Item | Value |
---|---|
geneid | 54625 |
ensemblid | ENSG00000173193.15 |
hgncid | 29232 |
symbol | PARP14 |
name | poly(ADP-ribose) polymerase family member 14 |
refseq_nuc | NM_017554.3 |
refseq_prot | NP_060024.2 |
ensembl_nuc | ENST00000474629.7 |
ensembl_prot | ENSP00000418194.2 |
mane_status | MANE Select |
chr | chr3 |
start | 122680839 |
end | 122730840 |
strand | + |
ver | v1.2 |
region | chr3:122680839-122730840 |
region5000 | chr3:122675839-122735840 |
regionname0 | PARP14_chr3_122680839_122730840 |
regionname5000 | PARP14_chr3_122675839_122735840 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1801 | 299 | 70 | 44 | 126 | 13 | 44 | 93 | PARP14_chr3_122675839_122735840 | PARP14 | MAVPG others(1796): Show |
chr3 | 122675839 | 122735840 |
a0002 | 0/0 | 1801 | 35 | 4 | 4 | 24 | 0 | 3 | 21 | PARP14_chr3_122675839_122735840 | PARP14 | MAVPG others(1796): Show |
chr3 | 122675839 | 122735840 |
a0003 | 0/0 | 1801 | 10 | 3 | 6 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | MAVPG others(1796): Show |
chr3 | 122675839 | 122735840 |
a0004 | 0/0 | 1801 | 8 | 5 | 3 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | MAVPG others(1796): Show |
chr3 | 122675839 | 122735840 |
a0005 | 0/0 | 1801 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | MAVPG others(1796): Show |
chr3 | 122675839 | 122735840 |
a0006 | 0/0 | 1801 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | MAVPG others(1796): Show |
chr3 | 122675839 | 122735840 |
a0007 | 0/0 | 1801 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | MAVPG others(1796): Show |
chr3 | 122675839 | 122735840 |
a0008 | 0/0 | 1801 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | MAVPG others(1796): Show |
chr3 | 122675839 | 122735840 |
a0009 | 0/0 | 1801 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | MAVPG others(1796): Show |
chr3 | 122675839 | 122735840 |
a0010 | 0/0 | 1801 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | MAVPG others(1796): Show |
chr3 | 122675839 | 122735840 |
a0011 | 0/0 | 1801 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | MAVPG others(1796): Show |
chr3 | 122675839 | 122735840 |
a0012 | 0/0 | 1801 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | MAVPG others(1796): Show |
chr3 | 122675839 | 122735840 |
a0013 | 0/0 | 1801 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | MAVPG others(1796): Show |
chr3 | 122675839 | 122735840 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 5403 | 262 | 60 | 33 | 115 | 11 | 42 | PARP14_chr3_122675839_122735840 | PARP14 | ATGGC others(5398): Show |
chr3 | 122675839 | 122735840 | ||
a0001c0003 | 1/0 | 5403 | 19 | 7 | 7 | 3 | 1 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | ATGGC others(5398): Show |
chr3 | 122675839 | 122735840 | ||
a0001c0005 | 0/0 | 5403 | 6 | 0 | 1 | 5 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | ATGGC others(5398): Show |
chr3 | 122675839 | 122735840 | ||
a0001c0007 | 0/0 | 5403 | 4 | 1 | 3 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | ATGGC others(5398): Show |
chr3 | 122675839 | 122735840 | ||
a0001c0012 | 0/0 | 5403 | 2 | 0 | 0 | 2 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | ATGGC others(5398): Show |
chr3 | 122675839 | 122735840 | ||
a0001c0016 | 0/0 | 5403 | 1 | 0 | 0 | 0 | 1 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | ATGGC others(5398): Show |
chr3 | 122675839 | 122735840 | ||
a0001c0018 | 0/0 | 5403 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | ATGGC others(5398): Show |
chr3 | 122675839 | 122735840 | ||
a0001c0021 | 0/0 | 5403 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | ATGGC others(5398): Show |
chr3 | 122675839 | 122735840 | ||
a0001c0022 | 0/0 | 5403 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | ATGGC others(5398): Show |
chr3 | 122675839 | 122735840 | ||
a0001c0023 | 0/0 | 5403 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | ATGGC others(5398): Show |
chr3 | 122675839 | 122735840 | ||
a0001c0024 | 0/0 | 5403 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | ATGGC others(5398): Show |
chr3 | 122675839 | 122735840 | ||
a0002c0002 | 0/0 | 5403 | 35 | 4 | 4 | 24 | 0 | 3 | PARP14_chr3_122675839_122735840 | PARP14 | ATGGC others(5398): Show |
chr3 | 122675839 | 122735840 | ||
a0003c0004 | 0/0 | 5403 | 9 | 2 | 6 | 0 | 1 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | ATGGC others(5398): Show |
chr3 | 122675839 | 122735840 | ||
a0003c0015 | 0/0 | 5403 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | ATGGC others(5398): Show |
chr3 | 122675839 | 122735840 | ||
a0004c0008 | 0/0 | 5403 | 3 | 0 | 3 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | ATGGC others(5398): Show |
chr3 | 122675839 | 122735840 | ||
a0004c0009 | 0/0 | 5403 | 3 | 3 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | ATGGC others(5398): Show |
chr3 | 122675839 | 122735840 | ||
a0004c0011 | 0/0 | 5403 | 2 | 2 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | ATGGC others(5398): Show |
chr3 | 122675839 | 122735840 | ||
a0005c0006 | 0/0 | 5403 | 4 | 3 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | ATGGC others(5398): Show |
chr3 | 122675839 | 122735840 | ||
a0006c0010 | 0/0 | 5403 | 3 | 2 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | ATGGC others(5398): Show |
chr3 | 122675839 | 122735840 | ||
a0007c0017 | 0/0 | 5403 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | ATGGC others(5398): Show |
chr3 | 122675839 | 122735840 | ||
a0008c0026 | 0/0 | 5403 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | ATGGC others(5398): Show |
chr3 | 122675839 | 122735840 | ||
a0009c0014 | 0/0 | 5403 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | ATGGC others(5398): Show |
chr3 | 122675839 | 122735840 | ||
a0010c0019 | 0/0 | 5403 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | ATGGC others(5398): Show |
chr3 | 122675839 | 122735840 | ||
a0011c0025 | 0/0 | 5403 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | ATGGC others(5398): Show |
chr3 | 122675839 | 122735840 | ||
a0012c0020 | 0/0 | 5403 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | ATGGC others(5398): Show |
chr3 | 122675839 | 122735840 | ||
a0013c0013 | 0/0 | 5403 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | ATGGC others(5398): Show |
chr3 | 122675839 | 122735840 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7694 | 104 | 25 | 14 | 44 | 3 | 18 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7689): Show |
chr3 | 122675839 | 122735840 |
a0001c0001t0002 | 0/0 | 7693 | 64 | 4 | 7 | 46 | 0 | 7 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7688): Show |
chr3 | 122675839 | 122735840 |
a0001c0001t0003 | 0/0 | 7693 | 45 | 19 | 4 | 18 | 1 | 3 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7688): Show |
chr3 | 122675839 | 122735840 |
a0001c0001t0005 | 0/1 | 7695 | 17 | 6 | 2 | 1 | 4 | 3 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7690): Show |
chr3 | 122675839 | 122735840 |
a0001c0001t0006 | 0/0 | 7694 | 11 | 4 | 1 | 1 | 0 | 5 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7689): Show |
chr3 | 122675839 | 122735840 |
a0001c0001t0009 | 0/0 | 7694 | 6 | 0 | 0 | 0 | 2 | 4 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7689): Show |
chr3 | 122675839 | 122735840 |
a0001c0001t0012 | 0/0 | 7694 | 2 | 0 | 0 | 2 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7689): Show |
chr3 | 122675839 | 122735840 |
a0001c0001t0014 | 0/0 | 7693 | 2 | 1 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7688): Show |
chr3 | 122675839 | 122735840 |
a0001c0001t0015 | 0/0 | 7695 | 2 | 0 | 2 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7690): Show |
chr3 | 122675839 | 122735840 |
a0001c0001t0016 | 0/0 | 7693 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7688): Show |
chr3 | 122675839 | 122735840 |
a0001c0001t0017 | 0/0 | 7693 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7688): Show |
chr3 | 122675839 | 122735840 |
a0001c0001t0021 | 0/0 | 7694 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7689): Show |
chr3 | 122675839 | 122735840 |
a0001c0001t0022 | 0/0 | 7693 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7688): Show |
chr3 | 122675839 | 122735840 |
a0001c0001t0023 | 0/0 | 7693 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7688): Show |
chr3 | 122675839 | 122735840 |
a0001c0001t0024 | 0/0 | 7693 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7688): Show |
chr3 | 122675839 | 122735840 |
a0001c0001t0028 | 0/0 | 7694 | 1 | 0 | 0 | 0 | 1 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7689): Show |
chr3 | 122675839 | 122735840 |
a0001c0001t0030 | 0/0 | 7694 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7689): Show |
chr3 | 122675839 | 122735840 |
a0001c0001t0031 | 0/0 | 7694 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7689): Show |
chr3 | 122675839 | 122735840 |
a0001c0003t0001 | 0/0 | 7694 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7689): Show |
chr3 | 122675839 | 122735840 |
a0001c0003t0006 | 0/0 | 7694 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7689): Show |
chr3 | 122675839 | 122735840 |
a0001c0003t0007 | 0/0 | 7694 | 12 | 2 | 6 | 3 | 1 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7689): Show |
chr3 | 122675839 | 122735840 |
a0001c0003t0010 | 1/0 | 7694 | 4 | 3 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7689): Show |
chr3 | 122675839 | 122735840 |
a0001c0003t0020 | 0/0 | 7694 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7689): Show |
chr3 | 122675839 | 122735840 |
a0001c0005t0002 | 0/0 | 7693 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7688): Show |
chr3 | 122675839 | 122735840 |
a0001c0005t0003 | 0/0 | 7693 | 5 | 0 | 1 | 4 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7688): Show |
chr3 | 122675839 | 122735840 |
a0001c0007t0005 | 0/0 | 7695 | 4 | 1 | 3 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7690): Show |
chr3 | 122675839 | 122735840 |
a0001c0012t0003 | 0/0 | 7693 | 2 | 0 | 0 | 2 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7688): Show |
chr3 | 122675839 | 122735840 |
a0001c0016t0027 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 1 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7690): Show |
chr3 | 122675839 | 122735840 |
a0001c0018t0007 | 0/0 | 7694 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7689): Show |
chr3 | 122675839 | 122735840 |
a0001c0021t0029 | 0/0 | 7694 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7689): Show |
chr3 | 122675839 | 122735840 |
a0001c0022t0001 | 0/0 | 7694 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7689): Show |
chr3 | 122675839 | 122735840 |
a0001c0023t0006 | 0/0 | 7694 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7689): Show |
chr3 | 122675839 | 122735840 |
a0001c0024t0001 | 0/0 | 7694 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7689): Show |
chr3 | 122675839 | 122735840 |
a0002c0002t0004 | 0/0 | 7694 | 32 | 4 | 4 | 22 | 0 | 2 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7689): Show |
chr3 | 122675839 | 122735840 |
a0002c0002t0013 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7690): Show |
chr3 | 122675839 | 122735840 |
a0002c0002t0025 | 0/0 | 7693 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7688): Show |
chr3 | 122675839 | 122735840 |
a0002c0002t0026 | 0/0 | 7694 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7689): Show |
chr3 | 122675839 | 122735840 |
a0003c0004t0003 | 0/0 | 7693 | 5 | 2 | 3 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7688): Show |
chr3 | 122675839 | 122735840 |
a0003c0004t0006 | 0/0 | 7694 | 3 | 0 | 2 | 0 | 1 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7689): Show |
chr3 | 122675839 | 122735840 |
a0003c0004t0019 | 0/0 | 7693 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7688): Show |
chr3 | 122675839 | 122735840 |
a0003c0015t0018 | 0/0 | 7693 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7688): Show |
chr3 | 122675839 | 122735840 |
a0004c0008t0008 | 0/0 | 7695 | 3 | 0 | 3 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7690): Show |
chr3 | 122675839 | 122735840 |
a0004c0009t0008 | 0/0 | 7695 | 3 | 3 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7690): Show |
chr3 | 122675839 | 122735840 |
a0004c0011t0008 | 0/0 | 7695 | 2 | 2 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7690): Show |
chr3 | 122675839 | 122735840 |
a0005c0006t0008 | 0/0 | 7695 | 4 | 3 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7690): Show |
chr3 | 122675839 | 122735840 |
a0006c0010t0011 | 0/0 | 7693 | 3 | 2 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7688): Show |
chr3 | 122675839 | 122735840 |
a0007c0017t0005 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7690): Show |
chr3 | 122675839 | 122735840 |
a0008c0026t0003 | 0/0 | 7693 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7688): Show |
chr3 | 122675839 | 122735840 |
a0009c0014t0004 | 0/0 | 7694 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7689): Show |
chr3 | 122675839 | 122735840 |
a0010c0019t0003 | 0/0 | 7693 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7688): Show |
chr3 | 122675839 | 122735840 |
a0011c0025t0001 | 0/0 | 7694 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7689): Show |
chr3 | 122675839 | 122735840 |
a0012c0020t0003 | 0/0 | 7693 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7688): Show |
chr3 | 122675839 | 122735840 |
a0013c0013t0013 | 0/0 | 7695 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | GGAGT others(7690): Show |
chr3 | 122675839 | 122735840 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0005g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0005g0016 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0005g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0005g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0005g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0005g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0005g0129 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0005g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0005g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0006g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0006g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0006g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0006g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0006g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0006g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0006g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0006g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0006g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0006g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0009g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0009g0029 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0009g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0009g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0012g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0012g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0014g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0014g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0015g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0015g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0016g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0017g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0021g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0022g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0023g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0024g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0028g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0030g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0001t0031g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0003t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0003t0006g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0003t0007g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0003t0007g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0003t0007g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0003t0007g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0003t0007g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0003t0007g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0003t0007g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0003t0007g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0003t0007g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0003t0007g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0003t0007g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0003t0007g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0003t0010g0098 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0003t0010g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0003t0010g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0003t0010g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0003t0020g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0005t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0005t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0005t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0005t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0005t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0005t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0007t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0007t0005g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0007t0005g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0007t0005g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0012t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0012t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0016t0027g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0018t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0021t0029g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0022t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0023t0006g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0001c0024t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0004g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0004g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0004g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0004g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0004g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0004g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0013g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0025g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0002c0002t0026g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0003c0004t0003g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0003c0004t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0003c0004t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0003c0004t0003g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0003c0004t0006g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0003c0004t0006g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0003c0004t0006g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0003c0004t0019g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0003c0015t0018g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0004c0008t0008g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0004c0008t0008g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0004c0008t0008g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0004c0009t0008g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0004c0009t0008g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0004c0009t0008g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0004c0011t0008g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0005c0006t0008g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0005c0006t0008g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0005c0006t0008g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0006c0010t0011g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0006c0010t0011g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0006c0010t0011g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0007c0017t0005g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0008c0026t0003g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0009c0014t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0010c0019t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0011c0025t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0012c0020t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
a0013c0013t0013g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0166 | EUR | GBR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00099 | hp2 | a0001 | c0001 | t0005 | g0016 | EUR | GBR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00280 | hp1 | a0001 | c0003 | t0007 | g0324 | EUR | FIN | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00280 | hp2 | a0001 | c0016 | t0027 | g0292 | EUR | FIN | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | FIN | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | FIN | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00408 | hp1 | a0002 | c0002 | t0004 | g0058 | EAS | CHS | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00408 | hp2 | a0001 | c0005 | t0003 | g0126 | EAS | CHS | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00544 | hp1 | a0002 | c0002 | t0004 | g0044 | EAS | CHS | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00558 | hp2 | a0002 | c0002 | t0026 | g0005 | EAS | CHS | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | CHS | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | CHS | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | CHS | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | CHS | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00621 | hp1 | a0001 | c0001 | t0030 | g0297 | EAS | CHS | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00639 | hp1 | a0001 | c0001 | t0017 | g0039 | AMR | PUR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00642 | hp2 | a0001 | c0003 | t0007 | g0323 | AMR | PUR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | CHS | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00735 | hp1 | a0005 | c0006 | t0008 | g0027 | AMR | PUR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00735 | hp2 | a0002 | c0002 | t0004 | g0052 | AMR | PUR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00741 | hp1 | a0007 | c0017 | t0005 | g0090 | AMR | PUR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG00741 | hp2 | a0008 | c0026 | t0003 | g0002 | AMR | PUR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01069 | hp1 | a0002 | c0002 | t0004 | g0031 | AMR | PUR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01069 | hp2 | a0001 | c0001 | t0005 | g0091 | AMR | PUR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01070 | hp1 | a0001 | c0003 | t0007 | g0321 | AMR | PUR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01071 | hp1 | a0002 | c0002 | t0004 | g0031 | AMR | PUR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01071 | hp2 | a0001 | c0003 | t0007 | g0325 | AMR | PUR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01167 | hp2 | a0004 | c0008 | t0008 | g0081 | AMR | PUR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01168 | hp1 | a0003 | c0004 | t0006 | g0159 | AMR | PUR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01169 | hp1 | a0003 | c0004 | t0006 | g0160 | AMR | PUR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01169 | hp2 | a0004 | c0008 | t0008 | g0078 | AMR | PUR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01243 | hp2 | a0001 | c0001 | t0021 | g0307 | AMR | PUR | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01255 | hp1 | a0002 | c0002 | t0004 | g0068 | AMR | CLM | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01255 | hp2 | a0001 | c0007 | t0005 | g0097 | AMR | CLM | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01256 | hp1 | a0001 | c0003 | t0001 | g0079 | AMR | CLM | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01256 | hp2 | a0003 | c0004 | t0019 | g0157 | AMR | CLM | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01257 | hp1 | a0001 | c0001 | t0015 | g0120 | AMR | CLM | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01257 | hp2 | a0004 | c0008 | t0008 | g0080 | AMR | CLM | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01261 | hp2 | a0001 | c0007 | t0005 | g0095 | AMR | CLM | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01346 | hp1 | a0001 | c0003 | t0007 | g0141 | AMR | CLM | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0248 | AMR | CLM | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01358 | hp1 | a0001 | c0001 | t0024 | g0215 | AMR | CLM | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | CLM | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01361 | hp1 | a0001 | c0007 | t0005 | g0096 | AMR | CLM | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01361 | hp2 | a0003 | c0004 | t0003 | g0002 | AMR | CLM | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01433 | hp2 | a0006 | c0010 | t0011 | g0305 | AMR | CLM | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0250 | AMR | CLM | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01496 | hp2 | a0001 | c0001 | t0015 | g0100 | AMR | CLM | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01515 | hp1 | a0001 | c0001 | t0028 | g0030 | EUR | IBS | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01515 | hp2 | a0001 | c0001 | t0005 | g0131 | EUR | IBS | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | IBS | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01516 | hp2 | a0001 | c0001 | t0009 | g0029 | EUR | IBS | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01517 | hp1 | a0001 | c0001 | t0009 | g0029 | EUR | IBS | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01517 | hp2 | a0001 | c0001 | t0005 | g0130 | EUR | IBS | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0187 | AFR | ACB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01884 | hp2 | a0004 | c0009 | t0008 | g0273 | AFR | ACB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | ACB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | ACB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01934 | hp1 | a0003 | c0004 | t0003 | g0291 | AMR | PEL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0227 | AMR | PEL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01943 | hp1 | a0001 | c0003 | t0007 | g0276 | AMR | PEL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PEL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01975 | hp2 | a0001 | c0005 | t0003 | g0226 | AMR | PEL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0220 | AMR | PEL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | PEL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0233 | AMR | PEL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01981 | hp2 | a0001 | c0001 | t0006 | g0301 | AMR | PEL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02015 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | KHV | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | KHV | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | KHV | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02055 | hp2 | a0001 | c0003 | t0010 | g0329 | AFR | ACB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02056 | hp1 | a0001 | c0001 | t0006 | g0300 | EAS | KHV | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0258 | EAS | KHV | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | KHV | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | KHV | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | KHV | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | KHV | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | KHV | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02135 | hp2 | a0001 | c0022 | t0001 | g0086 | EAS | KHV | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0281 | AFR | ACB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02148 | hp1 | a0003 | c0004 | t0003 | g0156 | AMR | PEL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02148 | hp2 | a0001 | c0003 | t0007 | g0322 | AMR | PEL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | CDX | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | CDX | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | ACB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02280 | hp2 | a0002 | c0002 | t0004 | g0001 | AFR | ACB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02293 | hp1 | a0009 | c0014 | t0004 | g0069 | AMR | PEL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | PEL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02451 | hp1 | a0001 | c0001 | t0006 | g0265 | AFR | ACB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02451 | hp2 | a0001 | c0001 | t0005 | g0173 | AFR | ACB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | KHV | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02572 | hp1 | a0006 | c0010 | t0011 | g0306 | AFR | GWD | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02572 | hp2 | a0002 | c0002 | t0004 | g0057 | AFR | GWD | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02602 | hp1 | a0001 | c0001 | t0023 | g0228 | SAS | PJL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02615 | hp1 | a0003 | c0004 | t0003 | g0286 | AFR | GWD | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02615 | hp2 | a0001 | c0001 | t0005 | g0174 | AFR | GWD | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | GWD | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02630 | hp1 | a0005 | c0006 | t0008 | g0027 | AFR | GWD | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02647 | hp1 | a0005 | c0006 | t0008 | g0275 | AFR | GWD | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02683 | hp1 | a0001 | c0001 | t0006 | g0034 | SAS | PJL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02698 | hp1 | a0001 | c0001 | t0006 | g0185 | SAS | PJL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0264 | SAS | PJL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0175 | AFR | GWD | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02723 | hp2 | a0006 | c0010 | t0011 | g0191 | AFR | GWD | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02735 | hp1 | a0001 | c0001 | t0005 | g0016 | SAS | PJL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02735 | hp2 | a0001 | c0001 | t0009 | g0028 | SAS | PJL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02738 | hp1 | a0002 | c0002 | t0013 | g0051 | SAS | PJL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02809 | hp1 | a0002 | c0002 | t0004 | g0001 | AFR | GWD | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | GWD | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | GWD | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02895 | hp1 | a0001 | c0001 | t0014 | g0182 | AFR | GWD | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02896 | hp2 | a0005 | c0006 | t0008 | g0272 | AFR | GWD | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02922 | hp2 | a0001 | c0003 | t0010 | g0167 | AFR | ESN | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02965 | hp1 | a0004 | c0011 | t0008 | g0026 | AFR | ESN | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | ESN | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0267 | AFR | ESN | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | ESN | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03017 | hp1 | a0001 | c0001 | t0005 | g0082 | SAS | PJL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03017 | hp2 | a0001 | c0001 | t0006 | g0184 | SAS | PJL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0311 | AFR | MSL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03098 | hp2 | a0002 | c0002 | t0004 | g0001 | AFR | MSL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03139 | hp1 | a0001 | c0001 | t0006 | g0304 | AFR | ESN | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03139 | hp2 | a0004 | c0011 | t0008 | g0026 | AFR | ESN | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | ESN | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03195 | hp2 | a0010 | c0019 | t0003 | g0234 | AFR | ESN | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03209 | hp1 | a0003 | c0015 | t0018 | g0158 | AFR | MSL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03209 | hp2 | a0001 | c0003 | t0007 | g0326 | AFR | MSL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03225 | hp2 | a0001 | c0018 | t0007 | g0075 | AFR | MSL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03239 | hp1 | a0011 | c0025 | t0001 | g0041 | SAS | PJL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0212 | SAS | PJL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0048 | AFR | MSL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | MSL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03490 | hp1 | a0001 | c0001 | t0006 | g0021 | SAS | PJL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03491 | hp1 | a0002 | c0002 | t0004 | g0172 | SAS | PJL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03491 | hp2 | a0001 | c0001 | t0014 | g0293 | SAS | PJL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03492 | hp2 | a0001 | c0001 | t0006 | g0021 | SAS | PJL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0280 | AFR | ESN | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03540 | hp1 | a0001 | c0023 | t0006 | g0302 | AFR | GWD | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03540 | hp2 | a0001 | c0007 | t0005 | g0094 | AFR | GWD | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03579 | hp2 | a0004 | c0009 | t0008 | g0271 | AFR | MSL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03688 | hp1 | a0001 | c0001 | t0009 | g0028 | SAS | STU | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | STU | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03704 | hp2 | a0001 | c0021 | t0029 | g0164 | SAS | PJL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03710 | hp1 | a0001 | c0001 | t0009 | g0298 | SAS | PJL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | BEB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0330 | SAS | BEB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0249 | SAS | BEB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0252 | SAS | BEB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03927 | hp2 | a0001 | c0024 | t0001 | g0040 | SAS | BEB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0217 | SAS | BEB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | STU | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG04184 | hp2 | a0002 | c0002 | t0004 | g0050 | SAS | BEB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG04199 | hp1 | a0001 | c0001 | t0005 | g0093 | SAS | STU | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0145 | SAS | STU | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0225 | SAS | STU | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0232 | SAS | STU | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0240 | SAS | STU | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | STU | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18522 | hp1 | a0001 | c0001 | t0006 | g0186 | AFR | YRI | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18747 | hp1 | a0001 | c0003 | t0007 | g0171 | EAS | CHB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | CHB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | YRI | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18906 | hp2 | a0004 | c0009 | t0008 | g0282 | AFR | YRI | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18941 | hp2 | a0002 | c0002 | t0004 | g0140 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18945 | hp1 | a0001 | c0001 | t0031 | g0109 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18962 | hp1 | a0012 | c0020 | t0003 | g0224 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18964 | hp1 | a0002 | c0002 | t0004 | g0061 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18968 | hp2 | a0001 | c0001 | t0012 | g0245 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18969 | hp2 | a0002 | c0002 | t0004 | g0064 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18977 | hp2 | a0001 | c0001 | t0016 | g0151 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18983 | hp1 | a0002 | c0002 | t0004 | g0059 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18983 | hp2 | a0002 | c0002 | t0004 | g0066 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18984 | hp2 | a0002 | c0002 | t0004 | g0053 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18990 | hp2 | a0002 | c0002 | t0004 | g0188 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18992 | hp1 | a0002 | c0002 | t0004 | g0161 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18994 | hp2 | a0001 | c0005 | t0003 | g0223 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18995 | hp1 | a0001 | c0012 | t0003 | g0285 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19000 | hp2 | a0002 | c0002 | t0004 | g0056 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19002 | hp2 | a0002 | c0002 | t0025 | g0062 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19005 | hp2 | a0002 | c0002 | t0004 | g0035 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19009 | hp1 | a0001 | c0012 | t0003 | g0070 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19011 | hp1 | a0002 | c0002 | t0004 | g0055 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19030 | hp1 | a0001 | c0003 | t0006 | g0313 | AFR | LWK | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | LWK | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19043 | hp1 | a0001 | c0003 | t0007 | g0274 | AFR | LWK | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0261 | AFR | LWK | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19056 | hp1 | a0002 | c0002 | t0004 | g0308 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19056 | hp2 | a0001 | c0005 | t0003 | g0222 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19058 | hp1 | a0002 | c0002 | t0004 | g0005 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19060 | hp1 | a0001 | c0003 | t0007 | g0169 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19060 | hp2 | a0001 | c0005 | t0003 | g0127 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19067 | hp1 | a0001 | c0001 | t0012 | g0244 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19067 | hp2 | a0002 | c0002 | t0004 | g0067 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19072 | hp2 | a0013 | c0013 | t0013 | g0060 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19074 | hp2 | a0002 | c0002 | t0004 | g0022 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19077 | hp2 | a0001 | c0003 | t0007 | g0168 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19078 | hp1 | a0002 | c0002 | t0004 | g0054 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19079 | hp2 | a0002 | c0002 | t0004 | g0065 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19082 | hp2 | a0002 | c0002 | t0004 | g0063 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19085 | hp1 | a0002 | c0002 | t0004 | g0049 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19086 | hp2 | a0002 | c0002 | t0004 | g0022 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19089 | hp1 | a0001 | c0005 | t0002 | g0219 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | YRI | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA20129 | hp1 | a0001 | c0001 | t0022 | g0144 | AFR | ASW | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ASW | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA20805 | hp1 | a0003 | c0004 | t0006 | g0155 | EUR | TSI | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA20805 | hp2 | a0001 | c0001 | t0005 | g0290 | EUR | TSI | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA20905 | hp1 | a0001 | c0001 | t0009 | g0299 | SAS | GIH | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | GIH | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0229 | AMR | CLM | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG01123 | hp2 | a0001 | c0001 | t0005 | g0092 | AMR | CLM | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0328 | AFR | ACB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0270 | AFR | ACB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0310 | AFR | ACB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0268 | AFR | ACB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | ACB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0303 | AFR | ACB | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0189 | AFR | MSL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0266 | AFR | MSL | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG06807 | hp1 | a0001 | c0003 | t0010 | g0170 | AFR | USA | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
HG06807 | hp2 | a0003 | c0004 | t0003 | g0002 | AFR | USA | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
NA20300 | hp2 | a0001 | c0003 | t0020 | g0142 | AFR | USA | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0129 | REF | REF | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
homoSapiens | grch38p0 | a0001 | c0003 | t0010 | g0098 | REF | REF | PARP14_chr3_122675839_122735840 | PARP14 | chr3 | 122675839 | 122735840 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:122692319 | A | T | 1 | a0008 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.374A>T | p.Asp125Val | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/17 | 419/7694 | 374/5406 | 125/1801 | chr3 | 122692319 | |||
chr3:122699416 | C | T | 1 | a0011 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.862C>T | p.Leu288Phe | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/17 | 907/7694 | 862/5406 | 288/1801 | chr3 | 122699416 | |||
chr3:122699903 | G | A | 7 | a0002 a0003 a0004 others(4): Show |
60 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(57): Show |
missense_variant | MODERATE | c.1349G>A | p.Arg450Lys | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/17 | 1394/7694 | 1349/5406 | 450/1801 | chr3 | 122699903 | |||
chr3:122700236 | C | A | 3 | a0002 a0009 a0013 |
37 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(34): Show |
missense_variant | MODERATE | c.1682C>A | p.Ala561Glu | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/17 | 1727/7694 | 1682/5406 | 561/1801 | chr3 | 122700236 | |||
chr3:122700445 | A | G | 2 | a0004 a0005 |
12 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
missense_variant | MODERATE | c.1891A>G | p.Thr631Ala | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/17 | 1936/7694 | 1891/5406 | 631/1801 | chr3 | 122700445 | |||
chr3:122701295 | G | A | 1 | a0007 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.2741G>A | p.Arg914Gln | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/17 | 2786/7694 | 2741/5406 | 914/1801 | chr3 | 122701295 | |||
chr3:122703763 | G | A | 1 | a0010 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.3103G>A | p.Val1035Ile | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 7/17 | 3148/7694 | 3103/5406 | 1035/1801 | chr3 | 122703763 | |||
chr3:122703848 | A | T | 1 | a0013 | 1 | NA19072.hp2 | missense_variant | MODERATE | c.3188A>T | p.Asp1063Val | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 7/17 | 3233/7694 | 3188/5406 | 1063/1801 | chr3 | 122703848 | |||
chr3:122704707 | G | A | 1 | a0012 | 1 | NA18962.hp1 | missense_variant | MODERATE | c.3499G>A | p.Val1167Ile | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/17 | 3544/7694 | 3499/5406 | 1167/1801 | chr3 | 122704707 | |||
chr3:122718389 | A | C | 1 | a0006 | 3 | HG01433.hp2 HG02572.hp1 HG02723.hp2 |
missense_variant | MODERATE | c.4238A>C | p.Gln1413Pro | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 14/17 | 4283/7694 | 4238/5406 | 1413/1801 | chr3 | 122718389 | |||
chr3:122718689 | C | T | 1 | a0005 | 4 | HG00735.hp1 HG02630.hp1 HG02647.hp1 others(1): Show |
missense_variant | MODERATE | c.4538C>T | p.Ala1513Val | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 14/17 | 4583/7694 | 4538/5406 | 1513/1801 | chr3 | 122718689 | |||
chr3:122728368 | C | T | 1 | a0009 | 1 | HG02293.hp1 | missense_variant | MODERATE | c.5177C>T | p.Thr1726Met | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 5222/7694 | 5177/5406 | 1726/1801 | chr3 | 122728368 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:122692425 | G | C | 1 | a0013c0013 | 1 | NA19072.hp2 | synonymous_variant | LOW | c.480G>C | p.Val160Val | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/17 | 525/7694 | 480/5406 | 160/1801 | chr3 | 122692425 | |||
chr3:122699409 | C | T | 1 | a0001c0012 | 2 | NA18995.hp1 NA19009.hp1 |
synonymous_variant | LOW | c.855C>T | p.Ala285Ala | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/17 | 900/7694 | 855/5406 | 285/1801 | chr3 | 122699409 | |||
chr3:122699589 | C | T | 2 | a0001c0024 a0011c0025 |
2 | HG03239.hp1 HG03927.hp2 |
synonymous_variant | LOW | c.1035C>T | p.Asn345Asn | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/17 | 1080/7694 | 1035/5406 | 345/1801 | chr3 | 122699589 | |||
chr3:122700030 | G | A | 1 | a0001c0016 | 1 | HG00280.hp2 | synonymous_variant | LOW | c.1476G>A | p.Thr492Thr | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/17 | 1521/7694 | 1476/5406 | 492/1801 | chr3 | 122700030 | |||
chr3:122700288 | C | G | 1 | a0001c0023 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.1734C>G | p.Thr578Thr | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/17 | 1779/7694 | 1734/5406 | 578/1801 | chr3 | 122700288 | |||
chr3:122701146 | C | T | 3 | a0004c0009 a0004c0011 a0005c0006 |
9 | HG00735.hp1 HG01884.hp2 HG02630.hp1 others(6): Show |
synonymous_variant | LOW | c.2592C>T | p.Ala864Ala | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/17 | 2637/7694 | 2592/5406 | 864/1801 | chr3 | 122701146 | |||
chr3:122701203 | C | T | 1 | a0001c0007 | 4 | HG01255.hp2 HG01261.hp2 HG01361.hp1 others(1): Show |
synonymous_variant | LOW | c.2649C>T | p.Pro883Pro | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/17 | 2694/7694 | 2649/5406 | 883/1801 | chr3 | 122701203 | |||
chr3:122701353 | C | T | 1 | a0001c0005 | 6 | HG00408.hp2 HG01975.hp2 NA18994.hp2 others(3): Show |
synonymous_variant | LOW | c.2799C>T | p.Cys933Cys | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/17 | 2844/7694 | 2799/5406 | 933/1801 | chr3 | 122701353 | |||
chr3:122701401 | G | A | 1 | a0001c0018 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.2847G>A | p.Lys949Lys | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/17 | 2892/7694 | 2847/5406 | 949/1801 | chr3 | 122701401 | |||
chr3:122703744 | C | T | 1 | a0004c0011 | 2 | HG02965.hp1 HG03139.hp2 |
splice_region_variant&synonymous_variant | LOW | c.3084C>T | p.Thr1028Thr | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 7/17 | 3129/7694 | 3084/5406 | 1028/1801 | chr3 | 122703744 | |||
chr3:122703777 | C | T | 1 | a0001c0022 | 1 | HG02135.hp2 | synonymous_variant | LOW | c.3117C>T | p.Leu1039Leu | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 7/17 | 3162/7694 | 3117/5406 | 1039/1801 | chr3 | 122703777 | |||
chr3:122718087 | C | T | 1 | a0001c0021 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.4017C>T | p.His1339His | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 13/17 | 4062/7694 | 4017/5406 | 1339/1801 | chr3 | 122718087 | |||
chr3:122718474 | T | C | 24 | a0001c0001 a0001c0005 a0001c0007 others(21): Show |
345 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(342): Show |
synonymous_variant | LOW | c.4323T>C | p.Tyr1441Tyr | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 14/17 | 4368/7694 | 4323/5406 | 1441/1801 | chr3 | 122718474 | |||
chr3:122718618 | C | T | 1 | a0003c0015 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.4467C>T | p.Asp1489Asp | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 14/17 | 4512/7694 | 4467/5406 | 1489/1801 | chr3 | 122718618 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:122728727 | A | C | 16 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0014 others(13): Show |
141 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*130A>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 130 | chr3 | 122728727 | ||||||
chr3:122728749 | C | T | 52 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(49): Show |
361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
3_prime_UTR_variant | MODIFIER | c.*152C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 152 | chr3 | 122728749 | ||||||
chr3:122728754 | C | A | 4 | a0004c0008t0008 a0004c0009t0008 a0004c0011t0008 others(1): Show |
12 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*157C>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 157 | chr3 | 122728754 | ||||||
chr3:122729064 | A | G | 10 | a0002c0002t0004 a0002c0002t0013 a0002c0002t0025 others(7): Show |
49 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*467A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 467 | chr3 | 122729064 | ||||||
chr3:122729079 | C | T | 1 | a0001c0001t0024 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*482C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 482 | chr3 | 122729079 | ||||||
chr3:122729092 | G | A | 1 | a0001c0016t0027 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*495G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 495 | chr3 | 122729092 | ||||||
chr3:122729120 | C | T | 1 | a0001c0001t0031 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*523C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 523 | chr3 | 122729120 | ||||||
chr3:122729305 | G | T | 1 | a0002c0002t0026 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*708G>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 708 | chr3 | 122729305 | ||||||
chr3:122729314 | G | C | 1 | a0001c0001t0016 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*717G>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 717 | chr3 | 122729314 | ||||||
chr3:122729319 | A | G | 1 | a0001c0001t0030 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*722A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 722 | chr3 | 122729319 | ||||||
chr3:122729356 | C | T | 7 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0016 others(4): Show |
71 | HG00597.hp1 HG00597.hp2 HG00673.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*759C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 759 | chr3 | 122729356 | ||||||
chr3:122729391 | C | T | 6 | a0002c0002t0004 a0002c0002t0013 a0002c0002t0025 others(3): Show |
37 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*794C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 794 | chr3 | 122729391 | ||||||
chr3:122729434 | C | CT | 11 | a0001c0001t0005 a0001c0001t0015 a0001c0007t0005 others(8): Show |
38 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*854dupT | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 855 | INFO_REALIGN_3_PRIME | chr3 | 122729434 | |||||
chr3:122729434 | CT | C | 19 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0014 others(16): Show |
138 | HG00099.hp1 HG00408.hp2 HG00597.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*854delT | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 854 | INFO_REALIGN_3_PRIME | chr3 | 122729434 | |||||
chr3:122729496 | G | A | 2 | a0001c0001t0028 a0001c0003t0020 |
2 | HG01515.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*899G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 899 | chr3 | 122729496 | ||||||
chr3:122729497 | C | T | 1 | a0001c0001t0009 | 6 | HG01516.hp2 HG01517.hp1 HG02735.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*900C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 900 | chr3 | 122729497 | ||||||
chr3:122729498 | G | T | 1 | a0001c0001t0023 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*901G>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 901 | chr3 | 122729498 | ||||||
chr3:122729560 | G | A | 1 | a0001c0001t0022 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*963G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 963 | chr3 | 122729560 | ||||||
chr3:122729704 | C | T | 2 | a0001c0003t0007 a0001c0018t0007 |
13 | HG00280.hp1 HG00642.hp2 HG01070.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1107C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 1107 | chr3 | 122729704 | ||||||
chr3:122729717 | T | A | 1 | a0001c0001t0021 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1120T>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 1120 | chr3 | 122729717 | ||||||
chr3:122729797 | A | G | 1 | a0003c0004t0019 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1200A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 1200 | chr3 | 122729797 | ||||||
chr3:122729963 | G | C | 1 | a0001c0001t0017 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1366G>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 1366 | chr3 | 122729963 | ||||||
chr3:122729969 | G | C | 1 | a0001c0001t0022 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1372G>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 1372 | chr3 | 122729969 | ||||||
chr3:122730067 | T | C | 15 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0014 others(12): Show |
138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*1470T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 1470 | chr3 | 122730067 | ||||||
chr3:122730282 | T | C | 1 | a0001c0021t0029 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1685T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 1685 | chr3 | 122730282 | ||||||
chr3:122730284 | T | C | 1 | a0001c0001t0015 | 2 | HG01257.hp1 HG01496.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1687T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 1687 | chr3 | 122730284 | ||||||
chr3:122730736 | G | A | 1 | a0003c0015t0018 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2139G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 2139 | chr3 | 122730736 | ||||||
chr3:122730810 | A | G | 15 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0014 others(12): Show |
138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*2213A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 17/17 | 2213 | chr3 | 122730810 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:122681702 | G | C | 45 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(42): Show |
48 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.187+632G>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122681702 | |||||||
chr3:122681785 | A | G | 232 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(229): Show |
250 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.187+715A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122681785 | |||||||
chr3:122681943 | C | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0020 others(114): Show |
126 | HG00099.hp1 HG00597.hp2 HG00609.hp2 others(123): Show |
intron_variant | MODIFIER | c.187+873C>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122681943 | |||||||
chr3:122682015 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.187+945A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122682015 | |||||||
chr3:122682086 | G | C | 125 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0020 others(122): Show |
136 | HG00099.hp1 HG00597.hp2 HG00609.hp2 others(133): Show |
intron_variant | MODIFIER | c.187+1016G>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122682086 | |||||||
chr3:122682113 | T | C | 231 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(228): Show |
249 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.187+1043T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122682113 | |||||||
chr3:122682117 | C | A | 1 | a0001c0003t0007g0276 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.187+1047C>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122682117 | |||||||
chr3:122682659 | T | C | 1 | a0001c0001t0001g0074 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.187+1589T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122682659 | |||||||
chr3:122682789 | C | A | 1 | a0001c0018t0007g0075 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.187+1719C>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122682789 | |||||||
chr3:122682848 | C | G | 1 | a0001c0001t0001g0330 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.187+1778C>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122682848 | |||||||
chr3:122682871 | G | A | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG02055.hp1 HG02145.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.187+1801G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122682871 | |||||||
chr3:122682898 | C | G | 1 | a0005c0006t0008g0275 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.187+1828C>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122682898 | |||||||
chr3:122682962 | G | A | 29 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0287 others(26): Show |
31 | HG00280.hp2 HG00621.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.187+1892G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122682962 | |||||||
chr3:122683040 | C | A | 3 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0012t0003g0285 |
3 | NA18982.hp1 NA18995.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.187+1970C>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122683040 | |||||||
chr3:122683082 | GAAAC | G | 4 | a0001c0001t0001g0309 a0001c0001t0001g0312 a0001c0001t0003g0310 others(1): Show |
4 | HG02486.hp1 HG02818.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+2024_187+2027d others(6): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 122683082 | ||||||
chr3:122683376 | C | T | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG02055.hp1 HG02145.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-1809C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122683376 | |||||||
chr3:122683495 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.188-1690G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122683495 | |||||||
chr3:122683559 | C | T | 19 | a0001c0001t0001g0030 a0001c0001t0001g0316 a0001c0001t0001g0317 others(16): Show |
21 | HG00280.hp1 HG00642.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.188-1626C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122683559 | |||||||
chr3:122683609 | T | C | 1 | a0001c0001t0002g0077 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.188-1576T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122683609 | |||||||
chr3:122683723 | A | G | 8 | a0001c0001t0001g0312 a0001c0003t0007g0274 a0004c0009t0008g0271 others(5): Show |
10 | HG00735.hp1 HG01884.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.188-1462A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122683723 | |||||||
chr3:122683927 | A | T | 53 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(50): Show |
58 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.188-1258A>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122683927 | |||||||
chr3:122683979 | T | G | 3 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0012t0003g0285 |
3 | NA18982.hp1 NA18995.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.188-1206T>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122683979 | |||||||
chr3:122683990 | G | A | 1 | a0001c0001t0003g0280 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.188-1195G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122683990 | |||||||
chr3:122684182 | A | G | 8 | a0003c0004t0003g0002 a0003c0004t0003g0156 a0003c0004t0006g0155 others(5): Show |
9 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.188-1003A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122684182 | |||||||
chr3:122684424 | T | C | 1 | a0001c0001t0017g0039 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.188-761T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122684424 | |||||||
chr3:122684515 | T | C | 2 | a0001c0024t0001g0040 a0011c0025t0001g0041 |
2 | HG03239.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.188-670T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122684515 | |||||||
chr3:122684633 | C | T | 158 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0071 others(155): Show |
170 | HG00280.hp2 HG00597.hp2 HG00609.hp2 others(167): Show |
intron_variant | MODIFIER | c.188-552C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122684633 | |||||||
chr3:122684687 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.188-498C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122684687 | |||||||
chr3:122684697 | C | T | 235 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0020 others(232): Show |
254 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(251): Show |
intron_variant | MODIFIER | c.188-488C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122684697 | |||||||
chr3:122684839 | G | T | 1 | a0001c0001t0001g0076 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.188-346G>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 1/16 | chr3 | 122684839 | |||||||
chr3:122685510 | CT | C | 70 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0178 others(67): Show |
77 | HG00280.hp1 HG00621.hp1 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.321+209delT | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 122685510 | ||||||
chr3:122685532 | C | T | 1 | a0001c0001t0002g0269 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.321+214C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 2/16 | chr3 | 122685532 | |||||||
chr3:122685533 | G | A | 38 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(35): Show |
42 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.321+215G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 2/16 | chr3 | 122685533 | |||||||
chr3:122685550 | A | C | 53 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(50): Show |
58 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.321+232A>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 2/16 | chr3 | 122685550 | |||||||
chr3:122685574 | A | G | 1 | a0001c0012t0003g0070 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.321+256A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 2/16 | chr3 | 122685574 | |||||||
chr3:122685586 | T | A | 1 | a0001c0001t0002g0145 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.321+268T>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 2/16 | chr3 | 122685586 | |||||||
chr3:122685613 | G | C | 1 | a0001c0003t0010g0167 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.321+295G>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 2/16 | chr3 | 122685613 | |||||||
chr3:122685661 | C | T | 169 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0178 others(166): Show |
179 | HG00280.hp1 HG00597.hp2 HG00609.hp1 others(176): Show |
intron_variant | MODIFIER | c.321+343C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 2/16 | chr3 | 122685661 | |||||||
chr3:122685663 | C | T | 4 | a0001c0001t0003g0266 a0001c0001t0003g0267 a0001c0001t0003g0268 others(1): Show |
4 | HG02486.hp2 HG02976.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.321+345C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 2/16 | chr3 | 122685663 | |||||||
chr3:122685710 | A | T | 50 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0178 others(47): Show |
56 | HG00280.hp1 HG00621.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.321+392A>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 2/16 | chr3 | 122685710 | |||||||
chr3:122685750 | G | C | 238 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0020 others(235): Show |
257 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(254): Show |
intron_variant | MODIFIER | c.321+432G>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 2/16 | chr3 | 122685750 | |||||||
chr3:122685750 | G | T | 1 | a0001c0001t0002g0264 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.321+432G>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 2/16 | chr3 | 122685750 | |||||||
chr3:122685830 | T | A | 1 | a0004c0011t0008g0026 | 2 | HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.321+512T>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 2/16 | chr3 | 122685830 | |||||||
chr3:122685898 | T | G | 1 | a0002c0002t0004g0044 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.321+580T>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 2/16 | chr3 | 122685898 | |||||||
chr3:122685959 | A | G | 14 | a0001c0001t0001g0018 a0001c0001t0005g0018 a0001c0001t0005g0019 others(11): Show |
16 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+641A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 2/16 | chr3 | 122685959 | |||||||
chr3:122686002 | C | A | 2 | a0001c0001t0001g0314 a0001c0001t0003g0032 |
3 | HG02895.hp2 HG02897.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.321+684C>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 2/16 | chr3 | 122686002 | |||||||
chr3:122686146 | T | C | 235 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0020 others(232): Show |
252 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.321+828T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 2/16 | chr3 | 122686146 | |||||||
chr3:122686309 | A | G | 2 | a0003c0004t0006g0159 a0003c0004t0006g0160 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.322-771A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 2/16 | chr3 | 122686309 | |||||||
chr3:122686390 | T | C | 3 | a0006c0010t0011g0191 a0006c0010t0011g0305 a0006c0010t0011g0306 |
3 | HG01433.hp2 HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.322-690T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 2/16 | chr3 | 122686390 | |||||||
chr3:122686398 | A | T | 1 | a0001c0003t0007g0171 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.322-682A>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 2/16 | chr3 | 122686398 | |||||||
chr3:122686487 | T | C | 14 | a0001c0001t0001g0018 a0001c0001t0005g0018 a0001c0001t0005g0019 others(11): Show |
16 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-593T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 2/16 | chr3 | 122686487 | |||||||
chr3:122686677 | G | A | 3 | a0006c0010t0011g0191 a0006c0010t0011g0305 a0006c0010t0011g0306 |
3 | HG01433.hp2 HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.322-403G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 2/16 | chr3 | 122686677 | |||||||
chr3:122686937 | A | G | 1 | a0001c0018t0007g0075 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.322-143A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 2/16 | chr3 | 122686937 | |||||||
chr3:122687018 | A | T | 1 | a0001c0018t0007g0075 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.322-62A>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 2/16 | chr3 | 122687018 | |||||||
chr3:122687177 | A | G | 1 | a0001c0001t0002g0263 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.355+64A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122687177 | |||||||
chr3:122687213 | T | A | 14 | a0001c0001t0001g0018 a0001c0001t0005g0018 a0001c0001t0005g0019 others(11): Show |
16 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.355+100T>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122687213 | |||||||
chr3:122687230 | G | A | 178 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0020 others(175): Show |
189 | HG00280.hp1 HG00597.hp2 HG00609.hp1 others(186): Show |
intron_variant | MODIFIER | c.355+117G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122687230 | |||||||
chr3:122687293 | T | C | 34 | a0001c0024t0001g0040 a0002c0002t0004g0001 a0002c0002t0004g0005 others(31): Show |
38 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.355+180T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122687293 | |||||||
chr3:122687340 | A | G | 14 | a0001c0001t0001g0018 a0001c0001t0005g0018 a0001c0001t0005g0019 others(11): Show |
16 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.355+227A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122687340 | |||||||
chr3:122687370 | G | A | 1 | a0001c0018t0007g0075 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.355+257G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122687370 | |||||||
chr3:122687387 | G | A | 23 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0045 others(20): Show |
26 | HG02258.hp1 HG02523.hp2 HG02622.hp1 others(23): Show |
intron_variant | MODIFIER | c.355+274G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122687387 | |||||||
chr3:122687418 | C | A | 110 | a0001c0001t0001g0198 a0001c0001t0001g0309 a0001c0001t0002g0017 others(107): Show |
114 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.355+305C>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122687418 | |||||||
chr3:122687467 | A | G | 45 | a0001c0024t0001g0040 a0002c0002t0004g0001 a0002c0002t0004g0005 others(42): Show |
51 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.355+354A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122687467 | |||||||
chr3:122687551 | T | C | 14 | a0001c0001t0001g0018 a0001c0001t0005g0018 a0001c0001t0005g0019 others(11): Show |
16 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.355+438T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122687551 | |||||||
chr3:122687608 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | NA18940.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.355+495C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122687608 | |||||||
chr3:122687660 | C | T | 4 | a0001c0001t0003g0310 a0001c0001t0003g0311 a0002c0002t0004g0068 others(1): Show |
4 | HG01255.hp1 HG02293.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.355+547C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122687660 | |||||||
chr3:122687699 | G | A | 1 | a0001c0001t0005g0082 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.355+586G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122687699 | |||||||
chr3:122687733 | C | T | 14 | a0001c0001t0001g0018 a0001c0001t0005g0018 a0001c0001t0005g0019 others(11): Show |
16 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.355+620C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122687733 | |||||||
chr3:122687820 | A | T | 1 | a0001c0001t0001g0309 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.355+707A>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122687820 | |||||||
chr3:122687843 | C | T | 2 | a0001c0001t0003g0033 a0001c0001t0003g0048 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.355+730C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122687843 | |||||||
chr3:122687855 | T | C | 14 | a0001c0001t0001g0018 a0001c0001t0005g0018 a0001c0001t0005g0019 others(11): Show |
16 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.355+742T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122687855 | |||||||
chr3:122688012 | C | G | 230 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0020 others(227): Show |
247 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(244): Show |
intron_variant | MODIFIER | c.355+899C>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122688012 | |||||||
chr3:122688085 | A | AT | 45 | a0001c0001t0001g0018 a0001c0001t0005g0018 a0001c0001t0005g0019 others(42): Show |
50 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.355+983dupT | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 122688085 | ||||||
chr3:122688097 | G | T | 14 | a0001c0001t0001g0018 a0001c0001t0005g0018 a0001c0001t0005g0019 others(11): Show |
16 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.355+984G>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122688097 | |||||||
chr3:122688173 | G | C | 14 | a0001c0001t0001g0018 a0001c0001t0005g0018 a0001c0001t0005g0019 others(11): Show |
16 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.355+1060G>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122688173 | |||||||
chr3:122688242 | C | A | 8 | a0003c0004t0003g0002 a0003c0004t0003g0156 a0003c0004t0006g0155 others(5): Show |
9 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.355+1129C>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122688242 | |||||||
chr3:122688492 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.355+1379C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122688492 | |||||||
chr3:122688527 | T | G | 14 | a0001c0001t0001g0018 a0001c0001t0005g0018 a0001c0001t0005g0019 others(11): Show |
16 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.355+1414T>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122688527 | |||||||
chr3:122688565 | TA | T | 14 | a0001c0001t0001g0018 a0001c0001t0005g0018 a0001c0001t0005g0019 others(11): Show |
16 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.355+1455delA | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 122688565 | ||||||
chr3:122688701 | G | A | 14 | a0001c0001t0001g0018 a0001c0001t0005g0018 a0001c0001t0005g0019 others(11): Show |
16 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.355+1588G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122688701 | |||||||
chr3:122688752 | T | C | 14 | a0001c0001t0001g0018 a0001c0001t0005g0018 a0001c0001t0005g0019 others(11): Show |
16 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.355+1639T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122688752 | |||||||
chr3:122688853 | C | G | 1 | a0001c0001t0003g0038 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.355+1740C>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122688853 | |||||||
chr3:122688897 | A | G | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG02055.hp1 HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.355+1784A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122688897 | |||||||
chr3:122689066 | G | A | 1 | a0001c0001t0003g0038 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.355+1953G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122689066 | |||||||
chr3:122689174 | G | A | 1 | a0003c0004t0003g0286 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.355+2061G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122689174 | |||||||
chr3:122689251 | T | C | 14 | a0001c0001t0001g0018 a0001c0001t0005g0018 a0001c0001t0005g0019 others(11): Show |
16 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.355+2138T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122689251 | |||||||
chr3:122689371 | T | C | 17 | a0001c0001t0006g0021 a0001c0001t0006g0034 a0001c0001t0006g0184 others(14): Show |
20 | HG00621.hp1 HG01243.hp2 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.355+2258T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122689371 | |||||||
chr3:122689497 | C | T | 8 | a0003c0004t0003g0286 a0004c0009t0008g0271 a0004c0009t0008g0273 others(5): Show |
10 | HG00735.hp1 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.355+2384C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122689497 | |||||||
chr3:122689606 | G | C | 14 | a0001c0001t0001g0018 a0001c0001t0005g0018 a0001c0001t0005g0019 others(11): Show |
16 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.355+2493G>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122689606 | |||||||
chr3:122689652 | C | T | 1 | a0001c0001t0002g0262 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.355+2539C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122689652 | |||||||
chr3:122689682 | A | G | 14 | a0001c0001t0001g0018 a0001c0001t0005g0018 a0001c0001t0005g0019 others(11): Show |
16 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.355+2569A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122689682 | |||||||
chr3:122689778 | C | G | 8 | a0002c0002t0004g0035 a0002c0002t0004g0061 a0002c0002t0004g0063 others(5): Show |
8 | NA18964.hp1 NA18969.hp2 NA18983.hp2 others(5): Show |
intron_variant | MODIFIER | c.356-2523C>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122689778 | |||||||
chr3:122689949 | T | TTGCA | 2 | a0002c0002t0004g0022 a0002c0002t0004g0188 |
3 | NA18990.hp2 NA19074.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.356-2351_356-2348d others(6): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 122689949 | ||||||
chr3:122689950 | T | C | 1 | a0002c0002t0004g0049 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.356-2351T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122689950 | |||||||
chr3:122689987 | C | T | 14 | a0001c0001t0001g0018 a0001c0001t0005g0018 a0001c0001t0005g0019 others(11): Show |
16 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.356-2314C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122689987 | |||||||
chr3:122690429 | C | A | 1 | a0001c0001t0003g0194 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.356-1872C>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122690429 | |||||||
chr3:122690498 | C | T | 14 | a0001c0001t0001g0018 a0001c0001t0005g0018 a0001c0001t0005g0019 others(11): Show |
16 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.356-1803C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122690498 | |||||||
chr3:122690545 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.356-1756G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122690545 | |||||||
chr3:122690615 | G | A | 1 | a0001c0001t0003g0195 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.356-1686G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122690615 | |||||||
chr3:122690657 | G | A | 175 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0045 others(172): Show |
185 | HG00280.hp1 HG00597.hp2 HG00609.hp1 others(182): Show |
intron_variant | MODIFIER | c.356-1644G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122690657 | |||||||
chr3:122690764 | G | A | 176 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0045 others(173): Show |
186 | HG00280.hp1 HG00597.hp2 HG00609.hp1 others(183): Show |
intron_variant | MODIFIER | c.356-1537G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122690764 | |||||||
chr3:122690803 | C | T | 3 | a0001c0001t0005g0016 a0001c0001t0005g0130 a0001c0001t0005g0131 |
4 | HG00099.hp2 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.356-1498C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122690803 | |||||||
chr3:122690816 | C | T | 8 | a0003c0004t0003g0002 a0003c0004t0003g0156 a0003c0004t0006g0155 others(5): Show |
9 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.356-1485C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122690816 | |||||||
chr3:122690925 | C | G | 2 | a0001c0003t0006g0313 a0001c0003t0020g0142 |
2 | NA19030.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.356-1376C>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122690925 | |||||||
chr3:122691118 | C | T | 8 | a0003c0004t0003g0002 a0003c0004t0003g0156 a0003c0004t0006g0155 others(5): Show |
9 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.356-1183C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122691118 | |||||||
chr3:122691152 | T | C | 251 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0018 others(248): Show |
270 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.356-1149T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122691152 | |||||||
chr3:122691361 | G | A | 38 | a0001c0024t0001g0040 a0002c0002t0004g0001 a0002c0002t0004g0005 others(35): Show |
42 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.356-940G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122691361 | |||||||
chr3:122691467 | G | A | 1 | a0001c0001t0001g0309 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.356-834G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122691467 | |||||||
chr3:122691564 | T | A | 3 | a0001c0001t0001g0314 a0001c0001t0003g0032 a0001c0003t0010g0329 |
4 | HG02055.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.356-737T>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122691564 | |||||||
chr3:122691599 | A | G | 2 | a0001c0001t0003g0270 a0001c0001t0003g0280 |
2 | HG02109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.356-702A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122691599 | |||||||
chr3:122691681 | T | C | 251 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0018 others(248): Show |
270 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.356-620T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122691681 | |||||||
chr3:122691713 | G | A | 1 | a0001c0001t0001g0312 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.356-588G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122691713 | |||||||
chr3:122691807 | G | A | 6 | a0001c0001t0001g0018 a0001c0001t0005g0018 a0001c0001t0005g0019 others(3): Show |
7 | HG01891.hp2 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.356-494G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122691807 | |||||||
chr3:122692031 | C | T | 1 | a0003c0015t0018g0158 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.356-270C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122692031 | |||||||
chr3:122692081 | C | T | 38 | a0001c0024t0001g0040 a0002c0002t0004g0001 a0002c0002t0004g0005 others(35): Show |
42 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.356-220C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 3/16 | chr3 | 122692081 | |||||||
chr3:122692698 | G | T | 1 | a0001c0001t0005g0082 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.598+155G>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122692698 | |||||||
chr3:122692793 | G | A | 1 | a0001c0022t0001g0086 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.598+250G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122692793 | |||||||
chr3:122692801 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.598+258G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122692801 | |||||||
chr3:122692914 | T | C | 10 | a0001c0003t0007g0141 a0001c0003t0007g0168 a0001c0003t0007g0169 others(7): Show |
10 | HG00280.hp1 HG00642.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.598+371T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122692914 | |||||||
chr3:122692931 | T | C | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02647.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.598+388T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122692931 | |||||||
chr3:122692999 | G | T | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG02055.hp1 HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.598+456G>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122692999 | |||||||
chr3:122693034 | A | G | 2 | a0001c0001t0003g0025 a0001c0001t0003g0261 |
3 | HG02809.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.598+491A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122693034 | |||||||
chr3:122693104 | G | T | 176 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0045 others(173): Show |
186 | HG00280.hp1 HG00597.hp2 HG00609.hp1 others(183): Show |
intron_variant | MODIFIER | c.598+561G>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122693104 | |||||||
chr3:122693111 | T | C | 201 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0018 others(198): Show |
213 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(210): Show |
intron_variant | MODIFIER | c.598+568T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122693111 | |||||||
chr3:122693292 | GAAGAGAG others(17): Show |
G | 14 | a0001c0001t0001g0018 a0001c0001t0005g0018 a0001c0001t0005g0019 others(11): Show |
16 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.598+753_598+776del others(24): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 122693292 | ||||||
chr3:122693675 | CA | C | 190 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0020 others(187): Show |
202 | HG00280.hp1 HG00597.hp2 HG00609.hp1 others(199): Show |
intron_variant | MODIFIER | c.598+1140delA | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 122693675 | ||||||
chr3:122693710 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | NA18994.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.598+1167G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122693710 | |||||||
chr3:122693842 | G | GA | 190 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0020 others(187): Show |
202 | HG00280.hp1 HG00597.hp2 HG00609.hp1 others(199): Show |
intron_variant | MODIFIER | c.598+1312dupA | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 122693842 | ||||||
chr3:122693854 | AAGAAAAG others(5): Show |
A | 1 | a0013c0013t0013g0060 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.598+1313_598+1324d others(14): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 122693854 | ||||||
chr3:122693856 | GAAAAGAA others(4): Show |
G | 45 | a0001c0024t0001g0040 a0002c0002t0004g0001 a0002c0002t0004g0005 others(42): Show |
51 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.598+1324_598+1334d others(13): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr3 | 122693856 | ||||||
chr3:122693867 | A | G | 1 | a0013c0013t0013g0060 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.598+1324A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122693867 | |||||||
chr3:122693908 | G | A | 176 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0045 others(173): Show |
186 | HG00280.hp1 HG00597.hp2 HG00609.hp1 others(183): Show |
intron_variant | MODIFIER | c.598+1365G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122693908 | |||||||
chr3:122694016 | T | G | 1 | a0002c0002t0004g0308 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.599-1410T>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122694016 | |||||||
chr3:122694054 | C | T | 182 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0020 others(179): Show |
193 | HG00280.hp1 HG00597.hp2 HG00609.hp1 others(190): Show |
intron_variant | MODIFIER | c.599-1372C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122694054 | |||||||
chr3:122694126 | A | C | 182 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0020 others(179): Show |
193 | HG00280.hp1 HG00597.hp2 HG00609.hp1 others(190): Show |
intron_variant | MODIFIER | c.599-1300A>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122694126 | |||||||
chr3:122694169 | G | A | 16 | a0001c0001t0006g0021 a0001c0001t0006g0034 a0001c0001t0006g0184 others(13): Show |
19 | HG00621.hp1 HG01516.hp2 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.599-1257G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122694169 | |||||||
chr3:122694241 | A | G | 14 | a0001c0001t0001g0018 a0001c0001t0005g0018 a0001c0001t0005g0019 others(11): Show |
16 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.599-1185A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122694241 | |||||||
chr3:122694300 | T | A | 1 | a0001c0001t0002g0196 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.599-1126T>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122694300 | |||||||
chr3:122694381 | T | A | 3 | a0006c0010t0011g0191 a0006c0010t0011g0305 a0006c0010t0011g0306 |
3 | HG01433.hp2 HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.599-1045T>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122694381 | |||||||
chr3:122694468 | A | T | 1 | a0001c0016t0027g0292 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.599-958A>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122694468 | |||||||
chr3:122694689 | T | G | 195 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0020 others(192): Show |
206 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(203): Show |
intron_variant | MODIFIER | c.599-737T>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122694689 | |||||||
chr3:122694739 | C | T | 1 | a0001c0001t0001g0047 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.599-687C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122694739 | |||||||
chr3:122694929 | C | G | 1 | a0001c0001t0001g0128 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.599-497C>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122694929 | |||||||
chr3:122694946 | G | T | 1 | a0001c0001t0002g0183 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.599-480G>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122694946 | |||||||
chr3:122694982 | C | T | 227 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0020 others(224): Show |
243 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(240): Show |
intron_variant | MODIFIER | c.599-444C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122694982 | |||||||
chr3:122695013 | G | A | 3 | a0001c0001t0001g0314 a0001c0001t0003g0032 a0001c0003t0010g0329 |
4 | HG02055.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-413G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122695013 | |||||||
chr3:122695019 | G | A | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG02055.hp1 HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.599-407G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122695019 | |||||||
chr3:122695107 | G | A | 1 | a0001c0001t0002g0197 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.599-319G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122695107 | |||||||
chr3:122695261 | T | G | 3 | a0006c0010t0011g0191 a0006c0010t0011g0305 a0006c0010t0011g0306 |
3 | HG01433.hp2 HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.599-165T>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122695261 | |||||||
chr3:122695370 | C | T | 1 | a0001c0001t0003g0280 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.599-56C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 4/16 | chr3 | 122695370 | |||||||
chr3:122695805 | C | T | 2 | a0001c0001t0002g0259 a0001c0001t0002g0260 |
2 | HG00597.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.835+143C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | chr3 | 122695805 | |||||||
chr3:122695823 | G | A | 1 | a0001c0018t0007g0075 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.835+161G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | chr3 | 122695823 | |||||||
chr3:122695922 | T | C | 2 | a0001c0001t0003g0038 a0001c0001t0003g0189 |
2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.835+260T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | chr3 | 122695922 | |||||||
chr3:122696118 | C | T | 1 | a0001c0003t0010g0170 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.835+456C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | chr3 | 122696118 | |||||||
chr3:122696139 | T | C | 1 | a0001c0001t0003g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.835+477T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | chr3 | 122696139 | |||||||
chr3:122696300 | G | T | 1 | a0002c0002t0004g0059 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.835+638G>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | chr3 | 122696300 | |||||||
chr3:122696479 | T | C | 1 | a0003c0004t0003g0286 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.835+817T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | chr3 | 122696479 | |||||||
chr3:122696537 | C | T | 2 | a0002c0002t0004g0059 a0002c0002t0004g0172 |
2 | HG03491.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.835+875C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | chr3 | 122696537 | |||||||
chr3:122696883 | C | T | 10 | a0001c0001t0002g0255 a0001c0001t0003g0135 a0001c0001t0003g0136 others(7): Show |
10 | HG00609.hp1 HG00609.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.835+1221C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | chr3 | 122696883 | |||||||
chr3:122696934 | C | A | 1 | a0002c0002t0004g0050 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.835+1272C>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | chr3 | 122696934 | |||||||
chr3:122697040 | C | T | 1 | a0001c0001t0006g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.835+1378C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | chr3 | 122697040 | |||||||
chr3:122697042 | C | T | 1 | a0001c0001t0014g0182 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.835+1380C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | chr3 | 122697042 | |||||||
chr3:122697046 | A | G | 323 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(320): Show |
352 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(349): Show |
intron_variant | MODIFIER | c.835+1384A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | chr3 | 122697046 | |||||||
chr3:122697145 | A | G | 241 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0018 others(238): Show |
261 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.835+1483A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | chr3 | 122697145 | |||||||
chr3:122697578 | T | C | 37 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0045 others(34): Show |
40 | HG00280.hp1 HG00621.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.836-1812T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | chr3 | 122697578 | |||||||
chr3:122697669 | G | A | 2 | a0001c0001t0003g0032 a0001c0003t0010g0329 |
3 | HG02055.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.836-1721G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | chr3 | 122697669 | |||||||
chr3:122697742 | G | A | 34 | a0001c0001t0001g0099 a0002c0002t0004g0001 a0002c0002t0004g0005 others(31): Show |
38 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.836-1648G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | chr3 | 122697742 | |||||||
chr3:122697903 | G | A | 1 | a0002c0002t0004g0308 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.836-1487G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | chr3 | 122697903 | |||||||
chr3:122698084 | A | T | 1 | a0001c0001t0002g0253 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.836-1306A>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | chr3 | 122698084 | |||||||
chr3:122698169 | G | A | 10 | a0004c0008t0008g0078 a0004c0008t0008g0080 a0004c0008t0008g0081 others(7): Show |
12 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.836-1221G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | chr3 | 122698169 | |||||||
chr3:122698218 | C | G | 1 | a0001c0001t0001g0125 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.836-1172C>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | chr3 | 122698218 | |||||||
chr3:122698238 | C | A | 1 | a0001c0001t0017g0039 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.836-1152C>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | chr3 | 122698238 | |||||||
chr3:122698395 | C | T | 1 | a0001c0001t0003g0252 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.836-995C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | chr3 | 122698395 | |||||||
chr3:122698524 | T | C | 3 | a0006c0010t0011g0191 a0006c0010t0011g0305 a0006c0010t0011g0306 |
3 | HG01433.hp2 HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.836-866T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | chr3 | 122698524 | |||||||
chr3:122698691 | G | A | 18 | a0001c0001t0002g0023 a0001c0001t0002g0146 a0001c0001t0002g0147 others(15): Show |
19 | HG02074.hp2 HG02135.hp1 HG02165.hp1 others(16): Show |
intron_variant | MODIFIER | c.836-699G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | chr3 | 122698691 | |||||||
chr3:122698874 | CACTTTGA others(19): Show |
C | 1 | a0001c0001t0002g0212 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.836-486_836-461del others(26): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr3 | 122698874 | ||||||
chr3:122699043 | A | G | 9 | a0003c0004t0003g0002 a0003c0004t0003g0156 a0003c0004t0003g0291 others(6): Show |
10 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.836-347A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | chr3 | 122699043 | |||||||
chr3:122699223 | G | T | 1 | a0001c0001t0001g0124 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.836-167G>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | chr3 | 122699223 | |||||||
chr3:122699264 | A | C | 1 | a0003c0004t0003g0286 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.836-126A>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 5/16 | chr3 | 122699264 | |||||||
chr3:122701813 | C | T | 3 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0211 |
3 | HG02165.hp1 NA18986.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3081+178C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | chr3 | 122701813 | |||||||
chr3:122701898 | C | A | 333 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(330): Show |
363 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.3081+263C>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | chr3 | 122701898 | |||||||
chr3:122701946 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3081+311G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | chr3 | 122701946 | |||||||
chr3:122702092 | G | A | 9 | a0003c0004t0003g0002 a0003c0004t0003g0156 a0003c0004t0003g0291 others(6): Show |
10 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.3081+457G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | chr3 | 122702092 | |||||||
chr3:122702092 | G | T | 1 | a0002c0002t0004g0140 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.3081+457G>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | chr3 | 122702092 | |||||||
chr3:122702278 | A | G | 1 | a0004c0009t0008g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3081+643A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | chr3 | 122702278 | |||||||
chr3:122702285 | C | T | 12 | a0003c0004t0003g0002 a0003c0004t0003g0156 a0003c0004t0003g0291 others(9): Show |
13 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.3081+650C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | chr3 | 122702285 | |||||||
chr3:122702347 | G | A | 10 | a0004c0008t0008g0078 a0004c0008t0008g0080 a0004c0008t0008g0081 others(7): Show |
12 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.3081+712G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | chr3 | 122702347 | |||||||
chr3:122702373 | C | T | 3 | a0001c0001t0003g0270 a0001c0001t0003g0280 a0001c0001t0003g0328 |
3 | HG02109.hp1 HG02109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3081+738C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | chr3 | 122702373 | |||||||
chr3:122702557 | C | T | 9 | a0003c0004t0003g0002 a0003c0004t0003g0156 a0003c0004t0003g0291 others(6): Show |
10 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.3081+922C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | chr3 | 122702557 | |||||||
chr3:122702701 | T | C | 23 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0045 others(20): Show |
26 | HG00621.hp1 HG02258.hp1 HG02523.hp2 others(23): Show |
intron_variant | MODIFIER | c.3082-1041T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | chr3 | 122702701 | |||||||
chr3:122702728 | ATGT | A | 9 | a0003c0004t0003g0002 a0003c0004t0003g0156 a0003c0004t0003g0291 others(6): Show |
10 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.3082-1010_3082-100 others(7): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 122702728 | ||||||
chr3:122702866 | T | C | 1 | a0001c0001t0015g0100 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3082-876T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | chr3 | 122702866 | |||||||
chr3:122702993 | TA | T | 142 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0128 others(139): Show |
149 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.3082-732delA | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 122702993 | ||||||
chr3:122702997 | AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0003g0251 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3082-732_3082-719d others(16): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 122702997 | ||||||
chr3:122702998 | AAAAAAAA others(6): Show |
A | 2 | a0001c0001t0005g0093 a0007c0017t0005g0090 |
2 | HG00741.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.3082-724_3082-712d others(15): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 122702998 | ||||||
chr3:122703001 | A | C | 1 | a0003c0004t0003g0286 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3082-741A>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | chr3 | 122703001 | |||||||
chr3:122703002 | A | C | 1 | a0001c0003t0007g0274 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3082-740A>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | chr3 | 122703002 | |||||||
chr3:122703004 | A | C | 15 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0030 others(12): Show |
16 | HG00323.hp2 HG00642.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.3082-738A>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | chr3 | 122703004 | |||||||
chr3:122703005 | AAAAAACA others(12): Show |
A | 9 | a0003c0004t0003g0002 a0003c0004t0003g0156 a0003c0004t0003g0291 others(6): Show |
10 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.3082-731_3082-713d others(21): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 122703005 | ||||||
chr3:122703005 | AAAAAACA others(19): Show |
A | 10 | a0004c0008t0008g0078 a0004c0008t0008g0080 a0004c0008t0008g0081 others(7): Show |
12 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.3082-731_3082-706d others(28): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 122703005 | ||||||
chr3:122703008 | AAACAAAA others(16): Show |
A | 30 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(27): Show |
34 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.3082-731_3082-709d others(25): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 122703008 | ||||||
chr3:122703009 | AACAAAAA others(15): Show |
A | 3 | a0002c0002t0004g0054 a0002c0002t0004g0067 a0002c0002t0004g0188 |
3 | NA18990.hp2 NA19067.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.3082-731_3082-710d others(24): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 122703009 | ||||||
chr3:122703010 | A | C | 4 | a0001c0001t0001g0330 a0006c0010t0011g0191 a0006c0010t0011g0305 others(1): Show |
4 | HG01433.hp2 HG02572.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.3082-732A>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | chr3 | 122703010 | |||||||
chr3:122703010 | AC | A | 20 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(17): Show |
22 | HG01243.hp2 HG01516.hp2 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.3082-731delC | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | chr3 | 122703010 | |||||||
chr3:122703011 | C | A | 10 | a0001c0001t0001g0010 a0001c0001t0001g0119 a0001c0001t0001g0330 others(7): Show |
10 | HG00673.hp2 HG01433.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.3082-731C>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | chr3 | 122703011 | |||||||
chr3:122703022 | A | C | 1 | a0003c0004t0003g0286 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3082-720A>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | chr3 | 122703022 | |||||||
chr3:122703023 | A | C | 1 | a0001c0012t0003g0070 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.3082-719A>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | chr3 | 122703023 | |||||||
chr3:122703031 | C | A | 9 | a0003c0004t0003g0002 a0003c0004t0003g0156 a0003c0004t0003g0291 others(6): Show |
10 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.3082-711C>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | chr3 | 122703031 | |||||||
chr3:122703140 | A | G | 1 | a0001c0001t0006g0034 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3082-602A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | chr3 | 122703140 | |||||||
chr3:122703356 | G | A | 1 | a0001c0001t0022g0144 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3082-386G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | chr3 | 122703356 | |||||||
chr3:122703453 | A | T | 9 | a0003c0004t0003g0002 a0003c0004t0003g0156 a0003c0004t0003g0291 others(6): Show |
10 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.3082-289A>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | chr3 | 122703453 | |||||||
chr3:122703689 | T | C | 9 | a0003c0004t0003g0002 a0003c0004t0003g0156 a0003c0004t0003g0291 others(6): Show |
10 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.3082-53T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 6/16 | chr3 | 122703689 | |||||||
chr3:122704054 | C | T | 8 | a0001c0001t0002g0017 a0001c0001t0002g0152 a0001c0001t0002g0153 others(5): Show |
9 | HG01074.hp2 HG01346.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.3318+76C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 7/16 | chr3 | 122704054 | |||||||
chr3:122704404 | C | T | 15 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0030 others(12): Show |
16 | HG00323.hp2 HG00642.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.3319-123C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 7/16 | chr3 | 122704404 | |||||||
chr3:122704409 | A | G | 33 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(30): Show |
37 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.3319-118A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 7/16 | chr3 | 122704409 | |||||||
chr3:122704851 | T | G | 9 | a0003c0004t0003g0002 a0003c0004t0003g0156 a0003c0004t0003g0291 others(6): Show |
10 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.3540+103T>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122704851 | |||||||
chr3:122705090 | C | A | 9 | a0003c0004t0003g0002 a0003c0004t0003g0156 a0003c0004t0003g0291 others(6): Show |
10 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.3540+342C>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122705090 | |||||||
chr3:122705229 | A | C | 33 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(30): Show |
37 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.3540+481A>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122705229 | |||||||
chr3:122705232 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3540+484C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122705232 | |||||||
chr3:122705594 | T | C | 3 | a0001c0001t0003g0266 a0001c0001t0003g0267 a0001c0001t0003g0268 |
3 | HG02486.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3540+846T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122705594 | |||||||
chr3:122705622 | A | G | 2 | a0001c0001t0003g0025 a0001c0001t0003g0261 |
3 | HG02809.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3540+874A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122705622 | |||||||
chr3:122705657 | C | T | 1 | a0001c0001t0003g0247 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.3540+909C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122705657 | |||||||
chr3:122705703 | C | T | 3 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0289 |
3 | HG02523.hp2 NA19010.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.3540+955C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122705703 | |||||||
chr3:122705766 | T | C | 52 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(49): Show |
59 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.3540+1018T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122705766 | |||||||
chr3:122705990 | C | G | 1 | a0001c0001t0002g0246 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.3540+1242C>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122705990 | |||||||
chr3:122706003 | C | T | 2 | a0001c0001t0012g0244 a0001c0001t0012g0245 |
2 | NA18968.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.3540+1255C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122706003 | |||||||
chr3:122706371 | A | T | 278 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(275): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.3540+1623A>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122706371 | |||||||
chr3:122706413 | G | T | 1 | a0001c0001t0002g0243 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3540+1665G>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122706413 | |||||||
chr3:122706414 | T | G | 1 | a0001c0001t0001g0327 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3540+1666T>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122706414 | |||||||
chr3:122706444 | C | T | 36 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0045 others(33): Show |
39 | HG00280.hp1 HG00621.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.3540+1696C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122706444 | |||||||
chr3:122706474 | A | T | 52 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(49): Show |
59 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.3541-1716A>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122706474 | |||||||
chr3:122706529 | A | C | 3 | a0004c0008t0008g0078 a0004c0008t0008g0080 a0004c0008t0008g0081 |
3 | HG01167.hp2 HG01169.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.3541-1661A>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122706529 | |||||||
chr3:122706694 | T | G | 9 | a0003c0004t0003g0002 a0003c0004t0003g0156 a0003c0004t0003g0291 others(6): Show |
10 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.3541-1496T>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122706694 | |||||||
chr3:122706797 | T | C | 1 | a0001c0001t0024g0215 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3541-1393T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122706797 | |||||||
chr3:122706817 | C | CA | 26 | a0001c0001t0001g0020 a0001c0001t0001g0178 a0001c0001t0001g0288 others(23): Show |
31 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.3541-1359dupA | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 122706817 | ||||||
chr3:122706844 | G | C | 3 | a0004c0008t0008g0078 a0004c0008t0008g0080 a0004c0008t0008g0081 |
3 | HG01167.hp2 HG01169.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.3541-1346G>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122706844 | |||||||
chr3:122706924 | T | G | 10 | a0004c0008t0008g0078 a0004c0008t0008g0080 a0004c0008t0008g0081 others(7): Show |
12 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.3541-1266T>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122706924 | |||||||
chr3:122706996 | G | A | 32 | a0001c0001t0002g0255 a0001c0001t0003g0024 a0001c0001t0003g0072 others(29): Show |
33 | HG00099.hp1 HG00408.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.3541-1194G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122706996 | |||||||
chr3:122707035 | G | C | 1 | a0001c0001t0003g0328 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3541-1155G>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122707035 | |||||||
chr3:122707195 | G | C | 1 | a0003c0004t0006g0155 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3541-995G>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122707195 | |||||||
chr3:122707242 | G | A | 1 | a0001c0001t0017g0039 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3541-948G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122707242 | |||||||
chr3:122707380 | C | CAAAT | 32 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0071 others(29): Show |
36 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.3541-774_3541-771d others(6): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 122707380 | ||||||
chr3:122707380 | C | CAAATAAA others(1): Show |
121 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0099 others(118): Show |
131 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.3541-778_3541-771d others(10): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 122707380 | ||||||
chr3:122707380 | C | CAAATAAA others(5): Show |
115 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(112): Show |
126 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.3541-782_3541-771d others(14): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 122707380 | ||||||
chr3:122707380 | C | CAAATAAA others(9): Show |
19 | a0001c0001t0001g0030 a0001c0001t0001g0084 a0001c0001t0001g0119 others(16): Show |
20 | HG00738.hp2 HG01257.hp1 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.3541-786_3541-771d others(18): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 122707380 | ||||||
chr3:122707380 | C | CAAATAAA others(13): Show |
3 | a0001c0001t0001g0015 a0001c0001t0001g0123 a0001c0001t0003g0033 |
4 | HG00738.hp1 HG01070.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.3541-790_3541-771d others(22): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 122707380 | ||||||
chr3:122707627 | A | C | 115 | a0001c0001t0002g0017 a0001c0001t0002g0023 a0001c0001t0002g0036 others(112): Show |
119 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.3541-563A>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122707627 | |||||||
chr3:122707764 | A | G | 1 | a0001c0001t0002g0264 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3541-426A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122707764 | |||||||
chr3:122707778 | G | A | 1 | a0001c0001t0002g0235 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3541-412G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122707778 | |||||||
chr3:122707968 | A | G | 31 | a0002c0002t0004g0005 a0002c0002t0004g0022 a0002c0002t0004g0031 others(28): Show |
33 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.3541-222A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 8/16 | chr3 | 122707968 | |||||||
chr3:122708367 | A | G | 33 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(30): Show |
37 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.3619+99A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122708367 | |||||||
chr3:122708532 | G | A | 3 | a0001c0001t0003g0194 a0001c0001t0003g0218 a0001c0001t0003g0247 |
3 | NA18943.hp2 NA18963.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.3619+264G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122708532 | |||||||
chr3:122708823 | C | T | 3 | a0004c0008t0008g0078 a0004c0008t0008g0080 a0004c0008t0008g0081 |
3 | HG01167.hp2 HG01169.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.3619+555C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122708823 | |||||||
chr3:122708879 | C | T | 2 | a0001c0012t0003g0070 a0001c0012t0003g0285 |
2 | NA18995.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.3619+611C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122708879 | |||||||
chr3:122709001 | T | A | 1 | a0001c0001t0001g0314 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3619+733T>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122709001 | |||||||
chr3:122709166 | T | C | 115 | a0001c0001t0002g0017 a0001c0001t0002g0023 a0001c0001t0002g0036 others(112): Show |
119 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.3619+898T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122709166 | |||||||
chr3:122709414 | A | G | 124 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(121): Show |
139 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.3619+1146A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122709414 | |||||||
chr3:122709449 | G | T | 33 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(30): Show |
37 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.3619+1181G>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122709449 | |||||||
chr3:122709654 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3619+1386G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122709654 | |||||||
chr3:122709832 | A | G | 33 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(30): Show |
37 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.3619+1564A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122709832 | |||||||
chr3:122709892 | G | GT | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(120): Show |
138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.3619+1635dupT | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 122709892 | ||||||
chr3:122709900 | T | G | 3 | a0001c0001t0001g0294 a0001c0001t0014g0293 a0003c0004t0003g0286 |
3 | HG02615.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3619+1632T>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122709900 | |||||||
chr3:122709900 | T | TG | 6 | a0001c0001t0001g0018 a0001c0001t0005g0018 a0001c0001t0005g0019 others(3): Show |
7 | HG01891.hp2 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.3619+1632_3619+163 others(5): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122709900 | |||||||
chr3:122709900 | T | TTTG | 33 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(30): Show |
37 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.3619+1634_3619+163 others(7): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 122709900 | ||||||
chr3:122709904 | G | T | 1 | a0001c0005t0003g0226 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3619+1636G>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122709904 | |||||||
chr3:122710011 | A | G | 10 | a0004c0008t0008g0078 a0004c0008t0008g0080 a0004c0008t0008g0081 others(7): Show |
12 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.3619+1743A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122710011 | |||||||
chr3:122710281 | G | A | 1 | a0001c0001t0003g0033 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3619+2013G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122710281 | |||||||
chr3:122710353 | G | A | 33 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(30): Show |
37 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.3619+2085G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122710353 | |||||||
chr3:122710436 | A | G | 3 | a0001c0001t0001g0087 a0001c0001t0001g0118 a0001c0001t0001g0123 |
3 | HG00323.hp1 HG00738.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.3619+2168A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122710436 | |||||||
chr3:122710622 | T | C | 33 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(30): Show |
37 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.3619+2354T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122710622 | |||||||
chr3:122710791 | T | TTTTA | 10 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0101 others(7): Show |
10 | HG00642.hp1 HG00741.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.3619+2571_3619+257 others(8): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 122710791 | ||||||
chr3:122710791 | T | TTTTATTT others(5): Show |
1 | a0006c0010t0011g0305 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3619+2563_3619+257 others(16): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 122710791 | ||||||
chr3:122710791 | TTTTA | T | 171 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(168): Show |
188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.3619+2571_3619+257 others(8): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 122710791 | ||||||
chr3:122710791 | TTTTATTT others(1): Show |
T | 22 | a0001c0001t0001g0176 a0001c0001t0002g0241 a0001c0001t0002g0243 others(19): Show |
25 | HG00408.hp1 HG00642.hp2 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.3619+2567_3619+257 others(12): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 122710791 | ||||||
chr3:122710791 | TTTTATTT others(5): Show |
T | 5 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0003c0004t0019g0157 others(2): Show |
5 | HG01256.hp2 HG01884.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.3619+2563_3619+257 others(16): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 122710791 | ||||||
chr3:122710791 | TTTTATTT others(9): Show |
T | 7 | a0003c0004t0003g0002 a0003c0004t0003g0156 a0003c0004t0003g0291 others(4): Show |
8 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.3619+2559_3619+257 others(20): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 122710791 | ||||||
chr3:122710795 | A | T | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG02055.hp1 HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.3619+2527A>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122710795 | |||||||
chr3:122710906 | T | C | 1 | a0001c0001t0003g0328 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3620-2518T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122710906 | |||||||
chr3:122710973 | A | T | 52 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(49): Show |
59 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.3620-2451A>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122710973 | |||||||
chr3:122711020 | A | G | 52 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(49): Show |
59 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.3620-2404A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122711020 | |||||||
chr3:122711029 | G | T | 2 | a0002c0002t0004g0063 a0002c0002t0004g0064 |
2 | NA18969.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.3620-2395G>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122711029 | |||||||
chr3:122711091 | C | T | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(313): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(343): Show |
intron_variant | MODIFIER | c.3620-2333C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122711091 | |||||||
chr3:122711209 | T | A | 1 | a0001c0001t0003g0195 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.3620-2215T>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122711209 | |||||||
chr3:122711260 | C | T | 1 | a0001c0003t0007g0322 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3620-2164C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122711260 | |||||||
chr3:122711438 | C | T | 10 | a0004c0008t0008g0078 a0004c0008t0008g0080 a0004c0008t0008g0081 others(7): Show |
12 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.3620-1986C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122711438 | |||||||
chr3:122711535 | G | C | 2 | a0001c0001t0001g0018 a0001c0001t0005g0018 |
2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3620-1889G>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122711535 | |||||||
chr3:122711651 | A | G | 1 | a0001c0016t0027g0292 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3620-1773A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122711651 | |||||||
chr3:122711739 | T | A | 1 | a0001c0001t0022g0144 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3620-1685T>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122711739 | |||||||
chr3:122711901 | T | G | 2 | a0001c0001t0001g0006 a0001c0001t0005g0006 |
2 | HG02015.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.3620-1523T>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122711901 | |||||||
chr3:122711950 | T | C | 1 | a0001c0001t0006g0186 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3620-1474T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122711950 | |||||||
chr3:122712052 | A | G | 1 | a0001c0001t0002g0242 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3620-1372A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122712052 | |||||||
chr3:122712066 | G | T | 1 | a0001c0001t0002g0250 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3620-1358G>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122712066 | |||||||
chr3:122712189 | T | C | 1 | a0001c0001t0006g0186 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3620-1235T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122712189 | |||||||
chr3:122712240 | CT | C | 150 | a0001c0001t0001g0132 a0001c0001t0002g0017 a0001c0001t0002g0023 others(147): Show |
159 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(156): Show |
intron_variant | MODIFIER | c.3620-1169delT | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 122712240 | ||||||
chr3:122712240 | CTT | C | 166 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(163): Show |
187 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.3620-1170_3620-116 others(6): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr3 | 122712240 | ||||||
chr3:122712247 | T | A | 2 | a0001c0012t0003g0070 a0001c0012t0003g0285 |
2 | NA18995.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.3620-1177T>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122712247 | |||||||
chr3:122712329 | C | T | 1 | a0001c0001t0001g0284 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3620-1095C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122712329 | |||||||
chr3:122712336 | C | T | 1 | a0001c0001t0003g0252 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3620-1088C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122712336 | |||||||
chr3:122712399 | C | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG02896.hp1 HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3620-1025C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122712399 | |||||||
chr3:122712439 | G | A | 7 | a0004c0009t0008g0271 a0004c0009t0008g0273 a0004c0009t0008g0282 others(4): Show |
9 | HG00735.hp1 HG01884.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.3620-985G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122712439 | |||||||
chr3:122712450 | G | A | 1 | a0001c0022t0001g0086 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3620-974G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122712450 | |||||||
chr3:122712499 | C | T | 1 | a0009c0014t0004g0069 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3620-925C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122712499 | |||||||
chr3:122712564 | T | C | 1 | a0001c0001t0003g0254 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3620-860T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122712564 | |||||||
chr3:122712634 | C | T | 1 | a0001c0001t0003g0261 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3620-790C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122712634 | |||||||
chr3:122712658 | A | T | 33 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(30): Show |
37 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.3620-766A>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122712658 | |||||||
chr3:122712729 | T | C | 1 | a0001c0001t0001g0327 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3620-695T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122712729 | |||||||
chr3:122712942 | T | G | 43 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(40): Show |
49 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.3620-482T>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122712942 | |||||||
chr3:122713168 | G | A | 1 | a0001c0001t0003g0136 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3620-256G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122713168 | |||||||
chr3:122713194 | C | T | 1 | a0001c0001t0003g0225 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3620-230C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122713194 | |||||||
chr3:122713213 | A | G | 33 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(30): Show |
37 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.3620-211A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122713213 | |||||||
chr3:122713277 | G | A | 1 | a0001c0023t0006g0302 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3620-147G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122713277 | |||||||
chr3:122713324 | G | A | 43 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(40): Show |
49 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.3620-100G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 9/16 | chr3 | 122713324 | |||||||
chr3:122714122 | A | G | 9 | a0003c0004t0003g0002 a0003c0004t0003g0156 a0003c0004t0003g0291 others(6): Show |
10 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.3833-140A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 11/16 | chr3 | 122714122 | |||||||
chr3:122714151 | G | GT | 38 | a0001c0001t0001g0179 a0001c0001t0003g0270 a0001c0001t0003g0280 others(35): Show |
43 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.3833-99dupT | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 122714151 | ||||||
chr3:122714511 | G | T | 1 | a0001c0023t0006g0302 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4000+82G>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | chr3 | 122714511 | |||||||
chr3:122714576 | A | G | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG02738.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.4000+147A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | chr3 | 122714576 | |||||||
chr3:122714690 | TA | T | 33 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(30): Show |
37 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.4000+263delA | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 122714690 | ||||||
chr3:122714690 | TAAG | T | 24 | a0001c0001t0002g0208 a0001c0001t0002g0255 a0001c0001t0003g0072 others(21): Show |
24 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.4000+262_4000+264d others(5): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | chr3 | 122714690 | |||||||
chr3:122714715 | G | A | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(313): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(343): Show |
intron_variant | MODIFIER | c.4000+286G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | chr3 | 122714715 | |||||||
chr3:122714789 | C | T | 9 | a0003c0004t0003g0002 a0003c0004t0003g0156 a0003c0004t0003g0291 others(6): Show |
10 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.4000+360C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | chr3 | 122714789 | |||||||
chr3:122715077 | G | A | 1 | a0001c0001t0003g0310 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4000+648G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | chr3 | 122715077 | |||||||
chr3:122715083 | G | A | 74 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(71): Show |
84 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.4000+654G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | chr3 | 122715083 | |||||||
chr3:122715129 | T | C | 124 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(121): Show |
139 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.4000+700T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | chr3 | 122715129 | |||||||
chr3:122715249 | C | T | 1 | a0001c0001t0003g0328 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4000+820C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | chr3 | 122715249 | |||||||
chr3:122715357 | G | C | 7 | a0004c0009t0008g0271 a0004c0009t0008g0273 a0004c0009t0008g0282 others(4): Show |
9 | HG00735.hp1 HG01884.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.4000+928G>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | chr3 | 122715357 | |||||||
chr3:122715404 | T | C | 1 | a0001c0001t0003g0217 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4000+975T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | chr3 | 122715404 | |||||||
chr3:122715595 | C | CATCT | 48 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(45): Show |
55 | HG00621.hp1 HG00738.hp1 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.4000+1222_4000+122 others(8): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 122715595 | ||||||
chr3:122715595 | C | CATCTATC others(1): Show |
24 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0122 others(21): Show |
24 | HG00673.hp1 HG01261.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.4000+1218_4000+122 others(12): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 122715595 | ||||||
chr3:122715595 | C | CATCTATC others(5): Show |
1 | a0001c0001t0001g0178 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4000+1214_4000+122 others(16): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 122715595 | ||||||
chr3:122715595 | CATCT | C | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(94): Show |
112 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.4000+1222_4000+122 others(8): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 122715595 | ||||||
chr3:122715595 | CATCTATC others(1): Show |
C | 47 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0071 others(44): Show |
51 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.4000+1218_4000+122 others(12): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 122715595 | ||||||
chr3:122715595 | CATCTATC others(5): Show |
C | 19 | a0001c0001t0001g0099 a0001c0001t0003g0025 a0001c0001t0003g0073 others(16): Show |
20 | HG00621.hp2 HG01433.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.4000+1214_4000+122 others(16): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 122715595 | ||||||
chr3:122715595 | CATCTATC others(9): Show |
C | 7 | a0001c0001t0002g0196 a0001c0001t0002g0241 a0001c0001t0002g0269 others(4): Show |
7 | HG02559.hp2 HG03139.hp1 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.4000+1210_4000+122 others(20): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 122715595 | ||||||
chr3:122715595 | CATCTATC others(13): Show |
C | 1 | a0001c0003t0007g0322 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.4000+1206_4000+122 others(24): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 122715595 | ||||||
chr3:122715595 | CATCTATC others(17): Show |
C | 2 | a0001c0003t0007g0276 a0001c0003t0007g0323 |
2 | HG00642.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.4000+1202_4000+122 others(28): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 122715595 | ||||||
chr3:122715595 | CATCTATC others(21): Show |
C | 7 | a0001c0003t0007g0141 a0001c0003t0007g0168 a0001c0003t0007g0169 others(4): Show |
7 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.4000+1198_4000+122 others(32): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 122715595 | ||||||
chr3:122715884 | C | T | 2 | a0004c0009t0008g0273 a0004c0009t0008g0282 |
2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4000+1455C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | chr3 | 122715884 | |||||||
chr3:122716078 | G | A | 1 | a0006c0010t0011g0306 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4000+1649G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | chr3 | 122716078 | |||||||
chr3:122716742 | C | T | 1 | a0001c0012t0003g0285 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.4001-1329C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | chr3 | 122716742 | |||||||
chr3:122716882 | G | A | 52 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(49): Show |
59 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.4001-1189G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | chr3 | 122716882 | |||||||
chr3:122716903 | G | A | 52 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(49): Show |
59 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.4001-1168G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | chr3 | 122716903 | |||||||
chr3:122716906 | T | C | 16 | a0001c0001t0006g0021 a0001c0001t0006g0034 a0001c0001t0006g0184 others(13): Show |
19 | HG01243.hp2 HG01516.hp2 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.4001-1165T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | chr3 | 122716906 | |||||||
chr3:122717174 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.4001-897C>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | chr3 | 122717174 | |||||||
chr3:122717215 | A | G | 1 | a0003c0004t0003g0286 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4001-856A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | chr3 | 122717215 | |||||||
chr3:122717239 | T | C | 1 | a0001c0001t0003g0032 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.4001-832T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | chr3 | 122717239 | |||||||
chr3:122717410 | C | T | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0327 |
3 | HG03041.hp1 HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.4001-661C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | chr3 | 122717410 | |||||||
chr3:122717638 | G | T | 1 | a0004c0009t0008g0271 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4001-433G>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | chr3 | 122717638 | |||||||
chr3:122717683 | A | G | 2 | a0001c0001t0001g0004 a0001c0001t0001g0165 |
3 | HG00639.hp2 HG01074.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.4001-388A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | chr3 | 122717683 | |||||||
chr3:122717703 | T | C | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | NA18982.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.4001-368T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | chr3 | 122717703 | |||||||
chr3:122717750 | G | T | 1 | a0001c0001t0002g0148 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.4001-321G>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | chr3 | 122717750 | |||||||
chr3:122717827 | G | T | 1 | a0002c0002t0004g0059 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.4001-244G>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 12/16 | chr3 | 122717827 | |||||||
chr3:122718987 | A | G | 126 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(123): Show |
141 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.4807+29A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 14/16 | chr3 | 122718987 | |||||||
chr3:122718987 | A | T | 1 | a0001c0001t0030g0297 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4807+29A>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 14/16 | chr3 | 122718987 | |||||||
chr3:122719016 | C | T | 9 | a0003c0004t0003g0002 a0003c0004t0003g0156 a0003c0004t0003g0291 others(6): Show |
10 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.4807+58C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 14/16 | chr3 | 122719016 | |||||||
chr3:122719054 | A | G | 3 | a0004c0008t0008g0078 a0004c0008t0008g0080 a0004c0008t0008g0081 |
3 | HG01167.hp2 HG01169.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.4807+96A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 14/16 | chr3 | 122719054 | |||||||
chr3:122719066 | C | T | 1 | a0001c0003t0007g0274 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4807+108C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 14/16 | chr3 | 122719066 | |||||||
chr3:122719368 | G | A | 4 | a0001c0001t0003g0270 a0001c0001t0003g0280 a0001c0001t0003g0328 others(1): Show |
4 | HG00639.hp1 HG02109.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.4807+410G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 14/16 | chr3 | 122719368 | |||||||
chr3:122719544 | A | G | 33 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(30): Show |
37 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.4807+586A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 14/16 | chr3 | 122719544 | |||||||
chr3:122719671 | G | A | 16 | a0001c0001t0006g0021 a0001c0001t0006g0034 a0001c0001t0006g0184 others(13): Show |
19 | HG01243.hp2 HG01516.hp2 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.4808-584G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 14/16 | chr3 | 122719671 | |||||||
chr3:122720055 | CT | C | 16 | a0001c0001t0006g0021 a0001c0001t0006g0034 a0001c0001t0006g0184 others(13): Show |
19 | HG01243.hp2 HG01516.hp2 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.4808-192delT | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 122720055 | ||||||
chr3:122720061 | T | A | 2 | a0001c0001t0001g0294 a0001c0001t0014g0293 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.4808-194T>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 14/16 | chr3 | 122720061 | |||||||
chr3:122720100 | G | A | 1 | a0001c0001t0006g0265 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4808-155G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 14/16 | chr3 | 122720100 | |||||||
chr3:122720191 | G | A | 1 | a0001c0001t0002g0209 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.4808-64G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 14/16 | chr3 | 122720191 | |||||||
chr3:122720215 | C | T | 10 | a0004c0008t0008g0078 a0004c0008t0008g0080 a0004c0008t0008g0081 others(7): Show |
12 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.4808-40C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 14/16 | chr3 | 122720215 | |||||||
chr3:122720432 | G | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | NA18940.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.4941+44G>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122720432 | |||||||
chr3:122720524 | T | C | 10 | a0004c0008t0008g0078 a0004c0008t0008g0080 a0004c0008t0008g0081 others(7): Show |
12 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.4941+136T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122720524 | |||||||
chr3:122720616 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0121 |
2 | HG01261.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.4941+228A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122720616 | |||||||
chr3:122720664 | A | G | 3 | a0004c0008t0008g0078 a0004c0008t0008g0080 a0004c0008t0008g0081 |
3 | HG01167.hp2 HG01169.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.4941+276A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122720664 | |||||||
chr3:122720712 | T | C | 6 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(3): Show |
6 | HG02647.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.4941+324T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122720712 | |||||||
chr3:122720782 | T | A | 10 | a0004c0008t0008g0078 a0004c0008t0008g0080 a0004c0008t0008g0081 others(7): Show |
12 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.4941+394T>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122720782 | |||||||
chr3:122720907 | C | G | 43 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(40): Show |
49 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.4941+519C>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122720907 | |||||||
chr3:122720939 | C | G | 1 | a0001c0001t0002g0212 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.4941+551C>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122720939 | |||||||
chr3:122721088 | G | C | 10 | a0004c0008t0008g0078 a0004c0008t0008g0080 a0004c0008t0008g0081 others(7): Show |
12 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.4941+700G>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122721088 | |||||||
chr3:122721196 | G | A | 33 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(30): Show |
37 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.4941+808G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122721196 | |||||||
chr3:122721202 | A | G | 9 | a0003c0004t0003g0002 a0003c0004t0003g0156 a0003c0004t0003g0291 others(6): Show |
10 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.4941+814A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122721202 | |||||||
chr3:122721205 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.4941+817A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122721205 | |||||||
chr3:122721218 | C | T | 116 | a0001c0001t0002g0017 a0001c0001t0002g0023 a0001c0001t0002g0036 others(113): Show |
120 | HG00099.hp1 HG00408.hp2 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.4941+830C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122721218 | |||||||
chr3:122721219 | A | G | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(313): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(343): Show |
intron_variant | MODIFIER | c.4941+831A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122721219 | |||||||
chr3:122721359 | T | C | 52 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(49): Show |
59 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.4941+971T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122721359 | |||||||
chr3:122721443 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0190 |
2 | NA18962.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.4941+1055C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122721443 | |||||||
chr3:122721515 | T | C | 318 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(315): Show |
345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.4941+1127T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122721515 | |||||||
chr3:122721568 | C | CAG | 52 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(49): Show |
59 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.4941+1183_4941+118 others(6): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122721568 | ||||||
chr3:122721654 | G | A | 116 | a0001c0001t0002g0017 a0001c0001t0002g0023 a0001c0001t0002g0036 others(113): Show |
120 | HG00099.hp1 HG00408.hp2 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.4941+1266G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122721654 | |||||||
chr3:122721899 | T | C | 1 | a0006c0010t0011g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4941+1511T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122721899 | |||||||
chr3:122722124 | G | A | 2 | a0001c0001t0003g0038 a0001c0001t0003g0189 |
2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.4941+1736G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122722124 | |||||||
chr3:122722145 | G | C | 1 | a0001c0001t0002g0211 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.4941+1757G>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122722145 | |||||||
chr3:122722150 | T | C | 1 | a0001c0001t0003g0225 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.4941+1762T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122722150 | |||||||
chr3:122722217 | T | G | 33 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(30): Show |
37 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.4941+1829T>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122722217 | |||||||
chr3:122722251 | G | A | 1 | a0003c0004t0003g0286 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4941+1863G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122722251 | |||||||
chr3:122722465 | T | C | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.4941+2077T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122722465 | |||||||
chr3:122722560 | C | A | 1 | a0002c0002t0004g0052 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.4941+2172C>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122722560 | |||||||
chr3:122722619 | G | A | 1 | a0001c0001t0003g0254 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.4941+2231G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122722619 | |||||||
chr3:122722935 | A | AT | 19 | a0003c0004t0003g0002 a0003c0004t0003g0156 a0003c0004t0003g0291 others(16): Show |
22 | HG00735.hp1 HG00741.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.4941+2561dupT | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122722935 | ||||||
chr3:122722935 | AT | A | 124 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(121): Show |
128 | HG00099.hp1 HG00408.hp2 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.4941+2561delT | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122722935 | ||||||
chr3:122722949 | T | C | 2 | a0001c0001t0002g0150 a0001c0001t0002g0242 |
2 | HG00673.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.4941+2561T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122722949 | |||||||
chr3:122722991 | AG | A | 4 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(1): Show |
4 | NA18942.hp1 NA18955.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.4941+2604delG | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122722991 | |||||||
chr3:122722996 | C | T | 116 | a0001c0001t0002g0017 a0001c0001t0002g0023 a0001c0001t0002g0036 others(113): Show |
120 | HG00099.hp1 HG00408.hp2 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.4941+2608C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122722996 | |||||||
chr3:122723160 | G | A | 10 | a0004c0008t0008g0078 a0004c0008t0008g0080 a0004c0008t0008g0081 others(7): Show |
12 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.4941+2772G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122723160 | |||||||
chr3:122723187 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4941+2799G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122723187 | |||||||
chr3:122723204 | T | A | 7 | a0004c0009t0008g0271 a0004c0009t0008g0273 a0004c0009t0008g0282 others(4): Show |
9 | HG00735.hp1 HG01884.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.4941+2816T>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122723204 | |||||||
chr3:122723245 | C | T | 3 | a0001c0001t0003g0270 a0001c0001t0003g0280 a0001c0001t0003g0328 |
3 | HG02109.hp1 HG02109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.4941+2857C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122723245 | |||||||
chr3:122723280 | T | G | 1 | a0001c0003t0007g0324 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.4941+2892T>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122723280 | |||||||
chr3:122723509 | A | G | 1 | a0001c0001t0006g0301 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.4941+3121A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122723509 | |||||||
chr3:122723534 | T | C | 10 | a0004c0008t0008g0078 a0004c0008t0008g0080 a0004c0008t0008g0081 others(7): Show |
12 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.4941+3146T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122723534 | |||||||
chr3:122723697 | C | T | 126 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(123): Show |
141 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.4941+3309C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122723697 | |||||||
chr3:122723935 | T | C | 1 | a0001c0001t0001g0296 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4941+3547T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122723935 | |||||||
chr3:122724009 | T | C | 1 | a0001c0001t0003g0217 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4941+3621T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122724009 | |||||||
chr3:122724131 | C | T | 2 | a0001c0001t0002g0204 a0001c0001t0002g0205 |
2 | NA18957.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.4942-3681C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122724131 | |||||||
chr3:122724206 | C | T | 1 | a0001c0001t0002g0253 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.4942-3606C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122724206 | |||||||
chr3:122724207 | G | A | 33 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(30): Show |
37 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.4942-3605G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122724207 | |||||||
chr3:122724230 | A | G | 1 | a0001c0001t0002g0147 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.4942-3582A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122724230 | |||||||
chr3:122724302 | CT | C | 11 | a0001c0005t0003g0127 a0004c0008t0008g0078 a0004c0008t0008g0080 others(8): Show |
13 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.4942-3496delT | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122724302 | ||||||
chr3:122724302 | CTT | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(168): Show |
192 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.4942-3497_4942-349 others(6): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122724302 | ||||||
chr3:122724441 | G | A | 1 | a0010c0019t0003g0234 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4942-3371G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122724441 | |||||||
chr3:122724455 | C | T | 2 | a0001c0001t0003g0310 a0001c0001t0003g0311 |
2 | HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.4942-3357C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122724455 | |||||||
chr3:122724460 | A | AT | 49 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0176 others(46): Show |
55 | HG00621.hp2 HG01243.hp2 HG01516.hp2 others(52): Show |
intron_variant | MODIFIER | c.4942-3330dupT | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122724460 | ||||||
chr3:122724460 | A | ATT | 6 | a0001c0001t0006g0300 a0001c0001t0006g0301 a0002c0002t0004g0057 others(3): Show |
7 | HG00735.hp1 HG01981.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.4942-3331_4942-333 others(6): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122724460 | ||||||
chr3:122724460 | AT | A | 10 | a0001c0001t0003g0032 a0002c0002t0004g0140 a0003c0004t0003g0002 others(7): Show |
12 | HG00741.hp2 HG01168.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.4942-3330delT | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122724460 | ||||||
chr3:122724497 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4942-3315C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122724497 | |||||||
chr3:122724645 | A | T | 9 | a0003c0004t0003g0002 a0003c0004t0003g0156 a0003c0004t0003g0291 others(6): Show |
10 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.4942-3167A>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122724645 | |||||||
chr3:122724646 | T | A | 1 | a0001c0001t0001g0112 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.4942-3166T>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122724646 | |||||||
chr3:122724796 | G | A | 1 | a0004c0011t0008g0026 | 2 | HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4942-3016G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122724796 | |||||||
chr3:122724824 | T | C | 3 | a0004c0008t0008g0078 a0004c0008t0008g0080 a0004c0008t0008g0081 |
3 | HG01167.hp2 HG01169.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.4942-2988T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122724824 | |||||||
chr3:122724920 | A | T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG02738.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.4942-2892A>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122724920 | |||||||
chr3:122724957 | G | A | 2 | a0002c0002t0004g0050 a0002c0002t0013g0051 |
2 | HG02738.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.4942-2855G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122724957 | |||||||
chr3:122725099 | T | C | 43 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(40): Show |
49 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.4942-2713T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122725099 | |||||||
chr3:122725204 | A | AAGGCGCT others(27): Show |
1 | a0001c0001t0003g0033 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4942-2593_4942-256 others(38): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122725204 | ||||||
chr3:122725229 | G | A | 1 | a0001c0005t0003g0223 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.4942-2583G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122725229 | |||||||
chr3:122725242 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4942-2570C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122725242 | |||||||
chr3:122725389 | A | G | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(313): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(343): Show |
intron_variant | MODIFIER | c.4942-2423A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122725389 | |||||||
chr3:122725403 | C | G | 1 | a0001c0001t0001g0278 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4942-2409C>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122725403 | |||||||
chr3:122725421 | G | A | 33 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(30): Show |
37 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.4942-2391G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122725421 | |||||||
chr3:122725730 | C | A | 1 | a0001c0001t0003g0032 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.4942-2082C>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122725730 | |||||||
chr3:122725765 | C | G | 1 | a0001c0001t0001g0327 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4942-2047C>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122725765 | |||||||
chr3:122725781 | G | C | 1 | a0001c0001t0001g0312 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4942-2031G>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122725781 | |||||||
chr3:122725838 | T | C | 1 | a0001c0001t0002g0239 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4942-1974T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122725838 | |||||||
chr3:122725846 | A | T | 16 | a0001c0001t0006g0021 a0001c0001t0006g0034 a0001c0001t0006g0184 others(13): Show |
19 | HG01243.hp2 HG01516.hp2 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.4942-1966A>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122725846 | |||||||
chr3:122725852 | T | C | 2 | a0001c0001t0003g0033 a0001c0001t0003g0048 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4942-1960T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122725852 | |||||||
chr3:122725909 | CT | C | 10 | a0004c0008t0008g0078 a0004c0008t0008g0080 a0004c0008t0008g0081 others(7): Show |
12 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.4942-1902delT | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122725909 | |||||||
chr3:122726542 | A | G | 10 | a0004c0008t0008g0078 a0004c0008t0008g0080 a0004c0008t0008g0081 others(7): Show |
12 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.4942-1270A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122726542 | |||||||
chr3:122726550 | T | A | 1 | a0002c0002t0004g0049 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.4942-1262T>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122726550 | |||||||
chr3:122726561 | T | C | 1 | a0001c0001t0002g0235 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.4942-1251T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122726561 | |||||||
chr3:122726588 | A | T | 1 | a0001c0003t0007g0274 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4942-1224A>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122726588 | |||||||
chr3:122726667 | A | G | 2 | a0001c0001t0003g0038 a0001c0001t0003g0189 |
2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.4942-1145A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122726667 | |||||||
chr3:122726702 | A | C | 1 | a0001c0001t0017g0039 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.4942-1110A>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122726702 | |||||||
chr3:122726887 | G | GAAAAATA others(313): Show |
1 | a0001c0001t0003g0311 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4942-912_4942-911i others(322): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726887 | ||||||
chr3:122726887 | G | GAAAAATA others(314): Show |
1 | a0001c0001t0003g0310 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4942-912_4942-911i others(323): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726887 | ||||||
chr3:122726887 | G | GAAAAATA others(318): Show |
1 | a0001c0001t0003g0267 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4942-912_4942-911i others(327): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726887 | ||||||
chr3:122726887 | G | GAAAAATA others(330): Show |
3 | a0001c0001t0003g0187 a0001c0001t0003g0268 a0010c0019t0003g0234 |
3 | HG01884.hp1 HG02486.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.4942-912_4942-911i others(339): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726887 | ||||||
chr3:122726887 | G | GAAAAATA others(331): Show |
1 | a0001c0001t0003g0266 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4942-912_4942-911i others(340): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726887 | ||||||
chr3:122726890 | A | AAATAATT others(333): Show |
1 | a0001c0001t0003g0281 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4942-912_4942-911i others(342): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726890 | ||||||
chr3:122726893 | T | TAATTTTA others(309): Show |
1 | a0001c0001t0003g0218 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.4942-912_4942-911i others(318): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726893 | ||||||
chr3:122726893 | T | TAATTTTA others(324): Show |
1 | a0001c0001t0002g0183 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.4942-912_4942-911i others(333): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726893 | ||||||
chr3:122726893 | T | TAATTTTA others(303): Show |
2 | a0001c0001t0003g0220 a0001c0001t0012g0244 |
2 | HG01978.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.4942-912_4942-911i others(312): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726893 | ||||||
chr3:122726893 | T | TAATTTTA others(304): Show |
2 | a0001c0001t0002g0214 a0001c0001t0002g0243 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.4942-912_4942-911i others(313): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726893 | ||||||
chr3:122726893 | T | TAATTTTA others(305): Show |
1 | a0001c0001t0003g0225 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.4942-912_4942-911i others(314): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726893 | ||||||
chr3:122726893 | T | TAATTTTA others(306): Show |
1 | a0001c0001t0002g0260 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4942-912_4942-911i others(315): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726893 | ||||||
chr3:122726893 | T | TAATTTTA others(308): Show |
1 | a0001c0001t0003g0136 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.4942-912_4942-911i others(317): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726893 | ||||||
chr3:122726893 | T | TAATTTTA others(309): Show |
8 | a0001c0001t0003g0135 a0001c0001t0003g0137 a0001c0001t0003g0139 others(5): Show |
8 | HG00609.hp2 HG02074.hp1 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.4942-912_4942-911i others(318): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726893 | ||||||
chr3:122726893 | T | TAATTTTA others(310): Show |
3 | a0001c0001t0003g0138 a0001c0001t0003g0247 a0001c0001t0003g0256 |
3 | HG00609.hp1 NA19001.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.4942-912_4942-911i others(319): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726893 | ||||||
chr3:122726893 | T | TAATTTTA others(311): Show |
1 | a0001c0005t0003g0226 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.4942-912_4942-911i others(320): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726893 | ||||||
chr3:122726893 | T | TAATTTTA others(312): Show |
3 | a0001c0001t0002g0206 a0001c0001t0002g0248 a0001c0001t0003g0025 |
4 | HG01346.hp2 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.4942-912_4942-911i others(321): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726893 | ||||||
chr3:122726893 | T | TAATTTTA others(313): Show |
1 | a0001c0001t0003g0261 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4942-912_4942-911i others(322): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726893 | ||||||
chr3:122726893 | T | TAATTTTA others(321): Show |
1 | a0001c0001t0002g0199 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.4942-912_4942-911i others(330): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726893 | ||||||
chr3:122726893 | T | TAATTTTA others(323): Show |
1 | a0001c0001t0003g0024 | 2 | HG01081.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.4942-912_4942-911i others(332): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726893 | ||||||
chr3:122726893 | T | TAATTTTA others(324): Show |
7 | a0001c0001t0002g0017 a0001c0001t0002g0077 a0001c0001t0002g0154 others(4): Show |
8 | HG00099.hp1 HG00408.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.4942-912_4942-911i others(333): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726893 | ||||||
chr3:122726893 | T | TAATTTTA others(325): Show |
25 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0143 others(22): Show |
25 | HG02040.hp2 HG02129.hp1 HG02602.hp1 others(22): Show |
intron_variant | MODIFIER | c.4942-912_4942-911i others(334): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726893 | ||||||
chr3:122726893 | T | TAATTTTA others(326): Show |
12 | a0001c0001t0002g0145 a0001c0001t0002g0152 a0001c0001t0002g0213 others(9): Show |
12 | HG00597.hp2 HG00673.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.4942-912_4942-911i others(335): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726893 | ||||||
chr3:122726893 | T | TAATTTTA others(327): Show |
5 | a0001c0001t0002g0111 a0001c0001t0016g0151 a0001c0001t0024g0215 others(2): Show |
5 | HG00597.hp1 HG01358.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.4942-912_4942-911i others(336): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726893 | ||||||
chr3:122726893 | T | TAATTTTA others(328): Show |
4 | a0001c0001t0002g0203 a0001c0001t0002g0205 a0001c0001t0002g0253 others(1): Show |
4 | NA18957.hp1 NA18993.hp1 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.4942-912_4942-911i others(337): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726893 | ||||||
chr3:122726893 | T | TAATTTTA others(329): Show |
9 | a0001c0001t0002g0023 a0001c0001t0002g0201 a0001c0001t0002g0202 others(6): Show |
10 | HG01496.hp1 HG01934.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.4942-912_4942-911i others(338): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726893 | ||||||
chr3:122726893 | T | TAATTTTA others(330): Show |
6 | a0001c0001t0002g0147 a0001c0001t0002g0148 a0001c0001t0002g0149 others(3): Show |
6 | HG01978.hp2 HG02165.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.4942-912_4942-911i others(339): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726893 | ||||||
chr3:122726893 | T | TAATTTTA others(331): Show |
3 | a0001c0001t0002g0255 a0001c0001t0003g0033 a0001c0001t0003g0217 |
3 | HG03195.hp1 HG03942.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.4942-912_4942-911i others(340): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726893 | ||||||
chr3:122726893 | T | TAATTTTA others(332): Show |
1 | a0001c0001t0003g0048 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4942-912_4942-911i others(341): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726893 | ||||||
chr3:122726893 | T | TAATTTTA others(333): Show |
2 | a0001c0001t0002g0146 a0001c0001t0002g0209 |
2 | HG02165.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.4942-912_4942-911i others(342): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726893 | ||||||
chr3:122726893 | T | TAATTTTA others(339): Show |
1 | a0001c0001t0002g0208 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.4942-912_4942-911i others(348): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726893 | ||||||
chr3:122726893 | T | TAATTTTA others(325): Show |
1 | a0001c0001t0002g0235 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.4942-912_4942-911i others(334): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726893 | ||||||
chr3:122726896 | T | TTTTAGGC others(325): Show |
1 | a0001c0012t0003g0070 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.4942-912_4942-911i others(334): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726896 | ||||||
chr3:122726896 | T | TTTTAGGC others(326): Show |
1 | a0001c0001t0002g0262 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.4942-912_4942-911i others(335): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726896 | ||||||
chr3:122726896 | T | TTTTAGGC others(331): Show |
1 | a0001c0012t0003g0285 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.4942-912_4942-911i others(340): Show |
PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726896 | ||||||
chr3:122726931 | T | C | 33 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(30): Show |
37 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.4942-881T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122726931 | |||||||
chr3:122726945 | T | C | 1 | a0001c0001t0003g0328 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4942-867T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122726945 | |||||||
chr3:122726997 | G | GA | 56 | a0001c0001t0001g0045 a0001c0001t0001g0088 a0001c0001t0001g0104 others(53): Show |
63 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.4942-800dupA | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr3 | 122726997 | ||||||
chr3:122727081 | A | G | 1 | a0001c0001t0003g0135 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.4942-731A>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122727081 | |||||||
chr3:122727134 | C | T | 9 | a0003c0004t0003g0002 a0003c0004t0003g0156 a0003c0004t0003g0291 others(6): Show |
10 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.4942-678C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122727134 | |||||||
chr3:122727144 | C | A | 1 | a0001c0001t0003g0138 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.4942-668C>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122727144 | |||||||
chr3:122727149 | G | A | 1 | a0001c0003t0007g0141 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.4942-663G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122727149 | |||||||
chr3:122727274 | T | C | 3 | a0001c0003t0007g0276 a0001c0003t0007g0322 a0001c0003t0007g0323 |
3 | HG00642.hp2 HG01943.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.4942-538T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122727274 | |||||||
chr3:122727603 | G | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(114): Show |
131 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.4942-209G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122727603 | |||||||
chr3:122727736 | G | A | 1 | a0002c0002t0004g0058 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.4942-76G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122727736 | |||||||
chr3:122727737 | T | A | 1 | a0001c0001t0005g0174 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4942-75T>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122727737 | |||||||
chr3:122727795 | C | T | 43 | a0002c0002t0004g0001 a0002c0002t0004g0005 a0002c0002t0004g0022 others(40): Show |
49 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.4942-17C>T | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 15/16 | chr3 | 122727795 | |||||||
chr3:122728067 | T | C | 1 | a0001c0003t0006g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5116+81T>C | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 16/16 | chr3 | 122728067 | |||||||
chr3:122728104 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0084 |
3 | HG03688.hp2 HG03710.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.5116+118G>A | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 16/16 | chr3 | 122728104 | |||||||
chr3:122728156 | C | G | 1 | a0001c0003t0007g0141 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.5117-152C>G | PARP14 | ENSG00000173193.15 | transcript | ENST00000474629.7 | protein_coding | 16/16 | chr3 | 122728156 |