A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99006503 | |||||||
chr7:99006605 | A | G | 1 | a0001c0002t0010g0179 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.10753+1257A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99006605 | |||||||
chr7:99006773 | T | C | 2 | a0001c0001t0001g0084 a0001c0001t0001g0089 |
2 | HG00544.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.10753+1425T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99006773 | |||||||
chr7:99006849 | C | T | 1 | a0001c0002t0002g0166 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.10753+1501C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99006849 | |||||||
chr7:99007122 | A | G | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | NA18978.hp1 NA19000.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.10754-1255A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007122 | |||||||
chr7:99007142 | G | A | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0126 |
3 | HG02572.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.10754-1235G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007142 | |||||||
chr7:99007218 | C | T | 1 | a0001c0001t0002g0227 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.10754-1159C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007218 | |||||||
chr7:99007219 | G | A | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.10754-1158G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007219 | |||||||
chr7:99007221 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0133 |
2 | HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.10754-1156C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007221 | |||||||
chr7:99007240 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.10754-1137G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007240 | |||||||
chr7:99007461 | G | A | 3 | a0001c0001t0002g0195 a0001c0001t0002g0196 a0001c0001t0002g0197 |
3 | HG02258.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.10754-916G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007461 | |||||||
chr7:99007468 | C | T | 3 | a0001c0001t0002g0195 a0001c0001t0002g0196 a0001c0001t0002g0197 |
3 | HG02258.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.10754-909C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007468 | |||||||
chr7:99007506 | G | A | 1 | a0001c0001t0002g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.10754-871G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007506 | |||||||
chr7:99007667 | T | C | 1 | a0001c0005t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.10754-710T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007667 | |||||||
chr7:99007709 | C | T | 2 | a0001c0007t0001g0081 a0001c0007t0001g0105 |
2 | HG01891.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.10754-668C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007709 | |||||||
chr7:99007774 | G | A | 2 | a0001c0001t0002g0208 a0001c0001t0011g0209 |
2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.10754-603G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007774 | |||||||
chr7:99007824 | CT | C | 36 | a0001c0001t0002g0147 a0001c0001t0002g0195 a0001c0001t0002g0196 others(33): Show |
37 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.10754-537delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | INFO_REALIGN_3_PRIME | chr7 | 99007824 | ||||||
chr7:99007840 | T | C | 1 | a0001c0028t0002g0207 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.10754-537T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007840 | |||||||
chr7:99007936 | C | G | 1 | a0001c0001t0001g0111 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.10754-441C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007936 | |||||||
chr7:99007987 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.10754-390G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007987 | |||||||
chr7:99008014 | C | G | 1 | a0001c0017t0001g0116 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.10754-363C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99008014 | |||||||
chr7:99008032 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.10754-345A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99008032 | |||||||
chr7:99008038 | A | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0115 |
2 | HG00558.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.10754-339A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99008038 | |||||||
chr7:99008093 | T | G | 9 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0126 others(6): Show |
9 | HG01884.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.10754-284T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99008093 | |||||||
chr7:99008113 | T | C | 5 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0257 others(2): Show |
5 | HG02015.hp2 HG02040.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.10754-264T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99008113 | |||||||
chr7:99008152 | A | G | 1 | a0001c0001t0002g0232 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.10754-225A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99008152 | |||||||
chr7:99008195 | G | A | 1 | a0001c0002t0002g0187 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.10754-182G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99008195 | |||||||
chr7:99008307 | C | G | 6 | a0001c0001t0005g0159 a0001c0001t0005g0160 a0001c0001t0005g0162 others(3): Show |
6 | HG02055.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.10754-70C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99008307 | |||||||
chr7:99008311 | C | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0138 |
2 | NA19079.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.10754-66C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99008311 | |||||||
chr7:99008671 | C | G | 1 | a0001c0001t0001g0085 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.10938+110C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99008671 | |||||||
chr7:99008678 | G | T | 1 | a0001c0001t0002g0249 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.10938+117G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99008678 | |||||||
chr7:99008783 | G | A | 25 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0164 others(22): Show |
26 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.10938+222G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99008783 | |||||||
chr7:99008840 | C | T | 3 | a0001c0001t0001g0106 a0001c0001t0001g0114 a0001c0001t0001g0122 |
3 | HG03209.hp2 HG03579.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.10938+279C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99008840 | |||||||
chr7:99008885 | A | G | 1 | a0001c0025t0001g0118 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.10938+324A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99008885 | |||||||
chr7:99008900 | C | G | 43 | a0001c0001t0002g0147 a0001c0001t0005g0159 a0001c0001t0005g0160 others(40): Show |
44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.10938+339C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99008900 | |||||||
chr7:99009006 | T | C | 1 | a0001c0001t0001g0140 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.10938+445T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99009006 | |||||||
chr7:99009031 | T | C | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.10938+470T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99009031 | |||||||
chr7:99009032 | C | T | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.10938+471C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99009032 | |||||||
chr7:99009300 | C | T | 5 | a0001c0004t0002g0002 a0001c0004t0002g0168 a0001c0004t0002g0169 others(2): Show |
6 | HG02257.hp1 HG02647.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.10938+739C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99009300 | |||||||
chr7:99009371 | G | C | 2 | a0002c0008t0008g0192 a0002c0008t0008g0193 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.10938+810G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99009371 | |||||||
chr7:99009747 | G | A | 61 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0157 others(58): Show |
62 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.10938+1186G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99009747 | |||||||
chr7:99009880 | C | CT | 12 | a0001c0001t0001g0057 a0001c0001t0001g0062 a0001c0001t0001g0090 others(9): Show |
12 | HG00558.hp2 HG01261.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.10939-1147dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | INFO_REALIGN_3_PRIME | chr7 | 99009880 | ||||||
chr7:99009880 | CT | C | 27 | a0001c0001t0001g0059 a0001c0001t0001g0096 a0001c0001t0001g0130 others(24): Show |
27 | HG01884.hp2 HG01975.hp2 HG02451.hp1 others(24): Show |
intron_variant | MODIFIER | c.10939-1147delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | INFO_REALIGN_3_PRIME | chr7 | 99009880 | ||||||
chr7:99009880 | CTT | C | 87 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0195 others(84): Show |
89 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.10939-1148_10939-1 others(8): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | INFO_REALIGN_3_PRIME | chr7 | 99009880 | ||||||
chr7:99009880 | CTTT | C | 7 | a0001c0001t0002g0197 a0001c0001t0002g0222 a0001c0001t0002g0223 others(4): Show |
7 | HG01099.hp2 HG01943.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.10939-1149_10939-1 others(9): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | INFO_REALIGN_3_PRIME | chr7 | 99009880 | ||||||
chr7:99009882 | T | C | 1 | a0001c0001t0001g0013 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.10939-1170T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99009882 | |||||||
chr7:99009905 | T | A | 5 | a0001c0006t0002g0149 a0001c0006t0002g0150 a0001c0006t0002g0151 others(2): Show |
5 | HG02559.hp1 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.10939-1147T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99009905 | |||||||
chr7:99009964 | C | T | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.10939-1088C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99009964 | |||||||
chr7:99010108 | G | C | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.10939-944G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99010108 | |||||||
chr7:99010281 | T | C | 1 | a0001c0001t0003g0027 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.10939-771T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99010281 | |||||||
chr7:99010330 | C | G | 1 | a0001c0023t0002g0204 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.10939-722C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99010330 | |||||||
chr7:99010423 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG02109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.10939-629G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99010423 | |||||||
chr7:99010436 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.10939-616G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99010436 | |||||||
chr7:99010579 | A | G | 7 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0166 others(4): Show |
7 | HG01243.hp1 HG01884.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.10939-473A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99010579 | |||||||
chr7:99010581 | GAGTCTCT others(12): Show |
G | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.10939-463_10939-44 others(23): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | INFO_REALIGN_3_PRIME | chr7 | 99010581 | ||||||
chr7:99010609 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0089 |
2 | HG00544.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.10939-443G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99010609 | |||||||
chr7:99010697 | G | A | 6 | a0001c0005t0004g0004 a0001c0005t0004g0005 a0001c0005t0004g0006 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.10939-355G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99010697 | |||||||
chr7:99010862 | C | T | 1 | a0001c0019t0001g0112 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.10939-190C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99010862 | |||||||
chr7:99010892 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.10939-160C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99010892 | |||||||
chr7:99010982 | T | C | 1 | a0001c0002t0002g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.10939-70T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99010982 | |||||||
chr7:99010983 | T | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0019 others(41): Show |
45 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.10939-69T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99010983 | |||||||
chr7:99011288 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.11142+33C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 71/72 | chr7 | 99011288 | |||||||
chr7:99011952 | T | A | 3 | a0001c0002t0007g0154 a0001c0002t0007g0155 a0001c0002t0007g0156 |
3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.11338-119T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 72/72 | chr7 | 99011952 | |||||||
chr7:99012048 | G | C | 1 | a0001c0001t0002g0238 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.11338-23G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 72/72 | chr7 | 99012048 |