Item | Value |
---|---|
geneid | 10555 |
ensemblid | ENSG00000169692.14 |
hgncid | 325 |
symbol | AGPAT2 |
name | 1-acylglycerol-3-phosphate O-acyltransferase 2 |
refseq_nuc | NM_006412.4 |
refseq_prot | NP_006403.2 |
ensembl_nuc | ENST00000371696.7 |
ensembl_prot | ENSP00000360761.2 |
mane_status | MANE Select |
chr | chr9 |
start | 136673143 |
end | 136687457 |
strand | - |
ver | v1.2 |
region | chr9:136673143-136687457 |
region5000 | chr9:136668143-136692457 |
regionname0 | AGPAT2_chr9_136673143_136687457 |
regionname5000 | AGPAT2_chr9_136668143_136692457 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 278 | 348 | 90 | 62 | 147 | 11 | 36 | 104 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | MELWP others(273): Show |
chr9 | 136668143 | 136692457 |
a0002 | 0/0 | 279 | 18 | 0 | 10 | 5 | 1 | 2 | 4 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | MELWP others(274): Show |
chr9 | 136668143 | 136692457 |
a0003 | 0/0 | 278 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | MELWP others(273): Show |
chr9 | 136668143 | 136692457 |
a0004 | 0/0 | 278 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | MELWP others(273): Show |
chr9 | 136668143 | 136692457 |
a0005 | 0/0 | 278 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | MELWP others(273): Show |
chr9 | 136668143 | 136692457 |
a0006 | 0/0 | 278 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | MELWP others(273): Show |
chr9 | 136668143 | 136692457 |
a0007 | 0/0 | 278 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | MELWP others(273): Show |
chr9 | 136668143 | 136692457 |
a0008 | 0/0 | 278 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | MELWP others(273): Show |
chr9 | 136668143 | 136692457 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 834 | 328 | 86 | 59 | 135 | 11 | 35 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | ATGGA others(829): Show |
chr9 | 136668143 | 136692457 | ||
a0001c0003 | 0/0 | 834 | 9 | 0 | 0 | 9 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | ATGGA others(829): Show |
chr9 | 136668143 | 136692457 | ||
a0001c0004 | 0/0 | 834 | 6 | 3 | 3 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | ATGGA others(829): Show |
chr9 | 136668143 | 136692457 | ||
a0001c0008 | 0/0 | 834 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | ATGGA others(829): Show |
chr9 | 136668143 | 136692457 | ||
a0001c0012 | 0/0 | 834 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | ATGGA others(829): Show |
chr9 | 136668143 | 136692457 | ||
a0001c0013 | 0/0 | 834 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | ATGGA others(829): Show |
chr9 | 136668143 | 136692457 | ||
a0001c0014 | 0/0 | 834 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | ATGGA others(829): Show |
chr9 | 136668143 | 136692457 | ||
a0001c0016 | 0/0 | 834 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | ATGGA others(829): Show |
chr9 | 136668143 | 136692457 | ||
a0002c0002 | 0/0 | 837 | 17 | 0 | 9 | 5 | 1 | 2 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | ATGGA others(832): Show |
chr9 | 136668143 | 136692457 | ||
a0002c0007 | 0/0 | 837 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | ATGGA others(832): Show |
chr9 | 136668143 | 136692457 | ||
a0003c0005 | 0/0 | 834 | 2 | 1 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | ATGGA others(829): Show |
chr9 | 136668143 | 136692457 | ||
a0004c0006 | 0/0 | 834 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | ATGGA others(829): Show |
chr9 | 136668143 | 136692457 | ||
a0005c0010 | 0/0 | 834 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | ATGGA others(829): Show |
chr9 | 136668143 | 136692457 | ||
a0006c0011 | 0/0 | 834 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | ATGGA others(829): Show |
chr9 | 136668143 | 136692457 | ||
a0007c0009 | 0/0 | 834 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | ATGGA others(829): Show |
chr9 | 136668143 | 136692457 | ||
a0008c0015 | 0/0 | 834 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | ATGGA others(829): Show |
chr9 | 136668143 | 136692457 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1546 | 135 | 21 | 20 | 77 | 3 | 14 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
a0001c0001t0002 | 0/1 | 1546 | 122 | 33 | 29 | 33 | 6 | 20 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
a0001c0001t0003 | 1/0 | 1546 | 32 | 24 | 3 | 4 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
a0001c0001t0004 | 0/0 | 1546 | 9 | 0 | 0 | 9 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
a0001c0001t0005 | 0/0 | 1552 | 5 | 1 | 2 | 0 | 2 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1547): Show |
chr9 | 136668143 | 136692457 |
a0001c0001t0008 | 0/0 | 1546 | 6 | 0 | 0 | 6 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
a0001c0001t0010 | 0/0 | 1546 | 5 | 5 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
a0001c0001t0012 | 0/0 | 1546 | 3 | 0 | 3 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
a0001c0001t0013 | 0/0 | 1546 | 2 | 0 | 1 | 0 | 0 | 1 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
a0001c0001t0014 | 0/0 | 1546 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
a0001c0001t0016 | 0/0 | 1546 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
a0001c0001t0017 | 0/0 | 1546 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
a0001c0001t0018 | 0/0 | 1546 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
a0001c0001t0019 | 0/0 | 1552 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1547): Show |
chr9 | 136668143 | 136692457 |
a0001c0001t0020 | 0/0 | 1546 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
a0001c0001t0021 | 0/0 | 1546 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
a0001c0001t0022 | 0/0 | 1546 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
a0001c0003t0001 | 0/0 | 1546 | 9 | 0 | 0 | 9 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
a0001c0004t0003 | 0/0 | 1546 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
a0001c0004t0007 | 0/0 | 1546 | 5 | 2 | 3 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
a0001c0008t0002 | 0/0 | 1546 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
a0001c0012t0001 | 0/0 | 1546 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
a0001c0013t0002 | 0/0 | 1546 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
a0001c0014t0001 | 0/0 | 1546 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
a0001c0016t0004 | 0/0 | 1546 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
a0002c0002t0005 | 0/0 | 1555 | 3 | 0 | 1 | 0 | 0 | 2 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1550): Show |
chr9 | 136668143 | 136692457 |
a0002c0002t0006 | 0/0 | 1555 | 6 | 0 | 6 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1550): Show |
chr9 | 136668143 | 136692457 |
a0002c0002t0009 | 0/0 | 1549 | 5 | 0 | 2 | 3 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1544): Show |
chr9 | 136668143 | 136692457 |
a0002c0002t0011 | 0/0 | 1549 | 3 | 0 | 0 | 2 | 1 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1544): Show |
chr9 | 136668143 | 136692457 |
a0002c0007t0006 | 0/0 | 1555 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1550): Show |
chr9 | 136668143 | 136692457 |
a0003c0005t0015 | 0/0 | 1546 | 2 | 1 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
a0004c0006t0003 | 0/0 | 1546 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
a0005c0010t0001 | 0/0 | 1546 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
a0006c0011t0003 | 0/0 | 1546 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
a0007c0009t0001 | 0/0 | 1546 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
a0008c0015t0007 | 0/0 | 1546 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | AGCCC others(1541): Show |
chr9 | 136668143 | 136692457 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 18 | 0 | 3 | 13 | 0 | 2 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0003 | 0/0 | 11 | 0 | 6 | 3 | 2 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0007 | 0/0 | 7 | 0 | 1 | 4 | 0 | 2 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0009 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0010 | 0/0 | 5 | 0 | 1 | 1 | 0 | 3 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0011 | 0/0 | 5 | 2 | 3 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0021 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0002 | 0/0 | 13 | 2 | 5 | 0 | 0 | 6 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0004 | 0/0 | 10 | 0 | 4 | 5 | 0 | 1 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0005 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0012 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0013 | 0/0 | 4 | 2 | 0 | 0 | 0 | 2 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0031 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0168 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0003g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0003g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0003g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0003g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0003g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0003g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0003g0199 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0004g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0004g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0005g0018 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0005g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0008g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0008g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0008g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0008g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0010g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0010g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0010g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0012g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0012g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0012g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0013g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0013g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0014g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0016g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0017g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0018g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0019g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0020g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0021g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0001t0022g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0003t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0003t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0004t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0004t0007g0055 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0004t0007g0056 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0004t0007g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0008t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0012t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0013t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0014t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0001c0016t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0002c0002t0005g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0002c0002t0005g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0002c0002t0006g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0002c0002t0006g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0002c0002t0006g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0002c0002t0006g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0002c0002t0006g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0002c0002t0009g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0002c0002t0009g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0002c0002t0009g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0002c0002t0009g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0002c0002t0011g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0002c0002t0011g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0002c0002t0011g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0002c0007t0006g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0003c0005t0015g0053 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0004c0006t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0004c0006t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0005c0010t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0006c0011t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0007c0009t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
a0008c0015t0007g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00323 | hp1 | a0001 | c0001 | t0002 | g0126 | EUR | FIN | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0039 | EUR | FIN | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00408 | hp2 | a0001 | c0001 | t0022 | g0140 | EAS | CHS | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00558 | hp1 | a0001 | c0001 | t0004 | g0132 | EAS | CHS | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | CHS | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00609 | hp1 | a0002 | c0002 | t0011 | g0064 | EAS | CHS | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | CHS | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | CHS | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | CHS | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00735 | hp1 | a0001 | c0001 | t0012 | g0074 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG00738 | hp2 | a0001 | c0001 | t0005 | g0189 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01069 | hp2 | a0002 | c0002 | t0006 | g0065 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01074 | hp1 | a0001 | c0004 | t0007 | g0055 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01081 | hp2 | a0002 | c0002 | t0009 | g0026 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01106 | hp1 | a0001 | c0001 | t0005 | g0018 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01109 | hp2 | a0003 | c0005 | t0015 | g0053 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01192 | hp2 | a0002 | c0002 | t0006 | g0062 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01243 | hp1 | a0002 | c0007 | t0006 | g0066 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01243 | hp2 | a0005 | c0010 | t0001 | g0146 | AMR | PUR | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | CLM | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01255 | hp2 | a0001 | c0001 | t0013 | g0129 | AMR | CLM | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01256 | hp1 | a0001 | c0004 | t0007 | g0056 | AMR | CLM | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01256 | hp2 | a0001 | c0001 | t0012 | g0097 | AMR | CLM | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01258 | hp2 | a0001 | c0001 | t0012 | g0098 | AMR | CLM | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01261 | hp2 | a0002 | c0002 | t0006 | g0025 | AMR | CLM | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01358 | hp1 | a0001 | c0001 | t0019 | g0094 | AMR | CLM | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01358 | hp2 | a0002 | c0002 | t0006 | g0025 | AMR | CLM | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | CLM | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01496 | hp1 | a0002 | c0002 | t0006 | g0059 | AMR | CLM | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01515 | hp1 | a0001 | c0001 | t0005 | g0018 | EUR | IBS | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0108 | EUR | IBS | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0031 | EUR | IBS | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01517 | hp2 | a0001 | c0001 | t0005 | g0018 | EUR | IBS | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01884 | hp2 | a0001 | c0008 | t0002 | g0071 | AFR | ACB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | ACB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ACB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01934 | hp2 | a0002 | c0002 | t0009 | g0026 | AMR | PEL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01943 | hp1 | a0002 | c0002 | t0006 | g0057 | AMR | PEL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | PEL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PEL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | PEL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | KHV | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | KHV | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | ACB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | ACB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | KHV | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | KHV | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | KHV | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02135 | hp2 | a0001 | c0016 | t0004 | g0130 | EAS | KHV | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | ACB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | ACB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | PEL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02165 | hp1 | a0001 | c0001 | t0008 | g0047 | EAS | CDX | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CDX | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | ACB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02258 | hp2 | a0001 | c0001 | t0018 | g0188 | AFR | ACB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | ACB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0102 | AFR | ACB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0209 | AFR | ACB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0087 | AFR | GWD | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02615 | hp1 | a0001 | c0001 | t0010 | g0019 | AFR | GWD | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02622 | hp1 | a0001 | c0001 | t0010 | g0125 | AFR | GWD | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | GWD | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02647 | hp1 | a0001 | c0001 | t0010 | g0019 | AFR | GWD | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0127 | SAS | PJL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | GWD | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | GWD | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | GWD | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0128 | SAS | PJL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02738 | hp1 | a0002 | c0002 | t0005 | g0027 | SAS | PJL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0193 | SAS | PJL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02809 | hp1 | a0006 | c0011 | t0003 | g0110 | AFR | GWD | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02818 | hp1 | a0001 | c0001 | t0021 | g0178 | AFR | GWD | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | GWD | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02895 | hp2 | a0007 | c0009 | t0001 | g0175 | AFR | GWD | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | ESN | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | ESN | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | ESN | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | ESN | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02976 | hp1 | a0001 | c0004 | t0007 | g0055 | AFR | ESN | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02976 | hp2 | a0001 | c0001 | t0010 | g0158 | AFR | ESN | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0088 | SAS | PJL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03098 | hp1 | a0001 | c0001 | t0010 | g0019 | AFR | MSL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | MSL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | ESN | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | ESN | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | ESN | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | ESN | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | MSL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | MSL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03225 | hp1 | a0003 | c0005 | t0015 | g0053 | AFR | MSL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | PJL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | MSL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0073 | AFR | MSL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03486 | hp1 | a0004 | c0006 | t0003 | g0202 | AFR | MSL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03486 | hp2 | a0008 | c0015 | t0007 | g0223 | AFR | MSL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0101 | AFR | ESN | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | GWD | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | MSL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | STU | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | STU | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | BEB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | BEB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03927 | hp2 | a0002 | c0002 | t0005 | g0070 | SAS | BEB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | BEB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG04199 | hp1 | a0001 | c0001 | t0013 | g0174 | SAS | STU | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0124 | SAS | STU | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | STU | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0109 | SAS | STU | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | YRI | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | YRI | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18747 | hp2 | a0001 | c0001 | t0017 | g0069 | EAS | CHB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | YRI | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | YRI | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18939 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18940 | hp1 | a0001 | c0003 | t0001 | g0172 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18943 | hp1 | a0001 | c0001 | t0016 | g0068 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18950 | hp1 | a0001 | c0001 | t0008 | g0046 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18952 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18962 | hp1 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18962 | hp2 | a0001 | c0003 | t0001 | g0032 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18963 | hp1 | a0001 | c0001 | t0008 | g0079 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18967 | hp2 | a0001 | c0001 | t0004 | g0176 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18969 | hp2 | a0002 | c0002 | t0009 | g0063 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18971 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18975 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18983 | hp2 | a0001 | c0003 | t0001 | g0032 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18984 | hp1 | a0001 | c0003 | t0001 | g0156 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18987 | hp2 | a0002 | c0002 | t0009 | g0067 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18990 | hp2 | a0001 | c0001 | t0014 | g0041 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18998 | hp1 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18999 | hp1 | a0001 | c0003 | t0001 | g0171 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19000 | hp2 | a0001 | c0001 | t0008 | g0112 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19005 | hp1 | a0001 | c0001 | t0020 | g0113 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19007 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19009 | hp1 | a0001 | c0014 | t0001 | g0082 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19011 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19012 | hp2 | a0001 | c0001 | t0014 | g0041 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | LWK | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | LWK | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0214 | AFR | LWK | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19064 | hp2 | a0001 | c0001 | t0004 | g0116 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19067 | hp1 | a0002 | c0002 | t0011 | g0058 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19067 | hp2 | a0001 | c0012 | t0001 | g0137 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19074 | hp1 | a0001 | c0001 | t0008 | g0047 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19082 | hp2 | a0001 | c0001 | t0008 | g0046 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19088 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19090 | hp1 | a0002 | c0002 | t0009 | g0060 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | YRI | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | YRI | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ASW | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ASW | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0191 | EUR | TSI | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA20752 | hp2 | a0002 | c0002 | t0011 | g0061 | EUR | TSI | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0151 | EUR | TSI | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0147 | EUR | TSI | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA20905 | hp1 | a0001 | c0013 | t0002 | g0145 | SAS | GIH | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | GIH | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01123 | hp1 | a0002 | c0002 | t0005 | g0027 | AMR | CLM | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG01123 | hp2 | a0001 | c0004 | t0007 | g0215 | AMR | CLM | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | ACB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0211 | AFR | ACB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0212 | AFR | ACB | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
HG03471 | hp2 | a0004 | c0006 | t0003 | g0201 | AFR | MSL | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | USA | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA20300 | hp2 | a0001 | c0004 | t0007 | g0056 | AFR | USA | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | LWK | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
NA21309 | hp2 | a0001 | c0004 | t0003 | g0084 | AFR | LWK | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0168 | REF | REF | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0199 | REF | REF | AGPAT2_chr9_136668143_136692457 | AGPAT2 | chr9 | 136668143 | 136692457 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:136673780 | G | A | 1 | a0003 | 2 | HG01109.hp2 HG03225.hp1 |
missense_variant | MODERATE | c.809C>T | p.Ala270Val | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 6/6 | 909/1546 | 809/837 | 270/278 | chr9 | 136673780 | |||
chr9:136673828 | G | A | 1 | a0004 | 2 | HG03471.hp2 HG03486.hp1 |
missense_variant | MODERATE | c.761C>T | p.Thr254Ile | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 6/6 | 861/1546 | 761/837 | 254/278 | chr9 | 136673828 | |||
chr9:136673861 | G | T | 1 | a0006 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.728C>A | p.Ala243Glu | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 6/6 | 828/1546 | 728/837 | 243/278 | chr9 | 136673861 | |||
chr9:136676992 | G | T | 1 | a0005 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.461C>A | p.Ala154Asp | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 3/6 | 561/1546 | 461/837 | 154/278 | chr9 | 136676992 | |||
chr9:136677510 | G | A | 1 | a0008 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.229C>T | p.Arg77Cys | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 2/6 | 329/1546 | 229/837 | 77/278 | chr9 | 136677510 | |||
chr9:136677531 | A | C | 1 | a0007 | 1 | HG02895.hp2 | missense_variant | MODERATE | c.208T>G | p.Phe70Val | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 2/6 | 308/1546 | 208/837 | 70/278 | chr9 | 136677531 | |||
chr9:136687306 | C | CCAG | 1 | a0002 | 18 | HG00609.hp1 HG01069.hp2 HG01081.hp2 others(15): Show |
conservative_inframe_insertion | MODERATE | c.49_51dupCTG | p.Leu17dup | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/6 | 151/1546 | 51/837 | 17/278 | chr9 | 136687306 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:136673770 | G | A | 1 | a0001c0012 | 1 | NA19067.hp2 | synonymous_variant | LOW | c.819C>T | p.Gly273Gly | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 6/6 | 919/1546 | 819/837 | 273/278 | chr9 | 136673770 | |||
chr9:136673848 | G | A | 1 | a0001c0003 | 9 | NA18940.hp1 NA18962.hp1 NA18962.hp2 others(6): Show |
synonymous_variant | LOW | c.741C>T | p.Thr247Thr | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 6/6 | 841/1546 | 741/837 | 247/278 | chr9 | 136673848 | |||
chr9:136673860 | C | T | 1 | a0002c0007 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.729G>A | p.Ala243Ala | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 6/6 | 829/1546 | 729/837 | 243/278 | chr9 | 136673860 | |||
chr9:136673887 | G | A | 1 | a0001c0013 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.702C>T | p.Ser234Ser | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 6/6 | 802/1546 | 702/837 | 234/278 | chr9 | 136673887 | |||
chr9:136677042 | G | A | 1 | a0001c0014 | 1 | NA19009.hp1 | synonymous_variant | LOW | c.411C>T | p.Gly137Gly | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 3/6 | 511/1546 | 411/837 | 137/278 | chr9 | 136677042 | |||
chr9:136677108 | G | A | 1 | a0001c0004 | 6 | HG01074.hp1 HG01123.hp2 HG01256.hp1 others(3): Show |
synonymous_variant | LOW | c.345C>T | p.Cys115Cys | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 3/6 | 445/1546 | 345/837 | 115/278 | chr9 | 136677108 | |||
chr9:136677550 | G | A | 1 | a0001c0016 | 1 | HG02135.hp2 | synonymous_variant | LOW | c.189C>T | p.Ile63Ile | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 2/6 | 289/1546 | 189/837 | 63/278 | chr9 | 136677550 | |||
chr9:136687190 | C | G | 1 | a0001c0008 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.168G>C | p.Thr56Thr | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/6 | 268/1546 | 168/837 | 56/278 | chr9 | 136687190 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:136673217 | G | A | 4 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0017 others(1): Show |
17 | HG00558.hp1 HG02135.hp2 HG02165.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*535C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 6/6 | 535 | chr9 | 136673217 | ||||||
chr9:136673235 | G | A | 9 | a0001c0001t0001 a0001c0001t0014 a0001c0001t0022 others(6): Show |
154 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*517C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 6/6 | 517 | chr9 | 136673235 | ||||||
chr9:136673242 | G | A | 1 | a0001c0001t0018 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*510C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 6/6 | 510 | chr9 | 136673242 | ||||||
chr9:136673310 | G | C | 21 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0008 others(18): Show |
301 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(298): Show |
3_prime_UTR_variant | MODIFIER | c.*442C>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 6/6 | 442 | chr9 | 136673310 | ||||||
chr9:136673385 | T | C | 1 | a0001c0001t0021 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*367A>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 6/6 | 367 | chr9 | 136673385 | ||||||
chr9:136673437 | G | A | 1 | a0001c0001t0022 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*315C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 6/6 | 315 | chr9 | 136673437 | ||||||
chr9:136673513 | C | T | 1 | a0001c0001t0010 | 5 | HG02615.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*239G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 6/6 | 239 | chr9 | 136673513 | ||||||
chr9:136673522 | G | A | 1 | a0001c0001t0014 | 2 | NA18990.hp2 NA19012.hp2 |
3_prime_UTR_variant | MODIFIER | c.*230C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 6/6 | 230 | chr9 | 136673522 | ||||||
chr9:136673534 | T | TCGAGCC | 5 | a0001c0001t0005 a0001c0001t0019 a0002c0002t0005 others(2): Show |
16 | HG00738.hp2 HG01069.hp2 HG01106.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*212_*217dupGGCTCG | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 6/6 | 217 | chr9 | 136673534 | ||||||
chr9:136673541 | C | T | 1 | a0001c0001t0020 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*211G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 6/6 | 211 | chr9 | 136673541 | ||||||
chr9:136673595 | G | A | 19 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0008 others(16): Show |
296 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(293): Show |
3_prime_UTR_variant | MODIFIER | c.*157C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 6/6 | 157 | chr9 | 136673595 | ||||||
chr9:136673673 | G | C | 2 | a0001c0001t0010 a0003c0005t0015 |
7 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*79C>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 6/6 | 79 | chr9 | 136673673 | ||||||
chr9:136673704 | A | G | 1 | a0001c0001t0012 | 3 | HG00735.hp1 HG01256.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*48T>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 6/6 | 48 | chr9 | 136673704 | ||||||
chr9:136687398 | G | T | 1 | a0001c0001t0017 | 1 | NA18747.hp2 | 5_prime_UTR_variant | MODIFIER | c.-41C>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/6 | 41 | chr9 | 136687398 | ||||||
chr9:136687419 | C | T | 1 | a0001c0001t0016 | 1 | NA18943.hp1 | 5_prime_UTR_variant | MODIFIER | c.-62G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/6 | 62 | chr9 | 136687419 | ||||||
chr9:136687424 | C | G | 4 | a0002c0002t0006 a0002c0002t0009 a0002c0002t0011 others(1): Show |
15 | HG00609.hp1 HG01069.hp2 HG01081.hp2 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-67G>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/6 | 67 | chr9 | 136687424 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:136674012 | C | G | 1 | a0001c0001t0001g0045 | 2 | NA19064.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.662-85G>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 5/5 | chr9 | 136674012 | |||||||
chr9:136674023 | C | G | 1 | a0001c0001t0005g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.662-96G>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 5/5 | chr9 | 136674023 | |||||||
chr9:136674138 | C | T | 1 | a0001c0001t0010g0125 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.662-211G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 5/5 | chr9 | 136674138 | |||||||
chr9:136674163 | C | T | 1 | a0001c0001t0003g0038 | 2 | HG01099.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.662-236G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 5/5 | chr9 | 136674163 | |||||||
chr9:136674223 | C | G | 3 | a0001c0004t0007g0055 a0001c0004t0007g0056 a0001c0004t0007g0215 |
5 | HG01074.hp1 HG01123.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.662-296G>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 5/5 | chr9 | 136674223 | |||||||
chr9:136674235 | C | T | 11 | a0001c0001t0005g0018 a0001c0001t0005g0189 a0001c0001t0019g0094 others(8): Show |
15 | HG00738.hp2 HG01069.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.662-308G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 5/5 | chr9 | 136674235 | |||||||
chr9:136674389 | G | C | 12 | a0001c0001t0002g0031 a0001c0001t0005g0018 a0001c0001t0005g0189 others(9): Show |
17 | HG00738.hp2 HG01069.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.661+346C>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 5/5 | chr9 | 136674389 | |||||||
chr9:136674412 | C | A | 1 | a0001c0001t0001g0152 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.661+323G>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 5/5 | chr9 | 136674412 | |||||||
chr9:136674426 | G | A | 1 | a0001c0001t0003g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.661+309C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 5/5 | chr9 | 136674426 | |||||||
chr9:136674446 | G | A | 1 | a0008c0015t0007g0223 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.661+289C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 5/5 | chr9 | 136674446 | |||||||
chr9:136674581 | C | G | 2 | a0002c0002t0005g0027 a0002c0002t0005g0070 |
3 | HG01123.hp1 HG02738.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.661+154G>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 5/5 | chr9 | 136674581 | |||||||
chr9:136674614 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(156): Show |
269 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.661+121T>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 5/5 | chr9 | 136674614 | |||||||
chr9:136674632 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.661+103G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 5/5 | chr9 | 136674632 | |||||||
chr9:136674659 | A | ACGATGAG others(12): Show |
1 | a0001c0001t0002g0099 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.661+57_661+75dupAG others(17): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 5/5 | chr9 | 136674659 | |||||||
chr9:136674698 | C | T | 4 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0141 others(1): Show |
6 | HG00544.hp1 HG02273.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.661+37G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 5/5 | chr9 | 136674698 | |||||||
chr9:136674712 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0181 |
2 | HG00544.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.661+23G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 5/5 | chr9 | 136674712 | |||||||
chr9:136674900 | C | A | 1 | a0001c0001t0002g0163 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.589-93G>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136674900 | |||||||
chr9:136674903 | C | T | 1 | a0001c0001t0002g0109 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.589-96G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136674903 | |||||||
chr9:136675019 | T | G | 2 | a0001c0001t0002g0034 a0001c0001t0002g0115 |
3 | HG01167.hp2 HG01169.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.589-212A>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675019 | |||||||
chr9:136675045 | T | A | 1 | a0001c0001t0003g0028 | 2 | HG01106.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.589-238A>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675045 | |||||||
chr9:136675124 | G | A | 9 | a0001c0001t0001g0138 a0001c0001t0001g0142 a0001c0001t0001g0165 others(6): Show |
11 | HG00621.hp1 HG02129.hp1 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.589-317C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675124 | |||||||
chr9:136675187 | A | G | 3 | a0001c0001t0003g0028 a0001c0001t0010g0019 a0001c0001t0010g0125 |
6 | HG01106.hp2 HG02055.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.589-380T>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675187 | |||||||
chr9:136675240 | G | C | 1 | a0001c0001t0001g0139 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.589-433C>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675240 | |||||||
chr9:136675298 | G | A | 7 | a0001c0001t0001g0142 a0001c0001t0001g0165 a0001c0001t0001g0195 others(4): Show |
8 | HG00621.hp1 HG02129.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.589-491C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675298 | |||||||
chr9:136675317 | C | CAGGGGGC others(34): Show |
1 | a0001c0001t0003g0209 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.589-551_589-511dup others(41): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675317 | |||||||
chr9:136675317 | C | CAGGGGGC others(157): Show |
1 | a0001c0001t0002g0187 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.589-511_589-510ins others(164): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675317 | |||||||
chr9:136675317 | C | CAGGGGGC others(34): Show |
56 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0016 others(53): Show |
109 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.589-511_589-510ins others(41): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675317 | |||||||
chr9:136675317 | C | CAGGGGGC others(75): Show |
4 | a0001c0001t0002g0005 a0001c0001t0002g0154 a0001c0001t0002g0207 others(1): Show |
10 | HG02109.hp2 HG02809.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.589-511_589-510ins others(82): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675317 | |||||||
chr9:136675317 | C | CAGGGGGC others(116): Show |
2 | a0001c0001t0001g0169 a0001c0008t0002g0071 |
2 | HG01884.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.589-511_589-510ins others(123): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675317 | |||||||
chr9:136675317 | C | CAGGGGGC others(157): Show |
1 | a0001c0001t0001g0040 | 2 | NA19056.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.589-511_589-510ins others(164): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675317 | |||||||
chr9:136675317 | C | CAGGGGGC others(198): Show |
2 | a0001c0001t0001g0148 a0001c0001t0002g0203 |
2 | HG02486.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.589-511_589-510ins others(205): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675317 | |||||||
chr9:136675317 | C | CAGGGGGC others(280): Show |
1 | a0001c0001t0001g0134 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.589-511_589-510ins others(287): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675317 | |||||||
chr9:136675317 | C | CAGGGGGC others(239): Show |
1 | a0001c0001t0002g0133 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.589-511_589-510ins others(246): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675317 | |||||||
chr9:136675317 | C | CAGGGGGC others(321): Show |
1 | a0001c0001t0001g0224 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.589-511_589-510ins others(328): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675317 | |||||||
chr9:136675317 | C | CAGGGGGC others(403): Show |
1 | a0001c0001t0002g0192 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.589-511_589-510ins others(410): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675317 | |||||||
chr9:136675317 | C | CAGGGGGC others(34): Show |
2 | a0001c0001t0002g0017 a0001c0001t0002g0093 |
4 | HG03139.hp2 NA18990.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-511_589-510ins others(41): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675317 | |||||||
chr9:136675317 | C | CAGGGGGC others(280): Show |
2 | a0001c0001t0002g0103 a0001c0001t0002g0104 |
2 | HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.589-511_589-510ins others(287): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675317 | |||||||
chr9:136675317 | C | CAGGGGGC others(608): Show |
1 | a0001c0001t0002g0121 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.589-511_589-510ins others(615): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675317 | |||||||
chr9:136675317 | C | CAGGGGGC others(690): Show |
3 | a0001c0001t0002g0044 a0001c0001t0002g0120 a0001c0001t0002g0221 |
4 | NA18945.hp1 NA18952.hp2 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-511_589-510ins others(697): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675317 | |||||||
chr9:136675317 | C | CAGGGGGC others(690): Show |
1 | a0001c0001t0002g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.589-511_589-510ins others(697): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675317 | |||||||
chr9:136675317 | C | CAGGGGGC others(157): Show |
1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.589-511_589-510ins others(164): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675317 | |||||||
chr9:136675317 | C | CAGGGGGC others(321): Show |
1 | a0002c0002t0009g0067 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.589-511_589-510ins others(328): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675317 | |||||||
chr9:136675321 | GGGCCAGC others(116): Show |
G | 13 | a0001c0001t0001g0051 a0001c0001t0001g0190 a0001c0001t0005g0018 others(10): Show |
18 | HG01069.hp2 HG01106.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.589-637_589-515del | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675321 | |||||||
chr9:136675321 | GGGCCAGC others(157): Show |
G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(8): Show |
27 | HG00408.hp1 HG00609.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.589-678_589-515del | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675321 | |||||||
chr9:136675347 | C | CAGCAGGG others(75): Show |
7 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0011 others(4): Show |
7 | HG00423.hp1 HG00597.hp2 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.589-541_589-540ins others(82): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675347 | |||||||
chr9:136675347 | C | CAGCAGGG others(485): Show |
1 | a0001c0001t0002g0004 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.589-541_589-540ins others(492): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675347 | |||||||
chr9:136675347 | C | CAGCAGGG others(239): Show |
1 | a0001c0001t0001g0152 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.589-541_589-540ins others(246): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675347 | |||||||
chr9:136675347 | C | CAGCAGGG others(403): Show |
1 | a0001c0001t0002g0004 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.589-541_589-540ins others(410): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675347 | |||||||
chr9:136675347 | C | CAGCAGGG others(198): Show |
19 | a0001c0001t0001g0009 a0001c0001t0001g0210 a0001c0001t0002g0004 others(16): Show |
27 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.589-541_589-540ins others(205): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675347 | |||||||
chr9:136675347 | C | CAGCAGGG others(280): Show |
2 | a0001c0001t0002g0004 a0001c0001t0002g0205 |
2 | HG02523.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.589-541_589-540ins others(287): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675347 | |||||||
chr9:136675347 | C | CAGCAGGG others(239): Show |
1 | a0001c0001t0001g0107 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.589-541_589-540ins others(246): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675347 | |||||||
chr9:136675347 | C | CAGCAGGG others(321): Show |
3 | a0001c0001t0002g0004 a0001c0001t0002g0048 a0001c0001t0002g0185 |
3 | NA18975.hp1 NA19056.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.589-541_589-540ins others(328): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675347 | |||||||
chr9:136675347 | C | CAGCAGGG others(157): Show |
2 | a0001c0001t0002g0022 a0001c0001t0002g0218 |
2 | HG00639.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.589-541_589-540ins others(164): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675347 | |||||||
chr9:136675347 | C | CAGCAGGG others(567): Show |
2 | a0001c0001t0001g0011 a0001c0001t0001g0153 |
2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.589-541_589-540ins others(574): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675347 | |||||||
chr9:136675347 | C | CAGCAGGG others(403): Show |
1 | a0005c0010t0001g0146 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.589-541_589-540ins others(410): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675347 | |||||||
chr9:136675347 | C | CAGCAGGG others(239): Show |
1 | a0001c0001t0002g0211 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.589-541_589-540ins others(246): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675347 | |||||||
chr9:136675347 | C | CAGCAGGG others(444): Show |
1 | a0001c0001t0002g0004 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.589-541_589-540ins others(451): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675347 | |||||||
chr9:136675347 | C | CAGCAGGG others(116): Show |
1 | a0001c0001t0002g0186 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.589-541_589-540ins others(123): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675347 | |||||||
chr9:136675347 | C | CAGCAGGG others(403): Show |
1 | a0001c0001t0008g0046 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.589-541_589-540ins others(410): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675347 | |||||||
chr9:136675347 | C | G | 18 | a0001c0001t0001g0009 a0001c0001t0001g0213 a0001c0001t0002g0013 others(15): Show |
23 | HG01081.hp2 HG01934.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.589-540G>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675347 | |||||||
chr9:136675354 | A | AAGGGAGG others(116): Show |
1 | a0001c0001t0002g0049 | 2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.589-548_589-547ins others(123): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675354 | |||||||
chr9:136675354 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(156): Show |
267 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(264): Show |
intron_variant | MODIFIER | c.589-547T>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675354 | |||||||
chr9:136675362 | GGGCCAGC others(116): Show |
G | 2 | a0001c0001t0004g0176 a0003c0005t0015g0053 |
2 | HG03225.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.589-678_589-556del | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675362 | |||||||
chr9:136675388 | G | C | 96 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(93): Show |
136 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.589-581C>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675388 | |||||||
chr9:136675388 | G | CAGCAGGG others(34): Show |
3 | a0001c0001t0001g0007 a0001c0001t0001g0085 a0001c0001t0001g0089 |
3 | HG02132.hp2 NA18999.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.589-581_589-580ins others(41): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675388 | |||||||
chr9:136675388 | G | GAGCAGGG others(34): Show |
5 | a0001c0001t0002g0002 a0001c0001t0002g0050 a0001c0001t0002g0108 others(2): Show |
6 | HG00733.hp1 HG01074.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.589-622_589-582dup others(41): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675388 | |||||||
chr9:136675388 | G | GAGCAGGG others(75): Show |
4 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0138 others(1): Show |
5 | HG02273.hp1 NA18970.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.589-582_589-581ins others(82): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675388 | |||||||
chr9:136675388 | G | GAGCAGGG others(157): Show |
6 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0092 others(3): Show |
6 | HG01175.hp1 HG01346.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-582_589-581ins others(164): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675388 | |||||||
chr9:136675388 | G | GAGCAGGG others(280): Show |
1 | a0001c0001t0001g0011 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.589-582_589-581ins others(287): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675388 | |||||||
chr9:136675388 | G | GAGCAGGG others(280): Show |
1 | a0001c0001t0001g0011 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.589-582_589-581ins others(287): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675388 | |||||||
chr9:136675395 | G | A | 4 | a0001c0001t0002g0049 a0001c0001t0010g0019 a0001c0001t0010g0125 others(1): Show |
7 | HG02615.hp1 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.589-588C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675395 | |||||||
chr9:136675403 | GGGCCAGC others(34): Show |
G | 7 | a0001c0001t0001g0007 a0001c0001t0001g0141 a0001c0001t0003g0198 others(4): Show |
8 | HG01074.hp1 HG01109.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.589-637_589-597del others(41): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675403 | |||||||
chr9:136675403 | GGGCCAGC others(75): Show |
G | 5 | a0001c0001t0001g0191 a0001c0001t0010g0019 a0001c0001t0010g0125 others(2): Show |
7 | HG00408.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.589-678_589-597del others(82): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675403 | |||||||
chr9:136675406 | C | CCAGCAGG others(75): Show |
1 | a0001c0001t0005g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.589-600_589-599ins others(82): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675406 | |||||||
chr9:136675429 | C | CAGCAGGG others(649): Show |
1 | a0001c0001t0001g0009 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.589-623_589-622ins others(656): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675429 | |||||||
chr9:136675429 | C | CAGCAGGG others(567): Show |
1 | a0001c0001t0001g0009 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.589-623_589-622ins others(574): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675429 | |||||||
chr9:136675429 | C | CAGCAGGG others(485): Show |
1 | a0001c0001t0002g0013 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.589-623_589-622ins others(492): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675429 | |||||||
chr9:136675429 | C | CAGCAGGG others(363): Show |
1 | a0001c0001t0002g0002 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.589-623_589-622ins others(370): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675429 | |||||||
chr9:136675429 | C | CAGCAGGG others(198): Show |
2 | a0001c0001t0002g0013 a0001c0001t0002g0099 |
2 | HG02922.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.589-623_589-622ins others(205): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675429 | |||||||
chr9:136675429 | C | CAGCAGGG others(75): Show |
30 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0016 others(27): Show |
66 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.589-623_589-622ins others(82): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675429 | |||||||
chr9:136675429 | C | CAGCAGGG others(567): Show |
1 | a0001c0001t0002g0117 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.589-623_589-622ins others(574): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675429 | |||||||
chr9:136675429 | C | CAGCAGGG others(321): Show |
6 | a0001c0001t0002g0122 a0001c0001t0002g0226 a0001c0001t0003g0101 others(3): Show |
7 | HG01081.hp2 HG01934.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-623_589-622ins others(328): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675429 | |||||||
chr9:136675429 | C | CAGCAGGG others(157): Show |
18 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0167 others(15): Show |
28 | HG00323.hp1 HG00438.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.589-623_589-622ins others(164): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675429 | |||||||
chr9:136675429 | C | CAGCAGGG others(116): Show |
1 | a0001c0001t0002g0002 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.589-623_589-622ins others(123): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675429 | |||||||
chr9:136675429 | C | CAGCAGGG others(198): Show |
1 | a0001c0001t0002g0182 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.589-623_589-622ins others(205): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675429 | |||||||
chr9:136675429 | C | CAGCAGGG others(34): Show |
6 | a0001c0001t0001g0007 a0001c0001t0002g0002 a0001c0001t0002g0093 others(3): Show |
7 | HG01099.hp1 HG02055.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.589-623_589-622ins others(41): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675429 | |||||||
chr9:136675429 | C | CAGCAGGG others(280): Show |
1 | a0001c0001t0002g0102 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.589-623_589-622ins others(287): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675429 | |||||||
chr9:136675429 | C | CAGCAGGG others(239): Show |
2 | a0001c0001t0001g0009 a0001c0001t0002g0031 |
2 | HG01516.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.589-623_589-622ins others(246): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675429 | |||||||
chr9:136675429 | C | CAGCAGGG others(280): Show |
1 | a0001c0001t0002g0031 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.589-623_589-622ins others(287): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675429 | |||||||
chr9:136675429 | C | CAGCAGGG others(116): Show |
2 | a0006c0011t0003g0110 a0007c0009t0001g0175 |
2 | HG02809.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.589-623_589-622ins others(123): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675429 | |||||||
chr9:136675429 | C | CAGCAGGG others(321): Show |
1 | a0001c0001t0002g0162 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.589-623_589-622ins others(328): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675429 | |||||||
chr9:136675429 | C | CAGCAGGG others(157): Show |
1 | a0001c0001t0003g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.589-623_589-622ins others(164): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675429 | |||||||
chr9:136675429 | C | G | 58 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(55): Show |
88 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.589-622G>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675429 | |||||||
chr9:136675429 | CAGCAGGA others(75): Show |
C | 2 | a0001c0001t0001g0213 a0001c0001t0003g0073 |
2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.589-704_589-623del others(82): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675429 | |||||||
chr9:136675436 | A | AAGGGAGG others(34): Show |
1 | a0001c0001t0003g0209 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.589-630_589-629ins others(41): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675436 | |||||||
chr9:136675436 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
274 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(271): Show |
intron_variant | MODIFIER | c.589-629T>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675436 | |||||||
chr9:136675441 | A | T | 1 | a0001c0001t0002g0143 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.589-634T>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675441 | |||||||
chr9:136675444 | A | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
278 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(275): Show |
intron_variant | MODIFIER | c.589-637T>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675444 | |||||||
chr9:136675444 | AGGCCAGC others(75): Show |
A | 7 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0116 others(4): Show |
9 | HG00558.hp1 NA18747.hp2 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.589-719_589-638del others(82): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675444 | |||||||
chr9:136675470 | C | CAGCAGGG others(778): Show |
1 | a0001c0001t0002g0100 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.589-664_589-663ins others(785): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675470 | |||||||
chr9:136675470 | C | CAGCAGGG others(731): Show |
1 | a0001c0001t0002g0017 | 3 | NA18990.hp1 NA19005.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.589-664_589-663ins others(738): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675470 | |||||||
chr9:136675470 | C | CAGCAGGG others(34): Show |
3 | a0001c0001t0001g0007 a0001c0001t0001g0042 a0001c0001t0001g0090 |
3 | HG02071.hp1 HG03927.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.589-664_589-663ins others(41): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675470 | |||||||
chr9:136675470 | C | CAGCAGGG others(116): Show |
1 | a0001c0001t0002g0002 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.589-664_589-663ins others(123): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675470 | |||||||
chr9:136675470 | C | G | 23 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0051 others(20): Show |
28 | HG00621.hp1 HG01934.hp1 HG02129.hp1 others(25): Show |
intron_variant | MODIFIER | c.589-663G>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675470 | |||||||
chr9:136675477 | G | GAGGGAGG others(116): Show |
1 | a0001c0016t0004g0130 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.589-671_589-670ins others(123): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675477 | |||||||
chr9:136675485 | A | AGGCCAGC others(34): Show |
2 | a0001c0004t0007g0056 a0001c0004t0007g0215 |
3 | HG01123.hp2 HG01256.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.589-719_589-679dup others(41): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675485 | |||||||
chr9:136675485 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
295 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(292): Show |
intron_variant | MODIFIER | c.589-678T>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675485 | |||||||
chr9:136675511 | G | C | 34 | a0001c0001t0001g0020 a0001c0001t0001g0051 a0001c0001t0001g0141 others(31): Show |
47 | HG01069.hp2 HG01074.hp1 HG01106.hp1 others(44): Show |
intron_variant | MODIFIER | c.589-704C>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675511 | |||||||
chr9:136675511 | G | GAGCAGGG others(34): Show |
11 | a0001c0001t0002g0013 a0001c0001t0002g0099 a0001c0001t0002g0102 others(8): Show |
15 | HG01081.hp2 HG01934.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.589-745_589-705dup others(41): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675511 | |||||||
chr9:136675511 | G | GAGCAGGG others(687): Show |
1 | a0001c0001t0002g0078 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.589-705_589-704ins others(694): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675511 | |||||||
chr9:136675511 | G | GAGCAGGG others(690): Show |
1 | a0001c0001t0002g0118 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.589-705_589-704ins others(697): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675511 | |||||||
chr9:136675511 | G | GAGCAGGG others(75): Show |
1 | a0001c0001t0001g0160 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.589-705_589-704ins others(82): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675511 | |||||||
chr9:136675518 | G | A | 2 | a0001c0001t0003g0028 a0001c0001t0005g0087 |
3 | HG01106.hp2 HG02055.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.589-711C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675518 | |||||||
chr9:136675549 | T | C | 2 | a0004c0006t0003g0201 a0004c0006t0003g0202 |
2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.589-742A>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675549 | |||||||
chr9:136675552 | C | CAGCAGGG others(34): Show |
1 | a0001c0001t0002g0093 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.589-746_589-745ins others(41): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675552 | |||||||
chr9:136675552 | C | CAGCAGGG others(75): Show |
1 | a0001c0001t0003g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.589-746_589-745ins others(82): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675552 | |||||||
chr9:136675552 | C | G | 36 | a0001c0001t0001g0051 a0001c0001t0001g0142 a0001c0001t0001g0165 others(33): Show |
46 | HG00621.hp1 HG00738.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.589-745G>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675552 | |||||||
chr9:136675564 | A | AGGGGGCC others(76): Show |
1 | a0001c0001t0001g0170 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.589-758_589-757ins others(83): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675564 | |||||||
chr9:136675567 | G | GGGCCAGC others(75): Show |
7 | a0001c0001t0001g0142 a0001c0001t0001g0165 a0001c0001t0001g0195 others(4): Show |
8 | HG00621.hp1 HG02129.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.589-761_589-760ins others(82): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675567 | |||||||
chr9:136675568 | G | A | 1 | a0002c0002t0006g0065 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.589-761C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675568 | |||||||
chr9:136675590 | C | T | 9 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0116 others(6): Show |
11 | HG00558.hp1 HG02135.hp2 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.589-783G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675590 | |||||||
chr9:136675602 | C | A | 4 | a0001c0001t0002g0034 a0001c0001t0002g0114 a0001c0001t0002g0115 others(1): Show |
5 | HG01167.hp2 HG01169.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.589-795G>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675602 | |||||||
chr9:136675673 | T | C | 1 | a0001c0001t0002g0096 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.589-866A>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675673 | |||||||
chr9:136675737 | G | C | 2 | a0001c0001t0003g0198 a0003c0005t0015g0053 |
3 | HG01109.hp2 HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.588+848C>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675737 | |||||||
chr9:136675761 | C | T | 21 | a0001c0001t0001g0165 a0001c0001t0001g0195 a0001c0001t0001g0200 others(18): Show |
29 | HG00621.hp1 HG01074.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.588+824G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675761 | |||||||
chr9:136675813 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.588+772C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675813 | |||||||
chr9:136675832 | CCT | C | 2 | a0001c0001t0003g0198 a0003c0005t0015g0053 |
3 | HG01109.hp2 HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.588+751_588+752del others(2): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136675832 | |||||||
chr9:136676037 | G | A | 2 | a0001c0001t0003g0198 a0003c0005t0015g0053 |
3 | HG01109.hp2 HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.588+548C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136676037 | |||||||
chr9:136676040 | G | C | 4 | a0001c0004t0003g0084 a0001c0004t0007g0055 a0001c0004t0007g0056 others(1): Show |
6 | HG01074.hp1 HG01123.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+545C>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136676040 | |||||||
chr9:136676068 | C | T | 2 | a0001c0001t0003g0198 a0003c0005t0015g0053 |
3 | HG01109.hp2 HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.588+517G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136676068 | |||||||
chr9:136676128 | G | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0051 others(10): Show |
30 | HG00408.hp1 HG00609.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.588+457C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136676128 | |||||||
chr9:136676154 | C | G | 2 | a0001c0004t0003g0084 a0001c0004t0007g0055 |
3 | HG01074.hp1 HG02976.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.588+431G>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136676154 | |||||||
chr9:136676165 | T | C | 29 | a0001c0001t0001g0165 a0001c0001t0001g0195 a0001c0001t0001g0200 others(26): Show |
39 | HG00621.hp1 HG00738.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.588+420A>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136676165 | |||||||
chr9:136676210 | G | A | 1 | a0001c0001t0005g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.588+375C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136676210 | |||||||
chr9:136676293 | G | A | 4 | a0001c0001t0002g0049 a0001c0001t0002g0187 a0001c0001t0003g0028 others(1): Show |
6 | HG01106.hp2 HG02055.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.588+292C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136676293 | |||||||
chr9:136676354 | A | G | 1 | a0001c0001t0002g0204 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.588+231T>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136676354 | |||||||
chr9:136676386 | G | C | 6 | a0001c0001t0002g0049 a0001c0001t0002g0187 a0001c0001t0003g0028 others(3): Show |
8 | HG01106.hp2 HG02055.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.588+199C>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136676386 | |||||||
chr9:136676457 | A | G | 1 | a0001c0001t0004g0036 | 2 | NA18952.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.588+128T>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136676457 | |||||||
chr9:136676481 | T | A | 1 | a0001c0001t0002g0104 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.588+104A>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136676481 | |||||||
chr9:136676500 | G | A | 1 | a0001c0001t0002g0216 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.588+85C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136676500 | |||||||
chr9:136676543 | C | T | 1 | a0001c0001t0002g0031 | 2 | HG01516.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.588+42G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136676543 | |||||||
chr9:136676564 | G | C | 6 | a0001c0001t0001g0165 a0001c0001t0001g0195 a0001c0001t0001g0200 others(3): Show |
7 | HG00621.hp1 NA18947.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.588+21C>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 4/5 | chr9 | 136676564 | |||||||
chr9:136676842 | G | A | 2 | a0004c0006t0003g0201 a0004c0006t0003g0202 |
2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.492+119C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 3/5 | chr9 | 136676842 | |||||||
chr9:136676843 | G | T | 2 | a0004c0006t0003g0201 a0004c0006t0003g0202 |
2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.492+118C>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 3/5 | chr9 | 136676843 | |||||||
chr9:136676911 | C | T | 4 | a0001c0001t0003g0073 a0001c0001t0003g0208 a0001c0001t0003g0209 others(1): Show |
4 | HG02258.hp2 HG02451.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.492+50G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 3/5 | chr9 | 136676911 | |||||||
chr9:136677143 | G | A | 6 | a0001c0001t0002g0102 a0001c0001t0002g0103 a0001c0001t0002g0104 others(3): Show |
6 | HG02451.hp1 HG02622.hp2 HG02818.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.317-7C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 2/5 | chr9 | 136677143 | |||||||
chr9:136677205 | C | A | 1 | a0001c0003t0001g0014 | 4 | NA18962.hp1 NA18971.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-69G>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 2/5 | chr9 | 136677205 | |||||||
chr9:136677616 | C | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
233 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(230): Show |
intron_variant | MODIFIER | c.183-60G>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136677616 | |||||||
chr9:136677617 | G | A | 2 | a0004c0006t0003g0201 a0004c0006t0003g0202 |
2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.183-61C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136677617 | |||||||
chr9:136677668 | C | T | 2 | a0001c0001t0003g0023 a0001c0001t0003g0214 |
4 | HG02922.hp2 HG02970.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.183-112G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136677668 | |||||||
chr9:136677684 | G | A | 2 | a0001c0001t0002g0123 a0001c0001t0002g0143 |
2 | HG00558.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.183-128C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136677684 | |||||||
chr9:136677762 | G | A | 4 | a0001c0001t0002g0124 a0001c0001t0012g0074 a0001c0001t0012g0097 others(1): Show |
4 | HG00735.hp1 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.183-206C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136677762 | |||||||
chr9:136677827 | G | A | 2 | a0001c0001t0002g0049 a0001c0001t0002g0187 |
3 | HG02717.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.183-271C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136677827 | |||||||
chr9:136677986 | C | T | 3 | a0001c0001t0001g0131 a0001c0001t0001g0160 a0001c0001t0014g0041 |
4 | NA18942.hp2 NA18963.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.183-430G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136677986 | |||||||
chr9:136678089 | A | G | 4 | a0001c0004t0003g0084 a0001c0004t0007g0055 a0001c0004t0007g0056 others(1): Show |
6 | HG01074.hp1 HG01123.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.183-533T>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136678089 | |||||||
chr9:136678141 | G | A | 1 | a0007c0009t0001g0175 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.183-585C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136678141 | |||||||
chr9:136678175 | T | G | 2 | a0001c0001t0002g0049 a0001c0001t0002g0187 |
3 | HG02717.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.183-619A>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136678175 | |||||||
chr9:136678176 | C | A | 2 | a0001c0001t0002g0049 a0001c0001t0002g0187 |
3 | HG02717.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.183-620G>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136678176 | |||||||
chr9:136678223 | T | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(220): Show |
371 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(368): Show |
intron_variant | MODIFIER | c.183-667A>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136678223 | |||||||
chr9:136678393 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.183-837C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136678393 | |||||||
chr9:136678473 | G | A | 1 | a0001c0001t0003g0073 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.183-917C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136678473 | |||||||
chr9:136678519 | G | T | 1 | a0001c0001t0001g0040 | 2 | NA19056.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.183-963C>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136678519 | |||||||
chr9:136678547 | A | G | 2 | a0001c0001t0001g0180 a0001c0001t0008g0046 |
3 | NA18950.hp1 NA18969.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.183-991T>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136678547 | |||||||
chr9:136678550 | G | A | 2 | a0001c0001t0003g0198 a0003c0005t0015g0053 |
3 | HG01109.hp2 HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.183-994C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136678550 | |||||||
chr9:136678698 | G | C | 3 | a0001c0001t0010g0019 a0001c0001t0010g0125 a0001c0001t0010g0158 |
5 | HG02615.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.183-1142C>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136678698 | |||||||
chr9:136678766 | A | C | 1 | a0001c0001t0005g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.183-1210T>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136678766 | |||||||
chr9:136678767 | G | A | 1 | a0001c0001t0005g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.183-1211C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136678767 | |||||||
chr9:136678770 | TCCCCTTG others(31): Show |
T | 22 | a0001c0001t0002g0049 a0001c0001t0002g0187 a0001c0001t0003g0198 others(19): Show |
30 | HG00738.hp2 HG01069.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.183-1252_183-1215d others(40): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136678770 | |||||||
chr9:136678809 | A | G | 22 | a0001c0001t0002g0049 a0001c0001t0002g0187 a0001c0001t0003g0198 others(19): Show |
30 | HG00738.hp2 HG01069.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.183-1253T>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136678809 | |||||||
chr9:136678810 | T | G | 22 | a0001c0001t0002g0049 a0001c0001t0002g0187 a0001c0001t0003g0198 others(19): Show |
30 | HG00738.hp2 HG01069.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.183-1254A>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136678810 | |||||||
chr9:136678811 | T | A | 22 | a0001c0001t0002g0049 a0001c0001t0002g0187 a0001c0001t0003g0198 others(19): Show |
30 | HG00738.hp2 HG01069.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.183-1255A>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136678811 | |||||||
chr9:136678818 | T | G | 1 | a0001c0001t0005g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.183-1262A>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136678818 | |||||||
chr9:136678890 | C | T | 2 | a0004c0006t0003g0201 a0004c0006t0003g0202 |
2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.183-1334G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136678890 | |||||||
chr9:136678896 | A | G | 3 | a0001c0001t0002g0050 a0001c0001t0002g0108 a0001c0001t0002g0147 |
4 | HG00733.hp1 HG01361.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.183-1340T>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136678896 | |||||||
chr9:136678925 | G | A | 1 | a0008c0015t0007g0223 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.183-1369C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136678925 | |||||||
chr9:136679017 | G | A | 1 | a0001c0001t0002g0126 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.183-1461C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136679017 | |||||||
chr9:136679038 | G | A | 1 | a0002c0002t0006g0059 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.183-1482C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136679038 | |||||||
chr9:136679104 | G | T | 1 | a0002c0002t0009g0060 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.183-1548C>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136679104 | |||||||
chr9:136679205 | G | A | 3 | a0001c0001t0002g0029 a0001c0001t0002g0127 a0001c0001t0002g0128 |
4 | HG01069.hp1 HG01071.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.183-1649C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136679205 | |||||||
chr9:136679398 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.183-1842G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136679398 | |||||||
chr9:136679525 | C | T | 11 | a0001c0001t0005g0018 a0001c0001t0005g0189 a0001c0001t0019g0094 others(8): Show |
15 | HG00738.hp2 HG01069.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.183-1969G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136679525 | |||||||
chr9:136679620 | G | C | 1 | a0002c0002t0006g0059 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.183-2064C>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136679620 | |||||||
chr9:136679629 | C | A | 1 | a0001c0001t0004g0177 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.183-2073G>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136679629 | |||||||
chr9:136679685 | C | G | 2 | a0001c0004t0003g0084 a0001c0004t0007g0055 |
3 | HG01074.hp1 HG02976.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.183-2129G>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136679685 | |||||||
chr9:136679754 | G | A | 2 | a0001c0001t0002g0049 a0001c0001t0002g0187 |
3 | HG02717.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.183-2198C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136679754 | |||||||
chr9:136679800 | C | T | 1 | a0005c0010t0001g0146 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.183-2244G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136679800 | |||||||
chr9:136679918 | C | T | 4 | a0001c0001t0001g0225 a0001c0004t0003g0084 a0001c0004t0007g0056 others(1): Show |
5 | HG01123.hp2 HG01256.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.183-2362G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136679918 | |||||||
chr9:136679919 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.183-2363C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136679919 | |||||||
chr9:136679925 | C | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
271 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(268): Show |
intron_variant | MODIFIER | c.183-2369G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136679925 | |||||||
chr9:136680051 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.183-2495G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136680051 | |||||||
chr9:136680164 | C | T | 11 | a0001c0001t0005g0018 a0001c0001t0005g0189 a0001c0001t0019g0094 others(8): Show |
15 | HG00738.hp2 HG01069.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.183-2608G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136680164 | |||||||
chr9:136680208 | T | C | 22 | a0001c0001t0001g0224 a0001c0001t0002g0049 a0001c0001t0002g0187 others(19): Show |
34 | HG01099.hp2 HG01891.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.183-2652A>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136680208 | |||||||
chr9:136680319 | C | T | 4 | a0001c0001t0001g0165 a0001c0001t0003g0030 a0001c0001t0003g0166 others(1): Show |
5 | HG00621.hp1 NA18947.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.183-2763G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136680319 | |||||||
chr9:136680320 | G | A | 1 | a0001c0001t0002g0039 | 2 | HG00323.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.183-2764C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136680320 | |||||||
chr9:136680416 | G | A | 4 | a0001c0001t0001g0165 a0001c0001t0003g0030 a0001c0001t0003g0166 others(1): Show |
5 | HG00621.hp1 NA18947.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.183-2860C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136680416 | |||||||
chr9:136680584 | G | A | 1 | a0001c0001t0001g0052 | 2 | NA18612.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.183-3028C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136680584 | |||||||
chr9:136680674 | A | AT | 3 | a0001c0001t0001g0225 a0001c0004t0007g0056 a0001c0004t0007g0215 |
4 | HG01123.hp2 HG01256.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.183-3119dupA | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136680674 | |||||||
chr9:136680681 | A | AT | 5 | a0001c0001t0003g0073 a0001c0001t0003g0075 a0001c0004t0003g0084 others(2): Show |
6 | HG01074.hp1 HG02976.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.183-3126dupA | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136680681 | |||||||
chr9:136680681 | A | T | 3 | a0001c0001t0001g0225 a0001c0004t0007g0056 a0001c0004t0007g0215 |
4 | HG01123.hp2 HG01256.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.183-3125T>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136680681 | |||||||
chr9:136680681 | AT | A | 2 | a0001c0001t0003g0023 a0001c0001t0003g0214 |
4 | HG02922.hp2 HG02970.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.183-3126delA | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136680681 | |||||||
chr9:136680693 | A | G | 2 | a0001c0001t0003g0023 a0001c0001t0003g0214 |
4 | HG02922.hp2 HG02970.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.183-3137T>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136680693 | |||||||
chr9:136680798 | T | C | 3 | a0001c0001t0001g0165 a0001c0001t0003g0030 a0001c0001t0003g0166 |
4 | HG00621.hp1 NA18947.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.183-3242A>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136680798 | |||||||
chr9:136680816 | G | A | 1 | a0001c0001t0002g0205 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.183-3260C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136680816 | |||||||
chr9:136680856 | G | A | 3 | a0001c0001t0001g0224 a0001c0001t0003g0024 a0001c0001t0003g0212 |
5 | HG02559.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.183-3300C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136680856 | |||||||
chr9:136680908 | G | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0020 others(44): Show |
82 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.183-3352C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136680908 | |||||||
chr9:136680926 | A | T | 1 | a0001c0003t0001g0014 | 4 | NA18962.hp1 NA18971.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.183-3370T>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136680926 | |||||||
chr9:136680955 | G | A | 1 | a0001c0013t0002g0145 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.183-3399C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136680955 | |||||||
chr9:136681035 | G | A | 22 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0016 others(19): Show |
36 | HG00438.hp1 HG00642.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.183-3479C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136681035 | |||||||
chr9:136681049 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | NA18939.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.183-3493G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136681049 | |||||||
chr9:136681053 | G | A | 2 | a0001c0001t0003g0198 a0003c0005t0015g0053 |
3 | HG01109.hp2 HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.183-3497C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136681053 | |||||||
chr9:136681102 | C | CT | 16 | a0001c0001t0001g0105 a0001c0001t0001g0165 a0001c0001t0001g0190 others(13): Show |
20 | HG00621.hp1 HG00738.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.183-3547dupA | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136681102 | |||||||
chr9:136681102 | CT | C | 22 | a0001c0001t0001g0091 a0001c0001t0001g0157 a0001c0001t0001g0159 others(19): Show |
24 | HG01074.hp2 HG01192.hp2 HG01943.hp2 others(21): Show |
intron_variant | MODIFIER | c.183-3547delA | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136681102 | |||||||
chr9:136681205 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.183-3649C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136681205 | |||||||
chr9:136681341 | G | A | 1 | a0001c0001t0001g0045 | 2 | NA19064.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.183-3785C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136681341 | |||||||
chr9:136681377 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(209): Show |
355 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(352): Show |
intron_variant | MODIFIER | c.183-3821A>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136681377 | |||||||
chr9:136681382 | T | C | 1 | a0001c0001t0002g0162 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.183-3826A>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136681382 | |||||||
chr9:136681427 | A | C | 5 | a0001c0001t0002g0049 a0001c0001t0002g0187 a0001c0001t0002g0207 others(2): Show |
10 | HG01891.hp1 HG01891.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.183-3871T>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136681427 | |||||||
chr9:136681427 | A | T | 51 | a0001c0001t0001g0003 a0001c0001t0001g0051 a0001c0001t0001g0052 others(48): Show |
78 | HG00408.hp1 HG00639.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.183-3871T>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136681427 | |||||||
chr9:136681447 | C | T | 1 | a0001c0001t0002g0093 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.183-3891G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136681447 | |||||||
chr9:136681448 | G | A | 2 | a0001c0001t0002g0207 a0001c0001t0003g0015 |
5 | HG01891.hp2 HG02886.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.183-3892C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136681448 | |||||||
chr9:136681487 | G | A | 2 | a0001c0001t0002g0049 a0001c0001t0002g0187 |
3 | HG02717.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.183-3931C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136681487 | |||||||
chr9:136681516 | T | C | 1 | a0001c0001t0002g0185 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.183-3960A>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136681516 | |||||||
chr9:136681577 | A | C | 2 | a0001c0001t0003g0198 a0003c0005t0015g0053 |
3 | HG01109.hp2 HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.183-4021T>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136681577 | |||||||
chr9:136681743 | G | A | 1 | a0001c0001t0002g0163 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.183-4187C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136681743 | |||||||
chr9:136681946 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.183-4390T>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136681946 | |||||||
chr9:136681953 | C | T | 1 | a0001c0001t0002g0076 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.183-4397G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136681953 | |||||||
chr9:136681954 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.183-4398C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136681954 | |||||||
chr9:136682017 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0003g0166 |
2 | NA18947.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.183-4461C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136682017 | |||||||
chr9:136682049 | G | A | 3 | a0001c0001t0002g0049 a0001c0001t0002g0187 a0001c0001t0018g0188 |
4 | HG02258.hp2 HG02717.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.183-4493C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136682049 | |||||||
chr9:136682074 | G | C | 28 | a0001c0001t0001g0003 a0001c0001t0001g0051 a0001c0001t0001g0052 others(25): Show |
48 | HG00408.hp1 HG00639.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.183-4518C>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136682074 | |||||||
chr9:136682142 | G | A | 3 | a0001c0001t0001g0210 a0001c0001t0003g0208 a0001c0001t0003g0209 |
3 | HG02451.hp2 HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.183-4586C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136682142 | |||||||
chr9:136682169 | C | T | 5 | a0001c0001t0001g0085 a0001c0001t0001g0089 a0001c0001t0001g0090 others(2): Show |
5 | HG02071.hp1 HG02132.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.183-4613G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136682169 | |||||||
chr9:136682230 | G | T | 7 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0002g0204 others(4): Show |
8 | HG01256.hp1 HG02055.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.183-4674C>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136682230 | |||||||
chr9:136682301 | C | T | 1 | a0001c0001t0005g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.183-4745G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136682301 | |||||||
chr9:136682312 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0219 others(1): Show |
12 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.183-4756C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136682312 | |||||||
chr9:136682323 | C | T | 3 | a0001c0001t0002g0049 a0001c0001t0002g0187 a0001c0001t0018g0188 |
4 | HG02258.hp2 HG02717.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.183-4767G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136682323 | |||||||
chr9:136682341 | T | G | 6 | a0001c0001t0002g0049 a0001c0001t0002g0187 a0001c0001t0003g0198 others(3): Show |
8 | HG01109.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.183-4785A>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136682341 | |||||||
chr9:136682342 | C | T | 6 | a0001c0001t0002g0049 a0001c0001t0002g0187 a0001c0001t0003g0198 others(3): Show |
8 | HG01109.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.183-4786G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136682342 | |||||||
chr9:136682404 | G | A | 4 | a0001c0001t0002g0216 a0001c0001t0003g0023 a0001c0001t0003g0214 others(1): Show |
6 | HG01123.hp2 HG02922.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.182+4772C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136682404 | |||||||
chr9:136682515 | G | GTACCCC | 6 | a0001c0001t0002g0049 a0001c0001t0002g0187 a0001c0001t0003g0198 others(3): Show |
8 | HG01109.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.182+4660_182+4661i others(8): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136682515 | |||||||
chr9:136682539 | C | T | 1 | a0001c0001t0002g0076 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.182+4637G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136682539 | |||||||
chr9:136682638 | A | G | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(220): Show |
371 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(368): Show |
intron_variant | MODIFIER | c.182+4538T>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136682638 | |||||||
chr9:136682734 | C | G | 2 | a0001c0001t0002g0080 a0001c0001t0002g0088 |
2 | HG03017.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.182+4442G>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136682734 | |||||||
chr9:136682740 | C | T | 1 | a0001c0001t0002g0218 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.182+4436G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136682740 | |||||||
chr9:136682792 | C | T | 12 | a0002c0002t0006g0025 a0002c0002t0006g0057 a0002c0002t0006g0059 others(9): Show |
14 | HG00609.hp1 HG01069.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.182+4384G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136682792 | |||||||
chr9:136682929 | C | T | 1 | a0001c0001t0005g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.182+4247G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136682929 | |||||||
chr9:136683066 | G | GC | 6 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0052 others(3): Show |
6 | HG02615.hp1 HG03831.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.182+4109_182+4110i others(3): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136683066 | |||||||
chr9:136683067 | T | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(217): Show |
364 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(361): Show |
intron_variant | MODIFIER | c.182+4109A>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136683067 | |||||||
chr9:136683067 | T | G | 6 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0052 others(3): Show |
6 | HG02615.hp1 HG03831.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.182+4109A>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136683067 | |||||||
chr9:136683068 | G | C | 2 | a0001c0001t0002g0186 a0001c0001t0005g0087 |
2 | HG02572.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.182+4108C>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136683068 | |||||||
chr9:136683074 | G | T | 2 | a0001c0001t0002g0049 a0001c0001t0002g0187 |
3 | HG02717.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.182+4102C>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136683074 | |||||||
chr9:136683077 | G | T | 1 | a0001c0001t0002g0076 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.182+4099C>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136683077 | |||||||
chr9:136683232 | A | G | 2 | a0001c0001t0001g0225 a0001c0004t0007g0056 |
3 | HG01256.hp1 HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.182+3944T>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136683232 | |||||||
chr9:136683235 | G | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(220): Show |
371 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(368): Show |
intron_variant | MODIFIER | c.182+3941C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136683235 | |||||||
chr9:136683581 | C | T | 1 | a0001c0001t0005g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.182+3595G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136683581 | |||||||
chr9:136683631 | G | T | 1 | a0001c0001t0005g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.182+3545C>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136683631 | |||||||
chr9:136683644 | G | A | 4 | a0001c0001t0002g0049 a0001c0001t0002g0187 a0001c0001t0003g0073 others(1): Show |
5 | HG02258.hp2 HG02717.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.182+3532C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136683644 | |||||||
chr9:136683664 | T | C | 1 | a0002c0002t0006g0065 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.182+3512A>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136683664 | |||||||
chr9:136683683 | C | T | 1 | a0001c0001t0003g0073 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.182+3493G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136683683 | |||||||
chr9:136683763 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.182+3413G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136683763 | |||||||
chr9:136683771 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.182+3405C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136683771 | |||||||
chr9:136683793 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.182+3383G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136683793 | |||||||
chr9:136683839 | C | A | 1 | a0001c0001t0001g0083 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.182+3337G>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136683839 | |||||||
chr9:136683842 | C | T | 1 | a0001c0001t0002g0186 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.182+3334G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136683842 | |||||||
chr9:136683843 | G | A | 1 | a0001c0001t0002g0226 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.182+3333C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136683843 | |||||||
chr9:136683862 | G | A | 3 | a0001c0001t0001g0170 a0001c0003t0001g0171 a0001c0003t0001g0172 |
3 | NA18940.hp1 NA18999.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.182+3314C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136683862 | |||||||
chr9:136683898 | C | T | 2 | a0001c0001t0002g0204 a0001c0001t0002g0205 |
2 | HG02055.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.182+3278G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136683898 | |||||||
chr9:136683945 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.182+3231C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136683945 | |||||||
chr9:136683966 | T | C | 1 | a0001c0001t0013g0174 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.182+3210A>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136683966 | |||||||
chr9:136683970 | G | A | 1 | a0007c0009t0001g0175 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.182+3206C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136683970 | |||||||
chr9:136684133 | G | A | 2 | a0001c0001t0004g0176 a0001c0001t0004g0177 |
2 | NA18967.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.182+3043C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684133 | |||||||
chr9:136684226 | G | A | 3 | a0001c0001t0002g0049 a0001c0001t0002g0187 a0001c0001t0018g0188 |
4 | HG02258.hp2 HG02717.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.182+2950C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684226 | |||||||
chr9:136684355 | G | A | 4 | a0001c0001t0002g0049 a0001c0001t0002g0187 a0001c0001t0003g0073 others(1): Show |
5 | HG02258.hp2 HG02717.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.182+2821C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684355 | |||||||
chr9:136684395 | G | A | 1 | a0001c0001t0021g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.182+2781C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684395 | |||||||
chr9:136684396 | C | T | 15 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0213 others(12): Show |
29 | HG01074.hp1 HG01106.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.182+2780G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684396 | |||||||
chr9:136684404 | A | G | 4 | a0001c0001t0002g0049 a0001c0001t0002g0187 a0001c0001t0003g0073 others(1): Show |
5 | HG02258.hp2 HG02717.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.182+2772T>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684404 | |||||||
chr9:136684428 | G | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(155): Show |
267 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(264): Show |
intron_variant | MODIFIER | c.182+2748C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684428 | |||||||
chr9:136684476 | C | G | 4 | a0001c0001t0002g0049 a0001c0001t0002g0187 a0001c0001t0003g0073 others(1): Show |
5 | HG02258.hp2 HG02717.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.182+2700G>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684476 | |||||||
chr9:136684485 | T | C | 4 | a0001c0001t0002g0049 a0001c0001t0002g0187 a0001c0001t0003g0073 others(1): Show |
5 | HG02258.hp2 HG02717.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.182+2691A>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684485 | |||||||
chr9:136684493 | C | G | 1 | a0001c0001t0001g0083 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.182+2683G>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684493 | |||||||
chr9:136684512 | C | T | 2 | a0001c0001t0001g0081 a0001c0014t0001g0082 |
2 | NA18979.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.182+2664G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684512 | |||||||
chr9:136684516 | G | A | 6 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0219 others(3): Show |
16 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.182+2660C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684516 | |||||||
chr9:136684520 | A | G | 1 | a0001c0001t0002g0080 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.182+2656T>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684520 | |||||||
chr9:136684527 | G | A | 1 | a0001c0001t0002g0186 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.182+2649C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684527 | |||||||
chr9:136684543 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.182+2633C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684543 | |||||||
chr9:136684554 | C | T | 1 | a0001c0001t0003g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.182+2622G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684554 | |||||||
chr9:136684558 | G | C | 14 | a0002c0002t0005g0027 a0002c0002t0005g0070 a0002c0002t0006g0025 others(11): Show |
17 | HG00609.hp1 HG01069.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.182+2618C>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684558 | |||||||
chr9:136684594 | CAG | C | 4 | a0001c0001t0002g0049 a0001c0001t0002g0187 a0001c0001t0003g0073 others(1): Show |
5 | HG02258.hp2 HG02717.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.182+2580_182+2581d others(4): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684594 | |||||||
chr9:136684650 | C | G | 6 | a0001c0001t0002g0049 a0001c0001t0002g0187 a0001c0001t0002g0204 others(3): Show |
7 | HG02055.hp2 HG02258.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.182+2526G>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684650 | |||||||
chr9:136684677 | A | T | 1 | a0002c0002t0006g0057 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.182+2499T>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684677 | |||||||
chr9:136684678 | G | A | 12 | a0001c0001t0001g0008 a0001c0001t0001g0180 a0001c0001t0001g0181 others(9): Show |
21 | HG00544.hp1 HG00544.hp2 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.182+2498C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684678 | |||||||
chr9:136684696 | G | A | 2 | a0001c0001t0001g0225 a0001c0004t0007g0056 |
3 | HG01256.hp1 HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.182+2480C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684696 | |||||||
chr9:136684723 | C | T | 2 | a0001c0001t0002g0204 a0001c0001t0002g0205 |
2 | HG02055.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.182+2453G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684723 | |||||||
chr9:136684749 | C | G | 1 | a0001c0001t0008g0079 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.182+2427G>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684749 | |||||||
chr9:136684750 | T | C | 1 | a0001c0001t0008g0079 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.182+2426A>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684750 | |||||||
chr9:136684752 | G | T | 1 | a0001c0001t0008g0079 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.182+2424C>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684752 | |||||||
chr9:136684798 | C | G | 17 | a0001c0001t0001g0003 a0001c0001t0001g0051 a0001c0001t0001g0052 others(14): Show |
33 | HG00408.hp1 HG00639.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.182+2378G>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684798 | |||||||
chr9:136684805 | G | A | 3 | a0001c0001t0002g0049 a0001c0001t0002g0187 a0001c0001t0018g0188 |
4 | HG02258.hp2 HG02717.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.182+2371C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684805 | |||||||
chr9:136684820 | C | T | 3 | a0001c0001t0002g0049 a0001c0001t0002g0187 a0001c0001t0018g0188 |
4 | HG02258.hp2 HG02717.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.182+2356G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684820 | |||||||
chr9:136684822 | C | T | 3 | a0001c0001t0002g0049 a0001c0001t0002g0187 a0001c0001t0018g0188 |
4 | HG02258.hp2 HG02717.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.182+2354G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684822 | |||||||
chr9:136684852 | C | T | 1 | a0004c0006t0003g0201 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.182+2324G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136684852 | |||||||
chr9:136685009 | T | A | 8 | a0001c0001t0001g0210 a0001c0001t0002g0207 a0001c0001t0003g0015 others(5): Show |
12 | HG01891.hp1 HG01891.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.182+2167A>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136685009 | |||||||
chr9:136685188 | C | T | 1 | a0001c0001t0003g0073 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.182+1988G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136685188 | |||||||
chr9:136685203 | C | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(155): Show |
268 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(265): Show |
intron_variant | MODIFIER | c.182+1973G>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136685203 | |||||||
chr9:136685243 | A | G | 1 | a0001c0001t0002g0078 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.182+1933T>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136685243 | |||||||
chr9:136685301 | A | T | 1 | a0001c0001t0002g0077 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.182+1875T>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136685301 | |||||||
chr9:136685385 | G | T | 1 | a0001c0001t0003g0073 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.182+1791C>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136685385 | |||||||
chr9:136685441 | T | C | 1 | a0001c0001t0003g0073 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.182+1735A>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136685441 | |||||||
chr9:136685443 | G | C | 1 | a0001c0001t0002g0203 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.182+1733C>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136685443 | |||||||
chr9:136685539 | G | C | 1 | a0001c0001t0002g0218 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.182+1637C>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136685539 | |||||||
chr9:136685630 | G | A | 35 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0213 others(32): Show |
52 | HG00609.hp1 HG01069.hp2 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.182+1546C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136685630 | |||||||
chr9:136685678 | C | T | 1 | a0001c0001t0003g0073 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.182+1498G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136685678 | |||||||
chr9:136685703 | A | G | 1 | a0001c0001t0002g0076 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.182+1473T>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136685703 | |||||||
chr9:136685771 | G | A | 15 | a0002c0002t0005g0027 a0002c0002t0005g0070 a0002c0002t0006g0025 others(12): Show |
18 | HG00609.hp1 HG01069.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.182+1405C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136685771 | |||||||
chr9:136685775 | A | AG | 4 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0219 others(1): Show |
12 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.182+1400dupC | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136685775 | |||||||
chr9:136685936 | G | A | 1 | a0001c0001t0003g0073 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.182+1240C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136685936 | |||||||
chr9:136685982 | C | T | 1 | a0001c0001t0003g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.182+1194G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136685982 | |||||||
chr9:136686084 | G | C | 1 | a0001c0001t0003g0073 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.182+1092C>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136686084 | |||||||
chr9:136686113 | C | G | 6 | a0001c0001t0001g0210 a0001c0001t0002g0207 a0001c0001t0003g0015 others(3): Show |
10 | HG01891.hp1 HG01891.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.182+1063G>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136686113 | |||||||
chr9:136686488 | T | A | 1 | a0001c0001t0003g0206 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.182+688A>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136686488 | |||||||
chr9:136686493 | G | A | 1 | a0001c0001t0003g0073 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.182+683C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136686493 | |||||||
chr9:136686507 | A | G | 1 | a0001c0001t0003g0073 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.182+669T>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136686507 | |||||||
chr9:136686641 | A | AAGAGGAA others(4): Show |
1 | a0001c0001t0003g0073 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.182+534_182+535ins others(11): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136686641 | |||||||
chr9:136686649 | A | G | 1 | a0001c0001t0003g0073 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.182+527T>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136686649 | |||||||
chr9:136686711 | G | C | 1 | a0001c0001t0003g0073 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.182+465C>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136686711 | |||||||
chr9:136686714 | CGGAG | C | 6 | a0001c0001t0001g0210 a0001c0001t0002g0207 a0001c0001t0003g0015 others(3): Show |
10 | HG01891.hp1 HG01891.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.182+458_182+461del others(4): Show |
AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136686714 | |||||||
chr9:136686769 | G | A | 15 | a0002c0002t0005g0027 a0002c0002t0005g0070 a0002c0002t0006g0025 others(12): Show |
18 | HG00609.hp1 HG01069.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.182+407C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136686769 | |||||||
chr9:136686777 | T | TC | 4 | a0001c0001t0001g0219 a0002c0002t0005g0070 a0002c0002t0009g0067 others(1): Show |
4 | HG01243.hp1 HG03516.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.182+398dupG | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136686777 | |||||||
chr9:136686782 | G | C | 29 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0213 others(26): Show |
45 | HG00609.hp1 HG01069.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.182+394C>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136686782 | |||||||
chr9:136686796 | G | C | 3 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0004g0222 |
3 | NA18945.hp1 NA18993.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.182+380C>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136686796 | |||||||
chr9:136686805 | G | T | 1 | a0001c0001t0003g0073 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.182+371C>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136686805 | |||||||
chr9:136686858 | C | T | 1 | a0001c0001t0012g0074 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.182+318G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136686858 | |||||||
chr9:136686871 | A | G | 1 | a0001c0001t0003g0073 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.182+305T>C | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136686871 | |||||||
chr9:136687077 | G | C | 19 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0004t0007g0056 others(16): Show |
23 | HG00609.hp1 HG01069.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.182+99C>G | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136687077 | |||||||
chr9:136687089 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.182+87G>A | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136687089 | |||||||
chr9:136687161 | G | A | 1 | a0001c0001t0002g0226 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.182+15C>T | AGPAT2 | ENSG00000169692.14 | transcript | ENST00000371696.7 | protein_coding | 1/5 | chr9 | 136687161 |