Item | Value |
---|---|
geneid | 55615 |
ensemblid | ENSG00000186654.21 |
hgncid | 31682 |
symbol | PRR5 |
name | proline rich 5 |
refseq_nuc | NM_181333.4 |
refseq_prot | NP_851850.1 |
ensembl_nuc | ENST00000336985.11 |
ensembl_prot | ENSP00000337464.6 |
mane_status | MANE Select |
chr | chr22 |
start | 44702204 |
end | 44737681 |
strand | + |
ver | v1.2 |
region | chr22:44702204-44737681 |
region5000 | chr22:44697204-44742681 |
regionname0 | PRR5_chr22_44702204_44737681 |
regionname5000 | PRR5_chr22_44697204_44742681 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 388 | 385 | 90 | 76 | 158 | 13 | 46 | 121 | PRR5_chr22_44697204_44742681 | PRR5 | MRTLR others(383): Show |
chr22 | 44697204 | 44742681 |
a0002 | 0/0 | 388 | 51 | 4 | 1 | 42 | 0 | 4 | 33 | PRR5_chr22_44697204_44742681 | PRR5 | MRTLR others(383): Show |
chr22 | 44697204 | 44742681 |
a0003 | 0/0 | 388 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | MRTLR others(383): Show |
chr22 | 44697204 | 44742681 |
a0004 | 0/0 | 388 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | MRTLR others(383): Show |
chr22 | 44697204 | 44742681 |
a0005 | 0/0 | 388 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | MRTLR others(383): Show |
chr22 | 44697204 | 44742681 |
a0006 | 0/0 | 324 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | MRTLR others(319): Show |
chr22 | 44697204 | 44742681 |
a0007 | 0/0 | 388 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | MRTLR others(383): Show |
chr22 | 44697204 | 44742681 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1164 | 225 | 36 | 50 | 100 | 9 | 28 | PRR5_chr22_44697204_44742681 | PRR5 | ATGAG others(1159): Show |
chr22 | 44697204 | 44742681 | ||
a0001c0002 | 0/0 | 1164 | 103 | 47 | 13 | 27 | 3 | 13 | PRR5_chr22_44697204_44742681 | PRR5 | ATGAG others(1159): Show |
chr22 | 44697204 | 44742681 | ||
a0001c0004 | 0/0 | 1164 | 40 | 7 | 13 | 15 | 1 | 4 | PRR5_chr22_44697204_44742681 | PRR5 | ATGAG others(1159): Show |
chr22 | 44697204 | 44742681 | ||
a0001c0005 | 0/0 | 1164 | 8 | 0 | 0 | 8 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | ATGAG others(1159): Show |
chr22 | 44697204 | 44742681 | ||
a0001c0006 | 0/0 | 1164 | 3 | 0 | 0 | 3 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | ATGAG others(1159): Show |
chr22 | 44697204 | 44742681 | ||
a0001c0008 | 0/0 | 1164 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | ATGAG others(1159): Show |
chr22 | 44697204 | 44742681 | ||
a0001c0009 | 0/0 | 1164 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | ATGAG others(1159): Show |
chr22 | 44697204 | 44742681 | ||
a0001c0011 | 0/0 | 1164 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | ATGAG others(1159): Show |
chr22 | 44697204 | 44742681 | ||
a0001c0012 | 0/0 | 1164 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | ATGAG others(1159): Show |
chr22 | 44697204 | 44742681 | ||
a0001c0015 | 0/0 | 1164 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | ATGAG others(1159): Show |
chr22 | 44697204 | 44742681 | ||
a0001c0017 | 0/0 | 1164 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | ATGAG others(1159): Show |
chr22 | 44697204 | 44742681 | ||
a0002c0003 | 0/0 | 1164 | 51 | 4 | 1 | 42 | 0 | 4 | PRR5_chr22_44697204_44742681 | PRR5 | ATGAG others(1159): Show |
chr22 | 44697204 | 44742681 | ||
a0003c0007 | 0/0 | 1164 | 2 | 2 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | ATGAG others(1159): Show |
chr22 | 44697204 | 44742681 | ||
a0004c0014 | 0/0 | 1164 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | ATGAG others(1159): Show |
chr22 | 44697204 | 44742681 | ||
a0005c0016 | 0/0 | 1164 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | ATGAG others(1159): Show |
chr22 | 44697204 | 44742681 | ||
a0006c0013 | 0/0 | 1150 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | ATGAG others(1145): Show |
chr22 | 44697204 | 44742681 | ||
a0007c0010 | 0/0 | 1164 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | ATGAG others(1159): Show |
chr22 | 44697204 | 44742681 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1872 | 157 | 8 | 43 | 70 | 9 | 25 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0001t0003 | 0/0 | 1872 | 35 | 6 | 3 | 26 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0001t0006 | 0/0 | 1872 | 11 | 6 | 3 | 1 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0001t0007 | 0/0 | 1872 | 5 | 4 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0001t0009 | 0/0 | 1872 | 2 | 2 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0001t0012 | 0/0 | 1872 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0001t0014 | 0/0 | 1872 | 3 | 3 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0001t0015 | 0/0 | 1872 | 2 | 2 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0001t0018 | 0/0 | 1872 | 2 | 2 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0001t0020 | 0/0 | 1872 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0001t0024 | 0/0 | 1856 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1851): Show |
chr22 | 44697204 | 44742681 |
a0001c0001t0027 | 0/0 | 1872 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0001t0029 | 0/0 | 1872 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0001t0030 | 0/0 | 1872 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0001t0032 | 0/0 | 1872 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0002t0001 | 0/0 | 1872 | 25 | 2 | 4 | 6 | 2 | 11 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0002t0003 | 0/0 | 1872 | 10 | 6 | 2 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0002t0005 | 0/0 | 1872 | 32 | 11 | 5 | 15 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0002t0006 | 0/0 | 1872 | 2 | 1 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0002t0007 | 0/0 | 1872 | 2 | 2 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0002t0008 | 0/0 | 1872 | 7 | 7 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0002t0009 | 0/0 | 1872 | 3 | 3 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0002t0010 | 0/0 | 1872 | 4 | 4 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0002t0011 | 0/0 | 1872 | 3 | 1 | 0 | 1 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0002t0012 | 0/0 | 1872 | 2 | 2 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0002t0013 | 0/0 | 1872 | 3 | 0 | 0 | 3 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0002t0015 | 0/0 | 1872 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0002t0017 | 0/0 | 1872 | 2 | 2 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0002t0019 | 0/0 | 1872 | 2 | 2 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0002t0022 | 0/0 | 1872 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0002t0023 | 0/0 | 1872 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0002t0026 | 0/0 | 1856 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1851): Show |
chr22 | 44697204 | 44742681 |
a0001c0002t0028 | 0/0 | 1872 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0002t0033 | 0/0 | 1872 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0004t0004 | 0/0 | 1872 | 38 | 6 | 13 | 15 | 0 | 4 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0004t0016 | 0/0 | 1872 | 2 | 1 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0005t0001 | 0/0 | 1872 | 8 | 0 | 0 | 8 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0006t0001 | 0/0 | 1872 | 3 | 0 | 0 | 3 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0008t0001 | 0/0 | 1872 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0009t0001 | 0/0 | 1872 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0011t0001 | 0/0 | 1872 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0012t0004 | 0/0 | 1872 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0015t0031 | 0/0 | 1872 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0001c0017t0001 | 0/0 | 1872 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0002c0003t0002 | 0/0 | 1872 | 49 | 3 | 1 | 42 | 0 | 3 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0002c0003t0003 | 0/0 | 1872 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0002c0003t0021 | 0/0 | 1872 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0003c0007t0004 | 0/0 | 1872 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0003c0007t0025 | 0/0 | 1856 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1851): Show |
chr22 | 44697204 | 44742681 |
a0004c0014t0001 | 0/0 | 1872 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0005c0016t0001 | 0/0 | 1872 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
a0006c0013t0001 | 0/0 | 1858 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1853): Show |
chr22 | 44697204 | 44742681 |
a0007c0010t0002 | 0/0 | 1872 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | GGCCT others(1867): Show |
chr22 | 44697204 | 44742681 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0159 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0198 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0386 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0389 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0390 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0392 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0397 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0399 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0402 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0414 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0398 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0405 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0416 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0006g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0006g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0006g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0006g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0006g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0006g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0006g0412 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0007g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0007g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0007g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0007g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0009g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0009g0410 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0012g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0014g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0014g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0014g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0015g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0015g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0018g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0018g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0020g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0020g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0024g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0027g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0029g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0030g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0032g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0393 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0394 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0406 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0003g0407 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0401 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0006g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0007g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0008g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0008g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0008g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0008g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0008g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0008g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0008g0408 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0009g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0009g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0009g0411 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0010g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0010g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0010g0403 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0010g0404 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0011g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0011g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0011g0413 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0012g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0012g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0013g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0013g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0015g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0017g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0017g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0019g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0019g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0022g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0023g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0026g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0028g0396 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0033g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0391 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0409 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0016g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0016g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0005t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0005t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0005t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0005t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0005t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0005t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0005t0001g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0006t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0006t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0006t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0008t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0009t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0011t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0012t0004g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0015t0031g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0017t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0400 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0415 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0021g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0003c0007t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0003c0007t0025g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0004c0014t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0005c0016t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0006c0013t0001g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0007c0010t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0195 | EUR | GBR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0314 | EUR | GBR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00140 | hp1 | a0001 | c0004 | t0016 | g0040 | EUR | GBR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00140 | hp2 | a0004 | c0014 | t0001 | g0199 | EUR | GBR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | FIN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0107 | EUR | FIN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00323 | hp1 | a0001 | c0002 | t0005 | g0105 | EUR | FIN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | FIN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00408 | hp1 | a0002 | c0003 | t0002 | g0353 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00408 | hp2 | a0002 | c0003 | t0002 | g0147 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00423 | hp1 | a0002 | c0003 | t0002 | g0149 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00423 | hp2 | a0001 | c0004 | t0004 | g0248 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00438 | hp2 | a0002 | c0003 | t0002 | g0306 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0373 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0287 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0312 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00609 | hp1 | a0001 | c0011 | t0001 | g0281 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00609 | hp2 | a0001 | c0002 | t0005 | g0220 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00621 | hp1 | a0001 | c0002 | t0005 | g0374 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0360 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00639 | hp1 | a0001 | c0004 | t0004 | g0363 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0366 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00642 | hp2 | a0001 | c0004 | t0004 | g0011 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00673 | hp1 | a0002 | c0003 | t0002 | g0253 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0386 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00735 | hp2 | a0001 | c0001 | t0006 | g0047 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00738 | hp1 | a0001 | c0002 | t0028 | g0396 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0388 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01069 | hp2 | a0001 | c0004 | t0004 | g0018 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01070 | hp1 | a0001 | c0002 | t0005 | g0170 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01070 | hp2 | a0001 | c0002 | t0005 | g0379 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01071 | hp1 | a0001 | c0004 | t0004 | g0018 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01071 | hp2 | a0001 | c0002 | t0005 | g0338 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01099 | hp1 | a0002 | c0003 | t0002 | g0144 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0298 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0059 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01109 | hp2 | a0001 | c0001 | t0007 | g0025 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0183 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01168 | hp2 | a0001 | c0001 | t0006 | g0042 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01175 | hp2 | a0001 | c0004 | t0004 | g0011 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0397 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01243 | hp1 | a0001 | c0002 | t0003 | g0407 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01243 | hp2 | a0001 | c0002 | t0003 | g0071 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01255 | hp2 | a0001 | c0004 | t0004 | g0344 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01256 | hp1 | a0001 | c0004 | t0004 | g0134 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0390 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0345 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0389 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01433 | hp2 | a0001 | c0001 | t0006 | g0036 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01496 | hp2 | a0001 | c0002 | t0005 | g0084 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0151 | EUR | IBS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0362 | EUR | IBS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01884 | hp1 | a0001 | c0002 | t0003 | g0251 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01884 | hp2 | a0001 | c0002 | t0003 | g0191 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01891 | hp1 | a0001 | c0002 | t0007 | g0023 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01928 | hp1 | a0001 | c0004 | t0004 | g0354 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01934 | hp1 | a0001 | c0002 | t0022 | g0004 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01943 | hp1 | a0001 | c0002 | t0005 | g0250 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01943 | hp2 | a0001 | c0004 | t0004 | g0409 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0387 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01975 | hp1 | a0001 | c0004 | t0004 | g0391 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0398 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0365 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0357 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01993 | hp2 | a0001 | c0004 | t0004 | g0233 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0235 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02015 | hp1 | a0001 | c0004 | t0004 | g0285 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02015 | hp2 | a0002 | c0003 | t0002 | g0122 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0334 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02027 | hp2 | a0001 | c0002 | t0005 | g0333 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02055 | hp1 | a0001 | c0004 | t0004 | g0276 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02055 | hp2 | a0001 | c0001 | t0018 | g0058 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02056 | hp1 | a0002 | c0003 | t0002 | g0361 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0293 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02071 | hp2 | a0001 | c0004 | t0004 | g0307 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02080 | hp2 | a0001 | c0015 | t0031 | g0358 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0382 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02129 | hp2 | a0001 | c0002 | t0005 | g0162 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02132 | hp1 | a0001 | c0002 | t0005 | g0364 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02135 | hp2 | a0002 | c0003 | t0002 | g0324 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02145 | hp1 | a0002 | c0003 | t0002 | g0093 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02145 | hp2 | a0001 | c0002 | t0005 | g0022 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02165 | hp1 | a0001 | c0002 | t0005 | g0104 | EAS | CDX | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CDX | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02257 | hp1 | a0001 | c0002 | t0010 | g0403 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02258 | hp1 | a0001 | c0001 | t0024 | g0063 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02258 | hp2 | a0001 | c0001 | t0015 | g0266 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02273 | hp1 | a0001 | c0004 | t0004 | g0367 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02273 | hp2 | a0001 | c0004 | t0004 | g0238 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02280 | hp1 | a0001 | c0002 | t0008 | g0090 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02280 | hp2 | a0002 | c0003 | t0003 | g0114 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0359 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0392 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02451 | hp1 | a0001 | c0002 | t0026 | g0062 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02451 | hp2 | a0001 | c0001 | t0006 | g0046 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02523 | hp1 | a0002 | c0003 | t0002 | g0350 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02572 | hp1 | a0001 | c0002 | t0019 | g0021 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0402 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0351 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02615 | hp1 | a0001 | c0001 | t0006 | g0412 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02615 | hp2 | a0001 | c0002 | t0007 | g0024 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02622 | hp1 | a0001 | c0004 | t0016 | g0029 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02622 | hp2 | a0001 | c0002 | t0010 | g0088 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02630 | hp1 | a0001 | c0002 | t0019 | g0206 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02630 | hp2 | a0001 | c0002 | t0003 | g0200 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02647 | hp1 | a0001 | c0004 | t0004 | g0204 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02647 | hp2 | a0001 | c0002 | t0023 | g0133 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02683 | hp2 | a0001 | c0004 | t0004 | g0136 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02717 | hp1 | a0001 | c0001 | t0014 | g0265 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02717 | hp2 | a0001 | c0001 | t0027 | g0274 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02723 | hp1 | a0001 | c0002 | t0005 | g0067 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0077 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02738 | hp1 | a0001 | c0004 | t0004 | g0304 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0394 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0326 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02809 | hp2 | a0001 | c0004 | t0004 | g0262 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02818 | hp1 | a0001 | c0001 | t0014 | g0264 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02818 | hp2 | a0001 | c0002 | t0005 | g0128 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02886 | hp1 | a0001 | c0002 | t0017 | g0039 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02895 | hp1 | a0001 | c0002 | t0005 | g0249 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02895 | hp2 | a0001 | c0004 | t0004 | g0339 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02897 | hp1 | a0001 | c0001 | t0006 | g0035 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02897 | hp2 | a0001 | c0004 | t0004 | g0380 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02922 | hp1 | a0001 | c0001 | t0009 | g0410 | AFR | ESN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02922 | hp2 | a0001 | c0002 | t0005 | g0252 | AFR | ESN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02965 | hp1 | a0001 | c0002 | t0003 | g0301 | AFR | ESN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0406 | AFR | ESN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02970 | hp1 | a0001 | c0002 | t0009 | g0033 | AFR | ESN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02970 | hp2 | a0001 | c0001 | t0007 | g0030 | AFR | ESN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02976 | hp1 | a0001 | c0002 | t0006 | g0032 | AFR | ESN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02976 | hp2 | a0001 | c0002 | t0010 | g0404 | AFR | ESN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03017 | hp1 | a0001 | c0002 | t0006 | g0050 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0142 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03041 | hp1 | a0001 | c0002 | t0005 | g0181 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03041 | hp2 | a0001 | c0001 | t0015 | g0267 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03098 | hp1 | a0001 | c0001 | t0018 | g0131 | AFR | MSL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03098 | hp2 | a0001 | c0002 | t0008 | g0408 | AFR | MSL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03130 | hp1 | a0001 | c0001 | t0007 | g0034 | AFR | ESN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03130 | hp2 | a0001 | c0001 | t0007 | g0037 | AFR | ESN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03139 | hp1 | a0001 | c0002 | t0005 | g0275 | AFR | ESN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0201 | AFR | ESN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03195 | hp1 | a0001 | c0002 | t0003 | g0070 | AFR | ESN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03195 | hp2 | a0001 | c0002 | t0008 | g0180 | AFR | ESN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | MSL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03209 | hp2 | a0001 | c0002 | t0033 | g0060 | AFR | MSL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0027 | AFR | MSL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03225 | hp2 | a0001 | c0001 | t0009 | g0026 | AFR | MSL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0205 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03453 | hp1 | a0001 | c0001 | t0006 | g0028 | AFR | MSL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03453 | hp2 | a0001 | c0002 | t0005 | g0182 | AFR | MSL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03486 | hp1 | a0003 | c0007 | t0025 | g0064 | AFR | MSL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03486 | hp2 | a0001 | c0002 | t0008 | g0085 | AFR | MSL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03490 | hp1 | a0001 | c0004 | t0004 | g0355 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0208 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0209 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03540 | hp1 | a0001 | c0002 | t0008 | g0300 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03540 | hp2 | a0001 | c0004 | t0004 | g0202 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03579 | hp1 | a0001 | c0001 | t0006 | g0031 | AFR | MSL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03579 | hp2 | a0001 | c0002 | t0011 | g0413 | AFR | MSL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0299 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03669 | hp1 | a0002 | c0003 | t0002 | g0246 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03669 | hp2 | a0001 | c0001 | t0032 | g0219 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03688 | hp1 | a0001 | c0001 | t0006 | g0043 | SAS | STU | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | STU | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03704 | hp2 | a0001 | c0001 | t0030 | g0111 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03710 | hp2 | a0002 | c0003 | t0021 | g0049 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03831 | hp1 | a0001 | c0002 | t0011 | g0045 | SAS | BEB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03831 | hp2 | a0002 | c0003 | t0002 | g0310 | SAS | BEB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0393 | SAS | BEB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0244 | SAS | BEB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0121 | SAS | BEB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | BEB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG04115 | hp1 | a0001 | c0004 | t0004 | g0109 | SAS | STU | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | STU | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | BEB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG04199 | hp1 | a0002 | c0003 | t0002 | g0092 | SAS | STU | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0311 | SAS | STU | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0196 | SAS | STU | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG04204 | hp2 | a0001 | c0017 | t0001 | g0213 | SAS | STU | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | STU | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | STU | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | YRI | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18522 | hp2 | a0001 | c0002 | t0015 | g0269 | AFR | YRI | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0372 | EAS | CHB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | CHB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0377 | EAS | CHB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18906 | hp1 | a0001 | c0002 | t0012 | g0268 | AFR | YRI | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0405 | AFR | YRI | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18942 | hp1 | a0001 | c0002 | t0005 | g0247 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18942 | hp2 | a0002 | c0003 | t0002 | g0375 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18943 | hp1 | a0001 | c0002 | t0013 | g0008 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18943 | hp2 | a0002 | c0003 | t0002 | g0148 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18944 | hp1 | a0001 | c0002 | t0005 | g0228 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18945 | hp1 | a0001 | c0004 | t0004 | g0234 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18945 | hp2 | a0001 | c0002 | t0003 | g0019 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18946 | hp2 | a0001 | c0001 | t0020 | g0230 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18947 | hp1 | a0001 | c0002 | t0005 | g0368 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18947 | hp2 | a0001 | c0004 | t0004 | g0232 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18948 | hp1 | a0002 | c0003 | t0002 | g0135 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18948 | hp2 | a0006 | c0013 | t0001 | g0378 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18950 | hp1 | a0002 | c0003 | t0002 | g0120 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0295 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18951 | hp2 | a0001 | c0005 | t0001 | g0385 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18953 | hp1 | a0001 | c0002 | t0005 | g0125 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18954 | hp2 | a0002 | c0003 | t0002 | g0002 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18957 | hp2 | a0001 | c0004 | t0004 | g0013 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18960 | hp2 | a0002 | c0003 | t0002 | g0255 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18961 | hp1 | a0001 | c0004 | t0004 | g0261 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18961 | hp2 | a0001 | c0002 | t0013 | g0008 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18962 | hp1 | a0002 | c0003 | t0002 | g0332 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18962 | hp2 | a0001 | c0006 | t0001 | g0129 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0395 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18963 | hp2 | a0002 | c0003 | t0002 | g0153 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18964 | hp1 | a0001 | c0005 | t0001 | g0095 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18964 | hp2 | a0001 | c0001 | t0006 | g0048 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18965 | hp1 | a0001 | c0002 | t0003 | g0335 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18965 | hp2 | a0001 | c0002 | t0005 | g0211 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18966 | hp1 | a0002 | c0003 | t0002 | g0383 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18969 | hp2 | a0002 | c0003 | t0002 | g0168 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18970 | hp1 | a0002 | c0003 | t0002 | g0002 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18971 | hp2 | a0002 | c0003 | t0002 | g0124 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18973 | hp1 | a0002 | c0003 | t0002 | g0118 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0381 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18974 | hp1 | a0002 | c0003 | t0002 | g0415 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18974 | hp2 | a0002 | c0003 | t0002 | g0284 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18978 | hp1 | a0002 | c0003 | t0002 | g0099 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18978 | hp2 | a0001 | c0002 | t0005 | g0101 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18980 | hp2 | a0002 | c0003 | t0002 | g0302 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18981 | hp1 | a0007 | c0010 | t0002 | g0002 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18981 | hp2 | a0001 | c0001 | t0020 | g0237 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18982 | hp1 | a0001 | c0002 | t0005 | g0291 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18982 | hp2 | a0001 | c0002 | t0013 | g0166 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18983 | hp1 | a0002 | c0003 | t0002 | g0325 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18983 | hp2 | a0001 | c0004 | t0004 | g0343 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18984 | hp1 | a0001 | c0005 | t0001 | g0016 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18986 | hp1 | a0001 | c0005 | t0001 | g0169 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18986 | hp2 | a0002 | c0003 | t0002 | g0207 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18987 | hp1 | a0002 | c0003 | t0002 | g0331 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18987 | hp2 | a0001 | c0002 | t0005 | g0091 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18989 | hp2 | a0002 | c0003 | t0002 | g0116 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18990 | hp1 | a0001 | c0002 | t0005 | g0329 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18992 | hp1 | a0001 | c0004 | t0004 | g0013 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18992 | hp2 | a0001 | c0006 | t0001 | g0164 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0414 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18997 | hp1 | a0001 | c0005 | t0001 | g0224 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18997 | hp2 | a0002 | c0003 | t0002 | g0322 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18998 | hp1 | a0001 | c0004 | t0004 | g0319 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0416 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18999 | hp2 | a0001 | c0005 | t0001 | g0348 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19001 | hp1 | a0001 | c0002 | t0011 | g0044 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19003 | hp1 | a0002 | c0003 | t0002 | g0254 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19005 | hp1 | a0002 | c0003 | t0002 | g0289 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19007 | hp1 | a0002 | c0003 | t0002 | g0155 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19010 | hp1 | a0001 | c0001 | t0029 | g0014 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19012 | hp1 | a0001 | c0004 | t0004 | g0229 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19030 | hp1 | a0001 | c0001 | t0014 | g0263 | AFR | LWK | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19030 | hp2 | a0001 | c0002 | t0012 | g0132 | AFR | LWK | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19043 | hp1 | a0003 | c0007 | t0004 | g0069 | AFR | LWK | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19043 | hp2 | a0002 | c0003 | t0002 | g0257 | AFR | LWK | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0384 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19054 | hp2 | a0002 | c0003 | t0002 | g0154 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0399 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19056 | hp2 | a0001 | c0006 | t0001 | g0273 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0376 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19060 | hp2 | a0002 | c0003 | t0002 | g0305 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0369 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19063 | hp2 | a0002 | c0003 | t0002 | g0297 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19066 | hp1 | a0001 | c0004 | t0004 | g0210 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19068 | hp2 | a0001 | c0004 | t0004 | g0218 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19074 | hp1 | a0002 | c0003 | t0002 | g0119 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0346 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19079 | hp2 | a0001 | c0012 | t0004 | g0371 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19080 | hp2 | a0001 | c0004 | t0004 | g0212 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19081 | hp1 | a0001 | c0009 | t0001 | g0110 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19082 | hp1 | a0002 | c0003 | t0002 | g0317 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19084 | hp2 | a0001 | c0005 | t0001 | g0225 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19087 | hp1 | a0002 | c0003 | t0002 | g0337 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19087 | hp2 | a0001 | c0008 | t0001 | g0278 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19088 | hp1 | a0002 | c0003 | t0002 | g0065 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19088 | hp2 | a0001 | c0005 | t0001 | g0016 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19089 | hp1 | a0002 | c0003 | t0002 | g0318 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19089 | hp2 | a0001 | c0004 | t0004 | g0370 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0321 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19240 | hp1 | a0002 | c0003 | t0002 | g0400 | AFR | YRI | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19240 | hp2 | a0001 | c0002 | t0008 | g0089 | AFR | YRI | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA20129 | hp1 | a0001 | c0002 | t0005 | g0259 | AFR | ASW | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA20129 | hp2 | a0001 | c0002 | t0005 | g0401 | AFR | ASW | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0217 | EUR | TSI | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0272 | EUR | TSI | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0352 | EUR | TSI | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | TSI | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | GIH | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0327 | SAS | GIH | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01123 | hp1 | a0005 | c0016 | t0001 | g0137 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02109 | hp1 | a0001 | c0001 | t0006 | g0041 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02109 | hp2 | a0001 | c0002 | t0009 | g0004 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02486 | hp1 | a0001 | c0002 | t0010 | g0020 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02486 | hp2 | a0001 | c0002 | t0005 | g0068 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02559 | hp1 | a0001 | c0001 | t0012 | g0083 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02559 | hp2 | a0001 | c0002 | t0008 | g0086 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03471 | hp1 | a0001 | c0002 | t0009 | g0411 | AFR | MSL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03471 | hp2 | a0001 | c0002 | t0003 | g0256 | AFR | MSL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | USA | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0192 | AFR | USA | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | USA | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA20300 | hp2 | a0001 | c0002 | t0017 | g0038 | AFR | USA | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | LWK | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0179 | AFR | LWK | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0198 | REF | REF | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0159 | REF | REF | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:44732330 | C | T | 1 | a0005 | 1 | HG01123.hp1 | missense_variant | MODERATE | c.494C>T | p.Ala165Val | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/8 | 765/1872 | 494/1167 | 165/388 | chr22 | 44732330 | |||
chr22:44735067 | G | A | 1 | a0007 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.596G>A | p.Arg199His | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/8 | 867/1872 | 596/1167 | 199/388 | chr22 | 44735067 | |||
chr22:44735117 | G | A | 1 | a0003 | 2 | HG03486.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.646G>A | p.Gly216Ser | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/8 | 917/1872 | 646/1167 | 216/388 | chr22 | 44735117 | |||
chr22:44736807 | G | A | 2 | a0002 a0007 |
52 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(49): Show |
missense_variant | MODERATE | c.727G>A | p.Val243Met | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 998/1872 | 727/1167 | 243/388 | chr22 | 44736807 | |||
chr22:44736872 | GGAGCACG others(7): Show |
G | 1 | a0006 | 1 | NA18948.hp2 | frameshift_variant | HIGH | c.794_807delAGCACGAG others(6): Show |
p.Glu265fs | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 1065/1872 | 794/1167 | 265/388 | INFO_REALIGN_3_PRIME | chr22 | 44736872 | ||
chr22:44736951 | G | A | 1 | a0004 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.871G>A | p.Glu291Lys | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 1142/1872 | 871/1167 | 291/388 | chr22 | 44736951 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:44725280 | G | A | 1 | a0001c0008 | 1 | NA19087.hp2 | synonymous_variant | LOW | c.252G>A | p.Thr84Thr | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/8 | 523/1872 | 252/1167 | 84/388 | chr22 | 44725280 | |||
chr22:44726603 | G | C | 2 | a0001c0006 a0001c0009 |
4 | NA18962.hp2 NA18992.hp2 NA19056.hp2 others(1): Show |
synonymous_variant | LOW | c.291G>C | p.Val97Val | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/8 | 562/1872 | 291/1167 | 97/388 | chr22 | 44726603 | |||
chr22:44731782 | C | T | 1 | a0001c0017 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.375C>T | p.Asp125Asp | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/8 | 646/1872 | 375/1167 | 125/388 | chr22 | 44731782 | |||
chr22:44732352 | T | C | 7 | a0001c0002 a0001c0004 a0001c0006 others(4): Show |
201 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
synonymous_variant | LOW | c.516T>C | p.Arg172Arg | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/8 | 787/1872 | 516/1167 | 172/388 | chr22 | 44732352 | |||
chr22:44735077 | G | A | 1 | a0001c0005 | 8 | NA18951.hp2 NA18964.hp1 NA18984.hp1 others(5): Show |
synonymous_variant | LOW | c.606G>A | p.Thr202Thr | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/8 | 877/1872 | 606/1167 | 202/388 | chr22 | 44735077 | |||
chr22:44736824 | T | C | 4 | a0001c0004 a0001c0011 a0001c0012 others(1): Show |
44 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(41): Show |
synonymous_variant | LOW | c.744T>C | p.Pro248Pro | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 1015/1872 | 744/1167 | 248/388 | chr22 | 44736824 | |||
chr22:44736845 | C | T | 1 | a0001c0015 | 1 | HG02080.hp2 | synonymous_variant | LOW | c.765C>T | p.Tyr255Tyr | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 1036/1872 | 765/1167 | 255/388 | chr22 | 44736845 | |||
chr22:44736887 | G | A | 1 | a0006c0013 | 1 | NA18948.hp2 | synonymous_variant | LOW | c.807G>A | p.Glu269Glu | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 1078/1872 | 807/1167 | 269/388 | chr22 | 44736887 | |||
chr22:44736905 | T | C | 3 | a0001c0004 a0001c0012 a0003c0007 |
43 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(40): Show |
synonymous_variant | LOW | c.825T>C | p.Gly275Gly | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 1096/1872 | 825/1167 | 275/388 | chr22 | 44736905 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:44702227 | T | G | 11 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0009 others(8): Show |
34 | HG00140.hp1 HG00735.hp2 HG01109.hp2 others(31): Show |
5_prime_UTR_variant | MODIFIER | c.-248T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/8 | 248 | chr22 | 44702227 | ||||||
chr22:44702231 | G | T | 3 | a0001c0001t0014 a0001c0001t0015 a0001c0002t0015 |
6 | HG02258.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-244G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/8 | chr22 | 44702231 | |||||||
chr22:44702255 | T | C | 4 | a0001c0001t0012 a0001c0001t0018 a0001c0002t0012 others(1): Show |
6 | HG02055.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-220T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/8 | 220 | chr22 | 44702255 | ||||||
chr22:44702263 | TCCGTGCA others(9): Show |
T | 3 | a0001c0001t0024 a0001c0002t0026 a0003c0007t0025 |
3 | HG02258.hp1 HG02451.hp1 HG03486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-208_-193delTGCAAT others(10): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/8 | 193 | INFO_REALIGN_3_PRIME | chr22 | 44702263 | |||||
chr22:44702307 | A | G | 4 | a0001c0001t0012 a0001c0001t0018 a0001c0002t0012 others(1): Show |
6 | HG02055.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-168A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/8 | 168 | chr22 | 44702307 | ||||||
chr22:44702391 | C | A | 1 | a0001c0001t0027 | 1 | HG02717.hp2 | 5_prime_UTR_variant | MODIFIER | c.-84C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/8 | 84 | chr22 | 44702391 | ||||||
chr22:44702427 | G | T | 1 | a0001c0002t0033 | 1 | HG03209.hp2 | 5_prime_UTR_variant | MODIFIER | c.-48G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/8 | 48 | chr22 | 44702427 | ||||||
chr22:44737287 | T | C | 1 | a0001c0002t0019 | 2 | HG02572.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*40T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 40 | chr22 | 44737287 | ||||||
chr22:44737343 | C | T | 3 | a0001c0001t0032 a0001c0002t0010 a0001c0002t0017 |
7 | HG02257.hp1 HG02486.hp1 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*96C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 96 | chr22 | 44737343 | ||||||
chr22:44737349 | G | A | 2 | a0001c0001t0029 a0001c0002t0028 |
2 | HG00738.hp1 NA19010.hp1 |
3_prime_UTR_variant | MODIFIER | c.*102G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 102 | chr22 | 44737349 | ||||||
chr22:44737358 | A | G | 32 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0009 others(29): Show |
215 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*111A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 111 | chr22 | 44737358 | ||||||
chr22:44737378 | T | C | 5 | a0001c0004t0004 a0001c0004t0016 a0001c0012t0004 others(2): Show |
43 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*131T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 131 | chr22 | 44737378 | ||||||
chr22:44737414 | A | G | 6 | a0001c0001t0009 a0001c0002t0008 a0001c0002t0009 others(3): Show |
15 | HG01934.hp1 HG02109.hp2 HG02280.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*167A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 167 | chr22 | 44737414 | ||||||
chr22:44737453 | C | G | 6 | a0001c0001t0009 a0001c0002t0008 a0001c0002t0009 others(3): Show |
15 | HG01934.hp1 HG02109.hp2 HG02280.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*206C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 206 | chr22 | 44737453 | ||||||
chr22:44737460 | G | A | 9 | a0001c0002t0005 a0001c0002t0010 a0001c0002t0011 others(6): Show |
95 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*213G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 213 | chr22 | 44737460 | ||||||
chr22:44737530 | C | T | 1 | a0001c0015t0031 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*283C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 283 | chr22 | 44737530 | ||||||
chr22:44737574 | C | A | 1 | a0001c0002t0022 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*327C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 327 | chr22 | 44737574 | ||||||
chr22:44737577 | T | C | 1 | a0001c0001t0030 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*330T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 330 | chr22 | 44737577 | ||||||
chr22:44737587 | G | A | 3 | a0002c0003t0002 a0002c0003t0021 a0007c0010t0002 |
51 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*340G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 340 | chr22 | 44737587 | ||||||
chr22:44737595 | A | G | 1 | a0001c0001t0020 | 2 | NA18946.hp2 NA18981.hp2 |
3_prime_UTR_variant | MODIFIER | c.*348A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 348 | chr22 | 44737595 | ||||||
chr22:44737655 | G | T | 6 | a0001c0002t0013 a0001c0004t0004 a0001c0004t0016 others(3): Show |
46 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*408G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 408 | chr22 | 44737655 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:44702745 | C | G | 5 | a0001c0001t0001g0414 a0001c0001t0003g0019 a0001c0001t0003g0416 others(2): Show |
5 | NA18945.hp2 NA18974.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.134+137C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44702745 | |||||||
chr22:44702990 | C | T | 4 | a0001c0001t0006g0412 a0001c0001t0009g0410 a0001c0002t0009g0411 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.134+382C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44702990 | |||||||
chr22:44703028 | G | T | 1 | a0001c0004t0004g0409 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.134+420G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44703028 | |||||||
chr22:44703107 | G | A | 3 | a0001c0002t0005g0022 a0001c0002t0010g0020 a0001c0002t0019g0021 |
3 | HG02145.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.134+499G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44703107 | |||||||
chr22:44703211 | T | G | 34 | a0001c0001t0006g0028 a0001c0001t0006g0031 a0001c0001t0006g0035 others(31): Show |
34 | HG00140.hp1 HG00735.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.134+603T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44703211 | |||||||
chr22:44703310 | CGGGAGGC others(39): Show |
C | 11 | a0001c0001t0006g0041 a0001c0001t0006g0042 a0001c0001t0006g0043 others(8): Show |
11 | HG00140.hp1 HG00735.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.134+710_134+755del others(46): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44703310 | ||||||
chr22:44703318 | AGTGGACA others(16): Show |
A | 23 | a0001c0001t0006g0028 a0001c0001t0006g0031 a0001c0001t0006g0035 others(20): Show |
23 | HG01109.hp2 HG01433.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.134+740_134+762del others(23): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44703318 | ||||||
chr22:44703586 | T | G | 34 | a0001c0001t0006g0028 a0001c0001t0006g0031 a0001c0001t0006g0035 others(31): Show |
34 | HG00140.hp1 HG00735.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.134+978T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44703586 | |||||||
chr22:44703674 | G | T | 1 | a0001c0002t0008g0408 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.134+1066G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44703674 | |||||||
chr22:44703678 | C | G | 1 | a0001c0002t0003g0407 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.134+1070C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44703678 | |||||||
chr22:44703891 | A | G | 7 | a0001c0001t0001g0402 a0001c0001t0003g0405 a0001c0002t0001g0406 others(4): Show |
7 | HG02257.hp1 HG02572.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.134+1283A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44703891 | |||||||
chr22:44703946 | A | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0277 others(166): Show |
181 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.134+1338A>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44703946 | |||||||
chr22:44703974 | T | C | 6 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
6 | HG00323.hp2 HG01081.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.134+1366T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44703974 | |||||||
chr22:44704309 | G | A | 1 | a0001c0001t0003g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.134+1701G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44704309 | |||||||
chr22:44704312 | G | C | 34 | a0001c0001t0006g0028 a0001c0001t0006g0031 a0001c0001t0006g0035 others(31): Show |
34 | HG00140.hp1 HG00735.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.134+1704G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44704312 | |||||||
chr22:44704339 | A | T | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+1731A>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44704339 | |||||||
chr22:44704475 | C | G | 13 | a0001c0001t0001g0001 a0001c0001t0001g0387 a0001c0001t0001g0388 others(10): Show |
19 | HG00738.hp1 HG00738.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.134+1867C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44704475 | |||||||
chr22:44704610 | C | A | 1 | a0001c0001t0018g0058 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.134+2002C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44704610 | |||||||
chr22:44704747 | A | G | 3 | a0001c0002t0005g0022 a0001c0002t0010g0020 a0001c0002t0019g0021 |
3 | HG02145.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.134+2139A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44704747 | |||||||
chr22:44704794 | G | A | 1 | a0001c0002t0001g0059 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.134+2186G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44704794 | |||||||
chr22:44705049 | C | T | 1 | a0001c0001t0001g0386 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.134+2441C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705049 | |||||||
chr22:44705085 | G | A | 1 | a0001c0002t0033g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.134+2477G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705085 | |||||||
chr22:44705117 | A | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0303 others(105): Show |
118 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.134+2509A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705117 | |||||||
chr22:44705134 | A | C | 1 | a0001c0001t0001g0272 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.134+2526A>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705134 | |||||||
chr22:44705204 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.134+2596T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705204 | |||||||
chr22:44705283 | C | CT | 16 | a0001c0001t0001g0286 a0001c0001t0001g0290 a0001c0001t0001g0292 others(13): Show |
18 | HG00558.hp1 HG02015.hp1 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.134+2678dupT | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44705283 | ||||||
chr22:44705315 | TTC | T | 3 | a0001c0001t0024g0063 a0001c0002t0026g0062 a0003c0007t0025g0064 |
3 | HG02258.hp1 HG02451.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.134+2717_134+2718d others(4): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44705315 | ||||||
chr22:44705328 | T | C | 2 | a0001c0002t0007g0023 a0001c0002t0007g0024 |
2 | HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.134+2720T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705328 | |||||||
chr22:44705348 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.134+2740C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705348 | |||||||
chr22:44705349 | G | A | 1 | a0002c0003t0002g0065 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.134+2741G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705349 | |||||||
chr22:44705362 | T | C | 2 | a0001c0001t0027g0274 a0001c0002t0033g0060 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.134+2754T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705362 | |||||||
chr22:44705364 | T | G | 16 | a0001c0001t0001g0286 a0001c0001t0001g0290 a0001c0001t0001g0292 others(13): Show |
18 | HG00558.hp1 HG02015.hp1 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.134+2756T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705364 | |||||||
chr22:44705447 | T | A | 1 | a0001c0001t0001g0066 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.134+2839T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705447 | |||||||
chr22:44705490 | A | T | 1 | a0001c0005t0001g0385 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.134+2882A>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705490 | |||||||
chr22:44705501 | T | G | 1 | a0001c0001t0001g0185 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.134+2893T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705501 | |||||||
chr22:44705569 | C | T | 3 | a0001c0001t0007g0037 a0001c0002t0017g0038 a0001c0002t0017g0039 |
3 | HG02886.hp1 HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.134+2961C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705569 | |||||||
chr22:44705614 | C | T | 34 | a0001c0001t0006g0028 a0001c0001t0006g0031 a0001c0001t0006g0035 others(31): Show |
34 | HG00140.hp1 HG00735.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.134+3006C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705614 | |||||||
chr22:44705615 | G | A | 2 | a0001c0002t0005g0067 a0001c0002t0005g0068 |
2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.134+3007G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705615 | |||||||
chr22:44705717 | C | T | 1 | a0001c0002t0001g0406 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.134+3109C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705717 | |||||||
chr22:44705767 | G | T | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3159G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705767 | |||||||
chr22:44705768 | G | C | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3160G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705768 | |||||||
chr22:44705775 | C | T | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3167C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705775 | |||||||
chr22:44705778 | C | T | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3170C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705778 | |||||||
chr22:44705780 | A | T | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3172A>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705780 | |||||||
chr22:44705783 | C | T | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3175C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705783 | |||||||
chr22:44705784 | C | A | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3176C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705784 | |||||||
chr22:44705792 | T | G | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3184T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705792 | |||||||
chr22:44705794 | T | A | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3186T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705794 | |||||||
chr22:44705795 | T | A | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3187T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705795 | |||||||
chr22:44705797 | G | C | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3189G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705797 | |||||||
chr22:44705798 | T | A | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3190T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705798 | |||||||
chr22:44705799 | T | C | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3191T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705799 | |||||||
chr22:44705805 | T | C | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3197T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705805 | |||||||
chr22:44705806 | T | A | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3198T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705806 | |||||||
chr22:44705811 | G | C | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3203G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705811 | |||||||
chr22:44705812 | G | C | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3204G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705812 | |||||||
chr22:44705814 | G | C | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3206G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705814 | |||||||
chr22:44705817 | G | C | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3209G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705817 | |||||||
chr22:44705818 | T | C | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3210T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705818 | |||||||
chr22:44705820 | T | C | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3212T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705820 | |||||||
chr22:44705822 | A | G | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3214A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705822 | |||||||
chr22:44705832 | C | G | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3224C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705832 | |||||||
chr22:44705836 | G | C | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3228G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705836 | |||||||
chr22:44705839 | G | T | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3231G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705839 | |||||||
chr22:44705858 | T | C | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3250T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705858 | |||||||
chr22:44705859 | C | G | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3251C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705859 | |||||||
chr22:44705860 | A | T | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3252A>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705860 | |||||||
chr22:44705865 | A | T | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3257A>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705865 | |||||||
chr22:44705866 | T | A | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3258T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705866 | |||||||
chr22:44705869 | C | T | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3261C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705869 | |||||||
chr22:44705870 | A | C | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3262A>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705870 | |||||||
chr22:44705874 | T | A | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3266T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705874 | |||||||
chr22:44705878 | C | G | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3270C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705878 | |||||||
chr22:44705880 | C | T | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3272C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705880 | |||||||
chr22:44705881 | C | G | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3273C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705881 | |||||||
chr22:44705884 | C | CGGCTCAG others(8): Show |
1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3276_134+3277i others(17): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705884 | |||||||
chr22:44705910 | G | C | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3302G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705910 | |||||||
chr22:44705911 | C | G | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3303C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705911 | |||||||
chr22:44705931 | G | A | 35 | a0001c0001t0006g0028 a0001c0001t0006g0031 a0001c0001t0006g0035 others(32): Show |
35 | HG00140.hp1 HG00735.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.134+3323G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705931 | |||||||
chr22:44705936 | C | T | 1 | a0001c0002t0001g0059 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.134+3328C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705936 | |||||||
chr22:44706055 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.134+3447C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44706055 | |||||||
chr22:44706171 | G | C | 1 | a0001c0001t0027g0274 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.134+3563G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44706171 | |||||||
chr22:44706246 | CATTG | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0082 |
3 | NA18969.hp1 NA18999.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.134+3654_134+3657d others(6): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44706246 | ||||||
chr22:44706262 | G | C | 21 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(18): Show |
21 | HG00733.hp1 HG00735.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.134+3654G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44706262 | |||||||
chr22:44706266 | C | G | 2 | a0001c0001t0001g0384 a0002c0003t0002g0383 |
2 | NA18966.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.134+3658C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44706266 | |||||||
chr22:44706682 | C | T | 30 | a0001c0001t0006g0031 a0001c0001t0006g0035 a0001c0001t0006g0036 others(27): Show |
30 | HG00140.hp1 HG00735.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.134+4074C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44706682 | |||||||
chr22:44706700 | G | C | 1 | a0001c0002t0033g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.134+4092G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44706700 | |||||||
chr22:44706845 | GGAGCTAT others(12): Show |
G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0277 others(134): Show |
149 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.134+4239_134+4257d others(21): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44706845 | ||||||
chr22:44706860 | C | T | 30 | a0001c0001t0006g0031 a0001c0001t0006g0035 a0001c0001t0006g0036 others(27): Show |
30 | HG00140.hp1 HG00735.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.134+4252C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44706860 | |||||||
chr22:44706864 | T | A | 1 | a0001c0004t0004g0261 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.134+4256T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44706864 | |||||||
chr22:44706866 | G | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0277 others(134): Show |
149 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.134+4258G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44706866 | |||||||
chr22:44706877 | G | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0277 others(124): Show |
139 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.134+4269G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44706877 | |||||||
chr22:44706879 | G | C | 1 | a0001c0001t0003g0295 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.134+4271G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44706879 | |||||||
chr22:44706946 | G | T | 1 | a0001c0001t0001g0294 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.134+4338G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44706946 | |||||||
chr22:44706951 | G | C | 2 | a0001c0002t0003g0301 a0001c0002t0008g0300 |
2 | HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.134+4343G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44706951 | |||||||
chr22:44706958 | C | T | 4 | a0001c0001t0006g0028 a0001c0002t0005g0022 a0001c0002t0010g0020 others(1): Show |
4 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.134+4350C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44706958 | |||||||
chr22:44707060 | C | T | 1 | a0001c0004t0004g0261 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.134+4452C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44707060 | |||||||
chr22:44707139 | C | G | 1 | a0001c0001t0006g0036 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.134+4531C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44707139 | |||||||
chr22:44707155 | G | A | 1 | a0001c0004t0016g0040 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.134+4547G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44707155 | |||||||
chr22:44707193 | G | A | 1 | a0001c0002t0007g0023 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.134+4585G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44707193 | |||||||
chr22:44707199 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.134+4591A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44707199 | |||||||
chr22:44707386 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.134+4778C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44707386 | |||||||
chr22:44707437 | C | T | 1 | a0001c0002t0001g0382 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.134+4829C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44707437 | |||||||
chr22:44707528 | C | T | 3 | a0001c0001t0006g0035 a0001c0002t0009g0004 a0001c0002t0022g0004 |
3 | HG01934.hp1 HG02109.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.134+4920C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44707528 | |||||||
chr22:44707606 | C | T | 291 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(288): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.134+4998C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44707606 | |||||||
chr22:44707671 | C | T | 3 | a0001c0001t0001g0258 a0001c0002t0005g0259 a0002c0003t0002g0257 |
3 | NA18522.hp1 NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.134+5063C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44707671 | |||||||
chr22:44707755 | C | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0303 others(102): Show |
115 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.134+5147C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44707755 | |||||||
chr22:44707932 | T | C | 1 | a0001c0002t0033g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.134+5324T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44707932 | |||||||
chr22:44707935 | G | A | 2 | a0001c0001t0003g0179 a0001c0002t0008g0180 |
2 | HG03195.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.134+5327G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44707935 | |||||||
chr22:44708059 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.134+5451C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44708059 | |||||||
chr22:44708132 | G | A | 1 | a0001c0002t0008g0408 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.134+5524G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44708132 | |||||||
chr22:44708153 | A | G | 2 | a0001c0002t0005g0275 a0001c0004t0004g0276 |
2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.134+5545A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44708153 | |||||||
chr22:44708161 | C | G | 7 | a0001c0001t0014g0263 a0001c0001t0014g0264 a0001c0001t0014g0265 others(4): Show |
7 | HG02258.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.134+5553C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44708161 | |||||||
chr22:44708186 | C | G | 1 | a0001c0002t0003g0407 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.134+5578C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44708186 | |||||||
chr22:44708363 | G | A | 1 | a0001c0001t0012g0083 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.134+5755G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44708363 | |||||||
chr22:44708445 | C | T | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.134+5837C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44708445 | |||||||
chr22:44708468 | C | T | 30 | a0001c0001t0006g0031 a0001c0001t0006g0035 a0001c0001t0006g0036 others(27): Show |
30 | HG00140.hp1 HG00735.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.134+5860C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44708468 | |||||||
chr22:44708486 | A | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0277 others(165): Show |
180 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.134+5878A>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44708486 | |||||||
chr22:44708491 | A | T | 1 | a0001c0001t0001g0399 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+5883A>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44708491 | |||||||
chr22:44708670 | G | A | 3 | a0001c0002t0003g0070 a0001c0002t0003g0071 a0003c0007t0004g0069 |
3 | HG01243.hp2 HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.135-5921G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44708670 | |||||||
chr22:44708761 | G | C | 1 | a0001c0002t0005g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.135-5830G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44708761 | |||||||
chr22:44708792 | C | T | 32 | a0001c0001t0006g0031 a0001c0001t0006g0035 a0001c0001t0006g0036 others(29): Show |
32 | HG00140.hp1 HG00735.hp2 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.135-5799C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44708792 | |||||||
chr22:44708843 | T | C | 44 | a0001c0001t0001g0087 a0001c0001t0006g0031 a0001c0001t0006g0035 others(41): Show |
44 | HG00140.hp1 HG00735.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.135-5748T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44708843 | |||||||
chr22:44708966 | C | CA | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0072 others(107): Show |
120 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.135-5598dupA | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44708966 | ||||||
chr22:44708966 | C | CAA | 35 | a0001c0001t0001g0087 a0001c0001t0001g0286 a0001c0001t0001g0290 others(32): Show |
36 | HG00438.hp2 HG00558.hp1 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.135-5599_135-5598d others(4): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44708966 | ||||||
chr22:44708966 | CA | C | 14 | a0001c0001t0001g0082 a0001c0001t0001g0163 a0001c0001t0001g0165 others(11): Show |
14 | HG01069.hp1 HG01070.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.135-5598delA | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44708966 | ||||||
chr22:44708966 | CAA | C | 7 | a0001c0001t0014g0264 a0001c0001t0014g0265 a0001c0001t0015g0266 others(4): Show |
7 | HG02055.hp1 HG02258.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.135-5599_135-5598d others(4): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44708966 | ||||||
chr22:44708966 | CAAAAAA | C | 11 | a0001c0001t0006g0041 a0001c0001t0006g0042 a0001c0001t0006g0043 others(8): Show |
11 | HG00140.hp1 HG00735.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.135-5603_135-5598d others(8): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44708966 | ||||||
chr22:44708966 | CAAAAAAA | C | 22 | a0001c0001t0006g0031 a0001c0001t0006g0035 a0001c0001t0006g0036 others(19): Show |
22 | HG01433.hp2 HG01891.hp1 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.135-5604_135-5598d others(9): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44708966 | ||||||
chr22:44708966 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0414 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.135-5607_135-5598d others(12): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44708966 | ||||||
chr22:44708966 | CAAAAAAA others(4): Show |
C | 110 | a0001c0001t0001g0012 a0001c0001t0001g0078 a0001c0001t0001g0079 others(107): Show |
113 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.135-5608_135-5598d others(13): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44708966 | ||||||
chr22:44709036 | G | A | 1 | a0001c0002t0005g0181 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.135-5555G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709036 | |||||||
chr22:44709079 | A | AC | 43 | a0001c0001t0001g0087 a0001c0001t0006g0031 a0001c0001t0006g0035 others(40): Show |
43 | HG00140.hp1 HG00735.hp2 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.135-5512_135-5511i others(3): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709079 | |||||||
chr22:44709096 | C | A | 1 | a0001c0001t0001g0163 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.135-5495C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709096 | |||||||
chr22:44709136 | C | T | 1 | a0001c0002t0003g0256 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.135-5455C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709136 | |||||||
chr22:44709229 | C | T | 87 | a0001c0001t0001g0012 a0001c0001t0001g0078 a0001c0001t0001g0079 others(84): Show |
90 | HG00140.hp2 HG00423.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.135-5362C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709229 | |||||||
chr22:44709230 | G | A | 10 | a0001c0001t0001g0087 a0001c0001t0027g0274 a0001c0002t0003g0070 others(7): Show |
10 | HG01243.hp2 HG02280.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.135-5361G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709230 | |||||||
chr22:44709403 | C | T | 2 | a0001c0002t0005g0104 a0001c0002t0005g0162 |
2 | HG02129.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.135-5188C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709403 | |||||||
chr22:44709432 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.135-5159G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709432 | |||||||
chr22:44709491 | C | T | 1 | a0001c0002t0033g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.135-5100C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709491 | |||||||
chr22:44709492 | T | G | 1 | a0002c0003t0002g0310 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.135-5099T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709492 | |||||||
chr22:44709498 | C | G | 1 | a0001c0001t0001g0376 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.135-5093C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709498 | |||||||
chr22:44709503 | G | A | 1 | a0001c0002t0005g0105 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.135-5088G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709503 | |||||||
chr22:44709534 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.135-5057G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709534 | |||||||
chr22:44709622 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.135-4969C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709622 | |||||||
chr22:44709627 | G | A | 23 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0193 others(20): Show |
23 | HG01168.hp2 HG01433.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.135-4964G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709627 | |||||||
chr22:44709816 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.135-4775C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709816 | |||||||
chr22:44709827 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.135-4764A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709827 | |||||||
chr22:44709838 | C | T | 2 | a0001c0002t0001g0280 a0001c0011t0001g0281 |
2 | HG00609.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.135-4753C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709838 | |||||||
chr22:44709851 | C | CA | 21 | a0001c0001t0001g0286 a0001c0001t0001g0290 a0001c0001t0001g0292 others(18): Show |
23 | HG00558.hp1 HG01109.hp1 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.135-4733dupA | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44709851 | ||||||
chr22:44709881 | G | A | 1 | a0001c0002t0003g0191 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.135-4710G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709881 | |||||||
chr22:44710027 | G | A | 1 | a0001c0002t0001g0107 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.135-4564G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710027 | |||||||
chr22:44710137 | T | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(234): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.135-4454T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710137 | |||||||
chr22:44710285 | AC | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(216): Show |
234 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.135-4296delC | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44710285 | ||||||
chr22:44710285 | ACC | A | 59 | a0001c0001t0001g0097 a0001c0001t0001g0138 a0001c0001t0001g0171 others(56): Show |
62 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.135-4297_135-4296d others(4): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44710285 | ||||||
chr22:44710293 | C | A | 1 | a0001c0002t0001g0217 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.135-4298C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710293 | |||||||
chr22:44710293 | C | G | 60 | a0001c0001t0001g0001 a0001c0001t0001g0087 a0001c0001t0001g0184 others(57): Show |
67 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.135-4298C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710293 | |||||||
chr22:44710353 | C | T | 67 | a0001c0001t0001g0003 a0001c0001t0001g0073 a0001c0001t0001g0117 others(64): Show |
69 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.135-4238C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710353 | |||||||
chr22:44710488 | A | G | 9 | a0001c0001t0001g0066 a0001c0001t0014g0264 a0001c0001t0014g0265 others(6): Show |
9 | HG01243.hp2 HG02258.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.135-4103A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710488 | |||||||
chr22:44710513 | G | T | 4 | a0001c0002t0003g0251 a0001c0002t0005g0249 a0001c0002t0005g0250 others(1): Show |
4 | HG01884.hp1 HG01943.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.135-4078G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710513 | |||||||
chr22:44710515 | C | T | 4 | a0001c0002t0003g0251 a0001c0002t0005g0249 a0001c0002t0005g0250 others(1): Show |
4 | HG01884.hp1 HG01943.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.135-4076C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710515 | |||||||
chr22:44710516 | T | C | 4 | a0001c0002t0003g0251 a0001c0002t0005g0249 a0001c0002t0005g0250 others(1): Show |
4 | HG01884.hp1 HG01943.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.135-4075T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710516 | |||||||
chr22:44710626 | AGC | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0189 a0001c0001t0001g0277 others(36): Show |
46 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.135-3963_135-3962d others(4): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44710626 | ||||||
chr22:44710656 | T | C | 1 | a0002c0003t0002g0116 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.135-3935T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710656 | |||||||
chr22:44710731 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.135-3860G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710731 | |||||||
chr22:44710817 | G | A | 1 | a0001c0002t0005g0022 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.135-3774G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710817 | |||||||
chr22:44710906 | G | A | 100 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(97): Show |
104 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.135-3685G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710906 | |||||||
chr22:44710926 | C | T | 3 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0004t0004g0343 |
3 | NA18957.hp1 NA18983.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.135-3665C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710926 | |||||||
chr22:44710927 | G | A | 3 | a0001c0002t0003g0070 a0001c0002t0003g0071 a0003c0007t0004g0069 |
3 | HG01243.hp2 HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.135-3664G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710927 | |||||||
chr22:44710930 | C | T | 3 | a0001c0001t0001g0258 a0001c0002t0005g0259 a0002c0003t0002g0257 |
3 | NA18522.hp1 NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.135-3661C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710930 | |||||||
chr22:44711101 | A | C | 5 | a0001c0001t0001g0414 a0001c0001t0003g0019 a0001c0001t0003g0416 others(2): Show |
5 | NA18945.hp2 NA18974.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.135-3490A>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711101 | |||||||
chr22:44711102 | G | C | 5 | a0001c0001t0001g0414 a0001c0001t0003g0019 a0001c0001t0003g0416 others(2): Show |
5 | NA18945.hp2 NA18974.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.135-3489G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711102 | |||||||
chr22:44711114 | G | C | 1 | a0002c0003t0002g0302 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.135-3477G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711114 | |||||||
chr22:44711140 | T | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(225): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.135-3451T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711140 | |||||||
chr22:44711159 | T | G | 1 | a0001c0001t0001g0074 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.135-3432T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711159 | |||||||
chr22:44711190 | T | C | 1 | a0001c0001t0009g0410 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.135-3401T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711190 | |||||||
chr22:44711245 | A | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(230): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.135-3346A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711245 | |||||||
chr22:44711249 | G | A | 91 | a0001c0001t0001g0066 a0001c0001t0001g0073 a0001c0001t0001g0117 others(88): Show |
91 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.135-3342G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711249 | |||||||
chr22:44711262 | C | T | 2 | a0001c0002t0005g0022 a0001c0002t0005g0181 |
2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.135-3329C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711262 | |||||||
chr22:44711357 | G | T | 1 | a0001c0002t0001g0188 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.135-3234G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711357 | |||||||
chr22:44711380 | T | C | 413 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(410): Show |
435 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(432): Show |
intron_variant | MODIFIER | c.135-3211T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711380 | |||||||
chr22:44711416 | G | A | 10 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0214 others(7): Show |
10 | HG01168.hp2 HG01255.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.135-3175G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711416 | |||||||
chr22:44711486 | A | AG | 11 | a0001c0001t0001g0245 a0001c0001t0001g0308 a0001c0001t0001g0369 others(8): Show |
11 | HG00735.hp2 HG02451.hp2 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.135-3102dupG | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44711486 | ||||||
chr22:44711598 | A | C | 1 | a0001c0002t0003g0071 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.135-2993A>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711598 | |||||||
chr22:44711686 | C | T | 2 | a0001c0002t0001g0059 a0001c0002t0005g0128 |
2 | HG01109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.135-2905C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711686 | |||||||
chr22:44711797 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.135-2794C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711797 | |||||||
chr22:44711808 | C | G | 2 | a0001c0001t0006g0046 a0001c0001t0006g0047 |
2 | HG00735.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.135-2783C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711808 | |||||||
chr22:44711846 | C | G | 1 | a0001c0004t0004g0276 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.135-2745C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711846 | |||||||
chr22:44711928 | G | A | 4 | a0001c0001t0007g0037 a0001c0002t0017g0038 a0001c0002t0019g0206 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.135-2663G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711928 | |||||||
chr22:44711979 | T | C | 4 | a0001c0001t0001g0190 a0001c0001t0001g0216 a0001c0001t0001g0384 others(1): Show |
4 | NA18960.hp2 NA18967.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.135-2612T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711979 | |||||||
chr22:44711998 | G | C | 1 | a0002c0003t0002g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.135-2593G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711998 | |||||||
chr22:44712045 | C | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(166): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.135-2546C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44712045 | |||||||
chr22:44712081 | A | AGG | 6 | a0001c0001t0006g0035 a0001c0001t0014g0264 a0001c0001t0014g0265 others(3): Show |
6 | HG02258.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.135-2507_135-2506d others(4): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44712081 | ||||||
chr22:44712106 | C | G | 1 | a0001c0001t0001g0066 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.135-2485C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44712106 | |||||||
chr22:44712135 | C | T | 5 | a0001c0001t0001g0061 a0001c0001t0001g0313 a0001c0001t0001g0359 others(2): Show |
5 | HG01981.hp2 HG02293.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.135-2456C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44712135 | |||||||
chr22:44712204 | G | T | 1 | a0001c0005t0001g0385 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.135-2387G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44712204 | |||||||
chr22:44712312 | A | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(166): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.135-2279A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44712312 | |||||||
chr22:44712377 | C | T | 168 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(165): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.135-2214C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44712377 | |||||||
chr22:44712404 | T | C | 56 | a0001c0001t0001g0073 a0001c0001t0001g0117 a0001c0001t0001g0141 others(53): Show |
56 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.135-2187T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44712404 | |||||||
chr22:44712465 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(164): Show |
180 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.135-2126G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44712465 | |||||||
chr22:44712484 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0184 others(61): Show |
73 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.135-2107C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44712484 | |||||||
chr22:44712523 | G | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(165): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.135-2068G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44712523 | |||||||
chr22:44712706 | GCAGCATC others(20): Show |
G | 1 | a0002c0003t0002g0415 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.135-1882_135-1856d others(29): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44712706 | ||||||
chr22:44712709 | G | A | 4 | a0001c0002t0005g0170 a0001c0002t0005g0338 a0001c0002t0005g0379 others(1): Show |
4 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.135-1882G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44712709 | |||||||
chr22:44712800 | C | T | 3 | a0001c0001t0001g0003 a0002c0003t0002g0337 a0006c0013t0001g0378 |
5 | NA18948.hp2 NA18952.hp1 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.135-1791C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44712800 | |||||||
chr22:44712975 | A | G | 1 | a0001c0001t0001g0376 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.135-1616A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44712975 | |||||||
chr22:44713147 | C | T | 187 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(184): Show |
192 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.135-1444C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44713147 | |||||||
chr22:44713223 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(146): Show |
162 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.135-1368G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44713223 | |||||||
chr22:44713225 | G | A | 1 | a0001c0004t0004g0344 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.135-1366G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44713225 | |||||||
chr22:44713331 | A | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(166): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.135-1260A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44713331 | |||||||
chr22:44713413 | G | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(166): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.135-1178G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44713413 | |||||||
chr22:44713553 | G | T | 1 | a0001c0002t0003g0191 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.135-1038G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44713553 | |||||||
chr22:44713661 | C | T | 5 | a0001c0001t0014g0264 a0001c0001t0014g0265 a0001c0001t0015g0266 others(2): Show |
5 | HG02258.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.135-930C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44713661 | |||||||
chr22:44713682 | C | T | 1 | a0001c0002t0006g0050 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.135-909C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44713682 | |||||||
chr22:44713690 | C | T | 10 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0214 others(7): Show |
10 | HG01168.hp2 HG01255.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.135-901C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44713690 | |||||||
chr22:44713786 | C | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(166): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.135-805C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44713786 | |||||||
chr22:44713843 | G | A | 1 | a0001c0002t0003g0407 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.135-748G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44713843 | |||||||
chr22:44713889 | T | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0082 a0001c0001t0001g0158 others(4): Show |
8 | HG00621.hp1 NA18612.hp2 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.135-702T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44713889 | |||||||
chr22:44713948 | C | T | 97 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(94): Show |
102 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.135-643C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44713948 | |||||||
chr22:44714008 | T | G | 1 | a0001c0002t0009g0411 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.135-583T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44714008 | |||||||
chr22:44714123 | CAG | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(170): Show |
187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.135-467_135-466del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44714123 | |||||||
chr22:44714194 | G | A | 4 | a0001c0001t0007g0037 a0001c0002t0017g0038 a0001c0002t0019g0206 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.135-397G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44714194 | |||||||
chr22:44714403 | A | G | 6 | a0001c0001t0006g0035 a0001c0001t0014g0264 a0001c0001t0014g0265 others(3): Show |
6 | HG02258.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.135-188A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44714403 | |||||||
chr22:44714483 | T | TGGCTATC others(13): Show |
1 | a0001c0001t0003g0096 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.135-107_135-88dupG others(19): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44714483 | ||||||
chr22:44714541 | G | C | 1 | a0001c0002t0001g0196 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.135-50G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44714541 | |||||||
chr22:44714584 | C | A | 4 | a0001c0001t0007g0037 a0001c0002t0017g0038 a0001c0002t0019g0206 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG03130.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.135-7C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44714584 | |||||||
chr22:44714705 | T | C | 1 | a0001c0001t0012g0083 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.215+34T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44714705 | |||||||
chr22:44714852 | T | C | 55 | a0001c0001t0001g0073 a0001c0001t0001g0117 a0001c0001t0001g0141 others(52): Show |
55 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.215+181T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44714852 | |||||||
chr22:44714885 | T | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0184 others(64): Show |
76 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.215+214T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44714885 | |||||||
chr22:44714971 | G | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0184 others(58): Show |
70 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.215+300G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44714971 | |||||||
chr22:44714996 | A | G | 110 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(107): Show |
114 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.215+325A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44714996 | |||||||
chr22:44715101 | A | G | 1 | a0001c0001t0012g0083 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.215+430A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44715101 | |||||||
chr22:44715169 | G | A | 354 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(351): Show |
372 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(369): Show |
intron_variant | MODIFIER | c.215+498G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44715169 | |||||||
chr22:44715225 | A | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(138): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.215+554A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44715225 | |||||||
chr22:44715354 | T | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(138): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.215+683T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44715354 | |||||||
chr22:44715397 | G | A | 141 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(138): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.215+726G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44715397 | |||||||
chr22:44715440 | G | A | 55 | a0001c0001t0001g0073 a0001c0001t0001g0117 a0001c0001t0001g0141 others(52): Show |
55 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.215+769G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44715440 | |||||||
chr22:44715488 | A | T | 1 | a0001c0001t0001g0294 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.215+817A>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44715488 | |||||||
chr22:44715518 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.215+847G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44715518 | |||||||
chr22:44715529 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.215+858G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44715529 | |||||||
chr22:44715533 | C | T | 1 | a0002c0003t0002g0155 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.215+862C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44715533 | |||||||
chr22:44715631 | T | G | 2 | a0001c0002t0012g0268 a0001c0002t0015g0269 |
2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.215+960T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44715631 | |||||||
chr22:44715901 | A | G | 34 | a0001c0001t0001g0066 a0001c0001t0001g0245 a0001c0001t0001g0308 others(31): Show |
34 | HG00735.hp2 HG02145.hp2 HG02257.hp1 others(31): Show |
intron_variant | MODIFIER | c.215+1230A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44715901 | |||||||
chr22:44715959 | T | A | 1 | a0002c0003t0002g0310 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.215+1288T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44715959 | |||||||
chr22:44716188 | C | T | 1 | a0001c0001t0003g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.215+1517C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716188 | |||||||
chr22:44716268 | A | G | 12 | a0001c0001t0001g0402 a0001c0001t0018g0131 a0001c0002t0005g0022 others(9): Show |
12 | HG02145.hp2 HG02257.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.215+1597A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716268 | |||||||
chr22:44716308 | C | T | 4 | a0001c0001t0001g0239 a0001c0001t0003g0240 a0001c0001t0003g0241 others(1): Show |
4 | NA18960.hp1 NA18979.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.215+1637C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716308 | |||||||
chr22:44716337 | C | G | 13 | a0001c0001t0001g0066 a0001c0001t0006g0035 a0001c0001t0007g0037 others(10): Show |
13 | HG01109.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.215+1666C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716337 | |||||||
chr22:44716396 | T | C | 36 | a0001c0001t0001g0066 a0001c0001t0001g0245 a0001c0001t0001g0308 others(33): Show |
36 | HG00735.hp2 HG01109.hp1 HG02145.hp2 others(33): Show |
intron_variant | MODIFIER | c.215+1725T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716396 | |||||||
chr22:44716426 | A | G | 36 | a0001c0001t0001g0066 a0001c0001t0001g0245 a0001c0001t0001g0308 others(33): Show |
36 | HG00735.hp2 HG01109.hp1 HG02145.hp2 others(33): Show |
intron_variant | MODIFIER | c.215+1755A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716426 | |||||||
chr22:44716434 | G | A | 36 | a0001c0001t0001g0066 a0001c0001t0001g0245 a0001c0001t0001g0308 others(33): Show |
36 | HG00735.hp2 HG01109.hp1 HG02145.hp2 others(33): Show |
intron_variant | MODIFIER | c.215+1763G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716434 | |||||||
chr22:44716463 | G | C | 56 | a0001c0001t0001g0073 a0001c0001t0001g0117 a0001c0001t0001g0141 others(53): Show |
56 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.215+1792G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716463 | |||||||
chr22:44716500 | C | A | 36 | a0001c0001t0001g0066 a0001c0001t0001g0245 a0001c0001t0001g0308 others(33): Show |
36 | HG00735.hp2 HG01109.hp1 HG02145.hp2 others(33): Show |
intron_variant | MODIFIER | c.215+1829C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716500 | |||||||
chr22:44716640 | G | A | 1 | a0001c0002t0001g0227 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.215+1969G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716640 | |||||||
chr22:44716649 | T | C | 1 | a0001c0001t0001g0315 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.215+1978T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716649 | |||||||
chr22:44716750 | G | C | 2 | a0001c0001t0014g0264 a0001c0001t0014g0265 |
2 | HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.215+2079G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716750 | |||||||
chr22:44716827 | G | A | 1 | a0001c0001t0001g0316 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.215+2156G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716827 | |||||||
chr22:44716847 | G | A | 1 | a0001c0005t0001g0224 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.215+2176G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716847 | |||||||
chr22:44716874 | A | C | 1 | a0001c0001t0003g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.215+2203A>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716874 | |||||||
chr22:44716921 | G | A | 1 | a0001c0004t0004g0218 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.215+2250G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716921 | |||||||
chr22:44716976 | CAT | C | 7 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0214 others(4): Show |
7 | HG01168.hp2 HG01433.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.215+2306_215+2307d others(4): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716976 | |||||||
chr22:44717083 | T | C | 92 | a0001c0001t0001g0066 a0001c0001t0001g0073 a0001c0001t0001g0117 others(89): Show |
92 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.215+2412T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717083 | |||||||
chr22:44717189 | C | CT | 251 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(248): Show |
269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.215+2537dupT | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44717189 | ||||||
chr22:44717189 | C | CTT | 25 | a0001c0001t0001g0066 a0001c0001t0001g0115 a0001c0001t0001g0340 others(22): Show |
26 | HG01106.hp2 HG01243.hp2 HG02135.hp1 others(23): Show |
intron_variant | MODIFIER | c.215+2536_215+2537d others(4): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44717189 | ||||||
chr22:44717189 | C | CTTT | 9 | a0001c0001t0001g0308 a0001c0001t0001g0369 a0001c0001t0006g0047 others(6): Show |
9 | HG00735.hp2 HG03453.hp2 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.215+2535_215+2537d others(5): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44717189 | ||||||
chr22:44717193 | TTTTTTTT others(517): Show |
T | 1 | a0001c0004t0004g0109 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.215+2538_215+3061d others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44717193 | ||||||
chr22:44717206 | T | TG | 3 | a0001c0001t0018g0131 a0001c0002t0012g0132 a0001c0002t0023g0133 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.215+2535_215+2536i others(3): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717206 | |||||||
chr22:44717271 | G | A | 63 | a0001c0001t0001g0066 a0001c0001t0001g0073 a0001c0001t0001g0117 others(60): Show |
63 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.215+2600G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717271 | |||||||
chr22:44717308 | C | G | 1 | a0001c0001t0014g0263 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.215+2637C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717308 | |||||||
chr22:44717309 | G | A | 1 | a0001c0001t0001g0373 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.215+2638G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717309 | |||||||
chr22:44717371 | T | C | 2 | a0001c0002t0005g0170 a0001c0004t0004g0134 |
2 | HG01070.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.215+2700T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717371 | |||||||
chr22:44717374 | T | C | 1 | a0001c0001t0001g0330 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.215+2703T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717374 | |||||||
chr22:44717381 | G | C | 1 | a0001c0001t0003g0096 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.215+2710G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717381 | |||||||
chr22:44717407 | G | T | 1 | a0001c0001t0014g0263 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.215+2736G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717407 | |||||||
chr22:44717533 | C | A | 5 | a0001c0001t0001g0087 a0001c0002t0008g0085 a0001c0002t0008g0089 others(2): Show |
5 | HG02280.hp1 HG02622.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.215+2862C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717533 | |||||||
chr22:44717538 | C | T | 30 | a0001c0001t0001g0066 a0001c0001t0001g0245 a0001c0001t0001g0308 others(27): Show |
30 | HG00735.hp2 HG02145.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.215+2867C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717538 | |||||||
chr22:44717564 | A | G | 30 | a0001c0001t0001g0066 a0001c0001t0001g0245 a0001c0001t0001g0308 others(27): Show |
30 | HG00735.hp2 HG02145.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.215+2893A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717564 | |||||||
chr22:44717574 | G | T | 30 | a0001c0001t0001g0066 a0001c0001t0001g0245 a0001c0001t0001g0308 others(27): Show |
30 | HG00735.hp2 HG02145.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.215+2903G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717574 | |||||||
chr22:44717621 | A | G | 1 | a0002c0003t0002g0383 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.215+2950A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717621 | |||||||
chr22:44717654 | C | T | 4 | a0001c0001t0007g0037 a0001c0002t0017g0038 a0001c0002t0019g0206 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.215+2983C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717654 | |||||||
chr22:44717666 | AG | A | 6 | a0001c0001t0007g0037 a0001c0002t0001g0059 a0001c0002t0005g0128 others(3): Show |
6 | HG01109.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.215+2996delG | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717666 | |||||||
chr22:44717687 | G | A | 1 | a0001c0004t0004g0344 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.215+3016G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717687 | |||||||
chr22:44717697 | G | A | 166 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
171 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.215+3026G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717697 | |||||||
chr22:44717700 | T | C | 353 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(350): Show |
371 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(368): Show |
intron_variant | MODIFIER | c.215+3029T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717700 | |||||||
chr22:44717717 | C | CT | 10 | a0001c0001t0001g0308 a0001c0001t0001g0349 a0001c0001t0001g0369 others(7): Show |
10 | HG01109.hp1 HG01168.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.215+3062dupT | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44717717 | ||||||
chr22:44717717 | CT | C | 11 | a0001c0001t0001g0053 a0001c0001t0001g0171 a0001c0001t0003g0096 others(8): Show |
11 | HG01099.hp2 HG02129.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.215+3062delT | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44717717 | ||||||
chr22:44717773 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.215+3102A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717773 | |||||||
chr22:44717799 | C | T | 1 | a0001c0004t0004g0238 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.215+3128C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717799 | |||||||
chr22:44717851 | G | A | 6 | a0001c0001t0001g0309 a0001c0001t0001g0360 a0001c0001t0001g0381 others(3): Show |
6 | HG00621.hp2 HG02056.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.215+3180G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717851 | |||||||
chr22:44717874 | A | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(160): Show |
176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.215+3203A>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717874 | |||||||
chr22:44717876 | C | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(160): Show |
176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.215+3205C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717876 | |||||||
chr22:44717888 | T | G | 1 | a0001c0001t0027g0274 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.215+3217T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717888 | |||||||
chr22:44717953 | G | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(130): Show |
146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.215+3282G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717953 | |||||||
chr22:44717964 | C | T | 1 | a0001c0004t0004g0262 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.215+3293C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717964 | |||||||
chr22:44717995 | G | A | 16 | a0001c0001t0001g0115 a0001c0001t0003g0057 a0001c0001t0006g0031 others(13): Show |
16 | HG01106.hp2 HG01243.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.215+3324G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717995 | |||||||
chr22:44718014 | C | T | 1 | a0001c0001t0003g0377 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.215+3343C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44718014 | |||||||
chr22:44718024 | C | T | 1 | a0002c0003t0002g0331 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.215+3353C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44718024 | |||||||
chr22:44718042 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(160): Show |
176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.215+3371A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44718042 | |||||||
chr22:44718052 | A | G | 6 | a0001c0001t0007g0037 a0001c0002t0001g0059 a0001c0002t0005g0128 others(3): Show |
6 | HG01109.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.215+3381A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44718052 | |||||||
chr22:44718161 | A | G | 7 | a0001c0001t0001g0395 a0001c0001t0001g0397 a0001c0002t0001g0017 others(4): Show |
8 | HG00738.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.215+3490A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44718161 | |||||||
chr22:44718192 | C | CT | 127 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(124): Show |
131 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.215+3541dupT | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44718192 | ||||||
chr22:44718192 | C | CTT | 59 | a0001c0001t0001g0007 a0001c0001t0001g0073 a0001c0001t0001g0081 others(56): Show |
60 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.215+3540_215+3541d others(4): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44718192 | ||||||
chr22:44718192 | C | CTTTT | 6 | a0001c0001t0001g0390 a0001c0001t0012g0083 a0001c0004t0004g0355 others(3): Show |
6 | HG01256.hp2 HG01943.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.215+3538_215+3541d others(6): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44718192 | ||||||
chr22:44718192 | C | CTTTTT | 53 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0184 others(50): Show |
62 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.215+3537_215+3541d others(7): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44718192 | ||||||
chr22:44718192 | C | CTTTTTT | 65 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0061 others(62): Show |
69 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.215+3536_215+3541d others(8): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44718192 | ||||||
chr22:44718192 | C | CTTTTTTT | 12 | a0001c0001t0001g0051 a0001c0001t0001g0066 a0001c0001t0001g0103 others(9): Show |
12 | HG02258.hp2 HG02818.hp1 HG03486.hp1 others(9): Show |
intron_variant | MODIFIER | c.215+3535_215+3541d others(9): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44718192 | ||||||
chr22:44718192 | C | CTTTTTTT others(1): Show |
14 | a0001c0001t0001g0165 a0001c0001t0001g0245 a0001c0001t0001g0308 others(11): Show |
14 | HG00735.hp2 HG01167.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.215+3534_215+3541d others(10): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44718192 | ||||||
chr22:44718192 | C | CTTTTTTT others(2): Show |
10 | a0001c0001t0001g0369 a0001c0001t0001g0402 a0001c0001t0006g0035 others(7): Show |
10 | HG02572.hp2 HG02886.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.215+3533_215+3541d others(11): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44718192 | ||||||
chr22:44718192 | C | CTTTTTTT others(3): Show |
1 | a0001c0002t0010g0403 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.215+3532_215+3541d others(12): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44718192 | ||||||
chr22:44718297 | C | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(160): Show |
176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.215+3626C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44718297 | |||||||
chr22:44718342 | G | A | 1 | a0001c0006t0001g0273 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.215+3671G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44718342 | |||||||
chr22:44718440 | C | T | 1 | a0001c0001t0009g0410 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.215+3769C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44718440 | |||||||
chr22:44718637 | AG | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(161): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.215+3968delG | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44718637 | ||||||
chr22:44718749 | G | A | 6 | a0001c0001t0007g0037 a0001c0002t0001g0059 a0001c0002t0005g0128 others(3): Show |
6 | HG01109.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.215+4078G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44718749 | |||||||
chr22:44718962 | C | T | 1 | a0001c0001t0006g0035 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.215+4291C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44718962 | |||||||
chr22:44718968 | C | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(160): Show |
176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.215+4297C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44718968 | |||||||
chr22:44719089 | C | CT | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(162): Show |
178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.215+4433dupT | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44719089 | ||||||
chr22:44719089 | C | CTTT | 6 | a0001c0001t0007g0037 a0001c0002t0001g0059 a0001c0002t0005g0128 others(3): Show |
6 | HG01109.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.215+4431_215+4433d others(5): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44719089 | ||||||
chr22:44719120 | G | A | 3 | a0001c0001t0001g0056 a0001c0001t0001g0243 a0001c0001t0001g0362 |
3 | HG01261.hp2 HG01515.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.215+4449G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719120 | |||||||
chr22:44719142 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(160): Show |
176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.215+4471T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719142 | |||||||
chr22:44719145 | A | G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0127 |
2 | HG03704.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.215+4474A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719145 | |||||||
chr22:44719153 | C | G | 1 | a0001c0001t0001g0126 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.215+4482C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719153 | |||||||
chr22:44719160 | G | A | 1 | a0001c0004t0004g0363 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.215+4489G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719160 | |||||||
chr22:44719167 | C | A | 7 | a0001c0001t0001g0066 a0001c0001t0006g0035 a0001c0001t0014g0264 others(4): Show |
7 | HG02258.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.215+4496C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719167 | |||||||
chr22:44719240 | T | C | 6 | a0001c0001t0007g0037 a0001c0002t0001g0059 a0001c0002t0005g0128 others(3): Show |
6 | HG01109.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.215+4569T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719240 | |||||||
chr22:44719246 | AT | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(167): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.215+4585delT | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44719246 | ||||||
chr22:44719248 | T | A | 1 | a0001c0001t0014g0263 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.215+4577T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719248 | |||||||
chr22:44719499 | T | C | 1 | a0001c0001t0014g0263 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.215+4828T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719499 | |||||||
chr22:44719519 | A | G | 39 | a0001c0001t0001g0115 a0001c0001t0001g0245 a0001c0001t0001g0308 others(36): Show |
39 | HG00735.hp2 HG01106.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.215+4848A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719519 | |||||||
chr22:44719534 | G | A | 6 | a0001c0001t0007g0037 a0001c0002t0001g0059 a0001c0002t0005g0128 others(3): Show |
6 | HG01109.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.215+4863G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719534 | |||||||
chr22:44719538 | G | A | 3 | a0001c0001t0001g0195 a0001c0001t0001g0270 a0001c0002t0001g0205 |
3 | HG00099.hp1 HG03239.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.215+4867G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719538 | |||||||
chr22:44719544 | G | A | 6 | a0001c0001t0007g0037 a0001c0002t0001g0059 a0001c0002t0005g0128 others(3): Show |
6 | HG01109.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.215+4873G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719544 | |||||||
chr22:44719604 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(137): Show |
153 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.215+4933G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719604 | |||||||
chr22:44719617 | G | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(137): Show |
153 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.215+4946G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719617 | |||||||
chr22:44719652 | T | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(137): Show |
153 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.215+4981T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719652 | |||||||
chr22:44719671 | T | C | 6 | a0001c0001t0007g0037 a0001c0002t0001g0059 a0001c0002t0005g0128 others(3): Show |
6 | HG01109.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.215+5000T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719671 | |||||||
chr22:44719699 | A | G | 354 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(351): Show |
372 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(369): Show |
intron_variant | MODIFIER | c.215+5028A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719699 | |||||||
chr22:44719871 | GCAAACCC others(11): Show |
G | 1 | a0001c0002t0005g0291 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.215+5201_215+5218d others(20): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719871 | |||||||
chr22:44719877 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(176): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.215+5206C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719877 | |||||||
chr22:44720024 | G | A | 174 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(171): Show |
179 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.216-5220G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720024 | |||||||
chr22:44720076 | C | G | 1 | a0001c0002t0008g0085 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.216-5168C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720076 | |||||||
chr22:44720168 | C | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(129): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.216-5076C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720168 | |||||||
chr22:44720247 | G | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(129): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.216-4997G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720247 | |||||||
chr22:44720287 | C | T | 3 | a0001c0001t0018g0131 a0001c0002t0012g0132 a0001c0002t0023g0133 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.216-4957C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720287 | |||||||
chr22:44720290 | G | A | 75 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0051 others(72): Show |
79 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.216-4954G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720290 | |||||||
chr22:44720291 | G | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(129): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.216-4953G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720291 | |||||||
chr22:44720311 | C | T | 166 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
171 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.216-4933C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720311 | |||||||
chr22:44720323 | A | G | 339 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(336): Show |
357 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(354): Show |
intron_variant | MODIFIER | c.216-4921A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720323 | |||||||
chr22:44720364 | C | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(129): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.216-4880C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720364 | |||||||
chr22:44720561 | A | G | 168 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
173 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.216-4683A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720561 | |||||||
chr22:44720570 | G | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(129): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.216-4674G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720570 | |||||||
chr22:44720608 | C | T | 1 | a0001c0002t0033g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.216-4636C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720608 | |||||||
chr22:44720614 | G | A | 353 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(350): Show |
371 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(368): Show |
intron_variant | MODIFIER | c.216-4630G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720614 | |||||||
chr22:44720727 | T | C | 2 | a0001c0002t0001g0059 a0001c0002t0005g0128 |
2 | HG01109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.216-4517T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720727 | |||||||
chr22:44720727 | T | G | 4 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(1): Show |
4 | HG00323.hp2 HG01099.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.216-4517T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720727 | |||||||
chr22:44720784 | T | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(142): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.216-4460T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720784 | |||||||
chr22:44720814 | C | T | 1 | a0001c0001t0003g0416 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.216-4430C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720814 | |||||||
chr22:44720920 | A | G | 312 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(309): Show |
330 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.216-4324A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720920 | |||||||
chr22:44720982 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.216-4262G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720982 | |||||||
chr22:44721097 | C | A | 55 | a0001c0001t0001g0007 a0001c0001t0001g0073 a0001c0001t0001g0117 others(52): Show |
56 | HG00438.hp1 HG00609.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.216-4147C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721097 | |||||||
chr22:44721099 | G | A | 3 | a0001c0002t0003g0251 a0001c0002t0005g0249 a0001c0002t0005g0250 |
3 | HG01884.hp1 HG01943.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.216-4145G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721099 | |||||||
chr22:44721099 | G | T | 3 | a0001c0004t0004g0262 a0001c0004t0004g0339 a0001c0004t0004g0380 |
3 | HG02809.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.216-4145G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721099 | |||||||
chr22:44721248 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.216-3996G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721248 | |||||||
chr22:44721298 | C | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(135): Show |
151 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.216-3946C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721298 | |||||||
chr22:44721423 | C | T | 4 | a0001c0001t0001g0239 a0001c0001t0003g0240 a0001c0001t0003g0241 others(1): Show |
4 | NA18960.hp1 NA18979.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.216-3821C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721423 | |||||||
chr22:44721551 | G | A | 1 | a0001c0009t0001g0110 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.216-3693G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721551 | |||||||
chr22:44721554 | T | C | 280 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(277): Show |
295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.216-3690T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721554 | |||||||
chr22:44721676 | C | A | 110 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(107): Show |
113 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.216-3568C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721676 | |||||||
chr22:44721679 | C | G | 4 | a0001c0001t0001g0309 a0001c0001t0001g0381 a0001c0002t0005g0228 others(1): Show |
4 | NA18944.hp1 NA18973.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.216-3565C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721679 | |||||||
chr22:44721714 | T | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(218): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.216-3530T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721714 | |||||||
chr22:44721749 | C | G | 93 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(90): Show |
97 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.216-3495C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721749 | |||||||
chr22:44721750 | G | A | 1 | a0005c0016t0001g0137 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.216-3494G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721750 | |||||||
chr22:44721760 | C | A | 1 | a0001c0001t0001g0009 | 2 | NA19004.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.216-3484C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721760 | |||||||
chr22:44721917 | G | C | 283 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(280): Show |
300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.216-3327G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721917 | |||||||
chr22:44721993 | T | A | 1 | a0001c0001t0001g0314 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.216-3251T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721993 | |||||||
chr22:44722022 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.216-3222C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44722022 | |||||||
chr22:44722037 | G | A | 1 | a0001c0001t0024g0063 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.216-3207G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44722037 | |||||||
chr22:44722073 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0314 |
2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.216-3171C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44722073 | |||||||
chr22:44722086 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.216-3158G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44722086 | |||||||
chr22:44722183 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.216-3061G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44722183 | |||||||
chr22:44722239 | T | C | 1 | a0002c0003t0002g0099 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.216-3005T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44722239 | |||||||
chr22:44722401 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.216-2843C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44722401 | |||||||
chr22:44722435 | G | A | 1 | a0001c0002t0017g0038 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.216-2809G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44722435 | |||||||
chr22:44722653 | T | G | 107 | a0001c0001t0001g0009 a0001c0001t0001g0078 a0001c0001t0001g0079 others(104): Show |
110 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.216-2591T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44722653 | |||||||
chr22:44722670 | T | A | 324 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(321): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.216-2574T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44722670 | |||||||
chr22:44722744 | G | T | 105 | a0001c0001t0001g0009 a0001c0001t0001g0078 a0001c0001t0001g0079 others(102): Show |
108 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.216-2500G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44722744 | |||||||
chr22:44722767 | T | C | 128 | a0001c0001t0001g0009 a0001c0001t0001g0078 a0001c0001t0001g0079 others(125): Show |
132 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.216-2477T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44722767 | |||||||
chr22:44722983 | C | T | 1 | a0001c0002t0005g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.216-2261C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44722983 | |||||||
chr22:44722988 | CT | C | 76 | a0001c0001t0001g0007 a0001c0001t0001g0075 a0001c0001t0001g0079 others(73): Show |
78 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.216-2241delT | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44722988 | ||||||
chr22:44722988 | CTT | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(108): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.216-2242_216-2241d others(4): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44722988 | ||||||
chr22:44723048 | C | T | 64 | a0001c0001t0001g0007 a0001c0001t0001g0103 a0001c0001t0001g0112 others(61): Show |
66 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.216-2196C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723048 | |||||||
chr22:44723054 | C | G | 127 | a0001c0001t0001g0009 a0001c0001t0001g0078 a0001c0001t0001g0079 others(124): Show |
131 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.216-2190C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723054 | |||||||
chr22:44723059 | C | T | 1 | a0001c0002t0005g0368 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.216-2185C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723059 | |||||||
chr22:44723078 | C | T | 1 | a0001c0001t0007g0034 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.216-2166C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723078 | |||||||
chr22:44723143 | G | A | 53 | a0001c0001t0001g0007 a0001c0001t0001g0103 a0001c0001t0001g0112 others(50): Show |
55 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.216-2101G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723143 | |||||||
chr22:44723164 | TTAG | T | 4 | a0001c0001t0001g0145 a0001c0001t0001g0161 a0001c0001t0001g0174 others(1): Show |
4 | HG00558.hp2 NA18959.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.216-2076_216-2074d others(5): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44723164 | ||||||
chr22:44723203 | C | T | 1 | a0001c0001t0027g0274 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.216-2041C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723203 | |||||||
chr22:44723317 | G | A | 3 | a0001c0002t0008g0085 a0001c0002t0008g0089 a0001c0002t0008g0090 |
3 | HG02280.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.216-1927G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723317 | |||||||
chr22:44723421 | A | G | 1 | a0001c0001t0006g0412 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.216-1823A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723421 | |||||||
chr22:44723437 | G | T | 1 | a0001c0002t0005g0291 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.216-1807G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723437 | |||||||
chr22:44723458 | G | A | 5 | a0001c0001t0006g0036 a0001c0001t0007g0025 a0001c0001t0007g0034 others(2): Show |
5 | HG01109.hp2 HG01433.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.216-1786G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723458 | |||||||
chr22:44723523 | C | G | 1 | a0001c0002t0005g0182 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.216-1721C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723523 | |||||||
chr22:44723551 | C | G | 15 | a0001c0001t0001g0402 a0001c0001t0003g0077 a0001c0001t0014g0263 others(12): Show |
15 | HG02257.hp1 HG02486.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.216-1693C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723551 | |||||||
chr22:44723592 | C | T | 1 | a0001c0004t0016g0029 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.216-1652C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723592 | |||||||
chr22:44723593 | G | T | 2 | a0001c0004t0004g0011 a0001c0004t0004g0202 |
3 | HG00642.hp2 HG01175.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.216-1651G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723593 | |||||||
chr22:44723674 | C | T | 11 | a0001c0001t0001g0193 a0001c0001t0003g0179 a0001c0001t0003g0192 others(8): Show |
11 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.216-1570C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723674 | |||||||
chr22:44723779 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(109): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.216-1465G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723779 | |||||||
chr22:44723801 | A | G | 2 | a0002c0003t0002g0065 a0002c0003t0002g0254 |
2 | NA19003.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.216-1443A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723801 | |||||||
chr22:44724019 | T | C | 1 | a0001c0015t0031g0358 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.216-1225T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724019 | |||||||
chr22:44724048 | G | A | 15 | a0001c0001t0001g0402 a0001c0001t0003g0077 a0001c0001t0014g0263 others(12): Show |
15 | HG02257.hp1 HG02486.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.216-1196G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724048 | |||||||
chr22:44724080 | T | G | 1 | a0001c0001t0001g0330 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.216-1164T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724080 | |||||||
chr22:44724102 | C | T | 1 | a0001c0001t0006g0035 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.216-1142C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724102 | |||||||
chr22:44724320 | C | T | 1 | a0001c0004t0004g0367 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.216-924C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724320 | |||||||
chr22:44724333 | G | A | 1 | a0001c0002t0005g0401 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.216-911G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724333 | |||||||
chr22:44724424 | A | C | 1 | a0002c0003t0002g0284 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.216-820A>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724424 | |||||||
chr22:44724490 | T | C | 1 | a0002c0003t0002g0284 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.216-754T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724490 | |||||||
chr22:44724491 | C | T | 1 | a0002c0003t0002g0284 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.216-753C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724491 | |||||||
chr22:44724492 | T | G | 1 | a0002c0003t0002g0284 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.216-752T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724492 | |||||||
chr22:44724543 | G | A | 10 | a0001c0001t0001g0141 a0001c0001t0001g0277 a0001c0002t0001g0208 others(7): Show |
10 | HG00609.hp1 HG00673.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.216-701G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724543 | |||||||
chr22:44724625 | A | G | 1 | a0001c0002t0005g0291 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.216-619A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724625 | |||||||
chr22:44724719 | T | C | 4 | a0001c0001t0003g0183 a0001c0001t0014g0264 a0001c0004t0004g0136 others(1): Show |
4 | HG01168.hp1 HG02683.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.216-525T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724719 | |||||||
chr22:44724758 | A | G | 2 | a0001c0001t0001g0087 a0001c0002t0017g0038 |
2 | HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.216-486A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724758 | |||||||
chr22:44724769 | T | A | 1 | a0001c0002t0005g0291 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.216-475T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724769 | |||||||
chr22:44725058 | C | G | 15 | a0001c0002t0001g0059 a0001c0002t0005g0067 a0001c0002t0005g0068 others(12): Show |
15 | HG01109.hp1 HG01496.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.216-186C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44725058 | |||||||
chr22:44725070 | G | C | 1 | a0001c0002t0005g0291 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.216-174G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44725070 | |||||||
chr22:44725548 | G | A | 50 | a0001c0001t0001g0009 a0001c0001t0001g0056 a0001c0001t0001g0078 others(47): Show |
51 | HG00408.hp2 HG00423.hp1 HG01255.hp2 others(48): Show |
intron_variant | MODIFIER | c.264+256G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44725548 | |||||||
chr22:44725627 | C | T | 1 | a0001c0002t0001g0059 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.264+335C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44725627 | |||||||
chr22:44725659 | T | TTTG | 88 | a0001c0001t0001g0141 a0001c0001t0001g0143 a0001c0001t0001g0158 others(85): Show |
92 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.264+389_264+391dup others(3): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr22 | 44725659 | ||||||
chr22:44725659 | TTTGTTG | T | 4 | a0001c0001t0015g0267 a0001c0002t0003g0301 a0001c0002t0007g0023 others(1): Show |
4 | HG01891.hp1 HG02615.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.264+386_264+391del others(6): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr22 | 44725659 | ||||||
chr22:44725917 | A | G | 326 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(323): Show |
346 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(343): Show |
intron_variant | MODIFIER | c.264+625A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44725917 | |||||||
chr22:44725940 | C | T | 3 | a0001c0002t0003g0256 a0001c0002t0005g0250 a0001c0002t0023g0133 |
3 | HG01943.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.265-637C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44725940 | |||||||
chr22:44725945 | G | A | 36 | a0001c0001t0001g0009 a0001c0001t0001g0056 a0001c0001t0001g0078 others(33): Show |
37 | HG00408.hp2 HG00423.hp1 HG02015.hp2 others(34): Show |
intron_variant | MODIFIER | c.265-632G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44725945 | |||||||
chr22:44725957 | G | A | 1 | a0001c0008t0001g0278 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.265-620G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44725957 | |||||||
chr22:44725961 | G | A | 2 | a0001c0001t0001g0087 a0001c0002t0005g0252 |
2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.265-616G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44725961 | |||||||
chr22:44725984 | T | C | 344 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(341): Show |
365 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(362): Show |
intron_variant | MODIFIER | c.265-593T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44725984 | |||||||
chr22:44725999 | G | C | 1 | a0001c0002t0001g0080 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.265-578G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44725999 | |||||||
chr22:44726001 | C | G | 340 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(337): Show |
360 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(357): Show |
intron_variant | MODIFIER | c.265-576C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44726001 | |||||||
chr22:44726034 | A | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(172): Show |
189 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.265-543A>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44726034 | |||||||
chr22:44726097 | A | G | 14 | a0001c0001t0006g0028 a0001c0001t0018g0058 a0001c0002t0001g0059 others(11): Show |
14 | HG01109.hp1 HG01934.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.265-480A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44726097 | |||||||
chr22:44726184 | G | A | 1 | a0001c0001t0003g0077 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.265-393G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44726184 | |||||||
chr22:44726196 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.265-381T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44726196 | |||||||
chr22:44726379 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.265-198C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44726379 | |||||||
chr22:44726657 | C | T | 1 | a0001c0002t0012g0268 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.322+23C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44726657 | |||||||
chr22:44726696 | T | C | 5 | a0001c0001t0009g0410 a0001c0001t0014g0265 a0001c0002t0005g0182 others(2): Show |
5 | HG02717.hp1 HG02895.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.322+62T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44726696 | |||||||
chr22:44726767 | C | T | 1 | a0001c0001t0003g0077 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.322+133C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44726767 | |||||||
chr22:44726835 | C | T | 1 | a0001c0002t0005g0259 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.322+201C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44726835 | |||||||
chr22:44726881 | C | G | 1 | a0001c0001t0001g0178 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.322+247C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44726881 | |||||||
chr22:44726904 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.322+270C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44726904 | |||||||
chr22:44726986 | C | G | 325 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(322): Show |
346 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(343): Show |
intron_variant | MODIFIER | c.322+352C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44726986 | |||||||
chr22:44727126 | A | G | 1 | a0001c0012t0004g0371 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.322+492A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727126 | |||||||
chr22:44727140 | G | A | 1 | a0001c0001t0001g0341 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.322+506G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727140 | |||||||
chr22:44727155 | CA | C | 8 | a0001c0001t0006g0046 a0001c0001t0006g0047 a0001c0001t0006g0412 others(5): Show |
8 | HG00280.hp2 HG00735.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.322+522delA | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727155 | |||||||
chr22:44727161 | T | C | 1 | a0001c0002t0033g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.322+527T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727161 | |||||||
chr22:44727161 | T | G | 7 | a0001c0001t0006g0046 a0001c0001t0006g0047 a0001c0001t0006g0412 others(4): Show |
7 | HG00280.hp2 HG00735.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.322+527T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727161 | |||||||
chr22:44727204 | A | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(130): Show |
147 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.322+570A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727204 | |||||||
chr22:44727210 | T | C | 1 | a0001c0002t0008g0408 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.322+576T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727210 | |||||||
chr22:44727228 | C | T | 1 | a0002c0003t0002g0246 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.322+594C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727228 | |||||||
chr22:44727238 | C | T | 2 | a0001c0001t0003g0293 a0001c0005t0001g0016 |
3 | HG02071.hp1 NA18984.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.322+604C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727238 | |||||||
chr22:44727304 | G | A | 3 | a0001c0002t0005g0128 a0001c0002t0005g0275 a0001c0004t0004g0204 |
3 | HG02647.hp1 HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.322+670G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727304 | |||||||
chr22:44727335 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.322+701C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727335 | |||||||
chr22:44727339 | G | A | 1 | a0001c0001t0001g0395 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.322+705G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727339 | |||||||
chr22:44727370 | G | T | 1 | a0001c0001t0003g0167 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.322+736G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727370 | |||||||
chr22:44727480 | G | T | 1 | a0001c0001t0001g0349 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.322+846G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727480 | |||||||
chr22:44727536 | G | A | 6 | a0001c0002t0003g0191 a0001c0002t0003g0251 a0001c0002t0003g0301 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.322+902G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727536 | |||||||
chr22:44727601 | C | T | 3 | a0001c0001t0006g0035 a0001c0004t0004g0262 a0001c0004t0016g0029 |
3 | HG02622.hp1 HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.322+967C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727601 | |||||||
chr22:44727623 | G | C | 57 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(54): Show |
60 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.322+989G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727623 | |||||||
chr22:44727673 | C | T | 10 | a0001c0002t0008g0085 a0001c0002t0008g0086 a0001c0002t0008g0089 others(7): Show |
10 | HG01934.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.322+1039C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727673 | |||||||
chr22:44727685 | C | G | 1 | a0001c0001t0003g0293 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.322+1051C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727685 | |||||||
chr22:44727745 | G | A | 45 | a0001c0001t0001g0239 a0001c0001t0001g0258 a0001c0001t0003g0014 others(42): Show |
46 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.322+1111G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727745 | |||||||
chr22:44727800 | C | A | 1 | a0001c0002t0026g0062 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.322+1166C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727800 | |||||||
chr22:44727812 | A | G | 4 | a0001c0002t0001g0017 a0001c0002t0001g0080 a0001c0002t0001g0393 others(1): Show |
5 | HG01257.hp2 HG01258.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.322+1178A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727812 | |||||||
chr22:44727866 | C | G | 51 | a0001c0001t0001g0239 a0001c0001t0001g0258 a0001c0001t0003g0014 others(48): Show |
52 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.322+1232C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727866 | |||||||
chr22:44727874 | C | T | 1 | a0001c0002t0001g0244 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.322+1240C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727874 | |||||||
chr22:44727926 | C | T | 1 | a0001c0002t0005g0275 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.322+1292C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727926 | |||||||
chr22:44727961 | C | G | 386 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(383): Show |
408 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(405): Show |
intron_variant | MODIFIER | c.322+1327C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727961 | |||||||
chr22:44727994 | G | A | 4 | a0001c0002t0001g0017 a0001c0002t0001g0080 a0001c0002t0001g0393 others(1): Show |
5 | HG01257.hp2 HG01258.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.322+1360G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727994 | |||||||
chr22:44728093 | G | A | 1 | a0001c0002t0005g0101 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.322+1459G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728093 | |||||||
chr22:44728097 | G | C | 169 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(166): Show |
176 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.322+1463G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728097 | |||||||
chr22:44728099 | C | T | 1 | a0002c0003t0002g0289 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.322+1465C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728099 | |||||||
chr22:44728156 | A | G | 168 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
175 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.322+1522A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728156 | |||||||
chr22:44728283 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.322+1649G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728283 | |||||||
chr22:44728415 | A | C | 155 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
162 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.322+1781A>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728415 | |||||||
chr22:44728470 | C | T | 91 | a0001c0001t0001g0347 a0001c0001t0001g0360 a0001c0001t0003g0108 others(88): Show |
94 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.322+1836C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728470 | |||||||
chr22:44728471 | G | A | 2 | a0001c0001t0014g0265 a0001c0002t0026g0062 |
2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.322+1837G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728471 | |||||||
chr22:44728482 | T | C | 3 | a0001c0002t0005g0211 a0001c0009t0001g0110 a0002c0003t0002g0253 |
3 | HG00673.hp1 NA18965.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.322+1848T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728482 | |||||||
chr22:44728497 | G | A | 1 | a0001c0004t0004g0262 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.322+1863G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728497 | |||||||
chr22:44728540 | C | T | 4 | a0001c0001t0001g0193 a0001c0001t0009g0410 a0001c0001t0014g0265 others(1): Show |
4 | HG01891.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.322+1906C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728540 | |||||||
chr22:44728560 | T | G | 6 | a0001c0002t0003g0191 a0001c0002t0003g0251 a0001c0002t0003g0301 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.322+1926T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728560 | |||||||
chr22:44728634 | C | T | 2 | a0001c0001t0001g0245 a0002c0003t0002g0246 |
2 | HG02683.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.322+2000C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728634 | |||||||
chr22:44728661 | C | T | 1 | a0001c0002t0008g0408 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.322+2027C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728661 | |||||||
chr22:44728665 | T | C | 1 | a0002c0003t0002g0305 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.322+2031T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728665 | |||||||
chr22:44728715 | T | G | 64 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(61): Show |
75 | HG00280.hp1 HG00438.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.322+2081T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728715 | |||||||
chr22:44728729 | G | A | 1 | a0002c0003t0002g0297 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.322+2095G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728729 | |||||||
chr22:44728730 | A | G | 1 | a0002c0003t0002g0297 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.322+2096A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728730 | |||||||
chr22:44728731 | G | C | 1 | a0002c0003t0002g0297 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.322+2097G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728731 | |||||||
chr22:44728773 | G | A | 3 | a0001c0001t0001g0193 a0001c0001t0014g0265 a0001c0002t0026g0062 |
3 | HG01891.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.322+2139G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728773 | |||||||
chr22:44728782 | A | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0082 a0001c0001t0001g0141 others(1): Show |
5 | NA18969.hp1 NA18999.hp1 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.322+2148A>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728782 | |||||||
chr22:44728825 | C | G | 12 | a0001c0001t0006g0028 a0001c0001t0018g0058 a0001c0002t0008g0085 others(9): Show |
12 | HG01934.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.322+2191C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728825 | |||||||
chr22:44728883 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0082 a0001c0001t0009g0410 |
4 | HG02922.hp1 NA18969.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.322+2249G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728883 | |||||||
chr22:44728962 | G | A | 12 | a0001c0001t0006g0028 a0001c0001t0018g0058 a0001c0002t0008g0085 others(9): Show |
12 | HG01934.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.322+2328G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728962 | |||||||
chr22:44728966 | C | T | 59 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(56): Show |
63 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.322+2332C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728966 | |||||||
chr22:44728971 | G | T | 1 | a0001c0004t0004g0234 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.322+2337G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728971 | |||||||
chr22:44729015 | A | G | 172 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(169): Show |
180 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.322+2381A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729015 | |||||||
chr22:44729025 | A | G | 12 | a0001c0001t0006g0028 a0001c0001t0018g0058 a0001c0002t0008g0085 others(9): Show |
12 | HG01934.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.322+2391A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729025 | |||||||
chr22:44729026 | A | G | 12 | a0001c0001t0006g0028 a0001c0001t0018g0058 a0001c0002t0008g0085 others(9): Show |
12 | HG01934.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.322+2392A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729026 | |||||||
chr22:44729101 | C | T | 12 | a0001c0001t0006g0028 a0001c0001t0018g0058 a0001c0002t0008g0085 others(9): Show |
12 | HG01934.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.322+2467C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729101 | |||||||
chr22:44729201 | C | T | 4 | a0001c0002t0001g0017 a0001c0002t0001g0080 a0001c0002t0001g0393 others(1): Show |
5 | HG01257.hp2 HG01258.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.323-2529C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729201 | |||||||
chr22:44729233 | C | T | 12 | a0001c0001t0006g0028 a0001c0001t0018g0058 a0001c0002t0008g0085 others(9): Show |
12 | HG01934.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.323-2497C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729233 | |||||||
chr22:44729363 | C | G | 1 | a0001c0001t0001g0174 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.323-2367C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729363 | |||||||
chr22:44729430 | G | A | 82 | a0001c0001t0001g0347 a0001c0001t0001g0360 a0001c0001t0003g0108 others(79): Show |
85 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.323-2300G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729430 | |||||||
chr22:44729506 | G | A | 3 | a0001c0001t0009g0410 a0001c0001t0014g0265 a0001c0002t0026g0062 |
3 | HG02451.hp1 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.323-2224G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729506 | |||||||
chr22:44729533 | C | G | 1 | a0001c0002t0001g0227 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.323-2197C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729533 | |||||||
chr22:44729539 | T | C | 1 | a0001c0001t0009g0410 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.323-2191T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729539 | |||||||
chr22:44729577 | T | G | 12 | a0001c0001t0006g0028 a0001c0001t0018g0058 a0001c0002t0008g0085 others(9): Show |
12 | HG01934.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.323-2153T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729577 | |||||||
chr22:44729672 | C | CA | 6 | a0001c0001t0001g0087 a0001c0001t0001g0402 a0001c0001t0006g0036 others(3): Show |
6 | HG01433.hp2 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.323-2057dupA | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr22 | 44729672 | ||||||
chr22:44729731 | C | T | 1 | a0002c0003t0002g0207 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.323-1999C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729731 | |||||||
chr22:44729740 | G | A | 1 | a0002c0003t0002g0289 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.323-1990G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729740 | |||||||
chr22:44729766 | G | A | 1 | a0001c0001t0009g0410 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.323-1964G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729766 | |||||||
chr22:44729800 | C | T | 1 | a0001c0001t0001g0351 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.323-1930C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729800 | |||||||
chr22:44729877 | G | A | 54 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(51): Show |
57 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.323-1853G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729877 | |||||||
chr22:44729920 | G | T | 1 | a0001c0001t0001g0066 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.323-1810G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729920 | |||||||
chr22:44729952 | G | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0056 a0001c0001t0001g0316 others(2): Show |
6 | HG00738.hp2 HG01934.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.323-1778G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729952 | |||||||
chr22:44729961 | G | A | 2 | a0001c0001t0014g0265 a0001c0002t0026g0062 |
2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.323-1769G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729961 | |||||||
chr22:44729971 | G | A | 1 | a0001c0001t0009g0410 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.323-1759G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729971 | |||||||
chr22:44730195 | G | A | 1 | a0001c0001t0030g0111 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.323-1535G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730195 | |||||||
chr22:44730252 | C | T | 5 | a0001c0002t0001g0017 a0001c0002t0001g0080 a0001c0002t0001g0393 others(2): Show |
6 | HG01257.hp2 HG01258.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.323-1478C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730252 | |||||||
chr22:44730255 | G | A | 1 | a0002c0003t0002g0254 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.323-1475G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730255 | |||||||
chr22:44730277 | G | A | 1 | a0001c0002t0019g0206 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.323-1453G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730277 | |||||||
chr22:44730319 | C | T | 1 | a0001c0001t0003g0077 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.323-1411C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730319 | |||||||
chr22:44730423 | G | A | 1 | a0001c0002t0005g0329 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.323-1307G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730423 | |||||||
chr22:44730426 | C | G | 1 | a0002c0003t0002g0310 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.323-1304C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730426 | |||||||
chr22:44730524 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.323-1206C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730524 | |||||||
chr22:44730547 | T | C | 161 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(158): Show |
168 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.323-1183T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730547 | |||||||
chr22:44730580 | C | T | 1 | a0001c0001t0009g0410 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.323-1150C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730580 | |||||||
chr22:44730671 | C | T | 3 | a0001c0001t0015g0267 a0001c0002t0003g0200 a0001c0002t0012g0268 |
3 | HG02630.hp2 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.323-1059C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730671 | |||||||
chr22:44730725 | C | T | 1 | a0001c0001t0009g0410 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.323-1005C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730725 | |||||||
chr22:44730735 | C | T | 4 | a0001c0001t0001g0193 a0001c0001t0009g0410 a0001c0001t0014g0265 others(1): Show |
4 | HG01891.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.323-995C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730735 | |||||||
chr22:44730755 | A | C | 6 | a0001c0002t0003g0191 a0001c0002t0003g0251 a0001c0002t0003g0301 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.323-975A>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730755 | |||||||
chr22:44730758 | G | T | 172 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(169): Show |
180 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.323-972G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730758 | |||||||
chr22:44730766 | G | A | 1 | a0001c0002t0005g0022 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.323-964G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730766 | |||||||
chr22:44730772 | C | T | 3 | a0001c0001t0007g0027 a0001c0001t0007g0034 a0001c0001t0009g0026 |
3 | HG03130.hp1 HG03225.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.323-958C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730772 | |||||||
chr22:44730815 | T | A | 12 | a0001c0001t0006g0028 a0001c0001t0018g0058 a0001c0002t0008g0085 others(9): Show |
12 | HG01934.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.323-915T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730815 | |||||||
chr22:44730895 | T | C | 274 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(271): Show |
293 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.323-835T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730895 | |||||||
chr22:44730967 | G | C | 1 | a0002c0003t0002g0310 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.323-763G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730967 | |||||||
chr22:44731037 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.323-693A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44731037 | |||||||
chr22:44731051 | A | G | 1 | a0001c0002t0026g0062 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.323-679A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44731051 | |||||||
chr22:44731054 | G | A | 1 | a0001c0002t0026g0062 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.323-676G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44731054 | |||||||
chr22:44731063 | G | A | 1 | a0001c0001t0001g0292 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.323-667G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44731063 | |||||||
chr22:44731170 | G | A | 1 | a0001c0002t0001g0244 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.323-560G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44731170 | |||||||
chr22:44731186 | C | T | 1 | a0001c0001t0007g0034 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.323-544C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44731186 | |||||||
chr22:44731276 | G | A | 1 | a0001c0002t0006g0050 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.323-454G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44731276 | |||||||
chr22:44731452 | G | A | 6 | a0001c0002t0003g0191 a0001c0002t0003g0251 a0001c0002t0003g0301 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.323-278G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44731452 | |||||||
chr22:44731555 | G | T | 92 | a0001c0001t0001g0056 a0001c0001t0001g0151 a0001c0001t0001g0239 others(89): Show |
95 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.323-175G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44731555 | |||||||
chr22:44731600 | T | C | 1 | a0001c0002t0005g0250 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.323-130T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44731600 | |||||||
chr22:44731661 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.323-69C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44731661 | |||||||
chr22:44731688 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.323-42C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44731688 | |||||||
chr22:44731692 | C | T | 1 | a0001c0001t0001g0360 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.323-38C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44731692 | |||||||
chr22:44731701 | C | T | 2 | a0002c0003t0002g0147 a0002c0003t0002g0149 |
2 | HG00408.hp2 HG00423.hp1 |
intron_variant | MODIFIER | c.323-29C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44731701 | |||||||
chr22:44731859 | C | T | 43 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0019 others(40): Show |
44 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.414+38C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/7 | chr22 | 44731859 | |||||||
chr22:44731882 | A | G | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.414+61A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/7 | chr22 | 44731882 | |||||||
chr22:44731892 | G | C | 8 | a0001c0001t0001g0123 a0001c0001t0001g0141 a0001c0002t0003g0335 others(5): Show |
8 | NA18947.hp2 NA18961.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.414+71G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/7 | chr22 | 44731892 | |||||||
chr22:44731900 | G | A | 1 | a0001c0004t0004g0134 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.414+79G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/7 | chr22 | 44731900 | |||||||
chr22:44731926 | CTCTGCTC others(3): Show |
C | 47 | a0001c0002t0001g0017 a0001c0002t0001g0080 a0001c0002t0001g0188 others(44): Show |
49 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.414+106_414+115del others(10): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/7 | chr22 | 44731926 | |||||||
chr22:44731927 | T | G | 30 | a0001c0001t0001g0010 a0001c0001t0003g0077 a0001c0001t0007g0027 others(27): Show |
31 | HG00609.hp1 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.414+106T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/7 | chr22 | 44731927 | |||||||
chr22:44731936 | T | C | 19 | a0001c0001t0003g0077 a0001c0001t0007g0027 a0001c0001t0007g0034 others(16): Show |
19 | HG00408.hp1 HG00673.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.414+115T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/7 | chr22 | 44731936 | |||||||
chr22:44731937 | G | A | 1 | a0002c0003t0002g0122 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.414+116G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/7 | chr22 | 44731937 | |||||||
chr22:44731953 | T | C | 2 | a0001c0001t0015g0267 a0001c0002t0003g0200 |
2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.414+132T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/7 | chr22 | 44731953 | |||||||
chr22:44732011 | C | A | 5 | a0001c0002t0005g0128 a0001c0002t0005g0181 a0001c0002t0005g0259 others(2): Show |
5 | HG02818.hp2 HG03041.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.414+190C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/7 | chr22 | 44732011 | |||||||
chr22:44732031 | A | G | 26 | a0001c0001t0001g0178 a0001c0001t0003g0077 a0001c0001t0027g0274 others(23): Show |
26 | HG00140.hp1 HG01243.hp2 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.414+210A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/7 | chr22 | 44732031 | |||||||
chr22:44732043 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.415-208C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/7 | chr22 | 44732043 | |||||||
chr22:44732166 | C | G | 1 | a0001c0001t0001g0296 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.415-85C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/7 | chr22 | 44732166 | |||||||
chr22:44732234 | G | A | 1 | a0001c0002t0012g0268 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.415-17G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/7 | chr22 | 44732234 | |||||||
chr22:44732408 | G | C | 326 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(323): Show |
346 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(343): Show |
intron_variant | MODIFIER | c.555+17G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732408 | |||||||
chr22:44732494 | C | G | 1 | a0001c0001t0001g0156 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.555+103C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732494 | |||||||
chr22:44732569 | G | T | 241 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0052 others(238): Show |
249 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.555+178G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732569 | |||||||
chr22:44732625 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.555+234A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732625 | |||||||
chr22:44732667 | G | A | 1 | a0001c0004t0004g0319 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.555+276G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732667 | |||||||
chr22:44732673 | G | A | 2 | a0001c0002t0003g0407 a0001c0002t0012g0132 |
2 | HG01243.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.555+282G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732673 | |||||||
chr22:44732696 | T | C | 47 | a0001c0002t0003g0070 a0001c0002t0003g0071 a0001c0002t0003g0200 others(44): Show |
51 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.555+305T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732696 | |||||||
chr22:44732716 | T | C | 321 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(318): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.555+325T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732716 | |||||||
chr22:44732721 | G | A | 40 | a0001c0002t0003g0200 a0001c0002t0003g0335 a0001c0004t0004g0011 others(37): Show |
43 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.555+330G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732721 | |||||||
chr22:44732728 | T | C | 47 | a0001c0002t0003g0070 a0001c0002t0003g0071 a0001c0002t0003g0200 others(44): Show |
51 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.555+337T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732728 | |||||||
chr22:44732736 | CACCA | C | 9 | a0001c0002t0003g0200 a0001c0004t0004g0109 a0001c0004t0004g0136 others(6): Show |
9 | HG00140.hp1 HG01255.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.555+346_555+349del others(4): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732736 | |||||||
chr22:44732738 | CCA | C | 38 | a0001c0001t0001g0193 a0001c0001t0003g0241 a0001c0002t0001g0017 others(35): Show |
42 | HG00423.hp2 HG00609.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.555+353_555+354del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732738 | ||||||
chr22:44732739 | C | T | 1 | a0001c0002t0012g0268 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.555+348C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732739 | |||||||
chr22:44732744 | A | G | 1 | a0001c0002t0005g0250 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.555+353A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732744 | |||||||
chr22:44732752 | ACG | A | 15 | a0001c0001t0009g0026 a0001c0001t0009g0410 a0001c0002t0008g0085 others(12): Show |
15 | HG01934.hp1 HG02109.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.555+363_555+364del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732752 | ||||||
chr22:44732754 | G | A | 50 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0019 others(47): Show |
51 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.555+363G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732754 | |||||||
chr22:44732760 | G | A | 3 | a0001c0001t0015g0267 a0001c0002t0001g0059 a0001c0002t0012g0268 |
3 | HG01109.hp1 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.555+369G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732760 | |||||||
chr22:44732762 | TAC | T | 6 | a0001c0002t0003g0191 a0001c0002t0003g0251 a0001c0002t0003g0301 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.555+377_555+378del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732762 | ||||||
chr22:44732773 | CTGTGTGC others(14): Show |
C | 98 | a0001c0002t0005g0022 a0001c0002t0005g0067 a0001c0002t0005g0068 others(95): Show |
99 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.555+387_555+407del others(21): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732773 | ||||||
chr22:44732778 | T | C | 270 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(267): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.555+387T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732778 | |||||||
chr22:44732782 | C | T | 2 | a0001c0004t0004g0204 a0001c0004t0004g0276 |
2 | HG02055.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.555+391C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732782 | |||||||
chr22:44732787 | ATAC | A | 67 | a0001c0001t0001g0001 a0001c0001t0003g0014 a0001c0001t0003g0015 others(64): Show |
68 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.555+400_555+402del others(3): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732787 | ||||||
chr22:44732800 | A | G | 98 | a0001c0002t0005g0022 a0001c0002t0005g0067 a0001c0002t0005g0068 others(95): Show |
99 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.555+409A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732800 | |||||||
chr22:44732803 | C | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(157): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.555+412C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732803 | |||||||
chr22:44732804 | G | A | 1 | a0001c0001t0007g0030 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.555+413G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732804 | |||||||
chr22:44732807 | TAC | T | 44 | a0001c0002t0001g0059 a0001c0002t0003g0200 a0001c0002t0003g0335 others(41): Show |
48 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.555+421_555+422del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732807 | ||||||
chr22:44732813 | CTA | C | 6 | a0001c0002t0003g0191 a0001c0002t0003g0251 a0001c0002t0003g0301 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.555+423_555+424del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732813 | |||||||
chr22:44732819 | G | A | 2 | a0001c0001t0015g0267 a0001c0002t0012g0268 |
2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.555+428G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732819 | |||||||
chr22:44732822 | T | C | 43 | a0001c0002t0003g0200 a0001c0002t0003g0335 a0001c0002t0013g0008 others(40): Show |
47 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.555+431T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732822 | |||||||
chr22:44732826 | C | T | 2 | a0001c0001t0015g0266 a0001c0002t0033g0060 |
2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.555+435C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732826 | |||||||
chr22:44732827 | G | A | 9 | a0001c0002t0003g0200 a0001c0004t0004g0109 a0001c0004t0004g0136 others(6): Show |
9 | HG00140.hp1 HG01255.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.555+436G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732827 | |||||||
chr22:44732831 | ATAC | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(148): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.555+444_555+446del others(3): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732831 | ||||||
chr22:44732831 | ATACTACA others(29): Show |
A | 43 | a0001c0002t0003g0200 a0001c0002t0003g0335 a0001c0002t0013g0008 others(40): Show |
47 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.555+444_555+479del others(36): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732831 | ||||||
chr22:44732832 | TACTACAC others(6): Show |
T | 5 | a0001c0001t0014g0265 a0001c0002t0001g0017 a0001c0002t0001g0227 others(2): Show |
6 | HG01257.hp2 HG01258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.555+444_555+456del others(13): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732832 | ||||||
chr22:44732835 | TAC | T | 7 | a0001c0002t0003g0191 a0001c0002t0003g0251 a0001c0002t0003g0301 others(4): Show |
7 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.555+449_555+450del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732835 | ||||||
chr22:44732835 | TACACACG others(3): Show |
T | 98 | a0001c0002t0005g0022 a0001c0002t0005g0067 a0001c0002t0005g0068 others(95): Show |
99 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.555+459_555+468del others(10): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732835 | ||||||
chr22:44732836 | A | G | 4 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0081 others(1): Show |
4 | NA18612.hp1 NA19001.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.555+445A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732836 | |||||||
chr22:44732844 | GCA | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(147): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.555+459_555+460del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732844 | ||||||
chr22:44732860 | G | A | 1 | a0001c0001t0009g0410 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.555+469G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732860 | |||||||
chr22:44732868 | TAC | T | 15 | a0001c0001t0009g0026 a0001c0001t0009g0410 a0001c0002t0008g0085 others(12): Show |
15 | HG01934.hp1 HG02109.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.555+482_555+483del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732868 | ||||||
chr22:44732883 | C | T | 416 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(413): Show |
438 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(435): Show |
intron_variant | MODIFIER | c.555+492C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732883 | |||||||
chr22:44732887 | CCA | C | 11 | a0001c0001t0003g0057 a0001c0001t0003g0179 a0001c0001t0003g0192 others(8): Show |
11 | HG01109.hp2 HG02055.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.555+502_555+503del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732887 | ||||||
chr22:44732892 | C | T | 1 | a0001c0001t0006g0035 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.555+501C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732892 | |||||||
chr22:44732898 | C | T | 43 | a0001c0002t0003g0200 a0001c0002t0003g0335 a0001c0002t0013g0008 others(40): Show |
47 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.555+507C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732898 | |||||||
chr22:44732899 | A | G | 43 | a0001c0002t0003g0200 a0001c0002t0003g0335 a0001c0002t0013g0008 others(40): Show |
47 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.555+508A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732899 | |||||||
chr22:44732912 | C | T | 1 | a0001c0004t0004g0011 | 2 | HG00642.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.555+521C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732912 | |||||||
chr22:44732913 | TAC | T | 99 | a0001c0001t0003g0201 a0001c0002t0005g0022 a0001c0002t0005g0067 others(96): Show |
100 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.555+527_555+528del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732913 | ||||||
chr22:44732923 | C | T | 56 | a0001c0002t0003g0191 a0001c0002t0003g0251 a0001c0002t0003g0301 others(53): Show |
57 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.555+532C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732923 | |||||||
chr22:44732924 | G | A | 2 | a0001c0004t0004g0339 a0001c0004t0004g0380 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.555+533G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732924 | |||||||
chr22:44732927 | C | A | 2 | a0001c0001t0015g0267 a0001c0002t0012g0268 |
2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.555+536C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732927 | |||||||
chr22:44732928 | G | A | 1 | a0001c0001t0001g0009 | 2 | NA19004.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.555+537G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732928 | |||||||
chr22:44732936 | TAC | T | 43 | a0001c0002t0003g0200 a0001c0002t0003g0335 a0001c0002t0013g0008 others(40): Show |
47 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.555+550_555+551del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732936 | ||||||
chr22:44732943 | G | C | 1 | a0001c0001t0024g0063 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.555+552G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732943 | |||||||
chr22:44732946 | T | C | 65 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0019 others(62): Show |
66 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.555+555T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732946 | |||||||
chr22:44732946 | TGCACACA others(5): Show |
T | 1 | a0001c0001t0015g0266 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.555+557_555+568del others(12): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732946 | ||||||
chr22:44732947 | GCA | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(147): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.555+561_555+562del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732947 | ||||||
chr22:44732954 | TACGCGTG others(3): Show |
T | 1 | a0001c0002t0033g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.555+568_555+577del others(10): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732954 | ||||||
chr22:44732977 | TAC | T | 4 | a0001c0002t0001g0017 a0001c0002t0001g0080 a0001c0002t0001g0393 others(1): Show |
5 | HG01257.hp2 HG01258.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.555+592_555+593del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732977 | ||||||
chr22:44732981 | CACAT | C | 17 | a0001c0001t0009g0026 a0001c0001t0009g0410 a0001c0002t0008g0085 others(14): Show |
17 | HG01934.hp1 HG02109.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.555+595_555+598del others(4): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732981 | ||||||
chr22:44732983 | CAT | C | 6 | a0001c0002t0003g0191 a0001c0002t0003g0251 a0001c0002t0003g0301 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.555+594_555+595del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732983 | ||||||
chr22:44732990 | G | T | 40 | a0001c0002t0003g0200 a0001c0002t0003g0335 a0001c0004t0004g0011 others(37): Show |
43 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.555+599G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732990 | |||||||
chr22:44732998 | A | G | 270 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(267): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.555+607A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732998 | |||||||
chr22:44733013 | GTGCACA | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(153): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.555+630_555+635del others(6): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44733013 | ||||||
chr22:44733083 | T | C | 2 | a0001c0001t0015g0267 a0001c0002t0012g0268 |
2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.555+692T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733083 | |||||||
chr22:44733109 | G | A | 3 | a0001c0002t0001g0017 a0001c0002t0001g0393 a0001c0002t0001g0394 |
4 | HG01257.hp2 HG01258.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.555+718G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733109 | |||||||
chr22:44733126 | C | G | 1 | a0001c0004t0004g0218 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.555+735C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733126 | |||||||
chr22:44733196 | C | T | 65 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0019 others(62): Show |
66 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.555+805C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733196 | |||||||
chr22:44733219 | A | G | 370 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(367): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.555+828A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733219 | |||||||
chr22:44733228 | T | C | 43 | a0001c0002t0003g0200 a0001c0002t0003g0335 a0001c0002t0013g0008 others(40): Show |
47 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.555+837T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733228 | |||||||
chr22:44733276 | C | G | 1 | a0001c0001t0001g0270 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.555+885C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733276 | |||||||
chr22:44733277 | A | G | 43 | a0001c0002t0003g0200 a0001c0002t0003g0335 a0001c0002t0013g0008 others(40): Show |
47 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.555+886A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733277 | |||||||
chr22:44733280 | C | T | 1 | a0001c0002t0011g0045 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.555+889C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733280 | |||||||
chr22:44733359 | T | C | 42 | a0001c0002t0003g0200 a0001c0002t0013g0008 a0001c0002t0013g0166 others(39): Show |
46 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.555+968T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733359 | |||||||
chr22:44733365 | C | T | 42 | a0001c0002t0003g0200 a0001c0002t0013g0008 a0001c0002t0013g0166 others(39): Show |
46 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.555+974C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733365 | |||||||
chr22:44733377 | T | C | 1 | a0001c0001t0014g0265 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.555+986T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733377 | |||||||
chr22:44733382 | C | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(64): Show |
78 | HG00280.hp1 HG00438.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.555+991C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733382 | |||||||
chr22:44733386 | G | C | 42 | a0001c0002t0003g0200 a0001c0002t0013g0008 a0001c0002t0013g0166 others(39): Show |
46 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.555+995G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733386 | |||||||
chr22:44733391 | C | T | 2 | a0003c0007t0004g0069 a0003c0007t0025g0064 |
2 | HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.555+1000C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733391 | |||||||
chr22:44733434 | C | G | 1 | a0001c0001t0001g0226 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.555+1043C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733434 | |||||||
chr22:44733479 | G | C | 6 | a0001c0002t0003g0191 a0001c0002t0003g0251 a0001c0002t0003g0301 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.555+1088G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733479 | |||||||
chr22:44733594 | G | C | 6 | a0001c0002t0003g0191 a0001c0002t0003g0251 a0001c0002t0003g0301 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.555+1203G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733594 | |||||||
chr22:44733625 | C | T | 51 | a0002c0003t0002g0002 a0002c0003t0002g0065 a0002c0003t0002g0092 others(48): Show |
52 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.555+1234C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733625 | |||||||
chr22:44733651 | C | T | 33 | a0001c0002t0013g0008 a0001c0002t0013g0166 a0001c0004t0004g0011 others(30): Show |
37 | HG00423.hp2 HG00609.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.555+1260C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733651 | |||||||
chr22:44733727 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.556-1300G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733727 | |||||||
chr22:44733810 | A | G | 2 | a0001c0001t0015g0267 a0001c0002t0012g0268 |
2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.556-1217A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733810 | |||||||
chr22:44733823 | C | G | 3 | a0001c0002t0001g0080 a0001c0002t0001g0393 a0001c0002t0001g0394 |
3 | HG02738.hp2 HG03927.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.556-1204C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733823 | |||||||
chr22:44733929 | G | A | 1 | a0001c0001t0001g0386 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.556-1098G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733929 | |||||||
chr22:44733940 | T | G | 1 | a0001c0004t0004g0391 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.556-1087T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733940 | |||||||
chr22:44734052 | T | A | 2 | a0001c0001t0015g0267 a0001c0002t0012g0268 |
2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.556-975T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734052 | |||||||
chr22:44734103 | C | G | 1 | a0001c0002t0012g0268 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.556-924C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734103 | |||||||
chr22:44734131 | G | A | 6 | a0001c0004t0004g0109 a0001c0004t0004g0136 a0001c0004t0004g0304 others(3): Show |
6 | HG00140.hp1 HG01255.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.556-896G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734131 | |||||||
chr22:44734156 | C | T | 49 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0019 others(46): Show |
50 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.556-871C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734156 | |||||||
chr22:44734182 | G | A | 91 | a0001c0002t0005g0022 a0001c0002t0005g0067 a0001c0002t0005g0068 others(88): Show |
92 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.556-845G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734182 | |||||||
chr22:44734296 | A | G | 7 | a0001c0002t0003g0191 a0001c0002t0003g0251 a0001c0002t0003g0301 others(4): Show |
7 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.556-731A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734296 | |||||||
chr22:44734411 | G | C | 1 | a0001c0002t0015g0269 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.556-616G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734411 | |||||||
chr22:44734428 | A | C | 3 | a0001c0002t0001g0080 a0001c0002t0001g0393 a0001c0002t0001g0394 |
3 | HG02738.hp2 HG03927.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.556-599A>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734428 | |||||||
chr22:44734493 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(151): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.556-534A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734493 | |||||||
chr22:44734535 | G | A | 1 | a0001c0002t0033g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.556-492G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734535 | |||||||
chr22:44734548 | G | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(147): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.556-479G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734548 | |||||||
chr22:44734582 | G | T | 1 | a0001c0002t0005g0259 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.556-445G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734582 | |||||||
chr22:44734586 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(146): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.556-441G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734586 | |||||||
chr22:44734613 | C | T | 1 | a0001c0001t0003g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.556-414C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734613 | |||||||
chr22:44734632 | G | A | 5 | a0001c0001t0001g0087 a0001c0001t0001g0258 a0001c0001t0006g0031 others(2): Show |
5 | HG02615.hp1 HG02886.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.556-395G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734632 | |||||||
chr22:44734684 | T | G | 40 | a0001c0001t0006g0035 a0001c0002t0005g0022 a0001c0002t0005g0067 others(37): Show |
40 | HG00323.hp1 HG00609.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.556-343T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734684 | |||||||
chr22:44734778 | C | G | 1 | a0001c0001t0001g0193 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.556-249C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734778 | |||||||
chr22:44734811 | C | A | 39 | a0001c0002t0003g0200 a0001c0004t0004g0011 a0001c0004t0004g0013 others(36): Show |
42 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.556-216C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734811 | |||||||
chr22:44734815 | C | T | 40 | a0001c0001t0014g0263 a0001c0002t0003g0200 a0001c0004t0004g0011 others(37): Show |
43 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.556-212C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734815 | |||||||
chr22:44734968 | G | T | 2 | a0001c0001t0015g0266 a0001c0002t0033g0060 |
2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.556-59G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734968 | |||||||
chr22:44735014 | C | A | 10 | a0001c0001t0001g0145 a0001c0001t0001g0161 a0001c0001t0001g0174 others(7): Show |
10 | HG00544.hp2 HG00558.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.556-13C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44735014 | |||||||
chr22:44735020 | C | A | 2 | a0001c0002t0005g0338 a0001c0002t0005g0379 |
2 | HG01070.hp2 HG01071.hp2 |
splice_region_variant&intron_variant | LOW | c.556-7C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44735020 | |||||||
chr22:44735173 | G | A | 51 | a0002c0003t0002g0002 a0002c0003t0002g0065 a0002c0003t0002g0092 others(48): Show |
52 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.691+11G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735173 | |||||||
chr22:44735206 | G | T | 1 | a0001c0002t0006g0050 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.691+44G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735206 | |||||||
chr22:44735207 | G | T | 1 | a0001c0002t0006g0050 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.691+45G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735207 | |||||||
chr22:44735212 | C | T | 9 | a0001c0002t0003g0200 a0001c0004t0004g0109 a0001c0004t0004g0136 others(6): Show |
9 | HG00140.hp1 HG01255.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.691+50C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735212 | |||||||
chr22:44735238 | C | T | 4 | a0002c0003t0002g0116 a0002c0003t0002g0148 a0002c0003t0002g0254 others(1): Show |
4 | NA18943.hp2 NA18960.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.691+76C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735238 | |||||||
chr22:44735249 | G | A | 8 | a0001c0001t0003g0014 a0001c0001t0003g0019 a0001c0001t0003g0321 others(5): Show |
8 | HG01975.hp2 NA18945.hp2 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.691+87G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735249 | |||||||
chr22:44735286 | C | T | 39 | a0001c0002t0003g0200 a0001c0004t0004g0011 a0001c0004t0004g0013 others(36): Show |
42 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.691+124C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735286 | |||||||
chr22:44735310 | T | G | 1 | a0001c0004t0004g0204 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.691+148T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735310 | |||||||
chr22:44735311 | A | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0315 |
2 | HG02129.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.691+149A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735311 | |||||||
chr22:44735359 | C | G | 1 | a0001c0001t0001g0369 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.691+197C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735359 | |||||||
chr22:44735359 | C | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(145): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.691+197C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735359 | |||||||
chr22:44735426 | T | G | 4 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0081 others(1): Show |
4 | NA18612.hp1 NA19001.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.691+264T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735426 | |||||||
chr22:44735474 | C | G | 3 | a0001c0002t0001g0222 a0001c0002t0001g0280 a0001c0011t0001g0281 |
3 | HG00609.hp1 NA18990.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.691+312C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735474 | |||||||
chr22:44735480 | C | T | 39 | a0001c0002t0003g0200 a0001c0004t0004g0011 a0001c0004t0004g0013 others(36): Show |
42 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.691+318C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735480 | |||||||
chr22:44735533 | G | A | 51 | a0002c0003t0002g0002 a0002c0003t0002g0065 a0002c0003t0002g0092 others(48): Show |
52 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.691+371G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735533 | |||||||
chr22:44735539 | G | T | 2 | a0001c0001t0015g0266 a0001c0002t0033g0060 |
2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.691+377G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735539 | |||||||
chr22:44735543 | T | C | 2 | a0001c0001t0015g0266 a0001c0002t0033g0060 |
2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.691+381T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735543 | |||||||
chr22:44735548 | A | T | 2 | a0001c0001t0015g0266 a0001c0002t0033g0060 |
2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.691+386A>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735548 | |||||||
chr22:44735582 | T | A | 364 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(361): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.691+420T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735582 | |||||||
chr22:44735637 | T | A | 39 | a0001c0002t0003g0200 a0001c0004t0004g0011 a0001c0004t0004g0013 others(36): Show |
42 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.691+475T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735637 | |||||||
chr22:44735646 | A | G | 40 | a0001c0002t0003g0200 a0001c0004t0004g0011 a0001c0004t0004g0013 others(37): Show |
43 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.691+484A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735646 | |||||||
chr22:44735653 | C | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(150): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.691+491C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735653 | |||||||
chr22:44735675 | T | G | 364 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(361): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.691+513T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735675 | |||||||
chr22:44735718 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.691+556G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735718 | |||||||
chr22:44735732 | C | T | 41 | a0001c0002t0003g0200 a0001c0004t0004g0011 a0001c0004t0004g0013 others(38): Show |
44 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.691+570C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735732 | |||||||
chr22:44735786 | G | T | 1 | a0001c0002t0005g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.691+624G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735786 | |||||||
chr22:44735814 | C | T | 1 | a0002c0003t0002g0147 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.691+652C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735814 | |||||||
chr22:44735963 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.691+801G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735963 | |||||||
chr22:44735984 | T | C | 1 | a0002c0003t0002g0207 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.692-788T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735984 | |||||||
chr22:44735986 | T | C | 41 | a0001c0002t0003g0200 a0001c0004t0004g0011 a0001c0004t0004g0013 others(38): Show |
44 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.692-786T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735986 | |||||||
chr22:44736021 | C | T | 2 | a0001c0004t0004g0262 a0001c0004t0016g0029 |
2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.692-751C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736021 | |||||||
chr22:44736046 | T | C | 41 | a0001c0002t0003g0200 a0001c0004t0004g0011 a0001c0004t0004g0013 others(38): Show |
44 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.692-726T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736046 | |||||||
chr22:44736116 | C | T | 6 | a0002c0003t0002g0099 a0002c0003t0002g0147 a0002c0003t0002g0149 others(3): Show |
6 | HG00408.hp2 HG00423.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.692-656C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736116 | |||||||
chr22:44736239 | C | G | 1 | a0001c0001t0001g0384 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.692-533C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736239 | |||||||
chr22:44736259 | C | G | 3 | a0001c0002t0001g0080 a0001c0002t0001g0393 a0001c0002t0001g0394 |
3 | HG02738.hp2 HG03927.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.692-513C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736259 | |||||||
chr22:44736333 | G | A | 1 | a0001c0002t0012g0268 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.692-439G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736333 | |||||||
chr22:44736443 | A | G | 138 | a0001c0002t0003g0200 a0001c0002t0003g0256 a0001c0002t0005g0022 others(135): Show |
142 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.692-329A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736443 | |||||||
chr22:44736474 | CG | C | 41 | a0001c0002t0003g0200 a0001c0004t0004g0011 a0001c0004t0004g0013 others(38): Show |
44 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.692-293delG | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr22 | 44736474 | ||||||
chr22:44736475 | G | A | 6 | a0001c0002t0003g0191 a0001c0002t0003g0251 a0001c0002t0003g0301 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.692-297G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736475 | |||||||
chr22:44736479 | G | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(150): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.692-293G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736479 | |||||||
chr22:44736482 | A | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0395 a0001c0001t0001g0399 others(2): Show |
7 | NA18948.hp2 NA18952.hp1 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.692-290A>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736482 | |||||||
chr22:44736568 | G | T | 30 | a0001c0004t0004g0011 a0001c0004t0004g0013 a0001c0004t0004g0018 others(27): Show |
33 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.692-204G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736568 | |||||||
chr22:44736611 | G | A | 27 | a0001c0001t0001g0055 a0001c0001t0001g0072 a0001c0001t0001g0074 others(24): Show |
28 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.692-161G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736611 | |||||||
chr22:44736613 | CAG | C | 95 | a0001c0002t0005g0022 a0001c0002t0005g0067 a0001c0002t0005g0068 others(92): Show |
96 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.692-158_692-157del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736613 | |||||||
chr22:44736626 | G | A | 97 | a0001c0002t0005g0022 a0001c0002t0005g0067 a0001c0002t0005g0068 others(94): Show |
98 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.692-146G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736626 | |||||||
chr22:44736651 | G | C | 1 | a0001c0001t0001g0316 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.692-121G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736651 | |||||||
chr22:44736655 | C | T | 95 | a0001c0002t0005g0022 a0001c0002t0005g0067 a0001c0002t0005g0068 others(92): Show |
96 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.692-117C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736655 | |||||||
chr22:44736660 | C | T | 51 | a0002c0003t0002g0002 a0002c0003t0002g0065 a0002c0003t0002g0092 others(48): Show |
52 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.692-112C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736660 | |||||||
chr22:44736757 | C | T | 1 | a0001c0001t0006g0041 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.692-15C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736757 |