Item | Value |
---|---|
geneid | 79888 |
ensemblid | ENSG00000153395.10 |
hgncid | 25718 |
symbol | LPCAT1 |
name | lysophosphatidylcholine acyltransferase 1 |
refseq_nuc | NM_024830.5 |
refseq_prot | NP_079106.3 |
ensembl_nuc | ENST00000283415.4 |
ensembl_prot | ENSP00000283415.3 |
mane_status | MANE Select |
chr | chr5 |
start | 1461427 |
end | 1523960 |
strand | - |
ver | v1.2 |
region | chr5:1461427-1523960 |
region5000 | chr5:1456427-1528960 |
regionname0 | LPCAT1_chr5_1461427_1523960 |
regionname5000 | LPCAT1_chr5_1456427_1528960 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 534 | 328 | 83 | 54 | 146 | 11 | 32 | 105 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | MRLRG others(529): Show |
chr5 | 1456427 | 1528960 |
a0002 | 0/0 | 534 | 47 | 8 | 17 | 15 | 1 | 6 | 12 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | MRLRG others(529): Show |
chr5 | 1456427 | 1528960 |
a0003 | 0/0 | 534 | 6 | 0 | 1 | 0 | 4 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | MRLRG others(529): Show |
chr5 | 1456427 | 1528960 |
a0004 | 0/0 | 534 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | MRLRG others(529): Show |
chr5 | 1456427 | 1528960 |
a0005 | 0/0 | 534 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | MRLRG others(529): Show |
chr5 | 1456427 | 1528960 |
a0006 | 0/0 | 534 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | MRLRG others(529): Show |
chr5 | 1456427 | 1528960 |
a0007 | 0/0 | 534 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | MRLRG others(529): Show |
chr5 | 1456427 | 1528960 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1602 | 126 | 31 | 27 | 49 | 5 | 12 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | ATGAG others(1597): Show |
chr5 | 1456427 | 1528960 | ||
a0001c0002 | 0/0 | 1602 | 84 | 25 | 11 | 35 | 4 | 9 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | ATGAG others(1597): Show |
chr5 | 1456427 | 1528960 | ||
a0001c0003 | 0/0 | 1602 | 63 | 12 | 6 | 37 | 1 | 7 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | ATGAG others(1597): Show |
chr5 | 1456427 | 1528960 | ||
a0001c0004 | 0/0 | 1602 | 39 | 7 | 5 | 23 | 0 | 4 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | ATGAG others(1597): Show |
chr5 | 1456427 | 1528960 | ||
a0001c0007 | 0/0 | 1602 | 7 | 2 | 5 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | ATGAG others(1597): Show |
chr5 | 1456427 | 1528960 | ||
a0001c0009 | 0/0 | 1602 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | ATGAG others(1597): Show |
chr5 | 1456427 | 1528960 | ||
a0001c0010 | 0/0 | 1602 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | ATGAG others(1597): Show |
chr5 | 1456427 | 1528960 | ||
a0001c0015 | 0/0 | 1602 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | ATGAG others(1597): Show |
chr5 | 1456427 | 1528960 | ||
a0001c0018 | 0/0 | 1602 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | ATGAG others(1597): Show |
chr5 | 1456427 | 1528960 | ||
a0001c0019 | 0/0 | 1602 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | ATGAG others(1597): Show |
chr5 | 1456427 | 1528960 | ||
a0001c0020 | 0/0 | 1602 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | ATGAG others(1597): Show |
chr5 | 1456427 | 1528960 | ||
a0001c0021 | 0/0 | 1602 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | ATGAG others(1597): Show |
chr5 | 1456427 | 1528960 | ||
a0002c0005 | 0/0 | 1602 | 36 | 4 | 14 | 13 | 1 | 4 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | ATGAG others(1597): Show |
chr5 | 1456427 | 1528960 | ||
a0002c0006 | 0/0 | 1602 | 10 | 3 | 3 | 2 | 0 | 2 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | ATGAG others(1597): Show |
chr5 | 1456427 | 1528960 | ||
a0002c0016 | 0/0 | 1602 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | ATGAG others(1597): Show |
chr5 | 1456427 | 1528960 | ||
a0003c0008 | 0/0 | 1602 | 6 | 0 | 1 | 0 | 4 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | ATGAG others(1597): Show |
chr5 | 1456427 | 1528960 | ||
a0004c0012 | 0/0 | 1602 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | ATGAG others(1597): Show |
chr5 | 1456427 | 1528960 | ||
a0004c0014 | 0/0 | 1602 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | ATGAG others(1597): Show |
chr5 | 1456427 | 1528960 | ||
a0005c0013 | 0/0 | 1602 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | ATGAG others(1597): Show |
chr5 | 1456427 | 1528960 | ||
a0006c0017 | 0/0 | 1602 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | ATGAG others(1597): Show |
chr5 | 1456427 | 1528960 | ||
a0007c0011 | 0/0 | 1602 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | ATGAG others(1597): Show |
chr5 | 1456427 | 1528960 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 3945 | 62 | 12 | 14 | 29 | 2 | 5 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0001t0004 | 0/1 | 3945 | 22 | 5 | 8 | 0 | 1 | 7 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0001t0005 | 1/0 | 3945 | 17 | 2 | 2 | 12 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0001t0006 | 0/0 | 3945 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0001t0007 | 0/0 | 3945 | 10 | 9 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0001t0011 | 0/0 | 3945 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0001t0013 | 0/0 | 3945 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0001t0018 | 0/0 | 3945 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0001t0019 | 0/0 | 3945 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0001t0020 | 0/0 | 3945 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0001t0021 | 0/0 | 3944 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3939): Show |
chr5 | 1456427 | 1528960 |
a0001c0001t0025 | 0/0 | 3945 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0001t0026 | 0/0 | 3945 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0001t0027 | 0/0 | 3945 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0001t0028 | 0/0 | 3945 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0001t0029 | 0/0 | 3945 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0001t0030 | 0/0 | 3945 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0002t0001 | 0/0 | 3945 | 54 | 17 | 6 | 25 | 2 | 4 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0002t0002 | 0/0 | 3945 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0002t0004 | 0/0 | 3945 | 6 | 6 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0002t0006 | 0/0 | 3945 | 10 | 0 | 0 | 9 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0002t0008 | 0/0 | 3944 | 9 | 0 | 3 | 0 | 2 | 4 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3939): Show |
chr5 | 1456427 | 1528960 |
a0001c0002t0015 | 0/0 | 3944 | 2 | 1 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3939): Show |
chr5 | 1456427 | 1528960 |
a0001c0002t0023 | 0/0 | 3944 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3939): Show |
chr5 | 1456427 | 1528960 |
a0001c0002t0036 | 0/0 | 3944 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3939): Show |
chr5 | 1456427 | 1528960 |
a0001c0003t0001 | 0/0 | 3945 | 31 | 5 | 2 | 19 | 1 | 4 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0003t0006 | 0/0 | 3945 | 20 | 0 | 4 | 15 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0003t0009 | 0/0 | 3946 | 7 | 7 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3941): Show |
chr5 | 1456427 | 1528960 |
a0001c0003t0014 | 0/0 | 3945 | 2 | 0 | 0 | 0 | 0 | 2 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0003t0016 | 0/0 | 3945 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0003t0033 | 0/0 | 3945 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0004t0002 | 0/0 | 3945 | 11 | 2 | 1 | 8 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0004t0004 | 0/0 | 3945 | 4 | 0 | 1 | 0 | 0 | 3 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0004t0005 | 0/0 | 3945 | 15 | 3 | 3 | 9 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0004t0010 | 0/0 | 3945 | 4 | 0 | 0 | 4 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0004t0011 | 0/0 | 3945 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0004t0013 | 0/0 | 3945 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0004t0017 | 0/0 | 3931 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3926): Show |
chr5 | 1456427 | 1528960 |
a0001c0004t0024 | 0/0 | 3945 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0007t0004 | 0/0 | 3945 | 4 | 0 | 4 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0007t0005 | 0/0 | 3945 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0007t0007 | 0/0 | 3945 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0007t0022 | 0/0 | 3944 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3939): Show |
chr5 | 1456427 | 1528960 |
a0001c0009t0012 | 0/0 | 3944 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3939): Show |
chr5 | 1456427 | 1528960 |
a0001c0010t0001 | 0/0 | 3945 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0015t0004 | 0/0 | 3945 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0018t0010 | 0/0 | 3945 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0019t0012 | 0/0 | 3944 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3939): Show |
chr5 | 1456427 | 1528960 |
a0001c0020t0001 | 0/0 | 3945 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0001c0021t0002 | 0/0 | 3945 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0002c0005t0003 | 0/0 | 3945 | 32 | 4 | 12 | 11 | 1 | 4 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0002c0005t0004 | 0/0 | 3945 | 2 | 0 | 1 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0002c0005t0031 | 0/0 | 3945 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0002c0005t0037 | 0/0 | 3945 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0002c0006t0003 | 0/0 | 3945 | 8 | 3 | 3 | 0 | 0 | 2 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0002c0006t0032 | 0/0 | 3945 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0002c0006t0038 | 0/0 | 3945 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0002c0016t0003 | 0/0 | 3945 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0003c0008t0002 | 0/0 | 3945 | 6 | 0 | 1 | 0 | 4 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0004c0012t0035 | 0/0 | 3944 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3939): Show |
chr5 | 1456427 | 1528960 |
a0004c0014t0034 | 0/0 | 3944 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3939): Show |
chr5 | 1456427 | 1528960 |
a0005c0013t0003 | 0/0 | 3945 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0006c0017t0001 | 0/0 | 3945 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
a0007c0011t0001 | 0/0 | 3945 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | CCCGC others(3940): Show |
chr5 | 1456427 | 1528960 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0024 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0344 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0006g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0007g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0007g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0007g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0007g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0007g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0007g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0007g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0007g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0007g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0011g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0011g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0013g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0013g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0018g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0019g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0020g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0021g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0025g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0026g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0027g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0028g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0029g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0030g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0006g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0006g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0006g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0006g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0006g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0006g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0006g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0006g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0006g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0008g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0008g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0008g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0008g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0008g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0008g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0008g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0008g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0015g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0015g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0023g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0036g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0009g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0009g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0009g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0009g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0009g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0009g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0014g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0014g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0016g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0016g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0033g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0004g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0004g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0004g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0005g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0005g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0005g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0005g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0010g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0010g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0011g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0011g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0013g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0017g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0024g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0007t0004g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0007t0004g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0007t0004g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0007t0004g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0007t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0007t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0007t0022g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0009t0012g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0009t0012g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0010t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0010t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0015t0004g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0018t0010g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0019t0012g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0020t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0021t0002g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0031g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0037g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0006t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0006t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0006t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0006t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0006t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0006t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0006t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0006t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0006t0032g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0006t0038g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0016t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0003c0008t0002g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0003c0008t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0003c0008t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0003c0008t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0003c0008t0002g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0004c0012t0035g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0004c0014t0034g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0005c0013t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0006c0017t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0007c0011t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0015 | t0004 | g0252 | EUR | GBR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00099 | hp2 | a0003 | c0008 | t0002 | g0009 | EUR | GBR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00140 | hp1 | a0003 | c0008 | t0002 | g0047 | EUR | GBR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00140 | hp2 | a0001 | c0001 | t0029 | g0113 | EUR | GBR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00280 | hp1 | a0001 | c0002 | t0008 | g0130 | EUR | FIN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0221 | EUR | FIN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0358 | EUR | FIN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00323 | hp2 | a0003 | c0008 | t0002 | g0191 | EUR | FIN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0322 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0339 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00423 | hp2 | a0001 | c0003 | t0001 | g0065 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00438 | hp1 | a0001 | c0001 | t0005 | g0316 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00438 | hp2 | a0001 | c0004 | t0002 | g0355 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00544 | hp1 | a0002 | c0005 | t0003 | g0022 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00544 | hp2 | a0001 | c0003 | t0001 | g0226 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00558 | hp1 | a0001 | c0003 | t0006 | g0178 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00597 | hp1 | a0001 | c0001 | t0005 | g0058 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00597 | hp2 | a0001 | c0003 | t0033 | g0350 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00609 | hp2 | a0001 | c0004 | t0002 | g0341 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00621 | hp1 | a0001 | c0003 | t0006 | g0225 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00621 | hp2 | a0001 | c0003 | t0001 | g0336 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00639 | hp1 | a0002 | c0005 | t0031 | g0217 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0300 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00642 | hp1 | a0002 | c0005 | t0003 | g0188 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0051 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00673 | hp1 | a0002 | c0005 | t0004 | g0153 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00673 | hp2 | a0001 | c0003 | t0001 | g0310 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0222 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00733 | hp2 | a0002 | c0005 | t0004 | g0146 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00735 | hp1 | a0003 | c0008 | t0002 | g0125 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0345 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0044 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0360 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01069 | hp2 | a0001 | c0004 | t0004 | g0068 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01070 | hp1 | a0002 | c0006 | t0003 | g0202 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01074 | hp2 | a0002 | c0006 | t0003 | g0104 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01081 | hp1 | a0002 | c0005 | t0003 | g0328 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0026 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01099 | hp1 | a0002 | c0005 | t0003 | g0103 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01099 | hp2 | a0001 | c0003 | t0001 | g0270 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01106 | hp1 | a0001 | c0007 | t0004 | g0257 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0156 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01109 | hp1 | a0002 | c0005 | t0003 | g0184 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01109 | hp2 | a0001 | c0001 | t0026 | g0025 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01167 | hp1 | a0001 | c0003 | t0006 | g0231 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01167 | hp2 | a0002 | c0005 | t0003 | g0102 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01168 | hp1 | a0001 | c0001 | t0004 | g0135 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01168 | hp2 | a0001 | c0003 | t0006 | g0010 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01175 | hp1 | a0002 | c0005 | t0003 | g0301 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0329 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0080 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01192 | hp2 | a0001 | c0004 | t0005 | g0007 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0298 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0128 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01255 | hp2 | a0001 | c0002 | t0008 | g0155 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01256 | hp1 | a0001 | c0007 | t0004 | g0255 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01256 | hp2 | a0001 | c0002 | t0008 | g0004 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01257 | hp1 | a0001 | c0007 | t0022 | g0256 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01257 | hp2 | a0001 | c0004 | t0005 | g0101 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01258 | hp1 | a0001 | c0002 | t0008 | g0004 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01258 | hp2 | a0001 | c0004 | t0005 | g0159 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01261 | hp1 | a0001 | c0004 | t0002 | g0262 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0215 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01346 | hp1 | a0001 | c0007 | t0004 | g0254 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01346 | hp2 | a0001 | c0001 | t0028 | g0348 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01358 | hp1 | a0001 | c0007 | t0004 | g0218 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01358 | hp2 | a0001 | c0002 | t0036 | g0365 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01361 | hp1 | a0001 | c0001 | t0004 | g0299 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01361 | hp2 | a0001 | c0003 | t0001 | g0148 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01433 | hp1 | a0002 | c0005 | t0003 | g0081 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01433 | hp2 | a0001 | c0001 | t0005 | g0166 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01496 | hp1 | a0001 | c0001 | t0007 | g0281 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01496 | hp2 | a0002 | c0005 | t0003 | g0110 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01515 | hp1 | a0001 | c0002 | t0008 | g0114 | EUR | IBS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0239 | EUR | IBS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01516 | hp1 | a0003 | c0008 | t0002 | g0009 | EUR | IBS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0077 | EUR | IBS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01884 | hp1 | a0001 | c0004 | t0002 | g0244 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01884 | hp2 | a0001 | c0001 | t0021 | g0246 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01891 | hp1 | a0002 | c0005 | t0003 | g0149 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0302 | AMR | PEL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01928 | hp2 | a0002 | c0005 | t0003 | g0211 | AMR | PEL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01943 | hp1 | a0001 | c0001 | t0005 | g0171 | AMR | PEL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01943 | hp2 | a0002 | c0005 | t0003 | g0296 | AMR | PEL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01952 | hp1 | a0001 | c0003 | t0006 | g0157 | AMR | PEL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PEL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01975 | hp1 | a0002 | c0005 | t0003 | g0049 | AMR | PEL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01975 | hp2 | a0001 | c0002 | t0015 | g0297 | AMR | PEL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0293 | AMR | PEL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01978 | hp2 | a0002 | c0005 | t0003 | g0186 | AMR | PEL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01981 | hp1 | a0002 | c0006 | t0003 | g0200 | AMR | PEL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0308 | AMR | PEL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02004 | hp1 | a0001 | c0003 | t0006 | g0010 | AMR | PEL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02004 | hp2 | a0001 | c0001 | t0004 | g0134 | AMR | PEL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02015 | hp1 | a0001 | c0001 | t0005 | g0356 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02015 | hp2 | a0001 | c0004 | t0005 | g0219 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0307 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02040 | hp2 | a0001 | c0003 | t0006 | g0170 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02055 | hp1 | a0002 | c0016 | t0003 | g0147 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0245 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02056 | hp2 | a0001 | c0001 | t0018 | g0020 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02080 | hp1 | a0001 | c0001 | t0005 | g0314 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02080 | hp2 | a0001 | c0003 | t0001 | g0131 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02083 | hp1 | a0001 | c0001 | t0005 | g0357 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02083 | hp2 | a0002 | c0005 | t0003 | g0241 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02129 | hp1 | a0001 | c0003 | t0001 | g0325 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0122 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02132 | hp1 | a0001 | c0002 | t0006 | g0056 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02135 | hp1 | a0001 | c0004 | t0005 | g0007 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02135 | hp2 | a0001 | c0021 | t0002 | g0364 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02145 | hp1 | a0001 | c0001 | t0007 | g0034 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02145 | hp2 | a0001 | c0004 | t0017 | g0017 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | CDX | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02155 | hp2 | a0001 | c0004 | t0002 | g0117 | EAS | CDX | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02165 | hp1 | a0001 | c0003 | t0001 | g0334 | EAS | CDX | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02165 | hp2 | a0001 | c0003 | t0001 | g0342 | EAS | CDX | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0347 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0251 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0285 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02258 | hp2 | a0002 | c0005 | t0003 | g0330 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02451 | hp1 | a0001 | c0019 | t0012 | g0278 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02451 | hp2 | a0001 | c0003 | t0001 | g0279 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02523 | hp1 | a0001 | c0003 | t0001 | g0343 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02572 | hp1 | a0001 | c0001 | t0007 | g0138 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0132 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02602 | hp2 | a0001 | c0002 | t0006 | g0203 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0275 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02615 | hp2 | a0001 | c0009 | t0012 | g0116 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0076 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0250 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02630 | hp2 | a0001 | c0004 | t0005 | g0029 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0242 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02647 | hp2 | a0001 | c0004 | t0002 | g0261 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02683 | hp1 | a0001 | c0001 | t0004 | g0083 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02683 | hp2 | a0002 | c0005 | t0003 | g0361 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02698 | hp1 | a0002 | c0005 | t0003 | g0192 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0253 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0282 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02717 | hp2 | a0001 | c0003 | t0009 | g0237 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02723 | hp1 | a0001 | c0002 | t0004 | g0271 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02723 | hp2 | a0001 | c0002 | t0023 | g0243 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02735 | hp1 | a0001 | c0002 | t0008 | g0340 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02735 | hp2 | a0001 | c0003 | t0014 | g0019 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02738 | hp1 | a0001 | c0003 | t0001 | g0205 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02738 | hp2 | a0002 | c0006 | t0003 | g0204 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02809 | hp1 | a0001 | c0009 | t0012 | g0107 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0260 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02886 | hp1 | a0001 | c0003 | t0009 | g0238 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0362 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02895 | hp1 | a0001 | c0002 | t0004 | g0100 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0276 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02896 | hp1 | a0001 | c0001 | t0007 | g0003 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02896 | hp2 | a0001 | c0002 | t0004 | g0023 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02897 | hp1 | a0001 | c0001 | t0007 | g0003 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02897 | hp2 | a0001 | c0002 | t0004 | g0150 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0359 | AFR | ESN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02922 | hp2 | a0001 | c0020 | t0001 | g0265 | AFR | ESN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02965 | hp1 | a0002 | c0005 | t0003 | g0030 | AFR | ESN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02965 | hp2 | a0002 | c0006 | t0003 | g0031 | AFR | ESN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0287 | AFR | ESN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | ESN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03017 | hp2 | a0001 | c0003 | t0001 | g0213 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0090 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03041 | hp2 | a0004 | c0014 | t0034 | g0145 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03098 | hp1 | a0004 | c0012 | t0035 | g0280 | AFR | MSL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03098 | hp2 | a0001 | c0003 | t0009 | g0233 | AFR | MSL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03130 | hp1 | a0001 | c0007 | t0007 | g0112 | AFR | ESN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03130 | hp2 | a0001 | c0003 | t0001 | g0267 | AFR | ESN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03139 | hp1 | a0002 | c0006 | t0003 | g0032 | AFR | ESN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03139 | hp2 | a0001 | c0001 | t0007 | g0097 | AFR | ESN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03195 | hp1 | a0001 | c0003 | t0009 | g0041 | AFR | ESN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0263 | AFR | ESN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | MSL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | MSL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03225 | hp1 | a0001 | c0003 | t0001 | g0266 | AFR | MSL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0274 | AFR | MSL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03239 | hp2 | a0002 | c0006 | t0003 | g0214 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03453 | hp1 | a0001 | c0003 | t0009 | g0014 | AFR | MSL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0038 | AFR | MSL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0108 | AFR | MSL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03486 | hp2 | a0002 | c0006 | t0003 | g0142 | AFR | MSL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0012 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03490 | hp2 | a0001 | c0002 | t0008 | g0331 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0216 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03492 | hp2 | a0001 | c0001 | t0004 | g0012 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03516 | hp1 | a0001 | c0004 | t0024 | g0033 | AFR | ESN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0039 | AFR | ESN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0277 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0363 | AFR | MSL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03579 | hp2 | a0001 | c0003 | t0009 | g0268 | AFR | MSL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03654 | hp1 | a0001 | c0001 | t0004 | g0052 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03654 | hp2 | a0001 | c0001 | t0004 | g0075 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0320 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03669 | hp2 | a0001 | c0004 | t0004 | g0209 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0126 | SAS | STU | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03688 | hp2 | a0001 | c0002 | t0008 | g0333 | SAS | STU | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0085 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03704 | hp2 | a0001 | c0004 | t0004 | g0258 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03710 | hp1 | a0002 | c0005 | t0003 | g0326 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03710 | hp2 | a0001 | c0003 | t0006 | g0175 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03834 | hp1 | a0001 | c0001 | t0004 | g0079 | SAS | BEB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03834 | hp2 | a0002 | c0005 | t0003 | g0067 | SAS | BEB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03927 | hp1 | a0003 | c0008 | t0002 | g0351 | SAS | BEB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03927 | hp2 | a0001 | c0003 | t0001 | g0002 | SAS | BEB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0201 | SAS | BEB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03942 | hp2 | a0001 | c0003 | t0001 | g0002 | SAS | BEB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG04204 | hp1 | a0005 | c0013 | t0003 | g0189 | SAS | STU | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG04204 | hp2 | a0001 | c0002 | t0008 | g0332 | SAS | STU | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG04228 | hp1 | a0001 | c0004 | t0013 | g0196 | SAS | STU | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG04228 | hp2 | a0001 | c0003 | t0014 | g0018 | SAS | STU | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18522 | hp1 | a0001 | c0001 | t0007 | g0082 | AFR | YRI | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0284 | AFR | YRI | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18747 | hp1 | a0001 | c0004 | t0011 | g0168 | EAS | CHB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | CHB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18906 | hp1 | a0001 | c0002 | t0004 | g0143 | AFR | YRI | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18906 | hp2 | a0001 | c0010 | t0001 | g0264 | AFR | YRI | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18939 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18939 | hp2 | a0001 | c0004 | t0002 | g0304 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18942 | hp1 | a0002 | c0005 | t0003 | g0338 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18945 | hp1 | a0001 | c0002 | t0006 | g0120 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18945 | hp2 | a0002 | c0005 | t0003 | g0323 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18947 | hp1 | a0002 | c0005 | t0003 | g0118 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18948 | hp1 | a0001 | c0001 | t0005 | g0199 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0319 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18949 | hp1 | a0001 | c0003 | t0006 | g0235 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18952 | hp1 | a0001 | c0001 | t0005 | g0165 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18952 | hp2 | a0001 | c0003 | t0001 | g0093 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18953 | hp1 | a0001 | c0003 | t0006 | g0152 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18956 | hp1 | a0002 | c0006 | t0038 | g0368 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18956 | hp2 | a0001 | c0003 | t0001 | g0228 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18959 | hp2 | a0001 | c0001 | t0005 | g0291 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18963 | hp2 | a0001 | c0003 | t0006 | g0181 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18964 | hp1 | a0001 | c0001 | t0013 | g0042 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18964 | hp2 | a0001 | c0004 | t0010 | g0001 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18967 | hp2 | a0001 | c0002 | t0006 | g0167 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18970 | hp1 | a0001 | c0004 | t0010 | g0001 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18970 | hp2 | a0001 | c0003 | t0016 | g0366 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18971 | hp1 | a0001 | c0004 | t0005 | g0234 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18971 | hp2 | a0001 | c0004 | t0010 | g0001 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18972 | hp1 | a0001 | c0003 | t0001 | g0073 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18972 | hp2 | a0001 | c0001 | t0013 | g0055 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18973 | hp1 | a0001 | c0001 | t0005 | g0321 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18974 | hp2 | a0001 | c0003 | t0006 | g0207 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18977 | hp1 | a0001 | c0003 | t0006 | g0179 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18977 | hp2 | a0001 | c0003 | t0006 | g0074 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0312 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18978 | hp2 | a0002 | c0005 | t0003 | g0169 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18979 | hp1 | a0002 | c0006 | t0032 | g0247 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18982 | hp1 | a0001 | c0001 | t0011 | g0337 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18982 | hp2 | a0001 | c0004 | t0005 | g0154 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18983 | hp1 | a0001 | c0003 | t0001 | g0091 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18983 | hp2 | a0001 | c0004 | t0005 | g0160 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18986 | hp1 | a0001 | c0002 | t0006 | g0208 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18988 | hp1 | a0001 | c0004 | t0005 | g0105 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18988 | hp2 | a0001 | c0002 | t0006 | g0011 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18990 | hp2 | a0001 | c0018 | t0010 | g0177 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18991 | hp1 | a0001 | c0001 | t0011 | g0324 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18991 | hp2 | a0001 | c0004 | t0002 | g0173 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18993 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18993 | hp2 | a0001 | c0003 | t0006 | g0174 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18995 | hp1 | a0001 | c0003 | t0006 | g0190 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18995 | hp2 | a0001 | c0003 | t0001 | g0086 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18997 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18997 | hp2 | a0001 | c0001 | t0006 | g0136 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18999 | hp1 | a0001 | c0003 | t0001 | g0229 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18999 | hp2 | a0001 | c0004 | t0002 | g0335 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19002 | hp1 | a0001 | c0003 | t0001 | g0352 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19002 | hp2 | a0001 | c0001 | t0025 | g0061 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19003 | hp1 | a0001 | c0004 | t0002 | g0109 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19005 | hp2 | a0002 | c0005 | t0003 | g0306 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0349 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19009 | hp1 | a0001 | c0004 | t0002 | g0180 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19009 | hp2 | a0002 | c0005 | t0037 | g0369 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19010 | hp1 | a0002 | c0005 | t0003 | g0015 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19011 | hp1 | a0001 | c0003 | t0016 | g0367 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19011 | hp2 | a0001 | c0004 | t0005 | g0294 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19012 | hp1 | a0002 | c0005 | t0003 | g0119 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19012 | hp2 | a0001 | c0004 | t0005 | g0064 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0283 | AFR | LWK | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19030 | hp2 | a0001 | c0010 | t0001 | g0273 | AFR | LWK | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | LWK | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | LWK | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19056 | hp2 | a0001 | c0004 | t0010 | g0176 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19057 | hp1 | a0001 | c0001 | t0005 | g0292 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19059 | hp1 | a0001 | c0003 | t0006 | g0206 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19059 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19068 | hp1 | a0001 | c0003 | t0001 | g0094 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19070 | hp2 | a0002 | c0005 | t0003 | g0015 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19077 | hp1 | a0001 | c0002 | t0006 | g0313 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19077 | hp2 | a0001 | c0002 | t0006 | g0088 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19079 | hp1 | a0007 | c0011 | t0001 | g0133 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19079 | hp2 | a0001 | c0003 | t0006 | g0158 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0346 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19080 | hp2 | a0001 | c0003 | t0001 | g0162 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19081 | hp1 | a0001 | c0002 | t0006 | g0315 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19081 | hp2 | a0001 | c0001 | t0005 | g0066 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19083 | hp1 | a0001 | c0001 | t0020 | g0305 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19083 | hp2 | a0001 | c0003 | t0006 | g0137 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19084 | hp1 | a0001 | c0003 | t0001 | g0092 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19085 | hp2 | a0001 | c0004 | t0005 | g0063 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19086 | hp1 | a0002 | c0005 | t0003 | g0353 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19086 | hp2 | a0001 | c0002 | t0006 | g0011 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19088 | hp1 | a0001 | c0003 | t0006 | g0172 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19088 | hp2 | a0001 | c0004 | t0011 | g0354 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19240 | hp1 | a0001 | c0004 | t0005 | g0288 | AFR | YRI | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19240 | hp2 | a0001 | c0002 | t0004 | g0096 | AFR | YRI | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA20129 | hp1 | a0002 | c0005 | t0003 | g0050 | AFR | ASW | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA20129 | hp2 | a0001 | c0002 | t0015 | g0286 | AFR | ASW | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA20752 | hp1 | a0001 | c0001 | t0019 | g0072 | EUR | TSI | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0043 | EUR | TSI | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA20805 | hp1 | a0001 | c0003 | t0001 | g0249 | EUR | TSI | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA20805 | hp2 | a0002 | c0005 | t0003 | g0327 | EUR | TSI | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA20905 | hp1 | a0001 | c0004 | t0004 | g0210 | SAS | GIH | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0290 | SAS | GIH | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02109 | hp1 | a0001 | c0007 | t0005 | g0106 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02486 | hp1 | a0001 | c0003 | t0009 | g0014 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02559 | hp1 | a0001 | c0001 | t0007 | g0259 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03471 | hp1 | a0001 | c0001 | t0027 | g0272 | AFR | MSL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03471 | hp2 | a0001 | c0001 | t0007 | g0151 | AFR | MSL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG06807 | hp1 | a0001 | c0003 | t0001 | g0124 | AFR | USA | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG06807 | hp2 | a0006 | c0017 | t0001 | g0099 | AFR | USA | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0289 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18955 | hp2 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA20300 | hp1 | a0001 | c0001 | t0007 | g0269 | AFR | USA | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | USA | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA21309 | hp1 | a0001 | c0001 | t0030 | g0048 | AFR | LWK | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA21309 | hp2 | a0001 | c0004 | t0005 | g0139 | AFR | LWK | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0024 | REF | REF | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0344 | REF | REF | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:1463691 | G | A | 1 | a0004 | 2 | HG03041.hp2 HG03098.hp1 |
missense_variant | MODERATE | c.1565C>T | p.Ser522Leu | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1681/3945 | 1565/1605 | 522/534 | chr5 | 1463691 | |||
chr5:1463751 | G | A | 1 | a0005 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.1505C>T | p.Ala502Val | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1621/3945 | 1505/1605 | 502/534 | chr5 | 1463751 | |||
chr5:1466889 | A | G | 2 | a0002 a0005 |
48 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(45): Show |
missense_variant&splice_region_variant | MODERATE | c.1280T>C | p.Met427Thr | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/14 | 1396/3945 | 1280/1605 | 427/534 | chr5 | 1466889 | |||
chr5:1489771 | G | A | 1 | a0006 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.581C>T | p.Ala194Val | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/14 | 697/3945 | 581/1605 | 194/534 | chr5 | 1489771 | |||
chr5:1494820 | T | C | 1 | a0003 | 6 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(3): Show |
missense_variant | MODERATE | c.373A>G | p.Thr125Ala | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/14 | 489/3945 | 373/1605 | 125/534 | chr5 | 1494820 | |||
chr5:1494844 | C | T | 1 | a0007 | 1 | NA19079.hp1 | missense_variant | MODERATE | c.349G>A | p.Val117Met | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/14 | 465/3945 | 349/1605 | 117/534 | chr5 | 1494844 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:1466794 | G | A | 1 | a0001c0015 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.1375C>T | p.Leu459Leu | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/14 | 1491/3945 | 1375/1605 | 459/534 | chr5 | 1466794 | |||
chr5:1466804 | G | A | 6 | a0001c0002 a0001c0003 a0001c0010 others(3): Show |
152 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(149): Show |
synonymous_variant | LOW | c.1365C>T | p.Thr455Thr | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/14 | 1481/3945 | 1365/1605 | 455/534 | chr5 | 1466804 | |||
chr5:1470826 | C | T | 2 | a0001c0009 a0001c0019 |
3 | HG02451.hp1 HG02615.hp2 HG02809.hp1 |
splice_region_variant&synonymous_variant | LOW | c.1278G>A | p.Lys426Lys | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/14 | 1394/3945 | 1278/1605 | 426/534 | chr5 | 1470826 | |||
chr5:1477442 | G | A | 1 | a0002c0016 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.861C>T | p.Pro287Pro | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/14 | 977/3945 | 861/1605 | 287/534 | chr5 | 1477442 | |||
chr5:1477457 | C | T | 1 | a0004c0012 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.846G>A | p.Glu282Glu | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/14 | 962/3945 | 846/1605 | 282/534 | chr5 | 1477457 | |||
chr5:1494794 | C | T | 7 | a0001c0003 a0001c0004 a0001c0018 others(4): Show |
121 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(118): Show |
synonymous_variant | LOW | c.399G>A | p.Ala133Ala | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/14 | 515/3945 | 399/1605 | 133/534 | chr5 | 1494794 | |||
chr5:1494845 | G | C | 1 | a0001c0018 | 1 | NA18990.hp2 | synonymous_variant | LOW | c.348C>G | p.Ala116Ala | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/14 | 464/3945 | 348/1605 | 116/534 | chr5 | 1494845 | |||
chr5:1501543 | G | A | 1 | a0001c0019 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.196C>T | p.Leu66Leu | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/14 | 312/3945 | 196/1605 | 66/534 | chr5 | 1501543 | |||
chr5:1501580 | G | A | 3 | a0001c0007 a0001c0010 a0001c0020 |
10 | HG01106.hp1 HG01256.hp1 HG01257.hp1 others(7): Show |
synonymous_variant | LOW | c.159C>T | p.Leu53Leu | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/14 | 275/3945 | 159/1605 | 53/534 | chr5 | 1501580 | |||
chr5:1523785 | G | A | 1 | a0001c0021 | 1 | HG02135.hp2 | synonymous_variant | LOW | c.60C>T | p.Asp20Asp | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/14 | 176/3945 | 60/1605 | 20/534 | chr5 | 1523785 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:1461453 | C | T | 47 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(44): Show |
257 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*2198G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 2198 | chr5 | 1461453 | ||||||
chr5:1461819 | G | A | 1 | a0001c0001t0027 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1832C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1832 | chr5 | 1461819 | ||||||
chr5:1461868 | C | T | 1 | a0001c0001t0026 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1783G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1783 | chr5 | 1461868 | ||||||
chr5:1461949 | T | C | 1 | a0001c0001t0025 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1702A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1702 | chr5 | 1461949 | ||||||
chr5:1461983 | A | G | 17 | a0001c0001t0006 a0001c0001t0020 a0001c0002t0001 others(14): Show |
135 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*1668T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1668 | chr5 | 1461983 | ||||||
chr5:1462079 | T | A | 1 | a0001c0001t0028 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1572A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1572 | chr5 | 1462079 | ||||||
chr5:1462182 | G | A | 1 | a0004c0012t0035 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1469C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1469 | chr5 | 1462182 | ||||||
chr5:1462389 | G | A | 1 | a0004c0014t0034 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1262C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1262 | chr5 | 1462389 | ||||||
chr5:1462418 | C | T | 1 | a0002c0005t0031 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1233G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1233 | chr5 | 1462418 | ||||||
chr5:1462485 | G | A | 1 | a0001c0003t0009 | 7 | HG02486.hp1 HG02717.hp2 HG02886.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1166C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1166 | chr5 | 1462485 | ||||||
chr5:1462539 | C | A | 1 | a0004c0014t0034 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1112G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1112 | chr5 | 1462539 | ||||||
chr5:1462543 | G | A | 1 | a0004c0014t0034 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1108C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1108 | chr5 | 1462543 | ||||||
chr5:1462605 | G | A | 38 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0026 others(35): Show |
238 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
3_prime_UTR_variant | MODIFIER | c.*1046C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1046 | chr5 | 1462605 | ||||||
chr5:1462612 | A | T | 59 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(56): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
3_prime_UTR_variant | MODIFIER | c.*1039T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1039 | chr5 | 1462612 | ||||||
chr5:1462617 | G | C | 46 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(43): Show |
259 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
3_prime_UTR_variant | MODIFIER | c.*1034C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1034 | chr5 | 1462617 | ||||||
chr5:1462687 | G | A | 3 | a0001c0002t0008 a0001c0002t0023 a0001c0002t0036 |
11 | HG00280.hp1 HG01255.hp2 HG01256.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*964C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 964 | chr5 | 1462687 | ||||||
chr5:1462722 | C | A | 2 | a0001c0001t0007 a0001c0007t0007 |
11 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*929G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 929 | chr5 | 1462722 | ||||||
chr5:1462734 | G | C | 1 | a0001c0001t0029 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*917C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 917 | chr5 | 1462734 | ||||||
chr5:1462838 | T | TA | 1 | a0001c0003t0009 | 7 | HG02486.hp1 HG02717.hp2 HG02886.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*812dupT | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 812 | chr5 | 1462838 | ||||||
chr5:1462853 | C | A | 2 | a0001c0004t0010 a0001c0018t0010 |
5 | NA18964.hp2 NA18970.hp1 NA18971.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*798G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 798 | chr5 | 1462853 | ||||||
chr5:1462898 | C | T | 10 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0021 others(7): Show |
27 | HG01496.hp1 HG01884.hp2 HG02145.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*753G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 753 | chr5 | 1462898 | ||||||
chr5:1462931 | G | A | 1 | a0001c0001t0030 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*720C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 720 | chr5 | 1462931 | ||||||
chr5:1462936 | G | C | 8 | a0002c0005t0003 a0002c0005t0031 a0002c0005t0037 others(5): Show |
46 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*715C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 715 | chr5 | 1462936 | ||||||
chr5:1463009 | TA | T | 10 | a0001c0001t0021 a0001c0002t0008 a0001c0002t0015 others(7): Show |
20 | HG00280.hp1 HG01255.hp2 HG01256.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*641delT | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 641 | chr5 | 1463009 | ||||||
chr5:1463011 | A | T | 1 | a0001c0001t0021 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*640T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 640 | chr5 | 1463011 | ||||||
chr5:1463088 | A | T | 7 | a0001c0001t0006 a0001c0001t0020 a0001c0002t0006 others(4): Show |
39 | HG00558.hp1 HG00621.hp1 HG01167.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*563T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 563 | chr5 | 1463088 | ||||||
chr5:1463107 | C | T | 1 | a0001c0001t0019 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*544G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 544 | chr5 | 1463107 | ||||||
chr5:1463159 | T | C | 1 | a0004c0012t0035 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*492A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 492 | chr5 | 1463159 | ||||||
chr5:1463232 | G | A | 1 | a0002c0006t0038 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*419C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 419 | chr5 | 1463232 | ||||||
chr5:1463423 | C | T | 2 | a0004c0012t0035 a0004c0014t0034 |
2 | HG03041.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*228G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 228 | chr5 | 1463423 | ||||||
chr5:1463432 | C | T | 1 | a0001c0001t0018 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*219G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 219 | chr5 | 1463432 | ||||||
chr5:1463474 | T | C | 3 | a0001c0002t0008 a0001c0002t0036 a0001c0003t0033 |
11 | HG00280.hp1 HG00597.hp2 HG01255.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*177A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 177 | chr5 | 1463474 | ||||||
chr5:1463541 | C | T | 1 | a0004c0014t0034 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*110G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 110 | chr5 | 1463541 | ||||||
chr5:1463575 | C | A | 2 | a0001c0001t0011 a0001c0004t0011 |
4 | NA18747.hp1 NA18982.hp1 NA18991.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*76G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 76 | chr5 | 1463575 | ||||||
chr5:1463605 | G | C | 2 | a0004c0012t0035 a0004c0014t0034 |
2 | HG03041.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*46C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 46 | chr5 | 1463605 | ||||||
chr5:1523876 | G | A | 1 | a0001c0002t0036 | 1 | HG01358.hp2 | 5_prime_UTR_variant | MODIFIER | c.-32C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/14 | 32 | chr5 | 1523876 | ||||||
chr5:1523881 | C | T | 1 | a0001c0003t0014 | 2 | HG02735.hp2 HG04228.hp2 |
5_prime_UTR_variant | MODIFIER | c.-37G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/14 | 37 | chr5 | 1523881 | ||||||
chr5:1523904 | G | A | 3 | a0001c0003t0016 a0002c0005t0037 a0002c0006t0038 |
4 | NA18956.hp1 NA18970.hp2 NA19009.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-60C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/14 | 60 | chr5 | 1523904 | ||||||
chr5:1523910 | TGGGCGCG others(7): Show |
T | 1 | a0001c0004t0017 | 1 | HG02145.hp2 | 5_prime_UTR_variant | MODIFIER | c.-80_-67delCGAGACCC others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/14 | 67 | chr5 | 1523910 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:1463846 | A | C | 1 | a0001c0004t0013g0196 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1421-11T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1463846 | |||||||
chr5:1463913 | C | T | 219 | a0001c0001t0002g0043 a0001c0001t0002g0187 a0001c0001t0002g0253 others(216): Show |
227 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.1421-78G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1463913 | |||||||
chr5:1463924 | G | A | 10 | a0001c0001t0007g0003 a0001c0001t0007g0034 a0001c0001t0007g0082 others(7): Show |
11 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1421-89C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1463924 | |||||||
chr5:1463957 | C | T | 2 | a0004c0012t0035g0280 a0004c0014t0034g0145 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1421-122G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1463957 | |||||||
chr5:1464258 | C | T | 1 | a0001c0001t0004g0108 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1421-423G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464258 | |||||||
chr5:1464292 | C | T | 1 | a0001c0002t0001g0277 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1421-457G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464292 | |||||||
chr5:1464300 | C | T | 3 | a0001c0009t0012g0107 a0001c0009t0012g0116 a0001c0019t0012g0278 |
3 | HG02451.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1421-465G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464300 | |||||||
chr5:1464316 | C | A | 1 | a0001c0002t0008g0331 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1421-481G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464316 | |||||||
chr5:1464484 | ACAAACAT | A | 10 | a0001c0002t0008g0004 a0001c0002t0008g0114 a0001c0002t0008g0130 others(7): Show |
11 | HG00280.hp1 HG01255.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.1421-656_1421-650d others(9): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464484 | |||||||
chr5:1464553 | T | G | 1 | a0001c0001t0021g0246 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1421-718A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464553 | |||||||
chr5:1464643 | GCA | G | 58 | a0001c0002t0008g0004 a0001c0002t0008g0114 a0001c0002t0008g0130 others(55): Show |
61 | HG00280.hp1 HG00544.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.1421-810_1421-809d others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464643 | |||||||
chr5:1464645 | A | G | 1 | a0001c0001t0011g0337 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1421-810T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464645 | |||||||
chr5:1464665 | A | G | 259 | a0001c0001t0002g0036 a0001c0001t0002g0043 a0001c0001t0002g0111 others(256): Show |
270 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.1421-830T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464665 | |||||||
chr5:1464667 | G | A | 1 | a0001c0001t0004g0299 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1421-832C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464667 | |||||||
chr5:1464669 | A | G | 1 | a0004c0012t0035g0280 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1421-834T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464669 | |||||||
chr5:1464676 | C | T | 1 | a0001c0003t0001g0266 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1421-841G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464676 | |||||||
chr5:1464679 | TAAAC | T | 3 | a0001c0009t0012g0107 a0001c0009t0012g0116 a0001c0019t0012g0278 |
3 | HG02451.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1421-848_1421-845d others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464679 | |||||||
chr5:1464685 | AAC | A | 13 | a0001c0001t0004g0079 a0001c0001t0007g0003 a0001c0001t0007g0034 others(10): Show |
14 | HG01257.hp1 HG01496.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1421-852_1421-851d others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464685 | |||||||
chr5:1464696 | GCACA | G | 4 | a0001c0001t0004g0013 a0001c0001t0004g0347 a0001c0001t0004g0363 others(1): Show |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1421-865_1421-862d others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464696 | |||||||
chr5:1464705 | C | CACA | 11 | a0001c0001t0007g0003 a0001c0001t0007g0034 a0001c0001t0007g0082 others(8): Show |
12 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1421-871_1421-870i others(5): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464705 | |||||||
chr5:1464705 | C | G | 3 | a0001c0001t0002g0227 a0001c0001t0002g0309 a0001c0001t0002g0349 |
3 | HG00558.hp2 HG00609.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1421-870G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464705 | |||||||
chr5:1464718 | C | CAT | 10 | a0001c0001t0007g0003 a0001c0001t0007g0034 a0001c0001t0007g0082 others(7): Show |
11 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1421-884_1421-883i others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464718 | |||||||
chr5:1464719 | G | A | 1 | a0001c0001t0030g0048 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1421-884C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464719 | |||||||
chr5:1464736 | G | A | 6 | a0001c0003t0009g0014 a0001c0003t0009g0041 a0001c0003t0009g0233 others(3): Show |
7 | HG02486.hp1 HG02717.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1421-901C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464736 | |||||||
chr5:1464736 | GCAGA | G | 2 | a0001c0001t0002g0016 a0001c0001t0002g0346 |
3 | NA18960.hp1 NA19005.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1421-905_1421-902d others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464736 | |||||||
chr5:1464739 | GAC | G | 11 | a0001c0001t0004g0108 a0001c0001t0007g0003 a0001c0001t0007g0034 others(8): Show |
12 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1421-906_1421-905d others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464739 | |||||||
chr5:1464754 | A | C | 1 | a0004c0012t0035g0280 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1421-919T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464754 | |||||||
chr5:1464759 | G | GCA | 12 | a0001c0001t0007g0003 a0001c0001t0007g0034 a0001c0001t0007g0082 others(9): Show |
13 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1421-926_1421-925d others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464759 | |||||||
chr5:1464759 | GCA | G | 4 | a0001c0002t0001g0284 a0001c0009t0012g0107 a0001c0009t0012g0116 others(1): Show |
4 | HG02451.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1421-926_1421-925d others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464759 | |||||||
chr5:1464760 | C | G | 6 | a0001c0003t0009g0014 a0001c0003t0009g0041 a0001c0003t0009g0233 others(3): Show |
7 | HG02486.hp1 HG02717.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1421-925G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464760 | |||||||
chr5:1464762 | C | G | 3 | a0001c0009t0012g0107 a0001c0009t0012g0116 a0001c0019t0012g0278 |
3 | HG02451.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1421-927G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464762 | |||||||
chr5:1464783 | C | CAT | 357 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(354): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.1421-949_1421-948i others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464783 | |||||||
chr5:1464783 | C | T | 9 | a0001c0003t0009g0014 a0001c0003t0009g0041 a0001c0003t0009g0233 others(6): Show |
10 | HG02451.hp1 HG02486.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1421-948G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464783 | |||||||
chr5:1464787 | C | T | 2 | a0002c0005t0003g0169 a0002c0005t0003g0353 |
2 | NA18978.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1421-952G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464787 | |||||||
chr5:1464817 | G | A | 1 | a0001c0004t0005g0219 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1421-982C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464817 | |||||||
chr5:1464833 | C | T | 1 | a0001c0001t0005g0166 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1421-998G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464833 | |||||||
chr5:1464855 | C | G | 224 | a0001c0001t0002g0036 a0001c0001t0002g0043 a0001c0001t0002g0111 others(221): Show |
232 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.1421-1020G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464855 | |||||||
chr5:1464874 | T | C | 1 | a0001c0001t0021g0246 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1421-1039A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464874 | |||||||
chr5:1464880 | C | CACA | 258 | a0001c0001t0002g0036 a0001c0001t0002g0043 a0001c0001t0002g0111 others(255): Show |
269 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.1421-1046_1421-104 others(7): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464880 | |||||||
chr5:1464884 | C | A | 3 | a0001c0002t0001g0289 a0001c0003t0001g0228 a0001c0003t0001g0229 |
3 | NA18955.hp1 NA18956.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1421-1049G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464884 | |||||||
chr5:1464893 | A | G | 260 | a0001c0001t0002g0036 a0001c0001t0002g0043 a0001c0001t0002g0111 others(257): Show |
271 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1421-1058T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464893 | |||||||
chr5:1464898 | CACTA | C | 56 | a0001c0001t0002g0187 a0001c0001t0006g0136 a0001c0001t0013g0042 others(53): Show |
57 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.1421-1067_1421-106 others(8): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464898 | |||||||
chr5:1464929 | AAAC | A | 10 | a0001c0001t0007g0003 a0001c0001t0007g0034 a0001c0001t0007g0082 others(7): Show |
11 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1421-1097_1421-109 others(7): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464929 | |||||||
chr5:1464970 | G | A | 1 | a0001c0001t0027g0272 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1421-1135C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464970 | |||||||
chr5:1464977 | T | C | 10 | a0001c0001t0007g0003 a0001c0001t0007g0034 a0001c0001t0007g0082 others(7): Show |
11 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1421-1142A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464977 | |||||||
chr5:1464988 | T | C | 231 | a0001c0001t0002g0043 a0001c0001t0002g0187 a0001c0001t0002g0253 others(228): Show |
240 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.1421-1153A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464988 | |||||||
chr5:1465000 | A | C | 256 | a0001c0001t0002g0043 a0001c0001t0002g0187 a0001c0001t0002g0253 others(253): Show |
267 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1421-1165T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465000 | |||||||
chr5:1465007 | GCA | G | 9 | a0001c0003t0009g0014 a0001c0003t0009g0041 a0001c0003t0009g0233 others(6): Show |
10 | HG02451.hp1 HG02486.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1421-1174_1421-117 others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465007 | |||||||
chr5:1465009 | ACACACAC others(49): Show |
A | 1 | a0001c0002t0001g0045 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1421-1230_1421-117 others(60): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465009 | |||||||
chr5:1465033 | C | CACTA | 99 | a0001c0001t0002g0043 a0001c0001t0002g0187 a0001c0001t0002g0253 others(96): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1421-1202_1421-119 others(8): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465033 | |||||||
chr5:1465046 | T | G | 6 | a0001c0003t0009g0014 a0001c0003t0009g0041 a0001c0003t0009g0233 others(3): Show |
7 | HG02486.hp1 HG02717.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1421-1211A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465046 | |||||||
chr5:1465065 | GCA | G | 57 | a0001c0001t0007g0003 a0001c0001t0007g0034 a0001c0001t0007g0082 others(54): Show |
59 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.1421-1232_1421-123 others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465065 | |||||||
chr5:1465066 | C | A | 2 | a0004c0012t0035g0280 a0004c0014t0034g0145 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1421-1231G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465066 | |||||||
chr5:1465068 | C | A | 10 | a0001c0001t0007g0003 a0001c0001t0007g0034 a0001c0001t0007g0082 others(7): Show |
11 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1421-1233G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465068 | |||||||
chr5:1465078 | AAC | A | 172 | a0001c0001t0002g0043 a0001c0001t0002g0187 a0001c0001t0002g0253 others(169): Show |
179 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.1421-1245_1421-124 others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465078 | |||||||
chr5:1465116 | GCACA | G | 47 | a0001c0010t0001g0264 a0002c0005t0003g0015 a0002c0005t0003g0022 others(44): Show |
48 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1421-1285_1421-128 others(8): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465116 | |||||||
chr5:1465118 | A | G | 1 | a0001c0001t0002g0220 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1421-1283T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465118 | |||||||
chr5:1465125 | C | T | 1 | a0002c0006t0032g0247 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1421-1290G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465125 | |||||||
chr5:1465189 | G | A | 3 | a0001c0004t0013g0196 a0004c0012t0035g0280 a0004c0014t0034g0145 |
3 | HG03041.hp2 HG03098.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1421-1354C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465189 | |||||||
chr5:1465190 | C | T | 10 | a0001c0001t0007g0003 a0001c0001t0007g0034 a0001c0001t0007g0082 others(7): Show |
11 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1421-1355G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465190 | |||||||
chr5:1465199 | TAACTA | T | 3 | a0001c0001t0004g0013 a0001c0001t0004g0347 a0001c0001t0004g0363 |
4 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1421-1369_1421-136 others(9): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465199 | |||||||
chr5:1465270 | GCACA | G | 3 | a0001c0009t0012g0107 a0001c0009t0012g0116 a0001c0019t0012g0278 |
3 | HG02451.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1421-1439_1421-143 others(8): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465270 | |||||||
chr5:1465272 | A | G | 1 | a0001c0001t0011g0337 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1421-1437T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465272 | |||||||
chr5:1465284 | G | A | 5 | a0002c0005t0003g0081 a0002c0005t0003g0103 a0002c0005t0003g0192 others(2): Show |
5 | HG01099.hp1 HG01175.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1421-1449C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465284 | |||||||
chr5:1465299 | CAT | C | 3 | a0001c0001t0021g0246 a0001c0002t0001g0248 a0001c0002t0001g0322 |
3 | HG00408.hp2 HG01884.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1420+1448_1420+144 others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465299 | |||||||
chr5:1465303 | TGC | T | 10 | a0001c0001t0007g0003 a0001c0001t0007g0034 a0001c0001t0007g0082 others(7): Show |
11 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1420+1444_1420+144 others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465303 | |||||||
chr5:1465308 | G | A | 2 | a0004c0012t0035g0280 a0004c0014t0034g0145 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1420+1441C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465308 | |||||||
chr5:1465336 | GTAAC | G | 36 | a0001c0001t0002g0043 a0001c0001t0002g0187 a0001c0001t0002g0253 others(33): Show |
38 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.1420+1409_1420+141 others(8): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465336 | |||||||
chr5:1465360 | A | G | 1 | a0001c0019t0012g0278 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1420+1389T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465360 | |||||||
chr5:1465370 | G | A | 2 | a0001c0001t0002g0084 a0002c0005t0003g0049 |
2 | HG01975.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1420+1379C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465370 | |||||||
chr5:1465383 | AAC | A | 24 | a0001c0002t0001g0027 a0001c0002t0001g0035 a0001c0002t0001g0037 others(21): Show |
25 | HG01099.hp2 HG01106.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1420+1364_1420+136 others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465383 | |||||||
chr5:1465400 | A | T | 1 | a0001c0003t0001g0342 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1420+1349T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465400 | |||||||
chr5:1465421 | GCA | G | 5 | a0001c0002t0001g0302 a0001c0002t0004g0143 a0002c0006t0038g0368 others(2): Show |
5 | HG01928.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1420+1326_1420+132 others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465421 | |||||||
chr5:1465421 | GCACA | G | 11 | a0001c0002t0008g0004 a0001c0002t0008g0114 a0001c0002t0008g0130 others(8): Show |
12 | HG00280.hp1 HG00597.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.1420+1324_1420+132 others(8): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465421 | |||||||
chr5:1465454 | A | G | 263 | a0001c0001t0002g0036 a0001c0001t0002g0043 a0001c0001t0002g0111 others(260): Show |
274 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.1420+1295T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465454 | |||||||
chr5:1465471 | G | GCA | 245 | a0001c0001t0002g0043 a0001c0001t0002g0187 a0001c0001t0002g0253 others(242): Show |
255 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1420+1276_1420+127 others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465471 | |||||||
chr5:1465487 | C | T | 2 | a0001c0001t0013g0042 a0001c0001t0013g0055 |
2 | NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1420+1262G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465487 | |||||||
chr5:1465494 | G | A | 2 | a0001c0002t0001g0274 a0001c0002t0001g0362 |
2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1420+1255C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465494 | |||||||
chr5:1465502 | TAAACACG others(9): Show |
T | 2 | a0001c0004t0002g0261 a0001c0004t0002g0262 |
2 | HG01261.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1420+1231_1420+124 others(20): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465502 | |||||||
chr5:1465513 | GCA | G | 23 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0071 others(20): Show |
23 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1420+1234_1420+123 others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465513 | |||||||
chr5:1465613 | G | A | 1 | a0002c0005t0003g0067 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1420+1136C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465613 | |||||||
chr5:1465615 | A | G | 11 | a0001c0002t0008g0004 a0001c0002t0008g0114 a0001c0002t0008g0130 others(8): Show |
12 | HG00280.hp1 HG00597.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.1420+1134T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465615 | |||||||
chr5:1465617 | A | G | 11 | a0001c0002t0008g0004 a0001c0002t0008g0114 a0001c0002t0008g0130 others(8): Show |
12 | HG00280.hp1 HG00597.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.1420+1132T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465617 | |||||||
chr5:1465647 | C | G | 1 | a0004c0014t0034g0145 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1420+1102G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465647 | |||||||
chr5:1465711 | A | G | 1 | a0001c0001t0002g0220 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1420+1038T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465711 | |||||||
chr5:1465742 | A | G | 12 | a0001c0001t0007g0003 a0001c0001t0007g0034 a0001c0001t0007g0082 others(9): Show |
13 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1420+1007T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465742 | |||||||
chr5:1465778 | A | AAC | 246 | a0001c0001t0002g0043 a0001c0001t0002g0187 a0001c0001t0002g0253 others(243): Show |
254 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1420+969_1420+970d others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465778 | |||||||
chr5:1465778 | A | ACTAAAC | 8 | a0001c0001t0007g0003 a0001c0001t0007g0097 a0001c0001t0007g0138 others(5): Show |
9 | HG02572.hp1 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.1420+970_1420+971i others(8): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465778 | |||||||
chr5:1465833 | C | T | 4 | a0001c0001t0002g0087 a0001c0001t0002g0182 a0001c0001t0002g0197 others(1): Show |
4 | HG02132.hp2 NA18960.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420+916G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465833 | |||||||
chr5:1465868 | GAAAC | G | 85 | a0001c0001t0002g0043 a0001c0001t0002g0187 a0001c0001t0002g0253 others(82): Show |
88 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.1420+877_1420+880d others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465868 | |||||||
chr5:1465886 | C | T | 1 | a0001c0004t0004g0068 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1420+863G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465886 | |||||||
chr5:1465889 | AC | A | 33 | a0001c0001t0002g0043 a0001c0001t0002g0187 a0001c0001t0002g0253 others(30): Show |
34 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.1420+859delG | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465889 | |||||||
chr5:1465892 | C | CGCACACA others(7): Show |
1 | a0001c0007t0005g0106 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1420+843_1420+856d others(16): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465892 | |||||||
chr5:1465981 | C | G | 4 | a0001c0001t0002g0236 a0001c0004t0002g0117 a0001c0004t0002g0355 others(1): Show |
4 | HG00438.hp2 HG02135.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.1420+768G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465981 | |||||||
chr5:1466030 | G | A | 2 | a0001c0001t0004g0026 a0001c0001t0026g0025 |
2 | HG01081.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.1420+719C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466030 | |||||||
chr5:1466077 | G | C | 1 | a0001c0004t0005g0105 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1420+672C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466077 | |||||||
chr5:1466114 | C | A | 1 | a0001c0002t0001g0245 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1420+635G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466114 | |||||||
chr5:1466238 | T | A | 12 | a0001c0001t0007g0003 a0001c0001t0007g0034 a0001c0001t0007g0082 others(9): Show |
13 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1420+511A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466238 | |||||||
chr5:1466284 | C | G | 251 | a0001c0001t0002g0043 a0001c0001t0002g0187 a0001c0001t0002g0253 others(248): Show |
260 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.1420+465G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466284 | |||||||
chr5:1466371 | G | T | 24 | a0001c0002t0001g0027 a0001c0002t0001g0035 a0001c0002t0001g0037 others(21): Show |
25 | HG01099.hp2 HG01106.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1420+378C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466371 | |||||||
chr5:1466384 | C | T | 2 | a0001c0001t0013g0042 a0001c0001t0013g0055 |
2 | NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1420+365G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466384 | |||||||
chr5:1466428 | G | A | 1 | a0001c0002t0001g0054 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1420+321C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466428 | |||||||
chr5:1466440 | C | T | 1 | a0002c0005t0003g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1420+309G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466440 | |||||||
chr5:1466534 | C | G | 1 | a0001c0010t0001g0264 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1420+215G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466534 | |||||||
chr5:1466542 | C | G | 2 | a0001c0004t0017g0017 a0001c0004t0024g0033 |
2 | HG02145.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1420+207G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466542 | |||||||
chr5:1466571 | G | C | 245 | a0001c0001t0002g0043 a0001c0001t0002g0187 a0001c0001t0002g0253 others(242): Show |
254 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1420+178C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466571 | |||||||
chr5:1466698 | T | C | 242 | a0001c0001t0002g0043 a0001c0001t0002g0187 a0001c0001t0002g0253 others(239): Show |
250 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.1420+51A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466698 | |||||||
chr5:1466701 | A | C | 1 | a0001c0001t0002g0318 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1420+48T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466701 | |||||||
chr5:1466704 | C | T | 1 | a0001c0003t0001g0086 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1420+45G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466704 | |||||||
chr5:1466721 | G | A | 6 | a0001c0003t0009g0014 a0001c0003t0009g0041 a0001c0003t0009g0233 others(3): Show |
7 | HG02486.hp1 HG02717.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1420+28C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466721 | |||||||
chr5:1466979 | C | T | 2 | a0002c0005t0003g0169 a0002c0005t0003g0353 |
2 | NA18978.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1279-89G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1466979 | |||||||
chr5:1466996 | G | A | 1 | a0002c0005t0004g0153 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1279-106C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1466996 | |||||||
chr5:1467018 | G | A | 1 | a0001c0003t0009g0233 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1279-128C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467018 | |||||||
chr5:1467130 | G | A | 254 | a0001c0001t0002g0043 a0001c0001t0002g0187 a0001c0001t0002g0253 others(251): Show |
263 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.1279-240C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467130 | |||||||
chr5:1467160 | G | A | 2 | a0004c0012t0035g0280 a0004c0014t0034g0145 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1279-270C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467160 | |||||||
chr5:1467236 | C | T | 10 | a0001c0001t0007g0003 a0001c0001t0007g0034 a0001c0001t0007g0082 others(7): Show |
11 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279-346G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467236 | |||||||
chr5:1467239 | C | T | 1 | a0001c0001t0002g0087 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1279-349G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467239 | |||||||
chr5:1467315 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1279-425G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467315 | |||||||
chr5:1467385 | G | A | 10 | a0001c0001t0007g0003 a0001c0001t0007g0034 a0001c0001t0007g0082 others(7): Show |
11 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279-495C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467385 | |||||||
chr5:1467392 | G | A | 3 | a0001c0009t0012g0107 a0001c0009t0012g0116 a0001c0019t0012g0278 |
3 | HG02451.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1279-502C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467392 | |||||||
chr5:1467465 | C | T | 1 | a0002c0005t0003g0119 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1279-575G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467465 | |||||||
chr5:1467516 | T | C | 11 | a0001c0001t0002g0089 a0001c0001t0007g0003 a0001c0001t0007g0034 others(8): Show |
12 | HG01496.hp1 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1279-626A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467516 | |||||||
chr5:1467688 | TGCAGGGT others(57): Show |
T | 1 | a0004c0014t0034g0145 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1279-862_1279-799d others(66): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467688 | |||||||
chr5:1467702 | C | T | 1 | a0001c0001t0002g0187 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1279-812G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467702 | |||||||
chr5:1467753 | T | C | 1 | a0004c0014t0034g0145 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1279-863A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467753 | |||||||
chr5:1467762 | C | T | 1 | a0001c0003t0009g0237 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1279-872G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467762 | |||||||
chr5:1467797 | G | A | 4 | a0001c0002t0004g0023 a0001c0002t0004g0096 a0001c0002t0004g0100 others(1): Show |
4 | HG02895.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279-907C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467797 | |||||||
chr5:1467820 | T | G | 1 | a0001c0003t0001g0336 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1279-930A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467820 | |||||||
chr5:1467828 | G | T | 1 | a0004c0014t0034g0145 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1279-938C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467828 | |||||||
chr5:1467896 | C | T | 141 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(138): Show |
150 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.1279-1006G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467896 | |||||||
chr5:1467899 | T | C | 3 | a0001c0001t0013g0042 a0001c0001t0013g0055 a0001c0004t0013g0196 |
3 | HG04228.hp1 NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1279-1009A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467899 | |||||||
chr5:1467928 | T | G | 1 | a0001c0002t0004g0023 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1279-1038A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467928 | |||||||
chr5:1468008 | T | TGGGAGGG others(16): Show |
1 | a0001c0007t0004g0254 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1279-1141_1279-111 others(27): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468008 | |||||||
chr5:1468055 | C | A | 5 | a0001c0001t0002g0127 a0001c0001t0002g0239 a0003c0008t0002g0009 others(2): Show |
6 | HG00099.hp2 HG00323.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1279-1165G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468055 | |||||||
chr5:1468055 | C | G | 269 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(266): Show |
281 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.1279-1165G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468055 | |||||||
chr5:1468095 | C | G | 1 | a0001c0001t0002g0187 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1279-1205G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468095 | |||||||
chr5:1468098 | C | T | 1 | a0001c0001t0021g0246 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1279-1208G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468098 | |||||||
chr5:1468129 | G | C | 124 | a0001c0001t0004g0299 a0001c0001t0005g0066 a0001c0001t0005g0321 others(121): Show |
128 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1279-1239C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468129 | |||||||
chr5:1468172 | C | A | 161 | a0001c0001t0002g0043 a0001c0001t0002g0253 a0001c0001t0002g0260 others(158): Show |
167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1279-1282G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468172 | |||||||
chr5:1468280 | A | G | 1 | a0001c0001t0004g0135 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1279-1390T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468280 | |||||||
chr5:1468405 | C | G | 1 | a0001c0001t0002g0182 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1279-1515G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468405 | |||||||
chr5:1468618 | T | C | 31 | a0001c0001t0002g0043 a0001c0001t0002g0071 a0001c0001t0002g0253 others(28): Show |
32 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.1279-1728A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468618 | |||||||
chr5:1468682 | A | G | 1 | a0001c0001t0002g0140 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1279-1792T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468682 | |||||||
chr5:1468728 | C | T | 26 | a0001c0002t0001g0027 a0001c0002t0001g0035 a0001c0002t0001g0037 others(23): Show |
27 | HG01099.hp2 HG01106.hp2 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.1279-1838G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468728 | |||||||
chr5:1468741 | C | T | 1 | a0001c0001t0005g0314 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1279-1851G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468741 | |||||||
chr5:1468767 | T | C | 2 | a0001c0001t0013g0042 a0001c0001t0013g0055 |
2 | NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1279-1877A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468767 | |||||||
chr5:1468802 | G | T | 1 | a0001c0001t0021g0246 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1279-1912C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468802 | |||||||
chr5:1468874 | C | T | 4 | a0001c0001t0002g0239 a0003c0008t0002g0009 a0003c0008t0002g0191 others(1): Show |
5 | HG00099.hp2 HG00323.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.1278+1952G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468874 | |||||||
chr5:1469029 | G | A | 3 | a0001c0002t0001g0251 a0001c0002t0001g0275 a0006c0017t0001g0099 |
3 | HG02257.hp2 HG02615.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1278+1797C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1469029 | |||||||
chr5:1469055 | G | A | 1 | a0001c0002t0023g0243 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1278+1771C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1469055 | |||||||
chr5:1469107 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1278+1719G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1469107 | |||||||
chr5:1469147 | G | C | 11 | a0001c0001t0007g0003 a0001c0001t0007g0034 a0001c0001t0007g0082 others(8): Show |
12 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1278+1679C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1469147 | |||||||
chr5:1469283 | C | T | 1 | a0001c0001t0025g0061 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1278+1543G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1469283 | |||||||
chr5:1469322 | A | G | 100 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(97): Show |
106 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.1278+1504T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1469322 | |||||||
chr5:1469603 | C | G | 1 | a0001c0002t0001g0027 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1278+1223G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1469603 | |||||||
chr5:1469719 | T | G | 1 | a0001c0001t0004g0108 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1278+1107A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1469719 | |||||||
chr5:1469746 | A | G | 165 | a0001c0001t0002g0036 a0001c0001t0002g0111 a0001c0001t0002g0115 others(162): Show |
172 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.1278+1080T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1469746 | |||||||
chr5:1469800 | A | C | 3 | a0001c0001t0002g0141 a0001c0001t0006g0136 a0001c0004t0011g0168 |
3 | NA18747.hp1 NA18973.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.1278+1026T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1469800 | |||||||
chr5:1469845 | C | A | 1 | a0001c0001t0002g0224 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1278+981G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1469845 | |||||||
chr5:1469907 | G | A | 1 | a0001c0003t0006g0225 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1278+919C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1469907 | |||||||
chr5:1469954 | G | C | 316 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(313): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1278+872C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1469954 | |||||||
chr5:1469980 | C | A | 1 | a0001c0001t0027g0272 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1278+846G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1469980 | |||||||
chr5:1470000 | G | A | 1 | a0002c0005t0003g0327 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1278+826C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1470000 | |||||||
chr5:1470039 | G | A | 1 | a0001c0001t0004g0108 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1278+787C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1470039 | |||||||
chr5:1470307 | C | A | 11 | a0001c0001t0007g0003 a0001c0001t0007g0034 a0001c0001t0007g0082 others(8): Show |
12 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1278+519G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1470307 | |||||||
chr5:1470322 | G | A | 3 | a0001c0003t0006g0074 a0001c0003t0006g0175 a0001c0003t0016g0366 |
3 | HG03710.hp2 NA18970.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1278+504C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1470322 | |||||||
chr5:1470329 | T | C | 1 | a0001c0004t0005g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1278+497A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1470329 | |||||||
chr5:1470356 | CCAGGAGT others(6): Show |
C | 1 | a0001c0003t0016g0367 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1278+457_1278+469d others(15): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1470356 | |||||||
chr5:1470444 | G | A | 1 | a0001c0001t0027g0272 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1278+382C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1470444 | |||||||
chr5:1470463 | G | A | 316 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(313): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1278+363C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1470463 | |||||||
chr5:1470577 | C | T | 34 | a0001c0001t0002g0043 a0001c0001t0002g0253 a0001c0001t0004g0012 others(31): Show |
36 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.1278+249G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1470577 | |||||||
chr5:1470648 | C | G | 7 | a0001c0002t0001g0027 a0001c0002t0001g0035 a0001c0002t0001g0037 others(4): Show |
7 | HG02055.hp2 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1278+178G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1470648 | |||||||
chr5:1470721 | T | C | 1 | a0001c0001t0002g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1278+105A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1470721 | |||||||
chr5:1470774 | G | A | 1 | a0001c0001t0027g0272 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1278+52C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1470774 | |||||||
chr5:1470785 | G | A | 92 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(89): Show |
98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.1278+41C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1470785 | |||||||
chr5:1470994 | T | C | 317 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(314): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1180-70A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1470994 | |||||||
chr5:1471066 | TGGAA | T | 4 | a0002c0005t0003g0030 a0002c0006t0003g0031 a0002c0006t0003g0032 others(1): Show |
4 | HG02965.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180-146_1180-143d others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471066 | |||||||
chr5:1471078 | C | T | 11 | a0001c0001t0007g0003 a0001c0001t0007g0034 a0001c0001t0007g0082 others(8): Show |
12 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1180-154G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471078 | |||||||
chr5:1471098 | G | A | 1 | a0001c0001t0002g0060 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1180-174C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471098 | |||||||
chr5:1471157 | G | C | 3 | a0001c0009t0012g0107 a0001c0009t0012g0116 a0001c0019t0012g0278 |
3 | HG02451.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1180-233C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471157 | |||||||
chr5:1471190 | C | T | 1 | a0004c0012t0035g0280 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1180-266G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471190 | |||||||
chr5:1471194 | G | A | 33 | a0001c0001t0002g0043 a0001c0001t0002g0253 a0001c0001t0004g0012 others(30): Show |
35 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.1180-270C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471194 | |||||||
chr5:1471236 | C | G | 1 | a0001c0001t0007g0097 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1180-312G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471236 | |||||||
chr5:1471273 | G | A | 313 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(310): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.1180-349C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471273 | |||||||
chr5:1471643 | G | C | 1 | a0001c0002t0001g0311 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1180-719C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471643 | |||||||
chr5:1471713 | G | A | 1 | a0001c0003t0001g0352 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1180-789C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471713 | |||||||
chr5:1471715 | G | C | 3 | a0001c0009t0012g0107 a0001c0009t0012g0116 a0001c0019t0012g0278 |
3 | HG02451.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1180-791C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471715 | |||||||
chr5:1471758 | A | C | 1 | a0001c0003t0001g0205 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1180-834T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471758 | |||||||
chr5:1471766 | TA | T | 3 | a0001c0009t0012g0107 a0001c0009t0012g0116 a0001c0019t0012g0278 |
3 | HG02451.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1180-843delT | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471766 | |||||||
chr5:1471804 | A | ACTCAGGA others(55): Show |
1 | a0001c0003t0006g0137 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1180-942_1180-881d others(64): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471804 | |||||||
chr5:1471943 | G | A | 1 | a0002c0006t0038g0368 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1180-1019C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471943 | |||||||
chr5:1472011 | A | AGCAGAGA others(42): Show |
1 | a0001c0004t0010g0176 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1180-1088_1180-108 others(53): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472011 | |||||||
chr5:1472011 | A | AGCAGAGA others(42): Show |
1 | a0001c0001t0005g0066 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1180-1088_1180-108 others(53): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472011 | |||||||
chr5:1472011 | A | AGCAGAGA others(42): Show |
313 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(310): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.1180-1088_1180-108 others(53): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472011 | |||||||
chr5:1472129 | T | G | 11 | a0001c0001t0007g0003 a0001c0001t0007g0034 a0001c0001t0007g0082 others(8): Show |
12 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1180-1205A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472129 | |||||||
chr5:1472193 | A | C | 35 | a0001c0001t0002g0043 a0001c0001t0002g0253 a0001c0001t0002g0260 others(32): Show |
37 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.1180-1269T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472193 | |||||||
chr5:1472196 | C | A | 2 | a0001c0002t0001g0248 a0001c0002t0001g0322 |
2 | HG00408.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1180-1272G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472196 | |||||||
chr5:1472297 | C | T | 1 | a0001c0002t0002g0053 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1180-1373G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472297 | |||||||
chr5:1472415 | G | T | 1 | a0001c0001t0002g0089 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1180-1491C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472415 | |||||||
chr5:1472453 | G | A | 2 | a0001c0004t0005g0063 a0001c0004t0005g0064 |
2 | NA19012.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1179+1504C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472453 | |||||||
chr5:1472462 | GACT | G | 152 | a0001c0001t0002g0036 a0001c0001t0002g0111 a0001c0001t0002g0115 others(149): Show |
156 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.1179+1492_1179+149 others(7): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472462 | |||||||
chr5:1472584 | A | T | 109 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(106): Show |
118 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.1179+1373T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472584 | |||||||
chr5:1472586 | T | C | 316 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(313): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1179+1371A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472586 | |||||||
chr5:1472657 | A | G | 2 | a0001c0003t0001g0065 a0002c0005t0003g0338 |
2 | HG00423.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.1179+1300T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472657 | |||||||
chr5:1472795 | G | T | 8 | a0001c0001t0002g0043 a0001c0001t0002g0253 a0001c0001t0004g0012 others(5): Show |
9 | HG00099.hp1 HG01081.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1179+1162C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472795 | |||||||
chr5:1472879 | C | G | 2 | a0001c0001t0013g0042 a0001c0001t0013g0055 |
2 | NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1179+1078G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472879 | |||||||
chr5:1472956 | A | G | 317 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(314): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1179+1001T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472956 | |||||||
chr5:1472998 | T | G | 175 | a0001c0001t0002g0036 a0001c0001t0002g0111 a0001c0001t0002g0115 others(172): Show |
183 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.1179+959A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472998 | |||||||
chr5:1473035 | GCTCCTCT | G | 36 | a0001c0001t0002g0043 a0001c0001t0002g0253 a0001c0001t0002g0260 others(33): Show |
38 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.1179+915_1179+921d others(9): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473035 | |||||||
chr5:1473102 | C | T | 1 | a0001c0003t0001g0266 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1179+855G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473102 | |||||||
chr5:1473147 | C | T | 1 | a0001c0001t0005g0292 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1179+810G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473147 | |||||||
chr5:1473210 | G | C | 1 | a0001c0007t0005g0106 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1179+747C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473210 | |||||||
chr5:1473240 | G | T | 1 | a0002c0005t0004g0153 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1179+717C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473240 | |||||||
chr5:1473257 | C | A | 1 | a0001c0001t0004g0075 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1179+700G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473257 | |||||||
chr5:1473261 | C | A | 2 | a0001c0002t0004g0143 a0001c0002t0004g0271 |
2 | HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1179+696G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473261 | |||||||
chr5:1473382 | C | A | 1 | a0001c0003t0001g0205 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1179+575G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473382 | |||||||
chr5:1473445 | T | C | 317 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(314): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1179+512A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473445 | |||||||
chr5:1473590 | C | A | 1 | a0001c0001t0002g0320 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1179+367G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473590 | |||||||
chr5:1473591 | G | A | 1 | a0001c0001t0027g0272 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1179+366C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473591 | |||||||
chr5:1473611 | G | A | 4 | a0001c0002t0004g0023 a0001c0002t0004g0096 a0001c0002t0004g0100 others(1): Show |
4 | HG02895.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1179+346C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473611 | |||||||
chr5:1473637 | G | A | 1 | a0001c0002t0006g0208 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1179+320C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473637 | |||||||
chr5:1473862 | A | G | 318 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(315): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1179+95T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473862 | |||||||
chr5:1473933 | C | T | 2 | a0001c0002t0004g0100 a0001c0002t0004g0150 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1179+24G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473933 | |||||||
chr5:1474689 | C | T | 1 | a0001c0004t0004g0258 | 1 | HG03704.hp2 | splice_region_variant&intron_variant | LOW | c.900-4G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1474689 | |||||||
chr5:1474747 | C | T | 3 | a0001c0001t0013g0042 a0001c0001t0013g0055 a0001c0004t0013g0196 |
3 | HG04228.hp1 NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.900-62G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1474747 | |||||||
chr5:1474951 | TGAGAATT others(41): Show |
T | 1 | a0001c0001t0002g0295 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.900-314_900-267del others(48): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1474951 | |||||||
chr5:1474993 | A | T | 1 | a0001c0001t0025g0061 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.900-308T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1474993 | |||||||
chr5:1475065 | T | C | 1 | a0001c0004t0013g0196 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.900-380A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1475065 | |||||||
chr5:1475139 | C | T | 1 | a0001c0002t0001g0076 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.900-454G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1475139 | |||||||
chr5:1475148 | C | A | 1 | a0001c0002t0001g0194 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.900-463G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1475148 | |||||||
chr5:1475163 | C | T | 3 | a0001c0001t0004g0044 a0001c0001t0004g0134 a0001c0001t0004g0221 |
3 | HG00280.hp2 HG00741.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.900-478G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1475163 | |||||||
chr5:1475194 | A | G | 7 | a0001c0001t0018g0020 a0001c0002t0001g0057 a0001c0002t0001g0069 others(4): Show |
7 | HG02056.hp2 HG02155.hp1 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.900-509T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1475194 | |||||||
chr5:1475321 | C | T | 19 | a0001c0002t0001g0027 a0001c0002t0001g0035 a0001c0002t0001g0037 others(16): Show |
19 | HG01099.hp2 HG01106.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.900-636G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1475321 | |||||||
chr5:1475520 | C | A | 1 | a0001c0004t0005g0064 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.900-835G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1475520 | |||||||
chr5:1475656 | A | G | 1 | a0001c0004t0013g0196 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.900-971T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1475656 | |||||||
chr5:1475733 | CCCGAGTG others(61): Show |
C | 58 | a0001c0001t0002g0043 a0001c0001t0002g0127 a0001c0001t0002g0239 others(55): Show |
62 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.900-1116_900-1049d others(70): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1475733 | |||||||
chr5:1475817 | CGGCCCCG others(62): Show |
C | 2 | a0001c0001t0002g0089 a0001c0001t0021g0246 |
2 | HG01884.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.900-1201_900-1133d others(71): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1475817 | |||||||
chr5:1475844 | G | A | 307 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(304): Show |
322 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.900-1159C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1475844 | |||||||
chr5:1475913 | G | A | 1 | a0001c0001t0021g0246 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.900-1228C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1475913 | |||||||
chr5:1476165 | A | G | 1 | a0001c0004t0005g0154 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.899+1239T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1476165 | |||||||
chr5:1476255 | A | G | 3 | a0001c0001t0004g0013 a0001c0001t0004g0347 a0001c0001t0004g0363 |
4 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.899+1149T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1476255 | |||||||
chr5:1476271 | G | A | 1 | a0004c0014t0034g0145 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.899+1133C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1476271 | |||||||
chr5:1476290 | TTGTTCAG others(7): Show |
T | 1 | a0001c0001t0027g0272 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.899+1100_899+1113d others(16): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1476290 | |||||||
chr5:1476332 | G | A | 1 | a0001c0002t0001g0287 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.899+1072C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1476332 | |||||||
chr5:1476460 | C | T | 1 | a0001c0002t0001g0312 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.899+944G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1476460 | |||||||
chr5:1476592 | C | G | 73 | a0001c0001t0002g0043 a0001c0001t0002g0078 a0001c0001t0002g0087 others(70): Show |
74 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.899+812G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1476592 | |||||||
chr5:1476670 | C | A | 66 | a0001c0001t0002g0008 a0001c0001t0002g0028 a0001c0001t0002g0040 others(63): Show |
71 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.899+734G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1476670 | |||||||
chr5:1476763 | G | C | 1 | a0002c0005t0003g0211 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.899+641C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1476763 | |||||||
chr5:1476804 | TGGGGAGG others(33): Show |
T | 4 | a0001c0001t0004g0013 a0001c0001t0004g0347 a0001c0001t0004g0363 others(1): Show |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.899+560_899+599del others(40): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1476804 | |||||||
chr5:1476844 | G | C | 4 | a0002c0005t0003g0022 a0002c0005t0003g0119 a0002c0005t0003g0241 others(1): Show |
4 | HG00544.hp1 HG02083.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.899+560C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1476844 | |||||||
chr5:1476956 | C | T | 1 | a0004c0012t0035g0280 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.899+448G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1476956 | |||||||
chr5:1477068 | G | A | 3 | a0001c0001t0013g0042 a0001c0001t0013g0055 a0001c0004t0013g0196 |
3 | HG04228.hp1 NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.899+336C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1477068 | |||||||
chr5:1477073 | C | A | 3 | a0001c0001t0013g0042 a0001c0001t0013g0055 a0001c0004t0013g0196 |
3 | HG04228.hp1 NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.899+331G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1477073 | |||||||
chr5:1477074 | G | A | 1 | a0001c0001t0027g0272 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.899+330C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1477074 | |||||||
chr5:1477109 | C | T | 4 | a0001c0001t0013g0042 a0001c0001t0013g0055 a0001c0004t0013g0196 others(1): Show |
4 | HG03098.hp1 HG04228.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.899+295G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1477109 | |||||||
chr5:1477116 | A | C | 28 | a0001c0001t0002g0043 a0001c0001t0002g0253 a0001c0001t0002g0260 others(25): Show |
29 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.899+288T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1477116 | |||||||
chr5:1477195 | C | A | 314 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(311): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.899+209G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1477195 | |||||||
chr5:1477233 | A | G | 1 | a0003c0008t0002g0047 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.899+171T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1477233 | |||||||
chr5:1477259 | C | T | 1 | a0002c0016t0003g0147 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.899+145G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1477259 | |||||||
chr5:1477260 | G | A | 3 | a0001c0001t0013g0042 a0001c0001t0013g0055 a0001c0004t0013g0196 |
3 | HG04228.hp1 NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.899+144C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1477260 | |||||||
chr5:1477262 | TTCACCAA others(34): Show |
T | 3 | a0001c0001t0013g0042 a0001c0001t0013g0055 a0001c0004t0013g0196 |
3 | HG04228.hp1 NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.899+101_899+141del others(41): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1477262 | |||||||
chr5:1477290 | G | A | 1 | a0001c0021t0002g0364 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.899+114C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1477290 | |||||||
chr5:1477524 | G | A | 2 | a0001c0002t0004g0143 a0001c0002t0004g0271 |
2 | HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.817-38C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1477524 | |||||||
chr5:1477530 | C | G | 1 | a0001c0001t0002g0360 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.817-44G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1477530 | |||||||
chr5:1477567 | C | A | 1 | a0004c0012t0035g0280 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.817-81G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1477567 | |||||||
chr5:1477598 | T | C | 3 | a0001c0004t0017g0017 a0001c0004t0024g0033 a0004c0012t0035g0280 |
3 | HG02145.hp2 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.817-112A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1477598 | |||||||
chr5:1477691 | C | G | 1 | a0002c0005t0031g0217 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.817-205G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1477691 | |||||||
chr5:1477700 | T | C | 17 | a0001c0001t0007g0003 a0001c0001t0007g0034 a0001c0001t0007g0082 others(14): Show |
18 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.817-214A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1477700 | |||||||
chr5:1477717 | A | ACCTGCTG others(61): Show |
1 | a0001c0004t0010g0176 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.817-299_817-232dup others(68): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1477717 | |||||||
chr5:1477717 | ACCTGCTG others(61): Show |
A | 14 | a0001c0001t0004g0080 a0001c0001t0007g0003 a0001c0001t0007g0034 others(11): Show |
15 | HG01192.hp1 HG01496.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.817-299_817-232del others(68): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1477717 | |||||||
chr5:1477717 | ACCTGCTG others(129): Show |
A | 5 | a0001c0001t0013g0042 a0001c0001t0013g0055 a0001c0002t0004g0143 others(2): Show |
5 | HG02723.hp1 HG04228.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-367_817-232del | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1477717 | |||||||
chr5:1477834 | C | T | 5 | a0001c0001t0002g0005 a0001c0001t0002g0095 a0001c0001t0002g0144 others(2): Show |
6 | NA18947.hp2 NA18949.hp2 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.817-348G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1477834 | |||||||
chr5:1477921 | GCCTGCTG others(61): Show |
G | 1 | a0001c0001t0021g0246 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.817-503_817-436del others(68): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1477921 | |||||||
chr5:1478041 | C | T | 153 | a0001c0001t0002g0036 a0001c0001t0002g0111 a0001c0001t0002g0115 others(150): Show |
157 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.817-555G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1478041 | |||||||
chr5:1478220 | C | G | 3 | a0001c0001t0013g0042 a0001c0001t0013g0055 a0001c0004t0013g0196 |
3 | HG04228.hp1 NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.817-734G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1478220 | |||||||
chr5:1478280 | C | T | 10 | a0001c0001t0013g0042 a0001c0001t0013g0055 a0001c0002t0004g0143 others(7): Show |
10 | HG01975.hp1 HG02055.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.817-794G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1478280 | |||||||
chr5:1478332 | T | A | 1 | a0001c0003t0006g0137 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.817-846A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1478332 | |||||||
chr5:1478596 | A | G | 312 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(309): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.816+1025T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1478596 | |||||||
chr5:1478681 | C | T | 1 | a0004c0012t0035g0280 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.816+940G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1478681 | |||||||
chr5:1479214 | A | T | 1 | a0001c0002t0001g0245 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.816+407T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1479214 | |||||||
chr5:1479238 | T | A | 2 | a0001c0002t0004g0100 a0001c0002t0004g0150 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.816+383A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1479238 | |||||||
chr5:1479252 | G | A | 1 | a0002c0005t0003g0330 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.816+369C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1479252 | |||||||
chr5:1479356 | C | A | 2 | a0001c0002t0004g0143 a0001c0002t0004g0271 |
2 | HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.816+265G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1479356 | |||||||
chr5:1479433 | G | A | 5 | a0001c0001t0013g0042 a0001c0001t0013g0055 a0001c0002t0004g0143 others(2): Show |
5 | HG02723.hp1 HG04228.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+188C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1479433 | |||||||
chr5:1479563 | G | C | 304 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(301): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.816+58C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1479563 | |||||||
chr5:1479617 | G | A | 1 | a0001c0004t0004g0258 | 1 | HG03704.hp2 | splice_region_variant&intron_variant | LOW | c.816+4C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1479617 | |||||||
chr5:1479764 | G | A | 1 | a0004c0012t0035g0280 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.762-89C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1479764 | |||||||
chr5:1479888 | C | T | 1 | a0001c0004t0013g0196 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.762-213G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1479888 | |||||||
chr5:1479899 | C | T | 7 | a0001c0001t0013g0042 a0001c0001t0013g0055 a0001c0004t0013g0196 others(4): Show |
7 | HG02451.hp1 HG02615.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.762-224G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1479899 | |||||||
chr5:1479953 | T | A | 25 | a0001c0001t0002g0060 a0001c0001t0005g0039 a0001c0001t0005g0058 others(22): Show |
28 | HG00597.hp1 HG01192.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.762-278A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1479953 | |||||||
chr5:1480102 | T | C | 1 | a0001c0001t0027g0272 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.762-427A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1480102 | |||||||
chr5:1480143 | T | C | 3 | a0001c0001t0013g0042 a0001c0001t0013g0055 a0001c0004t0013g0196 |
3 | HG04228.hp1 NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.762-468A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1480143 | |||||||
chr5:1480211 | C | A | 1 | a0001c0003t0001g0092 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.762-536G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1480211 | |||||||
chr5:1480332 | C | T | 1 | a0001c0001t0002g0283 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.761+610G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1480332 | |||||||
chr5:1480353 | T | C | 2 | a0001c0001t0002g0028 a0001c0004t0002g0244 |
2 | HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.761+589A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1480353 | |||||||
chr5:1480356 | A | G | 3 | a0001c0001t0013g0042 a0001c0001t0013g0055 a0001c0004t0013g0196 |
3 | HG04228.hp1 NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.761+586T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1480356 | |||||||
chr5:1480494 | T | C | 5 | a0001c0003t0009g0014 a0001c0003t0009g0041 a0001c0003t0009g0237 others(2): Show |
6 | HG02486.hp1 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.761+448A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1480494 | |||||||
chr5:1480515 | G | A | 105 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(102): Show |
112 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.761+427C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1480515 | |||||||
chr5:1480737 | C | T | 3 | a0001c0001t0004g0013 a0001c0001t0004g0347 a0001c0001t0004g0363 |
4 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.761+205G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1480737 | |||||||
chr5:1480780 | C | T | 1 | a0001c0001t0002g0187 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.761+162G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1480780 | |||||||
chr5:1480791 | C | T | 2 | a0001c0002t0004g0143 a0001c0002t0004g0271 |
2 | HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.761+151G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1480791 | |||||||
chr5:1480860 | T | C | 1 | a0001c0001t0002g0140 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.761+82A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1480860 | |||||||
chr5:1480886 | C | T | 1 | a0001c0004t0005g0288 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.761+56G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1480886 | |||||||
chr5:1481020 | CAGGGCCT others(6): Show |
C | 111 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(108): Show |
119 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.727-57_727-45delTG others(11): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481020 | |||||||
chr5:1481033 | A | C | 86 | a0001c0001t0002g0043 a0001c0001t0002g0253 a0001c0001t0004g0012 others(83): Show |
89 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.727-57T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481033 | |||||||
chr5:1481098 | A | G | 1 | a0001c0003t0001g0092 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.727-122T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481098 | |||||||
chr5:1481100 | G | A | 1 | a0001c0003t0001g0092 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.727-124C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481100 | |||||||
chr5:1481110 | T | A | 1 | a0001c0003t0001g0092 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.727-134A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481110 | |||||||
chr5:1481148 | G | A | 46 | a0001c0001t0004g0108 a0001c0001t0004g0299 a0001c0002t0001g0027 others(43): Show |
47 | HG00280.hp1 HG01099.hp2 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.727-172C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481148 | |||||||
chr5:1481166 | C | G | 2 | a0001c0001t0013g0042 a0001c0001t0013g0055 |
2 | NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.727-190G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481166 | |||||||
chr5:1481224 | A | C | 30 | a0001c0002t0001g0027 a0001c0002t0001g0035 a0001c0002t0001g0037 others(27): Show |
30 | HG01099.hp2 HG01106.hp2 HG01261.hp1 others(27): Show |
intron_variant | MODIFIER | c.727-248T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481224 | |||||||
chr5:1481295 | A | G | 80 | a0001c0001t0002g0043 a0001c0001t0002g0253 a0001c0001t0004g0012 others(77): Show |
83 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.727-319T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481295 | |||||||
chr5:1481314 | C | A | 1 | a0001c0001t0004g0012 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.727-338G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481314 | |||||||
chr5:1481383 | C | T | 3 | a0001c0009t0012g0107 a0001c0009t0012g0116 a0001c0019t0012g0278 |
3 | HG02451.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.727-407G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481383 | |||||||
chr5:1481434 | C | A | 1 | a0001c0003t0001g0092 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.727-458G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481434 | |||||||
chr5:1481453 | C | G | 1 | a0001c0004t0002g0262 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.727-477G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481453 | |||||||
chr5:1481459 | C | G | 1 | a0001c0001t0002g0212 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.727-483G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481459 | |||||||
chr5:1481555 | C | A | 1 | a0001c0004t0004g0068 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.727-579G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481555 | |||||||
chr5:1481571 | C | T | 3 | a0001c0009t0012g0107 a0001c0009t0012g0116 a0001c0019t0012g0278 |
3 | HG02451.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.727-595G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481571 | |||||||
chr5:1481697 | T | G | 1 | a0001c0015t0004g0252 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.727-721A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481697 | |||||||
chr5:1481702 | G | A | 1 | a0001c0001t0002g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.727-726C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481702 | |||||||
chr5:1481747 | C | A | 1 | a0004c0014t0034g0145 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.727-771G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481747 | |||||||
chr5:1481767 | G | A | 1 | a0001c0001t0002g0198 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.727-791C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481767 | |||||||
chr5:1481826 | C | G | 1 | a0001c0004t0004g0209 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.727-850G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481826 | |||||||
chr5:1481877 | C | T | 4 | a0001c0004t0002g0117 a0001c0004t0002g0335 a0001c0004t0002g0355 others(1): Show |
4 | HG00438.hp2 HG02135.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.727-901G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481877 | |||||||
chr5:1481880 | C | T | 48 | a0001c0001t0004g0108 a0001c0001t0004g0299 a0001c0001t0027g0272 others(45): Show |
49 | HG00280.hp1 HG01099.hp2 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.727-904G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481880 | |||||||
chr5:1481883 | G | C | 3 | a0001c0001t0013g0042 a0001c0001t0013g0055 a0001c0004t0013g0196 |
3 | HG04228.hp1 NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.727-907C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481883 | |||||||
chr5:1481910 | C | T | 2 | a0001c0002t0001g0201 a0002c0005t0003g0184 |
2 | HG01109.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.727-934G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481910 | |||||||
chr5:1482047 | C | T | 1 | a0001c0004t0013g0196 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.727-1071G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482047 | |||||||
chr5:1482056 | C | T | 1 | a0001c0001t0002g0260 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.727-1080G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482056 | |||||||
chr5:1482132 | AGTGGGCT | A | 31 | a0001c0001t0004g0108 a0001c0002t0001g0027 a0001c0002t0001g0035 others(28): Show |
31 | HG01099.hp2 HG01106.hp2 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.727-1163_727-1157d others(9): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482132 | |||||||
chr5:1482318 | G | C | 5 | a0001c0001t0007g0003 a0001c0001t0007g0034 a0001c0001t0007g0082 others(2): Show |
6 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.726+1110C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482318 | |||||||
chr5:1482492 | AGGCTGGG others(13): Show |
A | 1 | a0001c0003t0001g0342 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.726+916_726+935del others(20): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482492 | |||||||
chr5:1482495 | CTGGGG | C | 138 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0028 others(135): Show |
145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.726+928_726+932del others(5): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482495 | |||||||
chr5:1482505 | GTGGGGTG others(121): Show |
G | 1 | a0001c0007t0004g0254 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.726+795_726+922del | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482505 | |||||||
chr5:1482507 | GGGGTGGG others(34): Show |
G | 10 | a0001c0002t0001g0038 a0001c0002t0001g0251 a0001c0002t0001g0275 others(7): Show |
10 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.726+880_726+920del others(41): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482507 | |||||||
chr5:1482527 | G | GGGGTGGG others(65): Show |
1 | a0002c0005t0003g0301 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.726+829_726+900dup others(72): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482527 | |||||||
chr5:1482527 | GGGGTGGG others(29): Show |
G | 1 | a0001c0002t0001g0122 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.726+865_726+900del others(36): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482527 | |||||||
chr5:1482551 | G | C | 10 | a0001c0002t0001g0038 a0001c0002t0001g0251 a0001c0002t0001g0275 others(7): Show |
10 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.726+877C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482551 | |||||||
chr5:1482563 | A | G | 10 | a0001c0002t0001g0038 a0001c0002t0001g0251 a0001c0002t0001g0275 others(7): Show |
10 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.726+865T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482563 | |||||||
chr5:1482579 | AGGGCAGG others(69): Show |
A | 34 | a0001c0001t0002g0043 a0001c0001t0002g0253 a0001c0001t0004g0012 others(31): Show |
36 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.726+773_726+848del others(76): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482579 | |||||||
chr5:1482655 | T | A | 2 | a0001c0007t0004g0254 a0001c0010t0001g0273 |
2 | HG01346.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.726+773A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482655 | |||||||
chr5:1482666 | G | A | 1 | a0001c0002t0001g0242 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.726+762C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482666 | |||||||
chr5:1482702 | T | C | 1 | a0001c0001t0002g0078 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.726+726A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482702 | |||||||
chr5:1482716 | C | CTGGGG | 49 | a0001c0001t0004g0108 a0001c0001t0004g0299 a0001c0001t0027g0272 others(46): Show |
50 | HG00280.hp1 HG01099.hp2 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.726+707_726+711dup others(5): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482716 | |||||||
chr5:1482752 | T | C | 82 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0028 others(79): Show |
88 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.726+676A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482752 | |||||||
chr5:1482790 | T | C | 163 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0028 others(160): Show |
172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.726+638A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482790 | |||||||
chr5:1482791 | G | A | 49 | a0001c0001t0004g0108 a0001c0001t0004g0299 a0001c0001t0027g0272 others(46): Show |
50 | HG00280.hp1 HG01099.hp2 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.726+637C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482791 | |||||||
chr5:1483144 | A | C | 1 | a0001c0002t0004g0096 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.726+284T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1483144 | |||||||
chr5:1483151 | C | A | 37 | a0001c0001t0004g0108 a0001c0001t0027g0272 a0001c0002t0001g0027 others(34): Show |
37 | HG01099.hp2 HG01106.hp2 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.726+277G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1483151 | |||||||
chr5:1483362 | G | A | 5 | a0001c0001t0027g0272 a0001c0002t0004g0023 a0001c0002t0004g0100 others(2): Show |
5 | HG02895.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.726+66C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1483362 | |||||||
chr5:1483706 | C | T | 1 | a0002c0016t0003g0147 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.668-220G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483706 | |||||||
chr5:1483711 | A | AAGGAACA others(93): Show |
1 | a0001c0003t0001g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.668-226_668-225ins others(100): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483711 | |||||||
chr5:1483726 | T | C | 1 | a0001c0004t0002g0244 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.668-240A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483726 | |||||||
chr5:1483728 | T | G | 1 | a0001c0004t0002g0244 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.668-242A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483728 | |||||||
chr5:1483728 | T | TTAACATC others(93): Show |
2 | a0001c0001t0002g0089 a0001c0001t0004g0044 |
2 | HG00741.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.668-243_668-242ins others(100): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483728 | |||||||
chr5:1483728 | T | TTAACATC others(193): Show |
4 | a0001c0001t0004g0026 a0001c0001t0026g0025 a0001c0001t0028g0348 others(1): Show |
4 | HG01081.hp2 HG01109.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.668-243_668-242ins others(200): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483728 | |||||||
chr5:1483728 | T | TTAACATC others(93): Show |
1 | a0001c0001t0013g0042 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.668-243_668-242ins others(100): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483728 | |||||||
chr5:1483728 | TTAACATC others(93): Show |
T | 13 | a0001c0001t0005g0166 a0001c0001t0005g0314 a0001c0001t0006g0136 others(10): Show |
14 | HG01106.hp1 HG01192.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.668-342_668-243del others(100): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483728 | |||||||
chr5:1483738 | G | A | 1 | a0001c0001t0005g0292 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.668-252C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483738 | |||||||
chr5:1483742 | G | A | 16 | a0001c0001t0004g0012 a0001c0001t0004g0079 a0001c0001t0004g0134 others(13): Show |
18 | HG00140.hp2 HG01069.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.668-256C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483742 | |||||||
chr5:1483742 | G | AAGCTGGA others(93): Show |
2 | a0001c0001t0002g0239 a0001c0001t0002g0360 |
2 | HG00741.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.668-256delCinsGGTG others(97): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483742 | |||||||
chr5:1483742 | G | AAGCTGGA others(193): Show |
2 | a0001c0002t0008g0130 a0001c0002t0036g0365 |
2 | HG00280.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.668-256delCinsGGTG others(197): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483742 | |||||||
chr5:1483742 | G | C | 17 | a0001c0001t0002g0060 a0001c0001t0004g0026 a0001c0001t0004g0044 others(14): Show |
19 | HG00741.hp1 HG01081.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.668-256C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483742 | |||||||
chr5:1483742 | G | GAGCTGGA others(93): Show |
27 | a0001c0001t0002g0089 a0001c0001t0002g0187 a0001c0001t0002g0345 others(24): Show |
28 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.668-356_668-257dup others(100): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483742 | |||||||
chr5:1483742 | G | GAGCTGGA others(193): Show |
2 | a0001c0003t0001g0065 a0001c0003t0016g0366 |
2 | HG00423.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.668-456_668-257dup others(200): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483742 | |||||||
chr5:1483742 | G | GAGCTGGA others(393): Show |
1 | a0001c0003t0006g0175 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.668-257_668-256ins others(400): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483742 | |||||||
chr5:1483742 | G | GAGCTGGA others(293): Show |
1 | a0001c0002t0001g0300 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.668-257_668-256ins others(300): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483742 | |||||||
chr5:1483742 | G | GAGCTGGA others(493): Show |
1 | a0001c0001t0002g0220 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.668-257_668-256ins others(500): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483742 | |||||||
chr5:1483742 | G | GAGCTGGA others(93): Show |
1 | a0001c0002t0001g0307 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.668-257_668-256ins others(100): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483742 | |||||||
chr5:1483742 | GAGCTGGA others(93): Show |
A | 1 | a0001c0004t0005g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.668-356_668-256del others(105): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483742 | |||||||
chr5:1483742 | GAGCTGGA others(93): Show |
G | 92 | a0001c0001t0002g0008 a0001c0001t0002g0016 a0001c0001t0002g0036 others(89): Show |
96 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.668-356_668-257del others(100): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483742 | |||||||
chr5:1483778 | A | ATAACATT others(93): Show |
2 | a0001c0001t0005g0039 a0001c0001t0005g0263 |
2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.668-293_668-292ins others(100): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483778 | |||||||
chr5:1483778 | A | G | 6 | a0001c0002t0001g0248 a0001c0003t0006g0170 a0001c0003t0006g0206 others(3): Show |
6 | HG00621.hp1 HG02040.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.668-292T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483778 | |||||||
chr5:1483787 | C | CGCACGAG others(93): Show |
1 | a0001c0002t0001g0230 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.668-302_668-301ins others(100): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483787 | |||||||
chr5:1483803 | C | T | 3 | a0001c0001t0002g0006 a0001c0001t0002g0140 a0001c0001t0002g0141 |
4 | HG00408.hp1 NA18953.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.668-317G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483803 | |||||||
chr5:1483826 | C | T | 14 | a0001c0001t0002g0005 a0001c0001t0002g0095 a0001c0001t0002g0223 others(11): Show |
15 | HG00438.hp2 HG02135.hp2 HG02155.hp2 others(12): Show |
intron_variant | MODIFIER | c.668-340G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483826 | |||||||
chr5:1483828 | G | T | 14 | a0001c0001t0002g0005 a0001c0001t0002g0095 a0001c0001t0002g0223 others(11): Show |
15 | HG00438.hp2 HG02135.hp2 HG02155.hp2 others(12): Show |
intron_variant | MODIFIER | c.668-342C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483828 | |||||||
chr5:1483842 | C | A | 2 | a0001c0004t0004g0210 a0001c0007t0004g0257 |
2 | HG01106.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.668-356G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483842 | |||||||
chr5:1483878 | A | G | 1 | a0001c0002t0001g0322 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.668-392T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483878 | |||||||
chr5:1483892 | G | GAGCTGGA others(43): Show |
2 | a0001c0001t0002g0098 a0001c0001t0002g0129 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.668-456_668-407dup others(50): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483892 | |||||||
chr5:1483928 | G | A | 1 | a0001c0004t0013g0196 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.668-442C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483928 | |||||||
chr5:1483936 | G | GCGCACCA others(93): Show |
1 | a0001c0002t0004g0023 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.668-451_668-450ins others(100): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483936 | |||||||
chr5:1483995 | C | T | 6 | a0001c0002t0001g0287 a0001c0002t0004g0100 a0001c0002t0004g0150 others(3): Show |
6 | HG01346.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.668-509G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483995 | |||||||
chr5:1484379 | C | T | 127 | a0001c0001t0002g0111 a0001c0001t0002g0127 a0001c0001t0002g0212 others(124): Show |
134 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.668-893G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484379 | |||||||
chr5:1484405 | T | C | 25 | a0001c0001t0002g0126 a0001c0001t0002g0253 a0001c0001t0002g0329 others(22): Show |
26 | HG00280.hp1 HG01081.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.668-919A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484405 | |||||||
chr5:1484422 | A | G | 1 | a0001c0003t0001g0094 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.668-936T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484422 | |||||||
chr5:1484495 | G | A | 19 | a0001c0001t0002g0126 a0001c0001t0002g0253 a0001c0001t0004g0026 others(16): Show |
20 | HG00280.hp1 HG01081.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.668-1009C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484495 | |||||||
chr5:1484670 | G | A | 2 | a0001c0001t0005g0039 a0001c0001t0005g0263 |
2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.668-1184C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484670 | |||||||
chr5:1484677 | T | C | 16 | a0001c0001t0002g0006 a0001c0001t0002g0127 a0001c0001t0002g0140 others(13): Show |
18 | HG00408.hp1 HG00738.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.668-1191A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484677 | |||||||
chr5:1484692 | G | A | 2 | a0001c0001t0002g0098 a0001c0001t0002g0129 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.668-1206C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484692 | |||||||
chr5:1484711 | G | A | 32 | a0001c0001t0002g0008 a0001c0001t0002g0071 a0001c0001t0002g0183 others(29): Show |
34 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.668-1225C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484711 | |||||||
chr5:1484720 | G | A | 13 | a0001c0001t0002g0360 a0001c0001t0004g0132 a0001c0001t0004g0135 others(10): Show |
13 | HG00140.hp2 HG00741.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.668-1234C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484720 | |||||||
chr5:1484769 | T | C | 1 | a0001c0007t0005g0106 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.668-1283A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484769 | |||||||
chr5:1484810 | G | A | 3 | a0001c0001t0002g0212 a0001c0002t0004g0096 a0002c0005t0003g0323 |
3 | HG00735.hp2 NA18945.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.668-1324C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484810 | |||||||
chr5:1484819 | CCT | C | 4 | a0001c0002t0004g0271 a0001c0003t0001g0279 a0001c0004t0004g0068 others(1): Show |
4 | HG01069.hp2 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.668-1335_668-1334d others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484819 | |||||||
chr5:1484877 | A | G | 179 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0089 others(176): Show |
189 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.668-1391T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484877 | |||||||
chr5:1484903 | C | G | 1 | a0002c0005t0003g0323 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.668-1417G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484903 | |||||||
chr5:1484908 | T | C | 1 | a0001c0002t0004g0096 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.668-1422A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484908 | |||||||
chr5:1484915 | G | C | 13 | a0001c0001t0002g0016 a0001c0001t0002g0346 a0001c0001t0004g0108 others(10): Show |
14 | HG00408.hp2 HG02723.hp2 HG02895.hp1 others(11): Show |
intron_variant | MODIFIER | c.668-1429C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484915 | |||||||
chr5:1484943 | G | A | 1 | a0001c0002t0004g0096 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.668-1457C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484943 | |||||||
chr5:1484949 | C | T | 1 | a0001c0002t0004g0096 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.668-1463G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484949 | |||||||
chr5:1484992 | G | A | 1 | a0001c0004t0005g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.668-1506C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484992 | |||||||
chr5:1485007 | C | T | 3 | a0003c0008t0002g0009 a0003c0008t0002g0191 a0003c0008t0002g0351 |
4 | HG00099.hp2 HG00323.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.668-1521G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485007 | |||||||
chr5:1485010 | A | C | 123 | a0001c0001t0002g0111 a0001c0001t0005g0171 a0001c0001t0005g0356 others(120): Show |
130 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.668-1524T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485010 | |||||||
chr5:1485079 | G | C | 2 | a0001c0001t0002g0359 a0001c0004t0002g0244 |
2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.668-1593C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485079 | |||||||
chr5:1485100 | G | T | 1 | a0001c0002t0004g0096 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.668-1614C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485100 | |||||||
chr5:1485102 | G | A | 1 | a0001c0001t0002g0089 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.668-1616C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485102 | |||||||
chr5:1485223 | C | A | 1 | a0001c0003t0001g0249 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.668-1737G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485223 | |||||||
chr5:1485354 | C | A | 2 | a0001c0001t0002g0111 a0004c0014t0034g0145 |
2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.668-1868G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485354 | |||||||
chr5:1485396 | G | C | 2 | a0001c0004t0005g0101 a0001c0004t0005g0159 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.668-1910C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485396 | |||||||
chr5:1485465 | G | T | 2 | a0001c0001t0002g0195 a0001c0001t0018g0020 |
2 | HG02056.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.668-1979C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485465 | |||||||
chr5:1485467 | G | A | 23 | a0001c0001t0002g0089 a0001c0001t0002g0359 a0001c0001t0004g0075 others(20): Show |
24 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.668-1981C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485467 | |||||||
chr5:1485628 | C | T | 1 | a0001c0001t0013g0042 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.668-2142G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485628 | |||||||
chr5:1485805 | C | T | 3 | a0001c0003t0001g0279 a0001c0004t0004g0068 a0001c0004t0005g0288 |
3 | HG01069.hp2 HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.668-2319G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485805 | |||||||
chr5:1485852 | G | A | 107 | a0001c0001t0002g0317 a0001c0001t0002g0318 a0001c0001t0005g0199 others(104): Show |
113 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.668-2366C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485852 | |||||||
chr5:1485932 | C | T | 20 | a0001c0001t0002g0126 a0001c0001t0002g0253 a0001c0001t0004g0026 others(17): Show |
21 | HG00280.hp1 HG01081.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.668-2446G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485932 | |||||||
chr5:1485933 | G | A | 1 | a0002c0005t0003g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.668-2447C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485933 | |||||||
chr5:1485960 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.667+2431G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485960 | |||||||
chr5:1485964 | G | C | 2 | a0001c0001t0002g0359 a0001c0004t0002g0244 |
2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.667+2427C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485964 | |||||||
chr5:1486064 | C | T | 1 | a0001c0001t0004g0135 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.667+2327G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1486064 | |||||||
chr5:1486190 | C | T | 1 | a0001c0002t0036g0365 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.667+2201G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1486190 | |||||||
chr5:1486412 | G | T | 4 | a0001c0003t0001g0325 a0001c0003t0001g0334 a0001c0003t0001g0336 others(1): Show |
4 | HG00597.hp2 HG00621.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.667+1979C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1486412 | |||||||
chr5:1486428 | C | T | 2 | a0001c0001t0002g0111 a0004c0014t0034g0145 |
2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.667+1963G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1486428 | |||||||
chr5:1486493 | C | T | 3 | a0001c0003t0001g0279 a0001c0004t0004g0068 a0001c0004t0005g0288 |
3 | HG01069.hp2 HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.667+1898G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1486493 | |||||||
chr5:1486628 | G | C | 2 | a0001c0001t0002g0111 a0004c0014t0034g0145 |
2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.667+1763C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1486628 | |||||||
chr5:1486639 | G | A | 1 | a0001c0001t0007g0281 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.667+1752C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1486639 | |||||||
chr5:1486868 | C | T | 1 | a0001c0001t0002g0126 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.667+1523G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1486868 | |||||||
chr5:1486895 | C | A | 1 | a0001c0003t0001g0073 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.667+1496G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1486895 | |||||||
chr5:1486965 | T | C | 1 | a0001c0001t0013g0042 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.667+1426A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1486965 | |||||||
chr5:1486995 | G | A | 1 | a0001c0003t0009g0233 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.667+1396C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1486995 | |||||||
chr5:1487004 | C | T | 1 | a0001c0002t0004g0096 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.667+1387G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487004 | |||||||
chr5:1487037 | T | A | 1 | a0001c0003t0001g0073 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.667+1354A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487037 | |||||||
chr5:1487046 | C | T | 1 | a0001c0002t0004g0096 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.667+1345G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487046 | |||||||
chr5:1487067 | G | A | 21 | a0001c0001t0002g0089 a0001c0001t0002g0359 a0001c0001t0007g0003 others(18): Show |
22 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.667+1324C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487067 | |||||||
chr5:1487155 | T | C | 193 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0089 others(190): Show |
204 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.667+1236A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487155 | |||||||
chr5:1487173 | C | T | 2 | a0001c0001t0002g0111 a0004c0014t0034g0145 |
2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.667+1218G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487173 | |||||||
chr5:1487309 | C | T | 117 | a0001c0001t0005g0356 a0001c0001t0005g0357 a0001c0001t0028g0348 others(114): Show |
124 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.667+1082G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487309 | |||||||
chr5:1487359 | G | A | 1 | a0001c0002t0004g0271 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.667+1032C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487359 | |||||||
chr5:1487361 | G | T | 1 | a0001c0001t0020g0305 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.667+1030C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487361 | |||||||
chr5:1487524 | G | A | 1 | a0001c0001t0007g0003 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.667+867C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487524 | |||||||
chr5:1487548 | G | A | 119 | a0001c0001t0002g0111 a0001c0001t0005g0356 a0001c0001t0005g0357 others(116): Show |
126 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.667+843C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487548 | |||||||
chr5:1487880 | T | C | 13 | a0001c0001t0002g0016 a0001c0001t0002g0346 a0001c0001t0004g0108 others(10): Show |
14 | HG00408.hp2 HG02723.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.667+511A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487880 | |||||||
chr5:1487923 | C | T | 1 | a0002c0005t0031g0217 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.667+468G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487923 | |||||||
chr5:1487942 | C | A | 1 | a0001c0001t0007g0138 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.667+449G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487942 | |||||||
chr5:1487991 | C | G | 1 | a0001c0002t0004g0096 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.667+400G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487991 | |||||||
chr5:1488032 | C | T | 7 | a0001c0001t0002g0040 a0001c0001t0002g0295 a0001c0001t0002g0303 others(4): Show |
7 | HG00423.hp1 NA18980.hp2 NA19002.hp2 others(4): Show |
intron_variant | MODIFIER | c.667+359G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1488032 | |||||||
chr5:1488035 | G | T | 20 | a0001c0001t0002g0126 a0001c0001t0002g0253 a0001c0001t0004g0026 others(17): Show |
21 | HG00280.hp1 HG01081.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.667+356C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1488035 | |||||||
chr5:1488102 | G | A | 11 | a0001c0001t0002g0016 a0001c0001t0002g0346 a0001c0001t0004g0108 others(8): Show |
12 | HG00408.hp2 HG02723.hp2 HG03098.hp2 others(9): Show |
intron_variant | MODIFIER | c.667+289C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1488102 | |||||||
chr5:1488387 | A | G | 1 | a0001c0003t0014g0018 | 1 | HG04228.hp2 | splice_region_variant&intron_variant | LOW | c.667+4T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1488387 | |||||||
chr5:1488626 | C | T | 2 | a0001c0001t0002g0111 a0004c0014t0034g0145 |
2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.607-175G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1488626 | |||||||
chr5:1488874 | T | A | 3 | a0001c0001t0002g0043 a0001c0002t0001g0290 a0001c0015t0004g0252 |
3 | HG00099.hp1 NA20752.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.607-423A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1488874 | |||||||
chr5:1488905 | C | T | 5 | a0001c0001t0002g0016 a0001c0001t0002g0346 a0001c0002t0001g0248 others(2): Show |
6 | HG00408.hp2 HG02723.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.607-454G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1488905 | |||||||
chr5:1488928 | G | A | 22 | a0001c0001t0002g0089 a0001c0001t0002g0359 a0001c0001t0004g0075 others(19): Show |
23 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.607-477C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1488928 | |||||||
chr5:1488958 | G | A | 118 | a0001c0001t0002g0111 a0001c0001t0005g0356 a0001c0001t0005g0357 others(115): Show |
125 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.607-507C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1488958 | |||||||
chr5:1488974 | T | C | 156 | a0001c0001t0002g0016 a0001c0001t0002g0111 a0001c0001t0002g0126 others(153): Show |
165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.607-523A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1488974 | |||||||
chr5:1489051 | G | A | 1 | a0001c0004t0005g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.607-600C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1489051 | |||||||
chr5:1489077 | C | T | 1 | a0001c0002t0008g0340 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.607-626G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1489077 | |||||||
chr5:1489133 | G | A | 13 | a0001c0001t0002g0006 a0001c0001t0002g0127 a0001c0001t0002g0140 others(10): Show |
14 | HG00408.hp1 HG00738.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.606+613C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1489133 | |||||||
chr5:1489194 | G | A | 13 | a0001c0001t0002g0006 a0001c0001t0002g0127 a0001c0001t0002g0140 others(10): Show |
14 | HG00408.hp1 HG00738.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.606+552C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1489194 | |||||||
chr5:1489239 | C | T | 11 | a0001c0001t0002g0016 a0001c0001t0002g0346 a0001c0001t0004g0108 others(8): Show |
12 | HG00408.hp2 HG02723.hp2 HG03098.hp2 others(9): Show |
intron_variant | MODIFIER | c.606+507G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1489239 | |||||||
chr5:1489270 | A | G | 1 | a0001c0007t0005g0106 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.606+476T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1489270 | |||||||
chr5:1489273 | G | A | 1 | a0001c0001t0002g0187 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.606+473C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1489273 | |||||||
chr5:1489286 | G | C | 1 | a0001c0001t0002g0212 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.606+460C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1489286 | |||||||
chr5:1489397 | G | A | 1 | a0001c0001t0004g0222 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.606+349C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1489397 | |||||||
chr5:1489465 | G | A | 1 | a0001c0003t0006g0074 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.606+281C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1489465 | |||||||
chr5:1489591 | A | G | 192 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0089 others(189): Show |
203 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.606+155T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1489591 | |||||||
chr5:1489616 | C | T | 1 | a0001c0002t0004g0271 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.606+130G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1489616 | |||||||
chr5:1489903 | C | T | 4 | a0001c0001t0004g0026 a0001c0001t0019g0072 a0001c0001t0026g0025 others(1): Show |
4 | HG01081.hp2 HG01109.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.494-45G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1489903 | |||||||
chr5:1489904 | C | G | 21 | a0001c0001t0002g0126 a0001c0001t0002g0212 a0001c0001t0002g0253 others(18): Show |
22 | HG00280.hp1 HG00735.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.494-46G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1489904 | |||||||
chr5:1489905 | G | A | 1 | a0001c0002t0004g0096 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.494-47C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1489905 | |||||||
chr5:1489956 | G | A | 1 | a0001c0002t0004g0271 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.494-98C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1489956 | |||||||
chr5:1490009 | A | C | 179 | a0001c0001t0002g0006 a0001c0001t0002g0089 a0001c0001t0002g0111 others(176): Show |
189 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.494-151T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490009 | |||||||
chr5:1490024 | A | C | 6 | a0001c0001t0002g0016 a0001c0001t0002g0346 a0001c0001t0027g0272 others(3): Show |
7 | HG00408.hp2 HG02723.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.494-166T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490024 | |||||||
chr5:1490033 | G | A | 2 | a0001c0002t0004g0096 a0001c0007t0005g0106 |
2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.494-175C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490033 | |||||||
chr5:1490080 | A | C | 119 | a0001c0001t0002g0111 a0001c0001t0005g0171 a0001c0001t0005g0356 others(116): Show |
126 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.494-222T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490080 | |||||||
chr5:1490121 | C | T | 1 | a0001c0010t0001g0264 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.494-263G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490121 | |||||||
chr5:1490134 | G | A | 1 | a0001c0001t0005g0321 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.494-276C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490134 | |||||||
chr5:1490229 | C | A | 2 | a0001c0003t0001g0205 a0001c0004t0004g0258 |
2 | HG02738.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.494-371G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490229 | |||||||
chr5:1490237 | T | G | 193 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0089 others(190): Show |
204 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.494-379A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490237 | |||||||
chr5:1490410 | G | T | 2 | a0001c0007t0004g0257 a0001c0007t0022g0256 |
2 | HG01106.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.494-552C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490410 | |||||||
chr5:1490418 | T | G | 2 | a0001c0004t0017g0017 a0001c0004t0024g0033 |
2 | HG02145.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.494-560A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490418 | |||||||
chr5:1490431 | C | T | 2 | a0001c0001t0002g0111 a0004c0014t0034g0145 |
2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.494-573G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490431 | |||||||
chr5:1490479 | T | C | 193 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0089 others(190): Show |
204 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.494-621A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490479 | |||||||
chr5:1490742 | G | A | 1 | a0001c0001t0004g0052 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.494-884C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490742 | |||||||
chr5:1490853 | G | T | 1 | a0001c0002t0001g0322 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.494-995C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490853 | |||||||
chr5:1490872 | C | T | 1 | a0001c0003t0001g0266 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.494-1014G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490872 | |||||||
chr5:1490889 | A | G | 1 | a0001c0001t0002g0212 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.494-1031T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490889 | |||||||
chr5:1490894 | A | G | 67 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0089 others(64): Show |
71 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.494-1036T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490894 | |||||||
chr5:1491099 | G | A | 1 | a0001c0001t0028g0348 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.494-1241C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491099 | |||||||
chr5:1491123 | T | C | 2 | a0001c0002t0004g0096 a0001c0007t0005g0106 |
2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.494-1265A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491123 | |||||||
chr5:1491214 | G | A | 114 | a0001c0001t0005g0356 a0001c0001t0005g0357 a0001c0001t0028g0348 others(111): Show |
121 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.494-1356C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491214 | |||||||
chr5:1491220 | G | A | 1 | a0001c0002t0001g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.494-1362C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491220 | |||||||
chr5:1491222 | A | AAGGGAAG others(46): Show |
2 | a0001c0001t0002g0006 a0001c0002t0001g0289 |
3 | NA18953.hp2 NA18955.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.494-1365_494-1364i others(55): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491222 | |||||||
chr5:1491222 | A | AAGGGAAG others(46): Show |
43 | a0001c0001t0002g0016 a0001c0001t0002g0111 a0001c0001t0002g0126 others(40): Show |
45 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.494-1365_494-1364i others(55): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491222 | |||||||
chr5:1491242 | G | A | 1 | a0001c0002t0001g0051 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.494-1384C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491242 | |||||||
chr5:1491262 | C | T | 1 | a0001c0001t0007g0138 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.494-1404G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491262 | |||||||
chr5:1491270 | A | C | 1 | a0001c0001t0013g0042 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.494-1412T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491270 | |||||||
chr5:1491391 | G | C | 1 | a0001c0003t0001g0229 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.494-1533C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491391 | |||||||
chr5:1491435 | C | T | 1 | a0001c0003t0009g0233 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.494-1577G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491435 | |||||||
chr5:1491561 | G | A | 3 | a0001c0003t0001g0279 a0001c0004t0004g0068 a0001c0004t0005g0288 |
3 | HG01069.hp2 HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.494-1703C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491561 | |||||||
chr5:1491621 | C | T | 4 | a0001c0001t0004g0108 a0001c0001t0007g0269 a0001c0001t0028g0348 others(1): Show |
4 | HG01346.hp2 HG01361.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-1763G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491621 | |||||||
chr5:1491653 | G | A | 2 | a0001c0001t0002g0111 a0004c0014t0034g0145 |
2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.494-1795C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491653 | |||||||
chr5:1491656 | G | A | 6 | a0001c0001t0004g0108 a0001c0001t0007g0269 a0001c0002t0004g0100 others(3): Show |
6 | HG02895.hp1 HG02897.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.494-1798C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491656 | |||||||
chr5:1491773 | G | A | 2 | a0001c0004t0004g0209 a0001c0004t0004g0210 |
2 | HG03669.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.494-1915C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491773 | |||||||
chr5:1491909 | A | T | 1 | a0002c0005t0003g0102 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.494-2051T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491909 | |||||||
chr5:1491967 | G | A | 2 | a0001c0001t0002g0220 a0001c0002t0001g0300 |
2 | HG00639.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.494-2109C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491967 | |||||||
chr5:1491974 | T | C | 2 | a0001c0002t0004g0096 a0001c0007t0005g0106 |
2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.494-2116A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491974 | |||||||
chr5:1492001 | G | A | 14 | a0001c0001t0002g0006 a0001c0001t0002g0127 a0001c0001t0002g0140 others(11): Show |
15 | HG00408.hp1 HG00738.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.494-2143C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492001 | |||||||
chr5:1492087 | G | T | 26 | a0001c0001t0002g0016 a0001c0001t0002g0111 a0001c0001t0002g0126 others(23): Show |
28 | HG00280.hp1 HG00408.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.494-2229C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492087 | |||||||
chr5:1492150 | C | T | 1 | a0004c0012t0035g0280 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.494-2292G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492150 | |||||||
chr5:1492250 | A | AGCCTGGG others(19): Show |
2 | a0001c0001t0002g0111 a0004c0014t0034g0145 |
2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.494-2418_494-2393d others(28): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492250 | |||||||
chr5:1492341 | G | A | 20 | a0001c0001t0002g0126 a0001c0001t0002g0253 a0001c0001t0004g0026 others(17): Show |
21 | HG00280.hp1 HG01081.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.493+2359C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492341 | |||||||
chr5:1492364 | G | A | 1 | a0001c0003t0006g0190 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.493+2336C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492364 | |||||||
chr5:1492444 | A | G | 193 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0089 others(190): Show |
204 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.493+2256T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492444 | |||||||
chr5:1492453 | G | A | 4 | a0001c0002t0004g0100 a0001c0002t0004g0150 a0001c0010t0001g0264 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.493+2247C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492453 | |||||||
chr5:1492527 | C | T | 121 | a0001c0001t0005g0171 a0001c0001t0005g0356 a0001c0001t0005g0357 others(118): Show |
128 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.493+2173G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492527 | |||||||
chr5:1492544 | C | CTTGT | 193 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0089 others(190): Show |
204 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.493+2152_493+2155d others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492544 | |||||||
chr5:1492640 | C | T | 1 | a0001c0002t0004g0271 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.493+2060G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492640 | |||||||
chr5:1492819 | GC | G | 5 | a0001c0001t0002g0028 a0001c0001t0007g0034 a0001c0001t0007g0082 others(2): Show |
5 | HG01243.hp1 HG01496.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.493+1880delG | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492819 | |||||||
chr5:1492826 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.493+1874G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492826 | |||||||
chr5:1492856 | C | T | 69 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0089 others(66): Show |
73 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.493+1844G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492856 | |||||||
chr5:1492910 | C | T | 1 | a0001c0002t0001g0230 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.493+1790G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492910 | |||||||
chr5:1492928 | A | C | 1 | a0001c0009t0012g0116 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.493+1772T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492928 | |||||||
chr5:1492957 | C | T | 11 | a0001c0001t0004g0075 a0001c0001t0007g0003 a0001c0001t0007g0138 others(8): Show |
12 | HG02055.hp2 HG02451.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.493+1743G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492957 | |||||||
chr5:1492966 | G | C | 69 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0089 others(66): Show |
73 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.493+1734C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492966 | |||||||
chr5:1492980 | C | T | 1 | a0001c0001t0027g0272 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.493+1720G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492980 | |||||||
chr5:1492983 | G | A | 1 | a0004c0012t0035g0280 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.493+1717C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492983 | |||||||
chr5:1493062 | G | A | 1 | a0001c0007t0005g0106 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.493+1638C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493062 | |||||||
chr5:1493423 | G | A | 1 | a0002c0005t0003g0361 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.493+1277C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493423 | |||||||
chr5:1493467 | G | A | 4 | a0001c0002t0004g0100 a0001c0002t0004g0150 a0001c0010t0001g0264 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.493+1233C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493467 | |||||||
chr5:1493493 | G | A | 119 | a0001c0001t0005g0356 a0001c0001t0005g0357 a0001c0001t0028g0348 others(116): Show |
126 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.493+1207C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493493 | |||||||
chr5:1493532 | G | A | 2 | a0001c0001t0004g0108 a0001c0001t0007g0269 |
2 | HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.493+1168C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493532 | |||||||
chr5:1493538 | C | T | 1 | a0001c0001t0021g0246 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.493+1162G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493538 | |||||||
chr5:1493631 | A | G | 1 | a0001c0001t0013g0042 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.493+1069T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493631 | |||||||
chr5:1493677 | G | A | 1 | a0001c0003t0001g0336 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.493+1023C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493677 | |||||||
chr5:1493702 | G | C | 1 | a0001c0007t0005g0106 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.493+998C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493702 | |||||||
chr5:1493711 | A | G | 1 | a0001c0002t0006g0203 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.493+989T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493711 | |||||||
chr5:1493712 | G | C | 4 | a0001c0001t0002g0005 a0001c0001t0002g0095 a0001c0001t0002g0223 others(1): Show |
5 | NA18947.hp2 NA18949.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.493+988C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493712 | |||||||
chr5:1493733 | G | A | 4 | a0001c0002t0004g0100 a0001c0002t0004g0150 a0001c0010t0001g0264 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.493+967C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493733 | |||||||
chr5:1493752 | A | G | 117 | a0001c0001t0005g0356 a0001c0001t0005g0357 a0001c0001t0028g0348 others(114): Show |
124 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.493+948T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493752 | |||||||
chr5:1493753 | G | C | 1 | a0001c0001t0004g0026 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.493+947C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493753 | |||||||
chr5:1493770 | G | A | 1 | a0001c0004t0002g0173 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.493+930C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493770 | |||||||
chr5:1493859 | G | A | 1 | a0001c0001t0011g0324 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.493+841C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493859 | |||||||
chr5:1493955 | G | A | 112 | a0001c0001t0005g0356 a0001c0001t0005g0357 a0001c0001t0028g0348 others(109): Show |
119 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.493+745C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493955 | |||||||
chr5:1494123 | T | C | 191 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0089 others(188): Show |
202 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.493+577A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1494123 | |||||||
chr5:1494148 | T | TG | 190 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0089 others(187): Show |
201 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.493+551dupC | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1494148 | |||||||
chr5:1494156 | G | A | 1 | a0005c0013t0003g0189 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.493+544C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1494156 | |||||||
chr5:1494278 | G | A | 1 | a0002c0005t0004g0153 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.493+422C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1494278 | |||||||
chr5:1494324 | C | T | 289 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(286): Show |
304 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.493+376G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1494324 | |||||||
chr5:1494394 | G | A | 2 | a0001c0001t0013g0042 a0001c0002t0004g0096 |
2 | NA18964.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.493+306C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1494394 | |||||||
chr5:1494412 | G | A | 2 | a0001c0001t0004g0108 a0001c0001t0007g0269 |
2 | HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.493+288C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1494412 | |||||||
chr5:1494414 | T | TG | 43 | a0001c0001t0002g0095 a0001c0001t0002g0283 a0001c0001t0002g0329 others(40): Show |
44 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.493+285dupC | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1494414 | |||||||
chr5:1494416 | G | C | 13 | a0001c0001t0002g0006 a0001c0001t0002g0127 a0001c0001t0002g0140 others(10): Show |
14 | HG00408.hp1 HG00738.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.493+284C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1494416 | |||||||
chr5:1494417 | G | T | 27 | a0001c0001t0002g0016 a0001c0001t0002g0111 a0001c0001t0002g0126 others(24): Show |
29 | HG00280.hp1 HG00408.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.493+283C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1494417 | |||||||
chr5:1494423 | G | T | 2 | a0001c0009t0012g0107 a0001c0009t0012g0116 |
2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.493+277C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1494423 | |||||||
chr5:1494428 | C | G | 1 | a0001c0002t0001g0319 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.493+272G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1494428 | |||||||
chr5:1494649 | C | T | 26 | a0001c0001t0002g0016 a0001c0001t0002g0111 a0001c0001t0002g0126 others(23): Show |
28 | HG00280.hp1 HG00408.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.493+51G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1494649 | |||||||
chr5:1494923 | G | A | 1 | a0001c0003t0001g0334 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.279-9C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1494923 | |||||||
chr5:1494950 | T | C | 2 | a0001c0001t0027g0272 a0001c0002t0004g0023 |
2 | HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.279-36A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1494950 | |||||||
chr5:1495104 | T | C | 59 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0060 others(56): Show |
63 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.279-190A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495104 | |||||||
chr5:1495140 | G | A | 1 | a0001c0001t0002g0212 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.279-226C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495140 | |||||||
chr5:1495162 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.279-248G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495162 | |||||||
chr5:1495169 | C | T | 11 | a0001c0002t0001g0274 a0001c0002t0004g0096 a0001c0002t0004g0100 others(8): Show |
11 | HG01069.hp2 HG02145.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.279-255G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495169 | |||||||
chr5:1495181 | T | C | 34 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0111 others(31): Show |
36 | HG00408.hp1 HG00408.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.279-267A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495181 | |||||||
chr5:1495181 | T | G | 1 | a0001c0001t0002g0089 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.279-267A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495181 | |||||||
chr5:1495250 | A | G | 2 | a0001c0002t0008g0004 a0001c0002t0008g0114 |
3 | HG01256.hp2 HG01258.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.279-336T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495250 | |||||||
chr5:1495316 | C | T | 1 | a0001c0004t0002g0244 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.279-402G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495316 | |||||||
chr5:1495330 | T | TG | 29 | a0001c0001t0002g0040 a0001c0001t0002g0095 a0001c0001t0002g0144 others(26): Show |
29 | HG00140.hp2 HG00597.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.279-417dupC | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495330 | |||||||
chr5:1495330 | TG | T | 195 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0016 others(192): Show |
208 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.279-417delC | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495330 | |||||||
chr5:1495334 | G | C | 140 | a0001c0001t0002g0016 a0001c0001t0002g0346 a0001c0001t0002g0359 others(137): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.279-420C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495334 | |||||||
chr5:1495336 | G | C | 2 | a0001c0004t0004g0209 a0001c0004t0004g0210 |
2 | HG03669.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.279-422C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495336 | |||||||
chr5:1495358 | C | T | 5 | a0001c0001t0002g0028 a0001c0001t0007g0034 a0001c0001t0007g0082 others(2): Show |
5 | HG01243.hp1 HG01496.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.279-444G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495358 | |||||||
chr5:1495395 | T | C | 1 | a0001c0001t0002g0140 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.279-481A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495395 | |||||||
chr5:1495398 | C | T | 1 | a0001c0010t0001g0264 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.279-484G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495398 | |||||||
chr5:1495615 | T | C | 2 | a0001c0009t0012g0107 a0001c0009t0012g0116 |
2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.279-701A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495615 | |||||||
chr5:1495648 | A | G | 233 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(230): Show |
242 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.279-734T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495648 | |||||||
chr5:1495649 | G | T | 3 | a0001c0003t0001g0279 a0001c0004t0004g0068 a0001c0004t0005g0288 |
3 | HG01069.hp2 HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.279-735C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495649 | |||||||
chr5:1495654 | G | A | 1 | a0001c0001t0002g0329 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.279-740C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495654 | |||||||
chr5:1495663 | G | A | 1 | a0001c0004t0002g0304 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.279-749C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495663 | |||||||
chr5:1495724 | C | T | 123 | a0001c0001t0002g0005 a0001c0001t0002g0036 a0001c0001t0002g0040 others(120): Show |
127 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.279-810G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495724 | |||||||
chr5:1495798 | T | C | 3 | a0001c0001t0005g0039 a0001c0001t0005g0263 a0001c0007t0005g0106 |
3 | HG02109.hp1 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.279-884A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495798 | |||||||
chr5:1496010 | A | G | 1 | a0001c0001t0013g0055 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.279-1096T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496010 | |||||||
chr5:1496098 | C | T | 1 | a0001c0002t0004g0096 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.279-1184G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496098 | |||||||
chr5:1496234 | G | A | 32 | a0001c0001t0002g0008 a0001c0001t0002g0071 a0001c0001t0002g0182 others(29): Show |
34 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.279-1320C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496234 | |||||||
chr5:1496289 | G | T | 1 | a0001c0002t0004g0271 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.279-1375C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496289 | |||||||
chr5:1496293 | G | A | 1 | a0001c0001t0002g0212 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.279-1379C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496293 | |||||||
chr5:1496310 | G | A | 1 | a0001c0002t0004g0271 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.279-1396C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496310 | |||||||
chr5:1496357 | T | C | 19 | a0001c0001t0002g0098 a0001c0001t0002g0129 a0001c0001t0002g0253 others(16): Show |
20 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(17): Show |
intron_variant | MODIFIER | c.279-1443A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496357 | |||||||
chr5:1496405 | T | C | 4 | a0001c0001t0007g0097 a0001c0001t0007g0151 a0001c0002t0001g0276 others(1): Show |
4 | HG02895.hp2 HG03098.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.279-1491A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496405 | |||||||
chr5:1496417 | C | CA | 39 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0126 others(36): Show |
43 | HG00408.hp1 HG00408.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.279-1504dupT | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496417 | |||||||
chr5:1496417 | CA | C | 10 | a0001c0001t0007g0097 a0001c0001t0007g0151 a0001c0001t0013g0042 others(7): Show |
10 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.279-1504delT | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496417 | |||||||
chr5:1496462 | T | C | 1 | a0001c0002t0006g0088 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.279-1548A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496462 | |||||||
chr5:1496471 | A | T | 1 | a0001c0001t0013g0055 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.279-1557T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496471 | |||||||
chr5:1496507 | C | T | 92 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(89): Show |
97 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.279-1593G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496507 | |||||||
chr5:1496531 | G | A | 131 | a0001c0001t0002g0016 a0001c0001t0002g0040 a0001c0001t0002g0084 others(128): Show |
139 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.279-1617C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496531 | |||||||
chr5:1496606 | C | T | 2 | a0001c0001t0007g0003 a0001c0001t0007g0138 |
3 | HG02572.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.279-1692G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496606 | |||||||
chr5:1496609 | C | T | 1 | a0001c0001t0002g0087 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.279-1695G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496609 | |||||||
chr5:1496675 | T | G | 11 | a0001c0001t0002g0006 a0001c0001t0002g0040 a0001c0001t0002g0140 others(8): Show |
12 | HG00408.hp1 HG00738.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.279-1761A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496675 | |||||||
chr5:1497018 | A | G | 4 | a0001c0001t0007g0097 a0001c0002t0004g0023 a0001c0004t0017g0017 others(1): Show |
4 | HG02145.hp2 HG02896.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.279-2104T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1497018 | |||||||
chr5:1497067 | G | A | 1 | a0001c0001t0013g0042 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.279-2153C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1497067 | |||||||
chr5:1497144 | T | G | 1 | a0001c0004t0005g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.279-2230A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1497144 | |||||||
chr5:1497237 | A | G | 9 | a0001c0001t0002g0253 a0001c0002t0008g0004 a0001c0002t0008g0114 others(6): Show |
10 | HG00280.hp1 HG01255.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.279-2323T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1497237 | |||||||
chr5:1497279 | G | A | 1 | a0001c0007t0004g0218 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.279-2365C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1497279 | |||||||
chr5:1497445 | G | C | 1 | a0001c0001t0013g0055 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.279-2531C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1497445 | |||||||
chr5:1497493 | G | A | 10 | a0001c0003t0001g0086 a0001c0003t0006g0170 a0001c0003t0006g0178 others(7): Show |
10 | HG00558.hp1 HG00621.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.279-2579C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1497493 | |||||||
chr5:1497504 | G | A | 1 | a0001c0001t0002g0349 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.279-2590C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1497504 | |||||||
chr5:1497511 | T | C | 245 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(242): Show |
255 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.279-2597A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1497511 | |||||||
chr5:1497578 | C | A | 1 | a0001c0004t0005g0160 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.279-2664G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1497578 | |||||||
chr5:1497579 | G | A | 1 | a0001c0001t0028g0348 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.279-2665C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1497579 | |||||||
chr5:1497851 | C | A | 1 | a0001c0001t0013g0055 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.279-2937G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1497851 | |||||||
chr5:1498066 | G | T | 1 | a0002c0005t0003g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.279-3152C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498066 | |||||||
chr5:1498225 | T | A | 41 | a0001c0001t0002g0008 a0001c0001t0002g0071 a0001c0001t0002g0183 others(38): Show |
43 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.278+3236A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498225 | |||||||
chr5:1498234 | C | T | 2 | a0001c0001t0002g0036 a0001c0002t0001g0037 |
2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.278+3227G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498234 | |||||||
chr5:1498249 | G | A | 1 | a0001c0001t0002g0183 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.278+3212C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498249 | |||||||
chr5:1498413 | G | A | 4 | a0001c0002t0001g0284 a0001c0002t0001g0285 a0001c0002t0001g0287 others(1): Show |
4 | HG02258.hp1 HG02976.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.278+3048C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498413 | |||||||
chr5:1498415 | G | A | 1 | a0001c0001t0002g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.278+3046C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498415 | |||||||
chr5:1498480 | A | G | 2 | a0001c0002t0001g0230 a0002c0005t0003g0118 |
2 | NA18947.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.278+2981T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498480 | |||||||
chr5:1498511 | G | A | 1 | a0001c0002t0023g0243 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.278+2950C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498511 | |||||||
chr5:1498539 | A | T | 1 | a0001c0001t0013g0055 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.278+2922T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498539 | |||||||
chr5:1498550 | T | A | 4 | a0001c0002t0001g0302 a0001c0002t0001g0308 a0001c0002t0015g0297 others(1): Show |
4 | HG01928.hp1 HG01943.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.278+2911A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498550 | |||||||
chr5:1498599 | T | G | 1 | a0001c0001t0004g0052 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.278+2862A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498599 | |||||||
chr5:1498618 | G | A | 1 | a0001c0003t0001g0266 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.278+2843C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498618 | |||||||
chr5:1498651 | CAG | C | 79 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0040 others(76): Show |
81 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.278+2808_278+2809d others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498651 | |||||||
chr5:1498668 | T | C | 11 | a0001c0001t0004g0026 a0001c0001t0019g0072 a0001c0001t0026g0025 others(8): Show |
11 | HG01081.hp2 HG01106.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.278+2793A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498668 | |||||||
chr5:1498679 | A | G | 7 | a0001c0002t0001g0076 a0001c0002t0001g0242 a0001c0002t0001g0250 others(4): Show |
7 | HG02451.hp1 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.278+2782T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498679 | |||||||
chr5:1498744 | A | G | 60 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0087 others(57): Show |
63 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.278+2717T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498744 | |||||||
chr5:1498789 | CAT | C | 6 | a0001c0003t0001g0162 a0001c0003t0001g0226 a0001c0003t0001g0228 others(3): Show |
6 | HG00544.hp2 HG02109.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.278+2670_278+2671d others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498789 | |||||||
chr5:1498838 | T | TACAC | 25 | a0001c0001t0002g0006 a0001c0001t0002g0089 a0001c0001t0002g0126 others(22): Show |
26 | HG00408.hp1 HG00738.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.278+2619_278+2622d others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498838 | |||||||
chr5:1498871 | G | A | 169 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(166): Show |
175 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.278+2590C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498871 | |||||||
chr5:1498877 | C | T | 7 | a0001c0002t0001g0076 a0001c0002t0001g0242 a0001c0002t0001g0250 others(4): Show |
7 | HG02451.hp1 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.278+2584G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498877 | |||||||
chr5:1498895 | A | G | 2 | a0001c0001t0004g0108 a0001c0001t0007g0269 |
2 | HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.278+2566T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498895 | |||||||
chr5:1498936 | T | TACAC | 60 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0087 others(57): Show |
63 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.278+2521_278+2524d others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498936 | |||||||
chr5:1498942 | C | T | 7 | a0001c0002t0001g0076 a0001c0002t0001g0242 a0001c0002t0001g0250 others(4): Show |
7 | HG02451.hp1 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.278+2519G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498942 | |||||||
chr5:1498994 | G | C | 93 | a0001c0001t0002g0008 a0001c0001t0002g0071 a0001c0001t0002g0089 others(90): Show |
97 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.278+2467C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498994 | |||||||
chr5:1499051 | G | A | 1 | a0001c0002t0001g0275 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.278+2410C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499051 | |||||||
chr5:1499060 | C | T | 79 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(76): Show |
83 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.278+2401G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499060 | |||||||
chr5:1499090 | G | A | 1 | a0001c0001t0005g0292 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.278+2371C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499090 | |||||||
chr5:1499251 | C | T | 79 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0040 others(76): Show |
81 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.278+2210G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499251 | |||||||
chr5:1499255 | C | T | 87 | a0001c0001t0002g0008 a0001c0001t0002g0071 a0001c0001t0002g0115 others(84): Show |
91 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.278+2206G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499255 | |||||||
chr5:1499351 | C | T | 79 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0040 others(76): Show |
81 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.278+2110G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499351 | |||||||
chr5:1499352 | G | C | 1 | a0001c0001t0002g0212 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.278+2109C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499352 | |||||||
chr5:1499368 | A | T | 31 | a0001c0001t0002g0089 a0001c0001t0002g0212 a0001c0001t0002g0240 others(28): Show |
31 | HG00735.hp2 HG01106.hp1 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.278+2093T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499368 | |||||||
chr5:1499494 | C | G | 1 | a0001c0001t0007g0138 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.278+1967G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499494 | |||||||
chr5:1499500 | T | G | 1 | a0001c0001t0013g0055 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.278+1961A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499500 | |||||||
chr5:1499691 | A | G | 165 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0016 others(162): Show |
172 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.278+1770T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499691 | |||||||
chr5:1499704 | C | T | 176 | a0001c0001t0002g0008 a0001c0001t0002g0028 a0001c0001t0002g0036 others(173): Show |
182 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.278+1757G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499704 | |||||||
chr5:1499750 | C | A | 1 | a0001c0001t0002g0318 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.278+1711G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499750 | |||||||
chr5:1499776 | C | G | 1 | a0001c0001t0005g0021 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.278+1685G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499776 | |||||||
chr5:1499802 | T | C | 87 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0040 others(84): Show |
89 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.278+1659A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499802 | |||||||
chr5:1499856 | C | T | 7 | a0001c0002t0001g0076 a0001c0002t0001g0242 a0001c0002t0001g0250 others(4): Show |
7 | HG02451.hp1 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.278+1605G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499856 | |||||||
chr5:1500001 | T | A | 178 | a0001c0001t0002g0008 a0001c0001t0002g0028 a0001c0001t0002g0036 others(175): Show |
184 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.278+1460A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500001 | |||||||
chr5:1500025 | T | A | 1 | a0001c0001t0002g0318 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.278+1436A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500025 | |||||||
chr5:1500045 | C | T | 87 | a0001c0001t0002g0008 a0001c0001t0002g0071 a0001c0001t0002g0115 others(84): Show |
91 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.278+1416G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500045 | |||||||
chr5:1500055 | C | G | 42 | a0001c0001t0002g0008 a0001c0001t0002g0071 a0001c0001t0002g0183 others(39): Show |
44 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.278+1406G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500055 | |||||||
chr5:1500134 | C | A | 2 | a0001c0001t0002g0282 a0001c0001t0002g0283 |
2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.278+1327G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500134 | |||||||
chr5:1500169 | A | G | 1 | a0001c0001t0004g0347 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.278+1292T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500169 | |||||||
chr5:1500198 | TGA | T | 4 | a0001c0003t0001g0325 a0001c0003t0001g0334 a0001c0003t0001g0336 others(1): Show |
4 | HG00597.hp2 HG00621.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.278+1261_278+1262d others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500198 | |||||||
chr5:1500240 | G | A | 1 | a0001c0002t0023g0243 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.278+1221C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500240 | |||||||
chr5:1500252 | G | A | 1 | a0001c0002t0023g0243 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.278+1209C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500252 | |||||||
chr5:1500307 | A | G | 1 | a0001c0001t0002g0212 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.278+1154T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500307 | |||||||
chr5:1500374 | G | T | 86 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0040 others(83): Show |
88 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.278+1087C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500374 | |||||||
chr5:1500385 | G | A | 1 | a0001c0004t0005g0288 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.278+1076C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500385 | |||||||
chr5:1500554 | G | A | 3 | a0001c0001t0007g0097 a0001c0004t0017g0017 a0001c0004t0024g0033 |
3 | HG02145.hp2 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.278+907C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500554 | |||||||
chr5:1500928 | G | A | 2 | a0002c0005t0003g0361 a0002c0005t0031g0217 |
2 | HG00639.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.278+533C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500928 | |||||||
chr5:1500970 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.278+491G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500970 | |||||||
chr5:1501064 | G | C | 60 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0087 others(57): Show |
63 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.278+397C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1501064 | |||||||
chr5:1501167 | T | C | 178 | a0001c0001t0002g0008 a0001c0001t0002g0028 a0001c0001t0002g0036 others(175): Show |
184 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.278+294A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1501167 | |||||||
chr5:1501239 | G | T | 1 | a0001c0002t0004g0096 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.278+222C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1501239 | |||||||
chr5:1501306 | C | T | 12 | a0001c0001t0002g0006 a0001c0001t0002g0126 a0001c0001t0002g0140 others(9): Show |
13 | HG00408.hp1 HG00738.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.278+155G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1501306 | |||||||
chr5:1501333 | G | A | 2 | a0001c0002t0006g0203 a0002c0005t0003g0192 |
2 | HG02602.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.278+128C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1501333 | |||||||
chr5:1501333 | G | C | 42 | a0001c0001t0002g0008 a0001c0001t0002g0071 a0001c0001t0002g0183 others(39): Show |
44 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.278+128C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1501333 | |||||||
chr5:1501409 | T | C | 14 | a0001c0002t0004g0100 a0001c0002t0004g0150 a0001c0003t0001g0090 others(11): Show |
15 | HG01099.hp2 HG01261.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.278+52A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1501409 | |||||||
chr5:1501420 | A | AC | 17 | a0001c0001t0002g0006 a0001c0001t0002g0127 a0001c0001t0002g0140 others(14): Show |
18 | HG00408.hp1 HG00738.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.278+40dupG | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1501420 | |||||||
chr5:1501427 | C | A | 87 | a0001c0001t0002g0008 a0001c0001t0002g0071 a0001c0001t0002g0115 others(84): Show |
91 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.278+34G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1501427 | |||||||
chr5:1501675 | T | C | 178 | a0001c0001t0002g0008 a0001c0001t0002g0028 a0001c0001t0002g0036 others(175): Show |
184 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.136-72A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1501675 | |||||||
chr5:1501766 | GAGGCTGA others(3): Show |
G | 1 | a0001c0002t0023g0243 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.136-173_136-164del others(10): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1501766 | |||||||
chr5:1501808 | C | T | 42 | a0001c0001t0002g0008 a0001c0001t0002g0071 a0001c0001t0002g0183 others(39): Show |
44 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.136-205G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1501808 | |||||||
chr5:1501836 | AGCACTGA others(13): Show |
A | 1 | a0001c0004t0002g0341 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.136-253_136-234del others(20): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1501836 | |||||||
chr5:1501887 | GCACTGAC others(43): Show |
G | 1 | a0001c0001t0002g0126 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.136-334_136-285del others(50): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1501887 | |||||||
chr5:1501915 | C | T | 42 | a0001c0001t0002g0008 a0001c0001t0002g0071 a0001c0001t0002g0183 others(39): Show |
44 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.136-312G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1501915 | |||||||
chr5:1502010 | T | C | 2 | a0001c0003t0016g0367 a0002c0006t0038g0368 |
2 | NA18956.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.136-407A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502010 | |||||||
chr5:1502087 | A | G | 178 | a0001c0001t0002g0008 a0001c0001t0002g0028 a0001c0001t0002g0036 others(175): Show |
184 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.136-484T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502087 | |||||||
chr5:1502091 | G | A | 1 | a0001c0002t0002g0053 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.136-488C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502091 | |||||||
chr5:1502122 | C | A | 1 | a0002c0006t0003g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.136-519G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502122 | |||||||
chr5:1502144 | C | A | 1 | a0001c0002t0023g0243 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.136-541G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502144 | |||||||
chr5:1502170 | A | C | 60 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0087 others(57): Show |
63 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.136-567T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502170 | |||||||
chr5:1502266 | C | G | 175 | a0001c0001t0002g0008 a0001c0001t0002g0028 a0001c0001t0002g0036 others(172): Show |
180 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.136-663G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502266 | |||||||
chr5:1502338 | A | T | 196 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0028 others(193): Show |
203 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.136-735T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502338 | |||||||
chr5:1502343 | A | C | 1 | a0001c0004t0002g0173 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.136-740T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502343 | |||||||
chr5:1502465 | C | T | 6 | a0001c0001t0002g0089 a0001c0001t0002g0240 a0001c0001t0007g0151 others(3): Show |
6 | HG02109.hp2 HG02895.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-862G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502465 | |||||||
chr5:1502469 | G | A | 2 | a0001c0003t0016g0367 a0002c0006t0038g0368 |
2 | NA18956.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.136-866C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502469 | |||||||
chr5:1502564 | G | A | 1 | a0001c0002t0023g0243 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.136-961C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502564 | |||||||
chr5:1502599 | G | A | 1 | a0001c0003t0001g0342 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.136-996C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502599 | |||||||
chr5:1502675 | A | G | 1 | a0001c0004t0004g0258 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.136-1072T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502675 | |||||||
chr5:1502683 | G | A | 1 | a0001c0001t0002g0283 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.136-1080C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502683 | |||||||
chr5:1502734 | T | C | 1 | a0001c0001t0004g0108 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.136-1131A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502734 | |||||||
chr5:1502893 | C | T | 1 | a0001c0001t0002g0183 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.136-1290G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502893 | |||||||
chr5:1502931 | C | T | 78 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(75): Show |
82 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.136-1328G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502931 | |||||||
chr5:1503090 | C | T | 78 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(75): Show |
82 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.136-1487G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503090 | |||||||
chr5:1503145 | G | A | 3 | a0001c0001t0002g0006 a0001c0001t0002g0141 a0001c0002t0001g0289 |
4 | NA18953.hp2 NA18955.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-1542C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503145 | |||||||
chr5:1503172 | C | A | 60 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0087 others(57): Show |
63 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.136-1569G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503172 | |||||||
chr5:1503279 | G | A | 7 | a0001c0001t0002g0115 a0001c0001t0007g0097 a0001c0002t0004g0100 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-1676C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503279 | |||||||
chr5:1503336 | GA | G | 11 | a0001c0001t0013g0055 a0001c0007t0004g0218 a0001c0007t0004g0254 others(8): Show |
11 | HG01106.hp1 HG01256.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.136-1734delT | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503336 | |||||||
chr5:1503418 | C | T | 1 | a0001c0003t0001g0205 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.136-1815G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503418 | |||||||
chr5:1503441 | G | A | 2 | a0001c0001t0002g0359 a0004c0014t0034g0145 |
2 | HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.136-1838C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503441 | |||||||
chr5:1503448 | A | T | 80 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(77): Show |
84 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.136-1845T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503448 | |||||||
chr5:1503495 | T | C | 61 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0087 others(58): Show |
64 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.136-1892A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503495 | |||||||
chr5:1503514 | C | T | 1 | a0001c0002t0002g0053 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.136-1911G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503514 | |||||||
chr5:1503541 | T | C | 1 | a0001c0002t0008g0340 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.136-1938A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503541 | |||||||
chr5:1503652 | C | G | 1 | a0002c0005t0031g0217 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.136-2049G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503652 | |||||||
chr5:1503696 | G | A | 1 | a0001c0002t0001g0027 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.136-2093C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503696 | |||||||
chr5:1503800 | A | AT | 87 | a0001c0001t0002g0008 a0001c0001t0002g0071 a0001c0001t0002g0115 others(84): Show |
91 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.136-2198dupA | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503800 | |||||||
chr5:1503815 | G | A | 1 | a0004c0014t0034g0145 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.136-2212C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503815 | |||||||
chr5:1503864 | C | T | 1 | a0001c0004t0011g0354 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.136-2261G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503864 | |||||||
chr5:1503981 | T | G | 1 | a0001c0002t0001g0232 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.136-2378A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503981 | |||||||
chr5:1504020 | T | C | 1 | a0001c0002t0008g0130 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.136-2417A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504020 | |||||||
chr5:1504116 | C | T | 56 | a0001c0001t0002g0005 a0001c0001t0002g0095 a0001c0001t0002g0127 others(53): Show |
58 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.136-2513G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504116 | |||||||
chr5:1504310 | G | GCGCAGCG others(8): Show |
1 | a0001c0002t0004g0271 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.136-2722_136-2708d others(17): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504310 | |||||||
chr5:1504312 | G | A | 1 | a0001c0002t0023g0243 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.136-2709C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504312 | |||||||
chr5:1504347 | A | G | 77 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(74): Show |
81 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.136-2744T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504347 | |||||||
chr5:1504357 | G | A | 10 | a0001c0007t0004g0218 a0001c0007t0004g0254 a0001c0007t0004g0255 others(7): Show |
10 | HG01106.hp1 HG01256.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.136-2754C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504357 | |||||||
chr5:1504418 | G | C | 3 | a0001c0003t0016g0366 a0001c0003t0016g0367 a0002c0006t0038g0368 |
3 | NA18956.hp1 NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.136-2815C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504418 | |||||||
chr5:1504427 | G | A | 1 | a0002c0006t0003g0032 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.136-2824C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504427 | |||||||
chr5:1504488 | G | A | 2 | a0001c0001t0002g0212 a0001c0001t0002g0260 |
2 | HG00735.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.136-2885C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504488 | |||||||
chr5:1504497 | G | A | 1 | a0001c0002t0004g0143 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.136-2894C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504497 | |||||||
chr5:1504597 | A | C | 161 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(158): Show |
169 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.136-2994T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504597 | |||||||
chr5:1504678 | C | A | 19 | a0001c0001t0002g0006 a0001c0001t0002g0089 a0001c0001t0002g0126 others(16): Show |
20 | HG00408.hp1 HG00738.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.136-3075G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504678 | |||||||
chr5:1504678 | C | T | 1 | a0002c0005t0003g0081 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.136-3075G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504678 | |||||||
chr5:1504710 | G | C | 1 | a0001c0001t0002g0144 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.136-3107C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504710 | |||||||
chr5:1504714 | C | CA | 165 | a0001c0001t0002g0008 a0001c0001t0002g0028 a0001c0001t0002g0036 others(162): Show |
171 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.136-3112dupT | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504714 | |||||||
chr5:1504714 | C | CAA | 25 | a0001c0001t0002g0006 a0001c0001t0002g0089 a0001c0001t0002g0126 others(22): Show |
26 | HG00408.hp1 HG00738.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.136-3113_136-3112d others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504714 | |||||||
chr5:1504714 | CA | C | 9 | a0001c0001t0004g0108 a0001c0001t0005g0039 a0001c0001t0005g0263 others(6): Show |
9 | HG02717.hp2 HG02723.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.136-3112delT | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504714 | |||||||
chr5:1504857 | C | T | 3 | a0001c0001t0002g0126 a0001c0002t0001g0156 a0001c0002t0008g0155 |
3 | HG01106.hp2 HG01255.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.136-3254G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504857 | |||||||
chr5:1504870 | G | C | 18 | a0001c0001t0002g0006 a0001c0001t0002g0089 a0001c0001t0002g0126 others(15): Show |
19 | HG00408.hp1 HG00738.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.136-3267C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504870 | |||||||
chr5:1504950 | C | CCA | 3 | a0001c0001t0002g0126 a0001c0002t0001g0156 a0001c0002t0008g0155 |
3 | HG01106.hp2 HG01255.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.136-3349_136-3348d others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504950 | |||||||
chr5:1504954 | A | G | 3 | a0001c0001t0002g0126 a0001c0002t0001g0156 a0001c0002t0008g0155 |
3 | HG01106.hp2 HG01255.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.136-3351T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504954 | |||||||
chr5:1504954 | AGTGTGGA others(66): Show |
A | 4 | a0001c0001t0007g0003 a0001c0001t0007g0138 a0001c0001t0007g0151 others(1): Show |
5 | HG02572.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-3424_136-3352d others(75): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504954 | |||||||
chr5:1504981 | C | T | 59 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0095 others(56): Show |
62 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.136-3378G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504981 | |||||||
chr5:1505104 | T | TGGAATAA others(64): Show |
6 | a0001c0001t0005g0356 a0001c0001t0005g0357 a0001c0004t0002g0117 others(3): Show |
6 | HG00438.hp2 HG02015.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-3572_136-3502d others(73): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505104 | |||||||
chr5:1505127 | C | T | 59 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0095 others(56): Show |
62 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.136-3524G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505127 | |||||||
chr5:1505129 | C | G | 1 | a0001c0002t0001g0285 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.136-3526G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505129 | |||||||
chr5:1505156 | CACTGCTT others(62): Show |
C | 1 | a0001c0002t0001g0284 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.136-3622_136-3554d others(71): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505156 | |||||||
chr5:1505223 | A | G | 1 | a0002c0005t0003g0330 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.136-3620T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505223 | |||||||
chr5:1505244 | C | T | 5 | a0001c0001t0002g0089 a0001c0001t0002g0240 a0001c0001t0027g0272 others(2): Show |
5 | HG02109.hp2 HG02895.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-3641G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505244 | |||||||
chr5:1505250 | A | G | 3 | a0001c0003t0016g0366 a0001c0003t0016g0367 a0002c0006t0038g0368 |
3 | NA18956.hp1 NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.136-3647T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505250 | |||||||
chr5:1505258 | A | G | 1 | a0001c0001t0002g0089 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.136-3655T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505258 | |||||||
chr5:1505414 | G | A | 1 | a0001c0001t0002g0197 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.136-3811C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505414 | |||||||
chr5:1505474 | A | G | 80 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(77): Show |
84 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.136-3871T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505474 | |||||||
chr5:1505559 | CCGGGT | C | 18 | a0001c0001t0002g0006 a0001c0001t0002g0089 a0001c0001t0002g0126 others(15): Show |
19 | HG00408.hp1 HG00738.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.136-3961_136-3957d others(7): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505559 | |||||||
chr5:1505560 | CGGGTA | C | 228 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0016 others(225): Show |
237 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.136-3962_136-3958d others(7): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505560 | |||||||
chr5:1505565 | A | T | 18 | a0001c0001t0002g0006 a0001c0001t0002g0089 a0001c0001t0002g0126 others(15): Show |
19 | HG00408.hp1 HG00738.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.136-3962T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505565 | |||||||
chr5:1505623 | G | A | 59 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0095 others(56): Show |
62 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.136-4020C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505623 | |||||||
chr5:1505656 | G | A | 7 | a0001c0002t0001g0076 a0001c0002t0001g0242 a0001c0002t0001g0250 others(4): Show |
7 | HG02451.hp1 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-4053C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505656 | |||||||
chr5:1505740 | C | T | 1 | a0001c0002t0023g0243 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.136-4137G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505740 | |||||||
chr5:1505749 | T | C | 3 | a0001c0003t0016g0366 a0001c0003t0016g0367 a0002c0006t0038g0368 |
3 | NA18956.hp1 NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.136-4146A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505749 | |||||||
chr5:1505767 | C | T | 1 | a0001c0003t0001g0073 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.136-4164G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505767 | |||||||
chr5:1505821 | C | T | 83 | a0001c0001t0002g0008 a0001c0001t0002g0071 a0001c0001t0002g0115 others(80): Show |
87 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.136-4218G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505821 | |||||||
chr5:1505843 | C | T | 1 | a0001c0001t0002g0346 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.136-4240G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505843 | |||||||
chr5:1506188 | A | G | 59 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0095 others(56): Show |
62 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.136-4585T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1506188 | |||||||
chr5:1506257 | G | A | 3 | a0001c0001t0007g0097 a0001c0004t0017g0017 a0001c0004t0024g0033 |
3 | HG02145.hp2 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.136-4654C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1506257 | |||||||
chr5:1506270 | G | A | 59 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0095 others(56): Show |
62 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.136-4667C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1506270 | |||||||
chr5:1506359 | G | A | 74 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0040 others(71): Show |
76 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.136-4756C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1506359 | |||||||
chr5:1506414 | G | A | 2 | a0001c0002t0004g0100 a0001c0002t0004g0150 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.136-4811C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1506414 | |||||||
chr5:1506504 | C | T | 59 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0095 others(56): Show |
62 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.136-4901G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1506504 | |||||||
chr5:1506629 | G | A | 1 | a0001c0003t0001g0131 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.136-5026C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1506629 | |||||||
chr5:1506804 | C | T | 1 | a0001c0003t0001g0148 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.136-5201G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1506804 | |||||||
chr5:1506859 | C | G | 5 | a0001c0002t0001g0215 a0001c0003t0001g0213 a0001c0003t0001g0249 others(2): Show |
5 | HG01261.hp2 HG01981.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-5256G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1506859 | |||||||
chr5:1507101 | C | T | 13 | a0001c0001t0002g0006 a0001c0001t0002g0126 a0001c0001t0002g0140 others(10): Show |
14 | HG00408.hp1 HG00738.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.136-5498G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507101 | |||||||
chr5:1507107 | G | C | 59 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0095 others(56): Show |
62 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.136-5504C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507107 | |||||||
chr5:1507183 | T | A | 11 | a0001c0001t0002g0005 a0001c0001t0002g0095 a0001c0001t0002g0198 others(8): Show |
12 | HG00423.hp2 HG00673.hp2 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.136-5580A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507183 | |||||||
chr5:1507199 | G | T | 7 | a0001c0002t0001g0076 a0001c0002t0001g0242 a0001c0002t0001g0250 others(4): Show |
7 | HG02451.hp1 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-5596C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507199 | |||||||
chr5:1507212 | G | A | 13 | a0001c0001t0002g0006 a0001c0001t0002g0126 a0001c0001t0002g0140 others(10): Show |
14 | HG00408.hp1 HG00738.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.136-5609C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507212 | |||||||
chr5:1507393 | G | C | 59 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0095 others(56): Show |
62 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.136-5790C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507393 | |||||||
chr5:1507419 | G | A | 1 | a0001c0003t0001g0002 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.136-5816C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507419 | |||||||
chr5:1507421 | T | G | 1 | a0001c0002t0004g0096 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.136-5818A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507421 | |||||||
chr5:1507532 | T | C | 4 | a0001c0002t0001g0193 a0001c0002t0001g0194 a0001c0004t0005g0160 others(1): Show |
4 | NA18983.hp2 NA19057.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-5929A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507532 | |||||||
chr5:1507547 | C | G | 1 | a0001c0002t0023g0243 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.136-5944G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507547 | |||||||
chr5:1507590 | C | T | 1 | a0001c0002t0001g0358 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.136-5987G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507590 | |||||||
chr5:1507591 | G | A | 1 | a0002c0006t0003g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.136-5988C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507591 | |||||||
chr5:1507593 | C | T | 2 | a0001c0003t0001g0279 a0001c0004t0005g0288 |
2 | HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.136-5990G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507593 | |||||||
chr5:1507628 | C | T | 1 | a0001c0003t0006g0172 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.136-6025G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507628 | |||||||
chr5:1507645 | G | A | 2 | a0001c0002t0001g0163 a0001c0002t0001g0164 |
2 | NA18994.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.136-6042C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507645 | |||||||
chr5:1507665 | C | T | 1 | a0002c0005t0003g0118 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.136-6062G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507665 | |||||||
chr5:1507666 | G | A | 1 | a0002c0005t0003g0015 | 2 | NA19010.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.136-6063C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507666 | |||||||
chr5:1507675 | C | T | 3 | a0001c0001t0002g0115 a0001c0001t0002g0282 a0001c0001t0002g0283 |
3 | HG01891.hp2 HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.136-6072G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507675 | |||||||
chr5:1507893 | GAACTCCA others(10): Show |
G | 3 | a0001c0003t0016g0366 a0001c0003t0016g0367 a0002c0006t0038g0368 |
3 | NA18956.hp1 NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.136-6307_136-6291d others(19): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507893 | |||||||
chr5:1507991 | G | C | 3 | a0001c0004t0002g0244 a0001c0007t0007g0112 a0004c0014t0034g0145 |
3 | HG01884.hp1 HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.136-6388C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507991 | |||||||
chr5:1508004 | C | T | 1 | a0001c0002t0004g0096 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.136-6401G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1508004 | |||||||
chr5:1508144 | C | T | 6 | a0001c0001t0002g0212 a0001c0001t0025g0061 a0001c0002t0001g0062 others(3): Show |
6 | HG00735.hp2 NA18939.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-6541G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1508144 | |||||||
chr5:1508145 | A | G | 9 | a0001c0001t0002g0212 a0001c0001t0025g0061 a0001c0002t0001g0062 others(6): Show |
9 | HG00735.hp2 NA18939.hp1 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.136-6542T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1508145 | |||||||
chr5:1508155 | T | C | 134 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(131): Show |
142 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.136-6552A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1508155 | |||||||
chr5:1508216 | C | T | 1 | a0001c0007t0004g0254 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.136-6613G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1508216 | |||||||
chr5:1508233 | G | A | 87 | a0001c0001t0002g0008 a0001c0001t0002g0060 a0001c0001t0002g0087 others(84): Show |
92 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.136-6630C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1508233 | |||||||
chr5:1508281 | T | A | 75 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0040 others(72): Show |
77 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.136-6678A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1508281 | |||||||
chr5:1508440 | T | A | 1 | a0001c0007t0007g0112 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.136-6837A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1508440 | |||||||
chr5:1508490 | C | T | 2 | a0001c0001t0007g0003 a0001c0001t0007g0151 |
3 | HG02896.hp1 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.136-6887G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1508490 | |||||||
chr5:1508566 | G | A | 3 | a0002c0006t0003g0031 a0002c0006t0003g0032 a0002c0006t0003g0142 |
3 | HG02965.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.136-6963C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1508566 | |||||||
chr5:1508722 | T | C | 146 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0040 others(143): Show |
149 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.136-7119A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1508722 | |||||||
chr5:1508862 | C | T | 2 | a0003c0008t0002g0009 a0003c0008t0002g0351 |
3 | HG00099.hp2 HG01516.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.136-7259G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1508862 | |||||||
chr5:1508905 | C | A | 1 | a0002c0005t0003g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.136-7302G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1508905 | |||||||
chr5:1508983 | C | T | 1 | a0002c0005t0003g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.136-7380G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1508983 | |||||||
chr5:1509030 | G | A | 7 | a0001c0002t0001g0201 a0001c0002t0006g0203 a0001c0003t0001g0205 others(4): Show |
7 | HG01070.hp1 HG01074.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-7427C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509030 | |||||||
chr5:1509031 | C | T | 2 | a0001c0001t0004g0108 a0001c0001t0007g0269 |
2 | HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.136-7428G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509031 | |||||||
chr5:1509078 | T | C | 3 | a0001c0001t0002g0043 a0001c0002t0001g0290 a0001c0015t0004g0252 |
3 | HG00099.hp1 NA20752.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.136-7475A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509078 | |||||||
chr5:1509095 | T | C | 4 | a0001c0003t0006g0170 a0001c0003t0006g0206 a0001c0003t0006g0207 others(1): Show |
4 | HG00621.hp1 HG02040.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-7492A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509095 | |||||||
chr5:1509141 | G | A | 1 | a0001c0003t0001g0334 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.136-7538C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509141 | |||||||
chr5:1509155 | G | A | 1 | a0002c0005t0003g0241 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.136-7552C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509155 | |||||||
chr5:1509170 | G | A | 15 | a0001c0001t0002g0115 a0001c0003t0009g0233 a0001c0004t0004g0258 others(12): Show |
15 | HG00140.hp1 HG00733.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.136-7567C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509170 | |||||||
chr5:1509194 | C | T | 1 | a0001c0003t0001g0266 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.136-7591G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509194 | |||||||
chr5:1509195 | G | A | 1 | a0001c0002t0008g0331 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.136-7592C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509195 | |||||||
chr5:1509289 | G | A | 1 | a0001c0004t0004g0210 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.136-7686C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509289 | |||||||
chr5:1509352 | G | A | 2 | a0001c0001t0021g0246 a0001c0002t0004g0096 |
2 | HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.136-7749C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509352 | |||||||
chr5:1509397 | G | A | 2 | a0001c0001t0007g0097 a0001c0003t0009g0233 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.136-7794C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509397 | |||||||
chr5:1509432 | G | C | 1 | a0001c0002t0001g0274 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.136-7829C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509432 | |||||||
chr5:1509461 | T | C | 79 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0040 others(76): Show |
82 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.136-7858A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509461 | |||||||
chr5:1509511 | C | A | 1 | a0001c0001t0002g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.136-7908G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509511 | |||||||
chr5:1509528 | C | A | 1 | a0001c0003t0001g0090 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.136-7925G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509528 | |||||||
chr5:1509633 | G | A | 2 | a0001c0001t0002g0359 a0001c0002t0004g0143 |
2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.136-8030C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509633 | |||||||
chr5:1509772 | C | T | 4 | a0001c0002t0001g0284 a0001c0002t0001g0285 a0001c0002t0001g0287 others(1): Show |
4 | HG02258.hp1 HG02976.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-8169G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509772 | |||||||
chr5:1509789 | T | C | 1 | a0001c0003t0009g0014 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.136-8186A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509789 | |||||||
chr5:1509815 | G | C | 137 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0040 others(134): Show |
141 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.136-8212C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509815 | |||||||
chr5:1509836 | G | A | 2 | a0001c0001t0004g0108 a0001c0001t0007g0269 |
2 | HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.136-8233C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509836 | |||||||
chr5:1509849 | G | C | 13 | a0001c0001t0002g0115 a0001c0001t0004g0108 a0001c0001t0007g0269 others(10): Show |
13 | HG01891.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.136-8246C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509849 | |||||||
chr5:1509865 | T | C | 1 | a0001c0003t0001g0090 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.136-8262A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509865 | |||||||
chr5:1509903 | G | A | 201 | a0001c0001t0002g0005 a0001c0001t0002g0028 a0001c0001t0002g0036 others(198): Show |
206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.136-8300C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509903 | |||||||
chr5:1510082 | GTTTC | G | 8 | a0001c0002t0001g0076 a0001c0002t0001g0245 a0001c0002t0001g0250 others(5): Show |
8 | HG02055.hp2 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.136-8483_136-8480d others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1510082 | |||||||
chr5:1510200 | G | A | 32 | a0001c0001t0002g0089 a0001c0001t0002g0111 a0001c0001t0002g0359 others(29): Show |
33 | HG00140.hp1 HG01106.hp1 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.136-8597C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1510200 | |||||||
chr5:1510226 | C | G | 5 | a0001c0001t0002g0089 a0001c0001t0002g0111 a0001c0001t0007g0259 others(2): Show |
5 | HG02109.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-8623G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1510226 | |||||||
chr5:1510257 | T | A | 2 | a0001c0001t0025g0061 a0001c0002t0001g0062 |
2 | NA18939.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.136-8654A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1510257 | |||||||
chr5:1510350 | G | A | 1 | a0001c0001t0007g0082 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.136-8747C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1510350 | |||||||
chr5:1510398 | G | A | 3 | a0001c0001t0002g0115 a0001c0002t0001g0274 a0001c0002t0004g0271 |
3 | HG01891.hp2 HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.136-8795C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1510398 | |||||||
chr5:1510453 | T | A | 3 | a0001c0001t0002g0087 a0001c0002t0001g0248 a0001c0003t0001g0343 |
3 | HG02523.hp1 NA18942.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.136-8850A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1510453 | |||||||
chr5:1510506 | A | G | 1 | a0001c0002t0001g0054 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.136-8903T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1510506 | |||||||
chr5:1510695 | G | A | 1 | a0001c0001t0002g0239 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.136-9092C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1510695 | |||||||
chr5:1510772 | A | G | 1 | a0001c0002t0001g0319 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.136-9169T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1510772 | |||||||
chr5:1510925 | C | T | 11 | a0001c0002t0001g0242 a0001c0002t0023g0243 a0001c0004t0002g0244 others(8): Show |
11 | HG01106.hp1 HG01256.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.136-9322G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1510925 | |||||||
chr5:1510937 | C | T | 1 | a0001c0001t0002g0087 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.136-9334G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1510937 | |||||||
chr5:1510938 | G | A | 3 | a0001c0003t0016g0366 a0001c0003t0016g0367 a0002c0006t0038g0368 |
3 | NA18956.hp1 NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.136-9335C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1510938 | |||||||
chr5:1511017 | C | T | 1 | a0003c0008t0002g0125 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.136-9414G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511017 | |||||||
chr5:1511107 | C | T | 18 | a0001c0001t0007g0281 a0001c0002t0001g0242 a0001c0002t0023g0243 others(15): Show |
18 | HG00140.hp1 HG01106.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.136-9504G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511107 | |||||||
chr5:1511169 | G | A | 3 | a0001c0003t0016g0366 a0001c0003t0016g0367 a0002c0006t0038g0368 |
3 | NA18956.hp1 NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.136-9566C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511169 | |||||||
chr5:1511170 | T | A | 3 | a0001c0003t0016g0366 a0001c0003t0016g0367 a0002c0006t0038g0368 |
3 | NA18956.hp1 NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.136-9567A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511170 | |||||||
chr5:1511246 | G | A | 1 | a0001c0001t0004g0363 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.136-9643C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511246 | |||||||
chr5:1511261 | G | A | 1 | a0001c0001t0002g0115 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.136-9658C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511261 | |||||||
chr5:1511308 | G | A | 1 | a0004c0014t0034g0145 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.136-9705C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511308 | |||||||
chr5:1511363 | C | T | 1 | a0001c0003t0006g0225 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.136-9760G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511363 | |||||||
chr5:1511410 | A | ATGGGGAT others(62): Show |
67 | a0001c0001t0002g0005 a0001c0001t0002g0095 a0001c0001t0002g0220 others(64): Show |
68 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.136-9808_136-9807i others(71): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511410 | |||||||
chr5:1511410 | ATGGGGAT others(62): Show |
A | 6 | a0001c0001t0004g0108 a0001c0001t0005g0263 a0001c0001t0007g0269 others(3): Show |
6 | HG02922.hp2 HG03041.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.136-9876_136-9808d others(71): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511410 | |||||||
chr5:1511548 | T | TTGGGGAT others(96): Show |
3 | a0001c0003t0016g0366 a0001c0003t0016g0367 a0002c0006t0038g0368 |
3 | NA18956.hp1 NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.136-9946_136-9945i others(105): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511548 | |||||||
chr5:1511582 | G | A | 1 | a0001c0001t0004g0052 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.136-9979C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511582 | |||||||
chr5:1511582 | G | GTGGGGAC others(62): Show |
1 | a0001c0002t0001g0051 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.136-9980_136-9979i others(71): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511582 | |||||||
chr5:1511582 | G | T | 1 | a0001c0002t0001g0302 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.136-9979C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511582 | |||||||
chr5:1511589 | T | C | 1 | a0001c0001t0004g0083 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.136-9986A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511589 | |||||||
chr5:1511594 | T | C | 1 | a0001c0002t0001g0302 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.136-9991A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511594 | |||||||
chr5:1511605 | T | C | 1 | a0001c0002t0001g0302 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.136-10002A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511605 | |||||||
chr5:1511773 | C | T | 2 | a0001c0007t0004g0218 a0002c0005t0003g0361 |
2 | HG01358.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.136-10170G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511773 | |||||||
chr5:1511823 | G | C | 3 | a0001c0001t0007g0097 a0001c0002t0001g0276 a0001c0004t0017g0017 |
3 | HG02145.hp2 HG02895.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.136-10220C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511823 | |||||||
chr5:1512092 | C | T | 1 | a0001c0003t0006g0170 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.136-10489G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512092 | |||||||
chr5:1512093 | G | A | 14 | a0001c0001t0007g0281 a0001c0002t0001g0242 a0001c0002t0023g0243 others(11): Show |
14 | HG01106.hp1 HG01256.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.136-10490C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512093 | |||||||
chr5:1512200 | C | G | 2 | a0001c0001t0004g0135 a0001c0003t0001g0249 |
2 | HG01168.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.136-10597G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512200 | |||||||
chr5:1512206 | T | A | 3 | a0001c0001t0004g0363 a0001c0001t0027g0272 a0001c0002t0001g0362 |
3 | HG02886.hp2 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.136-10603A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512206 | |||||||
chr5:1512207 | C | G | 22 | a0001c0001t0002g0089 a0001c0001t0002g0111 a0001c0001t0002g0115 others(19): Show |
22 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.136-10604G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512207 | |||||||
chr5:1512382 | T | C | 26 | a0001c0001t0002g0089 a0001c0001t0002g0111 a0001c0001t0002g0115 others(23): Show |
27 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.136-10779A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512382 | |||||||
chr5:1512504 | C | G | 1 | a0001c0003t0001g0266 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.136-10901G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512504 | |||||||
chr5:1512538 | C | G | 10 | a0001c0001t0002g0144 a0001c0001t0002g0295 a0001c0001t0005g0291 others(7): Show |
10 | NA18939.hp2 NA18959.hp2 NA18973.hp1 others(7): Show |
intron_variant | MODIFIER | c.136-10935G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512538 | |||||||
chr5:1512613 | T | C | 3 | a0001c0001t0004g0363 a0001c0001t0027g0272 a0001c0002t0001g0362 |
3 | HG02886.hp2 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.136-11010A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512613 | |||||||
chr5:1512627 | C | T | 104 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0043 others(101): Show |
107 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.136-11024G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512627 | |||||||
chr5:1512721 | C | G | 1 | a0001c0001t0002g0359 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.135+10989G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512721 | |||||||
chr5:1512753 | T | C | 207 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0040 others(204): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.135+10957A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512753 | |||||||
chr5:1512814 | C | T | 2 | a0001c0001t0002g0043 a0001c0015t0004g0252 |
2 | HG00099.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.135+10896G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512814 | |||||||
chr5:1512848 | T | C | 1 | a0001c0001t0002g0359 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.135+10862A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512848 | |||||||
chr5:1512901 | C | T | 1 | a0001c0002t0001g0358 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.135+10809G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512901 | |||||||
chr5:1512945 | C | T | 1 | a0001c0001t0004g0221 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.135+10765G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512945 | |||||||
chr5:1512961 | G | A | 1 | a0001c0019t0012g0278 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.135+10749C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512961 | |||||||
chr5:1512997 | C | T | 8 | a0001c0001t0002g0115 a0001c0001t0002g0260 a0001c0002t0004g0100 others(5): Show |
8 | HG01099.hp2 HG01261.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+10713G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512997 | |||||||
chr5:1513041 | A | T | 1 | a0002c0005t0003g0169 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.135+10669T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513041 | |||||||
chr5:1513194 | C | T | 1 | a0001c0002t0002g0053 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.135+10516G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513194 | |||||||
chr5:1513308 | C | G | 30 | a0001c0001t0002g0115 a0001c0001t0002g0260 a0001c0001t0002g0282 others(27): Show |
30 | HG01099.hp2 HG01261.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.135+10402G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513308 | |||||||
chr5:1513399 | G | A | 16 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0004g0013 others(13): Show |
17 | HG01243.hp1 HG02145.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.135+10311C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513399 | |||||||
chr5:1513588 | G | T | 21 | a0001c0001t0002g0071 a0001c0001t0002g0078 a0001c0001t0002g0098 others(18): Show |
22 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.135+10122C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513588 | |||||||
chr5:1513628 | G | A | 1 | a0001c0001t0002g0359 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.135+10082C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513628 | |||||||
chr5:1513636 | C | G | 4 | a0001c0001t0002g0359 a0001c0001t0007g0281 a0001c0003t0001g0279 others(1): Show |
4 | HG01496.hp1 HG02451.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+10074G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513636 | |||||||
chr5:1513647 | T | C | 1 | a0001c0002t0001g0319 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.135+10063A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513647 | |||||||
chr5:1513648 | GTTTCCTC others(47): Show |
G | 4 | a0001c0001t0004g0108 a0001c0001t0007g0269 a0001c0003t0009g0237 others(1): Show |
4 | HG02717.hp2 HG02886.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+10008_135+1006 others(58): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513648 | |||||||
chr5:1513702 | A | G | 4 | a0001c0002t0001g0284 a0001c0002t0001g0285 a0001c0002t0001g0287 others(1): Show |
4 | HG02258.hp1 HG02976.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+10008T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513702 | |||||||
chr5:1513773 | G | A | 59 | a0001c0001t0002g0043 a0001c0001t0002g0220 a0001c0001t0002g0295 others(56): Show |
59 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.135+9937C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513773 | |||||||
chr5:1513784 | T | C | 2 | a0001c0003t0001g0266 a0001c0003t0001g0267 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.135+9926A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513784 | |||||||
chr5:1513819 | G | C | 2 | a0001c0003t0001g0266 a0001c0003t0001g0267 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.135+9891C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513819 | |||||||
chr5:1513823 | A | G | 2 | a0001c0003t0001g0266 a0001c0003t0001g0267 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.135+9887T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513823 | |||||||
chr5:1513827 | G | A | 55 | a0001c0001t0002g0043 a0001c0001t0002g0220 a0001c0001t0002g0295 others(52): Show |
56 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.135+9883C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513827 | |||||||
chr5:1513862 | A | G | 2 | a0001c0003t0001g0266 a0001c0003t0001g0267 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.135+9848T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513862 | |||||||
chr5:1513916 | G | A | 10 | a0001c0001t0002g0253 a0001c0004t0004g0209 a0001c0004t0004g0210 others(7): Show |
10 | HG01106.hp1 HG01256.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.135+9794C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513916 | |||||||
chr5:1513918 | A | G | 1 | a0001c0003t0009g0014 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.135+9792T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513918 | |||||||
chr5:1513956 | C | G | 1 | a0001c0003t0009g0014 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.135+9754G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513956 | |||||||
chr5:1513970 | G | A | 1 | a0001c0001t0004g0363 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.135+9740C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513970 | |||||||
chr5:1513982 | G | A | 2 | a0001c0001t0005g0039 a0001c0002t0001g0038 |
2 | HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.135+9728C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513982 | |||||||
chr5:1513995 | C | T | 8 | a0001c0001t0002g0115 a0001c0001t0002g0260 a0001c0002t0004g0100 others(5): Show |
8 | HG01099.hp2 HG01261.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+9715G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513995 | |||||||
chr5:1513996 | A | G | 34 | a0001c0001t0002g0115 a0001c0001t0002g0260 a0001c0001t0002g0282 others(31): Show |
34 | HG01099.hp2 HG01261.hp1 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.135+9714T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513996 | |||||||
chr5:1514045 | A | G | 1 | a0001c0001t0002g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.135+9665T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1514045 | |||||||
chr5:1514091 | C | A | 3 | a0001c0001t0004g0363 a0001c0001t0027g0272 a0001c0002t0001g0362 |
3 | HG02886.hp2 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.135+9619G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1514091 | |||||||
chr5:1514324 | C | T | 1 | a0001c0010t0001g0273 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.135+9386G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1514324 | |||||||
chr5:1514339 | G | A | 27 | a0001c0001t0002g0253 a0001c0002t0001g0076 a0001c0002t0001g0242 others(24): Show |
27 | HG01106.hp1 HG01256.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.135+9371C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1514339 | |||||||
chr5:1514347 | A | G | 190 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0040 others(187): Show |
195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.135+9363T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1514347 | |||||||
chr5:1514522 | G | A | 100 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0040 others(97): Show |
105 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.135+9188C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1514522 | |||||||
chr5:1514666 | T | C | 1 | a0002c0005t0003g0149 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.135+9044A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1514666 | |||||||
chr5:1514705 | C | T | 2 | a0001c0001t0004g0108 a0001c0001t0007g0269 |
2 | HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.135+9005G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1514705 | |||||||
chr5:1514715 | A | G | 49 | a0001c0001t0002g0028 a0001c0001t0002g0115 a0001c0001t0002g0260 others(46): Show |
50 | HG01099.hp2 HG01243.hp1 HG01261.hp1 others(47): Show |
intron_variant | MODIFIER | c.135+8995T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1514715 | |||||||
chr5:1514781 | T | C | 3 | a0001c0003t0016g0366 a0001c0003t0016g0367 a0002c0006t0038g0368 |
3 | NA18956.hp1 NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.135+8929A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1514781 | |||||||
chr5:1514797 | A | G | 3 | a0001c0003t0016g0366 a0001c0003t0016g0367 a0002c0006t0038g0368 |
3 | NA18956.hp1 NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.135+8913T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1514797 | |||||||
chr5:1514908 | A | C | 1 | a0002c0005t0003g0353 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.135+8802T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1514908 | |||||||
chr5:1514965 | G | A | 4 | a0001c0001t0002g0282 a0001c0001t0002g0283 a0001c0003t0009g0237 others(1): Show |
4 | HG02717.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+8745C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1514965 | |||||||
chr5:1515066 | ACCCCCAG others(89): Show |
A | 4 | a0001c0001t0002g0359 a0001c0002t0001g0242 a0001c0002t0023g0243 others(1): Show |
4 | HG01884.hp1 HG02647.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+8548_135+8643d others(98): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515066 | |||||||
chr5:1515072 | A | G | 2 | a0001c0001t0005g0039 a0001c0002t0001g0038 |
2 | HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.135+8638T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515072 | |||||||
chr5:1515123 | T | C | 59 | a0001c0001t0002g0043 a0001c0001t0002g0115 a0001c0001t0002g0253 others(56): Show |
61 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.135+8587A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515123 | |||||||
chr5:1515123 | TGGCCCTT others(89): Show |
T | 1 | a0001c0001t0002g0140 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.135+8491_135+8586d others(98): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515123 | |||||||
chr5:1515219 | C | T | 14 | a0001c0001t0002g0008 a0001c0001t0005g0165 a0001c0001t0005g0166 others(11): Show |
16 | HG01069.hp1 HG01071.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.135+8491G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515219 | |||||||
chr5:1515278 | C | T | 1 | a0001c0003t0001g0270 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.135+8432G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515278 | |||||||
chr5:1515367 | G | C | 2 | a0001c0002t0008g0332 a0001c0002t0008g0333 |
2 | HG03688.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.135+8343C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515367 | |||||||
chr5:1515420 | G | C | 120 | a0001c0001t0002g0043 a0001c0001t0002g0111 a0001c0001t0002g0115 others(117): Show |
121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.135+8290C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515420 | |||||||
chr5:1515539 | G | A | 1 | a0002c0005t0003g0149 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.135+8171C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515539 | |||||||
chr5:1515672 | A | G | 59 | a0001c0001t0002g0115 a0001c0001t0002g0253 a0001c0001t0002g0260 others(56): Show |
60 | HG01099.hp2 HG01106.hp1 HG01256.hp1 others(57): Show |
intron_variant | MODIFIER | c.135+8038T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515672 | |||||||
chr5:1515706 | A | T | 1 | a0001c0002t0001g0274 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.135+8004T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515706 | |||||||
chr5:1515744 | C | T | 1 | a0002c0005t0003g0149 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.135+7966G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515744 | |||||||
chr5:1515768 | T | A | 81 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0040 others(78): Show |
85 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.135+7942A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515768 | |||||||
chr5:1515874 | C | G | 1 | a0001c0001t0002g0046 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.135+7836G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515874 | |||||||
chr5:1515894 | G | A | 2 | a0001c0001t0007g0003 a0001c0001t0007g0151 |
3 | HG02896.hp1 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.135+7816C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515894 | |||||||
chr5:1515979 | G | A | 60 | a0001c0001t0002g0043 a0001c0001t0002g0220 a0001c0001t0002g0295 others(57): Show |
60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.135+7731C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515979 | |||||||
chr5:1516041 | A | G | 3 | a0001c0001t0011g0324 a0001c0003t0001g0325 a0001c0003t0033g0350 |
3 | HG00597.hp2 HG02129.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.135+7669T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1516041 | |||||||
chr5:1516123 | G | A | 1 | a0001c0001t0007g0082 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.135+7587C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1516123 | |||||||
chr5:1516252 | G | A | 1 | a0001c0001t0004g0347 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.135+7458C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1516252 | |||||||
chr5:1516299 | T | A | 33 | a0001c0001t0002g0115 a0001c0001t0002g0260 a0001c0001t0002g0282 others(30): Show |
34 | HG01099.hp2 HG01261.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.135+7411A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1516299 | |||||||
chr5:1516422 | G | A | 3 | a0001c0003t0016g0366 a0001c0003t0016g0367 a0002c0006t0038g0368 |
3 | NA18956.hp1 NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.135+7288C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1516422 | |||||||
chr5:1516461 | C | T | 1 | a0001c0002t0001g0045 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.135+7249G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1516461 | |||||||
chr5:1516468 | G | C | 2 | a0001c0001t0007g0259 a0001c0007t0007g0112 |
2 | HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.135+7242C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1516468 | |||||||
chr5:1516632 | C | CT | 36 | a0001c0001t0002g0115 a0001c0001t0002g0260 a0001c0001t0002g0282 others(33): Show |
37 | HG01099.hp2 HG01261.hp1 HG01496.hp1 others(34): Show |
intron_variant | MODIFIER | c.135+7077dupA | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1516632 | |||||||
chr5:1516632 | CT | C | 8 | a0001c0001t0007g0097 a0001c0002t0001g0069 a0001c0002t0001g0070 others(5): Show |
8 | HG01069.hp2 HG01928.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+7077delA | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1516632 | |||||||
chr5:1516770 | C | G | 55 | a0001c0001t0002g0111 a0001c0001t0002g0220 a0001c0001t0002g0295 others(52): Show |
55 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.135+6940G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1516770 | |||||||
chr5:1516886 | G | C | 4 | a0001c0001t0002g0111 a0001c0001t0007g0259 a0001c0003t0009g0041 others(1): Show |
4 | HG02486.hp2 HG02559.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+6824C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1516886 | |||||||
chr5:1517009 | C | T | 4 | a0001c0001t0002g0282 a0001c0001t0002g0283 a0001c0003t0009g0237 others(1): Show |
4 | HG02717.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+6701G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517009 | |||||||
chr5:1517083 | C | T | 58 | a0001c0001t0002g0111 a0001c0001t0002g0220 a0001c0001t0002g0295 others(55): Show |
58 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.135+6627G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517083 | |||||||
chr5:1517124 | T | A | 20 | a0001c0001t0002g0282 a0001c0001t0002g0283 a0001c0001t0004g0108 others(17): Show |
20 | HG01891.hp1 HG02055.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.135+6586A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517124 | |||||||
chr5:1517161 | G | A | 3 | a0001c0001t0007g0097 a0001c0002t0001g0276 a0001c0004t0017g0017 |
3 | HG02145.hp2 HG02895.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.135+6549C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517161 | |||||||
chr5:1517200 | C | A | 5 | a0001c0001t0002g0043 a0001c0001t0004g0044 a0001c0001t0004g0221 others(2): Show |
5 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+6510G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517200 | |||||||
chr5:1517207 | T | G | 205 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0040 others(202): Show |
211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.135+6503A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517207 | |||||||
chr5:1517215 | A | T | 1 | a0001c0002t0001g0216 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.135+6495T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517215 | |||||||
chr5:1517216 | C | A | 1 | a0001c0002t0001g0216 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.135+6494G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517216 | |||||||
chr5:1517370 | C | T | 1 | a0001c0003t0006g0157 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.135+6340G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517370 | |||||||
chr5:1517430 | C | T | 33 | a0001c0001t0002g0115 a0001c0001t0002g0260 a0001c0001t0002g0282 others(30): Show |
34 | HG01099.hp2 HG01261.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.135+6280G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517430 | |||||||
chr5:1517433 | C | T | 1 | a0001c0003t0009g0014 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.135+6277G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517433 | |||||||
chr5:1517466 | C | T | 1 | a0001c0003t0001g0002 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.135+6244G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517466 | |||||||
chr5:1517518 | T | C | 1 | a0001c0001t0002g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.135+6192A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517518 | |||||||
chr5:1517527 | A | G | 102 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0040 others(99): Show |
106 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+6183T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517527 | |||||||
chr5:1517542 | C | T | 1 | a0001c0001t0027g0272 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.135+6168G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517542 | |||||||
chr5:1517586 | T | C | 168 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0040 others(165): Show |
173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.135+6124A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517586 | |||||||
chr5:1517599 | A | C | 168 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0040 others(165): Show |
173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.135+6111T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517599 | |||||||
chr5:1517654 | C | T | 165 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0040 others(162): Show |
170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.135+6056G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517654 | |||||||
chr5:1517661 | T | C | 1 | a0001c0001t0007g0151 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.135+6049A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517661 | |||||||
chr5:1517676 | C | CAA | 102 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0040 others(99): Show |
106 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+6032_135+6033d others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517676 | |||||||
chr5:1517677 | A | C | 113 | a0001c0001t0002g0008 a0001c0001t0002g0087 a0001c0001t0002g0182 others(110): Show |
121 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.135+6033T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517677 | |||||||
chr5:1517766 | T | C | 59 | a0001c0001t0002g0089 a0001c0001t0002g0220 a0001c0001t0002g0295 others(56): Show |
60 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.135+5944A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517766 | |||||||
chr5:1517768 | G | A | 1 | a0001c0004t0005g0219 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.135+5942C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517768 | |||||||
chr5:1517787 | G | A | 1 | a0001c0001t0002g0071 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.135+5923C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517787 | |||||||
chr5:1517853 | C | G | 1 | a0001c0003t0009g0014 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.135+5857G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517853 | |||||||
chr5:1517866 | C | A | 1 | a0001c0001t0004g0012 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.135+5844G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517866 | |||||||
chr5:1517868 | C | G | 92 | a0001c0001t0002g0111 a0001c0001t0002g0115 a0001c0001t0002g0220 others(89): Show |
93 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.135+5842G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517868 | |||||||
chr5:1517889 | A | G | 3 | a0001c0003t0016g0366 a0001c0003t0016g0367 a0002c0006t0038g0368 |
3 | NA18956.hp1 NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.135+5821T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517889 | |||||||
chr5:1517920 | C | T | 9 | a0001c0001t0005g0263 a0001c0001t0007g0281 a0001c0003t0001g0279 others(6): Show |
9 | HG01496.hp1 HG02451.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.135+5790G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517920 | |||||||
chr5:1517938 | T | A | 1 | a0001c0003t0009g0014 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.135+5772A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517938 | |||||||
chr5:1518102 | C | T | 11 | a0001c0001t0002g0098 a0001c0001t0002g0126 a0001c0001t0002g0127 others(8): Show |
11 | HG00280.hp1 HG00735.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.135+5608G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518102 | |||||||
chr5:1518244 | C | T | 1 | a0001c0001t0002g0253 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.135+5466G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518244 | |||||||
chr5:1518320 | G | A | 2 | a0002c0005t0004g0146 a0002c0016t0003g0147 |
2 | HG00733.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.135+5390C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518320 | |||||||
chr5:1518369 | C | T | 3 | a0001c0001t0005g0263 a0001c0010t0001g0264 a0001c0020t0001g0265 |
3 | HG02922.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.135+5341G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518369 | |||||||
chr5:1518376 | T | A | 183 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0040 others(180): Show |
188 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.135+5334A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518376 | |||||||
chr5:1518379 | C | T | 16 | a0001c0001t0002g0220 a0001c0001t0002g0295 a0001c0001t0002g0298 others(13): Show |
16 | HG00408.hp2 HG00639.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.135+5331G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518379 | |||||||
chr5:1518397 | G | C | 1 | a0001c0010t0001g0273 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.135+5313C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518397 | |||||||
chr5:1518426 | C | T | 53 | a0001c0001t0002g0220 a0001c0001t0002g0295 a0001c0001t0002g0298 others(50): Show |
53 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.135+5284G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518426 | |||||||
chr5:1518486 | A | G | 212 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0040 others(209): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.135+5224T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518486 | |||||||
chr5:1518511 | T | C | 3 | a0001c0001t0005g0263 a0001c0010t0001g0264 a0001c0020t0001g0265 |
3 | HG02922.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.135+5199A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518511 | |||||||
chr5:1518572 | C | T | 18 | a0001c0001t0002g0282 a0001c0001t0002g0283 a0001c0001t0007g0281 others(15): Show |
18 | HG01496.hp1 HG01891.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.135+5138G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518572 | |||||||
chr5:1518577 | T | C | 1 | a0001c0004t0005g0288 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.135+5133A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518577 | |||||||
chr5:1518583 | G | A | 4 | a0001c0001t0028g0348 a0001c0003t0001g0148 a0001c0007t0004g0218 others(1): Show |
4 | HG00639.hp1 HG01346.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+5127C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518583 | |||||||
chr5:1518604 | T | C | 1 | a0001c0001t0002g0320 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.135+5106A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518604 | |||||||
chr5:1518679 | C | T | 1 | a0001c0003t0009g0014 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.135+5031G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518679 | |||||||
chr5:1518740 | G | T | 5 | a0001c0001t0002g0111 a0001c0001t0007g0259 a0001c0001t0027g0272 others(2): Show |
5 | HG02486.hp2 HG02559.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+4970C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518740 | |||||||
chr5:1518774 | G | A | 21 | a0001c0001t0002g0282 a0001c0001t0002g0283 a0001c0001t0002g0359 others(18): Show |
21 | HG01496.hp1 HG01891.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.135+4936C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518774 | |||||||
chr5:1518797 | G | C | 1 | a0001c0002t0001g0276 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.135+4913C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518797 | |||||||
chr5:1518804 | G | A | 1 | a0001c0004t0005g0219 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.135+4906C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518804 | |||||||
chr5:1518830 | T | C | 2 | a0001c0002t0004g0100 a0001c0002t0004g0150 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.135+4880A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518830 | |||||||
chr5:1518908 | G | A | 2 | a0001c0001t0004g0108 a0001c0001t0007g0269 |
2 | HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.135+4802C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518908 | |||||||
chr5:1518964 | C | T | 38 | a0001c0001t0002g0040 a0001c0001t0002g0220 a0001c0001t0002g0295 others(35): Show |
38 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.135+4746G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518964 | |||||||
chr5:1519016 | G | A | 1 | a0001c0004t0002g0262 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.135+4694C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519016 | |||||||
chr5:1519082 | T | C | 17 | a0001c0001t0002g0078 a0001c0001t0002g0253 a0001c0001t0004g0079 others(14): Show |
19 | HG00738.hp1 HG01106.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.135+4628A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519082 | |||||||
chr5:1519149 | A | G | 17 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0004g0013 others(14): Show |
18 | HG01243.hp1 HG02145.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.135+4561T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519149 | |||||||
chr5:1519202 | T | C | 1 | a0001c0002t0001g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.135+4508A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519202 | |||||||
chr5:1519307 | A | G | 2 | a0001c0003t0001g0266 a0001c0003t0001g0267 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.135+4403T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519307 | |||||||
chr5:1519389 | T | C | 2 | a0001c0001t0007g0082 a0001c0002t0001g0276 |
2 | HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.135+4321A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519389 | |||||||
chr5:1519475 | C | T | 1 | a0001c0004t0002g0109 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.135+4235G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519475 | |||||||
chr5:1519503 | T | A | 4 | a0001c0002t0001g0250 a0001c0002t0001g0251 a0001c0002t0001g0277 others(1): Show |
4 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+4207A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519503 | |||||||
chr5:1519534 | T | C | 7 | a0001c0001t0002g0282 a0001c0001t0002g0283 a0001c0002t0001g0242 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.135+4176A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519534 | |||||||
chr5:1519578 | G | A | 120 | a0001c0001t0002g0008 a0001c0001t0002g0095 a0001c0001t0002g0182 others(117): Show |
128 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.135+4132C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519578 | |||||||
chr5:1519710 | C | T | 3 | a0001c0001t0004g0026 a0001c0001t0026g0025 a0001c0002t0036g0365 |
3 | HG01081.hp2 HG01109.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.135+4000G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519710 | |||||||
chr5:1519718 | T | C | 25 | a0001c0001t0002g0220 a0001c0001t0002g0253 a0001c0001t0004g0221 others(22): Show |
25 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.135+3992A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519718 | |||||||
chr5:1519755 | C | T | 4 | a0001c0001t0004g0108 a0001c0003t0009g0233 a0001c0007t0005g0106 others(1): Show |
4 | HG02109.hp1 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+3955G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519755 | |||||||
chr5:1519912 | G | C | 5 | a0001c0001t0005g0356 a0001c0001t0005g0357 a0001c0004t0002g0355 others(2): Show |
5 | HG00438.hp2 HG02015.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+3798C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519912 | |||||||
chr5:1519974 | T | G | 1 | a0001c0001t0002g0084 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.135+3736A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519974 | |||||||
chr5:1519990 | G | A | 7 | a0001c0001t0002g0223 a0001c0001t0002g0224 a0001c0001t0002g0227 others(4): Show |
7 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(4): Show |
intron_variant | MODIFIER | c.135+3720C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519990 | |||||||
chr5:1520095 | T | C | 1 | a0001c0002t0001g0230 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.135+3615A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520095 | |||||||
chr5:1520100 | G | A | 2 | a0001c0001t0002g0359 a0001c0002t0001g0358 |
2 | HG00323.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.135+3610C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520100 | |||||||
chr5:1520317 | C | T | 1 | a0001c0004t0005g0294 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.135+3393G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520317 | |||||||
chr5:1520326 | G | T | 1 | a0001c0001t0005g0292 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.135+3384C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520326 | |||||||
chr5:1520470 | G | A | 4 | a0001c0003t0016g0366 a0001c0003t0016g0367 a0002c0005t0037g0369 others(1): Show |
4 | NA18956.hp1 NA18970.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+3240C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520470 | |||||||
chr5:1520499 | G | A | 1 | a0001c0003t0006g0231 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.135+3211C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520499 | |||||||
chr5:1520507 | T | C | 1 | a0001c0002t0001g0232 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.135+3203A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520507 | |||||||
chr5:1520550 | C | G | 174 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(171): Show |
185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.135+3160G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520550 | |||||||
chr5:1520583 | G | A | 6 | a0001c0001t0021g0246 a0001c0002t0001g0242 a0001c0002t0001g0245 others(3): Show |
7 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+3127C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520583 | |||||||
chr5:1520643 | A | C | 2 | a0001c0001t0002g0089 a0001c0003t0001g0090 |
2 | HG02109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.135+3067T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520643 | |||||||
chr5:1520695 | C | T | 1 | a0001c0004t0005g0105 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.135+3015G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520695 | |||||||
chr5:1520795 | A | G | 293 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(290): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.135+2915T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520795 | |||||||
chr5:1520801 | T | C | 1 | a0001c0002t0001g0085 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.135+2909A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520801 | |||||||
chr5:1520817 | C | T | 1 | a0001c0002t0001g0290 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.135+2893G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520817 | |||||||
chr5:1520818 | G | A | 2 | a0001c0003t0014g0018 a0001c0003t0014g0019 |
2 | HG02735.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.135+2892C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520818 | |||||||
chr5:1520820 | A | G | 4 | a0001c0003t0016g0366 a0001c0003t0016g0367 a0002c0005t0037g0369 others(1): Show |
4 | NA18956.hp1 NA18970.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+2890T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520820 | |||||||
chr5:1520860 | C | CA | 15 | a0001c0001t0002g0282 a0001c0001t0002g0283 a0001c0001t0002g0360 others(12): Show |
15 | HG00741.hp2 HG01496.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.135+2849dupT | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520860 | |||||||
chr5:1520860 | CA | C | 19 | a0001c0001t0002g0087 a0001c0001t0002g0236 a0001c0001t0005g0263 others(16): Show |
19 | HG02145.hp2 HG02523.hp2 HG02735.hp2 others(16): Show |
intron_variant | MODIFIER | c.135+2849delT | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520860 | |||||||
chr5:1520860 | CAA | C | 220 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(217): Show |
233 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.135+2848_135+2849d others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520860 | |||||||
chr5:1520860 | CAAA | C | 14 | a0001c0001t0002g0098 a0001c0001t0021g0246 a0001c0002t0001g0242 others(11): Show |
15 | HG01070.hp2 HG01074.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.135+2847_135+2849d others(5): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520860 | |||||||
chr5:1520876 | A | AG | 4 | a0001c0001t0002g0260 a0001c0001t0007g0259 a0001c0004t0002g0261 others(1): Show |
4 | HG01261.hp1 HG02559.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+2833_135+2834i others(3): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520876 | |||||||
chr5:1521130 | T | C | 3 | a0001c0001t0004g0363 a0001c0002t0001g0362 a0001c0004t0005g0288 |
3 | HG02886.hp2 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.135+2580A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1521130 | |||||||
chr5:1521147 | C | G | 7 | a0001c0001t0002g0253 a0001c0004t0004g0258 a0001c0007t0004g0254 others(4): Show |
7 | HG00099.hp1 HG01106.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.135+2563G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1521147 | |||||||
chr5:1521273 | C | A | 1 | a0001c0001t0002g0239 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.135+2437G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1521273 | |||||||
chr5:1521302 | C | T | 1 | a0001c0002t0001g0290 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.135+2408G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1521302 | |||||||
chr5:1521313 | C | T | 1 | a0001c0002t0001g0289 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.135+2397G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1521313 | |||||||
chr5:1521332 | A | G | 2 | a0001c0003t0014g0018 a0001c0003t0014g0019 |
2 | HG02735.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.135+2378T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1521332 | |||||||
chr5:1521361 | T | C | 1 | a0001c0001t0021g0246 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.135+2349A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1521361 | |||||||
chr5:1521384 | G | A | 1 | a0001c0001t0002g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.135+2326C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1521384 | |||||||
chr5:1521393 | A | G | 2 | a0001c0001t0007g0097 a0001c0004t0017g0017 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.135+2317T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1521393 | |||||||
chr5:1521458 | C | T | 85 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0040 others(82): Show |
89 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.135+2252G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1521458 | |||||||
chr5:1521778 | A | G | 74 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0040 others(71): Show |
77 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.135+1932T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1521778 | |||||||
chr5:1521955 | A | T | 2 | a0001c0003t0014g0018 a0001c0003t0014g0019 |
2 | HG02735.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.135+1755T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1521955 | |||||||
chr5:1522038 | C | T | 1 | a0001c0002t0004g0096 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.135+1672G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1522038 | |||||||
chr5:1522354 | C | G | 1 | a0001c0002t0001g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.135+1356G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1522354 | |||||||
chr5:1522371 | T | G | 73 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0040 others(70): Show |
76 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.135+1339A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1522371 | |||||||
chr5:1522374 | C | T | 73 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0040 others(70): Show |
76 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.135+1336G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1522374 | |||||||
chr5:1522425 | C | A | 1 | a0002c0005t0003g0241 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.135+1285G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1522425 | |||||||
chr5:1522463 | C | G | 3 | a0001c0001t0002g0095 a0001c0003t0001g0093 a0001c0003t0001g0094 |
3 | NA18952.hp2 NA18994.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.135+1247G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1522463 | |||||||
chr5:1522465 | G | C | 2 | a0001c0001t0002g0089 a0001c0003t0001g0090 |
2 | HG02109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.135+1245C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1522465 | |||||||
chr5:1522620 | G | C | 81 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0040 others(78): Show |
85 | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.135+1090C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1522620 | |||||||
chr5:1523036 | G | A | 2 | a0001c0002t0001g0248 a0002c0006t0032g0247 |
2 | NA18942.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.135+674C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1523036 | |||||||
chr5:1523137 | C | A | 1 | a0001c0003t0001g0249 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.135+573G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1523137 | |||||||
chr5:1523206 | A | C | 292 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(289): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.135+504T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1523206 | |||||||
chr5:1523241 | G | A | 2 | a0001c0001t0004g0363 a0001c0002t0001g0362 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.135+469C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1523241 | |||||||
chr5:1523306 | A | C | 1 | a0001c0002t0001g0250 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.135+404T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1523306 | |||||||
chr5:1523396 | C | T | 2 | a0001c0003t0001g0091 a0001c0003t0001g0092 |
2 | NA18983.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.135+314G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1523396 | |||||||
chr5:1523428 | C | G | 75 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0040 others(72): Show |
78 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.135+282G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1523428 | |||||||
chr5:1523518 | A | G | 249 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(246): Show |
262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.135+192T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1523518 | |||||||
chr5:1523697 | C | T | 1 | a0001c0001t0018g0020 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.135+13G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1523697 |