Item | Value |
---|---|
geneid | 84725 |
ensemblid | ENSG00000106086.21 |
hgncid | 30037 |
symbol | PLEKHA8 |
name | pleckstrin homology domain containing A8 |
refseq_nuc | NM_001197026.2 |
refseq_prot | NP_001183955.1 |
ensembl_nuc | ENST00000449726.6 |
ensembl_prot | ENSP00000397947.1 |
mane_status | MANE Select |
chr | chr7 |
start | 30028412 |
end | 30084650 |
strand | + |
ver | v1.2 |
region | chr7:30028412-30084650 |
region5000 | chr7:30023412-30089650 |
regionname0 | PLEKHA8_chr7_30028412_30084650 |
regionname5000 | PLEKHA8_chr7_30023412_30089650 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 519 | 232 | 75 | 38 | 89 | 10 | 18 | 72 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | MEGVL others(514): Show |
chr7 | 30023412 | 30089650 |
a0002 | 0/0 | 519 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | MEGVL others(514): Show |
chr7 | 30023412 | 30089650 |
a0003 | 0/0 | 519 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | MEGVL others(514): Show |
chr7 | 30023412 | 30089650 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1557 | 126 | 33 | 23 | 50 | 6 | 12 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | ATGGA others(1552): Show |
chr7 | 30023412 | 30089650 | ||
a0001c0002 | 0/0 | 1557 | 103 | 40 | 14 | 39 | 4 | 6 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | ATGGA others(1552): Show |
chr7 | 30023412 | 30089650 | ||
a0001c0003 | 0/0 | 1557 | 3 | 2 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | ATGGA others(1552): Show |
chr7 | 30023412 | 30089650 | ||
a0002c0005 | 0/0 | 1557 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | ATGGA others(1552): Show |
chr7 | 30023412 | 30089650 | ||
a0003c0004 | 0/0 | 1557 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | ATGGA others(1552): Show |
chr7 | 30023412 | 30089650 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 7774 | 109 | 27 | 19 | 46 | 6 | 9 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | GGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0001t0010 | 0/0 | 7774 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | GGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0001t0011 | 0/0 | 7774 | 3 | 0 | 1 | 1 | 0 | 1 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | GGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0001t0012 | 0/0 | 7774 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | GGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0001t0013 | 0/0 | 7774 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | GGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0001t0027 | 0/0 | 7774 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | GGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0001t0028 | 0/0 | 7774 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | GGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0001t0029 | 0/0 | 7774 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | GGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0001t0030 | 0/0 | 7774 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | GGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0001t0031 | 0/0 | 7774 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | GGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0001t0032 | 0/0 | 7774 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | GGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0002t0001 | 0/0 | 7774 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | GGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0002t0002 | 0/0 | 7774 | 35 | 12 | 7 | 10 | 2 | 4 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | AGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0002t0003 | 0/0 | 7774 | 18 | 3 | 2 | 13 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | AGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0002t0004 | 0/0 | 7774 | 18 | 3 | 0 | 14 | 0 | 1 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | AGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0002t0005 | 0/0 | 7774 | 6 | 4 | 1 | 0 | 1 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | GGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0002t0006 | 0/0 | 7774 | 5 | 4 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | AGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0002t0007 | 0/0 | 7774 | 3 | 0 | 2 | 0 | 1 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | AGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0002t0009 | 0/0 | 7775 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | AGTGC others(7770): Show |
chr7 | 30023412 | 30089650 |
a0001c0002t0014 | 0/0 | 7774 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | GGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0002t0015 | 0/0 | 7774 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | AGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0002t0016 | 0/0 | 7774 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | AGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0002t0017 | 0/0 | 7774 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | AGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0002t0018 | 0/0 | 7774 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | AGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0002t0019 | 0/0 | 7774 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | AGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0002t0020 | 0/0 | 7774 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | AGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0002t0021 | 0/0 | 7774 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | AGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0002t0022 | 0/0 | 7774 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | AGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0002t0023 | 0/0 | 7774 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | AGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0002t0024 | 0/0 | 7774 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | AGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0001c0002t0025 | 0/0 | 7775 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | AGTGC others(7770): Show |
chr7 | 30023412 | 30089650 |
a0001c0002t0026 | 0/0 | 7775 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | AGTGC others(7770): Show |
chr7 | 30023412 | 30089650 |
a0001c0003t0008 | 0/0 | 7774 | 3 | 2 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | AGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0002c0005t0001 | 0/0 | 7774 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | GGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
a0003c0004t0001 | 0/0 | 7774 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | GGTGC others(7769): Show |
chr7 | 30023412 | 30089650 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 2 | 1 | 1 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0003 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0041 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0010g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0010g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0010g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0011g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0011g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0011g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0012g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0012g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0012g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0013g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0027g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0028g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0029g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0030g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0031g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0001t0032g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0005 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0004g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0004g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0005g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0005g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0006g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0006g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0007g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0007g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0007g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0009g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0009g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0009g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0014g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0014g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0015g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0016g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0017g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0018g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0019g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0020g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0021g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0022g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0023g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0024g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0025g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0002t0026g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0003t0008g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0003t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0001c0003t0008g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0002c0005t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
a0003c0004t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00323 | hp1 | a0001 | c0002 | t0007 | g0055 | EUR | FIN | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0068 | EUR | FIN | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG00423 | hp1 | a0001 | c0002 | t0004 | g0006 | EAS | CHS | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG00558 | hp2 | a0001 | c0002 | t0003 | g0174 | EAS | CHS | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG00609 | hp1 | a0001 | c0001 | t0031 | g0135 | EAS | CHS | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG00609 | hp2 | a0001 | c0001 | t0028 | g0001 | EAS | CHS | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0197 | AMR | PUR | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG00741 | hp1 | a0001 | c0002 | t0003 | g0167 | AMR | PUR | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG00741 | hp2 | a0001 | c0001 | t0013 | g0004 | AMR | PUR | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01069 | hp2 | a0001 | c0002 | t0002 | g0194 | AMR | PUR | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01070 | hp1 | a0001 | c0002 | t0005 | g0208 | AMR | PUR | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01074 | hp2 | a0001 | c0001 | t0013 | g0004 | AMR | PUR | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01081 | hp1 | a0001 | c0002 | t0006 | g0020 | AMR | PUR | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01169 | hp1 | a0001 | c0002 | t0002 | g0196 | AMR | PUR | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01175 | hp1 | a0001 | c0002 | t0002 | g0214 | AMR | PUR | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01192 | hp1 | a0001 | c0002 | t0003 | g0166 | AMR | PUR | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01192 | hp2 | a0001 | c0001 | t0011 | g0115 | AMR | PUR | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01243 | hp1 | a0001 | c0003 | t0008 | g0023 | AMR | PUR | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01243 | hp2 | a0001 | c0002 | t0007 | g0034 | AMR | PUR | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01256 | hp1 | a0001 | c0002 | t0002 | g0013 | AMR | CLM | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01258 | hp1 | a0001 | c0002 | t0002 | g0013 | AMR | CLM | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01261 | hp1 | a0001 | c0002 | t0007 | g0057 | AMR | CLM | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0204 | AMR | CLM | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | IBS | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01515 | hp2 | a0001 | c0002 | t0002 | g0187 | EUR | IBS | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | IBS | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01516 | hp2 | a0001 | c0002 | t0002 | g0199 | EUR | IBS | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01891 | hp1 | a0001 | c0002 | t0002 | g0188 | AFR | ACB | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0058 | AFR | ACB | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01981 | hp2 | a0001 | c0002 | t0015 | g0056 | AMR | PEL | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG01993 | hp2 | a0001 | c0001 | t0029 | g0097 | AMR | PEL | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02027 | hp2 | a0001 | c0002 | t0003 | g0211 | EAS | KHV | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02055 | hp1 | a0001 | c0002 | t0004 | g0179 | AFR | ACB | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02055 | hp2 | a0001 | c0002 | t0005 | g0184 | AFR | ACB | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02071 | hp1 | a0002 | c0005 | t0001 | g0086 | EAS | KHV | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02129 | hp1 | a0001 | c0001 | t0011 | g0114 | EAS | KHV | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02165 | hp1 | a0001 | c0002 | t0016 | g0163 | EAS | CDX | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CDX | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02258 | hp2 | a0001 | c0002 | t0002 | g0212 | AFR | ACB | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02280 | hp2 | a0001 | c0002 | t0021 | g0033 | AFR | ACB | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02451 | hp2 | a0001 | c0002 | t0026 | g0050 | AFR | ACB | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02572 | hp2 | a0001 | c0003 | t0008 | g0024 | AFR | GWD | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02615 | hp1 | a0001 | c0002 | t0002 | g0202 | AFR | GWD | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02615 | hp2 | a0001 | c0001 | t0012 | g0149 | AFR | GWD | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02622 | hp2 | a0001 | c0002 | t0003 | g0182 | AFR | GWD | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02630 | hp1 | a0001 | c0002 | t0002 | g0200 | AFR | GWD | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02647 | hp1 | a0001 | c0001 | t0012 | g0083 | AFR | GWD | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02647 | hp2 | a0001 | c0002 | t0009 | g0053 | AFR | GWD | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02723 | hp1 | a0001 | c0002 | t0005 | g0185 | AFR | GWD | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02723 | hp2 | a0001 | c0002 | t0009 | g0052 | AFR | GWD | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02735 | hp1 | a0001 | c0002 | t0004 | g0065 | SAS | PJL | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02735 | hp2 | a0001 | c0002 | t0017 | g0164 | SAS | PJL | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02738 | hp1 | a0001 | c0001 | t0032 | g0105 | SAS | PJL | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02818 | hp2 | a0001 | c0002 | t0002 | g0195 | AFR | GWD | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02896 | hp1 | a0001 | c0002 | t0002 | g0189 | AFR | GWD | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02896 | hp2 | a0001 | c0001 | t0010 | g0102 | AFR | GWD | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02897 | hp2 | a0001 | c0001 | t0010 | g0103 | AFR | GWD | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02922 | hp2 | a0001 | c0002 | t0002 | g0203 | AFR | ESN | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02970 | hp1 | a0001 | c0002 | t0002 | g0201 | AFR | ESN | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02976 | hp1 | a0001 | c0003 | t0008 | g0025 | AFR | ESN | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02976 | hp2 | a0001 | c0002 | t0018 | g0061 | AFR | ESN | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03041 | hp2 | a0001 | c0002 | t0005 | g0183 | AFR | GWD | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03098 | hp1 | a0001 | c0002 | t0014 | g0127 | AFR | MSL | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03130 | hp1 | a0001 | c0002 | t0020 | g0067 | AFR | ESN | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03139 | hp1 | a0001 | c0002 | t0006 | g0019 | AFR | ESN | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03139 | hp2 | a0001 | c0002 | t0004 | g0177 | AFR | ESN | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03209 | hp1 | a0001 | c0002 | t0002 | g0213 | AFR | MSL | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03225 | hp1 | a0001 | c0002 | t0003 | g0181 | AFR | MSL | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03239 | hp2 | a0001 | c0001 | t0011 | g0116 | SAS | PJL | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03453 | hp1 | a0001 | c0002 | t0005 | g0186 | AFR | MSL | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03516 | hp2 | a0001 | c0002 | t0002 | g0191 | AFR | ESN | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03579 | hp2 | a0001 | c0002 | t0004 | g0178 | AFR | MSL | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03704 | hp1 | a0001 | c0002 | t0002 | g0207 | SAS | PJL | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0205 | SAS | BEB | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0192 | SAS | BEB | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | STU | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG04204 | hp2 | a0001 | c0001 | t0030 | g0094 | SAS | STU | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18522 | hp1 | a0001 | c0002 | t0009 | g0051 | AFR | YRI | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18522 | hp2 | a0001 | c0002 | t0006 | g0021 | AFR | YRI | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18940 | hp2 | a0001 | c0002 | t0004 | g0066 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18941 | hp2 | a0001 | c0002 | t0004 | g0062 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18942 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18947 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18959 | hp2 | a0001 | c0002 | t0004 | g0037 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18960 | hp1 | a0001 | c0002 | t0003 | g0175 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18960 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18961 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18963 | hp1 | a0001 | c0002 | t0023 | g0002 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18967 | hp1 | a0001 | c0002 | t0004 | g0063 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18968 | hp1 | a0001 | c0002 | t0004 | g0035 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18974 | hp2 | a0001 | c0002 | t0003 | g0176 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18977 | hp1 | a0001 | c0002 | t0004 | g0054 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18979 | hp1 | a0001 | c0001 | t0027 | g0069 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18986 | hp2 | a0001 | c0002 | t0004 | g0042 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18990 | hp1 | a0001 | c0002 | t0003 | g0168 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18991 | hp2 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18992 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19002 | hp1 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19010 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19010 | hp2 | a0001 | c0002 | t0004 | g0036 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19011 | hp1 | a0001 | c0002 | t0004 | g0006 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19012 | hp1 | a0001 | c0002 | t0003 | g0169 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19012 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19030 | hp1 | a0001 | c0002 | t0025 | g0156 | AFR | LWK | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | LWK | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | LWK | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19043 | hp2 | a0001 | c0002 | t0002 | g0193 | AFR | LWK | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19060 | hp2 | a0001 | c0002 | t0004 | g0049 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19064 | hp2 | a0001 | c0002 | t0003 | g0173 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19068 | hp2 | a0001 | c0002 | t0003 | g0165 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19070 | hp1 | a0001 | c0002 | t0002 | g0206 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19076 | hp1 | a0001 | c0002 | t0004 | g0038 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19079 | hp1 | a0001 | c0002 | t0003 | g0170 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19080 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19088 | hp1 | a0001 | c0002 | t0003 | g0171 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19088 | hp2 | a0001 | c0002 | t0004 | g0064 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19090 | hp1 | a0001 | c0002 | t0003 | g0172 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | YRI | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA19240 | hp2 | a0001 | c0002 | t0014 | g0126 | AFR | YRI | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ASW | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA20129 | hp2 | a0001 | c0002 | t0022 | g0048 | AFR | ASW | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA20752 | hp2 | a0001 | c0002 | t0005 | g0209 | EUR | TSI | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | TSI | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | TSI | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | GIH | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA20905 | hp2 | a0001 | c0002 | t0002 | g0005 | SAS | GIH | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02486 | hp1 | a0001 | c0002 | t0019 | g0060 | AFR | ACB | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02486 | hp2 | a0001 | c0001 | t0010 | g0104 | AFR | ACB | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02559 | hp1 | a0001 | c0002 | t0003 | g0180 | AFR | ACB | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG02559 | hp2 | a0003 | c0004 | t0001 | g0098 | AFR | ACB | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03471 | hp1 | a0001 | c0002 | t0002 | g0190 | AFR | MSL | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG03471 | hp2 | a0001 | c0001 | t0012 | g0136 | AFR | MSL | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG06807 | hp1 | a0001 | c0002 | t0006 | g0022 | AFR | USA | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
HG06807 | hp2 | a0001 | c0002 | t0024 | g0029 | AFR | USA | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18955 | hp1 | a0001 | c0002 | t0004 | g0059 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA20300 | hp1 | a0001 | c0002 | t0006 | g0018 | AFR | USA | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | USA | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0041 | REF | REF | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0003 | REF | REF | PLEKHA8_chr7_30023412_30089650 | PLEKHA8 | chr7 | 30023412 | 30089650 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:30047892 | A | G | 1 | a0002 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.374A>G | p.Asp125Gly | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 4/14 | 725/7774 | 374/1560 | 125/519 | chr7 | 30047892 | |||
chr7:30078656 | C | T | 1 | a0003 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.1429C>T | p.His477Tyr | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 1780/7774 | 1429/1560 | 477/519 | chr7 | 30078656 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:30054713 | A | G | 1 | a0001c0003 | 3 | HG01243.hp1 HG02572.hp2 HG02976.hp1 |
synonymous_variant | LOW | c.801A>G | p.Gln267Gln | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 8/14 | 1152/7774 | 801/1560 | 267/519 | chr7 | 30054713 | |||
chr7:30074090 | A | G | 2 | a0001c0002 a0001c0003 |
106 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(103): Show |
synonymous_variant | LOW | c.1320A>G | p.Thr440Thr | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/14 | 1671/7774 | 1320/1560 | 440/519 | chr7 | 30074090 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:30028412 | G | A | 19 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0004 others(16): Show |
97 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(94): Show |
5_prime_UTR_variant | MODIFIER | c.-351G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/14 | 351 | chr7 | 30028412 | ||||||
chr7:30028571 | G | T | 1 | a0001c0001t0012 | 3 | HG02615.hp2 HG02647.hp1 HG03471.hp2 |
5_prime_UTR_variant | MODIFIER | c.-192G>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/14 | 192 | chr7 | 30028571 | ||||||
chr7:30028576 | C | T | 3 | a0001c0002t0009 a0001c0002t0025 a0001c0002t0026 |
5 | HG02451.hp2 HG02647.hp2 HG02723.hp2 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-187C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/14 | chr7 | 30028576 | |||||||
chr7:30028648 | G | A | 5 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0015 others(2): Show |
24 | HG00323.hp1 HG00558.hp2 HG00741.hp1 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-115G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/14 | 115 | chr7 | 30028648 | ||||||
chr7:30078892 | C | T | 10 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0005 others(7): Show |
68 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*105C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 105 | chr7 | 30078892 | ||||||
chr7:30078995 | A | C | 1 | a0001c0002t0026 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*208A>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 208 | chr7 | 30078995 | ||||||
chr7:30079261 | G | A | 1 | a0001c0002t0021 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*474G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 474 | chr7 | 30079261 | ||||||
chr7:30079270 | T | C | 1 | a0001c0002t0022 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*483T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 483 | chr7 | 30079270 | ||||||
chr7:30079385 | A | G | 1 | a0001c0002t0006 | 5 | HG01081.hp1 HG03139.hp1 HG06807.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*598A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 598 | chr7 | 30079385 | ||||||
chr7:30079496 | C | T | 1 | a0001c0002t0014 | 2 | HG03098.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*709C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 709 | chr7 | 30079496 | ||||||
chr7:30079529 | C | G | 3 | a0001c0002t0003 a0001c0002t0016 a0001c0002t0017 |
20 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*742C>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 742 | chr7 | 30079529 | ||||||
chr7:30079541 | C | G | 1 | a0001c0003t0008 | 3 | HG01243.hp1 HG02572.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*754C>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 754 | chr7 | 30079541 | ||||||
chr7:30079638 | T | A | 1 | a0001c0001t0027 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*851T>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 851 | chr7 | 30079638 | ||||||
chr7:30079794 | G | A | 7 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0005 others(4): Show |
63 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*1007G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 1007 | chr7 | 30079794 | ||||||
chr7:30079854 | G | A | 1 | a0001c0003t0008 | 3 | HG01243.hp1 HG02572.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1067G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 1067 | chr7 | 30079854 | ||||||
chr7:30080069 | A | C | 1 | a0001c0002t0022 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1282A>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 1282 | chr7 | 30080069 | ||||||
chr7:30080205 | A | G | 1 | a0001c0001t0032 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1418A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 1418 | chr7 | 30080205 | ||||||
chr7:30080246 | C | G | 2 | a0001c0002t0007 a0001c0002t0015 |
4 | HG00323.hp1 HG01243.hp2 HG01261.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1459C>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 1459 | chr7 | 30080246 | ||||||
chr7:30080514 | T | C | 3 | a0001c0002t0006 a0001c0002t0018 a0001c0002t0019 |
7 | HG01081.hp1 HG02486.hp1 HG02976.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1727T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 1727 | chr7 | 30080514 | ||||||
chr7:30080685 | T | C | 3 | a0001c0002t0003 a0001c0002t0016 a0001c0002t0017 |
20 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1898T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 1898 | chr7 | 30080685 | ||||||
chr7:30080729 | T | A | 1 | a0001c0002t0016 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1942T>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 1942 | chr7 | 30080729 | ||||||
chr7:30080735 | C | T | 3 | a0001c0002t0009 a0001c0002t0025 a0001c0002t0026 |
5 | HG02451.hp2 HG02647.hp2 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1948C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 1948 | chr7 | 30080735 | ||||||
chr7:30080786 | A | G | 2 | a0001c0002t0009 a0001c0002t0026 |
4 | HG02451.hp2 HG02647.hp2 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1999A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 1999 | chr7 | 30080786 | ||||||
chr7:30081029 | C | T | 1 | a0001c0002t0020 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2242C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 2242 | chr7 | 30081029 | ||||||
chr7:30081462 | G | C | 1 | a0001c0001t0028 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2675G>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 2675 | chr7 | 30081462 | ||||||
chr7:30081625 | T | A | 1 | a0001c0001t0013 | 2 | HG00741.hp2 HG01074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2838T>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 2838 | chr7 | 30081625 | ||||||
chr7:30081659 | C | T | 1 | a0001c0002t0017 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2872C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 2872 | chr7 | 30081659 | ||||||
chr7:30082006 | A | G | 1 | a0001c0002t0021 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3219A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 3219 | chr7 | 30082006 | ||||||
chr7:30082047 | G | T | 1 | a0001c0002t0024 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3260G>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 3260 | chr7 | 30082047 | ||||||
chr7:30082305 | A | C | 1 | a0001c0001t0011 | 3 | HG01192.hp2 HG02129.hp1 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3518A>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 3518 | chr7 | 30082305 | ||||||
chr7:30082307 | C | G | 3 | a0001c0002t0002 a0001c0002t0005 a0001c0002t0023 |
42 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*3520C>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 3520 | chr7 | 30082307 | ||||||
chr7:30082333 | T | C | 4 | a0001c0002t0004 a0001c0002t0006 a0001c0002t0018 others(1): Show |
27 | HG00423.hp1 HG01081.hp1 HG01243.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*3546T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 3546 | chr7 | 30082333 | ||||||
chr7:30082412 | G | A | 1 | a0001c0002t0018 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3625G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 3625 | chr7 | 30082412 | ||||||
chr7:30082417 | T | C | 9 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0005 others(6): Show |
65 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*3630T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 3630 | chr7 | 30082417 | ||||||
chr7:30082434 | G | A | 1 | a0001c0001t0029 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3647G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 3647 | chr7 | 30082434 | ||||||
chr7:30082580 | C | T | 1 | a0001c0002t0024 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3793C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 3793 | chr7 | 30082580 | ||||||
chr7:30082809 | C | A | 9 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0005 others(6): Show |
65 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*4022C>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 4022 | chr7 | 30082809 | ||||||
chr7:30082942 | T | G | 1 | a0001c0002t0007 | 3 | HG00323.hp1 HG01243.hp2 HG01261.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4155T>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 4155 | chr7 | 30082942 | ||||||
chr7:30083205 | G | C | 1 | a0001c0001t0030 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4418G>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 4418 | chr7 | 30083205 | ||||||
chr7:30083385 | G | A | 1 | a0001c0001t0031 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4598G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 4598 | chr7 | 30083385 | ||||||
chr7:30083525 | C | CT | 3 | a0001c0002t0009 a0001c0002t0025 a0001c0002t0026 |
5 | HG02451.hp2 HG02647.hp2 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4739dupT | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 4740 | INFO_REALIGN_3_PRIME | chr7 | 30083525 | |||||
chr7:30083529 | A | G | 3 | a0001c0002t0003 a0001c0002t0016 a0001c0002t0017 |
20 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4742A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 4742 | chr7 | 30083529 | ||||||
chr7:30083639 | A | C | 1 | a0001c0001t0010 | 3 | HG02486.hp2 HG02896.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4852A>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 4852 | chr7 | 30083639 | ||||||
chr7:30084321 | T | G | 1 | a0001c0002t0023 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5534T>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 5534 | chr7 | 30084321 | ||||||
chr7:30084488 | G | A | 1 | a0001c0002t0022 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5701G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 14/14 | 5701 | chr7 | 30084488 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:30028812 | C | A | 6 | a0001c0002t0002g0002 a0001c0002t0002g0014 a0001c0002t0002g0015 others(3): Show |
7 | NA18947.hp2 NA18960.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.40+10C>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30028812 | |||||||
chr7:30028885 | T | A | 5 | a0001c0002t0006g0018 a0001c0002t0006g0019 a0001c0002t0006g0020 others(2): Show |
5 | HG01081.hp1 HG03139.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.40+83T>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30028885 | |||||||
chr7:30028904 | C | T | 3 | a0001c0002t0002g0212 a0001c0002t0002g0213 a0001c0002t0002g0214 |
3 | HG01175.hp1 HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.40+102C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30028904 | |||||||
chr7:30028936 | T | C | 3 | a0001c0003t0008g0023 a0001c0003t0008g0024 a0001c0003t0008g0025 |
3 | HG01243.hp1 HG02572.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.40+134T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30028936 | |||||||
chr7:30028978 | C | A | 3 | a0001c0003t0008g0023 a0001c0003t0008g0024 a0001c0003t0008g0025 |
3 | HG01243.hp1 HG02572.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.40+176C>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30028978 | |||||||
chr7:30029182 | A | G | 1 | a0001c0002t0002g0214 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.40+380A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30029182 | |||||||
chr7:30029217 | C | G | 1 | a0001c0002t0003g0211 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.40+415C>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30029217 | |||||||
chr7:30029317 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02451.hp1 HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.40+515G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30029317 | |||||||
chr7:30029325 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.40+523A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30029325 | |||||||
chr7:30029512 | A | T | 2 | a0001c0002t0005g0208 a0001c0002t0005g0209 |
2 | HG01070.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.40+710A>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30029512 | |||||||
chr7:30029791 | A | G | 36 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(33): Show |
40 | HG00735.hp2 HG01069.hp2 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.40+989A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30029791 | |||||||
chr7:30030297 | G | A | 1 | a0001c0002t0024g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.40+1495G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30030297 | |||||||
chr7:30030302 | G | T | 3 | a0001c0003t0008g0023 a0001c0003t0008g0024 a0001c0003t0008g0025 |
3 | HG01243.hp1 HG02572.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.40+1500G>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30030302 | |||||||
chr7:30030386 | T | G | 1 | a0001c0001t0001g0030 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.40+1584T>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30030386 | |||||||
chr7:30030607 | T | C | 1 | a0001c0001t0001g0031 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.40+1805T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30030607 | |||||||
chr7:30030683 | A | G | 1 | a0001c0001t0001g0031 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.40+1881A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30030683 | |||||||
chr7:30030700 | T | C | 1 | a0001c0001t0001g0032 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.40+1898T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30030700 | |||||||
chr7:30030785 | C | T | 3 | a0001c0002t0003g0180 a0001c0002t0003g0181 a0001c0002t0003g0182 |
3 | HG02559.hp1 HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.40+1983C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30030785 | |||||||
chr7:30030863 | T | C | 1 | a0001c0002t0006g0018 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.40+2061T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30030863 | |||||||
chr7:30030871 | C | T | 3 | a0001c0002t0004g0177 a0001c0002t0004g0178 a0001c0002t0004g0179 |
3 | HG02055.hp1 HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.40+2069C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30030871 | |||||||
chr7:30030928 | C | G | 52 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(49): Show |
57 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.40+2126C>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30030928 | |||||||
chr7:30031008 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.40+2206C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30031008 | |||||||
chr7:30031058 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.40+2256C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30031058 | |||||||
chr7:30031192 | C | A | 1 | a0001c0002t0005g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.40+2390C>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30031192 | |||||||
chr7:30031826 | G | A | 32 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(29): Show |
36 | HG00735.hp2 HG01069.hp2 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.40+3024G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30031826 | |||||||
chr7:30031888 | G | A | 2 | a0001c0002t0005g0208 a0001c0002t0005g0209 |
2 | HG01070.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.40+3086G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30031888 | |||||||
chr7:30032012 | G | A | 1 | a0001c0002t0021g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.40+3210G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30032012 | |||||||
chr7:30032033 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.40+3231A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30032033 | |||||||
chr7:30032526 | G | A | 1 | a0001c0002t0007g0034 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.40+3724G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30032526 | |||||||
chr7:30032545 | C | G | 1 | a0001c0002t0003g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.40+3743C>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30032545 | |||||||
chr7:30032774 | A | G | 1 | a0001c0002t0024g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.40+3972A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30032774 | |||||||
chr7:30032795 | A | G | 36 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(33): Show |
40 | HG00735.hp2 HG01069.hp2 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.40+3993A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30032795 | |||||||
chr7:30032961 | A | G | 19 | a0001c0002t0003g0012 a0001c0002t0003g0165 a0001c0002t0003g0166 others(16): Show |
20 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.40+4159A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30032961 | |||||||
chr7:30032988 | T | C | 5 | a0001c0002t0004g0006 a0001c0002t0004g0035 a0001c0002t0004g0036 others(2): Show |
6 | HG00423.hp1 NA18959.hp2 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.40+4186T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30032988 | |||||||
chr7:30033050 | G | A | 1 | a0001c0001t0001g0007 | 2 | NA18947.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.40+4248G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30033050 | |||||||
chr7:30033075 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0039 |
3 | NA18947.hp1 NA18990.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.40+4273T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30033075 | |||||||
chr7:30033428 | G | A | 3 | a0001c0003t0008g0023 a0001c0003t0008g0024 a0001c0003t0008g0025 |
3 | HG01243.hp1 HG02572.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.40+4626G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30033428 | |||||||
chr7:30033878 | T | A | 2 | a0001c0002t0005g0183 a0001c0002t0005g0184 |
2 | HG02055.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.40+5076T>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30033878 | |||||||
chr7:30033938 | A | G | 4 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
4 | HG00408.hp2 NA18941.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+5136A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30033938 | |||||||
chr7:30034010 | C | CT | 8 | a0001c0001t0001g0010 a0001c0001t0001g0082 a0001c0001t0001g0084 others(5): Show |
9 | HG02055.hp1 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.40+5240dupT | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30034010 | ||||||
chr7:30034010 | CT | C | 23 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0032 others(20): Show |
23 | HG00408.hp1 HG00423.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.40+5240delT | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30034010 | ||||||
chr7:30034010 | CTT | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(105): Show |
115 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.40+5239_40+5240del others(2): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30034010 | ||||||
chr7:30034010 | CTTT | C | 7 | a0001c0001t0001g0027 a0001c0001t0001g0106 a0001c0002t0004g0038 others(4): Show |
7 | HG01243.hp1 HG02055.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.40+5238_40+5240del others(3): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30034010 | ||||||
chr7:30034010 | CTTTTT | C | 33 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(30): Show |
37 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.40+5236_40+5240del others(5): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30034010 | ||||||
chr7:30034010 | CTTTTTT | C | 16 | a0001c0002t0002g0189 a0001c0002t0003g0012 a0001c0002t0003g0165 others(13): Show |
17 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.40+5235_40+5240del others(6): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30034010 | ||||||
chr7:30034010 | CTTTTTTT others(5): Show |
C | 1 | a0001c0002t0002g0202 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.40+5229_40+5240del others(12): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30034010 | ||||||
chr7:30034010 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0011g0115 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.40+5228_40+5240del others(13): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30034010 | ||||||
chr7:30034015 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.40+5213T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30034015 | |||||||
chr7:30034015 | T | G | 1 | a0001c0002t0002g0187 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.40+5213T>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30034015 | |||||||
chr7:30034053 | C | A | 1 | a0001c0002t0004g0042 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40+5251C>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30034053 | |||||||
chr7:30034095 | G | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 |
3 | HG01175.hp2 HG01256.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.40+5293G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30034095 | |||||||
chr7:30034198 | T | C | 54 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(51): Show |
59 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.40+5396T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30034198 | |||||||
chr7:30034260 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.40+5458C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30034260 | |||||||
chr7:30034627 | A | G | 1 | a0001c0002t0025g0156 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.40+5825A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30034627 | |||||||
chr7:30035025 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | NA18950.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.40+6223G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30035025 | |||||||
chr7:30035050 | T | C | 1 | a0001c0002t0016g0163 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.40+6248T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30035050 | |||||||
chr7:30035144 | T | C | 3 | a0001c0003t0008g0023 a0001c0003t0008g0024 a0001c0003t0008g0025 |
3 | HG01243.hp1 HG02572.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.40+6342T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30035144 | |||||||
chr7:30035295 | T | C | 38 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(35): Show |
42 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.40+6493T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30035295 | |||||||
chr7:30035344 | A | T | 2 | a0001c0002t0003g0180 a0001c0002t0003g0181 |
2 | HG02559.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.40+6542A>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30035344 | |||||||
chr7:30035418 | T | C | 1 | a0001c0002t0017g0164 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.40+6616T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30035418 | |||||||
chr7:30035587 | A | C | 38 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(35): Show |
42 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.40+6785A>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30035587 | |||||||
chr7:30035789 | G | A | 1 | a0001c0002t0022g0048 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.40+6987G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30035789 | |||||||
chr7:30035809 | G | A | 59 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(56): Show |
64 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.40+7007G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30035809 | |||||||
chr7:30035822 | A | AT | 19 | a0001c0002t0003g0012 a0001c0002t0003g0165 a0001c0002t0003g0166 others(16): Show |
20 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.40+7025dupT | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30035822 | ||||||
chr7:30035912 | T | C | 94 | a0001c0002t0001g0058 a0001c0002t0002g0002 a0001c0002t0002g0005 others(91): Show |
100 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.40+7110T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30035912 | |||||||
chr7:30036085 | G | A | 3 | a0001c0002t0005g0183 a0001c0002t0005g0184 a0001c0002t0005g0185 |
3 | HG02055.hp2 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.40+7283G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30036085 | |||||||
chr7:30036138 | C | A | 2 | a0001c0002t0021g0033 a0001c0002t0022g0048 |
2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.40+7336C>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30036138 | |||||||
chr7:30036407 | A | AATAG | 14 | a0001c0001t0001g0008 a0001c0001t0001g0043 a0001c0001t0001g0084 others(11): Show |
16 | HG00423.hp1 HG00544.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.40+7660_40+7663dup others(4): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30036407 | ||||||
chr7:30036407 | A | AATAGATA others(1): Show |
3 | a0001c0001t0001g0082 a0001c0002t0002g0188 a0001c0002t0004g0035 |
3 | HG01891.hp1 HG02965.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.40+7656_40+7663dup others(8): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30036407 | ||||||
chr7:30036407 | AATAG | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0032 others(64): Show |
70 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.40+7660_40+7663del others(4): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30036407 | ||||||
chr7:30036407 | AATAGATA others(1): Show |
A | 48 | a0001c0001t0001g0031 a0001c0001t0001g0068 a0001c0001t0001g0125 others(45): Show |
49 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.40+7656_40+7663del others(8): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30036407 | ||||||
chr7:30036407 | AATAGATA others(5): Show |
A | 27 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0026 others(24): Show |
33 | HG01074.hp1 HG01081.hp2 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.40+7652_40+7663del others(12): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30036407 | ||||||
chr7:30036407 | AATAGATA others(9): Show |
A | 2 | a0001c0001t0001g0155 a0001c0002t0003g0173 |
2 | NA19064.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.40+7648_40+7663del others(16): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30036407 | ||||||
chr7:30036407 | AATAGATA others(13): Show |
A | 3 | a0001c0002t0003g0180 a0001c0002t0003g0181 a0001c0002t0003g0182 |
3 | HG02559.hp1 HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.40+7644_40+7663del others(20): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30036407 | ||||||
chr7:30036407 | AATAGATA others(21): Show |
A | 4 | a0001c0002t0003g0174 a0001c0002t0003g0175 a0001c0002t0003g0176 others(1): Show |
4 | HG00558.hp2 HG02027.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.40+7636_40+7663del others(28): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30036407 | ||||||
chr7:30036451 | G | C | 16 | a0001c0001t0001g0030 a0001c0001t0001g0068 a0001c0001t0001g0070 others(13): Show |
16 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(13): Show |
intron_variant | MODIFIER | c.40+7649G>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30036451 | |||||||
chr7:30036563 | C | T | 13 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0121 others(10): Show |
13 | HG00408.hp2 HG00544.hp2 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.40+7761C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30036563 | |||||||
chr7:30036566 | T | A | 1 | a0001c0001t0001g0142 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.40+7764T>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30036566 | |||||||
chr7:30036605 | C | A | 3 | a0001c0003t0008g0023 a0001c0003t0008g0024 a0001c0003t0008g0025 |
3 | HG01243.hp1 HG02572.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.40+7803C>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30036605 | |||||||
chr7:30036985 | A | C | 6 | a0001c0002t0001g0058 a0001c0002t0007g0034 a0001c0002t0007g0055 others(3): Show |
6 | HG00323.hp1 HG01243.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.41-8100A>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30036985 | |||||||
chr7:30037058 | T | C | 63 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(60): Show |
68 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.41-8027T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30037058 | |||||||
chr7:30037173 | C | A | 1 | a0001c0001t0001g0089 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.41-7912C>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30037173 | |||||||
chr7:30037385 | T | C | 1 | a0001c0002t0024g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.41-7700T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30037385 | |||||||
chr7:30037705 | TG | T | 4 | a0001c0002t0007g0034 a0001c0002t0007g0055 a0001c0002t0007g0057 others(1): Show |
4 | HG00323.hp1 HG01243.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-7378delG | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30037705 | ||||||
chr7:30037710 | A | G | 1 | a0001c0002t0004g0064 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.41-7375A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30037710 | |||||||
chr7:30037771 | A | G | 4 | a0001c0002t0004g0054 a0001c0002t0004g0062 a0001c0002t0004g0063 others(1): Show |
4 | NA18940.hp2 NA18941.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-7314A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30037771 | |||||||
chr7:30037868 | A | G | 38 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(35): Show |
42 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.41-7217A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30037868 | |||||||
chr7:30038164 | T | C | 38 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(35): Show |
42 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.41-6921T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30038164 | |||||||
chr7:30038263 | AT | A | 38 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(35): Show |
42 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.41-6820delT | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30038263 | ||||||
chr7:30038602 | C | T | 2 | a0001c0002t0021g0033 a0001c0002t0022g0048 |
2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.41-6483C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30038602 | |||||||
chr7:30038713 | A | T | 5 | a0001c0002t0006g0018 a0001c0002t0006g0019 a0001c0002t0006g0020 others(2): Show |
5 | HG01081.hp1 HG03139.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.41-6372A>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30038713 | |||||||
chr7:30038972 | T | TATA | 38 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(35): Show |
42 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.41-6111_41-6109dup others(3): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30038972 | ||||||
chr7:30039012 | C | CAT | 98 | a0001c0002t0001g0058 a0001c0002t0002g0002 a0001c0002t0002g0005 others(95): Show |
104 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.41-6073_41-6072ins others(2): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30039012 | |||||||
chr7:30039280 | C | T | 41 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(38): Show |
45 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.41-5805C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30039280 | |||||||
chr7:30039333 | G | A | 1 | a0001c0002t0003g0180 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.41-5752G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30039333 | |||||||
chr7:30039362 | A | G | 19 | a0001c0002t0003g0012 a0001c0002t0003g0165 a0001c0002t0003g0166 others(16): Show |
20 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.41-5723A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30039362 | |||||||
chr7:30039380 | T | C | 1 | a0001c0001t0001g0125 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.41-5705T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30039380 | |||||||
chr7:30039439 | C | T | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG01074.hp1 HG01981.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.41-5646C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30039439 | |||||||
chr7:30039551 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.41-5534C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30039551 | |||||||
chr7:30039722 | C | T | 1 | a0001c0002t0002g0197 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.41-5363C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30039722 | |||||||
chr7:30039738 | G | A | 1 | a0001c0002t0022g0048 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.41-5347G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30039738 | |||||||
chr7:30039767 | TAGAGCTA others(52): Show |
T | 1 | a0001c0002t0021g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.41-5257_41-5199del others(59): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30039767 | ||||||
chr7:30039854 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.41-5231A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30039854 | |||||||
chr7:30040312 | C | G | 4 | a0001c0002t0007g0034 a0001c0002t0007g0055 a0001c0002t0007g0057 others(1): Show |
4 | HG00323.hp1 HG01243.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-4773C>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30040312 | |||||||
chr7:30040355 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.41-4730G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30040355 | |||||||
chr7:30040718 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.41-4367A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30040718 | |||||||
chr7:30040721 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.41-4364G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30040721 | |||||||
chr7:30040743 | C | T | 1 | a0001c0002t0024g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.41-4342C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30040743 | |||||||
chr7:30040874 | G | C | 2 | a0001c0002t0014g0126 a0001c0002t0014g0127 |
2 | HG03098.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.41-4211G>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30040874 | |||||||
chr7:30040887 | G | T | 1 | a0001c0001t0001g0088 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.41-4198G>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30040887 | |||||||
chr7:30041117 | C | A | 34 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(31): Show |
38 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.41-3968C>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30041117 | |||||||
chr7:30041194 | A | G | 1 | a0001c0002t0021g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.41-3891A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30041194 | |||||||
chr7:30041356 | G | A | 38 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(35): Show |
42 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.41-3729G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30041356 | |||||||
chr7:30041419 | A | AT | 56 | a0001c0001t0001g0030 a0001c0001t0001g0068 a0001c0001t0001g0071 others(53): Show |
60 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.41-3646dupT | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30041419 | ||||||
chr7:30041419 | AT | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(90): Show |
99 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.41-3646delT | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30041419 | ||||||
chr7:30041419 | ATT | A | 5 | a0001c0001t0001g0089 a0001c0001t0001g0160 a0001c0002t0004g0037 others(2): Show |
5 | HG00323.hp1 HG00558.hp1 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.41-3647_41-3646del others(2): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30041419 | ||||||
chr7:30041419 | ATTT | A | 12 | a0001c0002t0004g0006 a0001c0002t0004g0035 a0001c0002t0004g0036 others(9): Show |
13 | HG00423.hp1 HG02735.hp1 NA18941.hp2 others(10): Show |
intron_variant | MODIFIER | c.41-3648_41-3646del others(3): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30041419 | ||||||
chr7:30041752 | C | T | 1 | a0001c0002t0004g0064 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.41-3333C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30041752 | |||||||
chr7:30041814 | G | A | 4 | a0001c0002t0007g0034 a0001c0002t0007g0055 a0001c0002t0007g0057 others(1): Show |
4 | HG00323.hp1 HG01243.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-3271G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30041814 | |||||||
chr7:30041874 | G | A | 1 | a0001c0002t0024g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.41-3211G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30041874 | |||||||
chr7:30042198 | C | T | 1 | a0001c0002t0009g0053 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.41-2887C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30042198 | |||||||
chr7:30042277 | A | C | 18 | a0001c0002t0003g0012 a0001c0002t0003g0165 a0001c0002t0003g0166 others(15): Show |
19 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.41-2808A>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30042277 | |||||||
chr7:30042281 | T | G | 38 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(35): Show |
42 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.41-2804T>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30042281 | |||||||
chr7:30042394 | T | C | 62 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(59): Show |
67 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.41-2691T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30042394 | |||||||
chr7:30042508 | C | T | 1 | a0001c0002t0002g0196 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.41-2577C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30042508 | |||||||
chr7:30042887 | A | G | 18 | a0001c0002t0003g0012 a0001c0002t0003g0165 a0001c0002t0003g0166 others(15): Show |
19 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.41-2198A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30042887 | |||||||
chr7:30043006 | T | TTTTGTTT others(1): Show |
18 | a0001c0002t0002g0191 a0001c0002t0003g0012 a0001c0002t0003g0165 others(15): Show |
19 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.41-2069_41-2062dup others(8): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30043006 | ||||||
chr7:30043006 | T | TTTTGTTT others(5): Show |
1 | a0001c0002t0016g0163 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.41-2073_41-2062dup others(12): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30043006 | ||||||
chr7:30043006 | T | TTTTGTTT others(9): Show |
32 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(29): Show |
36 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.41-2077_41-2062dup others(16): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30043006 | ||||||
chr7:30043006 | T | TTTTGTTT others(13): Show |
1 | a0001c0002t0002g0195 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.41-2062_41-2061ins others(20): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30043006 | ||||||
chr7:30043051 | G | C | 1 | a0001c0001t0001g0091 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.41-2034G>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30043051 | |||||||
chr7:30043086 | CG | C | 18 | a0001c0002t0003g0012 a0001c0002t0003g0165 a0001c0002t0003g0166 others(15): Show |
19 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.41-1998delG | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30043086 | |||||||
chr7:30043087 | G | A | 1 | a0001c0002t0024g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.41-1998G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30043087 | |||||||
chr7:30043202 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.41-1883G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30043202 | |||||||
chr7:30043237 | T | C | 1 | a0001c0002t0004g0065 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.41-1848T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30043237 | |||||||
chr7:30043386 | C | A | 1 | a0001c0002t0022g0048 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.41-1699C>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30043386 | |||||||
chr7:30043405 | A | C | 35 | a0001c0002t0001g0058 a0001c0002t0004g0006 a0001c0002t0004g0035 others(32): Show |
36 | HG00323.hp1 HG00423.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.41-1680A>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30043405 | |||||||
chr7:30043525 | A | G | 38 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(35): Show |
42 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.41-1560A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30043525 | |||||||
chr7:30043779 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.41-1306A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30043779 | |||||||
chr7:30043812 | C | T | 1 | a0002c0005t0001g0086 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.41-1273C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30043812 | |||||||
chr7:30043882 | G | A | 1 | a0001c0003t0008g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.41-1203G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30043882 | |||||||
chr7:30044032 | A | AT | 36 | a0001c0001t0001g0080 a0001c0001t0001g0117 a0001c0001t0001g0150 others(33): Show |
37 | HG00423.hp1 HG01069.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.41-1035dupT | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30044032 | ||||||
chr7:30044032 | A | ATT | 5 | a0001c0002t0006g0021 a0001c0002t0007g0034 a0001c0002t0007g0055 others(2): Show |
5 | HG00323.hp1 HG01243.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.41-1036_41-1035dup others(2): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30044032 | ||||||
chr7:30044079 | T | G | 1 | a0001c0002t0002g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.41-1006T>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30044079 | |||||||
chr7:30044131 | T | C | 1 | a0001c0002t0024g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.41-954T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30044131 | |||||||
chr7:30044634 | CTTATTTC others(11): Show |
C | 1 | a0001c0001t0001g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.41-449_41-432delTA others(16): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 30044634 | ||||||
chr7:30044816 | G | T | 1 | a0001c0002t0003g0168 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.41-269G>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30044816 | |||||||
chr7:30045003 | A | G | 1 | a0001c0001t0029g0097 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.41-82A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 1/13 | chr7 | 30045003 | |||||||
chr7:30045213 | A | T | 1 | a0001c0002t0021g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.157+12A>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 2/13 | chr7 | 30045213 | |||||||
chr7:30045696 | TG | T | 4 | a0001c0001t0001g0141 a0001c0001t0011g0115 a0001c0001t0011g0116 others(1): Show |
4 | HG01192.hp2 HG02735.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+498delG | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr7 | 30045696 | ||||||
chr7:30045699 | G | A | 3 | a0001c0003t0008g0023 a0001c0003t0008g0024 a0001c0003t0008g0025 |
3 | HG01243.hp1 HG02572.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.157+498G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 2/13 | chr7 | 30045699 | |||||||
chr7:30045719 | T | A | 1 | a0001c0001t0001g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.158-491T>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 2/13 | chr7 | 30045719 | |||||||
chr7:30045963 | G | A | 38 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(35): Show |
42 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.158-247G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 2/13 | chr7 | 30045963 | |||||||
chr7:30045972 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.158-238G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 2/13 | chr7 | 30045972 | |||||||
chr7:30046016 | T | C | 2 | a0001c0002t0003g0012 a0001c0002t0003g0169 |
3 | NA18991.hp2 NA19002.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.158-194T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 2/13 | chr7 | 30046016 | |||||||
chr7:30046126 | A | G | 1 | a0001c0002t0024g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.158-84A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 2/13 | chr7 | 30046126 | |||||||
chr7:30046150 | T | G | 58 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(55): Show |
63 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.158-60T>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 2/13 | chr7 | 30046150 | |||||||
chr7:30046528 | C | T | 1 | a0001c0001t0001g0009 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.313+163C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 3/13 | chr7 | 30046528 | |||||||
chr7:30046796 | C | T | 3 | a0001c0001t0010g0102 a0001c0001t0010g0103 a0001c0001t0010g0104 |
3 | HG02486.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.313+431C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 3/13 | chr7 | 30046796 | |||||||
chr7:30047126 | A | G | 2 | a0001c0002t0021g0033 a0001c0002t0022g0048 |
2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.314-706A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 3/13 | chr7 | 30047126 | |||||||
chr7:30047258 | T | C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0210 |
2 | HG02273.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.314-574T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 3/13 | chr7 | 30047258 | |||||||
chr7:30047324 | A | G | 1 | a0001c0001t0011g0114 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.314-508A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 3/13 | chr7 | 30047324 | |||||||
chr7:30047765 | A | G | 97 | a0001c0002t0001g0058 a0001c0002t0002g0002 a0001c0002t0002g0005 others(94): Show |
103 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.314-67A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 3/13 | chr7 | 30047765 | |||||||
chr7:30047767 | A | G | 1 | a0001c0002t0024g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.314-65A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 3/13 | chr7 | 30047767 | |||||||
chr7:30048432 | A | G | 1 | a0001c0002t0021g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.438+476A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 4/13 | chr7 | 30048432 | |||||||
chr7:30048789 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.439-435G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 4/13 | chr7 | 30048789 | |||||||
chr7:30048790 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.439-434G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 4/13 | chr7 | 30048790 | |||||||
chr7:30048857 | A | T | 1 | a0001c0001t0001g0031 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.439-367A>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 4/13 | chr7 | 30048857 | |||||||
chr7:30048889 | CTCTTGGG others(5): Show |
C | 1 | a0001c0002t0026g0050 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.439-333_439-322del others(12): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 30048889 | ||||||
chr7:30048982 | T | G | 18 | a0001c0002t0003g0012 a0001c0002t0003g0165 a0001c0002t0003g0166 others(15): Show |
19 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.439-242T>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 4/13 | chr7 | 30048982 | |||||||
chr7:30049060 | CTTGA | C | 19 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(16): Show |
23 | HG00735.hp2 HG01070.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.439-161_439-158del others(4): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 30049060 | ||||||
chr7:30049199 | G | A | 2 | a0001c0002t0014g0126 a0001c0002t0014g0127 |
2 | HG03098.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.439-25G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 4/13 | chr7 | 30049199 | |||||||
chr7:30049586 | C | A | 30 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(27): Show |
34 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.597+204C>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 5/13 | chr7 | 30049586 | |||||||
chr7:30049586 | C | T | 3 | a0001c0002t0004g0177 a0001c0002t0004g0178 a0001c0002t0004g0179 |
3 | HG02055.hp1 HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.597+204C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 5/13 | chr7 | 30049586 | |||||||
chr7:30049863 | A | C | 1 | a0001c0002t0003g0167 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.597+481A>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 5/13 | chr7 | 30049863 | |||||||
chr7:30050253 | A | G | 1 | a0001c0002t0021g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.598-181A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 5/13 | chr7 | 30050253 | |||||||
chr7:30050386 | T | A | 1 | a0001c0002t0022g0048 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.598-48T>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 5/13 | chr7 | 30050386 | |||||||
chr7:30050396 | T | G | 1 | a0001c0002t0004g0038 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.598-38T>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 5/13 | chr7 | 30050396 | |||||||
chr7:30050410 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.598-24T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 5/13 | chr7 | 30050410 | |||||||
chr7:30050540 | A | T | 2 | a0001c0002t0001g0058 a0001c0002t0020g0067 |
2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.638+66A>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | chr7 | 30050540 | |||||||
chr7:30050802 | G | T | 52 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(49): Show |
57 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.638+328G>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | chr7 | 30050802 | |||||||
chr7:30050925 | T | TGCTCCTT others(33): Show |
1 | a0001c0002t0002g0212 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.638+460_638+461ins others(40): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr7 | 30050925 | ||||||
chr7:30050935 | A | G | 38 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(35): Show |
42 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.638+461A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | chr7 | 30050935 | |||||||
chr7:30051065 | A | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0101 others(3): Show |
8 | HG00741.hp2 HG01074.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.638+591A>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | chr7 | 30051065 | |||||||
chr7:30051133 | C | T | 18 | a0001c0002t0003g0012 a0001c0002t0003g0165 a0001c0002t0003g0166 others(15): Show |
19 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.638+659C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | chr7 | 30051133 | |||||||
chr7:30051162 | A | T | 3 | a0001c0003t0008g0023 a0001c0003t0008g0024 a0001c0003t0008g0025 |
3 | HG01243.hp1 HG02572.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.638+688A>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | chr7 | 30051162 | |||||||
chr7:30051192 | G | A | 1 | a0001c0002t0004g0178 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.638+718G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | chr7 | 30051192 | |||||||
chr7:30051194 | C | A | 1 | a0001c0002t0002g0197 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.638+720C>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | chr7 | 30051194 | |||||||
chr7:30051196 | G | A | 38 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(35): Show |
42 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.638+722G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | chr7 | 30051196 | |||||||
chr7:30051298 | A | G | 2 | a0001c0002t0002g0212 a0001c0002t0002g0213 |
2 | HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.638+824A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | chr7 | 30051298 | |||||||
chr7:30051396 | G | GT | 39 | a0001c0002t0001g0058 a0001c0002t0004g0006 a0001c0002t0004g0035 others(36): Show |
40 | HG00323.hp1 HG00423.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.638+934dupT | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr7 | 30051396 | ||||||
chr7:30051507 | G | A | 52 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(49): Show |
57 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.638+1033G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | chr7 | 30051507 | |||||||
chr7:30051629 | G | A | 3 | a0001c0002t0004g0049 a0001c0002t0004g0059 a0001c0002t0004g0064 |
3 | NA18955.hp1 NA19060.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.639-1080G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | chr7 | 30051629 | |||||||
chr7:30051730 | T | C | 4 | a0001c0001t0001g0093 a0001c0001t0001g0107 a0001c0001t0001g0145 others(1): Show |
4 | HG01069.hp1 HG01070.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.639-979T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | chr7 | 30051730 | |||||||
chr7:30051739 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.639-970C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | chr7 | 30051739 | |||||||
chr7:30051831 | G | A | 4 | a0001c0002t0007g0034 a0001c0002t0007g0055 a0001c0002t0007g0057 others(1): Show |
4 | HG00323.hp1 HG01243.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.639-878G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | chr7 | 30051831 | |||||||
chr7:30052015 | A | T | 1 | a0001c0002t0021g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.639-694A>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | chr7 | 30052015 | |||||||
chr7:30052055 | C | T | 34 | a0001c0002t0004g0006 a0001c0002t0004g0035 a0001c0002t0004g0036 others(31): Show |
35 | HG00323.hp1 HG00423.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.639-654C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | chr7 | 30052055 | |||||||
chr7:30052100 | C | T | 1 | a0001c0002t0024g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.639-609C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | chr7 | 30052100 | |||||||
chr7:30052160 | A | C | 1 | a0001c0001t0001g0113 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.639-549A>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | chr7 | 30052160 | |||||||
chr7:30052256 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.639-453G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | chr7 | 30052256 | |||||||
chr7:30052298 | A | G | 1 | a0001c0002t0002g0206 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.639-411A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | chr7 | 30052298 | |||||||
chr7:30052363 | G | A | 1 | a0001c0002t0024g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.639-346G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | chr7 | 30052363 | |||||||
chr7:30052436 | A | G | 4 | a0001c0002t0007g0034 a0001c0002t0007g0055 a0001c0002t0007g0057 others(1): Show |
4 | HG00323.hp1 HG01243.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.639-273A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | chr7 | 30052436 | |||||||
chr7:30052494 | G | A | 2 | a0001c0002t0005g0208 a0001c0002t0005g0209 |
2 | HG01070.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.639-215G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | chr7 | 30052494 | |||||||
chr7:30052520 | G | T | 1 | a0001c0001t0001g0128 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.639-189G>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | chr7 | 30052520 | |||||||
chr7:30052640 | C | CA | 6 | a0001c0001t0001g0117 a0001c0001t0011g0115 a0001c0002t0009g0051 others(3): Show |
6 | HG01192.hp2 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.639-49dupA | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr7 | 30052640 | ||||||
chr7:30052640 | C | CAAAAAAA others(3): Show |
14 | a0001c0002t0003g0012 a0001c0002t0003g0165 a0001c0002t0003g0166 others(11): Show |
15 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.639-58_639-49dupAA others(8): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr7 | 30052640 | ||||||
chr7:30052640 | C | CAAAAAAA others(4): Show |
5 | a0001c0002t0003g0169 a0001c0002t0003g0170 a0001c0002t0003g0173 others(2): Show |
5 | HG02027.hp2 HG02622.hp2 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.639-59_639-49dupAA others(9): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr7 | 30052640 | ||||||
chr7:30052640 | CAAAA | C | 34 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(31): Show |
38 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.639-52_639-49delAA others(2): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr7 | 30052640 | ||||||
chr7:30052672 | G | A | 1 | a0001c0002t0021g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.639-37G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 6/13 | chr7 | 30052672 | |||||||
chr7:30053147 | A | G | 3 | a0001c0003t0008g0023 a0001c0003t0008g0024 a0001c0003t0008g0025 |
3 | HG01243.hp1 HG02572.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.796+281A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 7/13 | chr7 | 30053147 | |||||||
chr7:30053267 | A | G | 19 | a0001c0002t0001g0058 a0001c0002t0003g0012 a0001c0002t0003g0165 others(16): Show |
20 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.796+401A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 7/13 | chr7 | 30053267 | |||||||
chr7:30053285 | C | G | 1 | a0001c0002t0003g0172 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.796+419C>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 7/13 | chr7 | 30053285 | |||||||
chr7:30053495 | C | T | 18 | a0001c0002t0003g0012 a0001c0002t0003g0165 a0001c0002t0003g0166 others(15): Show |
19 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.796+629C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 7/13 | chr7 | 30053495 | |||||||
chr7:30053884 | A | G | 2 | a0001c0002t0004g0035 a0001c0002t0004g0036 |
2 | NA18968.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.797-825A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 7/13 | chr7 | 30053884 | |||||||
chr7:30053885 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.797-824C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 7/13 | chr7 | 30053885 | |||||||
chr7:30053935 | T | C | 1 | a0001c0002t0022g0048 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.797-774T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 7/13 | chr7 | 30053935 | |||||||
chr7:30054139 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.797-570G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 7/13 | chr7 | 30054139 | |||||||
chr7:30054416 | C | A | 1 | a0001c0002t0024g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.797-293C>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 7/13 | chr7 | 30054416 | |||||||
chr7:30054575 | A | G | 2 | a0001c0002t0014g0126 a0001c0002t0014g0127 |
2 | HG03098.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.797-134A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 7/13 | chr7 | 30054575 | |||||||
chr7:30055152 | A | T | 7 | a0001c0001t0001g0079 a0001c0002t0002g0002 a0001c0002t0002g0014 others(4): Show |
8 | HG00735.hp1 NA18947.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.954-105A>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 8/13 | chr7 | 30055152 | |||||||
chr7:30055181 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.954-76A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 8/13 | chr7 | 30055181 | |||||||
chr7:30055455 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1039+113A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30055455 | |||||||
chr7:30055634 | A | C | 2 | a0001c0001t0001g0112 a0001c0001t0001g0117 |
2 | HG02572.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1039+292A>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30055634 | |||||||
chr7:30055677 | C | CT | 56 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(53): Show |
61 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.1039+341dupT | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30055677 | ||||||
chr7:30055781 | T | G | 3 | a0001c0002t0004g0177 a0001c0002t0004g0178 a0001c0002t0004g0179 |
3 | HG02055.hp1 HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1039+439T>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30055781 | |||||||
chr7:30055817 | C | T | 4 | a0001c0001t0012g0083 a0001c0001t0012g0136 a0001c0001t0012g0149 others(1): Show |
4 | HG02615.hp2 HG02647.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039+475C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30055817 | |||||||
chr7:30055945 | C | CT | 82 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(79): Show |
88 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.1039+618dupT | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30055945 | ||||||
chr7:30055965 | C | T | 1 | a0001c0002t0021g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1039+623C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30055965 | |||||||
chr7:30056074 | C | T | 18 | a0001c0002t0003g0012 a0001c0002t0003g0165 a0001c0002t0003g0166 others(15): Show |
19 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.1039+732C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056074 | |||||||
chr7:30056135 | G | A | 3 | a0001c0003t0008g0023 a0001c0003t0008g0024 a0001c0003t0008g0025 |
3 | HG01243.hp1 HG02572.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1039+793G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056135 | |||||||
chr7:30056222 | T | C | 56 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(53): Show |
61 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.1039+880T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056222 | |||||||
chr7:30056232 | C | G | 1 | a0001c0002t0003g0167 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1039+890C>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056232 | |||||||
chr7:30056238 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1039+896C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056238 | |||||||
chr7:30056278 | T | TTC | 5 | a0001c0001t0001g0009 a0001c0001t0001g0068 a0001c0001t0001g0081 others(2): Show |
6 | HG00323.hp2 HG02630.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1039+970_1039+971d others(4): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056278 | ||||||
chr7:30056278 | T | TTCTC | 12 | a0001c0001t0001g0008 a0001c0001t0001g0073 a0001c0001t0001g0074 others(9): Show |
13 | HG00544.hp1 HG01081.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1039+968_1039+971d others(6): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056278 | ||||||
chr7:30056278 | T | TTCTCTC | 12 | a0001c0001t0001g0075 a0001c0001t0001g0087 a0001c0001t0001g0088 others(9): Show |
12 | HG00544.hp2 HG01243.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1039+966_1039+971d others(8): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056278 | ||||||
chr7:30056278 | T | TTCTCTCT others(1): Show |
9 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0150 others(6): Show |
9 | HG00609.hp1 HG01074.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.1039+964_1039+971d others(10): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056278 | ||||||
chr7:30056278 | T | TTCTCTCT others(3): Show |
5 | a0001c0001t0001g0076 a0001c0001t0001g0128 a0001c0001t0001g0144 others(2): Show |
5 | HG01981.hp1 NA18961.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1039+962_1039+971d others(12): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056278 | ||||||
chr7:30056278 | T | TTCTCTCT others(5): Show |
2 | a0001c0001t0001g0140 a0001c0002t0021g0033 |
2 | HG02280.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1039+960_1039+971d others(14): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056278 | ||||||
chr7:30056278 | T | TTCTCTCT others(7): Show |
3 | a0001c0001t0001g0077 a0001c0001t0001g0121 a0001c0001t0001g0139 |
3 | HG02027.hp1 NA18971.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1039+958_1039+971d others(16): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056278 | ||||||
chr7:30056278 | T | TTCTCTCT others(9): Show |
1 | a0001c0001t0001g0078 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1039+956_1039+971d others(18): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056278 | ||||||
chr7:30056278 | TTCTC | T | 2 | a0001c0002t0003g0170 a0001c0002t0015g0056 |
2 | HG01981.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1039+968_1039+971d others(6): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056278 | ||||||
chr7:30056278 | TTCTCTC | T | 13 | a0001c0002t0004g0006 a0001c0002t0004g0035 a0001c0002t0004g0037 others(10): Show |
14 | HG00423.hp1 HG02735.hp1 NA18940.hp2 others(11): Show |
intron_variant | MODIFIER | c.1039+966_1039+971d others(8): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056278 | ||||||
chr7:30056278 | TTCTCTCT others(3): Show |
T | 3 | a0001c0002t0003g0180 a0001c0002t0003g0181 a0001c0002t0003g0182 |
3 | HG02559.hp1 HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1039+962_1039+971d others(12): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056278 | ||||||
chr7:30056305 | TCTCTCTC others(35): Show |
T | 5 | a0001c0002t0003g0012 a0001c0002t0003g0167 a0001c0002t0003g0169 others(2): Show |
6 | HG00741.hp1 HG02165.hp1 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.1039+964_1039+1005 others(45): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056305 | |||||||
chr7:30056307 | TCTCTCTA others(33): Show |
T | 8 | a0001c0002t0003g0165 a0001c0002t0003g0166 a0001c0002t0003g0171 others(5): Show |
8 | HG00558.hp2 HG01192.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.1039+966_1039+1005 others(43): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056307 | |||||||
chr7:30056308 | C | A | 1 | a0001c0002t0004g0049 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1039+966C>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056308 | |||||||
chr7:30056310 | C | A | 6 | a0001c0001t0001g0010 a0001c0002t0004g0006 a0001c0002t0004g0035 others(3): Show |
6 | HG00423.hp1 HG03098.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.1039+968C>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056310 | |||||||
chr7:30056310 | C | CTA | 2 | a0001c0002t0004g0177 a0001c0002t0004g0178 |
2 | HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1039+969_1039+970i others(4): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056310 | ||||||
chr7:30056310 | C | CTATA | 1 | a0001c0001t0013g0004 | 2 | HG00741.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1039+969_1039+970i others(6): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056310 | ||||||
chr7:30056310 | C | CTATATA | 5 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0117 others(2): Show |
6 | HG02071.hp1 HG02572.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1039+969_1039+970i others(8): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056310 | ||||||
chr7:30056310 | C | CTATATAT others(3): Show |
1 | a0001c0001t0001g0091 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1039+969_1039+970i others(12): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056310 | ||||||
chr7:30056310 | CTCTA | C | 3 | a0001c0002t0007g0034 a0001c0002t0007g0055 a0001c0002t0007g0057 |
3 | HG00323.hp1 HG01243.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1039+970_1039+973d others(6): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056310 | ||||||
chr7:30056312 | C | A | 21 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0031 others(18): Show |
25 | HG00423.hp1 HG00741.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.1039+970C>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056312 | |||||||
chr7:30056312 | C | CTA | 2 | a0001c0001t0001g0072 a0003c0004t0001g0098 |
2 | HG00423.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1039+989_1039+990d others(4): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056312 | ||||||
chr7:30056312 | C | CTATA | 6 | a0001c0001t0001g0001 a0001c0001t0001g0040 a0001c0001t0001g0111 others(3): Show |
6 | HG02055.hp1 HG02165.hp2 NA19064.hp1 others(3): Show |
intron_variant | MODIFIER | c.1039+987_1039+990d others(6): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056312 | ||||||
chr7:30056312 | C | CTATATA | 3 | a0001c0001t0001g0112 a0001c0001t0001g0158 a0001c0001t0001g0160 |
3 | HG02622.hp1 NA18964.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1039+985_1039+990d others(8): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056312 | ||||||
chr7:30056312 | C | CTATATAT others(1): Show |
5 | a0001c0001t0001g0079 a0001c0001t0001g0110 a0001c0001t0001g0129 others(2): Show |
5 | HG00735.hp1 HG01255.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1039+983_1039+990d others(10): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056312 | ||||||
chr7:30056312 | C | CTATATAT others(3): Show |
1 | a0001c0001t0001g0045 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1039+981_1039+990d others(12): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056312 | ||||||
chr7:30056312 | C | CTCTA | 3 | a0001c0001t0001g0004 a0001c0001t0001g0101 a0001c0002t0009g0051 |
3 | HG03669.hp1 NA18522.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1039+971_1039+972i others(6): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056312 | ||||||
chr7:30056312 | C | CTCTATA | 2 | a0001c0001t0001g0157 a0001c0001t0011g0115 |
2 | HG01192.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.1039+971_1039+972i others(8): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056312 | ||||||
chr7:30056312 | C | CTCTATAT others(1): Show |
9 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0032 others(6): Show |
9 | HG03239.hp2 HG03453.hp2 HG04204.hp2 others(6): Show |
intron_variant | MODIFIER | c.1039+971_1039+972i others(10): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056312 | ||||||
chr7:30056312 | C | CTCTATAT others(5): Show |
1 | a0001c0001t0001g0145 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1039+971_1039+972i others(14): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056312 | ||||||
chr7:30056312 | C | CTCTATAT others(9): Show |
1 | a0001c0001t0001g0106 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1039+971_1039+972i others(18): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056312 | ||||||
chr7:30056312 | C | CTCTCTA | 6 | a0001c0001t0001g0071 a0001c0001t0001g0090 a0001c0001t0001g0143 others(3): Show |
6 | HG02273.hp1 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1039+971_1039+972i others(8): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056312 | ||||||
chr7:30056312 | C | CTCTCTAT others(1): Show |
14 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0044 others(11): Show |
14 | HG00408.hp1 HG00408.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.1039+971_1039+972i others(10): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056312 | ||||||
chr7:30056312 | C | CTCTCTAT others(9): Show |
1 | a0001c0001t0001g0093 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1039+971_1039+972i others(18): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056312 | ||||||
chr7:30056312 | C | CTCTCTCT others(1): Show |
9 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0113 others(6): Show |
9 | HG00609.hp2 HG01169.hp2 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.1039+971_1039+972i others(10): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056312 | ||||||
chr7:30056312 | C | CTCTCTCT others(3): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0070 a0001c0001t0001g0089 |
3 | HG00558.hp1 HG01257.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1039+971_1039+972i others(12): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056312 | ||||||
chr7:30056312 | C | CTCTCTCT others(5): Show |
1 | a0001c0001t0001g0043 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1039+971_1039+972i others(14): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056312 | ||||||
chr7:30056312 | C | CTCTCTCT others(5): Show |
1 | a0001c0001t0011g0114 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1039+971_1039+972i others(14): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056312 | ||||||
chr7:30056312 | C | CTCTCTCT others(7): Show |
1 | a0001c0001t0001g0122 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1039+971_1039+972i others(16): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056312 | ||||||
chr7:30056312 | C | CTCTCTCT others(5): Show |
3 | a0001c0001t0001g0028 a0001c0001t0001g0080 a0001c0001t0001g0107 |
3 | HG01069.hp1 HG01515.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1039+971_1039+972i others(14): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056312 | ||||||
chr7:30056312 | C | CTCTCTCT others(7): Show |
2 | a0001c0001t0001g0027 a0001c0002t0019g0060 |
2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1039+971_1039+972i others(16): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056312 | ||||||
chr7:30056312 | C | CTCTCTCT others(11): Show |
1 | a0001c0002t0024g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1039+971_1039+972i others(20): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056312 | ||||||
chr7:30056312 | C | CTCTCTCT others(9): Show |
1 | a0001c0001t0001g0026 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1039+971_1039+972i others(18): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056312 | ||||||
chr7:30056312 | C | CTCTCTCT others(9): Show |
1 | a0001c0001t0001g0085 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1039+971_1039+972i others(18): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056312 | ||||||
chr7:30056312 | C | CTCTCTCT others(13): Show |
1 | a0001c0001t0001g0141 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1039+971_1039+972i others(22): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056312 | ||||||
chr7:30056314 | A | C | 68 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0073 others(65): Show |
73 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.1039+972A>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056314 | |||||||
chr7:30056316 | A | C | 44 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0081 others(41): Show |
48 | HG00609.hp1 HG00735.hp2 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.1039+974A>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056316 | |||||||
chr7:30056318 | A | C | 31 | a0001c0001t0001g0075 a0001c0001t0001g0081 a0001c0001t0001g0140 others(28): Show |
35 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.1039+976A>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056318 | |||||||
chr7:30056319 | TATATATA others(34): Show |
T | 2 | a0001c0002t0003g0168 a0001c0002t0003g0170 |
2 | NA18990.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1039+989_1039+1029 others(44): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056319 | ||||||
chr7:30056320 | A | C | 17 | a0001c0002t0002g0005 a0001c0002t0002g0187 a0001c0002t0002g0188 others(14): Show |
19 | HG01069.hp2 HG01070.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.1039+978A>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056320 | |||||||
chr7:30056322 | A | C | 12 | a0001c0002t0002g0005 a0001c0002t0002g0188 a0001c0002t0002g0190 others(9): Show |
14 | HG01069.hp2 HG01070.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1039+980A>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056322 | |||||||
chr7:30056324 | A | C | 9 | a0001c0002t0002g0005 a0001c0002t0002g0188 a0001c0002t0002g0193 others(6): Show |
10 | HG01069.hp2 HG01070.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1039+982A>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056324 | |||||||
chr7:30056325 | TATATATA others(28): Show |
T | 4 | a0001c0002t0002g0191 a0001c0002t0003g0180 a0001c0002t0003g0181 others(1): Show |
4 | HG02559.hp1 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039+991_1039+1025 others(38): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056325 | ||||||
chr7:30056326 | A | C | 5 | a0001c0002t0002g0188 a0001c0002t0002g0193 a0001c0002t0002g0194 others(2): Show |
5 | HG01069.hp2 HG01169.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.1039+984A>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056326 | |||||||
chr7:30056328 | A | C | 4 | a0001c0002t0002g0188 a0001c0002t0002g0193 a0001c0002t0002g0194 others(1): Show |
4 | HG01069.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039+986A>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056328 | |||||||
chr7:30056329 | TATAAATA others(11): Show |
T | 3 | a0001c0002t0002g0017 a0001c0002t0002g0188 a0001c0002t0002g0196 |
3 | HG01169.hp1 HG01891.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1039+991_1039+1008 others(21): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056329 | ||||||
chr7:30056329 | TATAAATA others(24): Show |
T | 2 | a0001c0002t0002g0202 a0001c0002t0002g0204 |
2 | HG01433.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1039+991_1039+1021 others(34): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056329 | ||||||
chr7:30056330 | A | C | 3 | a0001c0002t0002g0193 a0001c0002t0002g0194 a0001c0002t0002g0203 |
3 | HG01069.hp2 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1039+988A>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056330 | |||||||
chr7:30056331 | TAAATAAC others(9): Show |
T | 4 | a0001c0002t0002g0192 a0001c0002t0002g0193 a0001c0002t0002g0194 others(1): Show |
4 | HG01069.hp2 HG02922.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039+991_1039+1006 others(19): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056331 | ||||||
chr7:30056331 | TAAATAAC others(20): Show |
T | 19 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(16): Show |
21 | HG00735.hp2 HG01070.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.1039+991_1039+1017 others(30): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056331 | ||||||
chr7:30056331 | TAAATAAC others(22): Show |
T | 1 | a0001c0002t0002g0189 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1039+991_1039+1019 others(32): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056331 | ||||||
chr7:30056333 | A | T | 6 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(3): Show |
6 | HG02258.hp2 HG03704.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.1039+991A>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056333 | |||||||
chr7:30056335 | TAACATAT others(18): Show |
T | 6 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(3): Show |
6 | HG02258.hp2 HG03704.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.1039+995_1039+1019 others(28): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056335 | ||||||
chr7:30056348 | A | C | 3 | a0001c0002t0002g0193 a0001c0002t0002g0194 a0001c0002t0002g0203 |
3 | HG01069.hp2 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1039+1006A>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056348 | |||||||
chr7:30056350 | A | C | 1 | a0001c0002t0002g0194 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1039+1008A>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056350 | |||||||
chr7:30056355 | TAAC | T | 6 | a0001c0002t0002g0203 a0001c0002t0003g0012 a0001c0002t0003g0167 others(3): Show |
7 | HG00741.hp1 HG02165.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1039+1015_1039+101 others(7): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056355 | ||||||
chr7:30056355 | TAACAC | T | 14 | a0001c0002t0002g0017 a0001c0002t0002g0188 a0001c0002t0002g0192 others(11): Show |
14 | HG00558.hp2 HG01069.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1039+1015_1039+101 others(9): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056355 | ||||||
chr7:30056360 | C | CAT | 7 | a0001c0002t0014g0126 a0001c0002t0014g0127 a0001c0002t0021g0033 others(4): Show |
7 | HG01243.hp1 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1039+1028_1039+102 others(6): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056360 | ||||||
chr7:30056360 | C | T | 25 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(22): Show |
28 | HG00735.hp2 HG00741.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.1039+1018C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056360 | |||||||
chr7:30056386 | A | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(73): Show |
81 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1039+1044A>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056386 | |||||||
chr7:30056606 | G | A | 18 | a0001c0002t0003g0012 a0001c0002t0003g0165 a0001c0002t0003g0166 others(15): Show |
19 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.1039+1264G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056606 | |||||||
chr7:30056724 | C | CA | 8 | a0001c0001t0001g0112 a0001c0002t0007g0034 a0001c0002t0007g0055 others(5): Show |
8 | HG00323.hp1 HG01243.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1039+1400dupA | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056724 | ||||||
chr7:30056737 | AAAAAAGT others(4): Show |
A | 1 | a0001c0002t0009g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1039+1396_1039+140 others(15): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056737 | |||||||
chr7:30056737 | AAAAAAGT others(6): Show |
A | 3 | a0001c0002t0009g0052 a0001c0002t0009g0053 a0001c0002t0026g0050 |
3 | HG02451.hp2 HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1039+1396_1039+140 others(17): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056737 | |||||||
chr7:30056741 | AAGTGTGT others(6): Show |
A | 1 | a0001c0002t0002g0196 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1039+1400_1039+141 others(17): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056741 | |||||||
chr7:30056742 | A | AGT | 10 | a0001c0001t0001g0010 a0001c0001t0001g0068 a0001c0001t0001g0073 others(7): Show |
10 | HG00323.hp2 HG00544.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.1039+1443_1039+144 others(6): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056742 | ||||||
chr7:30056742 | AG | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0161 |
3 | HG02895.hp2 HG02897.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1039+1401delG | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056742 | |||||||
chr7:30056742 | AGT | A | 8 | a0001c0001t0001g0004 a0001c0002t0003g0012 a0001c0002t0003g0169 others(5): Show |
9 | HG02055.hp2 HG02976.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1039+1443_1039+144 others(6): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056742 | ||||||
chr7:30056742 | AGTG | A | 20 | a0001c0001t0001g0032 a0001c0001t0001g0044 a0001c0001t0001g0091 others(17): Show |
20 | HG01074.hp1 HG01433.hp1 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.1039+1401_1039+140 others(7): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056742 | |||||||
chr7:30056742 | AGTGT | A | 29 | a0001c0001t0001g0045 a0001c0001t0001g0077 a0001c0002t0003g0165 others(26): Show |
29 | HG00558.hp2 HG00741.hp1 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.1039+1441_1039+144 others(8): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056742 | ||||||
chr7:30056742 | AGTGTG | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0031 others(51): Show |
58 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.1039+1401_1039+140 others(9): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056742 | |||||||
chr7:30056742 | AGTGTGT | A | 5 | a0001c0002t0004g0006 a0001c0002t0004g0035 a0001c0002t0004g0036 others(2): Show |
6 | HG00423.hp1 HG02976.hp1 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.1039+1439_1039+144 others(10): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056742 | ||||||
chr7:30056742 | AGTGTGTG | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0093 a0001c0001t0001g0145 |
4 | HG01070.hp2 HG01516.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039+1401_1039+140 others(11): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056742 | |||||||
chr7:30056742 | AGTGTGTG others(2): Show |
A | 5 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0147 others(2): Show |
5 | HG01261.hp2 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1039+1401_1039+140 others(13): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056742 | |||||||
chr7:30056742 | AGTGTGTG others(4): Show |
A | 1 | a0001c0001t0001g0028 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1039+1401_1039+141 others(15): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056742 | |||||||
chr7:30056742 | AGTGTGTG others(9): Show |
A | 1 | a0001c0002t0024g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1039+1429_1039+144 others(20): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056742 | ||||||
chr7:30056743 | G | A | 2 | a0001c0001t0001g0131 a0001c0002t0020g0067 |
2 | HG03130.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.1039+1401G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056743 | |||||||
chr7:30056744 | T | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0131 a0001c0001t0001g0161 others(1): Show |
5 | HG02895.hp2 HG02897.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1039+1402T>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056744 | |||||||
chr7:30056745 | G | A | 3 | a0001c0002t0006g0019 a0001c0002t0006g0021 a0001c0002t0018g0061 |
3 | HG02976.hp2 HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1039+1403G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056745 | |||||||
chr7:30056746 | T | A | 23 | a0001c0001t0001g0032 a0001c0001t0001g0044 a0001c0001t0001g0091 others(20): Show |
23 | HG01074.hp1 HG01433.hp1 HG01981.hp1 others(20): Show |
intron_variant | MODIFIER | c.1039+1404T>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056746 | |||||||
chr7:30056747 | G | A | 13 | a0001c0001t0001g0045 a0001c0002t0004g0042 a0001c0002t0004g0049 others(10): Show |
13 | HG01081.hp1 HG01175.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1039+1405G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056747 | |||||||
chr7:30056748 | T | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0031 others(64): Show |
71 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.1039+1406T>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056748 | |||||||
chr7:30056749 | G | A | 7 | a0001c0002t0004g0006 a0001c0002t0004g0035 a0001c0002t0004g0036 others(4): Show |
8 | HG00423.hp1 HG01243.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1039+1407G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056749 | |||||||
chr7:30056750 | T | A | 10 | a0001c0001t0001g0011 a0001c0001t0001g0093 a0001c0001t0001g0145 others(7): Show |
12 | HG00423.hp1 HG01070.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1039+1408T>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056750 | |||||||
chr7:30056752 | T | A | 5 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0147 others(2): Show |
5 | HG01261.hp2 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1039+1410T>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056752 | |||||||
chr7:30056754 | T | A | 1 | a0001c0001t0001g0028 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1039+1412T>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056754 | |||||||
chr7:30056769 | GTGTGTGT others(11): Show |
G | 1 | a0001c0002t0002g0200 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1039+1429_1039+144 others(22): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056769 | ||||||
chr7:30056771 | GTGTGTGT others(9): Show |
G | 1 | a0001c0002t0002g0201 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1039+1431_1039+144 others(20): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056771 | ||||||
chr7:30056773 | GTGTGTGT others(7): Show |
G | 1 | a0001c0002t0002g0195 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1039+1433_1039+144 others(18): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056773 | ||||||
chr7:30056775 | GTGTGTGT others(5): Show |
G | 23 | a0001c0002t0002g0002 a0001c0002t0002g0014 a0001c0002t0002g0015 others(20): Show |
24 | HG01069.hp2 HG01070.hp1 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.1039+1435_1039+144 others(16): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056775 | ||||||
chr7:30056777 | GTGTGTGT others(3): Show |
G | 4 | a0001c0002t0002g0005 a0001c0002t0002g0197 a0001c0002t0002g0198 others(1): Show |
4 | HG00735.hp2 NA18942.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039+1437_1039+144 others(14): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056777 | ||||||
chr7:30056779 | GTGTGTGT others(3): Show |
G | 1 | a0001c0002t0002g0013 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1039+1439_1039+144 others(14): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30056779 | ||||||
chr7:30056785 | G | A | 3 | a0001c0002t0004g0177 a0001c0002t0004g0178 a0001c0002t0004g0179 |
3 | HG02055.hp1 HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1039+1443G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056785 | |||||||
chr7:30056787 | A | G | 19 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0096 others(16): Show |
21 | HG00609.hp1 HG01074.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.1039+1445A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056787 | |||||||
chr7:30056789 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1039+1447A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056789 | |||||||
chr7:30056840 | A | T | 56 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(53): Show |
61 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.1039+1498A>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056840 | |||||||
chr7:30056868 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1039+1526T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056868 | |||||||
chr7:30056927 | T | A | 1 | a0001c0001t0001g0161 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1039+1585T>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30056927 | |||||||
chr7:30057177 | A | G | 4 | a0001c0001t0001g0151 a0001c0001t0010g0102 a0001c0001t0010g0103 others(1): Show |
4 | HG02486.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039+1835A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30057177 | |||||||
chr7:30057232 | G | C | 1 | a0001c0002t0016g0163 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1039+1890G>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30057232 | |||||||
chr7:30057431 | G | A | 23 | a0001c0002t0004g0006 a0001c0002t0004g0035 a0001c0002t0004g0036 others(20): Show |
24 | HG00423.hp1 HG01081.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1039+2089G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30057431 | |||||||
chr7:30057624 | A | G | 18 | a0001c0002t0003g0012 a0001c0002t0003g0165 a0001c0002t0003g0166 others(15): Show |
19 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.1039+2282A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30057624 | |||||||
chr7:30057697 | A | G | 57 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(54): Show |
62 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.1039+2355A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30057697 | |||||||
chr7:30057936 | T | C | 53 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(50): Show |
58 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.1039+2594T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30057936 | |||||||
chr7:30058121 | G | A | 58 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(55): Show |
63 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1040-2763G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30058121 | |||||||
chr7:30058308 | C | T | 4 | a0001c0002t0002g0193 a0001c0002t0002g0194 a0001c0002t0002g0196 others(1): Show |
4 | HG01069.hp2 HG01169.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1040-2576C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30058308 | |||||||
chr7:30058368 | G | A | 2 | a0001c0002t0018g0061 a0001c0002t0019g0060 |
2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1040-2516G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30058368 | |||||||
chr7:30058444 | T | C | 1 | a0001c0001t0031g0135 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1040-2440T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30058444 | |||||||
chr7:30058471 | C | CT | 5 | a0001c0001t0001g0112 a0001c0001t0001g0161 a0001c0003t0008g0023 others(2): Show |
5 | HG01243.hp1 HG02572.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1040-2395dupT | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30058471 | ||||||
chr7:30058471 | CT | C | 20 | a0001c0001t0001g0145 a0001c0001t0001g0155 a0001c0001t0010g0102 others(17): Show |
21 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1040-2395delT | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30058471 | ||||||
chr7:30058471 | CTT | C | 33 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(30): Show |
37 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.1040-2396_1040-239 others(6): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30058471 | ||||||
chr7:30058472 | T | A | 1 | a0001c0002t0003g0165 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1040-2412T>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30058472 | |||||||
chr7:30058473 | T | A | 17 | a0001c0002t0003g0012 a0001c0002t0003g0166 a0001c0002t0003g0167 others(14): Show |
18 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.1040-2411T>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30058473 | |||||||
chr7:30058474 | T | A | 32 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(29): Show |
36 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1040-2410T>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30058474 | |||||||
chr7:30058475 | T | A | 2 | a0001c0002t0002g0199 a0001c0002t0002g0205 |
2 | HG01516.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1040-2409T>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30058475 | |||||||
chr7:30058556 | C | A | 18 | a0001c0002t0003g0012 a0001c0002t0003g0165 a0001c0002t0003g0166 others(15): Show |
19 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.1040-2328C>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30058556 | |||||||
chr7:30058574 | A | G | 1 | a0001c0002t0022g0048 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1040-2310A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30058574 | |||||||
chr7:30058580 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1040-2304C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30058580 | |||||||
chr7:30058631 | A | G | 1 | a0001c0002t0002g0196 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1040-2253A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30058631 | |||||||
chr7:30058634 | A | G | 5 | a0001c0002t0006g0018 a0001c0002t0006g0019 a0001c0002t0006g0020 others(2): Show |
5 | HG01081.hp1 HG03139.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1040-2250A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30058634 | |||||||
chr7:30058768 | T | C | 53 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(50): Show |
58 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.1040-2116T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30058768 | |||||||
chr7:30058902 | G | A | 18 | a0001c0002t0003g0012 a0001c0002t0003g0165 a0001c0002t0003g0166 others(15): Show |
19 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.1040-1982G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30058902 | |||||||
chr7:30059138 | G | A | 57 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(54): Show |
62 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.1040-1746G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30059138 | |||||||
chr7:30059178 | T | C | 38 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(35): Show |
42 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1040-1706T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30059178 | |||||||
chr7:30059276 | T | G | 58 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(55): Show |
63 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1040-1608T>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30059276 | |||||||
chr7:30059382 | C | T | 53 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(50): Show |
58 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.1040-1502C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30059382 | |||||||
chr7:30059578 | AT | A | 90 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(87): Show |
96 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.1040-1296delT | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30059578 | ||||||
chr7:30059657 | C | A | 1 | a0001c0002t0022g0048 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1040-1227C>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30059657 | |||||||
chr7:30059666 | AT | A | 10 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0084 others(7): Show |
10 | HG00323.hp1 HG01169.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.1040-1202delT | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30059666 | ||||||
chr7:30059809 | T | C | 1 | a0001c0003t0008g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1040-1075T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30059809 | |||||||
chr7:30059840 | T | TAATG | 58 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(55): Show |
63 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1040-1044_1040-104 others(8): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30059840 | |||||||
chr7:30059906 | G | A | 58 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(55): Show |
63 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1040-978G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30059906 | |||||||
chr7:30060024 | T | C | 63 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(60): Show |
68 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.1040-860T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30060024 | |||||||
chr7:30060068 | C | T | 58 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(55): Show |
63 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1040-816C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30060068 | |||||||
chr7:30060130 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1040-754C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30060130 | |||||||
chr7:30060269 | C | G | 1 | a0001c0002t0002g0195 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1040-615C>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30060269 | |||||||
chr7:30060321 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1040-563A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30060321 | |||||||
chr7:30060442 | AAAAC | A | 58 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(55): Show |
63 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1040-433_1040-430d others(6): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 30060442 | ||||||
chr7:30060559 | G | A | 1 | a0001c0002t0002g0207 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1040-325G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30060559 | |||||||
chr7:30060567 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1040-317T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 9/13 | chr7 | 30060567 | |||||||
chr7:30061003 | T | G | 3 | a0001c0003t0008g0023 a0001c0003t0008g0024 a0001c0003t0008g0025 |
3 | HG01243.hp1 HG02572.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1098+61T>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 10/13 | chr7 | 30061003 | |||||||
chr7:30061051 | CT | C | 58 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(55): Show |
63 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1098+113delT | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr7 | 30061051 | ||||||
chr7:30061484 | T | G | 4 | a0001c0002t0005g0183 a0001c0002t0005g0184 a0001c0002t0005g0185 others(1): Show |
4 | HG02055.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099-413T>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 10/13 | chr7 | 30061484 | |||||||
chr7:30061533 | G | A | 57 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(54): Show |
62 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.1099-364G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 10/13 | chr7 | 30061533 | |||||||
chr7:30061589 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1099-308A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 10/13 | chr7 | 30061589 | |||||||
chr7:30062067 | C | G | 57 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(54): Show |
62 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.1229+40C>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 11/13 | chr7 | 30062067 | |||||||
chr7:30062100 | C | T | 57 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(54): Show |
62 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.1229+73C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 11/13 | chr7 | 30062100 | |||||||
chr7:30062180 | A | AT | 19 | a0001c0002t0003g0012 a0001c0002t0003g0165 a0001c0002t0003g0166 others(16): Show |
20 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.1229+163dupT | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 30062180 | ||||||
chr7:30062464 | G | T | 2 | a0001c0002t0021g0033 a0001c0002t0022g0048 |
2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1230-208G>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 11/13 | chr7 | 30062464 | |||||||
chr7:30063112 | G | A | 1 | a0001c0002t0021g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1300+370G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30063112 | |||||||
chr7:30063116 | T | C | 3 | a0001c0003t0008g0023 a0001c0003t0008g0024 a0001c0003t0008g0025 |
3 | HG01243.hp1 HG02572.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1300+374T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30063116 | |||||||
chr7:30063218 | C | A | 19 | a0001c0002t0003g0012 a0001c0002t0003g0165 a0001c0002t0003g0166 others(16): Show |
20 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.1300+476C>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30063218 | |||||||
chr7:30063276 | C | G | 1 | a0001c0001t0001g0074 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1300+534C>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30063276 | |||||||
chr7:30063375 | C | G | 1 | a0001c0002t0002g0017 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1300+633C>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30063375 | |||||||
chr7:30063485 | G | A | 1 | a0001c0002t0022g0048 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1300+743G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30063485 | |||||||
chr7:30063493 | A | T | 4 | a0001c0002t0002g0193 a0001c0002t0002g0194 a0001c0002t0002g0196 others(1): Show |
4 | HG01069.hp2 HG01169.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300+751A>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30063493 | |||||||
chr7:30063579 | A | G | 1 | a0001c0002t0024g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1300+837A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30063579 | |||||||
chr7:30063950 | G | GGTCTCAG others(5): Show |
38 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(35): Show |
42 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1300+1209_1300+122 others(16): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 30063950 | ||||||
chr7:30064023 | C | T | 1 | a0001c0002t0003g0171 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1300+1281C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30064023 | |||||||
chr7:30064147 | A | T | 1 | a0001c0002t0020g0067 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1300+1405A>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30064147 | |||||||
chr7:30064369 | C | T | 58 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(55): Show |
63 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1300+1627C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30064369 | |||||||
chr7:30064495 | A | G | 58 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(55): Show |
63 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1300+1753A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30064495 | |||||||
chr7:30064504 | C | T | 1 | a0001c0002t0004g0038 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1300+1762C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30064504 | |||||||
chr7:30064549 | AAAAC | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0082 a0001c0001t0001g0084 |
4 | HG02258.hp1 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300+1823_1300+182 others(8): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 30064549 | ||||||
chr7:30064588 | A | C | 58 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(55): Show |
63 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1300+1846A>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30064588 | |||||||
chr7:30064821 | G | C | 1 | a0001c0001t0012g0136 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1300+2079G>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30064821 | |||||||
chr7:30064873 | T | C | 1 | a0003c0004t0001g0098 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1300+2131T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30064873 | |||||||
chr7:30064887 | A | G | 58 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(55): Show |
63 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1300+2145A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30064887 | |||||||
chr7:30065112 | G | C | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0106 others(1): Show |
4 | NA18950.hp1 NA18968.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300+2370G>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30065112 | |||||||
chr7:30065174 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1300+2432A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30065174 | |||||||
chr7:30065185 | C | T | 19 | a0001c0002t0003g0012 a0001c0002t0003g0165 a0001c0002t0003g0166 others(16): Show |
20 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.1300+2443C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30065185 | |||||||
chr7:30065214 | C | T | 1 | a0001c0002t0025g0156 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1300+2472C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30065214 | |||||||
chr7:30065239 | A | G | 38 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(35): Show |
42 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1300+2497A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30065239 | |||||||
chr7:30065407 | C | T | 1 | a0001c0001t0001g0007 | 2 | NA18947.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1300+2665C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30065407 | |||||||
chr7:30065427 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1300+2685C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30065427 | |||||||
chr7:30065481 | T | G | 1 | a0001c0002t0021g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1300+2739T>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30065481 | |||||||
chr7:30065626 | A | G | 5 | a0001c0002t0009g0051 a0001c0002t0009g0052 a0001c0002t0009g0053 others(2): Show |
5 | HG02451.hp2 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1300+2884A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30065626 | |||||||
chr7:30065713 | CACTT | C | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0106 others(1): Show |
4 | NA18950.hp1 NA18968.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300+2974_1300+297 others(8): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 30065713 | ||||||
chr7:30065802 | A | C | 1 | a0001c0002t0002g0207 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1300+3060A>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30065802 | |||||||
chr7:30065952 | A | ACT | 63 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(60): Show |
68 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.1300+3211_1300+321 others(6): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 30065952 | ||||||
chr7:30066125 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1300+3383A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30066125 | |||||||
chr7:30066264 | C | G | 6 | a0001c0002t0002g0002 a0001c0002t0002g0014 a0001c0002t0002g0015 others(3): Show |
7 | NA18947.hp2 NA18960.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.1300+3522C>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30066264 | |||||||
chr7:30066344 | A | G | 38 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(35): Show |
42 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1300+3602A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30066344 | |||||||
chr7:30066688 | T | C | 38 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(35): Show |
42 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1300+3946T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30066688 | |||||||
chr7:30066720 | T | C | 4 | a0001c0002t0005g0183 a0001c0002t0005g0184 a0001c0002t0005g0185 others(1): Show |
4 | HG02055.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300+3978T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30066720 | |||||||
chr7:30066854 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0082 a0001c0001t0001g0084 |
4 | HG02258.hp1 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300+4112G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30066854 | |||||||
chr7:30066948 | A | G | 1 | a0001c0002t0002g0202 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1300+4206A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30066948 | |||||||
chr7:30067036 | T | C | 16 | a0001c0002t0003g0012 a0001c0002t0003g0165 a0001c0002t0003g0166 others(13): Show |
17 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.1300+4294T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30067036 | |||||||
chr7:30067179 | G | A | 4 | a0001c0002t0007g0034 a0001c0002t0007g0055 a0001c0002t0007g0057 others(1): Show |
4 | HG00323.hp1 HG01243.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1300+4437G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30067179 | |||||||
chr7:30067622 | G | A | 1 | a0001c0002t0022g0048 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1300+4880G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30067622 | |||||||
chr7:30067648 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0130 |
2 | HG02129.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.1300+4906T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30067648 | |||||||
chr7:30067660 | ATATATT | A | 19 | a0001c0002t0003g0012 a0001c0002t0003g0165 a0001c0002t0003g0166 others(16): Show |
20 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.1300+4922_1300+492 others(10): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 30067660 | ||||||
chr7:30067692 | A | T | 1 | a0001c0002t0021g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1300+4950A>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30067692 | |||||||
chr7:30067810 | A | C | 61 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(58): Show |
66 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.1300+5068A>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30067810 | |||||||
chr7:30067858 | C | A | 38 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(35): Show |
42 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1300+5116C>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30067858 | |||||||
chr7:30068198 | T | C | 38 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(35): Show |
42 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1300+5456T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30068198 | |||||||
chr7:30068211 | C | G | 4 | a0001c0001t0001g0151 a0001c0001t0010g0102 a0001c0001t0010g0103 others(1): Show |
4 | HG02486.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300+5469C>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30068211 | |||||||
chr7:30068254 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1300+5512T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30068254 | |||||||
chr7:30068445 | A | G | 1 | a0001c0003t0008g0024 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1301-5626A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30068445 | |||||||
chr7:30068507 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1301-5564G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30068507 | |||||||
chr7:30068810 | G | A | 63 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(60): Show |
68 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.1301-5261G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30068810 | |||||||
chr7:30069008 | T | G | 38 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(35): Show |
42 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1301-5063T>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30069008 | |||||||
chr7:30069009 | T | TGA | 38 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(35): Show |
42 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1301-5047_1301-504 others(6): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 30069009 | ||||||
chr7:30069086 | C | G | 58 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(55): Show |
63 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1301-4985C>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30069086 | |||||||
chr7:30069393 | C | T | 57 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(54): Show |
62 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.1301-4678C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30069393 | |||||||
chr7:30069737 | G | A | 4 | a0001c0002t0007g0034 a0001c0002t0007g0055 a0001c0002t0007g0057 others(1): Show |
4 | HG00323.hp1 HG01243.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1301-4334G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30069737 | |||||||
chr7:30070102 | G | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(178): Show |
193 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.1301-3969G>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30070102 | |||||||
chr7:30070115 | A | C | 3 | a0001c0003t0008g0023 a0001c0003t0008g0024 a0001c0003t0008g0025 |
3 | HG01243.hp1 HG02572.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1301-3956A>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30070115 | |||||||
chr7:30070131 | G | GT | 7 | a0001c0001t0001g0113 a0001c0002t0004g0063 a0001c0002t0006g0018 others(4): Show |
7 | HG01081.hp1 HG03139.hp1 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.1301-3927dupT | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 30070131 | ||||||
chr7:30070131 | GT | G | 61 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(58): Show |
66 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.1301-3927delT | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 30070131 | ||||||
chr7:30070144 | T | A | 1 | a0001c0001t0001g0111 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1301-3927T>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30070144 | |||||||
chr7:30070547 | C | CT | 64 | a0001c0001t0001g0077 a0001c0001t0001g0122 a0001c0001t0001g0125 others(61): Show |
69 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.1301-3508dupT | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 30070547 | ||||||
chr7:30070746 | G | A | 58 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(55): Show |
63 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1301-3325G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30070746 | |||||||
chr7:30070746 | G | T | 1 | a0001c0001t0001g0087 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1301-3325G>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30070746 | |||||||
chr7:30070771 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1301-3300C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30070771 | |||||||
chr7:30070868 | T | G | 58 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(55): Show |
63 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1301-3203T>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30070868 | |||||||
chr7:30070882 | G | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0134 |
2 | HG00408.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1301-3189G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30070882 | |||||||
chr7:30070986 | A | G | 1 | a0001c0001t0001g0046 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1301-3085A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30070986 | |||||||
chr7:30071043 | A | G | 58 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(55): Show |
63 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1301-3028A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30071043 | |||||||
chr7:30071048 | C | G | 58 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(55): Show |
63 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1301-3023C>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30071048 | |||||||
chr7:30071051 | G | A | 200 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(197): Show |
212 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.1301-3020G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30071051 | |||||||
chr7:30071691 | A | C | 6 | a0001c0002t0009g0051 a0001c0002t0009g0052 a0001c0002t0009g0053 others(3): Show |
6 | HG02280.hp2 HG02451.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1301-2380A>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30071691 | |||||||
chr7:30071946 | G | A | 19 | a0001c0002t0003g0012 a0001c0002t0003g0165 a0001c0002t0003g0166 others(16): Show |
20 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.1301-2125G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30071946 | |||||||
chr7:30072124 | C | G | 1 | a0001c0002t0002g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1301-1947C>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30072124 | |||||||
chr7:30073284 | A | T | 58 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(55): Show |
63 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1301-787A>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30073284 | |||||||
chr7:30073385 | A | G | 1 | a0001c0002t0024g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1301-686A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30073385 | |||||||
chr7:30073532 | C | G | 1 | a0001c0001t0031g0135 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1301-539C>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30073532 | |||||||
chr7:30073563 | T | TA | 16 | a0001c0001t0001g0011 a0001c0001t0001g0045 a0001c0001t0001g0072 others(13): Show |
19 | HG00423.hp2 HG00544.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.1301-482dupA | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 30073563 | ||||||
chr7:30073563 | T | TAAA | 10 | a0001c0002t0004g0006 a0001c0002t0004g0035 a0001c0002t0004g0036 others(7): Show |
11 | HG00423.hp1 NA18940.hp2 NA18941.hp2 others(8): Show |
intron_variant | MODIFIER | c.1301-484_1301-482d others(5): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 30073563 | ||||||
chr7:30073563 | T | TAAAAAAA others(3): Show |
1 | a0001c0003t0008g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1301-491_1301-482d others(12): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 30073563 | ||||||
chr7:30073563 | T | TAAAAAAA others(4): Show |
1 | a0001c0003t0008g0024 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1301-492_1301-482d others(13): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 30073563 | ||||||
chr7:30073563 | T | TAAAAAAA others(5): Show |
1 | a0001c0002t0026g0050 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1301-493_1301-482d others(14): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 30073563 | ||||||
chr7:30073563 | T | TAAAAAAA others(6): Show |
3 | a0001c0002t0009g0051 a0001c0002t0009g0052 a0001c0002t0009g0053 |
3 | HG02647.hp2 HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1301-494_1301-482d others(15): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 30073563 | ||||||
chr7:30073563 | T | TAAAAAAA others(14): Show |
2 | a0001c0002t0006g0020 a0001c0002t0006g0021 |
2 | HG01081.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1301-502_1301-482d others(23): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 30073563 | ||||||
chr7:30073563 | T | TAAAAAAA others(18): Show |
1 | a0001c0002t0006g0019 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1301-506_1301-482d others(27): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 30073563 | ||||||
chr7:30073563 | T | TAAAAAAA others(19): Show |
1 | a0001c0002t0006g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1301-507_1301-482d others(28): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 30073563 | ||||||
chr7:30073563 | T | TAAAAAAA others(27): Show |
1 | a0001c0002t0006g0018 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1301-482_1301-481i others(36): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 30073563 | ||||||
chr7:30073563 | TA | T | 22 | a0001c0001t0001g0043 a0001c0001t0001g0082 a0001c0001t0001g0099 others(19): Show |
22 | HG01069.hp1 HG01069.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.1301-482delA | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 30073563 | ||||||
chr7:30073563 | TAA | T | 20 | a0001c0002t0003g0012 a0001c0002t0003g0165 a0001c0002t0003g0166 others(17): Show |
21 | HG00741.hp1 HG01192.hp1 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.1301-483_1301-482d others(4): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 30073563 | ||||||
chr7:30073739 | A | G | 19 | a0001c0002t0003g0012 a0001c0002t0003g0165 a0001c0002t0003g0166 others(16): Show |
20 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.1301-332A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30073739 | |||||||
chr7:30073929 | G | A | 3 | a0001c0003t0008g0023 a0001c0003t0008g0024 a0001c0003t0008g0025 |
3 | HG01243.hp1 HG02572.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1301-142G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30073929 | |||||||
chr7:30073982 | T | A | 2 | a0001c0002t0021g0033 a0001c0002t0022g0048 |
2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1301-89T>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30073982 | |||||||
chr7:30073988 | T | TA | 8 | a0001c0002t0003g0012 a0001c0002t0003g0169 a0001c0002t0003g0172 others(5): Show |
9 | HG02165.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1301-70dupA | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 30073988 | ||||||
chr7:30073988 | T | TAA | 11 | a0001c0002t0003g0165 a0001c0002t0003g0166 a0001c0002t0003g0167 others(8): Show |
11 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1301-71_1301-70dup others(2): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 30073988 | ||||||
chr7:30074001 | A | AG | 37 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(34): Show |
41 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.1301-69dupG | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 30074001 | ||||||
chr7:30074001 | A | G | 1 | a0001c0002t0002g0205 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1301-70A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 12/13 | chr7 | 30074001 | |||||||
chr7:30074182 | T | G | 1 | a0001c0002t0014g0126 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1362+50T>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30074182 | |||||||
chr7:30074246 | T | TTG | 128 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(125): Show |
136 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1362+140_1362+141d others(4): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 30074246 | ||||||
chr7:30074246 | T | TTGTG | 10 | a0001c0001t0001g0027 a0001c0001t0001g0039 a0001c0001t0001g0082 others(7): Show |
10 | HG00408.hp2 HG01081.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1362+138_1362+141d others(6): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 30074246 | ||||||
chr7:30074246 | T | TTGTGTG | 3 | a0001c0002t0002g0214 a0001c0002t0014g0126 a0001c0002t0014g0127 |
3 | HG01175.hp1 HG03098.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1362+136_1362+141d others(8): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 30074246 | ||||||
chr7:30074246 | T | TTGTGTGT others(1): Show |
7 | a0001c0002t0002g0188 a0001c0002t0002g0193 a0001c0002t0002g0196 others(4): Show |
7 | HG01169.hp1 HG01433.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1362+134_1362+141d others(10): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 30074246 | ||||||
chr7:30074246 | T | TTGTGTGT others(3): Show |
25 | a0001c0002t0002g0002 a0001c0002t0002g0013 a0001c0002t0002g0014 others(22): Show |
27 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.1362+132_1362+141d others(12): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 30074246 | ||||||
chr7:30074246 | T | TTGTGTGT others(5): Show |
7 | a0001c0002t0002g0005 a0001c0002t0002g0195 a0001c0002t0002g0198 others(4): Show |
9 | HG01243.hp1 HG02572.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1362+130_1362+141d others(14): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 30074246 | ||||||
chr7:30074246 | T | TTGTGTGT others(7): Show |
1 | a0001c0002t0002g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1362+128_1362+141d others(16): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 30074246 | ||||||
chr7:30074246 | T | TTGTGTGT others(9): Show |
1 | a0001c0002t0021g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1362+126_1362+141d others(18): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 30074246 | ||||||
chr7:30074246 | T | TTGTGTGT others(11): Show |
1 | a0001c0002t0002g0199 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1362+124_1362+141d others(20): Show |
PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 30074246 | ||||||
chr7:30074327 | TA | T | 58 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(55): Show |
63 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1362+196delA | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30074327 | |||||||
chr7:30074738 | C | T | 1 | a0001c0002t0024g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1362+606C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30074738 | |||||||
chr7:30074881 | C | A | 58 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(55): Show |
63 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1362+749C>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30074881 | |||||||
chr7:30074891 | A | T | 1 | a0001c0002t0022g0048 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1362+759A>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30074891 | |||||||
chr7:30075001 | T | C | 39 | a0001c0001t0001g0079 a0001c0002t0002g0002 a0001c0002t0002g0005 others(36): Show |
43 | HG00735.hp1 HG00735.hp2 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.1362+869T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30075001 | |||||||
chr7:30075174 | G | C | 63 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(60): Show |
68 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.1362+1042G>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30075174 | |||||||
chr7:30075530 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1362+1398A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30075530 | |||||||
chr7:30075707 | G | A | 20 | a0001c0002t0003g0012 a0001c0002t0003g0165 a0001c0002t0003g0166 others(17): Show |
21 | HG00558.hp2 HG00741.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1362+1575G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30075707 | |||||||
chr7:30075949 | A | G | 57 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(54): Show |
62 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.1362+1817A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30075949 | |||||||
chr7:30076265 | A | G | 58 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(55): Show |
63 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1362+2133A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30076265 | |||||||
chr7:30076275 | A | G | 1 | a0001c0002t0003g0180 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1362+2143A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30076275 | |||||||
chr7:30076291 | A | G | 2 | a0001c0002t0021g0033 a0001c0002t0022g0048 |
2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1362+2159A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30076291 | |||||||
chr7:30076384 | C | T | 58 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(55): Show |
63 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1363-2206C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30076384 | |||||||
chr7:30076471 | A | T | 3 | a0001c0002t0004g0177 a0001c0002t0004g0178 a0001c0002t0004g0179 |
3 | HG02055.hp1 HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1363-2119A>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30076471 | |||||||
chr7:30076753 | T | A | 1 | a0001c0002t0002g0198 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1363-1837T>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30076753 | |||||||
chr7:30076943 | A | G | 3 | a0001c0002t0004g0177 a0001c0002t0004g0178 a0001c0002t0004g0179 |
3 | HG02055.hp1 HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1363-1647A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30076943 | |||||||
chr7:30076948 | A | G | 2 | a0001c0001t0001g0109 a0001c0001t0001g0134 |
2 | HG00408.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1363-1642A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30076948 | |||||||
chr7:30077234 | A | G | 97 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(94): Show |
103 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.1363-1356A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30077234 | |||||||
chr7:30077255 | C | T | 1 | a0001c0002t0002g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1363-1335C>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30077255 | |||||||
chr7:30077525 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1363-1065A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30077525 | |||||||
chr7:30077639 | A | T | 1 | a0001c0002t0024g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1363-951A>T | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30077639 | |||||||
chr7:30077801 | C | A | 63 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(60): Show |
68 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.1363-789C>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30077801 | |||||||
chr7:30077886 | C | G | 58 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0013 others(55): Show |
63 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1363-704C>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30077886 | |||||||
chr7:30077973 | G | A | 2 | a0001c0002t0021g0033 a0001c0002t0022g0048 |
2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1363-617G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30077973 | |||||||
chr7:30078067 | T | C | 98 | a0001c0002t0001g0058 a0001c0002t0002g0002 a0001c0002t0002g0005 others(95): Show |
104 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.1363-523T>C | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30078067 | |||||||
chr7:30078095 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1363-495A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30078095 | |||||||
chr7:30078179 | A | G | 1 | a0001c0002t0002g0205 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1363-411A>G | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30078179 | |||||||
chr7:30078289 | G | A | 1 | a0001c0002t0025g0156 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1363-301G>A | PLEKHA8 | ENSG00000106086.21 | transcript | ENST00000449726.6 | protein_coding | 13/13 | chr7 | 30078289 |