Item | Value |
---|---|
geneid | 283659 |
ensemblid | ENSG00000166450.13 |
hgncid | 26373 |
symbol | PRTG |
name | protogenin |
refseq_nuc | NM_173814.6 |
refseq_prot | NP_776175.2 |
ensembl_nuc | ENST00000389286.9 |
ensembl_prot | ENSP00000373937.4 |
mane_status | MANE Select |
chr | chr15 |
start | 55611544 |
end | 55743152 |
strand | - |
ver | v1.2 |
region | chr15:55611544-55743152 |
region5000 | chr15:55606544-55748152 |
regionname0 | PRTG_chr15_55611544_55743152 |
regionname5000 | PRTG_chr15_55606544_55748152 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1150 | 181 | 44 | 47 | 53 | 7 | 28 | 41 | PRTG_chr15_55606544_55748152 | PRTG | MAPPL others(1145): Show |
chr15 | 55606544 | 55748152 |
a0002 | 0/0 | 1150 | 65 | 22 | 10 | 26 | 1 | 6 | 22 | PRTG_chr15_55606544_55748152 | PRTG | MAPPL others(1145): Show |
chr15 | 55606544 | 55748152 |
a0003 | 0/0 | 1150 | 11 | 0 | 5 | 0 | 5 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | MAPPL others(1145): Show |
chr15 | 55606544 | 55748152 |
a0004 | 0/0 | 1150 | 11 | 10 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | MAPPL others(1145): Show |
chr15 | 55606544 | 55748152 |
a0005 | 0/0 | 1150 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | MAPPL others(1145): Show |
chr15 | 55606544 | 55748152 |
a0006 | 0/0 | 1150 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | PRTG_chr15_55606544_55748152 | PRTG | MAPPL others(1145): Show |
chr15 | 55606544 | 55748152 |
a0007 | 0/0 | 1150 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | MAPPL others(1145): Show |
chr15 | 55606544 | 55748152 |
a0008 | 0/0 | 1150 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | MAPPL others(1145): Show |
chr15 | 55606544 | 55748152 |
a0009 | 0/0 | 1150 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | MAPPL others(1145): Show |
chr15 | 55606544 | 55748152 |
a0010 | 0/0 | 1150 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | MAPPL others(1145): Show |
chr15 | 55606544 | 55748152 |
a0011 | 0/0 | 1150 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | MAPPL others(1145): Show |
chr15 | 55606544 | 55748152 |
a0012 | 0/0 | 1150 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | MAPPL others(1145): Show |
chr15 | 55606544 | 55748152 |
a0013 | 0/0 | 1150 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | MAPPL others(1145): Show |
chr15 | 55606544 | 55748152 |
a0014 | 0/0 | 1150 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | MAPPL others(1145): Show |
chr15 | 55606544 | 55748152 |
a0015 | 0/0 | 1150 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | MARPL others(1145): Show |
chr15 | 55606544 | 55748152 |
a0016 | 0/0 | 1150 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | MAPPL others(1145): Show |
chr15 | 55606544 | 55748152 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 3450 | 154 | 29 | 43 | 46 | 6 | 28 | PRTG_chr15_55606544_55748152 | PRTG | ATGGC others(3445): Show |
chr15 | 55606544 | 55748152 | ||
a0001c0003 | 0/0 | 3450 | 11 | 0 | 3 | 7 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ATGGC others(3445): Show |
chr15 | 55606544 | 55748152 | ||
a0001c0007 | 0/0 | 3450 | 5 | 5 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ATGGC others(3445): Show |
chr15 | 55606544 | 55748152 | ||
a0001c0008 | 0/0 | 3450 | 4 | 4 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ATGGC others(3445): Show |
chr15 | 55606544 | 55748152 | ||
a0001c0009 | 0/0 | 3450 | 3 | 3 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ATGGC others(3445): Show |
chr15 | 55606544 | 55748152 | ||
a0001c0012 | 0/0 | 3450 | 3 | 2 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ATGGC others(3445): Show |
chr15 | 55606544 | 55748152 | ||
a0001c0020 | 0/0 | 3450 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ATGGC others(3445): Show |
chr15 | 55606544 | 55748152 | ||
a0002c0002 | 0/0 | 3450 | 65 | 22 | 10 | 26 | 1 | 6 | PRTG_chr15_55606544_55748152 | PRTG | ATGGC others(3445): Show |
chr15 | 55606544 | 55748152 | ||
a0003c0005 | 0/0 | 3450 | 6 | 0 | 3 | 0 | 2 | 1 | PRTG_chr15_55606544_55748152 | PRTG | ATGGC others(3445): Show |
chr15 | 55606544 | 55748152 | ||
a0003c0006 | 0/0 | 3450 | 5 | 0 | 2 | 0 | 3 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ATGGC others(3445): Show |
chr15 | 55606544 | 55748152 | ||
a0004c0004 | 0/0 | 3450 | 11 | 10 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ATGGC others(3445): Show |
chr15 | 55606544 | 55748152 | ||
a0005c0011 | 0/0 | 3450 | 3 | 3 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ATGGC others(3445): Show |
chr15 | 55606544 | 55748152 | ||
a0006c0010 | 0/0 | 3450 | 3 | 0 | 0 | 3 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ATGGC others(3445): Show |
chr15 | 55606544 | 55748152 | ||
a0007c0017 | 0/0 | 3450 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ATGGC others(3445): Show |
chr15 | 55606544 | 55748152 | ||
a0008c0022 | 0/0 | 3450 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ATGGC others(3445): Show |
chr15 | 55606544 | 55748152 | ||
a0009c0013 | 0/0 | 3450 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ATGGC others(3445): Show |
chr15 | 55606544 | 55748152 | ||
a0010c0021 | 0/0 | 3450 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ATGGC others(3445): Show |
chr15 | 55606544 | 55748152 | ||
a0011c0016 | 0/0 | 3450 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ATGGC others(3445): Show |
chr15 | 55606544 | 55748152 | ||
a0012c0019 | 0/0 | 3450 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ATGGC others(3445): Show |
chr15 | 55606544 | 55748152 | ||
a0013c0015 | 0/0 | 3450 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | ATGGC others(3445): Show |
chr15 | 55606544 | 55748152 | ||
a0014c0018 | 0/0 | 3450 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ATGGC others(3445): Show |
chr15 | 55606544 | 55748152 | ||
a0015c0023 | 0/0 | 3450 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ATGGC others(3445): Show |
chr15 | 55606544 | 55748152 | ||
a0016c0014 | 0/0 | 3450 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ATGGC others(3445): Show |
chr15 | 55606544 | 55748152 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 12112 | 47 | 3 | 8 | 26 | 2 | 8 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12107): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0002 | 0/1 | 12111 | 38 | 2 | 20 | 4 | 2 | 9 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12106): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0004 | 0/0 | 12114 | 2 | 0 | 0 | 2 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12109): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0005 | 0/0 | 12112 | 6 | 0 | 4 | 2 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12107): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0006 | 0/0 | 12114 | 3 | 0 | 0 | 2 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12109): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0008 | 0/0 | 12112 | 4 | 0 | 0 | 4 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12107): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0012 | 0/0 | 12112 | 2 | 0 | 1 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12107): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0015 | 0/0 | 12112 | 3 | 0 | 2 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12107): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0016 | 0/0 | 12141 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12136): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0018 | 0/0 | 12112 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12107): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0021 | 0/0 | 12145 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12140): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0024 | 0/0 | 12111 | 2 | 0 | 2 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12106): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0029 | 0/0 | 12139 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12134): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0032 | 0/0 | 12147 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12142): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0033 | 0/0 | 12143 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12138): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0034 | 0/0 | 12126 | 2 | 0 | 0 | 0 | 0 | 2 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12121): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0035 | 0/0 | 12140 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12135): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0036 | 0/0 | 12116 | 2 | 0 | 2 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12111): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0039 | 0/0 | 12111 | 2 | 0 | 0 | 1 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12106): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0040 | 0/0 | 12116 | 2 | 0 | 0 | 2 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12111): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0041 | 0/0 | 12112 | 2 | 0 | 2 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12107): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0051 | 0/0 | 12147 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12142): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0052 | 0/0 | 12143 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12138): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0054 | 0/0 | 12157 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12152): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0066 | 0/0 | 12121 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12116): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0070 | 0/0 | 12120 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12115): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0071 | 0/0 | 12112 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12107): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0075 | 0/0 | 12112 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12107): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0077 | 0/0 | 12114 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12109): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0078 | 0/0 | 12112 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12107): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0079 | 0/0 | 12112 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12107): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0080 | 0/0 | 12112 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12107): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0081 | 0/0 | 12112 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12107): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0082 | 0/0 | 12131 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12126): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0083 | 0/0 | 12151 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12146): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0084 | 0/0 | 12147 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12142): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0085 | 0/0 | 12145 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12140): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0086 | 1/0 | 12142 | 1 | 0 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12137): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0096 | 0/0 | 12142 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12137): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0097 | 0/0 | 12141 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12136): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0099 | 0/0 | 12137 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12132): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0100 | 0/0 | 12119 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12114): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0101 | 0/0 | 12111 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12106): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0102 | 0/0 | 12141 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12136): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0105 | 0/0 | 12139 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12134): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0111 | 0/0 | 12121 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12116): Show |
chr15 | 55606544 | 55748152 |
a0001c0001t0113 | 0/0 | 12113 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12108): Show |
chr15 | 55606544 | 55748152 |
a0001c0003t0003 | 0/0 | 12114 | 6 | 0 | 3 | 2 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12109): Show |
chr15 | 55606544 | 55748152 |
a0001c0003t0004 | 0/0 | 12114 | 2 | 0 | 0 | 2 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12109): Show |
chr15 | 55606544 | 55748152 |
a0001c0003t0017 | 0/0 | 12114 | 2 | 0 | 0 | 2 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12109): Show |
chr15 | 55606544 | 55748152 |
a0001c0003t0018 | 0/0 | 12112 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12107): Show |
chr15 | 55606544 | 55748152 |
a0001c0007t0038 | 0/0 | 12102 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12097): Show |
chr15 | 55606544 | 55748152 |
a0001c0007t0106 | 0/0 | 12102 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12097): Show |
chr15 | 55606544 | 55748152 |
a0001c0007t0107 | 0/0 | 12102 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12097): Show |
chr15 | 55606544 | 55748152 |
a0001c0007t0108 | 0/0 | 12102 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12097): Show |
chr15 | 55606544 | 55748152 |
a0001c0008t0037 | 0/0 | 12140 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12135): Show |
chr15 | 55606544 | 55748152 |
a0001c0008t0076 | 0/0 | 12144 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12139): Show |
chr15 | 55606544 | 55748152 |
a0001c0008t0093 | 0/0 | 12126 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12121): Show |
chr15 | 55606544 | 55748152 |
a0001c0009t0042 | 0/0 | 12140 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12135): Show |
chr15 | 55606544 | 55748152 |
a0001c0009t0087 | 0/0 | 12166 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12161): Show |
chr15 | 55606544 | 55748152 |
a0001c0009t0103 | 0/0 | 12165 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12160): Show |
chr15 | 55606544 | 55748152 |
a0001c0012t0002 | 0/0 | 12111 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12106): Show |
chr15 | 55606544 | 55748152 |
a0001c0012t0072 | 0/0 | 12140 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12135): Show |
chr15 | 55606544 | 55748152 |
a0001c0012t0074 | 0/0 | 12140 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12135): Show |
chr15 | 55606544 | 55748152 |
a0001c0020t0053 | 0/0 | 12131 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12126): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0003 | 0/0 | 12114 | 14 | 0 | 1 | 12 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12109): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0004 | 0/0 | 12114 | 6 | 0 | 0 | 6 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12109): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0006 | 0/0 | 12114 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12109): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0007 | 0/0 | 12116 | 4 | 0 | 0 | 4 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12111): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0011 | 0/0 | 12133 | 3 | 1 | 2 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12128): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0012 | 0/0 | 12112 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12107): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0013 | 0/0 | 12143 | 3 | 0 | 1 | 0 | 0 | 2 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12138): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0014 | 0/0 | 12131 | 3 | 3 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12126): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0016 | 0/0 | 12141 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12136): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0019 | 0/0 | 12121 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12116): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0020 | 0/0 | 12119 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12114): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0025 | 0/0 | 12118 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12113): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0026 | 0/0 | 12139 | 2 | 1 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12134): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0027 | 0/0 | 12137 | 2 | 1 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12132): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0028 | 0/0 | 12133 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12128): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0055 | 0/0 | 12137 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12132): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0056 | 0/0 | 12145 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12140): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0057 | 0/0 | 12139 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12134): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0058 | 0/0 | 12145 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12140): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0061 | 0/0 | 12147 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12142): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0062 | 0/0 | 12135 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12130): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0063 | 0/0 | 12131 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12126): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0064 | 0/0 | 12141 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12136): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0065 | 0/0 | 12137 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12132): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0067 | 0/0 | 12117 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12112): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0068 | 0/0 | 12117 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12112): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0088 | 0/0 | 12121 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12116): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0089 | 0/0 | 12119 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12114): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0090 | 0/0 | 12117 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12112): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0095 | 0/0 | 12119 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12114): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0104 | 0/0 | 12139 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12134): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0109 | 0/0 | 12143 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12138): Show |
chr15 | 55606544 | 55748152 |
a0002c0002t0110 | 0/0 | 12137 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12132): Show |
chr15 | 55606544 | 55748152 |
a0003c0005t0010 | 0/0 | 12130 | 3 | 0 | 2 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12125): Show |
chr15 | 55606544 | 55748152 |
a0003c0005t0022 | 0/0 | 12134 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12129): Show |
chr15 | 55606544 | 55748152 |
a0003c0005t0044 | 0/0 | 12136 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12131): Show |
chr15 | 55606544 | 55748152 |
a0003c0005t0045 | 0/0 | 12122 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12117): Show |
chr15 | 55606544 | 55748152 |
a0003c0006t0009 | 0/0 | 12132 | 3 | 0 | 1 | 0 | 2 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12127): Show |
chr15 | 55606544 | 55748152 |
a0003c0006t0022 | 0/0 | 12134 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12129): Show |
chr15 | 55606544 | 55748152 |
a0003c0006t0092 | 0/0 | 12130 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12125): Show |
chr15 | 55606544 | 55748152 |
a0004c0004t0023 | 0/0 | 12142 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12137): Show |
chr15 | 55606544 | 55748152 |
a0004c0004t0030 | 0/0 | 12142 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12137): Show |
chr15 | 55606544 | 55748152 |
a0004c0004t0031 | 0/0 | 12120 | 2 | 2 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12115): Show |
chr15 | 55606544 | 55748152 |
a0004c0004t0047 | 0/0 | 12140 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12135): Show |
chr15 | 55606544 | 55748152 |
a0004c0004t0048 | 0/0 | 12138 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12133): Show |
chr15 | 55606544 | 55748152 |
a0004c0004t0049 | 0/0 | 12136 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12131): Show |
chr15 | 55606544 | 55748152 |
a0004c0004t0050 | 0/0 | 12130 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12125): Show |
chr15 | 55606544 | 55748152 |
a0004c0004t0069 | 0/0 | 12112 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12107): Show |
chr15 | 55606544 | 55748152 |
a0005c0011t0035 | 0/0 | 12140 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12135): Show |
chr15 | 55606544 | 55748152 |
a0005c0011t0094 | 0/0 | 12141 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12136): Show |
chr15 | 55606544 | 55748152 |
a0005c0011t0098 | 0/0 | 12139 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12134): Show |
chr15 | 55606544 | 55748152 |
a0006c0010t0025 | 0/0 | 12118 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12113): Show |
chr15 | 55606544 | 55748152 |
a0006c0010t0059 | 0/0 | 12118 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12113): Show |
chr15 | 55606544 | 55748152 |
a0006c0010t0060 | 0/0 | 12120 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12115): Show |
chr15 | 55606544 | 55748152 |
a0007c0017t0002 | 0/0 | 12111 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12106): Show |
chr15 | 55606544 | 55748152 |
a0008c0022t0112 | 0/0 | 12119 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12114): Show |
chr15 | 55606544 | 55748152 |
a0009c0013t0002 | 0/0 | 12111 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12106): Show |
chr15 | 55606544 | 55748152 |
a0010c0021t0091 | 0/0 | 12137 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12132): Show |
chr15 | 55606544 | 55748152 |
a0011c0016t0029 | 0/0 | 12139 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12134): Show |
chr15 | 55606544 | 55748152 |
a0012c0019t0046 | 0/0 | 12113 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12108): Show |
chr15 | 55606544 | 55748152 |
a0013c0015t0043 | 0/0 | 12138 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12133): Show |
chr15 | 55606544 | 55748152 |
a0014c0018t0006 | 0/0 | 12114 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12109): Show |
chr15 | 55606544 | 55748152 |
a0015c0023t0001 | 0/0 | 12112 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12107): Show |
chr15 | 55606544 | 55748152 |
a0016c0014t0073 | 0/0 | 12168 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | ACTCC others(12163): Show |
chr15 | 55606544 | 55748152 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0245 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0005g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0005g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0005g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0005g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0005g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0006g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0008g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0008g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0008g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0008g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0012g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0012g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0015g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0015g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0015g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0016g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0016g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0018g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0021g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0021g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0024g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0024g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0029g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0032g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0032g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0033g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0033g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0034g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0035g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0036g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0036g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0039g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0039g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0040g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0040g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0041g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0041g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0051g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0052g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0054g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0066g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0070g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0071g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0075g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0077g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0078g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0079g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0080g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0081g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0082g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0083g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0084g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0085g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0086g0211 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0096g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0097g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0099g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0100g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0101g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0102g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0105g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0111g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0001t0113g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0003t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0003t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0003t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0003t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0003t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0003t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0003t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0003t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0003t0017g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0003t0017g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0003t0018g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0007t0038g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0007t0038g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0007t0106g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0007t0107g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0007t0108g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0008t0037g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0008t0037g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0008t0076g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0008t0093g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0009t0042g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0009t0087g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0009t0103g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0012t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0012t0072g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0012t0074g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0001c0020t0053g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0003g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0006g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0007g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0007g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0007g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0007g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0011g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0011g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0011g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0012g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0013g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0013g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0013g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0014g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0014g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0014g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0016g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0019g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0019g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0020g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0020g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0025g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0026g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0026g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0027g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0027g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0028g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0028g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0055g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0056g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0057g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0058g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0061g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0062g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0063g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0064g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0065g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0067g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0068g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0088g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0089g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0090g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0095g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0104g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0109g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0002c0002t0110g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0003c0005t0010g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0003c0005t0010g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0003c0005t0010g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0003c0005t0022g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0003c0005t0044g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0003c0005t0045g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0003c0006t0009g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0003c0006t0009g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0003c0006t0009g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0003c0006t0022g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0003c0006t0092g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0004c0004t0023g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0004c0004t0023g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0004c0004t0030g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0004c0004t0030g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0004c0004t0031g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0004c0004t0031g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0004c0004t0047g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0004c0004t0048g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0004c0004t0049g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0004c0004t0050g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0004c0004t0069g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0005c0011t0035g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0005c0011t0094g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0005c0011t0098g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0006c0010t0025g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0006c0010t0059g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0006c0010t0060g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0007c0017t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0008c0022t0112g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0009c0013t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0010c0021t0091g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0011c0016t0029g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0012c0019t0046g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0013c0015t0043g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0014c0018t0006g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0015c0023t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
a0016c0014t0073g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0005 | t0010 | g0038 | EUR | GBR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG00099 | hp2 | a0003 | c0006 | t0092 | g0146 | EUR | GBR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG00140 | hp1 | a0007 | c0017 | t0002 | g0254 | EUR | GBR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | GBR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG00280 | hp1 | a0001 | c0003 | t0003 | g0080 | EUR | FIN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | FIN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG00323 | hp1 | a0002 | c0002 | t0095 | g0212 | EUR | FIN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG00323 | hp2 | a0001 | c0001 | t0012 | g0091 | EUR | FIN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG00408 | hp2 | a0001 | c0003 | t0017 | g0090 | EAS | CHS | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG00438 | hp2 | a0002 | c0002 | t0003 | g0044 | EAS | CHS | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG00642 | hp1 | a0002 | c0002 | t0061 | g0027 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG00642 | hp2 | a0002 | c0002 | t0013 | g0018 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG00733 | hp2 | a0003 | c0006 | t0009 | g0015 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG00738 | hp1 | a0001 | c0001 | t0036 | g0151 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG00738 | hp2 | a0001 | c0001 | t0041 | g0263 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG00741 | hp1 | a0003 | c0005 | t0010 | g0039 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01071 | hp1 | a0008 | c0022 | t0112 | g0283 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01071 | hp2 | a0001 | c0001 | t0036 | g0157 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01074 | hp1 | a0002 | c0002 | t0110 | g0237 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01081 | hp1 | a0001 | c0001 | t0012 | g0083 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01081 | hp2 | a0001 | c0012 | t0002 | g0279 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01106 | hp2 | a0003 | c0005 | t0044 | g0040 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01109 | hp1 | a0002 | c0002 | t0056 | g0045 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01109 | hp2 | a0001 | c0001 | t0005 | g0185 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0277 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01167 | hp2 | a0002 | c0002 | t0011 | g0050 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0251 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01169 | hp1 | a0002 | c0002 | t0011 | g0049 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01243 | hp1 | a0003 | c0005 | t0010 | g0041 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01243 | hp2 | a0002 | c0002 | t0055 | g0046 | AMR | PUR | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0242 | AMR | CLM | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01255 | hp2 | a0004 | c0004 | t0049 | g0055 | AMR | CLM | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0267 | AMR | CLM | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01257 | hp1 | a0002 | c0002 | t0003 | g0081 | AMR | CLM | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01257 | hp2 | a0001 | c0001 | t0015 | g0116 | AMR | CLM | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01258 | hp1 | a0001 | c0001 | t0015 | g0169 | AMR | CLM | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0268 | AMR | CLM | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0250 | AMR | CLM | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01358 | hp2 | a0003 | c0006 | t0022 | g0012 | AMR | CLM | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01361 | hp1 | a0001 | c0001 | t0024 | g0013 | AMR | CLM | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01361 | hp2 | a0001 | c0001 | t0041 | g0280 | AMR | CLM | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01433 | hp1 | a0002 | c0002 | t0065 | g0014 | AMR | CLM | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01433 | hp2 | a0001 | c0001 | t0024 | g0031 | AMR | CLM | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01515 | hp1 | a0003 | c0006 | t0009 | g0008 | EUR | IBS | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0244 | EUR | IBS | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0255 | EUR | IBS | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01517 | hp2 | a0003 | c0006 | t0009 | g0007 | EUR | IBS | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01884 | hp2 | a0004 | c0004 | t0023 | g0056 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01891 | hp1 | a0001 | c0001 | t0016 | g0122 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01891 | hp2 | a0001 | c0001 | t0052 | g0006 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0265 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01928 | hp2 | a0001 | c0001 | t0005 | g0187 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0266 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01943 | hp1 | a0001 | c0003 | t0003 | g0075 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0271 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01952 | hp1 | a0001 | c0001 | t0005 | g0186 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0274 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01978 | hp1 | a0001 | c0001 | t0005 | g0180 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01981 | hp1 | a0001 | c0003 | t0003 | g0042 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0272 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02015 | hp1 | a0001 | c0003 | t0017 | g0076 | EAS | KHV | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02015 | hp2 | a0001 | c0001 | t0004 | g0142 | EAS | KHV | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02027 | hp1 | a0001 | c0001 | t0040 | g0135 | EAS | KHV | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02027 | hp2 | a0002 | c0002 | t0007 | g0043 | EAS | KHV | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02040 | hp1 | a0001 | c0001 | t0078 | g0149 | EAS | KHV | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02040 | hp2 | a0001 | c0001 | t0080 | g0202 | EAS | KHV | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02055 | hp1 | a0002 | c0002 | t0063 | g0026 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02055 | hp2 | a0001 | c0001 | t0066 | g0094 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02074 | hp1 | a0001 | c0003 | t0018 | g0073 | EAS | KHV | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02083 | hp2 | a0001 | c0003 | t0003 | g0079 | EAS | KHV | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02129 | hp1 | a0002 | c0002 | t0003 | g0063 | EAS | KHV | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02129 | hp2 | a0002 | c0002 | t0006 | g0227 | EAS | KHV | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02145 | hp1 | a0004 | c0004 | t0030 | g0097 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02145 | hp2 | a0001 | c0020 | t0053 | g0002 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02148 | hp2 | a0002 | c0002 | t0089 | g0163 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02257 | hp1 | a0009 | c0013 | t0002 | g0239 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02257 | hp2 | a0001 | c0001 | t0101 | g0217 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02273 | hp2 | a0001 | c0001 | t0075 | g0167 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02300 | hp1 | a0001 | c0001 | t0113 | g0276 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02300 | hp2 | a0001 | c0003 | t0003 | g0074 | AMR | PEL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02451 | hp1 | a0002 | c0002 | t0027 | g0028 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02451 | hp2 | a0002 | c0002 | t0019 | g0052 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02572 | hp1 | a0001 | c0001 | t0035 | g0219 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02572 | hp2 | a0005 | c0011 | t0098 | g0222 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02615 | hp1 | a0001 | c0009 | t0087 | g0112 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02615 | hp2 | a0002 | c0002 | t0026 | g0023 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02622 | hp1 | a0001 | c0001 | t0102 | g0126 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02622 | hp2 | a0001 | c0001 | t0032 | g0098 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02630 | hp1 | a0001 | c0007 | t0038 | g0230 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02630 | hp2 | a0001 | c0012 | t0074 | g0114 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02647 | hp1 | a0001 | c0001 | t0082 | g0128 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02647 | hp2 | a0001 | c0001 | t0096 | g0229 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02683 | hp1 | a0002 | c0002 | t0013 | g0016 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02698 | hp1 | a0002 | c0002 | t0013 | g0029 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0262 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02717 | hp1 | a0010 | c0021 | t0091 | g0204 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02717 | hp2 | a0002 | c0002 | t0057 | g0025 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02723 | hp1 | a0011 | c0016 | t0029 | g0093 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02723 | hp2 | a0001 | c0007 | t0038 | g0231 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02735 | hp1 | a0002 | c0002 | t0026 | g0030 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0238 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02738 | hp1 | a0001 | c0001 | t0079 | g0178 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0270 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02809 | hp1 | a0001 | c0001 | t0083 | g0125 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02809 | hp2 | a0012 | c0019 | t0046 | g0003 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02818 | hp1 | a0001 | c0001 | t0054 | g0005 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02818 | hp2 | a0005 | c0011 | t0035 | g0220 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02886 | hp1 | a0002 | c0002 | t0028 | g0021 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02886 | hp2 | a0002 | c0002 | t0088 | g0213 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02922 | hp1 | a0002 | c0002 | t0014 | g0020 | AFR | ESN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02922 | hp2 | a0002 | c0002 | t0016 | g0127 | AFR | ESN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02965 | hp1 | a0001 | c0001 | t0033 | g0102 | AFR | ESN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02965 | hp2 | a0004 | c0004 | t0048 | g0054 | AFR | ESN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02970 | hp1 | a0002 | c0002 | t0067 | g0104 | AFR | ESN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02970 | hp2 | a0001 | c0009 | t0103 | g0233 | AFR | ESN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02976 | hp1 | a0001 | c0001 | t0099 | g0228 | AFR | ESN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02976 | hp2 | a0005 | c0011 | t0094 | g0218 | AFR | ESN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03017 | hp1 | a0002 | c0002 | t0027 | g0019 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0247 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03041 | hp1 | a0001 | c0001 | t0085 | g0124 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03041 | hp2 | a0002 | c0002 | t0104 | g0215 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03098 | hp2 | a0002 | c0002 | t0020 | g0053 | AFR | MSL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03130 | hp1 | a0004 | c0004 | t0047 | g0061 | AFR | ESN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03130 | hp2 | a0002 | c0002 | t0020 | g0010 | AFR | ESN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03195 | hp1 | a0004 | c0004 | t0031 | g0096 | AFR | ESN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03195 | hp2 | a0001 | c0001 | t0033 | g0101 | AFR | ESN | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03209 | hp1 | a0002 | c0002 | t0019 | g0062 | AFR | MSL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03209 | hp2 | a0004 | c0004 | t0023 | g0057 | AFR | MSL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03225 | hp1 | a0002 | c0002 | t0011 | g0048 | AFR | MSL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03239 | hp2 | a0013 | c0015 | t0043 | g0011 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03453 | hp1 | a0001 | c0008 | t0037 | g0208 | AFR | MSL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03453 | hp2 | a0001 | c0012 | t0072 | g0113 | AFR | MSL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03486 | hp1 | a0001 | c0001 | t0105 | g0205 | AFR | MSL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03486 | hp2 | a0001 | c0008 | t0037 | g0210 | AFR | MSL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0282 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03490 | hp2 | a0003 | c0005 | t0022 | g0037 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03491 | hp2 | a0001 | c0001 | t0034 | g0001 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03492 | hp1 | a0001 | c0001 | t0034 | g0001 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0281 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03540 | hp1 | a0001 | c0001 | t0021 | g0051 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03540 | hp2 | a0001 | c0001 | t0029 | g0092 | AFR | GWD | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03579 | hp1 | a0004 | c0004 | t0050 | g0059 | AFR | MSL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03579 | hp2 | a0001 | c0001 | t0021 | g0060 | AFR | MSL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03669 | hp1 | a0001 | c0001 | t0006 | g0148 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03669 | hp2 | a0002 | c0002 | t0003 | g0009 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | STU | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0261 | SAS | STU | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0273 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03710 | hp2 | a0001 | c0001 | t0015 | g0201 | SAS | PJL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03831 | hp1 | a0001 | c0001 | t0018 | g0058 | SAS | BEB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03831 | hp2 | a0001 | c0001 | t0081 | g0171 | SAS | BEB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03834 | hp2 | a0001 | c0001 | t0039 | g0132 | SAS | BEB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03927 | hp2 | a0002 | c0002 | t0064 | g0017 | SAS | BEB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0260 | SAS | STU | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | STU | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | STU | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG04204 | hp2 | a0001 | c0001 | t0111 | g0278 | SAS | STU | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG04228 | hp1 | a0001 | c0001 | t0097 | g0221 | SAS | STU | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG04228 | hp2 | a0001 | c0001 | t0071 | g0143 | SAS | STU | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18522 | hp1 | a0002 | c0002 | t0028 | g0022 | AFR | YRI | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18522 | hp2 | a0004 | c0004 | t0031 | g0095 | AFR | YRI | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18906 | hp1 | a0002 | c0002 | t0068 | g0099 | AFR | YRI | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18906 | hp2 | a0001 | c0009 | t0042 | g0035 | AFR | YRI | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18942 | hp1 | a0002 | c0002 | t0003 | g0069 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18942 | hp2 | a0001 | c0001 | t0008 | g0145 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18943 | hp1 | a0002 | c0002 | t0004 | g0216 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18943 | hp2 | a0014 | c0018 | t0006 | g0170 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18944 | hp1 | a0006 | c0010 | t0025 | g0065 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18948 | hp1 | a0002 | c0002 | t0003 | g0087 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18951 | hp1 | a0001 | c0001 | t0005 | g0141 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18951 | hp2 | a0002 | c0002 | t0090 | g0214 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18952 | hp1 | a0001 | c0001 | t0008 | g0159 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18952 | hp2 | a0001 | c0001 | t0039 | g0199 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18953 | hp1 | a0001 | c0001 | t0005 | g0137 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18953 | hp2 | a0002 | c0002 | t0003 | g0067 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18954 | hp2 | a0006 | c0010 | t0060 | g0034 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18963 | hp1 | a0002 | c0002 | t0003 | g0071 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18964 | hp1 | a0002 | c0002 | t0004 | g0119 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18964 | hp2 | a0001 | c0001 | t0006 | g0140 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18966 | hp1 | a0006 | c0010 | t0059 | g0072 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18966 | hp2 | a0002 | c0002 | t0025 | g0070 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18971 | hp1 | a0002 | c0002 | t0003 | g0066 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18971 | hp2 | a0001 | c0001 | t0006 | g0138 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18973 | hp2 | a0001 | c0001 | t0077 | g0174 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18980 | hp1 | a0002 | c0002 | t0003 | g0078 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18981 | hp1 | a0002 | c0002 | t0004 | g0120 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18983 | hp1 | a0001 | c0001 | t0040 | g0136 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0188 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA18994 | hp2 | a0001 | c0003 | t0004 | g0225 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19000 | hp1 | a0002 | c0002 | t0007 | g0086 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19002 | hp1 | a0002 | c0002 | t0003 | g0084 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19002 | hp2 | a0001 | c0001 | t0008 | g0198 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19007 | hp2 | a0002 | c0002 | t0007 | g0085 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19009 | hp1 | a0015 | c0023 | t0001 | g0235 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19009 | hp2 | a0001 | c0003 | t0003 | g0089 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19011 | hp1 | a0002 | c0002 | t0003 | g0088 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19012 | hp2 | a0002 | c0002 | t0004 | g0108 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19030 | hp1 | a0001 | c0008 | t0076 | g0121 | AFR | LWK | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19030 | hp2 | a0001 | c0007 | t0108 | g0111 | AFR | LWK | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19043 | hp1 | a0001 | c0001 | t0100 | g0232 | AFR | LWK | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19043 | hp2 | a0001 | c0001 | t0051 | g0004 | AFR | LWK | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19054 | hp1 | a0001 | c0003 | t0004 | g0173 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19064 | hp2 | a0002 | c0002 | t0004 | g0118 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19066 | hp2 | a0002 | c0002 | t0003 | g0077 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19077 | hp2 | a0002 | c0002 | t0004 | g0117 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19078 | hp1 | a0002 | c0002 | t0012 | g0082 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19078 | hp2 | a0001 | c0001 | t0008 | g0197 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19080 | hp1 | a0002 | c0002 | t0007 | g0064 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19082 | hp2 | a0002 | c0002 | t0003 | g0068 | EAS | JPT | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19240 | hp1 | a0001 | c0001 | t0032 | g0103 | AFR | YRI | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA19240 | hp2 | a0001 | c0007 | t0107 | g0110 | AFR | YRI | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA20129 | hp1 | a0016 | c0014 | t0073 | g0234 | AFR | ASW | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA20129 | hp2 | a0001 | c0008 | t0093 | g0209 | AFR | ASW | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA20805 | hp1 | a0003 | c0005 | t0045 | g0036 | EUR | TSI | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA20805 | hp2 | a0001 | c0001 | t0070 | g0133 | EUR | TSI | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02109 | hp1 | a0001 | c0001 | t0016 | g0123 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02109 | hp2 | a0001 | c0007 | t0106 | g0109 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02486 | hp1 | a0002 | c0002 | t0014 | g0024 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02559 | hp1 | a0002 | c0002 | t0058 | g0047 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG02559 | hp2 | a0002 | c0002 | t0014 | g0033 | AFR | ACB | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03471 | hp1 | a0001 | c0001 | t0084 | g0129 | AFR | MSL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
HG03471 | hp2 | a0004 | c0004 | t0030 | g0105 | AFR | MSL | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA20300 | hp1 | a0002 | c0002 | t0109 | g0236 | AFR | USA | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA20300 | hp2 | a0002 | c0002 | t0062 | g0032 | AFR | USA | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA21309 | hp1 | a0004 | c0004 | t0069 | g0100 | AFR | LWK | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0259 | AFR | LWK | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0245 | REF | REF | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
homoSapiens | grch38p0 | a0001 | c0001 | t0086 | g0211 | REF | REF | PRTG_chr15_55606544_55748152 | PRTG | chr15 | 55606544 | 55748152 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:55620036 | T | C | 1 | a0010 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.3429A>G | p.Ile1143Met | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 3650/12142 | 3429/3453 | 1143/1150 | chr15 | 55620036 | |||
chr15:55620062 | C | T | 1 | a0011 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.3403G>A | p.Asp1135Asn | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 3624/12142 | 3403/3453 | 1135/1150 | chr15 | 55620062 | |||
chr15:55620193 | G | A | 1 | a0007 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.3272C>T | p.Ser1091Phe | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 3493/12142 | 3272/3453 | 1091/1150 | chr15 | 55620193 | |||
chr15:55620677 | T | A | 2 | a0003 a0013 |
12 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(9): Show |
missense_variant | MODERATE | c.3184A>T | p.Ile1062Leu | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 19/20 | 3405/12142 | 3184/3453 | 1062/1150 | chr15 | 55620677 | |||
chr15:55624362 | T | A | 1 | a0014 | 1 | NA18943.hp2 | missense_variant | MODERATE | c.3073A>T | p.Asn1025Tyr | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/20 | 3294/12142 | 3073/3453 | 1025/1150 | chr15 | 55624362 | |||
chr15:55624458 | G | A | 1 | a0012 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.2977C>T | p.Arg993Cys | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/20 | 3198/12142 | 2977/3453 | 993/1150 | chr15 | 55624458 | |||
chr15:55624487 | G | A | 1 | a0016 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.2948C>T | p.Thr983Met | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/20 | 3169/12142 | 2948/3453 | 983/1150 | chr15 | 55624487 | |||
chr15:55628845 | C | T | 1 | a0006 | 3 | NA18944.hp1 NA18954.hp2 NA18966.hp1 |
missense_variant | MODERATE | c.2783G>A | p.Arg928His | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/20 | 3004/12142 | 2783/3453 | 928/1150 | chr15 | 55628845 | |||
chr15:55637317 | C | G | 1 | a0004 | 11 | HG01255.hp2 HG01884.hp2 HG02145.hp1 others(8): Show |
missense_variant | MODERATE | c.2476G>C | p.Val826Leu | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/20 | 2697/12142 | 2476/3453 | 826/1150 | chr15 | 55637317 | |||
chr15:55672580 | C | G | 1 | a0013 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.1906G>C | p.Val636Leu | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/20 | 2127/12142 | 1906/3453 | 636/1150 | chr15 | 55672580 | |||
chr15:55680599 | T | C | 3 | a0002 a0006 a0010 |
69 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(66): Show |
missense_variant | MODERATE | c.706A>G | p.Thr236Ala | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 5/20 | 927/12142 | 706/3453 | 236/1150 | chr15 | 55680599 | |||
chr15:55683859 | T | C | 1 | a0005 | 3 | HG02572.hp2 HG02818.hp2 HG02976.hp2 |
missense_variant | MODERATE | c.470A>G | p.Lys157Arg | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/20 | 691/12142 | 470/3453 | 157/1150 | chr15 | 55683859 | |||
chr15:55740467 | C | G | 1 | a0009 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.312G>C | p.Glu104Asp | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/20 | 533/12142 | 312/3453 | 104/1150 | chr15 | 55740467 | |||
chr15:55742895 | G | A | 1 | a0008 | 1 | HG01071.hp1 | missense_variant | MODERATE | c.37C>T | p.Pro13Ser | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/20 | 258/12142 | 37/3453 | 13/1150 | chr15 | 55742895 | |||
chr15:55742924 | G | C | 1 | a0015 | 1 | NA19009.hp1 | missense_variant | MODERATE | c.8C>G | p.Pro3Arg | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/20 | 229/12142 | 8/3453 | 3/1150 | chr15 | 55742924 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:55638637 | G | A | 3 | a0001c0007 a0001c0008 a0004c0004 |
20 | HG01255.hp2 HG01884.hp2 HG02109.hp2 others(17): Show |
synonymous_variant | LOW | c.2364C>T | p.Asn788Asn | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 14/20 | 2585/12142 | 2364/3453 | 788/1150 | chr15 | 55638637 | |||
chr15:55641159 | G | A | 1 | a0001c0020 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.2091C>T | p.Asp697Asp | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/20 | 2312/12142 | 2091/3453 | 697/1150 | chr15 | 55641159 | |||
chr15:55673504 | C | T | 3 | a0001c0008 a0001c0009 a0016c0014 |
8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
synonymous_variant | LOW | c.1719G>A | p.Thr573Thr | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 10/20 | 1940/12142 | 1719/3453 | 573/1150 | chr15 | 55673504 | |||
chr15:55677843 | A | G | 4 | a0001c0003 a0002c0002 a0006c0010 others(1): Show |
80 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
synonymous_variant | LOW | c.1335T>C | p.Asn445Asn | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/20 | 1556/12142 | 1335/3453 | 445/1150 | chr15 | 55677843 | |||
chr15:55740509 | G | A | 1 | a0001c0012 | 3 | HG01081.hp2 HG02630.hp2 HG03453.hp2 |
synonymous_variant | LOW | c.270C>T | p.Asn90Asn | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/20 | 491/12142 | 270/3453 | 90/1150 | chr15 | 55740509 | |||
chr15:55740674 | G | A | 1 | a0003c0005 | 6 | HG00099.hp1 HG00741.hp1 HG01106.hp2 others(3): Show |
synonymous_variant | LOW | c.105C>T | p.Cys35Cys | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/20 | 326/12142 | 105/3453 | 35/1150 | chr15 | 55740674 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:55611551 | T | C | 1 | a0001c0001t0078 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8461A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 8461 | chr15 | 55611551 | ||||||
chr15:55611722 | A | G | 1 | a0001c0001t0101 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8290T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 8290 | chr15 | 55611722 | ||||||
chr15:55611731 | A | T | 1 | a0001c0001t0070 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8281T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 8281 | chr15 | 55611731 | ||||||
chr15:55611751 | A | G | 1 | a0002c0002t0062 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8261T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 8261 | chr15 | 55611751 | ||||||
chr15:55611892 | G | C | 33 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(30): Show |
122 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*8120C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 8120 | chr15 | 55611892 | ||||||
chr15:55611929 | T | C | 1 | a0001c0001t0096 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8083A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 8083 | chr15 | 55611929 | ||||||
chr15:55612019 | GA | G | 75 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(72): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*7992delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7992 | chr15 | 55612019 | ||||||
chr15:55612046 | T | C | 107 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(104): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*7966A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7966 | chr15 | 55612046 | ||||||
chr15:55612529 | G | A | 21 | a0001c0001t0002 a0001c0001t0024 a0001c0001t0032 others(18): Show |
61 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*7483C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7483 | chr15 | 55612529 | ||||||
chr15:55612575 | T | C | 1 | a0012c0019t0046 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7437A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7437 | chr15 | 55612575 | ||||||
chr15:55612633 | C | T | 1 | a0004c0004t0031 | 2 | HG03195.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7379G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7379 | chr15 | 55612633 | ||||||
chr15:55612696 | C | CCATATAT others(21): Show |
1 | a0016c0014t0073 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7315_*7316insCATA others(24): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7315 | chr15 | 55612696 | ||||||
chr15:55612696 | CAATATAT others(3): Show |
C | 1 | a0001c0001t0082 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7306_*7315delTATA others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7306 | chr15 | 55612696 | ||||||
chr15:55612697 | A | AAT | 7 | a0001c0001t0033 a0001c0001t0052 a0001c0001t0096 others(4): Show |
12 | HG00642.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*7313_*7314dupAT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7314 | chr15 | 55612697 | ||||||
chr15:55612697 | A | AATAT | 5 | a0001c0001t0021 a0001c0001t0085 a0001c0008t0076 others(2): Show |
6 | HG01109.hp1 HG02559.hp1 HG03041.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7311_*7314dupATAT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7314 | chr15 | 55612697 | ||||||
chr15:55612697 | A | AATATAT | 4 | a0001c0001t0032 a0001c0001t0051 a0001c0001t0084 others(1): Show |
5 | HG00642.hp1 HG02622.hp2 HG03471.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7309_*7314dupATAT others(2): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7314 | chr15 | 55612697 | ||||||
chr15:55612697 | A | AATATATA others(3): Show |
1 | a0001c0001t0083 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7305_*7314dupATAT others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7314 | chr15 | 55612697 | ||||||
chr15:55612697 | A | C | 4 | a0001c0001t0054 a0001c0009t0042 a0001c0009t0087 others(1): Show |
4 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7315T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7315 | chr15 | 55612697 | ||||||
chr15:55612697 | A | T | 5 | a0001c0001t0035 a0001c0001t0102 a0001c0012t0074 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7315T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7315 | chr15 | 55612697 | ||||||
chr15:55612697 | AAT | A | 9 | a0001c0001t0029 a0001c0001t0105 a0002c0002t0026 others(6): Show |
10 | HG02572.hp2 HG02615.hp2 HG02717.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*7313_*7314delAT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7313 | chr15 | 55612697 | ||||||
chr15:55612697 | AATAT | A | 8 | a0001c0001t0099 a0002c0002t0027 a0002c0002t0055 others(5): Show |
9 | HG01074.hp1 HG01106.hp2 HG01243.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*7311_*7314delATAT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7311 | chr15 | 55612697 | ||||||
chr15:55612697 | AATATAT | A | 3 | a0002c0002t0062 a0003c0005t0022 a0003c0006t0022 |
3 | HG01358.hp2 HG03490.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7309_*7314delATAT others(2): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7309 | chr15 | 55612697 | ||||||
chr15:55612697 | AATATATA others(1): Show |
A | 3 | a0002c0002t0011 a0002c0002t0028 a0003c0006t0009 |
8 | HG00733.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7307_*7314delATAT others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7307 | chr15 | 55612697 | ||||||
chr15:55612697 | AATATATA others(3): Show |
A | 6 | a0001c0020t0053 a0002c0002t0014 a0002c0002t0063 others(3): Show |
10 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*7305_*7314delATAT others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7305 | chr15 | 55612697 | ||||||
chr15:55612697 | AATATATA others(7): Show |
A | 2 | a0001c0001t0034 a0001c0008t0093 |
3 | HG03491.hp2 HG03492.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7301_*7314delATAT others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7301 | chr15 | 55612697 | ||||||
chr15:55612697 | AATATATA others(11): Show |
A | 1 | a0003c0005t0045 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7297_*7314delATAT others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7297 | chr15 | 55612697 | ||||||
chr15:55612697 | AATATATA others(13): Show |
A | 7 | a0001c0001t0066 a0001c0001t0070 a0001c0001t0111 others(4): Show |
9 | HG02055.hp2 HG02451.hp2 HG02886.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*7295_*7314delATAT others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7295 | chr15 | 55612697 | ||||||
chr15:55612697 | AATATATA others(15): Show |
A | 8 | a0001c0001t0100 a0002c0002t0020 a0002c0002t0025 others(5): Show |
9 | HG00323.hp1 HG01071.hp1 HG02148.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*7293_*7314delATAT others(18): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7293 | chr15 | 55612697 | ||||||
chr15:55612697 | AATATATA others(17): Show |
A | 6 | a0001c0001t0036 a0001c0001t0040 a0002c0002t0007 others(3): Show |
11 | HG00738.hp1 HG01071.hp2 HG02027.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*7291_*7314delATAT others(20): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7291 | chr15 | 55612697 | ||||||
chr15:55612697 | AATATATA others(19): Show |
A | 10 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0077 others(7): Show |
38 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*7289_*7314delATAT others(22): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7289 | chr15 | 55612697 | ||||||
chr15:55612697 | AATATATA others(21): Show |
A | 19 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(16): Show |
77 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*7287_*7314delATAT others(24): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7287 | chr15 | 55612697 | ||||||
chr15:55612697 | AATATATA others(23): Show |
A | 7 | a0001c0001t0002 a0001c0001t0024 a0001c0001t0039 others(4): Show |
45 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*7285_*7314delATAT others(26): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7285 | chr15 | 55612697 | ||||||
chr15:55612697 | AATATATA others(31): Show |
A | 4 | a0001c0007t0038 a0001c0007t0106 a0001c0007t0107 others(1): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7277_*7314delATAT others(34): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7277 | chr15 | 55612697 | ||||||
chr15:55612737 | T | C | 1 | a0016c0014t0073 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7275A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7275 | chr15 | 55612737 | ||||||
chr15:55612737 | T | TATATATA others(9): Show |
1 | a0001c0001t0054 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7274_*7275insGTAT others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7274 | chr15 | 55612737 | ||||||
chr15:55612737 | T | TATATATA others(17): Show |
1 | a0001c0009t0103 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7274_*7275insGTAT others(20): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7274 | chr15 | 55612737 | ||||||
chr15:55612737 | T | TATATATA others(19): Show |
1 | a0001c0009t0087 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7274_*7275insGTAT others(22): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7274 | chr15 | 55612737 | ||||||
chr15:55612747 | T | C | 8 | a0001c0001t0002 a0001c0001t0024 a0001c0001t0039 others(5): Show |
46 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*7265A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7265 | chr15 | 55612747 | ||||||
chr15:55612903 | C | A | 1 | a0001c0001t0079 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7109G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7109 | chr15 | 55612903 | ||||||
chr15:55612948 | T | C | 1 | a0001c0012t0074 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7064A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 7064 | chr15 | 55612948 | ||||||
chr15:55613098 | A | C | 5 | a0001c0001t0035 a0001c0001t0102 a0001c0012t0072 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6914T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 6914 | chr15 | 55613098 | ||||||
chr15:55613233 | T | C | 1 | a0002c0002t0063 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6779A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 6779 | chr15 | 55613233 | ||||||
chr15:55613491 | G | A | 1 | a0001c0001t0080 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6521C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 6521 | chr15 | 55613491 | ||||||
chr15:55613759 | C | CT | 22 | a0001c0001t0002 a0001c0001t0039 a0001c0001t0054 others(19): Show |
42 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*6252dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 6252 | chr15 | 55613759 | ||||||
chr15:55613759 | C | CTTT | 7 | a0003c0005t0010 a0003c0005t0044 a0003c0005t0045 others(4): Show |
9 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6250_*6252dupAAA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 6252 | chr15 | 55613759 | ||||||
chr15:55613759 | CT | C | 14 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(11): Show |
19 | HG01978.hp1 HG02109.hp2 HG02622.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*6252delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 6252 | chr15 | 55613759 | ||||||
chr15:55613759 | CTT | C | 38 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(35): Show |
119 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*6251_*6252delAA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 6251 | chr15 | 55613759 | ||||||
chr15:55613759 | CTTT | C | 4 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(1): Show |
7 | HG01168.hp2 HG01169.hp2 HG01257.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6250_*6252delAAA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 6250 | chr15 | 55613759 | ||||||
chr15:55613812 | A | G | 28 | a0001c0001t0029 a0001c0001t0066 a0001c0001t0111 others(25): Show |
39 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*6200T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 6200 | chr15 | 55613812 | ||||||
chr15:55614284 | T | C | 17 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(14): Show |
77 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*5728A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 5728 | chr15 | 55614284 | ||||||
chr15:55614359 | A | C | 2 | a0002c0002t0011 a0002c0002t0055 |
4 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5653T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 5653 | chr15 | 55614359 | ||||||
chr15:55614444 | A | C | 1 | a0002c0002t0068 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5568T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 5568 | chr15 | 55614444 | ||||||
chr15:55614616 | C | T | 4 | a0001c0001t0035 a0001c0012t0072 a0001c0012t0074 others(1): Show |
4 | HG02572.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5396G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 5396 | chr15 | 55614616 | ||||||
chr15:55614690 | T | C | 1 | a0001c0001t0081 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5322A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 5322 | chr15 | 55614690 | ||||||
chr15:55614898 | C | T | 1 | a0001c0007t0106 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5114G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 5114 | chr15 | 55614898 | ||||||
chr15:55614919 | C | T | 2 | a0001c0001t0034 a0001c0001t0070 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5093G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 5093 | chr15 | 55614919 | ||||||
chr15:55614983 | G | A | 2 | a0001c0001t0034 a0001c0001t0070 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5029C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 5029 | chr15 | 55614983 | ||||||
chr15:55615225 | G | A | 1 | a0002c0002t0064 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4787C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 4787 | chr15 | 55615225 | ||||||
chr15:55615239 | C | G | 1 | a0001c0001t0082 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4773G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 4773 | chr15 | 55615239 | ||||||
chr15:55615713 | A | G | 1 | a0005c0011t0094 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4299T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 4299 | chr15 | 55615713 | ||||||
chr15:55615776 | T | C | 15 | a0001c0007t0038 a0001c0007t0106 a0001c0007t0107 others(12): Show |
20 | HG01255.hp2 HG01884.hp2 HG02109.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4236A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 4236 | chr15 | 55615776 | ||||||
chr15:55616005 | T | C | 22 | a0001c0001t0002 a0001c0001t0024 a0001c0001t0032 others(19): Show |
62 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*4007A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 4007 | chr15 | 55616005 | ||||||
chr15:55616410 | A | C | 2 | a0001c0009t0103 a0016c0014t0073 |
2 | HG02970.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3602T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 3602 | chr15 | 55616410 | ||||||
chr15:55616419 | A | T | 1 | a0016c0014t0073 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3593T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 3593 | chr15 | 55616419 | ||||||
chr15:55616511 | A | C | 1 | a0002c0002t0067 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3501T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 3501 | chr15 | 55616511 | ||||||
chr15:55616685 | T | C | 3 | a0001c0001t0029 a0002c0002t0109 a0011c0016t0029 |
3 | HG02723.hp1 HG03540.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3327A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 3327 | chr15 | 55616685 | ||||||
chr15:55616907 | T | C | 2 | a0001c0001t0034 a0001c0001t0070 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3105A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 3105 | chr15 | 55616907 | ||||||
chr15:55616967 | T | C | 1 | a0016c0014t0073 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3045A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 3045 | chr15 | 55616967 | ||||||
chr15:55617223 | TA | T | 119 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(116): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*2788delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 2788 | chr15 | 55617223 | ||||||
chr15:55617391 | A | G | 4 | a0001c0001t0035 a0001c0012t0072 a0001c0012t0074 others(1): Show |
4 | HG02572.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2621T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 2621 | chr15 | 55617391 | ||||||
chr15:55617419 | T | C | 18 | a0001c0001t0029 a0002c0002t0011 a0002c0002t0013 others(15): Show |
27 | HG00642.hp1 HG00642.hp2 HG01109.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2593A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 2593 | chr15 | 55617419 | ||||||
chr15:55617752 | T | C | 2 | a0001c0009t0103 a0016c0014t0073 |
2 | HG02970.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2260A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 2260 | chr15 | 55617752 | ||||||
chr15:55617758 | T | C | 1 | a0002c0002t0104 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2254A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 2254 | chr15 | 55617758 | ||||||
chr15:55617807 | A | G | 1 | a0001c0009t0087 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2205T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 2205 | chr15 | 55617807 | ||||||
chr15:55617940 | T | C | 122 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(119): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*2072A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 2072 | chr15 | 55617940 | ||||||
chr15:55618059 | G | A | 1 | a0001c0001t0105 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1953C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 1953 | chr15 | 55618059 | ||||||
chr15:55618177 | T | C | 1 | a0002c0002t0065 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1835A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 1835 | chr15 | 55618177 | ||||||
chr15:55618199 | T | C | 8 | a0001c0001t0029 a0002c0002t0011 a0002c0002t0055 others(5): Show |
10 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1813A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 1813 | chr15 | 55618199 | ||||||
chr15:55618240 | A | T | 33 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(30): Show |
124 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*1772T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 1772 | chr15 | 55618240 | ||||||
chr15:55618465 | C | T | 1 | a0001c0008t0076 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1547G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 1547 | chr15 | 55618465 | ||||||
chr15:55618482 | C | G | 1 | a0006c0010t0059 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1530G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 1530 | chr15 | 55618482 | ||||||
chr15:55618562 | C | T | 2 | a0001c0007t0106 a0001c0007t0107 |
2 | HG02109.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1450G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 1450 | chr15 | 55618562 | ||||||
chr15:55618572 | A | G | 1 | a0001c0001t0008 | 4 | NA18942.hp2 NA18952.hp1 NA19002.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1440T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 1440 | chr15 | 55618572 | ||||||
chr15:55618755 | A | G | 1 | a0001c0001t0075 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1257T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 1257 | chr15 | 55618755 | ||||||
chr15:55618761 | C | T | 4 | a0001c0001t0035 a0001c0012t0072 a0001c0012t0074 others(1): Show |
4 | HG02572.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1251G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 1251 | chr15 | 55618761 | ||||||
chr15:55619008 | C | A | 3 | a0001c0007t0106 a0001c0007t0107 a0001c0007t0108 |
3 | HG02109.hp2 NA19030.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1004G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 1004 | chr15 | 55619008 | ||||||
chr15:55619342 | C | T | 2 | a0001c0001t0034 a0001c0001t0070 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*670G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 670 | chr15 | 55619342 | ||||||
chr15:55619367 | C | T | 1 | a0016c0014t0073 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*645G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 645 | chr15 | 55619367 | ||||||
chr15:55619470 | C | A | 14 | a0001c0001t0004 a0001c0001t0012 a0001c0001t0040 others(11): Show |
44 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*542G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 542 | chr15 | 55619470 | ||||||
chr15:55619497 | A | C | 1 | a0001c0012t0072 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*515T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 515 | chr15 | 55619497 | ||||||
chr15:55619500 | C | T | 1 | a0001c0001t0071 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*512G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 512 | chr15 | 55619500 | ||||||
chr15:55619615 | G | C | 10 | a0002c0002t0013 a0002c0002t0014 a0002c0002t0026 others(7): Show |
17 | HG00642.hp1 HG00642.hp2 HG01433.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*397C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 397 | chr15 | 55619615 | ||||||
chr15:55619656 | T | C | 1 | a0002c0002t0065 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*356A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 356 | chr15 | 55619656 | ||||||
chr15:55619674 | C | T | 2 | a0001c0001t0034 a0001c0001t0070 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*338G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 338 | chr15 | 55619674 | ||||||
chr15:55619859 | G | A | 1 | a0001c0001t0005 | 6 | HG01109.hp2 HG01928.hp2 HG01952.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*153C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 20/20 | 153 | chr15 | 55619859 | ||||||
chr15:55743041 | C | G | 7 | a0001c0001t0032 a0001c0001t0033 a0002c0002t0067 others(4): Show |
11 | HG02145.hp1 HG02622.hp2 HG02965.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-110G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/20 | 110 | chr15 | 55743041 | ||||||
chr15:55743043 | C | T | 3 | a0001c0001t0029 a0001c0001t0066 a0011c0016t0029 |
3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
5_prime_UTR_variant | MODIFIER | c.-112G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/20 | 112 | chr15 | 55743043 | ||||||
chr15:55743050 | G | A | 1 | a0002c0002t0109 | 1 | NA20300.hp1 | 5_prime_UTR_variant | MODIFIER | c.-119C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/20 | 119 | chr15 | 55743050 | ||||||
chr15:55743059 | C | G | 50 | a0001c0001t0012 a0001c0001t0018 a0001c0001t0021 others(47): Show |
91 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(88): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-128G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/20 | chr15 | 55743059 | |||||||
chr15:55743123 | G | A | 9 | a0001c0001t0002 a0001c0001t0041 a0001c0001t0111 others(6): Show |
46 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(43): Show |
5_prime_UTR_variant | MODIFIER | c.-192C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/20 | 192 | chr15 | 55743123 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:55620330 | C | T | 7 | a0003c0005t0010g0038 a0003c0005t0010g0039 a0003c0005t0010g0041 others(4): Show |
7 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.3199-64G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 19/19 | chr15 | 55620330 | |||||||
chr15:55620373 | G | A | 2 | a0004c0004t0031g0095 a0004c0004t0031g0096 |
2 | HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3199-107C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 19/19 | chr15 | 55620373 | |||||||
chr15:55620475 | T | C | 2 | a0004c0004t0030g0105 a0004c0004t0069g0100 |
2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3198+188A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 19/19 | chr15 | 55620475 | |||||||
chr15:55620580 | C | G | 5 | a0001c0001t0035g0219 a0001c0001t0102g0126 a0001c0012t0072g0113 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.3198+83G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 19/19 | chr15 | 55620580 | |||||||
chr15:55620655 | T | G | 1 | a0001c0003t0003g0075 | 1 | HG01943.hp1 | splice_region_variant&intron_variant | LOW | c.3198+8A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 19/19 | chr15 | 55620655 | |||||||
chr15:55621138 | G | A | 12 | a0003c0005t0010g0038 a0003c0005t0010g0039 a0003c0005t0010g0041 others(9): Show |
12 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.3094-371C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55621138 | |||||||
chr15:55621274 | C | G | 1 | a0001c0001t0012g0083 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3094-507G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55621274 | |||||||
chr15:55621344 | C | T | 12 | a0003c0005t0010g0038 a0003c0005t0010g0039 a0003c0005t0010g0041 others(9): Show |
12 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.3094-577G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55621344 | |||||||
chr15:55621357 | A | T | 1 | a0001c0001t0040g0136 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3094-590T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55621357 | |||||||
chr15:55621386 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3094-619C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55621386 | |||||||
chr15:55621428 | C | G | 1 | a0001c0001t0002g0251 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.3094-661G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55621428 | |||||||
chr15:55621432 | C | T | 2 | a0001c0001t0002g0281 a0001c0001t0002g0282 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3094-665G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55621432 | |||||||
chr15:55621527 | C | T | 80 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(77): Show |
80 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.3094-760G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55621527 | |||||||
chr15:55621583 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3094-816G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55621583 | |||||||
chr15:55621584 | G | A | 5 | a0001c0001t0035g0219 a0001c0001t0102g0126 a0001c0012t0072g0113 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.3094-817C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55621584 | |||||||
chr15:55621605 | C | T | 12 | a0003c0005t0010g0038 a0003c0005t0010g0039 a0003c0005t0010g0041 others(9): Show |
12 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.3094-838G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55621605 | |||||||
chr15:55621886 | T | C | 28 | a0001c0001t0035g0219 a0001c0001t0051g0004 a0001c0001t0052g0006 others(25): Show |
28 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.3094-1119A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55621886 | |||||||
chr15:55622150 | T | C | 12 | a0003c0005t0010g0038 a0003c0005t0010g0039 a0003c0005t0010g0041 others(9): Show |
12 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.3094-1383A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55622150 | |||||||
chr15:55622216 | G | GT | 85 | a0001c0001t0001g0206 a0001c0001t0002g0246 a0001c0001t0002g0257 others(82): Show |
85 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.3094-1450dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55622216 | |||||||
chr15:55622216 | G | GTT | 85 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(82): Show |
85 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.3094-1451_3094-145 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55622216 | |||||||
chr15:55622216 | GT | G | 9 | a0001c0001t0082g0128 a0001c0001t0083g0125 a0001c0001t0085g0124 others(6): Show |
9 | HG02145.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.3094-1450delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55622216 | |||||||
chr15:55622384 | AT | A | 14 | a0001c0001t0001g0155 a0001c0001t0001g0164 a0001c0001t0002g0272 others(11): Show |
14 | HG01891.hp2 HG01981.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.3094-1618delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55622384 | |||||||
chr15:55622384 | ATT | A | 257 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(254): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.3094-1619_3094-161 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55622384 | |||||||
chr15:55622415 | G | A | 3 | a0001c0001t0029g0092 a0002c0002t0109g0236 a0011c0016t0029g0093 |
3 | HG02723.hp1 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3094-1648C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55622415 | |||||||
chr15:55622564 | TA | T | 268 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(265): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.3093+1777delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55622564 | |||||||
chr15:55622565 | A | T | 1 | a0012c0019t0046g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3093+1777T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55622565 | |||||||
chr15:55622604 | G | A | 1 | a0001c0012t0002g0279 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3093+1738C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55622604 | |||||||
chr15:55622623 | C | T | 1 | a0001c0001t0041g0263 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3093+1719G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55622623 | |||||||
chr15:55622694 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3093+1648G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55622694 | |||||||
chr15:55622818 | G | C | 9 | a0001c0001t0035g0219 a0001c0001t0054g0005 a0001c0009t0042g0035 others(6): Show |
9 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.3093+1524C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55622818 | |||||||
chr15:55622870 | T | C | 1 | a0001c0001t0077g0174 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.3093+1472A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55622870 | |||||||
chr15:55623062 | C | A | 4 | a0001c0001t0035g0219 a0001c0012t0072g0113 a0001c0012t0074g0114 others(1): Show |
4 | HG02572.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.3093+1280G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55623062 | |||||||
chr15:55623084 | G | A | 8 | a0001c0001t0001g0144 a0001c0001t0001g0193 a0001c0001t0006g0138 others(5): Show |
8 | NA18942.hp2 NA18952.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.3093+1258C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55623084 | |||||||
chr15:55623435 | C | T | 12 | a0003c0005t0010g0038 a0003c0005t0010g0039 a0003c0005t0010g0041 others(9): Show |
12 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.3093+907G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55623435 | |||||||
chr15:55623452 | G | A | 59 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(56): Show |
59 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.3093+890C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55623452 | |||||||
chr15:55623497 | T | C | 232 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(229): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.3093+845A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55623497 | |||||||
chr15:55623520 | C | T | 1 | a0004c0004t0069g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3093+822G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55623520 | |||||||
chr15:55623563 | T | A | 6 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0040g0135 others(3): Show |
6 | HG00323.hp2 HG01081.hp1 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.3093+779A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55623563 | |||||||
chr15:55623702 | G | A | 272 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(269): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.3093+640C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55623702 | |||||||
chr15:55623835 | T | C | 40 | a0001c0001t0021g0051 a0001c0001t0021g0060 a0001c0001t0066g0094 others(37): Show |
40 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.3093+507A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55623835 | |||||||
chr15:55624158 | T | C | 1 | a0001c0001t0071g0143 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3093+184A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55624158 | |||||||
chr15:55624175 | CCCT | C | 12 | a0003c0005t0010g0038 a0003c0005t0010g0039 a0003c0005t0010g0041 others(9): Show |
12 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.3093+164_3093+166d others(5): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55624175 | |||||||
chr15:55624240 | G | C | 5 | a0001c0001t0054g0005 a0001c0009t0042g0035 a0001c0009t0087g0112 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3093+102C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55624240 | |||||||
chr15:55624241 | T | C | 1 | a0001c0020t0053g0002 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3093+101A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55624241 | |||||||
chr15:55624261 | A | G | 4 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(1): Show |
4 | HG03453.hp1 HG03486.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.3093+81T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 18/19 | chr15 | 55624261 | |||||||
chr15:55624636 | G | A | 1 | a0001c0001t0078g0149 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2928-129C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55624636 | |||||||
chr15:55624868 | G | T | 127 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(124): Show |
127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.2928-361C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55624868 | |||||||
chr15:55625353 | G | A | 1 | a0002c0002t0056g0045 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2928-846C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625353 | |||||||
chr15:55625432 | G | A | 1 | a0016c0014t0073g0234 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2928-925C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625432 | |||||||
chr15:55625469 | A | T | 1 | a0001c0003t0003g0042 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2928-962T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625469 | |||||||
chr15:55625515 | G | A | 1 | a0001c0001t0005g0141 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2928-1008C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625515 | |||||||
chr15:55625563 | C | T | 272 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(269): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.2928-1056G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625563 | |||||||
chr15:55625609 | T | A | 1 | a0001c0001t0101g0217 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2928-1102A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625609 | |||||||
chr15:55625626 | C | CT | 41 | a0001c0001t0021g0051 a0001c0001t0021g0060 a0001c0001t0066g0094 others(38): Show |
41 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.2928-1120dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625626 | |||||||
chr15:55625681 | T | C | 1 | a0002c0002t0003g0009 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2928-1174A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625681 | |||||||
chr15:55625707 | T | TC | 61 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(58): Show |
61 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.2928-1201dupG | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625707 | |||||||
chr15:55625768 | C | T | 48 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(45): Show |
48 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.2927+1240G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625768 | |||||||
chr15:55625819 | C | T | 19 | a0001c0001t0002g0249 a0001c0001t0002g0250 a0001c0001t0002g0251 others(16): Show |
19 | HG00733.hp1 HG01168.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.2927+1189G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625819 | |||||||
chr15:55625853 | C | T | 1 | a0004c0004t0069g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2927+1155G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625853 | |||||||
chr15:55625874 | C | T | 1 | a0001c0012t0002g0279 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2927+1134G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625874 | |||||||
chr15:55625948 | T | G | 8 | a0001c0001t0001g0144 a0001c0001t0001g0190 a0001c0001t0006g0138 others(5): Show |
8 | HG00408.hp1 NA18942.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.2927+1060A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625948 | |||||||
chr15:55625954 | T | C | 1 | a0001c0012t0072g0113 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2927+1054A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625954 | |||||||
chr15:55625979 | C | T | 1 | a0011c0016t0029g0093 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2927+1029G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55625979 | |||||||
chr15:55626298 | A | G | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2927+710T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55626298 | |||||||
chr15:55626314 | C | G | 1 | a0001c0001t0001g0160 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2927+694G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55626314 | |||||||
chr15:55626386 | G | A | 23 | a0002c0002t0011g0048 a0002c0002t0011g0049 a0002c0002t0011g0050 others(20): Show |
23 | HG00642.hp1 HG00642.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.2927+622C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55626386 | |||||||
chr15:55626460 | T | C | 4 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(1): Show |
4 | HG03453.hp1 HG03486.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2927+548A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55626460 | |||||||
chr15:55626500 | T | C | 2 | a0001c0001t0066g0094 a0002c0002t0019g0062 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2927+508A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55626500 | |||||||
chr15:55626515 | G | C | 47 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(44): Show |
47 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.2927+493C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55626515 | |||||||
chr15:55626576 | C | G | 1 | a0002c0002t0003g0009 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2927+432G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55626576 | |||||||
chr15:55626586 | T | TA | 5 | a0001c0001t0035g0219 a0001c0001t0102g0126 a0001c0012t0072g0113 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2927+421dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55626586 | |||||||
chr15:55626594 | C | CA | 7 | a0001c0001t0001g0162 a0001c0001t0001g0195 a0001c0001t0001g0200 others(4): Show |
7 | HG01934.hp2 HG02615.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.2927+413dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55626594 | |||||||
chr15:55626594 | CA | C | 37 | a0001c0001t0040g0135 a0001c0001t0066g0094 a0001c0001t0111g0278 others(34): Show |
37 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.2927+413delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55626594 | |||||||
chr15:55626706 | C | T | 5 | a0001c0001t0035g0219 a0001c0001t0102g0126 a0001c0012t0072g0113 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2927+302G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55626706 | |||||||
chr15:55626716 | C | G | 61 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(58): Show |
61 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.2927+292G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55626716 | |||||||
chr15:55626765 | TAAAAG | T | 4 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(1): Show |
4 | HG03453.hp1 HG03486.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2927+238_2927+242d others(7): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55626765 | |||||||
chr15:55626941 | T | G | 77 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.2927+67A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 17/19 | chr15 | 55626941 | |||||||
chr15:55627326 | G | GT | 47 | a0001c0001t0001g0144 a0001c0001t0002g0270 a0001c0001t0004g0142 others(44): Show |
47 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.2807-199dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627326 | |||||||
chr15:55627326 | G | GTT | 76 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(73): Show |
76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.2807-200_2807-199d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627326 | |||||||
chr15:55627326 | G | GTTT | 6 | a0001c0001t0001g0130 a0001c0001t0001g0162 a0001c0001t0001g0200 others(3): Show |
6 | HG00438.hp1 HG01361.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.2807-201_2807-199d others(5): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627326 | |||||||
chr15:55627326 | GT | G | 30 | a0001c0001t0035g0219 a0001c0001t0054g0005 a0001c0007t0038g0230 others(27): Show |
30 | HG01255.hp2 HG01884.hp2 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.2807-199delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627326 | |||||||
chr15:55627385 | G | A | 139 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.2807-257C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627385 | |||||||
chr15:55627492 | GT | G | 197 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(194): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.2807-365delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627492 | |||||||
chr15:55627515 | T | G | 3 | a0001c0001t0029g0092 a0002c0002t0109g0236 a0011c0016t0029g0093 |
3 | HG02723.hp1 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2807-387A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627515 | |||||||
chr15:55627582 | C | T | 44 | a0001c0001t0021g0051 a0001c0001t0021g0060 a0001c0001t0066g0094 others(41): Show |
44 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.2807-454G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627582 | |||||||
chr15:55627592 | G | A | 11 | a0003c0005t0010g0038 a0003c0005t0010g0039 a0003c0005t0010g0041 others(8): Show |
11 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.2807-464C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627592 | |||||||
chr15:55627715 | C | T | 1 | a0002c0002t0013g0016 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2807-587G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627715 | |||||||
chr15:55627830 | C | T | 1 | a0001c0001t0100g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2807-702G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627830 | |||||||
chr15:55627851 | T | C | 11 | a0003c0005t0010g0038 a0003c0005t0010g0039 a0003c0005t0010g0041 others(8): Show |
11 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.2807-723A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627851 | |||||||
chr15:55627881 | C | T | 2 | a0001c0009t0103g0233 a0016c0014t0073g0234 |
2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2807-753G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627881 | |||||||
chr15:55627911 | C | A | 5 | a0001c0001t0054g0005 a0001c0009t0042g0035 a0001c0009t0087g0112 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2807-783G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627911 | |||||||
chr15:55627931 | C | T | 3 | a0001c0001t0029g0092 a0002c0002t0109g0236 a0011c0016t0029g0093 |
3 | HG02723.hp1 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2807-803G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55627931 | |||||||
chr15:55628024 | C | T | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2806+798G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55628024 | |||||||
chr15:55628142 | T | G | 5 | a0002c0002t0011g0048 a0002c0002t0011g0049 a0002c0002t0011g0050 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.2806+680A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55628142 | |||||||
chr15:55628285 | G | A | 4 | a0001c0001t0040g0135 a0001c0001t0040g0136 a0001c0001t0071g0143 others(1): Show |
4 | HG02027.hp1 HG04228.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.2806+537C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55628285 | |||||||
chr15:55628358 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2806+464A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55628358 | |||||||
chr15:55628386 | GA | G | 239 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(236): Show |
239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.2806+435delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55628386 | |||||||
chr15:55628386 | GAA | G | 19 | a0001c0001t0001g0164 a0001c0001t0002g0265 a0001c0001t0004g0188 others(16): Show |
20 | HG00099.hp1 HG00438.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.2806+434_2806+435d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55628386 | |||||||
chr15:55628387 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2806+435T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55628387 | |||||||
chr15:55628389 | A | T | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2806+433T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55628389 | |||||||
chr15:55628514 | C | A | 1 | a0002c0002t0003g0063 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2806+308G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55628514 | |||||||
chr15:55628815 | T | C | 125 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(122): Show |
125 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(122): Show |
splice_region_variant&intron_variant | LOW | c.2806+7A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 16/19 | chr15 | 55628815 | |||||||
chr15:55629028 | T | G | 1 | a0001c0001t0096g0229 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2624-24A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629028 | |||||||
chr15:55629278 | T | C | 1 | a0002c0002t0012g0082 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2624-274A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629278 | |||||||
chr15:55629303 | T | C | 20 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(17): Show |
20 | HG01255.hp2 HG01884.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.2624-299A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629303 | |||||||
chr15:55629351 | T | C | 1 | a0002c0002t0003g0063 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2624-347A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629351 | |||||||
chr15:55629359 | GTA | G | 8 | a0001c0001t0002g0247 a0001c0001t0002g0255 a0001c0001t0002g0256 others(5): Show |
8 | HG00140.hp1 HG01517.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2624-357_2624-356d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629359 | |||||||
chr15:55629359 | GTATA | G | 3 | a0004c0004t0023g0056 a0004c0004t0030g0105 a0004c0004t0069g0100 |
3 | HG01884.hp2 HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2624-359_2624-356d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629359 | |||||||
chr15:55629363 | ATATATAT others(31): Show |
A | 1 | a0002c0002t0068g0099 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2624-397_2624-360d others(40): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629363 | |||||||
chr15:55629367 | ATATATAT others(3): Show |
A | 3 | a0001c0001t0001g0184 a0001c0001t0008g0197 a0001c0003t0018g0073 |
3 | HG01993.hp2 HG02074.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.2624-373_2624-364d others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629367 | |||||||
chr15:55629367 | ATATATAT others(5): Show |
A | 13 | a0001c0001t0001g0134 a0001c0001t0001g0154 a0001c0001t0001g0166 others(10): Show |
13 | HG01074.hp2 HG01975.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.2624-375_2624-364d others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629367 | |||||||
chr15:55629367 | ATATATAT others(7): Show |
A | 85 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(82): Show |
85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.2624-377_2624-364d others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629367 | |||||||
chr15:55629367 | ATATATAT others(9): Show |
A | 12 | a0001c0001t0001g0144 a0001c0001t0001g0153 a0001c0001t0001g0155 others(9): Show |
12 | HG00323.hp2 HG00408.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.2624-379_2624-364d others(18): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629367 | |||||||
chr15:55629367 | ATATATAT others(11): Show |
A | 9 | a0001c0001t0001g0168 a0001c0001t0001g0193 a0001c0001t0029g0092 others(6): Show |
9 | HG00738.hp2 HG02723.hp1 HG03540.hp2 others(6): Show |
intron_variant | MODIFIER | c.2624-381_2624-364d others(20): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629367 | |||||||
chr15:55629367 | ATATATAT others(13): Show |
A | 4 | a0001c0001t0001g0152 a0001c0001t0001g0160 a0001c0001t0001g0161 others(1): Show |
4 | HG00280.hp2 NA18953.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.2624-383_2624-364d others(22): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629367 | |||||||
chr15:55629367 | ATATATAT others(15): Show |
A | 1 | a0002c0002t0109g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2624-385_2624-364d others(24): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629367 | |||||||
chr15:55629367 | ATATATAT others(19): Show |
A | 1 | a0001c0001t0021g0060 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2624-389_2624-364d others(28): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629367 | |||||||
chr15:55629367 | ATATATAT others(21): Show |
A | 1 | a0001c0001t0021g0051 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2624-391_2624-364d others(30): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629367 | |||||||
chr15:55629367 | ATATATAT others(29): Show |
A | 1 | a0002c0002t0058g0047 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2624-399_2624-364d others(38): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629367 | |||||||
chr15:55629367 | ATATATAT others(31): Show |
A | 36 | a0001c0001t0066g0094 a0001c0001t0111g0278 a0002c0002t0011g0048 others(33): Show |
36 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2624-401_2624-364d others(40): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629367 | |||||||
chr15:55629369 | ATATATAT others(9): Show |
A | 1 | a0001c0001t0034g0001 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2624-381_2624-366d others(18): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629369 | |||||||
chr15:55629369 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0070g0133 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2624-383_2624-366d others(20): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629369 | |||||||
chr15:55629371 | A | ATGTG | 4 | a0001c0008t0093g0209 a0003c0006t0009g0015 a0004c0004t0048g0054 others(1): Show |
4 | HG00733.hp2 HG01255.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2624-368_2624-367i others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629371 | |||||||
chr15:55629371 | A | ATGTGTGT others(1): Show |
3 | a0001c0001t0102g0126 a0001c0008t0037g0210 a0004c0004t0030g0097 |
3 | HG02145.hp1 HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2624-368_2624-367i others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629371 | |||||||
chr15:55629371 | A | ATGTGTGT others(7): Show |
1 | a0001c0008t0076g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2624-368_2624-367i others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629371 | |||||||
chr15:55629371 | A | G | 1 | a0004c0004t0031g0096 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2624-367T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629371 | |||||||
chr15:55629371 | ATATATG | A | 3 | a0001c0001t0105g0205 a0001c0007t0038g0230 a0004c0004t0050g0059 |
3 | HG02630.hp1 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2624-373_2624-368d others(8): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629371 | |||||||
chr15:55629371 | ATATATGT others(5): Show |
A | 1 | a0001c0001t0035g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2624-379_2624-368d others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629371 | |||||||
chr15:55629371 | ATATATGT others(9): Show |
A | 1 | a0005c0011t0035g0220 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2624-383_2624-368d others(18): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629371 | |||||||
chr15:55629373 | A | ATG | 3 | a0001c0001t0002g0262 a0001c0001t0002g0264 a0009c0013t0002g0239 |
3 | HG00733.hp1 HG02257.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.2624-370_2624-369i others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629373 | |||||||
chr15:55629373 | A | G | 15 | a0001c0001t0101g0217 a0001c0001t0102g0126 a0001c0007t0038g0231 others(12): Show |
15 | HG00733.hp2 HG01255.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.2624-369T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629373 | |||||||
chr15:55629373 | ATATG | A | 3 | a0001c0001t0002g0250 a0001c0001t0002g0259 a0003c0005t0022g0037 |
3 | HG01358.hp1 HG03490.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2624-373_2624-370d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629373 | |||||||
chr15:55629373 | ATATGTG | A | 4 | a0001c0001t0002g0249 a0001c0001t0002g0258 a0003c0006t0009g0007 others(1): Show |
4 | HG01515.hp1 HG01517.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.2624-375_2624-370d others(8): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629373 | |||||||
chr15:55629373 | ATATGTGT others(1): Show |
A | 9 | a0001c0001t0002g0248 a0001c0001t0033g0102 a0001c0001t0039g0132 others(6): Show |
9 | HG00099.hp1 HG00741.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.2624-377_2624-370d others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629373 | |||||||
chr15:55629373 | ATATGTGT others(3): Show |
A | 3 | a0001c0001t0002g0251 a0001c0001t0033g0101 a0002c0002t0104g0215 |
3 | HG01168.hp1 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2624-379_2624-370d others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629373 | |||||||
chr15:55629373 | ATATGTGT others(5): Show |
A | 3 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0032g0098 |
3 | HG02622.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2624-381_2624-370d others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629373 | |||||||
chr15:55629373 | ATATGTGT others(7): Show |
A | 2 | a0001c0001t0032g0103 a0001c0001t0100g0232 |
2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2624-383_2624-370d others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629373 | |||||||
chr15:55629373 | ATATGTGT others(15): Show |
A | 1 | a0001c0001t0002g0257 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2624-391_2624-370d others(24): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629373 | |||||||
chr15:55629373 | ATATGTGT others(21): Show |
A | 1 | a0013c0015t0043g0011 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2624-397_2624-370d others(30): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629373 | |||||||
chr15:55629375 | A | ATG | 7 | a0001c0001t0002g0243 a0001c0001t0002g0246 a0001c0001t0002g0253 others(4): Show |
7 | HG00639.hp2 HG01081.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.2624-373_2624-372d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629375 | |||||||
chr15:55629375 | A | ATGTG | 5 | a0001c0001t0002g0244 a0001c0001t0002g0265 a0001c0001t0002g0266 others(2): Show |
5 | HG01515.hp2 HG01928.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.2624-375_2624-372d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629375 | |||||||
chr15:55629375 | A | ATGTGTG | 4 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0269 others(1): Show |
4 | HG00741.hp2 HG01943.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.2624-377_2624-372d others(8): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629375 | |||||||
chr15:55629375 | A | ATGTGTGT others(1): Show |
3 | a0001c0001t0002g0272 a0001c0009t0087g0112 a0002c0002t0016g0127 |
3 | HG01981.hp2 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2624-379_2624-372d others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629375 | |||||||
chr15:55629375 | A | ATGTGTGT others(7): Show |
1 | a0001c0001t0002g0277 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2624-385_2624-372d others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629375 | |||||||
chr15:55629375 | A | G | 27 | a0001c0001t0002g0262 a0001c0001t0002g0264 a0001c0001t0024g0013 others(24): Show |
27 | HG00733.hp1 HG00733.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.2624-371T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629375 | |||||||
chr15:55629375 | ATG | A | 6 | a0001c0001t0002g0274 a0001c0001t0054g0005 a0001c0001t0096g0229 others(3): Show |
6 | HG01952.hp2 HG02145.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.2624-373_2624-372d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629375 | |||||||
chr15:55629375 | ATGTG | A | 3 | a0001c0001t0016g0122 a0001c0001t0084g0129 a0003c0006t0022g0012 |
3 | HG01358.hp2 HG01891.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2624-375_2624-372d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629375 | |||||||
chr15:55629375 | ATGTGTGT others(3): Show |
A | 1 | a0005c0011t0098g0222 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2624-381_2624-372d others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629375 | |||||||
chr15:55629375 | ATGTGTGT others(7): Show |
A | 1 | a0001c0009t0042g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2624-385_2624-372d others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629375 | |||||||
chr15:55629375 | ATGTGTGT others(9): Show |
A | 2 | a0001c0001t0051g0004 a0001c0001t0052g0006 |
2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2624-387_2624-372d others(18): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629375 | |||||||
chr15:55629379 | G | A | 2 | a0001c0001t0096g0229 a0012c0019t0046g0003 |
2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2624-375C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629379 | |||||||
chr15:55629381 | G | A | 1 | a0001c0001t0096g0229 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2624-377C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629381 | |||||||
chr15:55629391 | G | T | 1 | a0001c0001t0001g0162 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2624-387C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629391 | |||||||
chr15:55629393 | G | T | 2 | a0001c0001t0001g0184 a0001c0003t0018g0073 |
2 | HG01993.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.2624-389C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629393 | |||||||
chr15:55629395 | G | T | 13 | a0001c0001t0001g0134 a0001c0001t0001g0154 a0001c0001t0001g0166 others(10): Show |
13 | HG01074.hp2 HG01975.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.2624-391C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629395 | |||||||
chr15:55629397 | G | T | 85 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(82): Show |
85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.2624-393C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629397 | |||||||
chr15:55629399 | G | T | 12 | a0001c0001t0001g0144 a0001c0001t0001g0153 a0001c0001t0001g0155 others(9): Show |
12 | HG00323.hp2 HG00408.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.2624-395C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629399 | |||||||
chr15:55629401 | G | T | 9 | a0001c0001t0001g0168 a0001c0001t0001g0193 a0001c0001t0029g0092 others(6): Show |
9 | HG00738.hp2 HG02723.hp1 HG03540.hp2 others(6): Show |
intron_variant | MODIFIER | c.2624-397C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629401 | |||||||
chr15:55629403 | G | T | 4 | a0001c0001t0001g0152 a0001c0001t0001g0160 a0001c0001t0001g0161 others(1): Show |
4 | HG00280.hp2 NA18953.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.2624-399C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629403 | |||||||
chr15:55629405 | G | A | 1 | a0002c0002t0068g0099 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2624-401C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629405 | |||||||
chr15:55629405 | G | T | 1 | a0002c0002t0109g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2624-401C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629405 | |||||||
chr15:55629537 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2624-533G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629537 | |||||||
chr15:55629694 | T | C | 5 | a0001c0001t0054g0005 a0001c0009t0042g0035 a0001c0009t0087g0112 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2624-690A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629694 | |||||||
chr15:55629790 | G | T | 128 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(125): Show |
128 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.2624-786C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629790 | |||||||
chr15:55629795 | CATGAATA others(1): Show |
C | 127 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(124): Show |
127 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.2624-799_2624-792d others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629795 | |||||||
chr15:55629858 | G | A | 1 | a0002c0002t0003g0063 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2624-854C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629858 | |||||||
chr15:55629881 | G | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0206 a0001c0001t0001g0207 |
3 | NA18948.hp2 NA18980.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.2624-877C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629881 | |||||||
chr15:55629936 | C | A | 1 | a0001c0001t0001g0144 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2624-932G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629936 | |||||||
chr15:55629984 | A | AT | 12 | a0001c0001t0001g0144 a0001c0001t0001g0165 a0001c0001t0001g0226 others(9): Show |
12 | HG01074.hp1 HG01934.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.2624-981dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629984 | |||||||
chr15:55629984 | AT | A | 9 | a0001c0001t0002g0244 a0001c0001t0002g0248 a0001c0001t0002g0262 others(6): Show |
10 | HG01515.hp2 HG01884.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.2624-981delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629984 | |||||||
chr15:55629985 | T | C | 1 | a0001c0009t0042g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2624-981A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55629985 | |||||||
chr15:55630110 | C | T | 1 | a0002c0002t0068g0099 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2624-1106G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630110 | |||||||
chr15:55630118 | C | A | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2624-1114G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630118 | |||||||
chr15:55630207 | C | T | 4 | a0001c0001t0032g0098 a0001c0001t0032g0103 a0001c0001t0033g0101 others(1): Show |
4 | HG02622.hp2 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2624-1203G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630207 | |||||||
chr15:55630245 | C | G | 1 | a0001c0001t0004g0142 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2624-1241G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630245 | |||||||
chr15:55630263 | G | C | 38 | a0001c0001t0066g0094 a0001c0001t0111g0278 a0002c0002t0011g0048 others(35): Show |
38 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2624-1259C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630263 | |||||||
chr15:55630281 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2624-1277G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630281 | |||||||
chr15:55630389 | C | T | 11 | a0003c0005t0010g0038 a0003c0005t0010g0039 a0003c0005t0010g0041 others(8): Show |
11 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.2624-1385G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630389 | |||||||
chr15:55630468 | G | T | 2 | a0001c0001t0021g0051 a0001c0001t0021g0060 |
2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2624-1464C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630468 | |||||||
chr15:55630469 | C | T | 2 | a0001c0001t0021g0051 a0001c0001t0021g0060 |
2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2624-1465G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630469 | |||||||
chr15:55630571 | A | T | 1 | a0001c0001t0001g0144 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2624-1567T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630571 | |||||||
chr15:55630573 | T | A | 1 | a0001c0001t0001g0144 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2624-1569A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630573 | |||||||
chr15:55630687 | T | G | 1 | a0002c0002t0007g0085 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2624-1683A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630687 | |||||||
chr15:55630698 | T | C | 1 | a0002c0002t0057g0025 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2624-1694A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630698 | |||||||
chr15:55630918 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2624-1914A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630918 | |||||||
chr15:55630940 | T | C | 1 | a0001c0001t0012g0083 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2624-1936A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55630940 | |||||||
chr15:55631198 | G | C | 1 | a0001c0001t0006g0138 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2624-2194C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55631198 | |||||||
chr15:55631266 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2624-2262G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55631266 | |||||||
chr15:55631465 | C | T | 3 | a0001c0001t0029g0092 a0002c0002t0109g0236 a0011c0016t0029g0093 |
3 | HG02723.hp1 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2624-2461G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55631465 | |||||||
chr15:55631710 | G | T | 1 | a0001c0001t0001g0144 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2624-2706C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55631710 | |||||||
chr15:55631757 | C | T | 61 | a0001c0001t0004g0142 a0001c0001t0004g0188 a0001c0001t0012g0083 others(58): Show |
61 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.2624-2753G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55631757 | |||||||
chr15:55631768 | T | G | 1 | a0001c0001t0001g0144 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2624-2764A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55631768 | |||||||
chr15:55631870 | G | A | 272 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(269): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.2624-2866C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55631870 | |||||||
chr15:55632074 | A | T | 1 | a0001c0001t0001g0144 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2624-3070T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632074 | |||||||
chr15:55632250 | T | C | 39 | a0001c0001t0002g0277 a0001c0001t0066g0094 a0001c0001t0111g0278 others(36): Show |
39 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.2624-3246A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632250 | |||||||
chr15:55632277 | T | C | 1 | a0001c0001t0096g0229 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2624-3273A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632277 | |||||||
chr15:55632316 | T | G | 1 | a0012c0019t0046g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2624-3312A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632316 | |||||||
chr15:55632411 | T | C | 139 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(136): Show |
139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.2624-3407A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632411 | |||||||
chr15:55632485 | T | A | 1 | a0001c0001t0018g0058 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2624-3481A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632485 | |||||||
chr15:55632521 | T | A | 1 | a0005c0011t0094g0218 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2624-3517A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632521 | |||||||
chr15:55632558 | A | C | 1 | a0001c0001t0001g0144 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2624-3554T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632558 | |||||||
chr15:55632666 | A | G | 1 | a0002c0002t0068g0099 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2624-3662T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632666 | |||||||
chr15:55632702 | G | A | 1 | a0002c0002t0013g0018 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2624-3698C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632702 | |||||||
chr15:55632755 | G | C | 6 | a0004c0004t0023g0056 a0004c0004t0023g0057 a0004c0004t0047g0061 others(3): Show |
6 | HG01255.hp2 HG01884.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2624-3751C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632755 | |||||||
chr15:55632828 | G | A | 273 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(270): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.2624-3824C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632828 | |||||||
chr15:55632881 | G | A | 1 | a0001c0009t0087g0112 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2624-3877C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632881 | |||||||
chr15:55632899 | T | A | 1 | a0001c0020t0053g0002 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2624-3895A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632899 | |||||||
chr15:55632906 | G | A | 1 | a0001c0001t0040g0135 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2624-3902C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55632906 | |||||||
chr15:55633191 | T | G | 1 | a0012c0019t0046g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2623+3979A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55633191 | |||||||
chr15:55633242 | C | CT | 10 | a0001c0001t0035g0219 a0001c0001t0054g0005 a0001c0001t0102g0126 others(7): Show |
10 | HG02572.hp1 HG02615.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2623+3927dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55633242 | |||||||
chr15:55633447 | T | C | 273 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(270): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.2623+3723A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55633447 | |||||||
chr15:55633463 | C | A | 1 | a0001c0001t0001g0166 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2623+3707G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55633463 | |||||||
chr15:55633631 | G | A | 20 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(17): Show |
20 | HG01255.hp2 HG01884.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.2623+3539C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55633631 | |||||||
chr15:55633749 | G | A | 76 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(73): Show |
76 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.2623+3421C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55633749 | |||||||
chr15:55633849 | C | T | 1 | a0001c0007t0106g0109 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2623+3321G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55633849 | |||||||
chr15:55633956 | T | C | 42 | a0001c0001t0021g0051 a0001c0001t0021g0060 a0001c0001t0034g0001 others(39): Show |
43 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.2623+3214A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55633956 | |||||||
chr15:55633965 | C | T | 42 | a0001c0001t0021g0051 a0001c0001t0021g0060 a0001c0001t0034g0001 others(39): Show |
43 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.2623+3205G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55633965 | |||||||
chr15:55633976 | T | C | 40 | a0001c0001t0021g0051 a0001c0001t0021g0060 a0001c0001t0066g0094 others(37): Show |
40 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.2623+3194A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55633976 | |||||||
chr15:55634063 | C | CTT | 36 | a0001c0001t0021g0051 a0001c0001t0021g0060 a0001c0001t0066g0094 others(33): Show |
36 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2623+3105_2623+310 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55634063 | |||||||
chr15:55634063 | CT | C | 200 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(197): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2623+3106delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55634063 | |||||||
chr15:55634063 | CTT | C | 13 | a0001c0001t0001g0131 a0001c0001t0001g0175 a0001c0001t0002g0249 others(10): Show |
13 | HG01074.hp1 HG01975.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.2623+3105_2623+310 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55634063 | |||||||
chr15:55634213 | G | A | 20 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(17): Show |
20 | HG01255.hp2 HG01884.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.2623+2957C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55634213 | |||||||
chr15:55634225 | G | A | 12 | a0003c0005t0010g0038 a0003c0005t0010g0039 a0003c0005t0010g0041 others(9): Show |
12 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.2623+2945C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55634225 | |||||||
chr15:55634427 | C | T | 1 | a0001c0020t0053g0002 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2623+2743G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55634427 | |||||||
chr15:55634535 | T | C | 48 | a0001c0001t0004g0142 a0001c0001t0004g0188 a0001c0001t0012g0083 others(45): Show |
48 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.2623+2635A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55634535 | |||||||
chr15:55634735 | G | A | 48 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(45): Show |
48 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.2623+2435C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55634735 | |||||||
chr15:55634831 | C | G | 2 | a0004c0004t0031g0095 a0004c0004t0031g0096 |
2 | HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2623+2339G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55634831 | |||||||
chr15:55634899 | G | A | 49 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0144 others(46): Show |
49 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.2623+2271C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55634899 | |||||||
chr15:55634902 | T | C | 167 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.2623+2268A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55634902 | |||||||
chr15:55634947 | GCCATGTA others(11): Show |
G | 1 | a0001c0008t0037g0208 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2623+2205_2623+222 others(22): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55634947 | |||||||
chr15:55634949 | C | G | 1 | a0002c0002t0003g0084 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2623+2221G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55634949 | |||||||
chr15:55635051 | G | A | 6 | a0001c0001t0054g0005 a0001c0009t0042g0035 a0001c0009t0087g0112 others(3): Show |
6 | HG02615.hp1 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2623+2119C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635051 | |||||||
chr15:55635061 | G | C | 273 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(270): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.2623+2109C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635061 | |||||||
chr15:55635069 | T | TTC | 6 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(3): Show |
6 | HG02145.hp1 HG03195.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2623+2099_2623+210 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635069 | |||||||
chr15:55635071 | C | CTG | 4 | a0001c0001t0029g0092 a0001c0003t0003g0074 a0011c0016t0029g0093 others(1): Show |
4 | HG02300.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2623+2097_2623+209 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635071 | |||||||
chr15:55635071 | C | CTGTGTGT others(1): Show |
6 | a0001c0009t0042g0035 a0003c0005t0010g0039 a0003c0005t0010g0041 others(3): Show |
6 | HG00741.hp1 HG01106.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.2623+2098_2623+209 others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635071 | |||||||
chr15:55635071 | C | CTGTGTGT others(3): Show |
7 | a0001c0001t0002g0255 a0001c0001t0054g0005 a0001c0001t0096g0229 others(4): Show |
7 | HG00140.hp1 HG01517.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2623+2098_2623+209 others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635071 | |||||||
chr15:55635071 | C | CTGTGTGT others(5): Show |
34 | a0001c0001t0001g0181 a0001c0001t0002g0240 a0001c0001t0002g0241 others(31): Show |
34 | HG00099.hp2 HG00733.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.2623+2098_2623+209 others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635071 | |||||||
chr15:55635071 | C | CTGTGTGT others(7): Show |
53 | a0001c0001t0001g0115 a0001c0001t0001g0130 a0001c0001t0001g0131 others(50): Show |
53 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.2623+2098_2623+209 others(18): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635071 | |||||||
chr15:55635071 | C | CTGTGTGT others(9): Show |
27 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0134 others(24): Show |
27 | HG01074.hp2 HG01891.hp2 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.2623+2098_2623+209 others(20): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635071 | |||||||
chr15:55635071 | C | CTGTGTGT others(11): Show |
5 | a0001c0001t0001g0200 a0001c0001t0002g0281 a0001c0001t0002g0282 others(2): Show |
5 | HG02572.hp1 HG02818.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.2623+2098_2623+209 others(22): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635071 | |||||||
chr15:55635071 | C | CTGTGTGT others(13): Show |
4 | a0001c0001t0002g0249 a0001c0001t0033g0102 a0001c0001t0039g0199 others(1): Show |
4 | HG01975.hp1 HG02572.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2623+2098_2623+209 others(24): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635071 | |||||||
chr15:55635071 | C | CTGTGTGT others(15): Show |
4 | a0001c0001t0002g0256 a0001c0001t0032g0098 a0001c0001t0032g0103 others(1): Show |
4 | HG02273.hp1 HG02622.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2623+2098_2623+209 others(26): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635071 | |||||||
chr15:55635071 | CTGGGTGT others(1): Show |
C | 3 | a0001c0001t0034g0001 a0001c0001t0070g0133 a0002c0002t0064g0017 |
4 | HG03491.hp2 HG03492.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.2623+2091_2623+209 others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635071 | |||||||
chr15:55635071 | CTGGGTGT others(3): Show |
C | 51 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0161 others(48): Show |
51 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.2623+2089_2623+209 others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635071 | |||||||
chr15:55635073 | G | C | 14 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(11): Show |
14 | HG01255.hp2 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2623+2097C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635073 | |||||||
chr15:55635074 | G | T | 217 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(214): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.2623+2096C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635074 | |||||||
chr15:55635103 | G | GTGTGTGT others(8): Show |
1 | a0001c0001t0006g0140 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2623+2066_2623+206 others(19): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635103 | |||||||
chr15:55635104 | T | TGTGTGTG others(8): Show |
3 | a0001c0001t0001g0144 a0001c0001t0001g0184 a0001c0001t0006g0148 |
3 | HG01993.hp2 HG03669.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.2623+2065_2623+206 others(19): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635104 | |||||||
chr15:55635105 | T | G | 65 | a0001c0001t0001g0152 a0001c0001t0001g0160 a0001c0001t0021g0051 others(62): Show |
65 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.2623+2065A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635105 | |||||||
chr15:55635124 | C | T | 44 | a0001c0001t0021g0051 a0001c0001t0021g0060 a0001c0001t0066g0094 others(41): Show |
44 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.2623+2046G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635124 | |||||||
chr15:55635216 | C | T | 1 | a0005c0011t0094g0218 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2623+1954G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635216 | |||||||
chr15:55635217 | G | A | 38 | a0001c0001t0066g0094 a0001c0001t0111g0278 a0002c0002t0011g0048 others(35): Show |
38 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2623+1953C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635217 | |||||||
chr15:55635223 | T | C | 267 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(264): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.2623+1947A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635223 | |||||||
chr15:55635235 | G | C | 4 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(1): Show |
4 | HG03453.hp1 HG03486.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2623+1935C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635235 | |||||||
chr15:55635423 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2623+1747T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635423 | |||||||
chr15:55635451 | G | A | 3 | a0001c0001t0021g0051 a0001c0001t0021g0060 a0002c0002t0058g0047 |
3 | HG02559.hp1 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2623+1719C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635451 | |||||||
chr15:55635500 | T | C | 137 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(134): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.2623+1670A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635500 | |||||||
chr15:55635521 | A | G | 1 | a0002c0002t0016g0127 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2623+1649T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635521 | |||||||
chr15:55635563 | T | C | 1 | a0001c0001t0002g0259 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2623+1607A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635563 | |||||||
chr15:55635733 | A | G | 11 | a0004c0004t0023g0056 a0004c0004t0023g0057 a0004c0004t0030g0097 others(8): Show |
11 | HG01255.hp2 HG01884.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2623+1437T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635733 | |||||||
chr15:55635934 | C | T | 50 | a0001c0001t0004g0142 a0001c0001t0004g0188 a0001c0001t0012g0083 others(47): Show |
50 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.2623+1236G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55635934 | |||||||
chr15:55636057 | G | T | 1 | a0001c0001t0054g0005 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2623+1113C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55636057 | |||||||
chr15:55636074 | T | G | 79 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(76): Show |
79 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.2623+1096A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55636074 | |||||||
chr15:55636369 | C | T | 1 | a0001c0001t0099g0228 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2623+801G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55636369 | |||||||
chr15:55636478 | T | A | 3 | a0001c0001t0029g0092 a0002c0002t0109g0236 a0011c0016t0029g0093 |
3 | HG02723.hp1 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2623+692A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55636478 | |||||||
chr15:55636578 | G | C | 1 | a0002c0002t0013g0016 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2623+592C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55636578 | |||||||
chr15:55636849 | G | T | 6 | a0004c0004t0023g0056 a0004c0004t0023g0057 a0004c0004t0047g0061 others(3): Show |
6 | HG01255.hp2 HG01884.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2623+321C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55636849 | |||||||
chr15:55636871 | T | A | 1 | a0014c0018t0006g0170 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2623+299A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55636871 | |||||||
chr15:55636929 | G | C | 25 | a0002c0002t0011g0048 a0002c0002t0011g0049 a0002c0002t0011g0050 others(22): Show |
25 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.2623+241C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55636929 | |||||||
chr15:55637087 | A | G | 4 | a0001c0001t0002g0255 a0001c0001t0002g0259 a0001c0001t0002g0262 others(1): Show |
4 | HG00733.hp1 HG01517.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.2623+83T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55637087 | |||||||
chr15:55637110 | T | C | 2 | a0002c0002t0003g0066 a0002c0002t0003g0071 |
2 | NA18963.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.2623+60A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55637110 | |||||||
chr15:55637129 | A | T | 1 | a0001c0001t0001g0203 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2623+41T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55637129 | |||||||
chr15:55637140 | T | C | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2623+30A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 15/19 | chr15 | 55637140 | |||||||
chr15:55637452 | G | A | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2453-112C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 14/19 | chr15 | 55637452 | |||||||
chr15:55637996 | G | T | 1 | a0007c0017t0002g0254 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2452+553C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 14/19 | chr15 | 55637996 | |||||||
chr15:55638028 | T | C | 1 | a0012c0019t0046g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2452+521A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 14/19 | chr15 | 55638028 | |||||||
chr15:55638033 | T | C | 50 | a0001c0001t0004g0142 a0001c0001t0004g0188 a0001c0001t0012g0083 others(47): Show |
50 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.2452+516A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 14/19 | chr15 | 55638033 | |||||||
chr15:55638042 | T | C | 1 | a0003c0005t0010g0038 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2452+507A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 14/19 | chr15 | 55638042 | |||||||
chr15:55638047 | C | A | 20 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(17): Show |
20 | HG01255.hp2 HG01884.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.2452+502G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 14/19 | chr15 | 55638047 | |||||||
chr15:55638051 | G | A | 1 | a0001c0001t0039g0132 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2452+498C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 14/19 | chr15 | 55638051 | |||||||
chr15:55638170 | T | C | 1 | a0012c0019t0046g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2452+379A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 14/19 | chr15 | 55638170 | |||||||
chr15:55638180 | A | G | 1 | a0001c0009t0087g0112 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2452+369T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 14/19 | chr15 | 55638180 | |||||||
chr15:55638337 | G | A | 12 | a0003c0005t0010g0038 a0003c0005t0010g0039 a0003c0005t0010g0041 others(9): Show |
12 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.2452+212C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 14/19 | chr15 | 55638337 | |||||||
chr15:55638344 | C | T | 143 | a0001c0001t0004g0142 a0001c0001t0004g0188 a0001c0001t0012g0083 others(140): Show |
144 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.2452+205G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 14/19 | chr15 | 55638344 | |||||||
chr15:55638379 | A | T | 144 | a0001c0001t0004g0142 a0001c0001t0004g0188 a0001c0001t0012g0083 others(141): Show |
145 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.2452+170T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 14/19 | chr15 | 55638379 | |||||||
chr15:55638528 | A | G | 1 | a0001c0001t0040g0136 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2452+21T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 14/19 | chr15 | 55638528 | |||||||
chr15:55638826 | T | C | 1 | a0001c0001t0105g0205 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2325-150A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55638826 | |||||||
chr15:55638928 | G | T | 1 | a0002c0002t0003g0071 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2325-252C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55638928 | |||||||
chr15:55638955 | A | ATCAT | 76 | a0001c0001t0002g0249 a0001c0001t0002g0250 a0001c0001t0002g0251 others(73): Show |
77 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.2325-283_2325-280d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55638955 | |||||||
chr15:55638955 | A | ATCATTCA others(1): Show |
3 | a0001c0001t0100g0232 a0002c0002t0013g0016 a0012c0019t0046g0003 |
3 | HG02683.hp1 HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2325-287_2325-280d others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55638955 | |||||||
chr15:55638955 | A | ATCATTCA others(5): Show |
1 | a0001c0001t0096g0229 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2325-291_2325-280d others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55638955 | |||||||
chr15:55638955 | ATCAT | A | 149 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(146): Show |
149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.2325-283_2325-280d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55638955 | |||||||
chr15:55638955 | ATCATTCA others(5): Show |
A | 1 | a0001c0001t0099g0228 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2325-291_2325-280d others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55638955 | |||||||
chr15:55638963 | T | A | 9 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(6): Show |
9 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2325-287A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55638963 | |||||||
chr15:55639007 | T | C | 5 | a0001c0001t0054g0005 a0001c0009t0042g0035 a0001c0009t0087g0112 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2325-331A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55639007 | |||||||
chr15:55639070 | C | G | 5 | a0001c0001t0054g0005 a0001c0009t0042g0035 a0001c0009t0087g0112 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2325-394G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55639070 | |||||||
chr15:55639085 | T | C | 5 | a0001c0001t0054g0005 a0001c0009t0042g0035 a0001c0009t0087g0112 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2325-409A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55639085 | |||||||
chr15:55639149 | T | A | 5 | a0001c0001t0054g0005 a0001c0009t0042g0035 a0001c0009t0087g0112 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2325-473A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55639149 | |||||||
chr15:55639407 | T | C | 1 | a0016c0014t0073g0234 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2324+235A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55639407 | |||||||
chr15:55639507 | C | T | 5 | a0001c0001t0054g0005 a0001c0009t0042g0035 a0001c0009t0087g0112 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2324+135G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55639507 | |||||||
chr15:55639518 | T | G | 5 | a0001c0001t0054g0005 a0001c0009t0042g0035 a0001c0009t0087g0112 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2324+124A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 13/19 | chr15 | 55639518 | |||||||
chr15:55639861 | G | A | 1 | a0001c0001t0006g0148 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2138-33C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55639861 | |||||||
chr15:55639989 | C | G | 76 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(73): Show |
76 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.2138-161G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55639989 | |||||||
chr15:55640029 | T | A | 1 | a0001c0001t0002g0273 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2138-201A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55640029 | |||||||
chr15:55640069 | T | C | 1 | a0002c0002t0026g0030 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2138-241A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55640069 | |||||||
chr15:55640108 | C | CAG | 10 | a0001c0001t0035g0219 a0001c0001t0054g0005 a0001c0001t0102g0126 others(7): Show |
10 | HG02572.hp1 HG02615.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2138-282_2138-281d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55640108 | |||||||
chr15:55640191 | A | G | 1 | a0004c0004t0030g0097 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2138-363T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55640191 | |||||||
chr15:55640419 | T | C | 189 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(186): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.2138-591A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55640419 | |||||||
chr15:55640427 | A | G | 11 | a0001c0001t0032g0098 a0001c0001t0032g0103 a0001c0001t0033g0101 others(8): Show |
11 | HG01891.hp2 HG02257.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2138-599T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55640427 | |||||||
chr15:55640567 | G | A | 1 | a0004c0004t0069g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2137+546C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55640567 | |||||||
chr15:55640688 | CTTAAATA others(20): Show |
C | 1 | a0001c0001t0006g0140 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2137+398_2137+424d others(29): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55640688 | |||||||
chr15:55640727 | T | C | 272 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(269): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.2137+386A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55640727 | |||||||
chr15:55640791 | C | G | 59 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(56): Show |
59 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.2137+322G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55640791 | |||||||
chr15:55640856 | C | CA | 46 | a0001c0001t0002g0257 a0001c0001t0021g0051 a0001c0001t0021g0060 others(43): Show |
47 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.2137+256dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55640856 | |||||||
chr15:55640967 | A | C | 1 | a0001c0001t0001g0223 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2137+146T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55640967 | |||||||
chr15:55641001 | G | T | 145 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(142): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.2137+112C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55641001 | |||||||
chr15:55641033 | T | C | 1 | a0001c0009t0042g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2137+80A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 12/19 | chr15 | 55641033 | |||||||
chr15:55641231 | T | C | 15 | a0001c0001t0066g0094 a0001c0001t0111g0278 a0002c0002t0019g0052 others(12): Show |
15 | HG00323.hp1 HG01071.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.2042-23A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55641231 | |||||||
chr15:55641354 | A | C | 2 | a0001c0001t0021g0051 a0001c0001t0021g0060 |
2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2042-146T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55641354 | |||||||
chr15:55641371 | T | C | 1 | a0001c0001t0004g0142 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2042-163A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55641371 | |||||||
chr15:55641459 | C | T | 1 | a0001c0001t0002g0255 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2042-251G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55641459 | |||||||
chr15:55641539 | G | A | 1 | a0004c0004t0069g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2042-331C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55641539 | |||||||
chr15:55641771 | A | T | 48 | a0001c0001t0004g0142 a0001c0001t0004g0188 a0001c0001t0012g0083 others(45): Show |
48 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.2042-563T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55641771 | |||||||
chr15:55641857 | C | A | 5 | a0001c0001t0054g0005 a0001c0009t0042g0035 a0001c0009t0087g0112 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2042-649G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55641857 | |||||||
chr15:55641939 | C | A | 5 | a0001c0001t0035g0219 a0001c0001t0102g0126 a0001c0012t0072g0113 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2042-731G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55641939 | |||||||
chr15:55641977 | A | T | 1 | a0012c0019t0046g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2042-769T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55641977 | |||||||
chr15:55641989 | A | G | 8 | a0001c0001t0016g0122 a0001c0001t0016g0123 a0001c0001t0082g0128 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2042-781T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55641989 | |||||||
chr15:55642101 | G | A | 3 | a0003c0005t0010g0038 a0003c0005t0010g0039 a0003c0005t0010g0041 |
3 | HG00099.hp1 HG00741.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.2042-893C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642101 | |||||||
chr15:55642136 | T | TGCAGTCC | 27 | a0001c0001t0051g0004 a0001c0001t0052g0006 a0001c0001t0054g0005 others(24): Show |
27 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.2042-935_2042-929d others(9): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642136 | |||||||
chr15:55642159 | C | T | 5 | a0001c0001t0054g0005 a0001c0009t0042g0035 a0001c0009t0087g0112 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2042-951G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642159 | |||||||
chr15:55642180 | C | CA | 38 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0001t0001g0158 others(35): Show |
38 | HG00140.hp2 HG01168.hp2 HG01169.hp2 others(35): Show |
intron_variant | MODIFIER | c.2042-973dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642180 | |||||||
chr15:55642180 | C | CAA | 8 | a0001c0001t0002g0269 a0001c0001t0052g0006 a0002c0002t0004g0117 others(5): Show |
8 | HG01255.hp2 HG01891.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.2042-974_2042-973d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642180 | |||||||
chr15:55642180 | CA | C | 53 | a0001c0001t0001g0130 a0001c0001t0002g0273 a0001c0001t0008g0145 others(50): Show |
53 | HG00323.hp1 HG00438.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.2042-973delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642180 | |||||||
chr15:55642180 | CAA | C | 11 | a0001c0001t0016g0122 a0001c0001t0016g0123 a0001c0001t0034g0001 others(8): Show |
12 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.2042-974_2042-973d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642180 | |||||||
chr15:55642192 | AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0101g0217 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2042-996_2042-985d others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642192 | |||||||
chr15:55642203 | AT | A | 3 | a0002c0002t0109g0236 a0003c0006t0009g0015 a0013c0015t0043g0011 |
3 | HG00733.hp2 HG03239.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2042-996delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642203 | |||||||
chr15:55642204 | T | A | 31 | a0001c0001t0051g0004 a0001c0001t0052g0006 a0001c0007t0038g0230 others(28): Show |
31 | HG00099.hp1 HG00741.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.2042-996A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642204 | |||||||
chr15:55642207 | T | G | 23 | a0001c0001t0051g0004 a0001c0001t0052g0006 a0001c0001t0101g0217 others(20): Show |
23 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.2042-999A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642207 | |||||||
chr15:55642315 | G | C | 63 | a0001c0001t0004g0142 a0001c0001t0004g0188 a0001c0001t0012g0083 others(60): Show |
63 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.2042-1107C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642315 | |||||||
chr15:55642381 | C | G | 5 | a0001c0001t0054g0005 a0001c0009t0042g0035 a0001c0009t0087g0112 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2042-1173G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642381 | |||||||
chr15:55642579 | C | G | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2042-1371G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642579 | |||||||
chr15:55642597 | CA | C | 157 | a0001c0001t0001g0107 a0001c0001t0001g0115 a0001c0001t0001g0130 others(154): Show |
158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.2042-1390delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642597 | |||||||
chr15:55642597 | CAA | C | 10 | a0001c0001t0001g0106 a0001c0001t0001g0177 a0001c0001t0002g0261 others(7): Show |
10 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2042-1391_2042-139 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642597 | |||||||
chr15:55642642 | T | C | 4 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0242 others(1): Show |
4 | HG00741.hp2 HG01106.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.2042-1434A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642642 | |||||||
chr15:55642812 | G | A | 2 | a0004c0004t0031g0095 a0004c0004t0031g0096 |
2 | HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2042-1604C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642812 | |||||||
chr15:55642858 | G | A | 1 | a0002c0002t0109g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2042-1650C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55642858 | |||||||
chr15:55643079 | AAACT | A | 5 | a0001c0001t0016g0122 a0001c0001t0016g0123 a0001c0001t0083g0125 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2042-1875_2042-187 others(8): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55643079 | |||||||
chr15:55643134 | G | C | 3 | a0001c0001t0029g0092 a0002c0002t0109g0236 a0011c0016t0029g0093 |
3 | HG02723.hp1 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2042-1926C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55643134 | |||||||
chr15:55643293 | G | A | 1 | a0001c0009t0103g0233 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2042-2085C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55643293 | |||||||
chr15:55643297 | G | A | 1 | a0001c0008t0093g0209 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2042-2089C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55643297 | |||||||
chr15:55643558 | C | G | 5 | a0001c0001t0054g0005 a0001c0009t0042g0035 a0001c0009t0087g0112 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2042-2350G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55643558 | |||||||
chr15:55643689 | G | A | 1 | a0004c0004t0069g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2042-2481C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55643689 | |||||||
chr15:55643864 | A | AT | 7 | a0001c0001t0002g0257 a0001c0001t0035g0219 a0001c0001t0080g0202 others(4): Show |
7 | HG02040.hp2 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2042-2657dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55643864 | |||||||
chr15:55643901 | C | A | 2 | a0001c0001t0051g0004 a0001c0001t0052g0006 |
2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2042-2693G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55643901 | |||||||
chr15:55643904 | C | T | 3 | a0001c0001t0029g0092 a0002c0002t0109g0236 a0011c0016t0029g0093 |
3 | HG02723.hp1 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2042-2696G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55643904 | |||||||
chr15:55643910 | C | A | 3 | a0001c0001t0029g0092 a0002c0002t0109g0236 a0011c0016t0029g0093 |
3 | HG02723.hp1 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2042-2702G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55643910 | |||||||
chr15:55644040 | C | T | 268 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(265): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.2042-2832G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55644040 | |||||||
chr15:55644126 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2042-2918T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55644126 | |||||||
chr15:55644151 | T | C | 1 | a0001c0001t0018g0058 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2042-2943A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55644151 | |||||||
chr15:55644391 | T | A | 4 | a0001c0001t0002g0255 a0001c0001t0002g0259 a0001c0001t0002g0262 others(1): Show |
4 | HG00733.hp1 HG01517.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.2042-3183A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55644391 | |||||||
chr15:55644421 | G | C | 5 | a0001c0001t0021g0051 a0001c0001t0021g0060 a0001c0001t0034g0001 others(2): Show |
6 | HG02809.hp2 HG03491.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.2042-3213C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55644421 | |||||||
chr15:55644643 | C | T | 1 | a0012c0019t0046g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2042-3435G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55644643 | |||||||
chr15:55644737 | G | A | 125 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(122): Show |
125 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.2042-3529C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55644737 | |||||||
chr15:55644742 | A | G | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2042-3534T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55644742 | |||||||
chr15:55644833 | G | C | 39 | a0001c0001t0066g0094 a0001c0001t0111g0278 a0002c0002t0011g0048 others(36): Show |
39 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.2042-3625C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55644833 | |||||||
chr15:55644862 | A | C | 1 | a0002c0002t0003g0084 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2042-3654T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55644862 | |||||||
chr15:55644972 | C | T | 1 | a0001c0001t0001g0223 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2042-3764G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55644972 | |||||||
chr15:55645164 | G | A | 59 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(56): Show |
59 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.2042-3956C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645164 | |||||||
chr15:55645201 | C | T | 9 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(6): Show |
9 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2042-3993G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645201 | |||||||
chr15:55645202 | G | A | 2 | a0001c0001t0001g0131 a0001c0001t0001g0144 |
2 | NA18974.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.2042-3994C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645202 | |||||||
chr15:55645210 | C | T | 5 | a0001c0001t0054g0005 a0001c0009t0042g0035 a0001c0009t0087g0112 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2042-4002G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645210 | |||||||
chr15:55645226 | G | C | 2 | a0001c0001t0040g0135 a0001c0001t0040g0136 |
2 | HG02027.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.2042-4018C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645226 | |||||||
chr15:55645304 | C | T | 1 | a0001c0001t0002g0241 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2042-4096G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645304 | |||||||
chr15:55645374 | C | G | 44 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(41): Show |
44 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.2042-4166G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645374 | |||||||
chr15:55645388 | C | T | 1 | a0012c0019t0046g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2042-4180G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645388 | |||||||
chr15:55645433 | C | CA | 6 | a0001c0001t0054g0005 a0001c0009t0042g0035 a0001c0009t0087g0112 others(3): Show |
6 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2042-4226dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | |||||||
chr15:55645433 | C | CAAAAA | 14 | a0001c0001t0034g0001 a0001c0001t0070g0133 a0002c0002t0006g0227 others(11): Show |
15 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.2042-4230_2042-422 others(9): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | |||||||
chr15:55645433 | C | CAAAAAAA others(2): Show |
11 | a0001c0001t0021g0060 a0004c0004t0023g0056 a0004c0004t0023g0057 others(8): Show |
11 | HG01255.hp2 HG01884.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2042-4234_2042-422 others(13): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | |||||||
chr15:55645433 | C | CAAAAAAA others(3): Show |
6 | a0001c0001t0001g0172 a0001c0001t0001g0196 a0001c0001t0015g0116 others(3): Show |
6 | HG00639.hp1 HG01256.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.2042-4235_2042-422 others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | |||||||
chr15:55645433 | C | CAAAAAAA others(4): Show |
6 | a0001c0001t0004g0142 a0001c0001t0024g0031 a0001c0001t0029g0092 others(3): Show |
6 | HG01433.hp2 HG02015.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.2042-4236_2042-422 others(15): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | |||||||
chr15:55645433 | C | CAAAAAAA others(5): Show |
32 | a0001c0001t0002g0247 a0001c0001t0004g0188 a0001c0001t0012g0083 others(29): Show |
32 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.2042-4237_2042-422 others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | |||||||
chr15:55645433 | C | CAAAAAAA others(6): Show |
14 | a0001c0001t0040g0135 a0001c0001t0071g0143 a0001c0003t0004g0225 others(11): Show |
14 | HG02027.hp1 HG02027.hp2 HG04228.hp2 others(11): Show |
intron_variant | MODIFIER | c.2042-4238_2042-422 others(17): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | |||||||
chr15:55645433 | C | CAAAAAAA others(7): Show |
3 | a0001c0001t0002g0269 a0001c0001t0002g0271 a0002c0002t0012g0082 |
3 | HG01943.hp2 HG01993.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.2042-4239_2042-422 others(18): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | |||||||
chr15:55645433 | C | CAAAAAAA others(8): Show |
1 | a0001c0012t0002g0279 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2042-4240_2042-422 others(19): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | |||||||
chr15:55645433 | C | CAAAAAAA others(12): Show |
7 | a0001c0001t0001g0106 a0001c0001t0001g0156 a0001c0001t0001g0177 others(4): Show |
7 | HG01168.hp2 HG01169.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.2042-4226_2042-422 others(23): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | |||||||
chr15:55645433 | C | CAAAAAAA others(13): Show |
35 | a0001c0001t0001g0107 a0001c0001t0001g0131 a0001c0001t0001g0158 others(32): Show |
35 | HG00280.hp2 HG00408.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.2042-4226_2042-422 others(24): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | |||||||
chr15:55645433 | C | CAAAAAAA others(14): Show |
33 | a0001c0001t0001g0130 a0001c0001t0001g0144 a0001c0001t0001g0147 others(30): Show |
33 | HG00140.hp2 HG00438.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.2042-4226_2042-422 others(25): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | |||||||
chr15:55645433 | C | CAAAAAAA others(15): Show |
12 | a0001c0001t0001g0115 a0001c0001t0001g0134 a0001c0001t0001g0152 others(9): Show |
12 | HG00738.hp1 HG01071.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.2042-4226_2042-422 others(26): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | |||||||
chr15:55645433 | C | CAAAAAAA others(16): Show |
5 | a0001c0001t0001g0139 a0001c0001t0001g0189 a0001c0001t0002g0251 others(2): Show |
5 | HG01168.hp1 HG02257.hp1 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.2042-4226_2042-422 others(27): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | |||||||
chr15:55645433 | C | CAAAAAAA others(17): Show |
17 | a0001c0001t0001g0191 a0001c0001t0002g0242 a0001c0001t0002g0243 others(14): Show |
17 | HG00639.hp2 HG00733.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.2042-4226_2042-422 others(28): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | |||||||
chr15:55645433 | C | CAAAAAAA others(18): Show |
13 | a0001c0001t0002g0241 a0001c0001t0002g0244 a0001c0001t0002g0246 others(10): Show |
13 | HG00140.hp1 HG01106.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.2042-4226_2042-422 others(29): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | |||||||
chr15:55645433 | C | CAAAAAAA others(19): Show |
7 | a0001c0001t0002g0265 a0001c0001t0002g0266 a0001c0001t0002g0267 others(4): Show |
7 | HG01256.hp2 HG01928.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2042-4226_2042-422 others(30): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | |||||||
chr15:55645433 | C | CAAAAAAA others(20): Show |
2 | a0001c0001t0002g0238 a0001c0001t0002g0268 |
2 | HG01258.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2042-4226_2042-422 others(31): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | |||||||
chr15:55645433 | C | CAAAAAAA others(22): Show |
2 | a0001c0001t0002g0260 a0001c0001t0002g0261 |
2 | HG03688.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2042-4226_2042-422 others(33): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | |||||||
chr15:55645433 | C | CAAAAAAA others(23): Show |
2 | a0001c0001t0002g0240 a0012c0019t0046g0003 |
2 | HG00741.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2042-4226_2042-422 others(34): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645433 | |||||||
chr15:55645511 | G | C | 10 | a0001c0001t0035g0219 a0001c0001t0054g0005 a0001c0001t0102g0126 others(7): Show |
10 | HG02572.hp1 HG02615.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2042-4303C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645511 | |||||||
chr15:55645785 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2042-4577G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645785 | |||||||
chr15:55645824 | C | T | 1 | a0001c0007t0038g0230 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2042-4616G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645824 | |||||||
chr15:55645848 | G | C | 9 | a0001c0001t0035g0219 a0001c0008t0037g0208 a0001c0008t0037g0210 others(6): Show |
9 | HG02572.hp1 HG02630.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2042-4640C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645848 | |||||||
chr15:55645909 | A | C | 6 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(3): Show |
6 | HG02970.hp2 HG03453.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2042-4701T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55645909 | |||||||
chr15:55646015 | T | A | 2 | a0001c0001t0051g0004 a0001c0001t0052g0006 |
2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2042-4807A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646015 | |||||||
chr15:55646081 | A | ACCGCAAC others(9): Show |
2 | a0001c0001t0077g0174 a0001c0003t0017g0090 |
2 | HG00408.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.2042-4889_2042-487 others(20): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646081 | |||||||
chr15:55646173 | G | GT | 108 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(105): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.2042-4966dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646173 | |||||||
chr15:55646173 | G | GTT | 6 | a0001c0001t0005g0180 a0001c0001t0008g0197 a0001c0001t0039g0199 others(3): Show |
6 | HG01109.hp1 HG01978.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2042-4967_2042-496 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646173 | |||||||
chr15:55646173 | GT | G | 31 | a0001c0001t0001g0155 a0001c0001t0001g0161 a0001c0001t0004g0188 others(28): Show |
31 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.2042-4966delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646173 | |||||||
chr15:55646175 | T | G | 1 | a0001c0001t0099g0228 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2042-4967A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646175 | |||||||
chr15:55646182 | T | G | 5 | a0001c0001t0035g0219 a0001c0012t0072g0113 a0002c0002t0028g0021 others(2): Show |
5 | HG02572.hp1 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2042-4974A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646182 | |||||||
chr15:55646292 | A | G | 63 | a0001c0001t0001g0150 a0001c0001t0001g0175 a0001c0001t0001g0226 others(60): Show |
63 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(60): Show |
intron_variant | MODIFIER | c.2042-5084T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646292 | |||||||
chr15:55646325 | CTCT | C | 12 | a0001c0001t0032g0098 a0004c0004t0023g0056 a0004c0004t0023g0057 others(9): Show |
12 | HG01255.hp2 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2042-5120_2042-511 others(7): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646325 | |||||||
chr15:55646327 | C | CT | 16 | a0001c0001t0001g0154 a0001c0001t0021g0051 a0001c0001t0021g0060 others(13): Show |
16 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.2042-5120dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646327 | |||||||
chr15:55646346 | G | A | 1 | a0001c0008t0093g0209 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2042-5138C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646346 | |||||||
chr15:55646351 | C | T | 2 | a0001c0007t0038g0230 a0001c0007t0038g0231 |
2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2042-5143G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646351 | |||||||
chr15:55646423 | C | T | 1 | a0004c0004t0069g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2042-5215G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646423 | |||||||
chr15:55646456 | A | C | 4 | a0001c0001t0051g0004 a0001c0001t0052g0006 a0001c0001t0054g0005 others(1): Show |
4 | HG01891.hp2 HG02818.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.2042-5248T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646456 | |||||||
chr15:55646456 | A | G | 3 | a0001c0001t0029g0092 a0001c0001t0066g0094 a0011c0016t0029g0093 |
3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2042-5248T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646456 | |||||||
chr15:55646468 | G | A | 43 | a0001c0001t0032g0103 a0001c0001t0033g0101 a0001c0001t0033g0102 others(40): Show |
43 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.2042-5260C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646468 | |||||||
chr15:55646478 | A | G | 1 | a0001c0001t0100g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2042-5270T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646478 | |||||||
chr15:55646479 | C | T | 1 | a0001c0001t0100g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2042-5271G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646479 | |||||||
chr15:55646480 | G | A | 14 | a0001c0001t0021g0051 a0001c0001t0021g0060 a0003c0005t0010g0038 others(11): Show |
14 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.2042-5272C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646480 | |||||||
chr15:55646499 | T | C | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2042-5291A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646499 | |||||||
chr15:55646554 | C | G | 1 | a0012c0019t0046g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2042-5346G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646554 | |||||||
chr15:55646569 | G | A | 3 | a0001c0001t0001g0155 a0001c0001t0001g0161 a0001c0001t0079g0178 |
3 | HG00280.hp2 HG02486.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2042-5361C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646569 | |||||||
chr15:55646634 | T | C | 1 | a0002c0002t0003g0087 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2042-5426A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646634 | |||||||
chr15:55646656 | G | C | 1 | a0001c0001t0105g0205 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2042-5448C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646656 | |||||||
chr15:55646681 | T | C | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2042-5473A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646681 | |||||||
chr15:55646685 | G | A | 1 | a0001c0001t0078g0149 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2042-5477C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646685 | |||||||
chr15:55646714 | A | G | 39 | a0001c0001t0111g0278 a0002c0002t0011g0048 a0002c0002t0011g0049 others(36): Show |
39 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.2042-5506T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646714 | |||||||
chr15:55646863 | A | C | 1 | a0002c0002t0057g0025 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2042-5655T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646863 | |||||||
chr15:55646922 | C | T | 8 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(5): Show |
8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.2042-5714G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55646922 | |||||||
chr15:55647153 | G | A | 1 | a0001c0001t0100g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2042-5945C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55647153 | |||||||
chr15:55647388 | G | C | 39 | a0001c0001t0111g0278 a0002c0002t0011g0048 a0002c0002t0011g0049 others(36): Show |
39 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.2042-6180C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55647388 | |||||||
chr15:55647503 | T | G | 3 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0099g0228 |
3 | HG02976.hp1 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2042-6295A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55647503 | |||||||
chr15:55647695 | G | A | 1 | a0001c0009t0042g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2042-6487C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55647695 | |||||||
chr15:55647761 | A | G | 62 | a0001c0001t0001g0226 a0001c0001t0002g0238 a0001c0001t0002g0240 others(59): Show |
62 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(59): Show |
intron_variant | MODIFIER | c.2042-6553T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55647761 | |||||||
chr15:55647778 | T | C | 2 | a0001c0009t0103g0233 a0016c0014t0073g0234 |
2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2042-6570A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55647778 | |||||||
chr15:55647923 | G | C | 8 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(5): Show |
8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.2042-6715C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55647923 | |||||||
chr15:55647989 | G | A | 1 | a0001c0007t0038g0231 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2042-6781C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55647989 | |||||||
chr15:55648002 | C | A | 6 | a0001c0001t0029g0092 a0001c0001t0051g0004 a0001c0001t0052g0006 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2042-6794G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55648002 | |||||||
chr15:55648041 | C | T | 1 | a0006c0010t0059g0072 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2042-6833G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55648041 | |||||||
chr15:55648219 | A | G | 2 | a0001c0001t0021g0051 a0001c0001t0021g0060 |
2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2042-7011T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55648219 | |||||||
chr15:55648274 | G | A | 6 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(3): Show |
6 | HG02615.hp1 HG03453.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2042-7066C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55648274 | |||||||
chr15:55648468 | A | AT | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2042-7261dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55648468 | |||||||
chr15:55648510 | G | A | 1 | a0015c0023t0001g0235 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2042-7302C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55648510 | |||||||
chr15:55648512 | C | T | 1 | a0012c0019t0046g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2042-7304G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55648512 | |||||||
chr15:55648533 | A | T | 3 | a0001c0012t0072g0113 a0001c0012t0074g0114 a0012c0019t0046g0003 |
3 | HG02630.hp2 HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2042-7325T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55648533 | |||||||
chr15:55648619 | T | G | 1 | a0001c0001t0001g0158 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2042-7411A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55648619 | |||||||
chr15:55648631 | C | G | 1 | a0002c0002t0025g0070 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2042-7423G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55648631 | |||||||
chr15:55648659 | A | G | 3 | a0001c0012t0072g0113 a0001c0012t0074g0114 a0012c0019t0046g0003 |
3 | HG02630.hp2 HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2042-7451T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55648659 | |||||||
chr15:55648778 | C | T | 17 | a0002c0002t0013g0016 a0002c0002t0013g0018 a0002c0002t0013g0029 others(14): Show |
17 | HG00642.hp1 HG00642.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.2042-7570G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55648778 | |||||||
chr15:55648793 | A | G | 1 | a0012c0019t0046g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2042-7585T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55648793 | |||||||
chr15:55649000 | C | G | 272 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(269): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.2042-7792G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55649000 | |||||||
chr15:55649088 | C | CA | 46 | a0001c0001t0001g0193 a0001c0001t0001g0226 a0001c0001t0002g0238 others(43): Show |
46 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.2042-7881dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55649088 | |||||||
chr15:55649105 | A | C | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2042-7897T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55649105 | |||||||
chr15:55649336 | T | C | 4 | a0001c0001t0001g0155 a0001c0001t0001g0161 a0001c0001t0001g0195 others(1): Show |
4 | HG00280.hp2 HG01934.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2042-8128A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55649336 | |||||||
chr15:55649427 | C | CA | 272 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(269): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.2042-8220_2042-821 others(5): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55649427 | |||||||
chr15:55649458 | C | T | 272 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(269): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.2042-8250G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55649458 | |||||||
chr15:55649643 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2042-8435G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55649643 | |||||||
chr15:55649762 | G | A | 17 | a0002c0002t0013g0016 a0002c0002t0013g0018 a0002c0002t0013g0029 others(14): Show |
17 | HG00642.hp1 HG00642.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.2042-8554C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55649762 | |||||||
chr15:55649791 | C | CAATA | 8 | a0001c0001t0077g0174 a0001c0001t0102g0126 a0001c0003t0003g0042 others(5): Show |
8 | HG00408.hp2 HG01943.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.2042-8587_2042-858 others(8): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55649791 | |||||||
chr15:55649791 | CAATA | C | 11 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0040g0135 others(8): Show |
11 | HG00323.hp2 HG01081.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.2042-8587_2042-858 others(8): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55649791 | |||||||
chr15:55649791 | CAATAAAT others(1): Show |
C | 41 | a0001c0001t0001g0192 a0001c0001t0029g0092 a0001c0001t0051g0004 others(38): Show |
41 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.2042-8591_2042-858 others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55649791 | |||||||
chr15:55649791 | CAATAAAT others(5): Show |
C | 175 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(172): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.2042-8595_2042-858 others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55649791 | |||||||
chr15:55649907 | T | C | 1 | a0002c0002t0012g0082 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2042-8699A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55649907 | |||||||
chr15:55650038 | T | G | 1 | a0001c0001t0070g0133 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2042-8830A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55650038 | |||||||
chr15:55650084 | T | G | 14 | a0001c0001t0021g0051 a0001c0001t0021g0060 a0003c0005t0010g0038 others(11): Show |
14 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.2042-8876A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55650084 | |||||||
chr15:55650130 | T | C | 1 | a0002c0002t0026g0030 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2042-8922A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55650130 | |||||||
chr15:55650276 | T | C | 1 | a0002c0002t0020g0053 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2042-9068A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55650276 | |||||||
chr15:55650374 | G | C | 204 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(201): Show |
205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.2042-9166C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55650374 | |||||||
chr15:55650757 | G | C | 1 | a0001c0001t0016g0123 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2042-9549C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55650757 | |||||||
chr15:55651001 | C | G | 13 | a0001c0001t0021g0051 a0001c0001t0021g0060 a0003c0005t0010g0038 others(10): Show |
13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.2042-9793G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55651001 | |||||||
chr15:55651086 | A | G | 1 | a0001c0001t0008g0159 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2042-9878T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55651086 | |||||||
chr15:55651344 | A | G | 180 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(177): Show |
180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.2042-10136T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55651344 | |||||||
chr15:55651375 | G | A | 1 | a0004c0004t0030g0097 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2042-10167C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55651375 | |||||||
chr15:55651648 | G | A | 1 | a0002c0002t0056g0045 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2042-10440C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55651648 | |||||||
chr15:55651669 | A | T | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2042-10461T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55651669 | |||||||
chr15:55652031 | T | C | 1 | a0006c0010t0025g0065 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2042-10823A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55652031 | |||||||
chr15:55652113 | C | G | 1 | a0001c0001t0001g0115 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2042-10905G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55652113 | |||||||
chr15:55652125 | C | T | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2042-10917G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55652125 | |||||||
chr15:55652194 | G | A | 5 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(2): Show |
5 | HG03453.hp1 HG03486.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.2042-10986C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55652194 | |||||||
chr15:55652319 | G | A | 86 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(83): Show |
86 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.2042-11111C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55652319 | |||||||
chr15:55652349 | A | G | 1 | a0001c0001t0002g0259 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2042-11141T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55652349 | |||||||
chr15:55652460 | G | A | 1 | a0006c0010t0025g0065 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2042-11252C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55652460 | |||||||
chr15:55652708 | G | A | 1 | a0001c0001t0096g0229 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2042-11500C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55652708 | |||||||
chr15:55652872 | G | A | 1 | a0001c0001t0018g0058 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2042-11664C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55652872 | |||||||
chr15:55653061 | T | C | 1 | a0002c0002t0006g0227 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2042-11853A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55653061 | |||||||
chr15:55653183 | T | A | 179 | a0001c0001t0001g0226 a0001c0001t0002g0238 a0001c0001t0002g0240 others(176): Show |
180 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.2042-11975A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55653183 | |||||||
chr15:55653255 | A | G | 161 | a0001c0001t0001g0226 a0001c0001t0002g0238 a0001c0001t0002g0240 others(158): Show |
162 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.2042-12047T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55653255 | |||||||
chr15:55653291 | T | C | 12 | a0001c0001t0032g0098 a0004c0004t0023g0056 a0004c0004t0023g0057 others(9): Show |
12 | HG01255.hp2 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2042-12083A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55653291 | |||||||
chr15:55653412 | C | A | 179 | a0001c0001t0001g0226 a0001c0001t0002g0238 a0001c0001t0002g0240 others(176): Show |
180 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.2042-12204G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55653412 | |||||||
chr15:55653463 | AT | A | 43 | a0001c0001t0001g0162 a0001c0001t0012g0083 a0001c0001t0012g0091 others(40): Show |
44 | HG00323.hp2 HG01081.hp1 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.2042-12256delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55653463 | |||||||
chr15:55653620 | A | T | 166 | a0001c0001t0001g0226 a0001c0001t0002g0238 a0001c0001t0002g0240 others(163): Show |
167 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2042-12412T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55653620 | |||||||
chr15:55653735 | A | C | 8 | a0001c0001t0096g0229 a0001c0001t0099g0228 a0001c0001t0100g0232 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2042-12527T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55653735 | |||||||
chr15:55654070 | C | T | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2042-12862G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654070 | |||||||
chr15:55654100 | T | C | 2 | a0001c0001t0001g0168 a0001c0001t0080g0202 |
2 | HG02040.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2042-12892A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654100 | |||||||
chr15:55654117 | C | T | 2 | a0003c0006t0009g0015 a0003c0006t0022g0012 |
2 | HG00733.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.2042-12909G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654117 | |||||||
chr15:55654184 | C | A | 162 | a0001c0001t0001g0226 a0001c0001t0002g0238 a0001c0001t0002g0240 others(159): Show |
163 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.2042-12976G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654184 | |||||||
chr15:55654206 | C | T | 5 | a0001c0001t0032g0103 a0001c0001t0033g0101 a0001c0001t0033g0102 others(2): Show |
5 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2042-12998G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654206 | |||||||
chr15:55654262 | G | C | 2 | a0001c0012t0072g0113 a0001c0012t0074g0114 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2042-13054C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654262 | |||||||
chr15:55654268 | A | C | 162 | a0001c0001t0001g0226 a0001c0001t0002g0238 a0001c0001t0002g0240 others(159): Show |
163 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.2042-13060T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654268 | |||||||
chr15:55654387 | C | T | 90 | a0001c0001t0032g0098 a0001c0001t0034g0001 a0001c0001t0070g0133 others(87): Show |
91 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.2042-13179G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654387 | |||||||
chr15:55654389 | A | G | 161 | a0001c0001t0001g0226 a0001c0001t0002g0238 a0001c0001t0002g0240 others(158): Show |
162 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.2042-13181T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654389 | |||||||
chr15:55654420 | C | T | 161 | a0001c0001t0001g0226 a0001c0001t0002g0238 a0001c0001t0002g0240 others(158): Show |
162 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.2042-13212G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654420 | |||||||
chr15:55654534 | C | T | 55 | a0001c0001t0001g0226 a0001c0001t0002g0238 a0001c0001t0002g0240 others(52): Show |
55 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.2042-13326G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654534 | |||||||
chr15:55654810 | C | T | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2042-13602G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654810 | |||||||
chr15:55654817 | G | A | 13 | a0001c0001t0021g0051 a0001c0001t0021g0060 a0003c0005t0010g0038 others(10): Show |
13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.2042-13609C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654817 | |||||||
chr15:55654830 | G | A | 5 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0040g0135 others(2): Show |
5 | HG00323.hp2 HG01081.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.2042-13622C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654830 | |||||||
chr15:55654918 | T | C | 2 | a0004c0004t0031g0095 a0004c0004t0031g0096 |
2 | HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2042-13710A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654918 | |||||||
chr15:55654984 | C | T | 9 | a0002c0002t0014g0020 a0002c0002t0014g0024 a0002c0002t0014g0033 others(6): Show |
9 | HG02055.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2042-13776G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55654984 | |||||||
chr15:55655110 | C | G | 8 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(5): Show |
8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.2042-13902G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55655110 | |||||||
chr15:55655152 | T | C | 2 | a0001c0007t0106g0109 a0001c0007t0107g0110 |
2 | HG02109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2042-13944A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55655152 | |||||||
chr15:55655168 | T | C | 1 | a0002c0002t0020g0053 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2042-13960A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55655168 | |||||||
chr15:55655352 | A | G | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2042-14144T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55655352 | |||||||
chr15:55655354 | G | A | 163 | a0001c0001t0001g0226 a0001c0001t0002g0238 a0001c0001t0002g0240 others(160): Show |
164 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.2042-14146C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55655354 | |||||||
chr15:55655355 | T | A | 1 | a0012c0019t0046g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2042-14147A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55655355 | |||||||
chr15:55655452 | A | C | 2 | a0001c0001t0001g0134 a0002c0002t0104g0215 |
2 | HG02683.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2042-14244T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55655452 | |||||||
chr15:55655463 | T | A | 1 | a0012c0019t0046g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2042-14255A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55655463 | |||||||
chr15:55655475 | T | C | 76 | a0001c0003t0003g0042 a0001c0003t0003g0074 a0001c0003t0003g0075 others(73): Show |
76 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.2042-14267A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55655475 | |||||||
chr15:55655786 | T | A | 3 | a0001c0001t0096g0229 a0001c0001t0099g0228 a0001c0001t0100g0232 |
3 | HG02647.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2042-14578A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55655786 | |||||||
chr15:55656240 | A | G | 1 | a0002c0002t0003g0081 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2042-15032T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55656240 | |||||||
chr15:55656245 | T | A | 1 | a0001c0001t0039g0199 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2042-15037A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55656245 | |||||||
chr15:55656321 | G | A | 2 | a0004c0004t0030g0097 a0004c0004t0030g0105 |
2 | HG02145.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2042-15113C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55656321 | |||||||
chr15:55656360 | C | T | 1 | a0001c0003t0017g0090 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2042-15152G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55656360 | |||||||
chr15:55656738 | G | A | 3 | a0001c0001t0029g0092 a0001c0001t0066g0094 a0011c0016t0029g0093 |
3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2042-15530C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55656738 | |||||||
chr15:55656887 | T | C | 3 | a0001c0001t0096g0229 a0001c0001t0099g0228 a0001c0001t0100g0232 |
3 | HG02647.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2041+15558A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55656887 | |||||||
chr15:55656937 | G | A | 5 | a0001c0001t0016g0122 a0001c0001t0016g0123 a0001c0001t0083g0125 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2041+15508C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55656937 | |||||||
chr15:55656942 | C | T | 2 | a0004c0004t0031g0095 a0004c0004t0031g0096 |
2 | HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2041+15503G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55656942 | |||||||
chr15:55656946 | C | T | 11 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0029g0092 others(8): Show |
11 | HG00323.hp2 HG01081.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2041+15499G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55656946 | |||||||
chr15:55657041 | T | C | 14 | a0001c0001t0021g0051 a0001c0001t0021g0060 a0003c0005t0010g0038 others(11): Show |
14 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.2041+15404A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55657041 | |||||||
chr15:55657149 | T | A | 1 | a0001c0001t0001g0147 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2041+15296A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55657149 | |||||||
chr15:55657175 | A | G | 1 | a0001c0001t0002g0259 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2041+15270T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55657175 | |||||||
chr15:55657293 | T | C | 1 | a0004c0004t0047g0061 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2041+15152A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55657293 | |||||||
chr15:55657375 | T | C | 3 | a0001c0001t0096g0229 a0001c0001t0099g0228 a0001c0001t0100g0232 |
3 | HG02647.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2041+15070A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55657375 | |||||||
chr15:55657477 | A | C | 1 | a0001c0001t0002g0272 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2041+14968T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55657477 | |||||||
chr15:55657551 | C | T | 177 | a0001c0001t0001g0226 a0001c0001t0002g0238 a0001c0001t0002g0240 others(174): Show |
178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.2041+14894G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55657551 | |||||||
chr15:55657778 | T | C | 1 | a0002c0002t0067g0104 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2041+14667A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55657778 | |||||||
chr15:55657884 | C | A | 45 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0021g0051 others(42): Show |
46 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.2041+14561G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55657884 | |||||||
chr15:55657905 | C | G | 1 | a0001c0001t0041g0263 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2041+14540G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55657905 | |||||||
chr15:55657971 | T | G | 8 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(5): Show |
8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.2041+14474A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55657971 | |||||||
chr15:55658219 | T | C | 3 | a0001c0001t0096g0229 a0001c0001t0099g0228 a0001c0001t0100g0232 |
3 | HG02647.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2041+14226A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55658219 | |||||||
chr15:55658313 | T | A | 9 | a0001c0001t0016g0122 a0001c0001t0016g0123 a0001c0001t0082g0128 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2041+14132A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55658313 | |||||||
chr15:55658319 | T | A | 272 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(269): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.2041+14126A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55658319 | |||||||
chr15:55658320 | T | A | 1 | a0001c0001t0012g0091 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2041+14125A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55658320 | |||||||
chr15:55658322 | T | A | 4 | a0001c0001t0096g0229 a0001c0001t0099g0228 a0001c0001t0100g0232 others(1): Show |
4 | HG02647.hp2 HG02976.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.2041+14123A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55658322 | |||||||
chr15:55658441 | G | A | 6 | a0001c0001t0029g0092 a0001c0001t0051g0004 a0001c0001t0052g0006 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2041+14004C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55658441 | |||||||
chr15:55658511 | C | T | 177 | a0001c0001t0001g0226 a0001c0001t0002g0238 a0001c0001t0002g0240 others(174): Show |
178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.2041+13934G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55658511 | |||||||
chr15:55658558 | C | T | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2041+13887G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55658558 | |||||||
chr15:55658587 | A | T | 5 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(2): Show |
5 | HG02615.hp1 HG03453.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041+13858T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55658587 | |||||||
chr15:55658743 | C | T | 161 | a0001c0001t0001g0226 a0001c0001t0002g0238 a0001c0001t0002g0240 others(158): Show |
162 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.2041+13702G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55658743 | |||||||
chr15:55659044 | T | C | 8 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(5): Show |
8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.2041+13401A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55659044 | |||||||
chr15:55659234 | A | G | 123 | a0001c0001t0001g0226 a0001c0001t0002g0238 a0001c0001t0002g0240 others(120): Show |
123 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.2041+13211T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55659234 | |||||||
chr15:55659317 | A | G | 3 | a0001c0001t0051g0004 a0001c0001t0052g0006 a0001c0001t0054g0005 |
3 | HG01891.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2041+13128T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55659317 | |||||||
chr15:55659327 | G | C | 1 | a0001c0003t0004g0225 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2041+13118C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55659327 | |||||||
chr15:55659588 | C | T | 16 | a0002c0002t0013g0018 a0002c0002t0013g0029 a0002c0002t0014g0020 others(13): Show |
16 | HG00642.hp1 HG00642.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.2041+12857G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55659588 | |||||||
chr15:55659867 | C | T | 1 | a0001c0001t0097g0221 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2041+12578G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55659867 | |||||||
chr15:55659927 | A | AAAAAC | 20 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0029g0092 others(17): Show |
21 | HG00323.hp2 HG01081.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.2041+12513_2041+12 others(11): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55659927 | |||||||
chr15:55659927 | A | AAAAACAA others(3): Show |
246 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(243): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.2041+12508_2041+12 others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55659927 | |||||||
chr15:55659927 | A | AAAAACAA others(8): Show |
8 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0246 others(5): Show |
8 | HG00741.hp2 HG01106.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.2041+12503_2041+12 others(21): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55659927 | |||||||
chr15:55659927 | A | AAAAACAA others(13): Show |
1 | a0001c0001t0002g0242 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2041+12498_2041+12 others(26): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55659927 | |||||||
chr15:55659927 | A | AAAAACAA others(18): Show |
2 | a0001c0001t0032g0098 a0012c0019t0046g0003 |
2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2041+12493_2041+12 others(31): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55659927 | |||||||
chr15:55660085 | G | A | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041+12360C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55660085 | |||||||
chr15:55660254 | T | A | 14 | a0001c0001t0021g0051 a0001c0001t0021g0060 a0003c0005t0010g0038 others(11): Show |
14 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.2041+12191A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55660254 | |||||||
chr15:55660431 | T | C | 1 | a0001c0003t0004g0173 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2041+12014A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55660431 | |||||||
chr15:55660892 | G | A | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041+11553C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55660892 | |||||||
chr15:55661056 | T | C | 3 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0081g0171 |
3 | HG03098.hp1 HG03225.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2041+11389A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55661056 | |||||||
chr15:55661402 | A | T | 77 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.2041+11043T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55661402 | |||||||
chr15:55661509 | C | CTTTA | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041+10932_2041+10 others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55661509 | |||||||
chr15:55661810 | C | T | 8 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(5): Show |
8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.2041+10635G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55661810 | |||||||
chr15:55661821 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2041+10624G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55661821 | |||||||
chr15:55661895 | TA | T | 166 | a0001c0001t0001g0226 a0001c0001t0002g0238 a0001c0001t0002g0240 others(163): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.2041+10549delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55661895 | |||||||
chr15:55661895 | TAA | T | 10 | a0001c0001t0002g0277 a0002c0002t0014g0020 a0002c0002t0014g0024 others(7): Show |
10 | HG01167.hp1 HG02055.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.2041+10548_2041+10 others(8): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55661895 | |||||||
chr15:55661920 | T | A | 11 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0029g0092 others(8): Show |
11 | HG00323.hp2 HG01081.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2041+10525A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55661920 | |||||||
chr15:55661965 | T | G | 6 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(3): Show |
6 | HG02615.hp1 HG03453.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2041+10480A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55661965 | |||||||
chr15:55662004 | A | G | 3 | a0001c0001t0021g0051 a0001c0001t0021g0060 a0012c0019t0046g0003 |
3 | HG02809.hp2 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2041+10441T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55662004 | |||||||
chr15:55662009 | G | T | 2 | a0002c0002t0026g0023 a0002c0002t0028g0022 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2041+10436C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55662009 | |||||||
chr15:55662211 | T | C | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2041+10234A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55662211 | |||||||
chr15:55662280 | T | C | 1 | a0002c0002t0004g0108 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2041+10165A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55662280 | |||||||
chr15:55662309 | T | C | 14 | a0001c0001t0021g0051 a0001c0001t0021g0060 a0003c0005t0010g0038 others(11): Show |
14 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.2041+10136A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55662309 | |||||||
chr15:55662385 | A | T | 6 | a0001c0001t0029g0092 a0001c0001t0051g0004 a0001c0001t0052g0006 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2041+10060T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55662385 | |||||||
chr15:55662498 | C | G | 15 | a0001c0001t0021g0051 a0001c0001t0021g0060 a0003c0005t0010g0038 others(12): Show |
15 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.2041+9947G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55662498 | |||||||
chr15:55662807 | A | G | 1 | a0002c0002t0003g0071 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2041+9638T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55662807 | |||||||
chr15:55662906 | C | T | 6 | a0002c0002t0011g0048 a0002c0002t0011g0049 a0002c0002t0011g0050 others(3): Show |
6 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.2041+9539G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55662906 | |||||||
chr15:55662907 | G | A | 6 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0001c0001t0001g0196 others(3): Show |
6 | HG00140.hp2 HG00639.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.2041+9538C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55662907 | |||||||
chr15:55663073 | C | T | 8 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(5): Show |
8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.2041+9372G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55663073 | |||||||
chr15:55663254 | A | G | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041+9191T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55663254 | |||||||
chr15:55663539 | C | CT | 9 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(6): Show |
9 | HG02630.hp2 HG02970.hp2 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.2041+8905dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55663539 | |||||||
chr15:55663539 | C | T | 2 | a0001c0001t0002g0243 a0001c0001t0002g0244 |
2 | HG00639.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.2041+8906G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55663539 | |||||||
chr15:55663591 | G | A | 2 | a0002c0002t0068g0099 a0002c0002t0109g0236 |
2 | NA18906.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2041+8854C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55663591 | |||||||
chr15:55663666 | G | C | 187 | a0001c0001t0001g0194 a0001c0001t0001g0226 a0001c0001t0002g0238 others(184): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.2041+8779C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55663666 | |||||||
chr15:55663692 | C | A | 4 | a0002c0002t0003g0084 a0006c0010t0025g0065 a0006c0010t0059g0072 others(1): Show |
4 | NA18944.hp1 NA18954.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.2041+8753G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55663692 | |||||||
chr15:55663774 | T | A | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041+8671A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55663774 | |||||||
chr15:55663807 | G | A | 12 | a0001c0001t0032g0098 a0004c0004t0023g0056 a0004c0004t0023g0057 others(9): Show |
12 | HG01255.hp2 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2041+8638C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55663807 | |||||||
chr15:55663944 | C | T | 10 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(7): Show |
10 | HG02615.hp1 HG02630.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.2041+8501G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55663944 | |||||||
chr15:55664017 | C | T | 10 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(7): Show |
10 | HG02615.hp1 HG02630.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.2041+8428G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664017 | |||||||
chr15:55664145 | T | C | 1 | a0001c0001t0006g0148 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2041+8300A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664145 | |||||||
chr15:55664186 | G | C | 3 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0192 |
3 | NA18962.hp1 NA18981.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.2041+8259C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664186 | |||||||
chr15:55664228 | G | GC | 8 | a0001c0001t0096g0229 a0001c0001t0099g0228 a0001c0001t0100g0232 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2041+8216dupG | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664228 | |||||||
chr15:55664360 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2041+8085G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664360 | |||||||
chr15:55664368 | C | T | 1 | a0001c0007t0038g0230 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2041+8077G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664368 | |||||||
chr15:55664423 | G | A | 4 | a0001c0001t0001g0226 a0001c0001t0002g0281 a0001c0001t0002g0282 others(1): Show |
4 | HG01361.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.2041+8022C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664423 | |||||||
chr15:55664567 | A | C | 3 | a0002c0002t0019g0052 a0002c0002t0019g0062 a0002c0002t0020g0010 |
3 | HG02451.hp2 HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2041+7878T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664567 | |||||||
chr15:55664672 | G | A | 248 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(245): Show |
249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.2041+7773C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664672 | |||||||
chr15:55664715 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2041+7730A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664715 | |||||||
chr15:55664769 | T | C | 1 | a0001c0001t0100g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2041+7676A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664769 | |||||||
chr15:55664842 | C | G | 1 | a0001c0001t0041g0263 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2041+7603G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664842 | |||||||
chr15:55664847 | T | A | 251 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(248): Show |
252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.2041+7598A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664847 | |||||||
chr15:55664926 | T | C | 8 | a0001c0001t0096g0229 a0001c0001t0099g0228 a0001c0001t0100g0232 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2041+7519A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664926 | |||||||
chr15:55664997 | G | A | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041+7448C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55664997 | |||||||
chr15:55665029 | C | T | 1 | a0001c0012t0002g0279 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2041+7416G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55665029 | |||||||
chr15:55665191 | T | A | 1 | a0002c0002t0007g0086 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2041+7254A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55665191 | |||||||
chr15:55665455 | G | C | 1 | a0004c0004t0069g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2041+6990C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55665455 | |||||||
chr15:55665506 | TG | T | 8 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(5): Show |
8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.2041+6938delC | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55665506 | |||||||
chr15:55665507 | G | GT | 8 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2041+6937dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55665507 | |||||||
chr15:55665507 | G | T | 4 | a0001c0012t0072g0113 a0001c0012t0074g0114 a0002c0002t0068g0099 others(1): Show |
4 | HG02630.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2041+6938C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55665507 | |||||||
chr15:55665507 | GT | G | 51 | a0001c0001t0001g0130 a0001c0001t0001g0226 a0001c0001t0002g0238 others(48): Show |
51 | HG00140.hp1 HG00438.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.2041+6937delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55665507 | |||||||
chr15:55665516 | T | C | 2 | a0001c0001t0005g0180 a0001c0001t0005g0187 |
2 | HG01928.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.2041+6929A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55665516 | |||||||
chr15:55665909 | A | G | 1 | a0001c0009t0042g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2041+6536T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55665909 | |||||||
chr15:55666219 | T | C | 143 | a0001c0001t0001g0226 a0001c0001t0002g0238 a0001c0001t0002g0240 others(140): Show |
143 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.2041+6226A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55666219 | |||||||
chr15:55666266 | C | T | 22 | a0001c0001t0021g0051 a0001c0001t0021g0060 a0001c0001t0096g0229 others(19): Show |
22 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.2041+6179G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55666266 | |||||||
chr15:55666531 | T | G | 4 | a0001c0001t0001g0226 a0001c0001t0002g0281 a0001c0001t0002g0282 others(1): Show |
4 | HG01361.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.2041+5914A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55666531 | |||||||
chr15:55666592 | A | G | 2 | a0002c0002t0004g0108 a0002c0002t0004g0216 |
2 | NA18943.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.2041+5853T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55666592 | |||||||
chr15:55666619 | C | T | 3 | a0001c0001t0029g0092 a0001c0001t0066g0094 a0011c0016t0029g0093 |
3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2041+5826G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55666619 | |||||||
chr15:55667158 | A | G | 2 | a0001c0001t0040g0135 a0001c0001t0040g0136 |
2 | HG02027.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.2041+5287T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55667158 | |||||||
chr15:55667193 | G | A | 1 | a0004c0004t0069g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2041+5252C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55667193 | |||||||
chr15:55667206 | A | G | 1 | a0001c0001t0002g0249 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2041+5239T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55667206 | |||||||
chr15:55667207 | GA | G | 108 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(105): Show |
109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.2041+5237delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55667207 | |||||||
chr15:55667207 | GAA | G | 20 | a0001c0001t0001g0164 a0001c0001t0001g0179 a0001c0001t0021g0051 others(17): Show |
20 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.2041+5236_2041+523 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55667207 | |||||||
chr15:55667220 | A | C | 143 | a0001c0001t0001g0226 a0001c0001t0002g0238 a0001c0001t0002g0240 others(140): Show |
143 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.2041+5225T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55667220 | |||||||
chr15:55667262 | T | C | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2041+5183A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55667262 | |||||||
chr15:55667431 | A | T | 5 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(2): Show |
5 | HG02615.hp1 HG03453.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041+5014T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55667431 | |||||||
chr15:55667457 | G | A | 1 | a0001c0001t0041g0263 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2041+4988C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55667457 | |||||||
chr15:55667553 | G | A | 1 | a0001c0003t0003g0042 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2041+4892C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55667553 | |||||||
chr15:55667762 | A | G | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041+4683T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55667762 | |||||||
chr15:55667834 | C | T | 2 | a0001c0001t0096g0229 a0001c0001t0099g0228 |
2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2041+4611G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55667834 | |||||||
chr15:55667912 | C | G | 1 | a0001c0001t0001g0154 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2041+4533G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55667912 | |||||||
chr15:55667967 | G | T | 1 | a0001c0001t0001g0165 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2041+4478C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55667967 | |||||||
chr15:55668001 | G | A | 1 | a0012c0019t0046g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2041+4444C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55668001 | |||||||
chr15:55668077 | T | A | 1 | a0001c0001t0002g0247 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2041+4368A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55668077 | |||||||
chr15:55668258 | A | G | 78 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(75): Show |
78 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.2041+4187T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55668258 | |||||||
chr15:55668491 | G | C | 6 | a0001c0001t0029g0092 a0001c0001t0051g0004 a0001c0001t0052g0006 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2041+3954C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55668491 | |||||||
chr15:55669174 | A | T | 33 | a0001c0001t0021g0051 a0001c0001t0021g0060 a0001c0001t0096g0229 others(30): Show |
33 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.2041+3271T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55669174 | |||||||
chr15:55669297 | C | T | 8 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(5): Show |
8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.2041+3148G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55669297 | |||||||
chr15:55669368 | A | G | 1 | a0001c0001t0001g0154 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2041+3077T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55669368 | |||||||
chr15:55670019 | A | C | 3 | a0001c0012t0072g0113 a0001c0012t0074g0114 a0012c0019t0046g0003 |
3 | HG02630.hp2 HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2041+2426T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670019 | |||||||
chr15:55670101 | T | C | 18 | a0001c0001t0021g0051 a0001c0001t0021g0060 a0001c0007t0038g0230 others(15): Show |
18 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.2041+2344A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670101 | |||||||
chr15:55670159 | C | T | 262 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(259): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.2041+2286G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670159 | |||||||
chr15:55670182 | T | G | 1 | a0012c0019t0046g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2041+2263A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670182 | |||||||
chr15:55670247 | G | GT | 265 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(262): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.2041+2197dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670247 | |||||||
chr15:55670326 | G | T | 1 | a0001c0001t0001g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2041+2119C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670326 | |||||||
chr15:55670490 | G | A | 1 | a0001c0001t0078g0149 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2041+1955C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670490 | |||||||
chr15:55670578 | C | T | 262 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(259): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.2041+1867G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670578 | |||||||
chr15:55670663 | G | A | 87 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(84): Show |
87 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.2041+1782C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670663 | |||||||
chr15:55670840 | C | T | 1 | a0001c0001t0001g0223 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2041+1605G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670840 | |||||||
chr15:55670895 | C | T | 1 | a0001c0001t0070g0133 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2041+1550G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670895 | |||||||
chr15:55670897 | TCACAAAC others(5): Show |
T | 1 | a0001c0001t0035g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2041+1536_2041+154 others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670897 | |||||||
chr15:55670901 | AAACACAC others(6): Show |
A | 1 | a0001c0001t0002g0270 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2041+1531_2041+154 others(17): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670901 | |||||||
chr15:55670901 | AAACACAC others(8): Show |
A | 1 | a0002c0002t0057g0025 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2041+1529_2041+154 others(19): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670901 | |||||||
chr15:55670901 | AAACACAC others(10): Show |
A | 1 | a0001c0001t0018g0058 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2041+1527_2041+154 others(21): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670901 | |||||||
chr15:55670901 | AAACACAC others(12): Show |
A | 2 | a0001c0001t0008g0159 a0001c0001t0039g0199 |
2 | NA18952.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.2041+1525_2041+154 others(23): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670901 | |||||||
chr15:55670902 | AACAC | A | 7 | a0001c0001t0016g0122 a0001c0001t0016g0123 a0001c0001t0066g0094 others(4): Show |
7 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.2041+1539_2041+154 others(8): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670902 | |||||||
chr15:55670902 | AACACACA others(3): Show |
A | 8 | a0001c0001t0033g0101 a0001c0001t0054g0005 a0001c0001t0097g0221 others(5): Show |
8 | HG02572.hp2 HG02818.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.2041+1533_2041+154 others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670902 | |||||||
chr15:55670902 | AACACACA others(5): Show |
A | 11 | a0001c0001t0002g0255 a0001c0001t0002g0258 a0001c0001t0032g0103 others(8): Show |
11 | HG01517.hp1 HG02965.hp1 HG03195.hp1 others(8): Show |
intron_variant | MODIFIER | c.2041+1531_2041+154 others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670902 | |||||||
chr15:55670902 | AACACACA others(7): Show |
A | 105 | a0001c0001t0001g0226 a0001c0001t0002g0238 a0001c0001t0002g0240 others(102): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.2041+1529_2041+154 others(18): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670902 | |||||||
chr15:55670902 | AACACACA others(9): Show |
A | 15 | a0001c0001t0002g0250 a0001c0001t0078g0149 a0001c0001t0081g0171 others(12): Show |
15 | HG01358.hp1 HG02040.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2041+1527_2041+154 others(20): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670902 | |||||||
chr15:55670902 | AACACACA others(11): Show |
A | 14 | a0001c0001t0001g0193 a0001c0001t0001g0223 a0001c0001t0008g0145 others(11): Show |
14 | HG00280.hp1 HG01361.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.2041+1525_2041+154 others(22): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670902 | |||||||
chr15:55670902 | AACACACA others(13): Show |
A | 76 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(73): Show |
77 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.2041+1523_2041+154 others(24): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670902 | |||||||
chr15:55670902 | AACACACA others(15): Show |
A | 13 | a0001c0001t0001g0160 a0001c0001t0001g0175 a0001c0001t0001g0207 others(10): Show |
13 | HG00099.hp1 HG01358.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.2041+1521_2041+154 others(26): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670902 | |||||||
chr15:55670902 | AACACACA others(17): Show |
A | 10 | a0001c0001t0021g0051 a0001c0001t0021g0060 a0003c0005t0010g0039 others(7): Show |
10 | HG00733.hp2 HG00741.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.2041+1519_2041+154 others(28): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670902 | |||||||
chr15:55670902 | AACACACA others(19): Show |
A | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041+1517_2041+154 others(30): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670902 | |||||||
chr15:55670902 | AACACACA others(21): Show |
A | 2 | a0001c0001t0096g0229 a0001c0001t0099g0228 |
2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2041+1515_2041+154 others(32): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670902 | |||||||
chr15:55670953 | A | T | 1 | a0001c0001t0105g0205 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2041+1492T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670953 | |||||||
chr15:55670971 | AAGAAG | A | 3 | a0001c0001t0096g0229 a0001c0001t0099g0228 a0001c0001t0100g0232 |
3 | HG02647.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2041+1469_2041+147 others(9): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55670971 | |||||||
chr15:55671037 | T | A | 1 | a0004c0004t0048g0054 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2041+1408A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55671037 | |||||||
chr15:55671204 | A | G | 263 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(260): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.2041+1241T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55671204 | |||||||
chr15:55671534 | G | A | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041+911C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55671534 | |||||||
chr15:55671549 | T | C | 3 | a0002c0002t0019g0052 a0002c0002t0019g0062 a0002c0002t0020g0010 |
3 | HG02451.hp2 HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2041+896A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55671549 | |||||||
chr15:55671566 | T | C | 5 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0040g0135 others(2): Show |
5 | HG00323.hp2 HG01081.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.2041+879A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55671566 | |||||||
chr15:55671574 | C | T | 272 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(269): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.2041+871G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55671574 | |||||||
chr15:55671588 | A | T | 265 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(262): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.2041+857T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55671588 | |||||||
chr15:55671642 | G | A | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2041+803C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55671642 | |||||||
chr15:55671646 | G | A | 43 | a0001c0001t0001g0226 a0001c0001t0002g0240 a0001c0001t0002g0241 others(40): Show |
43 | HG00140.hp1 HG00639.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.2041+799C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55671646 | |||||||
chr15:55671747 | C | T | 17 | a0001c0001t0032g0098 a0001c0001t0032g0103 a0001c0001t0033g0101 others(14): Show |
18 | HG01255.hp2 HG01884.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.2041+698G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55671747 | |||||||
chr15:55671755 | C | T | 1 | a0001c0001t0100g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2041+690G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55671755 | |||||||
chr15:55671970 | G | A | 1 | a0002c0002t0007g0086 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2041+475C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55671970 | |||||||
chr15:55672134 | C | T | 2 | a0003c0006t0009g0007 a0003c0006t0009g0008 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2041+311G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55672134 | |||||||
chr15:55672143 | CT | C | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041+301delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55672143 | |||||||
chr15:55672355 | G | C | 15 | a0001c0001t0032g0098 a0001c0001t0032g0103 a0001c0001t0033g0101 others(12): Show |
15 | HG01255.hp2 HG01884.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.2041+90C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 11/19 | chr15 | 55672355 | |||||||
chr15:55672782 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1853-149T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 10/19 | chr15 | 55672782 | |||||||
chr15:55673040 | C | CTGAA | 3 | a0001c0012t0072g0113 a0001c0012t0074g0114 a0012c0019t0046g0003 |
3 | HG02630.hp2 HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1852+327_1852+330d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 10/19 | chr15 | 55673040 | |||||||
chr15:55673259 | G | T | 1 | a0002c0002t0004g0216 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1852+112C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 10/19 | chr15 | 55673259 | |||||||
chr15:55673292 | TATAAAC | T | 13 | a0001c0001t0021g0051 a0001c0001t0021g0060 a0003c0005t0010g0038 others(10): Show |
13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.1852+73_1852+78del others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 10/19 | chr15 | 55673292 | |||||||
chr15:55673323 | T | C | 89 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(86): Show |
89 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.1852+48A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 10/19 | chr15 | 55673323 | |||||||
chr15:55673336 | A | G | 1 | a0001c0001t0001g0192 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1852+35T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 10/19 | chr15 | 55673336 | |||||||
chr15:55673344 | T | A | 1 | a0001c0001t0100g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1852+27A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 10/19 | chr15 | 55673344 | |||||||
chr15:55673773 | T | C | 78 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(75): Show |
78 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.1547-97A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 9/19 | chr15 | 55673773 | |||||||
chr15:55673911 | T | C | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1547-235A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 9/19 | chr15 | 55673911 | |||||||
chr15:55674043 | T | G | 188 | a0001c0001t0001g0226 a0001c0001t0002g0238 a0001c0001t0002g0240 others(185): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1547-367A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 9/19 | chr15 | 55674043 | |||||||
chr15:55674119 | A | G | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1547-443T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 9/19 | chr15 | 55674119 | |||||||
chr15:55674247 | G | C | 11 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0029g0092 others(8): Show |
11 | HG00323.hp2 HG01081.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1547-571C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 9/19 | chr15 | 55674247 | |||||||
chr15:55674416 | T | C | 2 | a0001c0009t0103g0233 a0016c0014t0073g0234 |
2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1547-740A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 9/19 | chr15 | 55674416 | |||||||
chr15:55674444 | C | A | 134 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0021g0051 others(131): Show |
135 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1547-768G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 9/19 | chr15 | 55674444 | |||||||
chr15:55674499 | T | C | 1 | a0001c0001t0001g0191 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1547-823A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 9/19 | chr15 | 55674499 | |||||||
chr15:55674782 | G | A | 12 | a0001c0001t0032g0098 a0004c0004t0023g0056 a0004c0004t0023g0057 others(9): Show |
12 | HG01255.hp2 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1546+737C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 9/19 | chr15 | 55674782 | |||||||
chr15:55675199 | A | G | 44 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0021g0051 others(41): Show |
44 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1546+320T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 9/19 | chr15 | 55675199 | |||||||
chr15:55675718 | T | C | 92 | a0001c0001t0032g0098 a0001c0003t0003g0042 a0001c0003t0003g0074 others(89): Show |
92 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1382-35A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55675718 | |||||||
chr15:55675752 | C | A | 1 | a0002c0002t0095g0212 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1382-69G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55675752 | |||||||
chr15:55675777 | C | G | 17 | a0002c0002t0013g0016 a0002c0002t0013g0018 a0002c0002t0013g0029 others(14): Show |
17 | HG00642.hp1 HG00642.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.1382-94G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55675777 | |||||||
chr15:55675784 | C | A | 8 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(5): Show |
8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.1382-101G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55675784 | |||||||
chr15:55676272 | GT | G | 90 | a0001c0001t0032g0098 a0001c0003t0003g0042 a0001c0003t0003g0074 others(87): Show |
90 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1382-590delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55676272 | |||||||
chr15:55676278 | T | C | 1 | a0001c0001t0005g0186 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1382-595A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55676278 | |||||||
chr15:55676341 | G | A | 82 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(79): Show |
82 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.1382-658C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55676341 | |||||||
chr15:55676401 | T | C | 1 | a0001c0001t0001g0160 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1382-718A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55676401 | |||||||
chr15:55676527 | A | G | 1 | a0001c0009t0103g0233 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1382-844T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55676527 | |||||||
chr15:55676657 | C | A | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1382-974G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55676657 | |||||||
chr15:55676726 | G | T | 2 | a0001c0012t0072g0113 a0001c0012t0074g0114 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1382-1043C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55676726 | |||||||
chr15:55676919 | A | G | 1 | a0001c0001t0084g0129 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1381+878T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55676919 | |||||||
chr15:55677013 | C | T | 2 | a0001c0001t0002g0259 a0001c0001t0002g0262 |
2 | HG02698.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1381+784G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55677013 | |||||||
chr15:55677046 | T | C | 3 | a0001c0001t0029g0092 a0001c0001t0066g0094 a0011c0016t0029g0093 |
3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1381+751A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55677046 | |||||||
chr15:55677380 | C | T | 1 | a0001c0007t0038g0231 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1381+417G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55677380 | |||||||
chr15:55677569 | T | C | 4 | a0002c0002t0013g0018 a0002c0002t0027g0019 a0002c0002t0061g0027 others(1): Show |
4 | HG00642.hp1 HG00642.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1381+228A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55677569 | |||||||
chr15:55677572 | T | C | 4 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(1): Show |
4 | HG03453.hp1 HG03486.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1381+225A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55677572 | |||||||
chr15:55677629 | A | C | 1 | a0001c0001t0071g0143 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1381+168T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 8/19 | chr15 | 55677629 | |||||||
chr15:55678091 | A | G | 1 | a0001c0007t0038g0230 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1134-47T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 7/19 | chr15 | 55678091 | |||||||
chr15:55678121 | A | G | 1 | a0012c0019t0046g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1134-77T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 7/19 | chr15 | 55678121 | |||||||
chr15:55678210 | T | C | 2 | a0001c0001t0051g0004 a0001c0001t0052g0006 |
2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1134-166A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 7/19 | chr15 | 55678210 | |||||||
chr15:55678386 | A | C | 1 | a0002c0002t0019g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1134-342T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 7/19 | chr15 | 55678386 | |||||||
chr15:55678395 | A | T | 6 | a0002c0002t0013g0018 a0002c0002t0013g0029 a0002c0002t0027g0019 others(3): Show |
6 | HG00642.hp1 HG00642.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1134-351T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 7/19 | chr15 | 55678395 | |||||||
chr15:55678725 | T | C | 1 | a0002c0002t0025g0070 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1133+561A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 7/19 | chr15 | 55678725 | |||||||
chr15:55678852 | T | C | 1 | a0002c0002t0057g0025 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1133+434A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 7/19 | chr15 | 55678852 | |||||||
chr15:55678854 | G | T | 1 | a0001c0001t0100g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1133+432C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 7/19 | chr15 | 55678854 | |||||||
chr15:55679031 | G | A | 1 | a0002c0002t0068g0099 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1133+255C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 7/19 | chr15 | 55679031 | |||||||
chr15:55679187 | A | T | 6 | a0001c0001t0029g0092 a0001c0001t0051g0004 a0001c0001t0052g0006 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1133+99T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 7/19 | chr15 | 55679187 | |||||||
chr15:55679458 | A | G | 1 | a0002c0002t0057g0025 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.974-13T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 6/19 | chr15 | 55679458 | |||||||
chr15:55679487 | T | C | 2 | a0001c0001t0051g0004 a0001c0001t0052g0006 |
2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.974-42A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 6/19 | chr15 | 55679487 | |||||||
chr15:55679539 | T | C | 15 | a0001c0001t0021g0051 a0001c0001t0021g0060 a0003c0005t0010g0038 others(12): Show |
15 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.974-94A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 6/19 | chr15 | 55679539 | |||||||
chr15:55679986 | A | G | 6 | a0001c0001t0029g0092 a0001c0001t0051g0004 a0001c0001t0052g0006 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.973+68T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 6/19 | chr15 | 55679986 | |||||||
chr15:55679988 | G | A | 1 | a0002c0002t0109g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.973+66C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 6/19 | chr15 | 55679988 | |||||||
chr15:55680011 | T | C | 1 | a0001c0001t0096g0229 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.973+43A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 6/19 | chr15 | 55680011 | |||||||
chr15:55680245 | T | C | 5 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0257 others(2): Show |
5 | HG03834.hp2 NA18962.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.815-33A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 5/19 | chr15 | 55680245 | |||||||
chr15:55680317 | A | G | 273 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(270): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.815-105T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 5/19 | chr15 | 55680317 | |||||||
chr15:55680453 | A | G | 2 | a0001c0001t0001g0226 a0001c0001t0041g0280 |
2 | HG01361.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.814+38T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 5/19 | chr15 | 55680453 | |||||||
chr15:55680646 | C | G | 1 | a0006c0010t0025g0065 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.677-18G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55680646 | |||||||
chr15:55680675 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.677-47A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55680675 | |||||||
chr15:55680940 | T | G | 52 | a0001c0001t0001g0226 a0001c0001t0002g0238 a0001c0001t0002g0240 others(49): Show |
52 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.677-312A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55680940 | |||||||
chr15:55681031 | A | C | 3 | a0001c0001t0021g0051 a0001c0001t0021g0060 a0012c0019t0046g0003 |
3 | HG02809.hp2 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.677-403T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55681031 | |||||||
chr15:55681200 | A | T | 7 | a0001c0001t0032g0103 a0001c0001t0033g0101 a0001c0001t0033g0102 others(4): Show |
7 | HG02257.hp2 HG02572.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.677-572T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55681200 | |||||||
chr15:55681318 | C | T | 2 | a0001c0001t0096g0229 a0001c0001t0099g0228 |
2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.677-690G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55681318 | |||||||
chr15:55681548 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.676+816C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55681548 | |||||||
chr15:55681572 | T | C | 5 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0040g0135 others(2): Show |
5 | HG00323.hp2 HG01081.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.676+792A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55681572 | |||||||
chr15:55681776 | G | C | 1 | a0001c0001t0001g0206 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.676+588C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55681776 | |||||||
chr15:55681847 | G | A | 1 | a0002c0002t0063g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.676+517C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55681847 | |||||||
chr15:55682111 | G | A | 8 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(5): Show |
8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.676+253C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55682111 | |||||||
chr15:55682121 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.676+243G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55682121 | |||||||
chr15:55682186 | T | C | 11 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0029g0092 others(8): Show |
11 | HG00323.hp2 HG01081.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.676+178A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55682186 | |||||||
chr15:55682228 | A | C | 2 | a0002c0002t0104g0215 a0002c0002t0110g0237 |
2 | HG01074.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.676+136T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55682228 | |||||||
chr15:55682297 | G | A | 2 | a0002c0002t0004g0108 a0002c0002t0004g0216 |
2 | NA18943.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.676+67C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55682297 | |||||||
chr15:55682330 | G | A | 1 | a0001c0001t0012g0083 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.676+34C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55682330 | |||||||
chr15:55682348 | C | T | 3 | a0001c0007t0106g0109 a0001c0007t0107g0110 a0001c0007t0108g0111 |
3 | HG02109.hp2 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.676+16G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55682348 | |||||||
chr15:55682357 | G | A | 2 | a0001c0001t0035g0219 a0001c0001t0101g0217 |
2 | HG02257.hp2 HG02572.hp1 |
splice_region_variant&intron_variant | LOW | c.676+7C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 4/19 | chr15 | 55682357 | |||||||
chr15:55682543 | A | ATTTT | 4 | a0001c0001t0001g0154 a0001c0001t0001g0160 a0001c0001t0077g0174 others(1): Show |
4 | HG04228.hp1 NA18973.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.543-50_543-47dupAA others(2): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682543 | |||||||
chr15:55682544 | T | TTTTA | 27 | a0001c0001t0021g0051 a0001c0001t0021g0060 a0001c0001t0024g0013 others(24): Show |
28 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.543-51_543-48dupTA others(2): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682544 | |||||||
chr15:55682544 | T | TTTTATTT others(1): Show |
36 | a0001c0001t0002g0246 a0001c0001t0002g0265 a0001c0001t0002g0266 others(33): Show |
36 | HG00323.hp1 HG01081.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.543-55_543-48dupTA others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682544 | |||||||
chr15:55682544 | T | TTTTATTT others(5): Show |
62 | a0001c0001t0001g0226 a0001c0001t0002g0238 a0001c0001t0002g0240 others(59): Show |
62 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.543-59_543-48dupTA others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682544 | |||||||
chr15:55682544 | T | TTTTATTT others(9): Show |
28 | a0001c0001t0002g0264 a0001c0001t0002g0273 a0001c0001t0002g0274 others(25): Show |
28 | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.543-63_543-48dupTA others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682544 | |||||||
chr15:55682544 | T | TTTTATTT others(13): Show |
3 | a0001c0001t0096g0229 a0001c0007t0106g0109 a0001c0007t0107g0110 |
3 | HG02109.hp2 HG02647.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.543-67_543-48dupTA others(18): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682544 | |||||||
chr15:55682544 | T | TTTTTTTT others(5): Show |
1 | a0001c0007t0038g0230 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.543-48_543-47insTA others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682544 | |||||||
chr15:55682544 | T | TTTTTTTT others(13): Show |
2 | a0001c0007t0038g0231 a0001c0007t0108g0111 |
2 | HG02723.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.543-48_543-47insTA others(18): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682544 | |||||||
chr15:55682544 | TTTTATTT others(5): Show |
T | 12 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0029g0092 others(9): Show |
12 | HG00323.hp2 HG01081.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.543-59_543-48delTA others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682544 | |||||||
chr15:55682548 | A | T | 69 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(66): Show |
69 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.543-51T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682548 | |||||||
chr15:55682553 | T | TTTATTTA others(9): Show |
7 | a0002c0002t0003g0044 a0002c0002t0003g0069 a0002c0002t0003g0088 others(4): Show |
7 | HG00438.hp2 HG02027.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.543-57_543-56insTT others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682553 | |||||||
chr15:55682560 | A | T | 1 | a0001c0001t0105g0205 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.543-63T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682560 | |||||||
chr15:55682676 | C | T | 1 | a0001c0012t0002g0279 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.543-179G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682676 | |||||||
chr15:55682756 | T | C | 52 | a0001c0001t0001g0226 a0001c0001t0002g0238 a0001c0001t0002g0240 others(49): Show |
52 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.543-259A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682756 | |||||||
chr15:55682796 | C | G | 1 | a0002c0002t0003g0084 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.543-299G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682796 | |||||||
chr15:55682887 | A | G | 80 | a0001c0003t0003g0042 a0001c0003t0003g0074 a0001c0003t0003g0075 others(77): Show |
80 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.543-390T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55682887 | |||||||
chr15:55683056 | C | T | 6 | a0001c0001t0029g0092 a0001c0001t0051g0004 a0001c0001t0052g0006 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.543-559G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55683056 | |||||||
chr15:55683185 | C | CT | 8 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(5): Show |
8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.542+601dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55683185 | |||||||
chr15:55683294 | T | C | 2 | a0001c0001t0002g0267 a0001c0001t0002g0268 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.542+493A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55683294 | |||||||
chr15:55683402 | T | C | 2 | a0001c0012t0072g0113 a0001c0012t0074g0114 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.542+385A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55683402 | |||||||
chr15:55683748 | A | C | 2 | a0001c0012t0072g0113 a0001c0012t0074g0114 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.542+39T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 3/19 | chr15 | 55683748 | |||||||
chr15:55684132 | C | T | 6 | a0001c0001t0029g0092 a0001c0001t0051g0004 a0001c0001t0052g0006 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.398-201G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55684132 | |||||||
chr15:55684510 | C | T | 11 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(8): Show |
11 | HG02615.hp1 HG02630.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.398-579G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55684510 | |||||||
chr15:55684628 | T | G | 1 | a0001c0001t0097g0221 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.398-697A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55684628 | |||||||
chr15:55684704 | T | TG | 266 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(263): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.398-774dupC | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55684704 | |||||||
chr15:55684762 | C | T | 19 | a0001c0001t0001g0224 a0001c0001t0021g0051 a0001c0001t0021g0060 others(16): Show |
19 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.398-831G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55684762 | |||||||
chr15:55684820 | A | C | 6 | a0001c0001t0029g0092 a0001c0001t0051g0004 a0001c0001t0052g0006 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.398-889T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55684820 | |||||||
chr15:55684861 | T | C | 3 | a0001c0001t0029g0092 a0001c0001t0066g0094 a0011c0016t0029g0093 |
3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.398-930A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55684861 | |||||||
chr15:55685102 | C | T | 79 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(76): Show |
79 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.398-1171G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55685102 | |||||||
chr15:55685382 | A | G | 7 | a0001c0001t0051g0004 a0001c0001t0052g0006 a0001c0001t0054g0005 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-1451T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55685382 | |||||||
chr15:55685544 | G | C | 2 | a0001c0001t0021g0051 a0001c0001t0021g0060 |
2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.398-1613C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55685544 | |||||||
chr15:55685569 | C | A | 5 | a0001c0001t0051g0004 a0001c0001t0052g0006 a0001c0001t0054g0005 others(2): Show |
5 | HG01891.hp2 HG02145.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-1638G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55685569 | |||||||
chr15:55685673 | A | T | 5 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(2): Show |
5 | HG02615.hp1 HG03453.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-1742T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55685673 | |||||||
chr15:55685826 | G | C | 87 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(84): Show |
87 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.398-1895C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55685826 | |||||||
chr15:55685992 | T | C | 1 | a0002c0002t0095g0212 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.398-2061A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55685992 | |||||||
chr15:55686243 | T | A | 88 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(85): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.398-2312A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55686243 | |||||||
chr15:55686348 | T | C | 11 | a0003c0005t0010g0038 a0003c0005t0010g0039 a0003c0005t0010g0041 others(8): Show |
11 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.398-2417A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55686348 | |||||||
chr15:55686469 | A | G | 1 | a0001c0001t0002g0243 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.398-2538T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55686469 | |||||||
chr15:55686612 | T | C | 7 | a0001c0001t0035g0219 a0001c0001t0101g0217 a0001c0007t0038g0230 others(4): Show |
7 | HG02109.hp2 HG02257.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.398-2681A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55686612 | |||||||
chr15:55686776 | C | T | 1 | a0001c0001t0035g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.398-2845G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55686776 | |||||||
chr15:55686932 | C | T | 8 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(5): Show |
8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.398-3001G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55686932 | |||||||
chr15:55687006 | C | T | 8 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(5): Show |
8 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.398-3075G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55687006 | |||||||
chr15:55687802 | T | C | 1 | a0002c0002t0110g0237 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.398-3871A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55687802 | |||||||
chr15:55687851 | G | A | 1 | a0001c0001t0021g0060 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.398-3920C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55687851 | |||||||
chr15:55688100 | G | A | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.398-4169C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55688100 | |||||||
chr15:55688401 | T | TTA | 99 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(96): Show |
99 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.398-4472_398-4471d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55688401 | |||||||
chr15:55688493 | C | T | 1 | a0001c0012t0074g0114 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.398-4562G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55688493 | |||||||
chr15:55688670 | C | G | 1 | a0006c0010t0059g0072 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.398-4739G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55688670 | |||||||
chr15:55688869 | G | A | 1 | a0006c0010t0059g0072 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.398-4938C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55688869 | |||||||
chr15:55689027 | G | A | 1 | a0001c0001t0051g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.398-5096C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55689027 | |||||||
chr15:55689408 | T | C | 1 | a0001c0001t0100g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.398-5477A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55689408 | |||||||
chr15:55689446 | C | G | 1 | a0001c0001t0041g0280 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.398-5515G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55689446 | |||||||
chr15:55689507 | G | A | 1 | a0002c0002t0025g0070 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.398-5576C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55689507 | |||||||
chr15:55689603 | G | A | 5 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0040g0135 others(2): Show |
5 | HG00323.hp2 HG01081.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.398-5672C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55689603 | |||||||
chr15:55689632 | T | TA | 266 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(263): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.398-5702dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55689632 | |||||||
chr15:55689743 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.398-5812G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55689743 | |||||||
chr15:55690014 | A | G | 1 | a0004c0004t0069g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.398-6083T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55690014 | |||||||
chr15:55690028 | T | C | 2 | a0005c0011t0035g0220 a0005c0011t0098g0222 |
2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.398-6097A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55690028 | |||||||
chr15:55690059 | T | C | 72 | a0001c0001t0024g0013 a0001c0001t0024g0031 a0001c0003t0017g0076 others(69): Show |
72 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.398-6128A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55690059 | |||||||
chr15:55690102 | T | C | 6 | a0001c0001t0002g0265 a0001c0001t0002g0266 a0001c0001t0002g0267 others(3): Show |
6 | HG01256.hp2 HG01258.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.398-6171A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55690102 | |||||||
chr15:55690321 | T | C | 2 | a0001c0001t0051g0004 a0001c0001t0052g0006 |
2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.398-6390A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55690321 | |||||||
chr15:55690373 | C | G | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-6442G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55690373 | |||||||
chr15:55690622 | C | T | 4 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(1): Show |
4 | HG03453.hp1 HG03486.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.398-6691G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55690622 | |||||||
chr15:55690643 | T | C | 2 | a0002c0002t0104g0215 a0002c0002t0110g0237 |
2 | HG01074.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.398-6712A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55690643 | |||||||
chr15:55690708 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.398-6777A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55690708 | |||||||
chr15:55690779 | G | C | 251 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(248): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.398-6848C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55690779 | |||||||
chr15:55691071 | G | C | 4 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(1): Show |
4 | HG03453.hp1 HG03486.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.398-7140C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691071 | |||||||
chr15:55691073 | T | C | 95 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(92): Show |
95 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.398-7142A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691073 | |||||||
chr15:55691111 | G | A | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.398-7180C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691111 | |||||||
chr15:55691147 | T | G | 4 | a0001c0001t0016g0122 a0001c0001t0016g0123 a0001c0001t0083g0125 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.398-7216A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691147 | |||||||
chr15:55691177 | T | C | 1 | a0001c0001t0002g0241 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.398-7246A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691177 | |||||||
chr15:55691296 | CA | C | 43 | a0001c0001t0001g0172 a0001c0001t0001g0179 a0001c0001t0001g0183 others(40): Show |
44 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.398-7366delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691296 | |||||||
chr15:55691296 | CAA | C | 44 | a0001c0001t0021g0051 a0001c0001t0021g0060 a0002c0002t0003g0009 others(41): Show |
44 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(41): Show |
intron_variant | MODIFIER | c.398-7367_398-7366d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691296 | |||||||
chr15:55691296 | CAAAAAAA | C | 7 | a0001c0001t0035g0219 a0001c0001t0097g0221 a0001c0001t0101g0217 others(4): Show |
7 | HG02257.hp2 HG02572.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-7372_398-7366d others(9): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691296 | |||||||
chr15:55691315 | A | AG | 3 | a0001c0001t0051g0004 a0001c0001t0052g0006 a0001c0001t0054g0005 |
3 | HG01891.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.398-7385dupC | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691315 | |||||||
chr15:55691315 | A | G | 2 | a0001c0012t0072g0113 a0001c0012t0074g0114 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.398-7384T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691315 | |||||||
chr15:55691393 | T | C | 4 | a0001c0001t0002g0259 a0001c0001t0002g0262 a0001c0001t0002g0264 others(1): Show |
4 | HG00733.hp1 HG00738.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-7462A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691393 | |||||||
chr15:55691509 | T | C | 1 | a0001c0001t0001g0207 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.398-7578A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691509 | |||||||
chr15:55691515 | C | T | 270 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(267): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.398-7584G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691515 | |||||||
chr15:55691549 | C | T | 1 | a0001c0001t0070g0133 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.398-7618G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691549 | |||||||
chr15:55691589 | A | G | 55 | a0001c0001t0001g0139 a0001c0001t0001g0144 a0001c0001t0002g0238 others(52): Show |
55 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.398-7658T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691589 | |||||||
chr15:55691636 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.398-7705C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691636 | |||||||
chr15:55691674 | C | A | 1 | a0014c0018t0006g0170 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.398-7743G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691674 | |||||||
chr15:55691680 | C | CA | 13 | a0001c0001t0032g0098 a0001c0001t0032g0103 a0001c0001t0033g0101 others(10): Show |
13 | HG02055.hp2 HG02145.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.398-7750dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691680 | |||||||
chr15:55691732 | A | G | 3 | a0001c0001t0029g0092 a0001c0001t0066g0094 a0011c0016t0029g0093 |
3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.398-7801T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55691732 | |||||||
chr15:55692067 | T | C | 79 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(76): Show |
79 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.398-8136A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55692067 | |||||||
chr15:55692097 | C | T | 1 | a0001c0009t0087g0112 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.398-8166G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55692097 | |||||||
chr15:55692241 | A | C | 46 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(43): Show |
46 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.398-8310T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55692241 | |||||||
chr15:55692334 | G | A | 2 | a0001c0012t0072g0113 a0001c0012t0074g0114 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.398-8403C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55692334 | |||||||
chr15:55692407 | A | C | 108 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(105): Show |
108 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.398-8476T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55692407 | |||||||
chr15:55692461 | C | T | 150 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(147): Show |
150 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.398-8530G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55692461 | |||||||
chr15:55692663 | T | G | 1 | a0003c0006t0009g0015 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.398-8732A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55692663 | |||||||
chr15:55692828 | G | A | 1 | a0007c0017t0002g0254 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.398-8897C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55692828 | |||||||
chr15:55692835 | C | CT | 162 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(159): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.398-8905dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55692835 | |||||||
chr15:55692835 | C | CTT | 10 | a0001c0001t0001g0164 a0001c0001t0002g0257 a0001c0001t0002g0261 others(7): Show |
11 | HG02040.hp1 HG02630.hp2 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.398-8906_398-8905d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55692835 | |||||||
chr15:55692835 | CT | C | 15 | a0001c0001t0012g0091 a0001c0001t0033g0102 a0002c0002t0016g0127 others(12): Show |
15 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.398-8905delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55692835 | |||||||
chr15:55692904 | G | A | 1 | a0001c0009t0103g0233 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.398-8973C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55692904 | |||||||
chr15:55692934 | G | A | 3 | a0001c0001t0034g0001 a0001c0001t0039g0132 a0001c0001t0070g0133 |
4 | HG03491.hp2 HG03492.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-9003C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55692934 | |||||||
chr15:55693008 | T | G | 51 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(48): Show |
51 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.398-9077A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55693008 | |||||||
chr15:55693241 | G | C | 1 | a0001c0001t0039g0132 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.398-9310C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55693241 | |||||||
chr15:55693303 | G | A | 54 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(51): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.398-9372C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55693303 | |||||||
chr15:55693322 | G | A | 2 | a0001c0001t0041g0263 a0002c0002t0003g0071 |
2 | HG00738.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.398-9391C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55693322 | |||||||
chr15:55693351 | G | C | 55 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(52): Show |
55 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.398-9420C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55693351 | |||||||
chr15:55693360 | GCAGGAGA others(5): Show |
G | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-9441_398-9430d others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55693360 | |||||||
chr15:55693373 | T | G | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-9442A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55693373 | |||||||
chr15:55693603 | T | C | 27 | a0001c0001t0024g0013 a0001c0001t0024g0031 a0002c0002t0011g0048 others(24): Show |
27 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.398-9672A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55693603 | |||||||
chr15:55694191 | T | C | 2 | a0005c0011t0035g0220 a0005c0011t0098g0222 |
2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.398-10260A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55694191 | |||||||
chr15:55694254 | G | C | 1 | a0002c0002t0109g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.398-10323C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55694254 | |||||||
chr15:55694582 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.398-10651A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55694582 | |||||||
chr15:55694869 | C | A | 1 | a0001c0001t0078g0149 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.398-10938G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55694869 | |||||||
chr15:55694987 | C | T | 4 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0258 others(1): Show |
4 | HG03834.hp2 NA18962.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.398-11056G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55694987 | |||||||
chr15:55695300 | A | G | 46 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(43): Show |
46 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.398-11369T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55695300 | |||||||
chr15:55695405 | C | T | 1 | a0002c0002t0003g0088 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.398-11474G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55695405 | |||||||
chr15:55695718 | C | A | 31 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(28): Show |
31 | HG00323.hp2 HG00438.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.398-11787G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55695718 | |||||||
chr15:55695744 | C | G | 1 | a0001c0001t0001g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.398-11813G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55695744 | |||||||
chr15:55695859 | T | C | 3 | a0001c0001t0029g0092 a0001c0001t0066g0094 a0011c0016t0029g0093 |
3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.398-11928A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55695859 | |||||||
chr15:55696184 | A | G | 45 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(42): Show |
45 | HG00323.hp2 HG00438.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.398-12253T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55696184 | |||||||
chr15:55696276 | G | A | 1 | a0002c0002t0090g0214 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.398-12345C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55696276 | |||||||
chr15:55696340 | A | G | 12 | a0003c0005t0010g0038 a0003c0005t0010g0039 a0003c0005t0010g0041 others(9): Show |
12 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.398-12409T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55696340 | |||||||
chr15:55696392 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.398-12461C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55696392 | |||||||
chr15:55696438 | T | G | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-12507A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55696438 | |||||||
chr15:55696617 | C | T | 1 | a0001c0001t0039g0132 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.398-12686G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55696617 | |||||||
chr15:55696738 | T | C | 2 | a0001c0001t0036g0151 a0001c0001t0036g0157 |
2 | HG00738.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.398-12807A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55696738 | |||||||
chr15:55696861 | T | C | 14 | a0001c0020t0053g0002 a0003c0005t0010g0038 a0003c0005t0010g0039 others(11): Show |
14 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.398-12930A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55696861 | |||||||
chr15:55696882 | G | A | 147 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(144): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.398-12951C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55696882 | |||||||
chr15:55696905 | T | A | 1 | a0002c0002t0110g0237 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.398-12974A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55696905 | |||||||
chr15:55697039 | G | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | NA18954.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.398-13108C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55697039 | |||||||
chr15:55697329 | G | C | 2 | a0001c0001t0001g0156 a0001c0001t0001g0177 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.398-13398C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55697329 | |||||||
chr15:55697512 | CTGTT | C | 7 | a0001c0001t0032g0098 a0002c0002t0068g0099 a0004c0004t0030g0097 others(4): Show |
7 | HG02145.hp1 HG02622.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.398-13585_398-1358 others(8): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55697512 | |||||||
chr15:55697543 | G | A | 1 | a0001c0009t0103g0233 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.398-13612C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55697543 | |||||||
chr15:55697594 | C | T | 32 | a0001c0001t0024g0013 a0001c0001t0024g0031 a0001c0001t0051g0004 others(29): Show |
32 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.398-13663G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55697594 | |||||||
chr15:55697741 | C | T | 46 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(43): Show |
46 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.398-13810G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55697741 | |||||||
chr15:55697831 | G | A | 87 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(84): Show |
87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.398-13900C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55697831 | |||||||
chr15:55698005 | T | C | 1 | a0003c0006t0092g0146 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.398-14074A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55698005 | |||||||
chr15:55698209 | T | A | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-14278A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55698209 | |||||||
chr15:55698404 | T | C | 1 | a0001c0008t0037g0210 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.398-14473A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55698404 | |||||||
chr15:55698520 | A | G | 1 | a0001c0003t0018g0073 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.398-14589T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55698520 | |||||||
chr15:55698566 | C | T | 1 | a0013c0015t0043g0011 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.398-14635G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55698566 | |||||||
chr15:55698860 | G | C | 7 | a0001c0001t0032g0098 a0002c0002t0068g0099 a0004c0004t0030g0097 others(4): Show |
7 | HG02145.hp1 HG02622.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.398-14929C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55698860 | |||||||
chr15:55698879 | G | A | 14 | a0001c0001t0002g0265 a0001c0001t0002g0266 a0001c0001t0002g0267 others(11): Show |
14 | HG01081.hp2 HG01167.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.398-14948C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55698879 | |||||||
chr15:55698885 | G | A | 1 | a0002c0002t0057g0025 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.398-14954C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55698885 | |||||||
chr15:55699058 | A | G | 2 | a0001c0012t0072g0113 a0001c0012t0074g0114 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.398-15127T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55699058 | |||||||
chr15:55699596 | A | G | 1 | a0016c0014t0073g0234 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.398-15665T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55699596 | |||||||
chr15:55699759 | G | A | 14 | a0001c0020t0053g0002 a0003c0005t0010g0038 a0003c0005t0010g0039 others(11): Show |
14 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.398-15828C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55699759 | |||||||
chr15:55699976 | T | G | 12 | a0003c0005t0010g0038 a0003c0005t0010g0039 a0003c0005t0010g0041 others(9): Show |
12 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.398-16045A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55699976 | |||||||
chr15:55700269 | T | G | 51 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(48): Show |
51 | HG00323.hp2 HG00438.hp2 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.398-16338A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55700269 | |||||||
chr15:55700447 | A | G | 3 | a0001c0001t0029g0092 a0001c0001t0066g0094 a0011c0016t0029g0093 |
3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.398-16516T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55700447 | |||||||
chr15:55700464 | T | G | 11 | a0003c0005t0010g0038 a0003c0005t0010g0039 a0003c0005t0010g0041 others(8): Show |
11 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.398-16533A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55700464 | |||||||
chr15:55700676 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.398-16745C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55700676 | |||||||
chr15:55700752 | G | A | 7 | a0001c0001t0032g0098 a0002c0002t0068g0099 a0004c0004t0030g0097 others(4): Show |
7 | HG02145.hp1 HG02622.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.398-16821C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55700752 | |||||||
chr15:55700762 | C | T | 75 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(72): Show |
75 | HG00323.hp2 HG00438.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.398-16831G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55700762 | |||||||
chr15:55700768 | C | G | 1 | a0001c0001t0005g0186 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.398-16837G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55700768 | |||||||
chr15:55700916 | G | A | 1 | a0002c0002t0088g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.398-16985C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55700916 | |||||||
chr15:55701118 | T | C | 1 | a0001c0001t0097g0221 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.398-17187A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55701118 | |||||||
chr15:55701163 | T | C | 3 | a0001c0001t0051g0004 a0001c0001t0052g0006 a0001c0001t0054g0005 |
3 | HG01891.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.398-17232A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55701163 | |||||||
chr15:55701244 | T | G | 2 | a0005c0011t0035g0220 a0005c0011t0098g0222 |
2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.398-17313A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55701244 | |||||||
chr15:55701262 | C | T | 3 | a0001c0001t0051g0004 a0001c0001t0052g0006 a0001c0001t0054g0005 |
3 | HG01891.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.398-17331G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55701262 | |||||||
chr15:55701294 | T | C | 10 | a0001c0001t0032g0098 a0001c0001t0032g0103 a0001c0001t0033g0101 others(7): Show |
10 | HG02145.hp1 HG02622.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.398-17363A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55701294 | |||||||
chr15:55701398 | G | C | 1 | a0002c0002t0003g0077 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.398-17467C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55701398 | |||||||
chr15:55701534 | A | AAAAAC | 4 | a0001c0001t0033g0102 a0001c0020t0053g0002 a0002c0002t0089g0163 others(1): Show |
4 | HG02145.hp2 HG02148.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-17608_398-1760 others(9): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55701534 | |||||||
chr15:55701607 | C | T | 13 | a0001c0020t0053g0002 a0003c0005t0010g0038 a0003c0005t0010g0039 others(10): Show |
13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.398-17676G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55701607 | |||||||
chr15:55701617 | A | C | 272 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(269): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.398-17686T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55701617 | |||||||
chr15:55702059 | T | C | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.398-18128A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55702059 | |||||||
chr15:55702160 | T | C | 94 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(91): Show |
94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.398-18229A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55702160 | |||||||
chr15:55702239 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.398-18308G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55702239 | |||||||
chr15:55702274 | G | A | 1 | a0001c0009t0103g0233 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.398-18343C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55702274 | |||||||
chr15:55702387 | C | CT | 3 | a0001c0001t0051g0004 a0001c0001t0052g0006 a0001c0001t0054g0005 |
3 | HG01891.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.398-18457dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55702387 | |||||||
chr15:55702393 | A | T | 3 | a0001c0001t0051g0004 a0001c0001t0052g0006 a0001c0001t0054g0005 |
3 | HG01891.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.398-18462T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55702393 | |||||||
chr15:55702711 | T | G | 94 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(91): Show |
94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.398-18780A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55702711 | |||||||
chr15:55702933 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.398-19002T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55702933 | |||||||
chr15:55702945 | G | A | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.398-19014C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55702945 | |||||||
chr15:55703116 | G | C | 2 | a0001c0001t0096g0229 a0001c0001t0099g0228 |
2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.398-19185C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55703116 | |||||||
chr15:55703146 | T | C | 1 | a0001c0001t0100g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.398-19215A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55703146 | |||||||
chr15:55703344 | G | A | 30 | a0001c0001t0024g0013 a0001c0001t0024g0031 a0001c0001t0051g0004 others(27): Show |
30 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.398-19413C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55703344 | |||||||
chr15:55703439 | C | T | 1 | a0001c0001t0100g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.398-19508G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55703439 | |||||||
chr15:55703489 | T | C | 3 | a0001c0001t0029g0092 a0001c0001t0066g0094 a0011c0016t0029g0093 |
3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.398-19558A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55703489 | |||||||
chr15:55703595 | T | C | 1 | a0001c0001t0101g0217 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.398-19664A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55703595 | |||||||
chr15:55703911 | G | A | 1 | a0002c0002t0027g0019 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.398-19980C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55703911 | |||||||
chr15:55703932 | T | C | 3 | a0001c0001t0002g0265 a0001c0001t0002g0266 a0001c0001t0002g0275 |
3 | HG01928.hp1 HG01934.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.398-20001A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55703932 | |||||||
chr15:55703937 | C | T | 1 | a0002c0002t0027g0019 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.398-20006G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55703937 | |||||||
chr15:55703940 | G | A | 11 | a0003c0005t0010g0038 a0003c0005t0010g0039 a0003c0005t0010g0041 others(8): Show |
11 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.398-20009C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55703940 | |||||||
chr15:55704007 | G | GA | 46 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(43): Show |
46 | HG00323.hp2 HG00438.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.398-20077dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55704007 | |||||||
chr15:55704072 | G | A | 1 | a0001c0001t0100g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.398-20141C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55704072 | |||||||
chr15:55704358 | T | G | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-20427A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55704358 | |||||||
chr15:55704504 | G | C | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-20573C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55704504 | |||||||
chr15:55704528 | C | T | 3 | a0001c0001t0029g0092 a0001c0001t0066g0094 a0011c0016t0029g0093 |
3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.398-20597G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55704528 | |||||||
chr15:55704587 | T | G | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-20656A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55704587 | |||||||
chr15:55704609 | G | A | 2 | a0001c0001t0002g0267 a0001c0001t0002g0268 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.398-20678C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55704609 | |||||||
chr15:55704637 | A | G | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG00438.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.398-20706T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55704637 | |||||||
chr15:55704898 | A | T | 128 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(125): Show |
128 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.398-20967T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55704898 | |||||||
chr15:55704939 | A | T | 1 | a0006c0010t0059g0072 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.398-21008T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55704939 | |||||||
chr15:55704955 | T | A | 1 | a0001c0007t0038g0230 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.398-21024A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55704955 | |||||||
chr15:55705283 | A | G | 2 | a0003c0006t0009g0015 a0003c0006t0022g0012 |
2 | HG00733.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.398-21352T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55705283 | |||||||
chr15:55705346 | A | T | 46 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(43): Show |
46 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.398-21415T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55705346 | |||||||
chr15:55705556 | C | T | 2 | a0001c0012t0072g0113 a0001c0012t0074g0114 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.398-21625G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55705556 | |||||||
chr15:55705854 | C | CT | 40 | a0001c0001t0001g0158 a0001c0001t0001g0224 a0001c0001t0024g0013 others(37): Show |
40 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.398-21924dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55705854 | |||||||
chr15:55705854 | C | CTT | 58 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(55): Show |
58 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.398-21925_398-2192 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55705854 | |||||||
chr15:55705882 | G | T | 129 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(126): Show |
129 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.398-21951C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55705882 | |||||||
chr15:55705910 | C | T | 1 | a0001c0001t0004g0188 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.398-21979G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55705910 | |||||||
chr15:55706014 | A | ATTTT | 21 | a0001c0001t0035g0219 a0001c0001t0097g0221 a0001c0001t0101g0217 others(18): Show |
21 | HG00323.hp1 HG02257.hp2 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.398-22087_398-2208 others(8): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706014 | |||||||
chr15:55706014 | A | ATTTTT | 55 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(52): Show |
55 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.398-22088_398-2208 others(9): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706014 | |||||||
chr15:55706014 | A | ATTTTTT | 15 | a0001c0001t0002g0253 a0001c0001t0002g0260 a0001c0001t0002g0270 others(12): Show |
15 | HG00323.hp2 HG00741.hp1 HG02148.hp1 others(12): Show |
intron_variant | MODIFIER | c.398-22089_398-2208 others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706014 | |||||||
chr15:55706014 | A | ATTTTTTT | 53 | a0001c0001t0012g0083 a0001c0001t0018g0058 a0001c0001t0021g0051 others(50): Show |
53 | HG00438.hp2 HG00642.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.398-22090_398-2208 others(11): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706014 | |||||||
chr15:55706014 | A | ATTTTTTT others(1): Show |
28 | a0001c0001t0024g0013 a0001c0001t0034g0001 a0001c0001t0070g0133 others(25): Show |
29 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.398-22091_398-2208 others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706014 | |||||||
chr15:55706014 | ATTT | A | 91 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(88): Show |
91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.398-22086_398-2208 others(7): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706014 | |||||||
chr15:55706050 | C | T | 46 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(43): Show |
46 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.398-22119G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706050 | |||||||
chr15:55706098 | C | G | 130 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(127): Show |
130 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.398-22167G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706098 | |||||||
chr15:55706200 | A | C | 1 | a0002c0002t0095g0212 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.398-22269T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706200 | |||||||
chr15:55706397 | A | C | 130 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(127): Show |
130 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.398-22466T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706397 | |||||||
chr15:55706405 | C | T | 2 | a0001c0001t0002g0255 a0007c0017t0002g0254 |
2 | HG00140.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.398-22474G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706405 | |||||||
chr15:55706539 | G | A | 2 | a0001c0001t0033g0101 a0001c0001t0033g0102 |
2 | HG02965.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.398-22608C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706539 | |||||||
chr15:55706582 | CA | C | 31 | a0001c0001t0002g0241 a0001c0001t0002g0270 a0001c0001t0012g0083 others(28): Show |
31 | HG00323.hp1 HG01081.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.398-22652delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706582 | |||||||
chr15:55706582 | CAA | C | 118 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0242 others(115): Show |
119 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.398-22653_398-2265 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706582 | |||||||
chr15:55706582 | CAAAAAAA | C | 96 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(93): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.398-22658_398-2265 others(11): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706582 | |||||||
chr15:55706659 | AG | A | 3 | a0001c0001t0029g0092 a0001c0001t0066g0094 a0011c0016t0029g0093 |
3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.398-22729delC | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706659 | |||||||
chr15:55706784 | G | A | 2 | a0004c0004t0031g0095 a0004c0004t0031g0096 |
2 | HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.398-22853C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706784 | |||||||
chr15:55706863 | A | G | 1 | a0009c0013t0002g0239 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.398-22932T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706863 | |||||||
chr15:55706958 | G | C | 265 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(262): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.398-23027C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55706958 | |||||||
chr15:55707083 | G | A | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.398-23152C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55707083 | |||||||
chr15:55707087 | T | C | 31 | a0001c0001t0024g0013 a0001c0001t0024g0031 a0001c0001t0051g0004 others(28): Show |
31 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.398-23156A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55707087 | |||||||
chr15:55707234 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.398-23303G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55707234 | |||||||
chr15:55707277 | C | T | 4 | a0002c0002t0003g0084 a0006c0010t0025g0065 a0006c0010t0059g0072 others(1): Show |
4 | NA18944.hp1 NA18954.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.398-23346G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55707277 | |||||||
chr15:55707296 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.398-23365T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55707296 | |||||||
chr15:55707499 | G | A | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.398-23568C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55707499 | |||||||
chr15:55707747 | A | G | 1 | a0001c0001t0054g0005 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.398-23816T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55707747 | |||||||
chr15:55707865 | C | T | 86 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(83): Show |
86 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.398-23934G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55707865 | |||||||
chr15:55707923 | A | T | 1 | a0004c0004t0069g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.398-23992T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55707923 | |||||||
chr15:55707985 | T | G | 1 | a0001c0001t0081g0171 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.398-24054A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55707985 | |||||||
chr15:55708034 | G | A | 3 | a0001c0001t0051g0004 a0001c0001t0052g0006 a0001c0001t0054g0005 |
3 | HG01891.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.398-24103C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708034 | |||||||
chr15:55708148 | T | TA | 51 | a0001c0001t0002g0238 a0001c0001t0002g0248 a0001c0001t0002g0249 others(48): Show |
51 | HG00140.hp1 HG00323.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.398-24218dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | |||||||
chr15:55708148 | T | TAA | 18 | a0001c0001t0002g0240 a0001c0001t0002g0242 a0001c0001t0002g0243 others(15): Show |
18 | HG00639.hp2 HG00741.hp2 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.398-24219_398-2421 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | |||||||
chr15:55708148 | T | TAAA | 12 | a0001c0001t0002g0241 a0001c0001t0002g0246 a0001c0001t0002g0269 others(9): Show |
12 | HG00438.hp2 HG01071.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.398-24220_398-2421 others(7): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | |||||||
chr15:55708148 | T | TAAAAAAA others(2): Show |
10 | a0002c0002t0013g0016 a0002c0002t0013g0029 a0002c0002t0014g0020 others(7): Show |
10 | HG02451.hp1 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.398-24226_398-2421 others(13): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | |||||||
chr15:55708148 | T | TAAAAAAA others(3): Show |
5 | a0001c0001t0051g0004 a0002c0002t0026g0023 a0002c0002t0057g0025 others(2): Show |
5 | HG01074.hp1 HG02055.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-24227_398-2421 others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | |||||||
chr15:55708148 | T | TAAAAAAA others(4): Show |
5 | a0001c0001t0052g0006 a0002c0002t0013g0018 a0002c0002t0026g0030 others(2): Show |
5 | HG00642.hp1 HG00642.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-24228_398-2421 others(15): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | |||||||
chr15:55708148 | T | TAAAAAAA others(5): Show |
3 | a0001c0001t0024g0031 a0001c0001t0054g0005 a0002c0002t0065g0014 |
3 | HG01433.hp1 HG01433.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.398-24229_398-2421 others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | |||||||
chr15:55708148 | T | TAAAAAAA others(6): Show |
1 | a0002c0002t0056g0045 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.398-24230_398-2421 others(17): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | |||||||
chr15:55708148 | T | TAAAAAAA others(7): Show |
1 | a0002c0002t0011g0048 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.398-24231_398-2421 others(18): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | |||||||
chr15:55708148 | T | TAAAAAAA others(9): Show |
1 | a0001c0001t0024g0013 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.398-24233_398-2421 others(20): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | |||||||
chr15:55708148 | T | TAAAAAAA others(14): Show |
2 | a0002c0002t0011g0049 a0002c0002t0011g0050 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.398-24238_398-2421 others(25): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | |||||||
chr15:55708148 | TAA | T | 6 | a0001c0001t0100g0232 a0003c0005t0010g0038 a0003c0005t0010g0041 others(3): Show |
6 | HG00099.hp1 HG00099.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.398-24219_398-2421 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | |||||||
chr15:55708148 | TAAA | T | 8 | a0001c0020t0053g0002 a0003c0005t0045g0036 a0003c0006t0009g0007 others(5): Show |
8 | HG00733.hp2 HG01358.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.398-24220_398-2421 others(7): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | |||||||
chr15:55708148 | TAAAAAAA others(3): Show |
T | 1 | a0002c0002t0058g0047 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.398-24227_398-2421 others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | |||||||
chr15:55708148 | TAAAAAAA others(4): Show |
T | 3 | a0001c0001t0082g0128 a0001c0001t0102g0126 a0002c0002t0055g0046 |
3 | HG01243.hp2 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.398-24228_398-2421 others(15): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | |||||||
chr15:55708148 | TAAAAAAA others(6): Show |
T | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-24230_398-2421 others(17): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | |||||||
chr15:55708148 | TAAAAAAA others(10): Show |
T | 86 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(83): Show |
86 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.398-24234_398-2421 others(21): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708148 | |||||||
chr15:55708272 | T | C | 100 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(97): Show |
100 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.398-24341A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708272 | |||||||
chr15:55708361 | C | T | 86 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(83): Show |
86 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.398-24430G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708361 | |||||||
chr15:55708523 | G | A | 30 | a0001c0001t0024g0013 a0001c0001t0024g0031 a0001c0001t0051g0004 others(27): Show |
30 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.398-24592C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708523 | |||||||
chr15:55708533 | G | A | 2 | a0001c0012t0072g0113 a0001c0012t0074g0114 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.398-24602C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708533 | |||||||
chr15:55708577 | T | C | 2 | a0001c0012t0072g0113 a0001c0012t0074g0114 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.398-24646A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708577 | |||||||
chr15:55708602 | C | T | 27 | a0001c0001t0024g0013 a0001c0001t0024g0031 a0002c0002t0011g0048 others(24): Show |
27 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.398-24671G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708602 | |||||||
chr15:55708996 | A | G | 2 | a0001c0001t0021g0051 a0001c0001t0021g0060 |
2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.398-25065T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55708996 | |||||||
chr15:55709102 | C | T | 6 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0161 others(3): Show |
6 | HG00280.hp2 HG01168.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.398-25171G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709102 | |||||||
chr15:55709145 | C | CA | 7 | a0001c0001t0002g0246 a0001c0001t0002g0250 a0001c0001t0016g0122 others(4): Show |
7 | HG00438.hp2 HG01358.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.398-25215dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709145 | |||||||
chr15:55709145 | C | CAAAAAAA others(4): Show |
4 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(1): Show |
4 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-25225_398-2521 others(15): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709145 | |||||||
chr15:55709145 | C | CAAAAAAA others(5): Show |
1 | a0001c0007t0107g0110 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.398-25226_398-2521 others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709145 | |||||||
chr15:55709145 | CA | C | 97 | a0001c0001t0002g0238 a0001c0001t0002g0243 a0001c0001t0002g0244 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.398-25215delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709145 | |||||||
chr15:55709145 | CAA | C | 9 | a0001c0001t0002g0251 a0001c0001t0024g0013 a0001c0001t0024g0031 others(6): Show |
9 | HG01109.hp1 HG01168.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.398-25216_398-2521 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709145 | |||||||
chr15:55709145 | CAAA | C | 26 | a0001c0001t0051g0004 a0001c0001t0054g0005 a0001c0001t0096g0229 others(23): Show |
26 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.398-25217_398-2521 others(7): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709145 | |||||||
chr15:55709145 | CAAAAAA | C | 79 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(76): Show |
79 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.398-25220_398-2521 others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709145 | |||||||
chr15:55709145 | CAAAAAAA others(2): Show |
C | 9 | a0001c0001t0032g0098 a0001c0001t0032g0103 a0001c0001t0033g0101 others(6): Show |
9 | HG02145.hp1 HG02622.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.398-25223_398-2521 others(13): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709145 | |||||||
chr15:55709186 | G | A | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-25255C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709186 | |||||||
chr15:55709220 | T | TAGTTA | 133 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(130): Show |
133 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.398-25290_398-2528 others(9): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709220 | |||||||
chr15:55709314 | T | C | 271 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(268): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.398-25383A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709314 | |||||||
chr15:55709349 | T | TATATATA others(29): Show |
1 | a0001c0001t0001g0106 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.398-25454_398-2541 others(40): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709349 | |||||||
chr15:55709376 | A | T | 3 | a0001c0001t0051g0004 a0001c0001t0052g0006 a0001c0001t0054g0005 |
3 | HG01891.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.398-25445T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709376 | |||||||
chr15:55709386 | T | G | 16 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0002g0274 others(13): Show |
16 | HG01255.hp2 HG01884.hp2 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.398-25455A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709386 | |||||||
chr15:55709388 | T | G | 144 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(141): Show |
144 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.398-25457A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709388 | |||||||
chr15:55709390 | G | T | 3 | a0001c0001t0006g0148 a0001c0001t0008g0159 a0001c0001t0078g0149 |
3 | HG02040.hp1 HG03669.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.398-25459C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709390 | |||||||
chr15:55709401 | C | T | 86 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(83): Show |
86 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.398-25470G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709401 | |||||||
chr15:55709403 | C | T | 13 | a0001c0001t0035g0219 a0001c0001t0097g0221 a0001c0001t0101g0217 others(10): Show |
13 | HG00323.hp1 HG02257.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.398-25472G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709403 | |||||||
chr15:55709404 | G | A | 1 | a0001c0001t0054g0005 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.398-25473C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709404 | |||||||
chr15:55709449 | G | A | 1 | a0001c0001t0041g0280 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.398-25518C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709449 | |||||||
chr15:55709501 | T | C | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.398-25570A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709501 | |||||||
chr15:55709507 | A | C | 9 | a0001c0003t0003g0042 a0001c0003t0003g0074 a0001c0003t0003g0075 others(6): Show |
9 | HG00280.hp1 HG00408.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.398-25576T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709507 | |||||||
chr15:55709550 | G | A | 2 | a0001c0001t0096g0229 a0001c0001t0099g0228 |
2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.398-25619C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709550 | |||||||
chr15:55709576 | C | T | 133 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(130): Show |
133 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.398-25645G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709576 | |||||||
chr15:55709759 | T | C | 242 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.398-25828A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709759 | |||||||
chr15:55709771 | C | A | 263 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(260): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.398-25840G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709771 | |||||||
chr15:55709837 | G | A | 4 | a0002c0002t0003g0084 a0006c0010t0025g0065 a0006c0010t0059g0072 others(1): Show |
4 | NA18944.hp1 NA18954.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.398-25906C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55709837 | |||||||
chr15:55710035 | A | C | 1 | a0001c0001t0101g0217 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.398-26104T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55710035 | |||||||
chr15:55710038 | C | T | 1 | a0001c0001t0099g0228 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.398-26107G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55710038 | |||||||
chr15:55710210 | G | C | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-26279C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55710210 | |||||||
chr15:55710300 | A | G | 3 | a0001c0001t0032g0103 a0001c0001t0033g0101 a0001c0001t0033g0102 |
3 | HG02965.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.398-26369T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55710300 | |||||||
chr15:55710325 | A | T | 1 | a0001c0001t0105g0205 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.398-26394T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55710325 | |||||||
chr15:55710621 | C | T | 13 | a0001c0020t0053g0002 a0003c0005t0010g0038 a0003c0005t0010g0039 others(10): Show |
13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.398-26690G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55710621 | |||||||
chr15:55710698 | TAA | T | 13 | a0001c0020t0053g0002 a0003c0005t0010g0038 a0003c0005t0010g0039 others(10): Show |
13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.398-26769_398-2676 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55710698 | |||||||
chr15:55710709 | G | C | 2 | a0001c0012t0072g0113 a0001c0012t0074g0114 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.398-26778C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55710709 | |||||||
chr15:55710821 | T | C | 77 | a0001c0001t0001g0155 a0001c0001t0002g0238 a0001c0001t0002g0240 others(74): Show |
77 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.398-26890A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55710821 | |||||||
chr15:55710938 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.398-27007G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55710938 | |||||||
chr15:55710943 | G | C | 1 | a0001c0001t0100g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.398-27012C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55710943 | |||||||
chr15:55711002 | G | A | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-27071C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55711002 | |||||||
chr15:55711081 | A | AT | 36 | a0001c0001t0002g0238 a0001c0001t0002g0250 a0001c0001t0002g0260 others(33): Show |
36 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.398-27151dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55711081 | |||||||
chr15:55711081 | A | ATT | 6 | a0001c0001t0002g0275 a0001c0001t0054g0005 a0001c0007t0108g0111 others(3): Show |
6 | HG02145.hp2 HG02148.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.398-27152_398-2715 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55711081 | |||||||
chr15:55711081 | AT | A | 55 | a0001c0001t0001g0172 a0001c0001t0012g0083 a0001c0001t0012g0091 others(52): Show |
55 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.398-27151delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55711081 | |||||||
chr15:55711168 | TG | T | 57 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(54): Show |
57 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.398-27238delC | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55711168 | |||||||
chr15:55711218 | G | T | 1 | a0016c0014t0073g0234 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.398-27287C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55711218 | |||||||
chr15:55711323 | A | G | 1 | a0002c0002t0028g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.398-27392T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55711323 | |||||||
chr15:55711507 | A | G | 134 | a0001c0001t0001g0155 a0001c0001t0002g0238 a0001c0001t0002g0240 others(131): Show |
134 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.398-27576T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55711507 | |||||||
chr15:55711511 | G | C | 3 | a0001c0001t0096g0229 a0001c0001t0099g0228 a0001c0001t0100g0232 |
3 | HG02647.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.398-27580C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55711511 | |||||||
chr15:55711654 | T | G | 3 | a0001c0001t0051g0004 a0001c0001t0052g0006 a0001c0001t0054g0005 |
3 | HG01891.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.398-27723A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55711654 | |||||||
chr15:55711718 | T | TA | 26 | a0001c0001t0024g0013 a0001c0001t0024g0031 a0002c0002t0011g0048 others(23): Show |
26 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.398-27788dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55711718 | |||||||
chr15:55711814 | G | A | 1 | a0001c0001t0100g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.398-27883C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55711814 | |||||||
chr15:55712020 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.398-28089T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55712020 | |||||||
chr15:55712026 | T | A | 3 | a0001c0007t0106g0109 a0001c0007t0107g0110 a0001c0007t0108g0111 |
3 | HG02109.hp2 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.398-28095A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55712026 | |||||||
chr15:55712061 | T | G | 4 | a0002c0002t0104g0215 a0005c0011t0035g0220 a0005c0011t0094g0218 others(1): Show |
4 | HG02572.hp2 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-28130A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55712061 | |||||||
chr15:55712152 | A | G | 2 | a0001c0020t0053g0002 a0012c0019t0046g0003 |
2 | HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.398-28221T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55712152 | |||||||
chr15:55712216 | G | A | 1 | a0001c0003t0003g0079 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.397+28166C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55712216 | |||||||
chr15:55712424 | AC | A | 6 | a0001c0001t0032g0098 a0002c0002t0068g0099 a0004c0004t0030g0097 others(3): Show |
6 | HG02145.hp1 HG02622.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.397+27957delG | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55712424 | |||||||
chr15:55712443 | A | G | 54 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(51): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.397+27939T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55712443 | |||||||
chr15:55712522 | T | TA | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.397+27859dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55712522 | |||||||
chr15:55712629 | A | G | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+27753T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55712629 | |||||||
chr15:55712909 | G | A | 86 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(83): Show |
86 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.397+27473C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55712909 | |||||||
chr15:55713137 | TTTATAA | T | 134 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(131): Show |
134 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.397+27239_397+2724 others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55713137 | |||||||
chr15:55713160 | G | A | 1 | a0002c0002t0027g0019 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.397+27222C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55713160 | |||||||
chr15:55713325 | C | A | 53 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(50): Show |
53 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.397+27057G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55713325 | |||||||
chr15:55713386 | C | T | 30 | a0001c0001t0024g0013 a0001c0001t0024g0031 a0001c0001t0051g0004 others(27): Show |
30 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.397+26996G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55713386 | |||||||
chr15:55713497 | A | G | 13 | a0001c0020t0053g0002 a0003c0005t0010g0038 a0003c0005t0010g0039 others(10): Show |
13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+26885T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55713497 | |||||||
chr15:55713534 | C | G | 83 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(80): Show |
83 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.397+26848G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55713534 | |||||||
chr15:55713557 | A | T | 2 | a0001c0001t0001g0152 a0001c0001t0077g0174 |
2 | NA18973.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.397+26825T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55713557 | |||||||
chr15:55713593 | T | A | 87 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(84): Show |
87 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.397+26789A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55713593 | |||||||
chr15:55713728 | T | C | 13 | a0001c0020t0053g0002 a0003c0005t0010g0038 a0003c0005t0010g0039 others(10): Show |
13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+26654A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55713728 | |||||||
chr15:55713733 | A | AT | 139 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(136): Show |
139 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.397+26648dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55713733 | |||||||
chr15:55714067 | T | G | 1 | a0002c0002t0003g0063 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.397+26315A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714067 | |||||||
chr15:55714157 | C | T | 1 | a0001c0001t0012g0091 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.397+26225G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714157 | |||||||
chr15:55714205 | G | GTC | 12 | a0001c0001t0001g0106 a0001c0001t0002g0250 a0001c0008t0037g0208 others(9): Show |
12 | HG01358.hp1 HG01515.hp1 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.397+26175_397+2617 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714205 | |||||||
chr15:55714205 | G | GTCTCTC | 27 | a0001c0001t0002g0247 a0001c0001t0002g0248 a0001c0001t0002g0251 others(24): Show |
27 | HG00140.hp1 HG00733.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.397+26171_397+2617 others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714205 | |||||||
chr15:55714205 | G | GTCTCTCT others(1): Show |
37 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0242 others(34): Show |
37 | HG00323.hp1 HG00639.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.397+26169_397+2617 others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714205 | |||||||
chr15:55714205 | G | GTCTCTCT others(3): Show |
24 | a0001c0001t0002g0238 a0001c0001t0002g0260 a0001c0001t0002g0261 others(21): Show |
24 | HG00642.hp2 HG01361.hp1 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.397+26167_397+2617 others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714205 | |||||||
chr15:55714205 | G | GTCTCTCT others(5): Show |
39 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0024g0031 others(36): Show |
40 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.397+26165_397+2617 others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714205 | |||||||
chr15:55714205 | G | GTCTCTCT others(7): Show |
6 | a0002c0002t0003g0081 a0002c0002t0003g0084 a0002c0002t0011g0048 others(3): Show |
6 | HG01257.hp1 HG02486.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.397+26163_397+2617 others(18): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714205 | |||||||
chr15:55714205 | G | GTCTCTCT others(9): Show |
5 | a0001c0001t0051g0004 a0001c0001t0054g0005 a0001c0001t0100g0232 others(2): Show |
5 | HG00280.hp1 HG02818.hp1 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+26161_397+2617 others(20): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714205 | |||||||
chr15:55714205 | G | GTCTCTCT others(13): Show |
1 | a0001c0001t0052g0006 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.397+26157_397+2617 others(24): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714205 | |||||||
chr15:55714205 | GTCTCTC | G | 11 | a0001c0001t0035g0219 a0001c0001t0097g0221 a0001c0001t0101g0217 others(8): Show |
11 | HG02257.hp2 HG02572.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.397+26171_397+2617 others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714205 | |||||||
chr15:55714297 | T | C | 13 | a0001c0020t0053g0002 a0003c0005t0010g0038 a0003c0005t0010g0039 others(10): Show |
13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+26085A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714297 | |||||||
chr15:55714387 | C | T | 1 | a0002c0002t0012g0082 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.397+25995G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714387 | |||||||
chr15:55714389 | C | T | 47 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(44): Show |
47 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.397+25993G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714389 | |||||||
chr15:55714390 | G | C | 6 | a0004c0004t0023g0056 a0004c0004t0023g0057 a0004c0004t0047g0061 others(3): Show |
6 | HG01255.hp2 HG01884.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.397+25992C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714390 | |||||||
chr15:55714473 | C | T | 1 | a0001c0001t0018g0058 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.397+25909G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714473 | |||||||
chr15:55714543 | C | A | 27 | a0001c0001t0024g0013 a0001c0001t0024g0031 a0002c0002t0011g0048 others(24): Show |
27 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.397+25839G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714543 | |||||||
chr15:55714806 | C | T | 138 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(135): Show |
138 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.397+25576G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55714806 | |||||||
chr15:55715004 | A | G | 16 | a0001c0001t0032g0103 a0001c0001t0033g0101 a0001c0001t0033g0102 others(13): Show |
16 | HG02257.hp2 HG02572.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.397+25378T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55715004 | |||||||
chr15:55715009 | A | T | 3 | a0001c0007t0106g0109 a0001c0007t0107g0110 a0001c0007t0108g0111 |
3 | HG02109.hp2 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.397+25373T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55715009 | |||||||
chr15:55715050 | C | G | 1 | a0006c0010t0059g0072 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.397+25332G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55715050 | |||||||
chr15:55715081 | A | G | 1 | a0002c0002t0003g0081 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.397+25301T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55715081 | |||||||
chr15:55715402 | T | C | 2 | a0001c0012t0072g0113 a0001c0012t0074g0114 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.397+24980A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55715402 | |||||||
chr15:55715497 | T | C | 16 | a0001c0001t0001g0224 a0001c0003t0004g0173 a0001c0003t0004g0225 others(13): Show |
16 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.397+24885A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55715497 | |||||||
chr15:55715716 | T | C | 2 | a0001c0012t0072g0113 a0001c0012t0074g0114 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.397+24666A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55715716 | |||||||
chr15:55715723 | T | G | 1 | a0004c0004t0048g0054 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.397+24659A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55715723 | |||||||
chr15:55715917 | A | C | 1 | a0002c0002t0016g0127 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.397+24465T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55715917 | |||||||
chr15:55716113 | G | A | 3 | a0001c0001t0029g0092 a0001c0001t0066g0094 a0011c0016t0029g0093 |
3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.397+24269C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716113 | |||||||
chr15:55716139 | G | C | 1 | a0001c0001t0001g0223 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.397+24243C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716139 | |||||||
chr15:55716227 | T | C | 15 | a0001c0001t0096g0229 a0001c0001t0099g0228 a0001c0020t0053g0002 others(12): Show |
15 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.397+24155A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716227 | |||||||
chr15:55716357 | T | C | 2 | a0001c0001t0002g0255 a0007c0017t0002g0254 |
2 | HG00140.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.397+24025A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716357 | |||||||
chr15:55716425 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.397+23957G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716425 | |||||||
chr15:55716509 | G | C | 2 | a0001c0020t0053g0002 a0012c0019t0046g0003 |
2 | HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.397+23873C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716509 | |||||||
chr15:55716565 | T | C | 1 | a0002c0002t0011g0048 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.397+23817A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716565 | |||||||
chr15:55716781 | G | T | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.397+23601C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716781 | |||||||
chr15:55716802 | T | C | 30 | a0001c0001t0032g0098 a0001c0001t0032g0103 a0001c0001t0033g0101 others(27): Show |
30 | HG02145.hp1 HG02257.hp2 HG02572.hp1 others(27): Show |
intron_variant | MODIFIER | c.397+23580A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716802 | |||||||
chr15:55716821 | T | C | 2 | a0001c0012t0072g0113 a0001c0012t0074g0114 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.397+23561A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716821 | |||||||
chr15:55716848 | T | C | 1 | a0001c0001t0100g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.397+23534A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716848 | |||||||
chr15:55716928 | G | C | 1 | a0001c0001t0100g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.397+23454C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716928 | |||||||
chr15:55716957 | G | A | 1 | a0010c0021t0091g0204 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.397+23425C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716957 | |||||||
chr15:55716980 | T | C | 3 | a0001c0001t0029g0092 a0001c0001t0066g0094 a0011c0016t0029g0093 |
3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.397+23402A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716980 | |||||||
chr15:55716996 | G | A | 272 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(269): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.397+23386C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55716996 | |||||||
chr15:55717446 | C | T | 1 | a0002c0002t0090g0214 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.397+22936G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55717446 | |||||||
chr15:55717450 | A | T | 84 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(81): Show |
84 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.397+22932T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55717450 | |||||||
chr15:55717745 | C | G | 2 | a0001c0001t0002g0260 a0001c0001t0002g0261 |
2 | HG03688.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.397+22637G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55717745 | |||||||
chr15:55717756 | A | G | 47 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(44): Show |
47 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.397+22626T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55717756 | |||||||
chr15:55718084 | T | C | 2 | a0001c0001t0002g0281 a0001c0001t0002g0282 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.397+22298A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55718084 | |||||||
chr15:55718482 | A | C | 28 | a0001c0001t0024g0013 a0001c0001t0024g0031 a0001c0001t0100g0232 others(25): Show |
28 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.397+21900T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55718482 | |||||||
chr15:55718609 | G | C | 12 | a0001c0001t0035g0219 a0001c0001t0097g0221 a0001c0001t0101g0217 others(9): Show |
12 | HG02257.hp2 HG02572.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.397+21773C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55718609 | |||||||
chr15:55718617 | C | CA | 9 | a0001c0001t0032g0098 a0001c0001t0032g0103 a0001c0001t0033g0101 others(6): Show |
9 | HG02145.hp1 HG02622.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.397+21764dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55718617 | |||||||
chr15:55718628 | C | CA | 60 | a0001c0001t0001g0154 a0001c0001t0001g0223 a0001c0001t0002g0238 others(57): Show |
60 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.397+21753dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55718628 | |||||||
chr15:55718632 | A | C | 3 | a0001c0001t0001g0134 a0001c0001t0001g0158 a0016c0014t0073g0234 |
3 | HG02683.hp2 NA19003.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.397+21750T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55718632 | |||||||
chr15:55718675 | T | C | 30 | a0001c0001t0024g0013 a0001c0001t0024g0031 a0001c0001t0051g0004 others(27): Show |
30 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.397+21707A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55718675 | |||||||
chr15:55718690 | T | A | 2 | a0005c0011t0035g0220 a0005c0011t0098g0222 |
2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.397+21692A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55718690 | |||||||
chr15:55718904 | G | A | 2 | a0004c0004t0031g0095 a0004c0004t0031g0096 |
2 | HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.397+21478C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55718904 | |||||||
chr15:55718909 | A | AT | 54 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(51): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.397+21472dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55718909 | |||||||
chr15:55719025 | A | G | 260 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(257): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.397+21357T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55719025 | |||||||
chr15:55719171 | G | A | 5 | a0001c0001t0024g0031 a0002c0002t0013g0018 a0002c0002t0013g0029 others(2): Show |
5 | HG00642.hp2 HG01433.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+21211C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55719171 | |||||||
chr15:55719227 | T | A | 1 | a0004c0004t0030g0097 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.397+21155A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55719227 | |||||||
chr15:55719392 | T | C | 2 | a0001c0001t0036g0151 a0001c0001t0036g0157 |
2 | HG00738.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.397+20990A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55719392 | |||||||
chr15:55719757 | G | T | 1 | a0001c0001t0083g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.397+20625C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55719757 | |||||||
chr15:55719792 | C | G | 2 | a0001c0001t0036g0151 a0001c0001t0036g0157 |
2 | HG00738.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.397+20590G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55719792 | |||||||
chr15:55719817 | C | T | 27 | a0001c0001t0024g0013 a0001c0001t0024g0031 a0002c0002t0011g0048 others(24): Show |
27 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.397+20565G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55719817 | |||||||
chr15:55719906 | A | C | 2 | a0001c0001t0024g0013 a0002c0002t0065g0014 |
2 | HG01361.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.397+20476T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55719906 | |||||||
chr15:55719919 | G | A | 1 | a0001c0001t0002g0247 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.397+20463C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55719919 | |||||||
chr15:55719929 | G | T | 53 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(50): Show |
53 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.397+20453C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55719929 | |||||||
chr15:55720060 | AAAAAG | A | 3 | a0001c0001t0051g0004 a0001c0001t0052g0006 a0001c0001t0054g0005 |
3 | HG01891.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.397+20317_397+2032 others(9): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55720060 | |||||||
chr15:55720188 | G | A | 1 | a0001c0001t0034g0001 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.397+20194C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55720188 | |||||||
chr15:55720391 | A | T | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+19991T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55720391 | |||||||
chr15:55720488 | T | C | 30 | a0001c0001t0024g0013 a0001c0001t0024g0031 a0001c0001t0051g0004 others(27): Show |
30 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.397+19894A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55720488 | |||||||
chr15:55720508 | T | A | 140 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(137): Show |
140 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.397+19874A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55720508 | |||||||
chr15:55720713 | C | A | 1 | a0001c0007t0038g0230 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.397+19669G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55720713 | |||||||
chr15:55720713 | C | T | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.397+19669G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55720713 | |||||||
chr15:55720850 | T | C | 1 | a0001c0001t0080g0202 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.397+19532A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55720850 | |||||||
chr15:55721065 | G | A | 30 | a0001c0001t0024g0013 a0001c0001t0024g0031 a0001c0001t0051g0004 others(27): Show |
30 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.397+19317C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55721065 | |||||||
chr15:55721113 | G | T | 2 | a0001c0020t0053g0002 a0012c0019t0046g0003 |
2 | HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.397+19269C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55721113 | |||||||
chr15:55721279 | C | A | 13 | a0001c0020t0053g0002 a0003c0005t0010g0038 a0003c0005t0010g0039 others(10): Show |
13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+19103G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55721279 | |||||||
chr15:55721387 | G | A | 2 | a0001c0001t0082g0128 a0001c0001t0102g0126 |
2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.397+18995C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55721387 | |||||||
chr15:55721453 | A | T | 2 | a0001c0001t0032g0098 a0002c0002t0068g0099 |
2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.397+18929T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55721453 | |||||||
chr15:55721607 | C | T | 2 | a0001c0012t0072g0113 a0001c0012t0074g0114 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.397+18775G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55721607 | |||||||
chr15:55721723 | C | T | 138 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(135): Show |
138 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.397+18659G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55721723 | |||||||
chr15:55721911 | A | G | 1 | a0001c0001t0021g0051 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.397+18471T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55721911 | |||||||
chr15:55721927 | T | A | 1 | a0001c0001t0002g0250 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.397+18455A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55721927 | |||||||
chr15:55722074 | A | G | 1 | a0002c0002t0061g0027 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.397+18308T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55722074 | |||||||
chr15:55722151 | A | C | 1 | a0001c0009t0042g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.397+18231T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55722151 | |||||||
chr15:55722153 | G | A | 1 | a0001c0009t0103g0233 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.397+18229C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55722153 | |||||||
chr15:55722183 | C | T | 13 | a0001c0020t0053g0002 a0003c0005t0010g0038 a0003c0005t0010g0039 others(10): Show |
13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+18199G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55722183 | |||||||
chr15:55722229 | T | A | 2 | a0001c0012t0072g0113 a0001c0012t0074g0114 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.397+18153A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55722229 | |||||||
chr15:55722285 | G | C | 7 | a0001c0001t0001g0139 a0001c0001t0001g0144 a0001c0001t0006g0140 others(4): Show |
7 | NA18942.hp2 NA18944.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+18097C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55722285 | |||||||
chr15:55722407 | AATAACT | A | 46 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(43): Show |
46 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.397+17969_397+1797 others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55722407 | |||||||
chr15:55722480 | T | C | 1 | a0002c0002t0095g0212 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.397+17902A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55722480 | |||||||
chr15:55722538 | T | C | 48 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(45): Show |
48 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.397+17844A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55722538 | |||||||
chr15:55722585 | CAG | C | 3 | a0001c0001t0029g0092 a0001c0001t0066g0094 a0011c0016t0029g0093 |
3 | HG02055.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.397+17795_397+1779 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55722585 | |||||||
chr15:55722785 | T | TG | 272 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(269): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.397+17596dupC | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55722785 | |||||||
chr15:55722984 | G | A | 13 | a0001c0020t0053g0002 a0003c0005t0010g0038 a0003c0005t0010g0039 others(10): Show |
13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+17398C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55722984 | |||||||
chr15:55723254 | T | C | 1 | a0001c0001t0018g0058 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.397+17128A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55723254 | |||||||
chr15:55723392 | T | TA | 31 | a0001c0001t0005g0186 a0001c0001t0024g0013 a0001c0001t0024g0031 others(28): Show |
31 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.397+16989dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55723392 | |||||||
chr15:55723569 | T | C | 84 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(81): Show |
84 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.397+16813A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55723569 | |||||||
chr15:55723730 | T | C | 272 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(269): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.397+16652A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55723730 | |||||||
chr15:55723736 | T | A | 272 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(269): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.397+16646A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55723736 | |||||||
chr15:55723752 | C | CT | 121 | a0001c0001t0001g0150 a0001c0001t0001g0153 a0001c0001t0001g0154 others(118): Show |
121 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.397+16629dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55723752 | |||||||
chr15:55723752 | C | CTT | 26 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0024g0031 others(23): Show |
26 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.397+16628_397+1662 others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55723752 | |||||||
chr15:55723783 | G | A | 1 | a0001c0001t0111g0278 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.397+16599C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55723783 | |||||||
chr15:55724005 | C | G | 1 | a0002c0002t0061g0027 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.397+16377G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55724005 | |||||||
chr15:55724110 | C | T | 2 | a0001c0001t0002g0249 a0001c0001t0002g0256 |
2 | HG01975.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.397+16272G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55724110 | |||||||
chr15:55724226 | C | G | 1 | a0006c0010t0059g0072 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.397+16156G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55724226 | |||||||
chr15:55724281 | G | A | 7 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(4): Show |
7 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.397+16101C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55724281 | |||||||
chr15:55724324 | G | A | 1 | a0002c0002t0109g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.397+16058C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55724324 | |||||||
chr15:55724548 | T | C | 46 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(43): Show |
46 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.397+15834A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55724548 | |||||||
chr15:55724551 | G | A | 1 | a0011c0016t0029g0093 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.397+15831C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55724551 | |||||||
chr15:55724601 | G | T | 6 | a0001c0001t0100g0232 a0001c0007t0038g0230 a0001c0007t0038g0231 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.397+15781C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55724601 | |||||||
chr15:55724616 | A | G | 272 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(269): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.397+15766T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55724616 | |||||||
chr15:55724629 | C | A | 1 | a0003c0005t0045g0036 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.397+15753G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55724629 | |||||||
chr15:55724699 | G | A | 5 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(2): Show |
5 | HG02615.hp1 HG03453.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+15683C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55724699 | |||||||
chr15:55724768 | AAAAAT | A | 58 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(55): Show |
58 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.397+15609_397+1561 others(9): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55724768 | |||||||
chr15:55724955 | G | A | 1 | a0002c0002t0088g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.397+15427C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55724955 | |||||||
chr15:55725224 | T | C | 59 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(56): Show |
59 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.397+15158A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55725224 | |||||||
chr15:55725357 | T | G | 2 | a0002c0002t0004g0108 a0002c0002t0004g0216 |
2 | NA18943.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.397+15025A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55725357 | |||||||
chr15:55725413 | A | G | 1 | a0001c0001t0066g0094 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.397+14969T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55725413 | |||||||
chr15:55725676 | A | G | 1 | a0001c0001t0016g0122 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.397+14706T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55725676 | |||||||
chr15:55725745 | T | G | 3 | a0001c0001t0051g0004 a0001c0001t0052g0006 a0001c0001t0054g0005 |
3 | HG01891.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.397+14637A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55725745 | |||||||
chr15:55725895 | C | T | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+14487G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55725895 | |||||||
chr15:55725896 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0077g0174 |
2 | NA18973.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.397+14486C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55725896 | |||||||
chr15:55726005 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.397+14377C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55726005 | |||||||
chr15:55726089 | C | T | 1 | a0002c0002t0110g0237 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.397+14293G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55726089 | |||||||
chr15:55726187 | C | T | 2 | a0001c0012t0072g0113 a0001c0012t0074g0114 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.397+14195G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55726187 | |||||||
chr15:55726395 | C | A | 1 | a0001c0003t0004g0225 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.397+13987G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55726395 | |||||||
chr15:55726403 | G | A | 1 | a0009c0013t0002g0239 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.397+13979C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55726403 | |||||||
chr15:55726617 | G | A | 5 | a0001c0001t0032g0098 a0002c0002t0068g0099 a0004c0004t0031g0095 others(2): Show |
5 | HG02622.hp2 HG03195.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+13765C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55726617 | |||||||
chr15:55726621 | A | G | 1 | a0001c0001t0002g0260 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.397+13761T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55726621 | |||||||
chr15:55726641 | C | CA | 17 | a0001c0001t0002g0246 a0001c0001t0002g0253 a0001c0001t0002g0270 others(14): Show |
17 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.397+13740dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55726641 | |||||||
chr15:55726641 | CA | C | 63 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(60): Show |
63 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.397+13740delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55726641 | |||||||
chr15:55726658 | T | A | 44 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0242 others(41): Show |
44 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.397+13724A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55726658 | |||||||
chr15:55726899 | G | A | 1 | a0004c0004t0031g0095 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.397+13483C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55726899 | |||||||
chr15:55726950 | CA | C | 185 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(182): Show |
186 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.397+13431delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55726950 | |||||||
chr15:55726959 | A | G | 2 | a0001c0012t0072g0113 a0001c0012t0074g0114 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.397+13423T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55726959 | |||||||
chr15:55727168 | T | C | 1 | a0016c0014t0073g0234 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.397+13214A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55727168 | |||||||
chr15:55727455 | T | C | 54 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(51): Show |
54 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.397+12927A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55727455 | |||||||
chr15:55727579 | T | C | 17 | a0001c0001t0032g0103 a0001c0001t0033g0101 a0001c0001t0033g0102 others(14): Show |
17 | HG00323.hp1 HG02257.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.397+12803A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55727579 | |||||||
chr15:55727697 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.397+12685C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55727697 | |||||||
chr15:55727723 | C | T | 3 | a0001c0003t0003g0042 a0001c0003t0003g0074 a0001c0003t0003g0075 |
3 | HG01943.hp1 HG01981.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.397+12659G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55727723 | |||||||
chr15:55727752 | C | T | 11 | a0003c0005t0010g0038 a0003c0005t0010g0039 a0003c0005t0010g0041 others(8): Show |
11 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.397+12630G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55727752 | |||||||
chr15:55727887 | G | A | 6 | a0001c0001t0100g0232 a0001c0007t0038g0230 a0001c0007t0038g0231 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.397+12495C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55727887 | |||||||
chr15:55727957 | C | A | 2 | a0001c0012t0072g0113 a0001c0012t0074g0114 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.397+12425G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55727957 | |||||||
chr15:55727979 | C | G | 6 | a0001c0001t0032g0098 a0002c0002t0068g0099 a0004c0004t0030g0097 others(3): Show |
6 | HG02145.hp1 HG02622.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.397+12403G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55727979 | |||||||
chr15:55728108 | C | T | 1 | a0004c0004t0030g0097 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.397+12274G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728108 | |||||||
chr15:55728117 | C | T | 54 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(51): Show |
54 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.397+12265G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728117 | |||||||
chr15:55728221 | C | A | 1 | a0001c0001t0054g0005 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.397+12161G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728221 | |||||||
chr15:55728521 | T | C | 2 | a0001c0001t0001g0175 a0001c0001t0001g0203 |
2 | HG03239.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.397+11861A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728521 | |||||||
chr15:55728529 | A | AG | 54 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(51): Show |
54 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.397+11852dupC | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728529 | |||||||
chr15:55728659 | A | G | 1 | a0001c0001t0002g0277 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.397+11723T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728659 | |||||||
chr15:55728722 | T | C | 1 | a0002c0002t0056g0045 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.397+11660A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728722 | |||||||
chr15:55728729 | T | C | 1 | a0001c0001t0002g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.397+11653A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728729 | |||||||
chr15:55728766 | A | AG | 272 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(269): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.397+11615_397+1161 others(5): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728766 | |||||||
chr15:55728770 | A | C | 272 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(269): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.397+11612T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728770 | |||||||
chr15:55728808 | T | C | 78 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(75): Show |
78 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.397+11574A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728808 | |||||||
chr15:55728821 | T | C | 13 | a0001c0020t0053g0002 a0003c0005t0010g0038 a0003c0005t0010g0039 others(10): Show |
13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+11561A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728821 | |||||||
chr15:55728959 | G | A | 1 | a0007c0017t0002g0254 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.397+11423C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728959 | |||||||
chr15:55728975 | T | C | 11 | a0003c0005t0010g0038 a0003c0005t0010g0039 a0003c0005t0010g0041 others(8): Show |
11 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.397+11407A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728975 | |||||||
chr15:55728980 | C | T | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.397+11402G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55728980 | |||||||
chr15:55729003 | A | G | 1 | a0001c0009t0103g0233 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.397+11379T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55729003 | |||||||
chr15:55729141 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0078g0149 |
2 | HG02040.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.397+11241C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55729141 | |||||||
chr15:55729223 | G | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0206 a0001c0001t0001g0207 |
3 | NA18948.hp2 NA18980.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.397+11159C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55729223 | |||||||
chr15:55729232 | C | G | 1 | a0001c0001t0001g0195 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.397+11150G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55729232 | |||||||
chr15:55729596 | T | A | 57 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(54): Show |
57 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.397+10786A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55729596 | |||||||
chr15:55729598 | A | T | 10 | a0002c0002t0019g0052 a0002c0002t0019g0062 a0002c0002t0020g0010 others(7): Show |
10 | HG01255.hp2 HG01884.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.397+10784T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55729598 | |||||||
chr15:55729739 | C | A | 1 | a0001c0003t0003g0089 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.397+10643G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55729739 | |||||||
chr15:55729748 | T | G | 4 | a0002c0002t0004g0117 a0002c0002t0004g0118 a0002c0002t0004g0119 others(1): Show |
4 | NA18964.hp1 NA18981.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+10634A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55729748 | |||||||
chr15:55729908 | G | A | 13 | a0001c0020t0053g0002 a0003c0005t0010g0038 a0003c0005t0010g0039 others(10): Show |
13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+10474C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55729908 | |||||||
chr15:55729943 | G | A | 13 | a0001c0020t0053g0002 a0003c0005t0010g0038 a0003c0005t0010g0039 others(10): Show |
13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+10439C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55729943 | |||||||
chr15:55730028 | T | C | 2 | a0001c0001t0096g0229 a0001c0001t0099g0228 |
2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.397+10354A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55730028 | |||||||
chr15:55730126 | G | A | 81 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(78): Show |
81 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.397+10256C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55730126 | |||||||
chr15:55730159 | C | A | 1 | a0001c0001t0041g0280 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.397+10223G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55730159 | |||||||
chr15:55730584 | C | T | 1 | a0002c0002t0110g0237 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.397+9798G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55730584 | |||||||
chr15:55730595 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.397+9787A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55730595 | |||||||
chr15:55730730 | G | T | 78 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(75): Show |
78 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.397+9652C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55730730 | |||||||
chr15:55730751 | G | C | 13 | a0001c0020t0053g0002 a0003c0005t0010g0038 a0003c0005t0010g0039 others(10): Show |
13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+9631C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55730751 | |||||||
chr15:55730792 | ACT | A | 6 | a0001c0001t0100g0232 a0001c0007t0038g0230 a0001c0007t0038g0231 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.397+9588_397+9589d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55730792 | |||||||
chr15:55731027 | A | T | 1 | a0001c0001t0006g0148 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.397+9355T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731027 | |||||||
chr15:55731031 | A | G | 1 | a0002c0002t0011g0048 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.397+9351T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731031 | |||||||
chr15:55731098 | G | C | 1 | a0002c0002t0003g0071 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.397+9284C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731098 | |||||||
chr15:55731115 | A | ACTTT | 136 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(133): Show |
136 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.397+9263_397+9266d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731115 | |||||||
chr15:55731234 | C | CTCT | 58 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(55): Show |
58 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.397+9145_397+9147d others(5): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731234 | |||||||
chr15:55731245 | G | C | 9 | a0001c0001t0016g0122 a0001c0001t0016g0123 a0001c0001t0082g0128 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.397+9137C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731245 | |||||||
chr15:55731304 | G | T | 242 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.397+9078C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731304 | |||||||
chr15:55731359 | TATCA | T | 6 | a0001c0001t0100g0232 a0001c0007t0038g0230 a0001c0007t0038g0231 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.397+9019_397+9022d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731359 | |||||||
chr15:55731366 | C | CT | 49 | a0001c0001t0001g0150 a0001c0001t0001g0153 a0001c0001t0001g0154 others(46): Show |
49 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.397+9015dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731366 | |||||||
chr15:55731366 | C | CTT | 69 | a0001c0001t0005g0187 a0001c0001t0012g0083 a0001c0001t0016g0122 others(66): Show |
69 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.397+9014_397+9015d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731366 | |||||||
chr15:55731366 | C | CTTT | 10 | a0001c0001t0018g0058 a0002c0002t0003g0067 a0002c0002t0003g0071 others(7): Show |
10 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.397+9013_397+9015d others(5): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731366 | |||||||
chr15:55731366 | CT | C | 6 | a0001c0001t0001g0179 a0001c0001t0002g0251 a0001c0001t0002g0277 others(3): Show |
6 | HG01074.hp2 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.397+9015delA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731366 | |||||||
chr15:55731410 | G | A | 1 | a0001c0001t0078g0149 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.397+8972C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731410 | |||||||
chr15:55731418 | TGGAGTAC others(3): Show |
T | 1 | a0001c0001t0041g0280 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.397+8954_397+8963d others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731418 | |||||||
chr15:55731440 | G | A | 1 | a0001c0001t0097g0221 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.397+8942C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731440 | |||||||
chr15:55731502 | C | T | 4 | a0001c0001t0029g0092 a0001c0001t0066g0094 a0002c0002t0020g0010 others(1): Show |
4 | HG02055.hp2 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+8880G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731502 | |||||||
chr15:55731573 | G | A | 135 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(132): Show |
135 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.397+8809C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731573 | |||||||
chr15:55731575 | C | T | 240 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(237): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.397+8807G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731575 | |||||||
chr15:55731711 | C | T | 13 | a0001c0020t0053g0002 a0003c0005t0010g0038 a0003c0005t0010g0039 others(10): Show |
13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+8671G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731711 | |||||||
chr15:55731717 | A | C | 57 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(54): Show |
57 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.397+8665T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731717 | |||||||
chr15:55731864 | T | C | 1 | a0001c0001t0002g0271 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.397+8518A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731864 | |||||||
chr15:55731892 | C | A | 7 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(4): Show |
7 | HG02615.hp1 HG02970.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.397+8490G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731892 | |||||||
chr15:55731968 | C | A | 1 | a0003c0006t0009g0015 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.397+8414G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55731968 | |||||||
chr15:55732031 | C | T | 242 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.397+8351G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55732031 | |||||||
chr15:55732069 | T | C | 90 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(87): Show |
90 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.397+8313A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55732069 | |||||||
chr15:55732133 | A | G | 1 | a0001c0009t0087g0112 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.397+8249T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55732133 | |||||||
chr15:55732348 | C | A | 1 | a0002c0002t0013g0016 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.397+8034G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55732348 | |||||||
chr15:55732493 | C | CT | 210 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(207): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.397+7888dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55732493 | |||||||
chr15:55732493 | C | CTT | 9 | a0001c0001t0001g0147 a0001c0001t0001g0152 a0001c0001t0001g0181 others(6): Show |
9 | HG00738.hp1 HG01978.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.397+7887_397+7888d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55732493 | |||||||
chr15:55732736 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.397+7646G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55732736 | |||||||
chr15:55732804 | T | A | 1 | a0003c0006t0022g0012 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.397+7578A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55732804 | |||||||
chr15:55732909 | C | T | 1 | a0002c0002t0003g0088 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.397+7473G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55732909 | |||||||
chr15:55732991 | C | T | 1 | a0002c0002t0020g0053 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.397+7391G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55732991 | |||||||
chr15:55733124 | G | A | 1 | a0001c0001t0105g0205 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.397+7258C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55733124 | |||||||
chr15:55733214 | T | C | 54 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(51): Show |
54 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.397+7168A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55733214 | |||||||
chr15:55733276 | T | G | 2 | a0001c0001t0032g0098 a0002c0002t0068g0099 |
2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.397+7106A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55733276 | |||||||
chr15:55733378 | C | T | 3 | a0001c0012t0072g0113 a0001c0012t0074g0114 a0002c0002t0012g0082 |
3 | HG02630.hp2 HG03453.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.397+7004G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55733378 | |||||||
chr15:55733433 | C | G | 1 | a0006c0010t0059g0072 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.397+6949G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55733433 | |||||||
chr15:55733514 | C | CA | 73 | a0001c0001t0001g0106 a0001c0001t0001g0200 a0001c0001t0001g0203 others(70): Show |
74 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.397+6867dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55733514 | |||||||
chr15:55733514 | CA | C | 7 | a0001c0001t0002g0243 a0001c0001t0032g0098 a0002c0002t0026g0030 others(4): Show |
7 | HG00639.hp2 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+6867delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55733514 | |||||||
chr15:55733514 | CAA | C | 20 | a0001c0001t0024g0013 a0001c0001t0024g0031 a0002c0002t0013g0016 others(17): Show |
20 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.397+6866_397+6867d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55733514 | |||||||
chr15:55733573 | T | C | 14 | a0001c0001t0035g0219 a0001c0001t0097g0221 a0001c0001t0101g0217 others(11): Show |
14 | HG00323.hp1 HG02257.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.397+6809A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55733573 | |||||||
chr15:55733622 | T | C | 2 | a0001c0020t0053g0002 a0012c0019t0046g0003 |
2 | HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.397+6760A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55733622 | |||||||
chr15:55733698 | G | A | 2 | a0002c0002t0004g0108 a0002c0002t0004g0216 |
2 | NA18943.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.397+6684C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55733698 | |||||||
chr15:55733720 | G | C | 1 | a0001c0001t0024g0031 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.397+6662C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55733720 | |||||||
chr15:55733853 | C | A | 14 | a0001c0001t0001g0179 a0001c0001t0001g0181 a0001c0001t0001g0182 others(11): Show |
14 | HG01074.hp2 HG01109.hp2 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.397+6529G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55733853 | |||||||
chr15:55733892 | G | A | 1 | a0002c0002t0057g0025 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.397+6490C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55733892 | |||||||
chr15:55734075 | G | A | 1 | a0002c0002t0007g0086 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.397+6307C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55734075 | |||||||
chr15:55734214 | C | T | 57 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(54): Show |
57 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.397+6168G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55734214 | |||||||
chr15:55734508 | T | A | 2 | a0001c0001t0082g0128 a0001c0001t0102g0126 |
2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.397+5874A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55734508 | |||||||
chr15:55734618 | T | C | 1 | a0001c0009t0042g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.397+5764A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55734618 | |||||||
chr15:55734748 | TA | T | 273 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(270): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.397+5633delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55734748 | |||||||
chr15:55734930 | A | G | 11 | a0003c0005t0010g0038 a0003c0005t0010g0039 a0003c0005t0010g0041 others(8): Show |
11 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.397+5452T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55734930 | |||||||
chr15:55734938 | T | C | 5 | a0001c0007t0038g0230 a0001c0007t0038g0231 a0001c0007t0106g0109 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+5444A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55734938 | |||||||
chr15:55734966 | T | A | 2 | a0001c0001t0096g0229 a0001c0001t0099g0228 |
2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.397+5416A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55734966 | |||||||
chr15:55734990 | T | C | 7 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(4): Show |
7 | HG00408.hp1 NA18954.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.397+5392A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55734990 | |||||||
chr15:55735111 | T | C | 83 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(80): Show |
83 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.397+5271A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55735111 | |||||||
chr15:55735116 | A | C | 1 | a0002c0002t0003g0071 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.397+5266T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55735116 | |||||||
chr15:55735269 | A | G | 1 | a0002c0002t0016g0127 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.397+5113T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55735269 | |||||||
chr15:55735312 | T | C | 58 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(55): Show |
58 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.397+5070A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55735312 | |||||||
chr15:55735420 | CTAAAACC others(5): Show |
C | 1 | a0001c0001t0051g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+4950_397+4961d others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55735420 | |||||||
chr15:55735532 | A | T | 1 | a0001c0001t0002g0270 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.397+4850T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55735532 | |||||||
chr15:55735718 | T | TA | 84 | a0001c0001t0001g0107 a0001c0001t0001g0194 a0001c0001t0001g0223 others(81): Show |
84 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.397+4663dupT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55735718 | |||||||
chr15:55735718 | T | TAA | 13 | a0001c0001t0002g0256 a0001c0001t0002g0257 a0001c0001t0002g0261 others(10): Show |
13 | HG01891.hp2 HG01943.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+4662_397+4663d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55735718 | |||||||
chr15:55735718 | T | TAAA | 11 | a0001c0001t0033g0102 a0001c0001t0054g0005 a0001c0001t0097g0221 others(8): Show |
11 | HG00323.hp1 HG02818.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.397+4661_397+4663d others(5): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55735718 | |||||||
chr15:55735718 | T | TAAAA | 44 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(41): Show |
44 | HG00280.hp1 HG00323.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.397+4660_397+4663d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55735718 | |||||||
chr15:55735718 | T | TAAAAA | 18 | a0001c0001t0021g0060 a0001c0001t0032g0103 a0001c0003t0003g0089 others(15): Show |
18 | HG00408.hp2 HG00438.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.397+4659_397+4663d others(7): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55735718 | |||||||
chr15:55735815 | G | T | 111 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(108): Show |
111 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.397+4567C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55735815 | |||||||
chr15:55735819 | A | G | 2 | a0001c0001t0096g0229 a0001c0001t0099g0228 |
2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.397+4563T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55735819 | |||||||
chr15:55736029 | C | T | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.397+4353G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55736029 | |||||||
chr15:55736110 | C | T | 57 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(54): Show |
57 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.397+4272G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55736110 | |||||||
chr15:55736205 | GA | G | 24 | a0001c0001t0024g0013 a0001c0001t0024g0031 a0001c0001t0051g0004 others(21): Show |
24 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.397+4176delT | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55736205 | |||||||
chr15:55736210 | G | C | 1 | a0001c0020t0053g0002 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.397+4172C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55736210 | |||||||
chr15:55736341 | C | G | 15 | a0001c0001t0002g0265 a0001c0001t0002g0275 a0001c0020t0053g0002 others(12): Show |
15 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.397+4041G>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55736341 | |||||||
chr15:55736364 | C | T | 48 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(45): Show |
48 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.397+4018G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55736364 | |||||||
chr15:55736365 | G | A | 2 | a0001c0012t0072g0113 a0001c0012t0074g0114 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.397+4017C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55736365 | |||||||
chr15:55736378 | A | C | 111 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(108): Show |
111 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.397+4004T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55736378 | |||||||
chr15:55736380 | C | CT | 16 | a0001c0001t0034g0001 a0001c0001t0070g0133 a0001c0012t0072g0113 others(13): Show |
17 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.397+4001dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55736380 | |||||||
chr15:55736380 | CTTTT | C | 57 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(54): Show |
57 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.397+3998_397+4001d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55736380 | |||||||
chr15:55736444 | G | T | 13 | a0001c0020t0053g0002 a0003c0005t0010g0038 a0003c0005t0010g0039 others(10): Show |
13 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+3938C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55736444 | |||||||
chr15:55736503 | T | C | 1 | a0001c0009t0103g0233 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.397+3879A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55736503 | |||||||
chr15:55736659 | C | A | 50 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(47): Show |
50 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.397+3723G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55736659 | |||||||
chr15:55736807 | T | C | 1 | a0001c0001t0012g0083 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.397+3575A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55736807 | |||||||
chr15:55737147 | T | C | 54 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(51): Show |
54 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.397+3235A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737147 | |||||||
chr15:55737180 | T | C | 54 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(51): Show |
54 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.397+3202A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737180 | |||||||
chr15:55737197 | T | C | 58 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(55): Show |
58 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.397+3185A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737197 | |||||||
chr15:55737276 | G | A | 4 | a0001c0001t0029g0092 a0001c0001t0066g0094 a0002c0002t0020g0010 others(1): Show |
4 | HG02055.hp2 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+3106C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737276 | |||||||
chr15:55737784 | GCA | G | 3 | a0001c0001t0051g0004 a0001c0001t0052g0006 a0001c0001t0054g0005 |
3 | HG01891.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.397+2596_397+2597d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737784 | |||||||
chr15:55737898 | G | GCTGCT | 89 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(86): Show |
89 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.397+2479_397+2483d others(7): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737898 | |||||||
chr15:55737976 | T | TTC | 23 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0200 others(20): Show |
23 | HG00639.hp1 HG01243.hp2 HG01934.hp2 others(20): Show |
intron_variant | MODIFIER | c.397+2404_397+2405d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737976 | |||||||
chr15:55737976 | T | TTCTC | 13 | a0001c0001t0001g0203 a0001c0001t0033g0101 a0001c0001t0035g0219 others(10): Show |
13 | HG00323.hp1 HG01891.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+2402_397+2405d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737976 | |||||||
chr15:55737976 | T | TTCTCTC | 5 | a0001c0001t0101g0217 a0002c0002t0004g0108 a0002c0002t0004g0216 others(2): Show |
5 | HG02257.hp2 NA18943.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+2400_397+2405d others(8): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737976 | |||||||
chr15:55737976 | T | TTCTCTCT others(1): Show |
3 | a0001c0001t0021g0060 a0002c0002t0019g0052 a0004c0004t0030g0105 |
3 | HG02451.hp2 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.397+2398_397+2405d others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737976 | |||||||
chr15:55737976 | T | TTCTCTCT others(3): Show |
25 | a0001c0001t0012g0083 a0001c0003t0003g0042 a0001c0003t0003g0074 others(22): Show |
25 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.397+2396_397+2405d others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737976 | |||||||
chr15:55737976 | T | TTCTCTCT others(5): Show |
5 | a0002c0002t0003g0084 a0002c0002t0007g0085 a0002c0002t0007g0086 others(2): Show |
5 | HG01255.hp2 HG03209.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+2394_397+2405d others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737976 | |||||||
chr15:55737976 | T | TTCTCTCT others(7): Show |
2 | a0001c0003t0003g0089 a0002c0002t0003g0087 |
2 | NA18948.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.397+2392_397+2405d others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737976 | |||||||
chr15:55737976 | T | TTCTCTCT others(9): Show |
1 | a0004c0004t0023g0057 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.397+2390_397+2405d others(18): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737976 | |||||||
chr15:55737976 | TTC | T | 3 | a0001c0001t0102g0126 a0002c0002t0014g0033 a0002c0002t0062g0032 |
3 | HG02559.hp2 HG02622.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.397+2404_397+2405d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737976 | |||||||
chr15:55737980 | C | T | 11 | a0003c0005t0010g0038 a0003c0005t0010g0039 a0003c0005t0010g0041 others(8): Show |
11 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.397+2402G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737980 | |||||||
chr15:55737996 | C | A | 1 | a0001c0001t0034g0001 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.397+2386G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737996 | |||||||
chr15:55737998 | C | A | 1 | a0001c0001t0034g0001 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.397+2384G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55737998 | |||||||
chr15:55738000 | C | A | 3 | a0001c0001t0034g0001 a0001c0001t0070g0133 a0002c0002t0011g0050 |
4 | HG01167.hp2 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.397+2382G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738000 | |||||||
chr15:55738000 | CTCTA | C | 9 | a0001c0001t0006g0138 a0001c0001t0024g0013 a0002c0002t0014g0020 others(6): Show |
9 | HG01361.hp1 HG02055.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.397+2378_397+2381d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738000 | |||||||
chr15:55738002 | C | A | 7 | a0001c0001t0001g0147 a0001c0001t0001g0224 a0001c0001t0032g0098 others(4): Show |
8 | HG01167.hp2 HG01169.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.397+2380G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738002 | |||||||
chr15:55738002 | C | CTCTCTCT others(3): Show |
4 | a0001c0001t0012g0091 a0001c0001t0018g0058 a0002c0002t0003g0068 others(1): Show |
4 | HG00323.hp2 HG02027.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.397+2379_397+2380i others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738002 | |||||||
chr15:55738002 | C | CTCTCTCT others(5): Show |
2 | a0002c0002t0006g0227 a0004c0004t0050g0059 |
2 | HG02129.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.397+2379_397+2380i others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738002 | |||||||
chr15:55738002 | C | CTCTCTCT others(7): Show |
1 | a0002c0002t0003g0069 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.397+2379_397+2380i others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738002 | |||||||
chr15:55738002 | CTA | C | 17 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0001t0001g0177 others(14): Show |
17 | HG00099.hp2 HG00733.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.397+2378_397+2379d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738002 | |||||||
chr15:55738002 | CTATA | C | 12 | a0001c0001t0002g0243 a0001c0001t0002g0244 a0001c0012t0002g0279 others(9): Show |
12 | HG00099.hp1 HG00639.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.397+2376_397+2379d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738002 | |||||||
chr15:55738002 | CTATATA | C | 5 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0242 others(2): Show |
5 | HG00741.hp2 HG01106.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+2374_397+2379d others(8): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738002 | |||||||
chr15:55738002 | CTATATAT others(3): Show |
C | 1 | a0001c0007t0108g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.397+2370_397+2379d others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738002 | |||||||
chr15:55738004 | A | C | 143 | a0001c0001t0001g0106 a0001c0001t0001g0115 a0001c0001t0001g0130 others(140): Show |
143 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.397+2378T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738004 | |||||||
chr15:55738004 | A | T | 2 | a0002c0002t0014g0033 a0002c0002t0062g0032 |
2 | HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.397+2378T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738004 | |||||||
chr15:55738006 | A | C | 95 | a0001c0001t0001g0115 a0001c0001t0001g0134 a0001c0001t0001g0139 others(92): Show |
95 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.397+2376T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738006 | |||||||
chr15:55738006 | A | T | 15 | a0001c0001t0024g0013 a0002c0002t0013g0018 a0002c0002t0013g0029 others(12): Show |
15 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.397+2376T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738006 | |||||||
chr15:55738008 | A | C | 54 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0207 others(51): Show |
54 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(51): Show |
intron_variant | MODIFIER | c.397+2374T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738008 | |||||||
chr15:55738008 | A | T | 1 | a0002c0002t0013g0016 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.397+2374T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738008 | |||||||
chr15:55738010 | A | C | 21 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0242 others(18): Show |
21 | HG00323.hp1 HG00408.hp2 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.397+2372T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738010 | |||||||
chr15:55738012 | A | C | 8 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0242 others(5): Show |
8 | HG00639.hp2 HG00741.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.397+2370T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738012 | |||||||
chr15:55738015 | T | C | 2 | a0001c0001t0034g0001 a0001c0001t0070g0133 |
3 | HG03491.hp2 HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.397+2367A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738015 | |||||||
chr15:55738017 | T | C | 3 | a0001c0001t0034g0001 a0001c0001t0070g0133 a0001c0001t0084g0129 |
4 | HG03471.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.397+2365A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738017 | |||||||
chr15:55738017 | TATATATA others(3): Show |
T | 3 | a0001c0007t0038g0231 a0001c0007t0106g0109 a0001c0007t0107g0110 |
3 | HG02109.hp2 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.397+2355_397+2364d others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738017 | |||||||
chr15:55738017 | TATATATA others(7): Show |
T | 1 | a0010c0021t0091g0204 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.397+2351_397+2364d others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738017 | |||||||
chr15:55738019 | T | C | 11 | a0001c0001t0029g0092 a0001c0001t0034g0001 a0001c0001t0070g0133 others(8): Show |
12 | HG01243.hp2 HG02559.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.397+2363A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738019 | |||||||
chr15:55738019 | T | TAC | 5 | a0001c0001t0066g0094 a0002c0002t0011g0048 a0002c0002t0011g0049 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+2362_397+2363i others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738019 | |||||||
chr15:55738021 | T | C | 38 | a0001c0001t0001g0144 a0001c0001t0001g0203 a0001c0001t0015g0201 others(35): Show |
39 | HG00733.hp2 HG01167.hp2 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.397+2361A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738021 | |||||||
chr15:55738021 | TATATAC | T | 25 | a0001c0001t0002g0238 a0001c0001t0002g0247 a0001c0001t0002g0248 others(22): Show |
25 | HG00140.hp1 HG00733.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.397+2355_397+2360d others(8): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738021 | |||||||
chr15:55738023 | T | C | 149 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(146): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.397+2359A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738023 | |||||||
chr15:55738023 | T | TACAC | 3 | a0001c0001t0032g0103 a0001c0001t0033g0102 a0002c0002t0068g0099 |
3 | HG02965.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.397+2358_397+2359i others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738023 | |||||||
chr15:55738023 | TATAC | T | 12 | a0001c0001t0002g0265 a0001c0001t0002g0266 a0001c0001t0002g0267 others(9): Show |
12 | HG01167.hp1 HG01256.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.397+2355_397+2358d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738023 | |||||||
chr15:55738025 | T | C | 174 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(171): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.397+2357A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738025 | |||||||
chr15:55738025 | T | TATAC | 3 | a0002c0002t0004g0118 a0002c0002t0004g0119 a0002c0002t0004g0120 |
3 | NA18964.hp1 NA18981.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.397+2356_397+2357i others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738025 | |||||||
chr15:55738025 | TAC | T | 3 | a0001c0001t0021g0051 a0001c0001t0096g0229 a0001c0001t0099g0228 |
3 | HG02647.hp2 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.397+2355_397+2356d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738025 | |||||||
chr15:55738027 | C | T | 5 | a0001c0001t0002g0269 a0001c0001t0002g0271 a0001c0001t0002g0281 others(2): Show |
5 | HG01943.hp2 HG01993.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+2355G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738027 | |||||||
chr15:55738029 | C | T | 3 | a0001c0001t0021g0051 a0001c0001t0096g0229 a0001c0001t0099g0228 |
3 | HG02647.hp2 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.397+2353G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738029 | |||||||
chr15:55738071 | A | AAT | 32 | a0001c0001t0001g0131 a0001c0001t0016g0122 a0001c0001t0016g0123 others(29): Show |
32 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.397+2309_397+2310d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | |||||||
chr15:55738071 | A | AATAT | 120 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0130 others(117): Show |
120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.397+2307_397+2310d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | |||||||
chr15:55738071 | A | AATATAT | 22 | a0001c0001t0001g0139 a0001c0001t0001g0144 a0001c0001t0001g0224 others(19): Show |
22 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.397+2305_397+2310d others(8): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | |||||||
chr15:55738071 | A | AATATATA others(1): Show |
15 | a0001c0001t0002g0275 a0001c0001t0005g0137 a0001c0001t0012g0091 others(12): Show |
15 | HG00323.hp2 HG01109.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.397+2303_397+2310d others(10): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | |||||||
chr15:55738071 | A | AATATATA others(3): Show |
16 | a0001c0001t0001g0115 a0001c0001t0001g0207 a0001c0001t0002g0246 others(13): Show |
16 | HG01256.hp2 HG01258.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.397+2301_397+2310d others(12): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | |||||||
chr15:55738071 | A | AATATATA others(5): Show |
4 | a0001c0001t0001g0134 a0001c0001t0002g0264 a0001c0001t0034g0001 others(1): Show |
5 | HG00733.hp1 HG02027.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+2299_397+2310d others(14): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | |||||||
chr15:55738071 | A | AATATATA others(7): Show |
1 | a0001c0001t0070g0133 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.397+2297_397+2310d others(16): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | |||||||
chr15:55738071 | A | AATATATA others(9): Show |
2 | a0001c0001t0002g0262 a0001c0001t0041g0263 |
2 | HG00738.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.397+2295_397+2310d others(18): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | |||||||
chr15:55738071 | A | AATATATA others(11): Show |
4 | a0001c0001t0002g0258 a0001c0001t0002g0259 a0001c0001t0002g0260 others(1): Show |
4 | HG03688.hp2 HG04115.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.397+2293_397+2310d others(20): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | |||||||
chr15:55738071 | A | AATATATA others(13): Show |
7 | a0001c0001t0001g0206 a0001c0001t0002g0256 a0001c0001t0002g0257 others(4): Show |
7 | HG02257.hp1 HG02273.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.397+2291_397+2310d others(22): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | |||||||
chr15:55738071 | A | AATATATA others(15): Show |
3 | a0001c0001t0002g0255 a0001c0001t0100g0232 a0007c0017t0002g0254 |
3 | HG00140.hp1 HG01517.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.397+2289_397+2310d others(24): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | |||||||
chr15:55738071 | A | AATATATA others(17): Show |
5 | a0001c0001t0002g0238 a0001c0001t0002g0243 a0001c0001t0002g0244 others(2): Show |
5 | HG00639.hp2 HG01515.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+2310_397+2311i others(26): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | |||||||
chr15:55738071 | A | AATATATA others(19): Show |
2 | a0001c0001t0002g0242 a0001c0001t0041g0280 |
2 | HG01255.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.397+2310_397+2311i others(28): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | |||||||
chr15:55738071 | A | AATATATA others(21): Show |
5 | a0001c0001t0002g0241 a0001c0001t0002g0249 a0001c0001t0002g0250 others(2): Show |
5 | HG01071.hp1 HG01106.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+2310_397+2311i others(30): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | |||||||
chr15:55738071 | A | AATATATA others(23): Show |
2 | a0001c0001t0002g0240 a0001c0001t0002g0248 |
2 | HG00741.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.397+2310_397+2311i others(32): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | |||||||
chr15:55738071 | A | AATATATA others(27): Show |
1 | a0001c0001t0002g0247 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.397+2310_397+2311i others(36): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738071 | |||||||
chr15:55738195 | TCAC | T | 6 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0242 others(3): Show |
6 | HG00639.hp2 HG00741.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.397+2184_397+2186d others(5): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738195 | |||||||
chr15:55738245 | G | A | 50 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(47): Show |
50 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.397+2137C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738245 | |||||||
chr15:55738345 | G | A | 51 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(48): Show |
51 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.397+2037C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738345 | |||||||
chr15:55738371 | A | G | 2 | a0001c0001t0096g0229 a0001c0001t0099g0228 |
2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.397+2011T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738371 | |||||||
chr15:55738372 | A | G | 3 | a0002c0002t0003g0044 a0002c0002t0003g0088 a0002c0002t0007g0043 |
3 | HG00438.hp2 HG02027.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.397+2010T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738372 | |||||||
chr15:55738503 | AAAGAT | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0206 a0001c0001t0001g0207 |
3 | NA18948.hp2 NA18980.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.397+1874_397+1878d others(7): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738503 | |||||||
chr15:55738539 | C | T | 2 | a0001c0001t0096g0229 a0001c0001t0099g0228 |
2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.397+1843G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738539 | |||||||
chr15:55738546 | T | G | 5 | a0001c0008t0037g0208 a0001c0008t0037g0210 a0001c0008t0076g0121 others(2): Show |
5 | HG02615.hp1 HG03453.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+1836A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738546 | |||||||
chr15:55738558 | T | C | 53 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(50): Show |
53 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.397+1824A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738558 | |||||||
chr15:55738648 | T | G | 57 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(54): Show |
57 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.397+1734A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738648 | |||||||
chr15:55738731 | A | C | 1 | a0001c0003t0003g0042 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.397+1651T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738731 | |||||||
chr15:55738774 | A | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG00438.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.397+1608T>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738774 | |||||||
chr15:55738801 | GAGGA | G | 3 | a0001c0001t0051g0004 a0001c0001t0052g0006 a0001c0001t0054g0005 |
3 | HG01891.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.397+1577_397+1580d others(6): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738801 | |||||||
chr15:55738828 | A | G | 218 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(215): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.397+1554T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738828 | |||||||
chr15:55738884 | A | G | 1 | a0001c0001t0051g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1498T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738884 | |||||||
chr15:55738887 | CAGAGGAA others(4): Show |
C | 8 | a0001c0001t0016g0122 a0001c0001t0016g0123 a0001c0001t0082g0128 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.397+1484_397+1494d others(13): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738887 | |||||||
chr15:55738888 | A | C | 1 | a0001c0001t0051g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1494T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738888 | |||||||
chr15:55738910 | A | C | 1 | a0001c0001t0051g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1472T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738910 | |||||||
chr15:55738917 | G | C | 1 | a0001c0001t0051g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1465C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738917 | |||||||
chr15:55738924 | A | C | 1 | a0001c0001t0051g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1458T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738924 | |||||||
chr15:55738926 | G | C | 1 | a0001c0001t0051g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1456C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738926 | |||||||
chr15:55738927 | A | C | 1 | a0001c0001t0051g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1455T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738927 | |||||||
chr15:55738928 | A | C | 1 | a0001c0001t0051g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1454T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738928 | |||||||
chr15:55738931 | A | C | 1 | a0001c0001t0051g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1451T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738931 | |||||||
chr15:55738932 | A | C | 1 | a0001c0001t0051g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1450T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738932 | |||||||
chr15:55738935 | A | C | 1 | a0001c0001t0051g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1447T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738935 | |||||||
chr15:55738939 | A | C | 1 | a0001c0001t0051g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1443T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738939 | |||||||
chr15:55738940 | G | T | 1 | a0001c0001t0051g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1442C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738940 | |||||||
chr15:55738943 | A | C | 1 | a0001c0001t0051g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1439T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738943 | |||||||
chr15:55738947 | A | C | 1 | a0001c0001t0051g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1435T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738947 | |||||||
chr15:55738949 | A | C | 1 | a0001c0001t0051g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1433T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738949 | |||||||
chr15:55738950 | G | T | 1 | a0001c0001t0051g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+1432C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738950 | |||||||
chr15:55738963 | G | A | 1 | a0001c0001t0001g0223 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.397+1419C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55738963 | |||||||
chr15:55739009 | G | A | 2 | a0001c0001t0001g0224 a0001c0003t0004g0225 |
2 | NA18994.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.397+1373C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55739009 | |||||||
chr15:55739042 | C | T | 51 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(48): Show |
51 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.397+1340G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55739042 | |||||||
chr15:55739171 | A | C | 1 | a0001c0008t0076g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.397+1211T>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55739171 | |||||||
chr15:55739263 | A | AT | 56 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0015g0116 others(53): Show |
56 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.397+1118dupA | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55739263 | |||||||
chr15:55739263 | ATT | A | 54 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(51): Show |
54 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.397+1117_397+1118d others(4): Show |
PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55739263 | |||||||
chr15:55739418 | G | C | 1 | a0001c0003t0017g0090 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.397+964C>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55739418 | |||||||
chr15:55739473 | G | A | 105 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(102): Show |
105 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.397+909C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55739473 | |||||||
chr15:55739606 | A | G | 1 | a0004c0004t0030g0097 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.397+776T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55739606 | |||||||
chr15:55739724 | T | A | 1 | a0001c0001t0001g0226 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.397+658A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55739724 | |||||||
chr15:55739880 | G | A | 1 | a0001c0001t0012g0091 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.397+502C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55739880 | |||||||
chr15:55739890 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.397+492T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55739890 | |||||||
chr15:55739901 | A | G | 108 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(105): Show |
108 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.397+481T>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55739901 | |||||||
chr15:55740068 | T | G | 2 | a0001c0020t0053g0002 a0012c0019t0046g0003 |
2 | HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.397+314A>C | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55740068 | |||||||
chr15:55740213 | T | C | 54 | a0001c0001t0012g0083 a0001c0001t0012g0091 a0001c0001t0018g0058 others(51): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.397+169A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55740213 | |||||||
chr15:55740242 | T | A | 2 | a0001c0001t0096g0229 a0001c0001t0099g0228 |
2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.397+140A>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55740242 | |||||||
chr15:55740321 | G | A | 45 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(42): Show |
45 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.397+61C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 2/19 | chr15 | 55740321 | |||||||
chr15:55740777 | G | A | 103 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(100): Show |
103 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.95-93C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55740777 | |||||||
chr15:55741398 | G | T | 2 | a0001c0012t0072g0113 a0001c0012t0074g0114 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.95-714C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55741398 | |||||||
chr15:55741399 | G | T | 2 | a0001c0012t0072g0113 a0001c0012t0074g0114 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.95-715C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55741399 | |||||||
chr15:55741649 | G | A | 52 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(49): Show |
52 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.95-965C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55741649 | |||||||
chr15:55741771 | C | T | 2 | a0001c0020t0053g0002 a0012c0019t0046g0003 |
2 | HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.94+1067G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55741771 | |||||||
chr15:55741866 | C | A | 3 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0041g0280 |
3 | HG01361.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.94+972G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55741866 | |||||||
chr15:55741906 | C | T | 2 | a0004c0004t0031g0095 a0004c0004t0031g0096 |
2 | HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.94+932G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55741906 | |||||||
chr15:55741909 | T | C | 53 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(50): Show |
53 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.94+929A>G | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55741909 | |||||||
chr15:55742333 | C | T | 4 | a0001c0007t0106g0109 a0001c0007t0107g0110 a0001c0007t0108g0111 others(1): Show |
4 | HG02109.hp2 HG02615.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+505G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55742333 | |||||||
chr15:55742397 | C | A | 1 | a0001c0001t0100g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.94+441G>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55742397 | |||||||
chr15:55742491 | C | T | 1 | a0002c0002t0004g0108 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.94+347G>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55742491 | |||||||
chr15:55742672 | G | A | 2 | a0001c0009t0103g0233 a0016c0014t0073g0234 |
2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.94+166C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55742672 | |||||||
chr15:55742680 | G | A | 45 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(42): Show |
45 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.94+158C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55742680 | |||||||
chr15:55742713 | G | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | NA18981.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.94+125C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55742713 | |||||||
chr15:55742787 | G | T | 1 | a0001c0001t0002g0238 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.94+51C>A | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55742787 | |||||||
chr15:55742812 | G | A | 45 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0002g0241 others(42): Show |
45 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.94+26C>T | PRTG | ENSG00000166450.13 | transcript | ENST00000389286.9 | protein_coding | 1/19 | chr15 | 55742812 |